Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.4382C>A | CA913177947 | |||
MT | m.4382C= | CA2573329762 | |||
MT | m.4382C>G | CA913177948 | |||
MT | m.4382C>T | CA913177949 | |||
MT | m.4383del | CA2573104465 | |||
MT | m.4383C>A | CA913177950 | |||
MT | m.4383C= | CA2573329771 | |||
MT | m.4383C>G | CA913177951 | |||
MT | m.4383C>T | CA913177952 | |||
MT | m.4384T>A | CA913177957 | ClinVar dbSNP | ||
MT | m.4384T>C | CA913177956 | ClinVar dbSNP | ||
MT | m.4384T>G | CA913177955 | |||
MT | m.4384T= | CA2499563859 | |||
MT | m.4385_4386del | CA2573104466 | |||
MT | m.4385A= | CA2499563860 | |||
MT | m.4385A>C | CA913177961 | |||
MT | m.4385A>G | CA913177962 | ClinVar dbSNP | ||
MT | m.4385A>T | CA337096869 | ClinVar dbSNP | ||
MT | m.4386T>A | CA913177965 | |||
MT | m.4386T>C | CA913177963 | ClinVar dbSNP | ||
MT | m.4386T>G | CA913177964 | |||
MT | m.4386T= | CA2499563861 | |||
MT | m.4387C>A | CA913177967 | |||
MT | m.4387C= | CA2499563862 | |||
MT | m.4387C>G | CA913177970 | |||
MT | m.4387C>T | CA913177969 | ClinVar dbSNP | ||
MT | m.4390_4391dup | CA2573104467 | |||
MT | m.4388A= | CA2499563863 | |||
MT | m.4388A>C | CA913177972 | |||
MT | m.4388A>G | CA10581310 | ClinVar dbSNP | ||
MT | m.4388A>T | CA913177976 | |||
MT | m.4389C>A | CA913177977 | |||
MT | m.4389C= | CA2573329785 | |||
MT | m.4389C>G | CA913177978 | |||
MT | m.4389C>T | CA913177979 | |||
MT | m.4390A= | CA2573329788 | |||
MT | m.4390A>C | CA913177980 | |||
MT | m.4390A>G | CA913177981 | |||
MT | m.4390A>T | CA913177982 | |||
MT | m.4391C>A | CA913177983 | |||
MT | m.4391C= | CA2573329790 | |||
MT | m.4391C>G | CA913177985 | |||
MT | m.4391C>T | CA913177984 | |||
MT | m.4392C>A | CA913177986 | |||
MT | m.4392C= | CA2573329791 | |||
MT | m.4392C>G | CA913177987 | |||
MT | m.4392C>T | CA913177988 | |||
MT | m.4393C>A | CA913177989 | |||
MT | m.4393C= | CA2573329792 | |||
MT | m.4393C>G | CA913177990 | |||
MT | m.4393C>T | CA913177992 | |||
MT | m.4394C>A | CA913177995 | ClinVar dbSNP | ||
MT | m.4394C= | CA2499563864 | |||
MT | m.4394C>G | CA913177996 | |||
MT | m.4394C>T | CA913177994 | dbSNP | ||
MT | m.4395A= | CA2499563865 | |||
MT | m.4395A>C | CA913177997 | |||
MT | m.4395A>G | CA913177998 | ClinVar dbSNP | ||
MT | m.4395A>T | CA913177999 | |||
MT | m.4396T>A | CA913178003 | |||
MT | m.4396T>C | CA913178004 | |||
MT | m.4396T>G | CA913178005 | |||
MT | m.4396T= | CA2573329797 | |||
MT | m.4397C>A | CA913178006 | |||
MT | m.4397C= | CA2573329799 | |||
MT | m.4397C>G | CA913178007 | |||
MT | m.4397C>T | CA913178008 | |||
MT | m.4398C>A | CA913178009 | |||
MT | m.4398C= | CA2573329801 | |||
MT | m.4398C>G | CA913178012 | |||
MT | m.4398C>T | CA913178010 | |||
MT | m.4399T>A | CA913178016 | |||
MT | m.4399T>C | CA913178017 | ClinVar dbSNP | ||
MT | m.4399T>G | CA913178018 | |||
MT | m.4399T= | CA2499563866 | |||
MT | m.4400A= | CA2499563867 | |||
MT | m.4400A>C | CA913178019 | |||
MT | m.4400A>G | CA913178020 | ClinVar dbSNP | ||
MT | m.4400A>T | CA913178021 | |||
MT | m.4401A= | CA2573329804 | |||
MT | m.4401A>C | CA2573329805 | |||
MT | m.4401A>G | CA2573104468 | dbSNP | ||
MT | m.4401A>T | CA2573329806 | |||
MT | m.4402A= | CA2573329807 | |||
MT | m.4402A>C | CA913178022 | |||
MT | m.4402A>G | CA913178023 | |||
MT | m.4402A>T | CA913178024 | |||
MT | m.4403G>A | CA913178026 | |||
MT | m.4403G>C | CA913178025 | |||
MT | m.4403G= | CA2573329808 | |||
MT | m.4403G>T | CA913178027 | |||
MT | m.4404T>A | CA913178029 | |||
MT | m.4404T>C | CA913178030 | dbSNP | ||
MT | m.4404T>G | CA913178031 | |||
MT | m.4404T= | CA2573329809 | |||
MT | m.4405A= | CA2573329811 | |||
MT | m.4405A>C | CA913178032 | |||
MT | m.4405A>G | CA913178033 | |||
MT | m.4405A>T | CA913178034 | |||
MT | m.4406A= | CA2573329814 | |||
MT | m.4406A>C | CA913178035 | |||
MT | m.4406A>G | CA913178036 | |||
MT | m.4406A>T | CA913178037 | |||
MT | m.4407G>A | CA913178040 | |||
MT | m.4407G>C | CA913178039 | |||
MT | m.4407G= | CA2573329816 | |||
MT | m.4407G>T | CA913178038 | |||
MT | m.4408G>A | CA913178042 | |||
MT | m.4408G>C | CA913178041 | |||
MT | m.4408G= | CA2573329819 | |||
MT | m.4408G>T | CA913178043 | |||
MT | m.4409T>A | CA913178047 | |||
MT | m.4409T>C | CA254835 | ClinVar dbSNP | ||
MT | m.4409T>G | CA913178046 | |||
MT | m.4409T= | CA2499563868 | |||
MT | m.4410C>A | CA913178048 | |||
MT | m.4410C= | CA2573329823 | |||
MT | m.4410C>G | CA913178049 | |||
MT | m.4410C>T | CA913178050 | |||
MT | m.4411A= | CA2573329824 | |||
MT | m.4411A>C | CA913178051 | |||
MT | m.4411A>G | CA913178052 | |||
MT | m.4411A>T | CA913178053 | |||
MT | m.4412G>A | CA658475630 | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC | ||
MT | m.4412G>C | CA913178058 | |||
MT | m.4412G= | CA2573329825 | |||
MT | m.4412G>T | CA913178055 | |||
MT | m.4413C>A | CA913178064 | |||
MT | m.4413C= | CA2573329827 | |||
MT | m.4413C>G | CA913178063 | |||
MT | m.4413C>T | CA913178062 | |||
MT | m.4414T>A | CA913178065 | |||
MT | m.4414T>C | CA913178066 | |||
MT | m.4414T>G | CA913178067 | |||
MT | m.4414T= | CA2573329828 | |||
MT | m.4415A= | CA2573329829 | |||
MT | m.4415A>C | CA913178070 | |||
MT | m.4415A>G | CA913178071 | |||
MT | m.4415A>T | CA913178068 | |||
MT | m.4416A= | CA2573329831 | |||
MT | m.4416A>C | CA913178077 | |||
MT | m.4416A>G | CA913178076 | |||
MT | m.4416A>T | CA913178075 | |||
MT | m.4417A= | CA2499563869 | |||
MT | m.4417A>C | CA913178080 | |||
MT | m.4417A>G | CA913178082 | ClinVar dbSNP | ||
MT | m.4417A>T | CA913178083 | |||
MT | m.4418T>A | CA913178086 | |||
MT | m.4418T>C | CA913178085 | ClinVar dbSNP | ||
MT | m.4418T>G | CA913178084 | |||
MT | m.4418T= | CA2499563870 | |||
MT | m.4419A= | CA2573329837 | |||
MT | m.4419A>C | CA913178089 | |||
MT | m.4419A>G | CA913178088 | |||
MT | m.4419A>T | CA913178087 | |||
MT | m.4420A= | CA2573329840 | |||
MT | m.4420A>C | CA913178092 | |||
MT | m.4420A>G | CA913178091 | |||
MT | m.4420A>T | CA913178090 | |||
MT | m.4421G>A | CA913178093 | |||
MT | m.4421G>C | CA913178094 | |||
MT | m.4421G= | CA2573329841 | |||
MT | m.4421G>T | CA913178095 | |||
MT | m.4422C>A | CA913178096 | |||
MT | m.4422C= | CA2573329843 | |||
MT | m.4422C>G | CA913178097 | |||
MT | m.4422C>T | CA913178098 | |||
MT | m.4423T>A | CA913178099 | |||
MT | m.4423T>C | CA913178100 | |||
MT | m.4423T>G | CA913178101 | |||
MT | m.4423T= | CA2573329846 | |||
MT | m.4424A= | CA2573329847 | |||
MT | m.4424A>C | CA913178102 | |||
MT | m.4424A>G | CA913178103 | |||
MT | m.4424A>T | CA913178104 | |||
MT | m.4425T>A | CA913178106 | |||
MT | m.4425T>C | CA913178108 | |||
MT | m.4425T>G | CA913178109 | |||
MT | m.4425T= | CA2573329850 | |||
MT | m.4426C>A | CA913178110 | |||
MT | m.4426C= | CA2573329852 | |||
MT | m.4426C>G | CA913178111 | |||
MT | m.4426C>T | CA913178112 | |||
MT | m.4427G>A | CA913178113 | |||
MT | m.4427G>C | CA913178114 | |||
MT | m.4427G= | CA2573329854 | |||
MT | m.4427G>T | CA913178116 | |||
MT | m.4429dup | CA2573104469 | |||
MT | m.4428G>A | CA913178119 | |||
MT | m.4428G>C | CA913178118 | |||
MT | m.4428G= | CA2573329856 | |||
MT | m.4428G>T | CA913178117 | |||
MT | m.4428_4430del | CA2740102073 | |||
MT | m.4429G>A | CA913178123 | ClinVar dbSNP | ||
MT | m.4429G>C | CA913178124 | |||
MT | m.4429G= | CA2499563871 | |||
MT | m.4429G>T | CA913178125 | |||
MT | m.4430C>A | CA913178126 | |||
MT | m.4430C= | CA2573329860 | |||
MT | m.4430C>G | CA913178128 | |||
MT | m.4430C>T | CA913178127 | |||
MT | m.4431C>A | CA913178130 | |||
MT | m.4431C= | CA2573329862 | |||
MT | m.4431C>G | CA913178129 | |||
MT | m.4431C>T | CA913178131 | |||
MT | m.4432C>A | CA913178132 | |||
MT | m.4432C= | CA2573329863 | |||
MT | m.4432C>G | CA913178133 | |||
MT | m.4432C>T | CA913178134 | |||
MT | m.4433A= | CA2573329864 | |||
MT | m.4433A>C | CA913178137 | |||
MT | m.4433A>G | CA913178136 | |||
MT | m.4433A>T | CA913178135 | |||
MT | m.4434T>A | CA913178140 | |||
MT | m.4434T>C | CA913178139 | |||
MT | m.4434T>G | CA913178138 | |||
MT | m.4434T= | CA2573329866 | |||
MT | m.4435A= | CA2499563872 | |||
MT | m.4435A>C | CA913178142 | |||
MT | m.4435A>G | CA337096873 | ClinVar dbSNP | ||
MT | m.4435A>T | CA913178141 | |||
MT | m.4436C>A | CA913178146 | |||
MT | m.4436C= | CA2573329871 | |||
MT | m.4436C>G | CA913178143 | |||
MT | m.4436C>T | CA913178145 | |||
MT | m.4437C>A | CA913178147 | |||
MT | m.4437C= | CA2499563873 | |||
MT | m.4437C>G | CA913178148 | |||
MT | m.4437C>T | CA913178150 | ClinVar dbSNP | ||
MT | m.4438C>A | CA913178151 | |||
MT | m.4438C= | CA2573329876 | |||
MT | m.4438C>G | CA913178152 | |||
MT | m.4438C>T | CA913178153 | |||
MT | m.4439C>A | CA913178154 | |||
MT | m.4439C= | CA2573329877 | |||
MT | m.4439C>G | CA913178155 | |||
MT | m.4439C>T | CA913178156 | |||
MT | m.4440G>A | CA913178157 | |||
MT | m.4440G>C | CA913178159 | |||
MT | m.4440G= | CA2573329878 | |||
MT | m.4440G>T | CA913178160 | |||
MT | m.4441A= | CA2573329879 | |||
MT | m.4441A>C | CA913178162 | |||
MT | m.4441A>G | CA913178163 | |||
MT | m.4441A>T | CA913178164 | |||
MT | m.4442A= | CA2573329881 | |||
MT | m.4442A>C | CA913178165 | |||
MT | m.4442A>G | CA913178167 | |||
MT | m.4442A>T | CA913178171 | |||
MT | m.4443A= | CA2573329883 | |||
MT | m.4443A>C | CA913178172 | |||
MT | m.4443A>G | CA913178173 | |||
MT | m.4443A>T | CA913178174 | |||
MT | m.4444A= | CA2573329884 | |||
MT | m.4444A>C | CA913178175 | |||
MT | m.4444A>G | CA913178179 | |||
MT | m.4444A>T | CA913178180 | |||
MT | m.4445T>A | CA913178181 | |||
MT | m.4445T>C | CA913178182 | |||
MT | m.4445T>G | CA913178184 | |||
MT | m.4445T= | CA2573329885 | |||
MT | m.4446G>A | CA913178186 | |||
MT | m.4446G>C | CA913178187 | |||
MT | m.4446G= | CA2573329889 | |||
MT | m.4446G>T | CA913178188 | |||
MT | m.4447T>A | CA913178191 | |||
MT | m.4447T>C | CA913178192 | |||
MT | m.4447T>G | CA913178193 | |||
MT | m.4447T= | CA2573329891 | |||
MT | m.4448T>A | CA913178194 | |||
MT | m.4448T>C | CA913178198 | |||
MT | m.4448T>G | CA913178199 | |||
MT | m.4448T= | CA2573329893 | |||
MT | m.4449G>A | CA913178203 | |||
MT | m.4449G>C | CA913178204 | |||
MT | m.4449G= | CA2573329895 | |||
MT | m.4449G>T | CA913178202 | |||
MT | m.4450G>A | CA913178210 | ClinVar | ||
MT | m.4450G>C | CA913178206 | |||
MT | m.4450G= | CA2573329896 | |||
MT | m.4450G>T | CA913178205 | |||
MT | m.4451T>A | CA913178211 | |||
MT | m.4451T>C | CA913178212 | |||
MT | m.4451T>G | CA913178213 | ClinVar dbSNP | ||
MT | m.4451T= | CA2499563874 | |||
MT | m.4452T>A | CA913178215 | |||
MT | m.4452T>C | CA337096875 | ClinVar dbSNP | ||
MT | m.4452T>G | CA913178216 | |||
MT | m.4452T= | CA2499563875 | |||
MT | m.4453A= | CA2513007329 | |||
MT | m.4453A>C | CA913178218 | |||
MT | m.4453A>G | CA913178219 | |||
MT | m.4453A>T | CA913178221 | |||
MT | m.4454T>A | CA337096879 | ClinVar dbSNP | ||
MT | m.4454T>C | CA337096877 | ClinVar dbSNP | ||
MT | m.4454T>G | CA913178223 | |||
MT | m.4454T= | CA2499563876 | |||
MT | m.4454dup | CA2741808802 | |||
MT | m.4455A= | CA2499563877 | |||
MT | m.4455A>C | CA913178224 | |||
MT | m.4455A>G | CA337096881 | ClinVar dbSNP | ||
MT | m.4455A>T | CA913178225 | |||
MT | m.4456C>A | CA913178226 | |||
MT | m.4456C= | CA2499563878 | |||
MT | m.4456C>G | CA913178230 | |||
MT | m.4456C>T | CA913178231 | ClinVar dbSNP | ||
MT | m.4457C>A | CA913178234 | |||
MT | m.4457C= | CA2573329909 | |||
MT | m.4457C>G | CA913178232 | |||
MT | m.4457C>T | CA913178233 | |||
MT | m.4458C>A | CA913178236 | |||
MT | m.4458C= | CA2573329911 | |||
MT | m.4458C>G | CA913178237 | |||
MT | m.4458C>T | CA913178238 | |||
MT | m.4459T>A | CA913178240 | |||
MT | m.4459T>C | CA913178242 | |||
MT | m.4459T>G | CA913178243 | |||
MT | m.4459T= | CA2573329912 | |||
MT | m.4460del | CA2573104470 | |||
MT | m.4460T>A | CA913178248 | |||
MT | m.4460T>C | CA913178244 | |||
MT | m.4460T>G | CA913178246 | |||
MT | m.4460T= | CA2573329914 | |||
MT | m.4461C>A | CA913178250 | |||
MT | m.4461C= | CA2573329916 | |||
MT | m.4461C>G | CA913178251 | |||
MT | m.4461C>T | CA913178249 | |||
MT | m.4462C>A | CA913178252 | |||
MT | m.4462C= | CA2573329919 | |||
MT | m.4462C>G | CA913178253 | |||
MT | m.4462C>T | CA913178254 | |||
MT | m.4463C>A | CA913178259 | |||
MT | m.4463C= | CA2573329921 | |||
MT | m.4463C>G | CA913178255 | |||
MT | m.4463C>T | CA913178256 | |||
MT | m.4464G>A | CA913178263 | ClinVar dbSNP | ||
MT | m.4464G>C | CA913178262 | |||
MT | m.4464G= | CA2499563879 | |||
MT | m.4464G>T | CA913178261 | |||
MT | m.4465T>A | CA913178266 | |||
MT | m.4465T>C | CA913178265 | |||
MT | m.4465T>G | CA913178264 | |||
MT | m.4465T= | CA2573329925 | |||
MT | m.4466A= | CA2499563880 | |||
MT | m.4466A>C | CA913178268 | |||
MT | m.4466A>G | CA913178270 | ClinVar dbSNP | ||
MT | m.4466A>T | CA913178267 | |||
MT | m.4467C>A | CA913178271 | |||
MT | m.4467C= | CA2573329928 | |||
MT | m.4467C>G | CA913178272 | |||
MT | m.4467C>T | CA913178274 | |||
MT | m.4468T>A | CA913178276 | |||
MT | m.4468T>C | CA913178277 | |||
MT | m.4468T>G | CA913178278 | |||
MT | m.4468T= | CA2573329931 | |||
MT | m.4469A= | CA2573329933 | |||
MT | m.4469A>C | CA913178279 | |||
MT | m.4469A>G | CA913178280 | |||
MT | m.4469A>T | CA913178281 | |||
MT | m.4470A= | CA2573329934 | MT-ND2 | c.1A= (p.Ile1=) | |
MT | m.4470A>C | CA414774540 | MT-ND2 | c.1A>C (p.Ile1Leu) | |
MT | m.4470A>G | CA414774541 | MT-ND2 | c.1A>G (p.Ile1Val) | |
MT | m.4470A>T | CA414774542 | MT-ND2 | c.1A>T (p.Ile1Phe) | |
MT | m.4471T>A | CA414774543 | MT-ND2 | c.2T>A (p.Ile1Asn) | |
MT | m.4471T>C | CA414774544 | MT-ND2 | c.2T>C (p.Ile1Thr) | |
MT | m.4471T>G | CA414774545 | MT-ND2 | c.2T>G (p.Ile1Ser) | |
MT | m.4471T= | CA2573329935 | MT-ND2 | c.2T= (p.Ile1=) | |
MT | m.4472T>A | CA913178286 | MT-ND2 | c.3T>A (p.Ile1=) | |
MT | m.4472T>C | CA16603181 | MT-ND2 | c.3T>C (p.Ile1=) | ClinVar dbSNP |
MT | m.4472T>G | CA414774546 | MT-ND2 | c.3T>G (p.Ile1Met) | |
MT | m.4472T= | CA2499563881 | MT-ND2 | c.3T= (p.Ile1=) | |
MT | m.4473A= | CA2573329938 | MT-ND2 | c.4A= (p.Asn2=) | |
MT | m.4473A>C | CA414774547 | MT-ND2 | c.4A>C (p.Asn2His) | |
MT | m.4473A>G | CA414774548 | MT-ND2 | c.4A>G (p.Asn2Asp) | |
MT | m.4473A>T | CA414774549 | MT-ND2 | c.4A>T (p.Asn2Tyr) | |
MT | m.4474A= | CA2573329942 | MT-ND2 | c.5A= (p.Asn2=) | |
MT | m.4474A>C | CA414774550 | MT-ND2 | c.5A>C (p.Asn2Thr) | |
MT | m.4474A>G | CA414774551 | MT-ND2 | c.5A>G (p.Asn2Ser) | |
MT | m.4474A>T | CA414774552 | MT-ND2 | c.5A>T (p.Asn2Ile) | |
MT | m.4475T>A | CA414774554 | MT-ND2 | c.6T>A (p.Asn2Lys) | |
MT | m.4475T>C | CA913178290 | MT-ND2 | c.6T>C (p.Asn2=) | |
MT | m.4475T>G | CA414774553 | MT-ND2 | c.6T>G (p.Asn2Lys) | |
MT | m.4475T= | CA2573329943 | MT-ND2 | c.6T= (p.Asn2=) | |
MT | m.4476C>A | CA414774555 | MT-ND2 | c.7C>A (p.Pro3Thr) | |
MT | m.4476C= | CA2573329944 | MT-ND2 | c.7C= (p.Pro3=) | |
MT | m.4476C>G | CA414774556 | MT-ND2 | c.7C>G (p.Pro3Ala) | |
MT | m.4476C>T | CA414774557 | MT-ND2 | c.7C>T (p.Pro3Ser) | |
MT | m.4479dup | CA2573104471 | MT-ND2 | c.10dup (p.Leu4ProfsTer?) | |
MT | m.4479del | CA2573104472 | MT-ND2 | c.10del (p.Leu4TrpfsTer19) | |
MT | m.4478_4490del | CA2740098105 | MT-ND2 | c.9_21del (p.Leu4SerfsTer15) | |
MT | m.4477C>A | CA414774558 | MT-ND2 | c.8C>A (p.Pro3His) | |
MT | m.4477C= | CA2499563882 | MT-ND2 | c.8C= (p.Pro3=) | |
MT | m.4477C>G | CA337096883 | MT-ND2 | c.8C>G (p.Pro3Arg) | dbSNP |
MT | m.4477C>T | CA414774559 | MT-ND2 | c.8C>T (p.Pro3Leu) | |
MT | m.4478C>A | CA913178291 | MT-ND2 | c.9C>A (p.Pro3=) | |
MT | m.4478C= | CA2573329947 | MT-ND2 | c.9C= (p.Pro3=) | |
MT | m.4478C>G | CA913178292 | MT-ND2 | c.9C>G (p.Pro3=) | |
MT | m.4478C>T | CA913178293 | MT-ND2 | c.9C>T (p.Pro3=) | |
MT | m.4479C>A | CA414774560 | MT-ND2 | c.10C>A (p.Leu4Met) | |
MT | m.4479C= | CA2573329948 | MT-ND2 | c.10C= (p.Leu4=) | |
MT | m.4479C>G | CA414774561 | MT-ND2 | c.10C>G (p.Leu4Val) | |
MT | m.4479C>T | CA913178294 | MT-ND2 | c.10C>T (p.Leu4=) | |
MT | m.4480del | CA2573104473 | MT-ND2 | c.11del (p.Leu4ArgfsTer19) | |
MT | m.4480T>A | CA414774562 | MT-ND2 | c.11T>A (p.Leu4Gln) | |
MT | m.4480T>C | CA414774563 | MT-ND2 | c.11T>C (p.Leu4Pro) | ClinVar dbSNP |
MT | m.4480T>G | CA414774564 | MT-ND2 | c.11T>G (p.Leu4Arg) | |
MT | m.4480T= | CA2499563883 | MT-ND2 | c.11T= (p.Leu4=) | |
MT | m.4481G>A | CA337096885 | MT-ND2 | c.12G>A (p.Leu4=) | dbSNP |
MT | m.4481G>C | CA913178298 | MT-ND2 | c.12G>C (p.Leu4=) | |
MT | m.4481G= | CA2499563884 | MT-ND2 | c.12G= (p.Leu4=) | |
MT | m.4481G>T | CA913178297 | MT-ND2 | c.12G>T (p.Leu4=) | |
MT | m.4482G>A | CA414774565 | MT-ND2 | c.13G>A (p.Ala5Thr) | ClinVar dbSNP |
MT | m.4482G>C | CA414774567 | MT-ND2 | c.13G>C (p.Ala5Pro) | |
MT | m.4482G= | CA2499563885 | MT-ND2 | c.13G= (p.Ala5=) | |
MT | m.4482G>T | CA414774566 | MT-ND2 | c.13G>T (p.Ala5Ser) |