Chr Mutation (hg38) CAid Gene Transcript Linkouts
MTm.5774_14768delCA2580610836
MTm.5780_14107delCA2580610932
MTm.5782_13922delCA250413 ClinVar
MTm.5788_13923delCA2580618295
MTm.5794_14876delCA250414 ClinVar
MTm.6470_15588delCA645373332 ClinVar
MTm.7129_13991delCA645373333 ClinVar
MTm.8815_13722delCA645373338 ClinVar
MTm.8839_14895delCA645373339 ClinVar
MTm.9062_16052delCA2580618296
MTm.10106_15067delCA645373340 ClinVar
MTm.10775_14941delCA2740090229 ClinVar
MTm.10950_15540delCA2580102079 ClinVar
MTm.11263_15374delCA645373341 ClinVar
MTm.12114_14420delCA645373342 ClinVar
MTm.13708_13755delCA2740098359MT-ND5c.1372_1419del (p.Ala458_Ser473del)
MTm.13716_13720delCA2740098361MT-ND5c.1380_1384del (p.Ser461IlefsTer8)
MTm.13720C>ACA414819218MT-ND5c.1384C>A (p.Leu462Ile)
MTm.13720C=CA2499568129MT-ND5c.1384C= (p.Leu462=)
MTm.13720C>GCA414819219MT-ND5c.1384C>G (p.Leu462Val)
MTm.13720C>TCA913171158MT-ND5c.1384C>T (p.Leu462=)
dbSNP
MTm.13721T>ACA414819225MT-ND5c.1385T>A (p.Leu462Gln)
MTm.13721T>CCA414819221MT-ND5c.1385T>C (p.Leu462Pro)
MTm.13721T>GCA414819223MT-ND5c.1385T>G (p.Leu462Arg)
MTm.13721T=CA2573325257MT-ND5c.1385T= (p.Leu462=)
MTm.13722delCA2740098362MT-ND5c.1386del (p.Phe463SerfsTer24)
MTm.13722A=CA2499568130MT-ND5c.1386A= (p.Leu462=)
MTm.13722A>CCA337099781MT-ND5c.1386A>C (p.Leu462=)
MTm.13722A>GCA16603314MT-ND5c.1386A>G (p.Leu462=)
ClinVar dbSNP
MTm.13722A>TCA337099783MT-ND5c.1386A>T (p.Leu462=)
MTm.13723T>ACA414819231MT-ND5c.1387T>A (p.Phe463Ile)
MTm.13723T>CCA414819232MT-ND5c.1387T>C (p.Phe463Leu)
MTm.13723T>GCA414819234MT-ND5c.1387T>G (p.Phe463Val)
MTm.13723T=CA2573325269MT-ND5c.1387T= (p.Phe463=)
MTm.13724T>ACA414819236MT-ND5c.1388T>A (p.Phe463Tyr)
MTm.13724T>CCA414819238MT-ND5c.1388T>C (p.Phe463Ser)
MTm.13724T>GCA414819239MT-ND5c.1388T>G (p.Phe463Cys)
MTm.13724T=CA2513284093MT-ND5c.1388T= (p.Phe463=)
MTm.13725C>ACA414819242MT-ND5c.1389C>A (p.Phe463Leu)
MTm.13725C=CA2499568131MT-ND5c.1389C= (p.Phe463=)
MTm.13725C>GCA414819243MT-ND5c.1389C>G (p.Phe463Leu)
MTm.13725C>TCA913171159MT-ND5c.1389C>T (p.Phe463=)
dbSNP
MTm.13726G>ACA414819246MT-ND5c.1390G>A (p.Ala464Thr)
ClinVar dbSNP
MTm.13726G>CCA414819249MT-ND5c.1390G>C (p.Ala464Pro)
MTm.13726G=CA2499568132MT-ND5c.1390G= (p.Ala464=)
MTm.13726G>TCA414819248MT-ND5c.1390G>T (p.Ala464Ser)
MTm.13727C>ACA414819252MT-ND5c.1391C>A (p.Ala464Glu)
MTm.13727C=CA2573325278MT-ND5c.1391C= (p.Ala464=)
MTm.13727C>GCA414819254MT-ND5c.1391C>G (p.Ala464Gly)
MTm.13727C>TCA414819255MT-ND5c.1391C>T (p.Ala464Val)

Number of alleles fetched