Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.5774_14768del | CA2580610836 | |||
MT | m.5780_14107del | CA2580610932 | |||
MT | m.5782_13922del | CA250413 | ClinVar | ||
MT | m.5788_13923del | CA2580618295 | |||
MT | m.5794_14876del | CA250414 | ClinVar | ||
MT | m.6470_15588del | CA645373332 | ClinVar | ||
MT | m.7129_13991del | CA645373333 | ClinVar | ||
MT | m.8815_13722del | CA645373338 | ClinVar | ||
MT | m.8839_14895del | CA645373339 | ClinVar | ||
MT | m.9062_16052del | CA2580618296 | |||
MT | m.10106_15067del | CA645373340 | ClinVar | ||
MT | m.10775_14941del | CA2740090229 | ClinVar | ||
MT | m.10950_15540del | CA2580102079 | ClinVar | ||
MT | m.11263_15374del | CA645373341 | ClinVar | ||
MT | m.12114_14420del | CA645373342 | ClinVar | ||
MT | m.13528A= | CA2499568041 | MT-ND5 | c.1192A= (p.Thr398=) | |
MT | m.13528A>C | CA414818389 | MT-ND5 | c.1192A>C (p.Thr398Pro) | |
MT | m.13528A>G | CA337099716 | MT-ND5 | c.1192A>G (p.Thr398Ala) | ClinVar dbSNP |
MT | m.13528A>T | CA414818390 | MT-ND5 | c.1192A>T (p.Thr398Ser) | |
MT | m.13529C>A | CA414818397 | MT-ND5 | c.1193C>A (p.Thr398Asn) | |
MT | m.13529C= | CA2573324681 | MT-ND5 | c.1193C= (p.Thr398=) | |
MT | m.13529C>G | CA414818399 | MT-ND5 | c.1193C>G (p.Thr398Ser) | |
MT | m.13529C>T | CA414818400 | MT-ND5 | c.1193C>T (p.Thr398Ile) | |
MT | m.13530C>A | CA913171024 | MT-ND5 | c.1194C>A (p.Thr398=) | |
MT | m.13530C= | CA2499568042 | MT-ND5 | c.1194C= (p.Thr398=) | |
MT | m.13530C>G | CA913171025 | MT-ND5 | c.1194C>G (p.Thr398=) | |
MT | m.13530C>T | CA913171026 | MT-ND5 | c.1194C>T (p.Thr398=) | dbSNP |
MT | m.13531G>A | CA414818402 | MT-ND5 | c.1195G>A (p.Ala399Thr) | COSMIC |
MT | m.13531G>C | CA414818404 | MT-ND5 | c.1195G>C (p.Ala399Pro) | |
MT | m.13531G= | CA2573324685 | MT-ND5 | c.1195G= (p.Ala399=) | |
MT | m.13531G>T | CA414818406 | MT-ND5 | c.1195G>T (p.Ala399Ser) | |
MT | m.13532C>A | CA414818408 | MT-ND5 | c.1196C>A (p.Ala399Glu) | |
MT | m.13532C= | CA2573324687 | MT-ND5 | c.1196C= (p.Ala399=) | |
MT | m.13532C>G | CA414818409 | MT-ND5 | c.1196C>G (p.Ala399Gly) | |
MT | m.13532C>T | CA414818411 | MT-ND5 | c.1196C>T (p.Ala399Val) | COSMIC |
MT | m.13533A= | CA2499568043 | MT-ND5 | c.1197A= (p.Ala399=) | |
MT | m.13533A>C | CA913171027 | MT-ND5 | c.1197A>C (p.Ala399=) | |
MT | m.13533A>G | CA913171028 | MT-ND5 | c.1197A>G (p.Ala399=) | dbSNP |
MT | m.13533A>T | CA913171029 | MT-ND5 | c.1197A>T (p.Ala399=) | dbSNP |
MT | m.13534A= | CA2573324695 | MT-ND5 | c.1198A= (p.Asn400=) | |
MT | m.13534A>C | CA414818417 | MT-ND5 | c.1198A>C (p.Asn400His) | |
MT | m.13534A>G | CA414818415 | MT-ND5 | c.1198A>G (p.Asn400Asp) | |
MT | m.13534A>T | CA414818413 | MT-ND5 | c.1198A>T (p.Asn400Tyr) | |
MT | m.13535A= | CA2499568044 | MT-ND5 | c.1199A= (p.Asn400=) | |
MT | m.13535A>C | CA414818419 | MT-ND5 | c.1199A>C (p.Asn400Thr) | |
MT | m.13535A>G | CA414818423 | MT-ND5 | c.1199A>G (p.Asn400Ser) | ClinVar dbSNP |
MT | m.13535A>T | CA414818421 | MT-ND5 | c.1199A>T (p.Asn400Ile) | |
MT | m.13536C>A | CA414818424 | MT-ND5 | c.1200C>A (p.Asn400Lys) | |
MT | m.13536C= | CA2573324700 | MT-ND5 | c.1200C= (p.Asn400=) | |
MT | m.13536C>G | CA414818426 | MT-ND5 | c.1200C>G (p.Asn400Lys) |