Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23425309A>C | CA389048506 | MYH7 | c.2396T>G (p.Met799Arg) n.2502T>G | |
14 | g.23425309A>G | CA389048507 | MYH7 | c.2396T>C (p.Met799Thr) n.2502T>C | |
14 | g.23425309A>T | CA389048508 | MYH7 | c.2396T>A (p.Met799Lys) n.2502T>A | |
14 | g.23425310T>A | CA389048511 | MYH7 | c.2395A>T (p.Met799Leu) n.2501A>T | |
14 | g.23425310T>C | CA389048509 | MYH7 | c.2395A>G (p.Met799Val) n.2501A>G | |
14 | g.23425310T>G | CA389048510 | MYH7 | c.2395A>C (p.Met799Leu) n.2501A>C | |
14 | g.23425311T>A | CA389048512 | MYH7 | c.2394A>T (p.Arg798Ser) n.2500A>T | |
14 | g.23425311T>C | CA485622652 | MYH7 | c.2394A>G (p.Arg798=) n.2500A>G | |
14 | g.23425311T>G | CA389048513 | MYH7 | c.2394A>C (p.Arg798Ser) n.2500A>C | |
14 | g.23425312C>A | CA389048514 | MYH7 | c.2393G>T (p.Arg798Ile) n.2499G>T | |
14 | g.23425312C= | CA2123457338 | MYH7 | c.2393G= (p.Arg798=) n.2499G= | |
14 | g.23425312C>G | CA389048515 | MYH7 | c.2393G>C (p.Arg798Thr) n.2499G>C | |
14 | g.23425312C>T | CA389048516 | MYH7 | c.2393G>A (p.Arg798Lys) n.2499G>A | ClinVar dbSNP COSMIC |
14 | g.23425313T>A | CA389048517 | MYH7 | c.2392A>T (p.Arg798Ter) n.2498A>T | |
14 | g.23425313T>C | CA389048518 | MYH7 | c.2392A>G (p.Arg798Gly) n.2498A>G | |
14 | g.23425313T>G | CA485622657 | MYH7 | c.2392A>C (p.Arg798=) n.2498A>C | |
14 | g.23425314G>A | CA485622658 | MYH7 | c.2391C>T (p.Ala797=) n.2497C>T | |
14 | g.23425314G>C | CA485622659 | MYH7 | c.2391C>G (p.Ala797=) n.2497C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23425314G= | CA2123457345 | MYH7 | c.2391C= (p.Ala797=) n.2497C= | |
14 | g.23425314G>T | CA485622660 | MYH7 | c.2391C>A (p.Ala797=) n.2497C>A | |
14 | g.23425315del | CA485622661 | MYH7 | c.2391del (p.Arg798GlufsTer16) n.2497del | COSMIC |
14 | g.23425315G>A | CA389048519 | MYH7 | c.2390C>T (p.Ala797Val) n.2496C>T | ClinVar |
14 | g.23425315G>C | CA389048520 | MYH7 | c.2390C>G (p.Ala797Gly) n.2496C>G | |
14 | g.23425315G>T | CA389048521 | MYH7 | c.2390C>A (p.Ala797Asp) n.2496C>A | |
14 | g.23425316C>A | CA389048522 | MYH7 | c.2389G>T (p.Ala797Ser) n.2495G>T | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23425316C= | CA2123457354 | MYH7 | c.2389G= (p.Ala797=) n.2495G= | |
14 | g.23425316C>G | CA389048523 | MYH7 | c.2389G>C (p.Ala797Pro) n.2495G>C | ClinVar dbSNP |
14 | g.23425316C>T | CA012268 | MYH7 | c.2389G>A (p.Ala797Thr) n.2495G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23425317G>A | CA012263 | MYH7 | c.2388C>T (p.Leu796=) n.2494C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23425317G>C | CA485622665 | MYH7 | c.2388C>G (p.Leu796=) n.2494C>G | |
14 | g.23425317G= | CA2123457362 | MYH7 | c.2388C= (p.Leu796=) n.2494C= | |
14 | g.23425317G>T | CA485622666 | MYH7 | c.2388C>A (p.Leu796=) n.2494C>A | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23425318A>C | CA389048526 | MYH7 | c.2387T>G (p.Leu796Arg) n.2493T>G | |
14 | g.23425318A>G | CA389048524 | MYH7 | c.2387T>C (p.Leu796Pro) n.2493T>C | |
14 | g.23425318A>T | CA389048525 | MYH7 | c.2387T>A (p.Leu796His) n.2493T>A | |
14 | g.23425319G>A | CA389048527 | MYH7 | c.2386C>T (p.Leu796Phe) n.2492C>T | ClinVar dbSNP |
14 | g.23425319G>C | CA389048528 | MYH7 | c.2386C>G (p.Leu796Val) n.2492C>G | |
14 | g.23425319G= | CA2123457367 | MYH7 | c.2386C= (p.Leu796=) n.2492C= | |
14 | g.23425319G>T | CA389048529 | MYH7 | c.2386C>A (p.Leu796Ile) n.2492C>A | |
14 | g.23425320C>A | CA485622671 | MYH7 | c.2385G>T (p.Val795=) n.2491G>T | gnomAD v4 |
14 | g.23425320C>G | CA485622669 | MYH7 | c.2385G>C (p.Val795=) n.2491G>C | |
14 | g.23425320C>T | CA485622667 | MYH7 | c.2385G>A (p.Val795=) n.2491G>A | gnomAD v4 |
14 | g.23425321A>C | CA389048532 | MYH7 | c.2384T>G (p.Val795Gly) n.2490T>G | |
14 | g.23425321A>G | CA389048531 | MYH7 | c.2384T>C (p.Val795Ala) n.2490T>C | |
14 | g.23425321A>T | CA389048530 | MYH7 | c.2384T>A (p.Val795Glu) n.2490T>A | gnomAD v4 |
14 | g.23425322C>A | CA257819681 | MYH7 | c.2383G>T (p.Val795Leu) n.2489G>T | dbSNP gnomAD v3 gnomAD v4 |
14 | g.23425322C= | CA2123457377 | MYH7 | c.2383G= (p.Val795=) n.2489G= | |
14 | g.23425322C>G | CA389048533 | MYH7 | c.2383G>C (p.Val795Leu) n.2489G>C | |
14 | g.23425322C>T | CA389048534 | MYH7 | c.2383G>A (p.Val795Met) n.2489G>A | dbSNP gnomAD v4 |
14 | g.23425323A= | CA2123457384 | MYH7 | c.2382T= (p.Gly794=) n.2488T= |