| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23425281C>A | CA389048446 | MYH7 | c.2423+1G>T (n.2423+1G>T) n.2529+1G>T | |
| 14 | g.23425281C= | CA2123457247 | MYH7 | c.2423+1G= (n.2423+1G=) n.2529+1G= | |
| 14 | g.23425281C>G | CA257819654 | MYH7 | c.2423+1G>C (n.2423+1G>C) n.2529+1G>C | dbSNP |
| 14 | g.23425281C>T | CA257819656 | MYH7 | c.2423+1G>A (n.2423+1G>A) n.2529+1G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425282C>A | CA389048447 | MYH7 | c.2423G>T (p.Arg808Ile) n.2529G>T | |
| 14 | g.23425282C>G | CA389048448 | MYH7 | c.2423G>C (p.Arg808Thr) n.2529G>C | |
| 14 | g.23425282C>T | CA389048449 | MYH7 | c.2423G>A (p.Arg808Lys) n.2529G>A | |
| 14 | g.23425283T>A | CA389048450 | MYH7 | c.2422A>T (p.Arg808Ter) n.2528A>T | |
| 14 | g.23425283T>C | CA389048451 | MYH7 | c.2422A>G (p.Arg808Gly) n.2528A>G | |
| 14 | g.23425283T>G | CA485622618 | MYH7 | c.2422A>C (p.Arg808=) n.2528A>C | |
| 14 | g.23425284A>C | CA485622619 | MYH7 | c.2421T>G (p.Arg807=) n.2527T>G | |
| 14 | g.23425284A>G | CA485622620 | MYH7 | c.2421T>C (p.Arg807=) n.2527T>C | |
| 14 | g.23425284A>T | CA485622621 | MYH7 | c.2421T>A (p.Arg807=) n.2527T>A | gnomAD v4 |
| 14 | g.23425285C>A | CA389048452 | MYH7 | c.2420G>T (p.Arg807Leu) n.2526G>T | gnomAD v4 |
| 14 | g.23425285C= | CA2123457248 | MYH7 | c.2420G= (p.Arg807=) n.2526G= | |
| 14 | g.23425285C>G | CA389048453 | MYH7 | c.2420G>C (p.Arg807Pro) n.2526G>C | ClinVar dbSNP |
| 14 | g.23425285C>T | CA032556 | MYH7 | c.2420G>A (p.Arg807His) n.2526G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425286G>A | CA389048454 | MYH7 | c.2419C>T (p.Arg807Cys) n.2525C>T | ClinVar gnomAD v4 |
| 14 | g.23425286G>C | CA389048456 | MYH7 | c.2419C>G (p.Arg807Gly) n.2525C>G | ClinVar dbSNP |
| 14 | g.23425286G>T | CA389048455 | MYH7 | c.2419C>A (p.Arg807Ser) n.2525C>A | COSMIC |
| 14 | g.23425287T>A | CA389048457 | MYH7 | c.2418A>T (p.Glu806Asp) n.2524A>T | dbSNP |
| 14 | g.23425287T>C | CA485622622 | MYH7 | c.2418A>G (p.Glu806=) n.2524A>G | |
| 14 | g.23425287T>G | CA389048458 | MYH7 | c.2418A>C (p.Glu806Asp) n.2524A>C | |
| 14 | g.23425287T= | CA2123457255 | MYH7 | c.2418A= (p.Glu806=) n.2524A= | |
| 14 | g.23425288T>A | CA389048459 | MYH7 | c.2417A>T (p.Glu806Val) n.2523A>T | |
| 14 | g.23425288T>C | CA389048460 | MYH7 | c.2417A>G (p.Glu806Gly) n.2523A>G | ClinVar dbSNP |
| 14 | g.23425288T>G | CA389048461 | MYH7 | c.2417A>C (p.Glu806Ala) n.2523A>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425288T= | CA2123457257 | MYH7 | c.2417A= (p.Glu806=) n.2523A= | |
| 14 | g.23425289C>A | CA389048462 | MYH7 | c.2416G>T (p.Glu806Ter) n.2522G>T | COSMIC |
| 14 | g.23425289C= | CA2123457265 | MYH7 | c.2416G= (p.Glu806=) n.2522G= | |
| 14 | g.23425289C>G | CA389048463 | MYH7 | c.2416G>C (p.Glu806Gln) n.2522G>C | |
| 14 | g.23425289C>T | CA012304 | MYH7 | c.2416G>A (p.Glu806Lys) n.2522G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23425290C>A | CA485622626 | MYH7 | c.2415G>T (p.Leu805=) n.2521G>T | |
| 14 | g.23425290C>G | CA485622627 | MYH7 | c.2415G>C (p.Leu805=) n.2521G>C | |
| 14 | g.23425290C>T | CA485622628 | MYH7 | c.2415G>A (p.Leu805=) n.2521G>A | gnomAD v4 |
| 14 | g.23425291A= | CA2123457300 | MYH7 | c.2414T= (p.Leu805=) n.2520T= | |
| 14 | g.23425291A>C | CA389048464 | MYH7 | c.2414T>G (p.Leu805Arg) n.2520T>G | dbSNP |
| 14 | g.23425291A>G | CA389048465 | MYH7 | c.2414T>C (p.Leu805Pro) n.2520T>C | |
| 14 | g.23425291A>T | CA389048466 | MYH7 | c.2414T>A (p.Leu805Gln) n.2520T>A | |
| 14 | g.23425292G>A | CA485622629 | MYH7 | c.2413C>T (p.Leu805=) n.2519C>T | |
| 14 | g.23425292G>C | CA389048467 | MYH7 | c.2413C>G (p.Leu805Val) n.2519C>G | |
| 14 | g.23425292G>T | CA389048468 | MYH7 | c.2413C>A (p.Leu805Met) n.2519C>A | |
| 14 | g.23425293C>A | CA485622634 | MYH7 | c.2412G>T (p.Leu804=) n.2518G>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425293C>G | CA485622632 | MYH7 | c.2412G>C (p.Leu804=) n.2518G>C | |
| 14 | g.23425293C>T | CA485622630 | MYH7 | c.2412G>A (p.Leu804=) n.2518G>A | |
| 14 | g.23425293_23425294delinsCA | CA2123457304 | MYH7 | c.2411_2412delinsTG (p.Leu804=) n.2517_2518delinsTG | |
| 14 | g.23425294del | CA2123457309 | MYH7 | c.2411del (p.Leu804ArgfsTer10) n.2517del | ClinVar dbSNP |
| 14 | g.23425294A= | CA2123457310 | MYH7 | c.2411T= (p.Leu804=) n.2517T= | |
| 14 | g.23425294A>C | CA389048469 | MYH7 | c.2411T>G (p.Leu804Arg) n.2517T>G | |
| 14 | g.23425294A>G | CA389048470 | MYH7 | c.2411T>C (p.Leu804Pro) n.2517T>C | ClinVar dbSNP |
| 14 | g.23425294A>T | CA389048471 | MYH7 | c.2411T>A (p.Leu804Gln) n.2517T>A | |
| 14 | g.23425295G>A | CA485622635 | MYH7 | c.2410C>T (p.Leu804=) n.2516C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425295G>C | CA389048472 | MYH7 | c.2410C>G (p.Leu804Val) n.2516C>G | |
| 14 | g.23425295G= | CA2123457316 | MYH7 | c.2410C= (p.Leu804=) n.2516C= | |
| 14 | g.23425295G>T | CA389048473 | MYH7 | c.2410C>A (p.Leu804Met) n.2516C>A | |
| 14 | g.23425296C>A | CA389048474 | MYH7 | c.2409G>T (p.Lys803Asn) n.2515G>T | |
| 14 | g.23425296C>G | CA389048475 | MYH7 | c.2409G>C (p.Lys803Asn) n.2515G>C | |
| 14 | g.23425296C>T | CA485622636 | MYH7 | c.2409G>A (p.Lys803=) n.2515G>A | gnomAD v4 |
| 14 | g.23425297T>A | CA389048476 | MYH7 | c.2408A>T (p.Lys803Met) n.2514A>T | |
| 14 | g.23425297T>C | CA389048477 | MYH7 | c.2408A>G (p.Lys803Arg) n.2514A>G | |
| 14 | g.23425297T>G | CA389048478 | MYH7 | c.2408A>C (p.Lys803Thr) n.2514A>C | |
| 14 | g.23425301del | CA2575486613 | MYH7 | c.2408del (p.Lys803SerfsTer11) n.2514del | ClinVar gnomAD v4 |
| 14 | g.23425298T>A | CA389048479 | MYH7 | c.2407A>T (p.Lys803Ter) n.2513A>T | |
| 14 | g.23425298T>C | CA389048480 | MYH7 | c.2407A>G (p.Lys803Glu) n.2513A>G | |
| 14 | g.23425298T>G | CA389048481 | MYH7 | c.2407A>C (p.Lys803Gln) n.2513A>C | |
| 14 | g.23425299T>A | CA389048482 | MYH7 | c.2406A>T (p.Lys802Asn) n.2512A>T | |
| 14 | g.23425299T>C | CA485622641 | MYH7 | c.2406A>G (p.Lys802=) n.2512A>G | |
| 14 | g.23425299T>G | CA389048483 | MYH7 | c.2406A>C (p.Lys802Asn) n.2512A>C | COSMIC |
| 14 | g.23425300T>A | CA389048484 | MYH7 | c.2405A>T (p.Lys802Ile) n.2511A>T | |
| 14 | g.23425300T>C | CA389048485 | MYH7 | c.2405A>G (p.Lys802Arg) n.2511A>G | |
| 14 | g.23425300T>G | CA389048486 | MYH7 | c.2405A>C (p.Lys802Thr) n.2511A>C | |
| 14 | g.23425301T>A | CA389048487 | MYH7 | c.2404A>T (p.Lys802Ter) n.2510A>T | |
| 14 | g.23425301T>C | CA389048488 | MYH7 | c.2404A>G (p.Lys802Glu) n.2510A>G | |
| 14 | g.23425301T>G | CA389048489 | MYH7 | c.2404A>C (p.Lys802Gln) n.2510A>C | gnomAD v4 COSMIC |
| 14 | g.23425302del | CA2575486614 | MYH7 | c.2403del (p.Tyr801Ter) n.2509del | |
| 14 | g.23425302G>A | CA032522 | MYH7 | c.2403C>T (p.Tyr801=) n.2509C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425302G>C | CA389048490 | MYH7 | c.2403C>G (p.Tyr801Ter) n.2509C>G | ClinVar dbSNP |
| 14 | g.23425302G= | CA2123457319 | MYH7 | c.2403C= (p.Tyr801=) n.2509C= | |
| 14 | g.23425302G>T | CA389048491 | MYH7 | c.2403C>A (p.Tyr801Ter) n.2509C>A | |
| 14 | g.23425303T>A | CA389048492 | MYH7 | c.2402A>T (p.Tyr801Phe) n.2508A>T | gnomAD v4 |
| 14 | g.23425303T>C | CA389048493 | MYH7 | c.2402A>G (p.Tyr801Cys) n.2508A>G | |
| 14 | g.23425303T>G | CA389048494 | MYH7 | c.2402A>C (p.Tyr801Ser) n.2508A>C | |
| 14 | g.23425304A= | CA2123457325 | MYH7 | c.2401T= (p.Tyr801=) n.2507T= | |
| 14 | g.23425304A>C | CA257819671 | MYH7 | c.2401T>G (p.Tyr801Asp) n.2507T>G | dbSNP |
| 14 | g.23425304A>G | CA389048495 | MYH7 | c.2401T>C (p.Tyr801His) n.2507T>C | |
| 14 | g.23425304A>T | CA012286 | MYH7 | c.2401T>A (p.Tyr801Asn) n.2507T>A | ClinVar dbSNP |
| 14 | g.23425305C>A | CA012281 | MYH7 | c.2400G>T (p.Glu800Asp) n.2506G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425305C= | CA2123457330 | MYH7 | c.2400G= (p.Glu800=) n.2506G= | |
| 14 | g.23425305C>G | CA389048496 | MYH7 | c.2400G>C (p.Glu800Asp) n.2506G>C | gnomAD v4 |
| 14 | g.23425305C>T | CA485622645 | MYH7 | c.2400G>A (p.Glu800=) n.2506G>A | dbSNP |
| 14 | g.23425306del | CA2739277785 | MYH7 | c.2399del (p.Glu800GlyfsTer14) n.2505del | ClinVar |
| 14 | g.23425306T>A | CA389048497 | MYH7 | c.2399A>T (p.Glu800Val) n.2505A>T | |
| 14 | g.23425306T>C | CA389048498 | MYH7 | c.2399A>G (p.Glu800Gly) n.2505A>G | |
| 14 | g.23425306T>G | CA389048499 | MYH7 | c.2399A>C (p.Glu800Ala) n.2505A>C | |
| 14 | g.23425307C>A | CA389048500 | MYH7 | c.2398G>T (p.Glu800Ter) n.2504G>T | |
| 14 | g.23425307C>G | CA389048501 | MYH7 | c.2398G>C (p.Glu800Gln) n.2504G>C | |
| 14 | g.23425307C>T | CA389048502 | MYH7 | c.2398G>A (p.Glu800Lys) n.2504G>A | gnomAD v4 COSMIC |
| 14 | g.23425308C>A | CA389048503 | MYH7 | c.2397G>T (p.Met799Ile) n.2503G>T | |
| 14 | g.23425308C>G | CA389048504 | MYH7 | c.2397G>C (p.Met799Ile) n.2503G>C | |
| 14 | g.23425308C>T | CA389048505 | MYH7 | c.2397G>A (p.Met799Ile) n.2503G>A | COSMIC |
| 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 | ClinVar 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= | |
| 14 | g.23425323A>C | CA485622673 | MYH7 | c.2382T>G (p.Gly794=) n.2488T>G | gnomAD v4 |
| 14 | g.23425323A>G | CA485622674 | MYH7 | c.2382T>C (p.Gly794=) n.2488T>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425323A>T | CA485622676 | MYH7 | c.2382T>A (p.Gly794=) n.2488T>A | |
| 14 | g.23425324C>A | CA389048535 | MYH7 | c.2381G>T (p.Gly794Val) n.2487G>T | |
| 14 | g.23425324C>G | CA389048536 | MYH7 | c.2381G>C (p.Gly794Ala) n.2487G>C | |
| 14 | g.23425324C>T | CA389048537 | MYH7 | c.2381G>A (p.Gly794Asp) n.2487G>A | ClinVar |
| 14 | g.23425325C>A | CA389048538 | MYH7 | c.2380G>T (p.Gly794Cys) n.2486G>T | |
| 14 | g.23425325C>G | CA389048540 | MYH7 | c.2380G>C (p.Gly794Arg) n.2486G>C | |
| 14 | g.23425325C>T | CA389048539 | MYH7 | c.2380G>A (p.Gly794Ser) n.2486G>A | |
| 14 | g.23425326T>A | CA485622679 | MYH7 | c.2379A>T (p.Arg793=) n.2485A>T | |
| 14 | g.23425326T>C | CA485622680 | MYH7 | c.2379A>G (p.Arg793=) n.2485A>G | ClinVar dbSNP |
| 14 | g.23425326T>G | CA485622681 | MYH7 | c.2379A>C (p.Arg793=) n.2485A>C | |
| 14 | g.23425326T= | CA2123457389 | MYH7 | c.2379A= (p.Arg793=) n.2485A= | |
| 14 | g.23425327C>A | CA389048541 | MYH7 | c.2378G>T (p.Arg793Leu) n.2484G>T | |
| 14 | g.23425327C= | CA2123457402 | MYH7 | c.2378G= (p.Arg793=) n.2484G= | |
| 14 | g.23425327C>G | CA389048542 | MYH7 | c.2378G>C (p.Arg793Pro) n.2484G>C | ClinVar dbSNP |
| 14 | g.23425327C>T | CA012259 | MYH7 | c.2378G>A (p.Arg793Gln) n.2484G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425328G>A | CA257819682 | MYH7 | c.2377C>T (p.Arg793Ter) n.2483C>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23425328G>C | CA389048543 | MYH7 | c.2377C>G (p.Arg793Gly) n.2483C>G | |
| 14 | g.23425328G= | CA2123457410 | MYH7 | c.2377C= (p.Arg793=) n.2483C= | |
| 14 | g.23425328G>T | CA032455 | MYH7 | c.2377C>A (p.Arg793=) n.2483C>A | dbSNP ExAC gnomAD v2 |
| 14 | g.23425329G>A | CA485622682 | MYH7 | c.2376C>T (p.Ser792=) n.2482C>T | gnomAD v4 |
| 14 | g.23425329G>C | CA485622684 | MYH7 | c.2376C>G (p.Ser792=) n.2482C>G | |
| 14 | g.23425329G>T | CA485622686 | MYH7 | c.2376C>A (p.Ser792=) n.2482C>A | |
| 14 | g.23425330G>A | CA389048544 | MYH7 | c.2375C>T (p.Ser792Phe) n.2481C>T | ClinVar dbSNP |
| 14 | g.23425330G>C | CA389048545 | MYH7 | c.2375C>G (p.Ser792Cys) n.2481C>G | gnomAD v4 |
| 14 | g.23425330G= | CA2123457413 | MYH7 | c.2375C= (p.Ser792=) n.2481C= | |
| 14 | g.23425330G>T | CA389048546 | MYH7 | c.2375C>A (p.Ser792Tyr) n.2481C>A | ClinVar |
| 14 | g.23425331A>C | CA389048547 | MYH7 | c.2374T>G (p.Ser792Ala) n.2480T>G | |
| 14 | g.23425331A>G | CA389048548 | MYH7 | c.2374T>C (p.Ser792Pro) n.2480T>C | ClinVar dbSNP |
| 14 | g.23425331A>T | CA389048549 | MYH7 | c.2374T>A (p.Ser792Thr) n.2480T>A | |
| 14 | g.23425332C>A | CA389048550 | MYH7 | c.2373G>T (p.Gln791His) n.2479G>T | |
| 14 | g.23425332C>G | CA389048551 | MYH7 | c.2373G>C (p.Gln791His) n.2479G>C | |
| 14 | g.23425332C>T | CA485622688 | MYH7 | c.2373G>A (p.Gln791=) n.2479G>A | ClinVar |
| 14 | g.23425333T>A | CA389048552 | MYH7 | c.2372A>T (p.Gln791Leu) n.2478A>T | |
| 14 | g.23425333T>C | CA389048554 | MYH7 | c.2372A>G (p.Gln791Arg) n.2478A>G | |
| 14 | g.23425333T>G | CA389048553 | MYH7 | c.2372A>C (p.Gln791Pro) n.2478A>C | ClinVar dbSNP |
| 14 | g.23425333T= | CA2123457419 | MYH7 | c.2372A= (p.Gln791=) n.2478A= | |
| 14 | g.23425333_23425334delinsTG | CA2123457417 | MYH7 | c.2371_2372delinsCA (p.Gln791=) n.2477_2478delinsCA | |
| 14 | g.23425334G>A | CA389048555 | MYH7 | c.2371C>T (p.Gln791Ter) n.2477C>T | dbSNP |
| 14 | g.23425334G>C | CA389048556 | MYH7 | c.2371C>G (p.Gln791Glu) n.2477C>G | |
| 14 | g.23425334G= | CA2123457490 | MYH7 | c.2371C= (p.Gln791=) n.2477C= | |
| 14 | g.23425334G>T | CA032435 | MYH7 | c.2371C>A (p.Gln791Lys) n.2477C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425336del | CA612937573 | MYH7 | c.2371del (p.Gln791SerfsTer23) n.2477del | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425335G>A | CA485622690 | MYH7 | c.2370C>T (p.Ala790=) n.2476C>T | gnomAD v4 |
| 14 | g.23425335G>C | CA485622691 | MYH7 | c.2370C>G (p.Ala790=) n.2476C>G | |
| 14 | g.23425335G>T | CA485622693 | MYH7 | c.2370C>A (p.Ala790=) n.2476C>A | COSMIC |
| 14 | g.23425336G>A | CA389048557 | MYH7 | c.2369C>T (p.Ala790Val) n.2475C>T | |
| 14 | g.23425336G>C | CA389048559 | MYH7 | c.2369C>G (p.Ala790Gly) n.2475C>G | |
| 14 | g.23425336G>T | CA389048558 | MYH7 | c.2369C>A (p.Ala790Asp) n.2475C>A | |
| 14 | g.23425338_23425347del | CA2573149868 | MYH7 | c.2360_2369del (p.Arg787ProfsTer24) n.2466_2475del | ClinVar dbSNP |
| 14 | g.23425337C>A | CA389048560 | MYH7 | c.2368G>T (p.Ala790Ser) n.2474G>T | |
| 14 | g.23425337C>G | CA389048561 | MYH7 | c.2368G>C (p.Ala790Pro) n.2474G>C | |
| 14 | g.23425337C>T | CA389048562 | MYH7 | c.2368G>A (p.Ala790Thr) n.2474G>A | |
| 14 | g.23425338C>A | CA389048563 | MYH7 | c.2367G>T (p.Gln789His) n.2473G>T | |
| 14 | g.23425338C>G | CA389048564 | MYH7 | c.2367G>C (p.Gln789His) n.2473G>C | |
| 14 | g.23425338C>T | CA485622694 | MYH7 | c.2367G>A (p.Gln789=) n.2473G>A | |
| 14 | g.23425338_23425339delinsCT | CA2123457493 | MYH7 | c.2366_2367delinsAG (p.Gln789=) n.2472_2473delinsAG | |
| 14 | g.23425339del | CA012249 | MYH7 | c.2366del (p.Gln789ArgfsTer25) n.2472del | ClinVar dbSNP |
| 14 | g.23425339T>A | CA389048565 | MYH7 | c.2366A>T (p.Gln789Leu) n.2472A>T | |
| 14 | g.23425339T>C | CA389048566 | MYH7 | c.2366A>G (p.Gln789Arg) n.2472A>G | ClinVar gnomAD v4 |
| 14 | g.23425339T>G | CA389048567 | MYH7 | c.2366A>C (p.Gln789Pro) n.2472A>C | |
| 14 | g.23425340G>A | CA389048570 | MYH7 | c.2365C>T (p.Gln789Ter) n.2471C>T | dbSNP |
| 14 | g.23425340G>C | CA389048569 | MYH7 | c.2365C>G (p.Gln789Glu) n.2471C>G | |
| 14 | g.23425340G= | CA2123457499 | MYH7 | c.2365C= (p.Gln789=) n.2471C= | |
| 14 | g.23425340G>T | CA389048568 | MYH7 | c.2365C>A (p.Gln789Lys) n.2471C>A | |
| 14 | g.23425341G>A | CA032413 | MYH7 | c.2364C>T (p.Ile788=) n.2470C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425341G>C | CA389048571 | MYH7 | c.2364C>G (p.Ile788Met) n.2470C>G | |
| 14 | g.23425341G= | CA2123457507 | MYH7 | c.2364C= (p.Ile788=) n.2470C= | |
| 14 | g.23425341G>T | CA485622698 | MYH7 | c.2364C>A (p.Ile788=) n.2470C>A | |
| 14 | g.23425342A>C | CA389048572 | MYH7 | c.2363T>G (p.Ile788Ser) n.2469T>G | |
| 14 | g.23425342A>G | CA389048573 | MYH7 | c.2363T>C (p.Ile788Thr) n.2469T>C | |
| 14 | g.23425342A>T | CA389048574 | MYH7 | c.2363T>A (p.Ile788Asn) n.2469T>A | |
| 14 | g.23425343T>A | CA389048575 | MYH7 | c.2362A>T (p.Ile788Phe) n.2468A>T | |
| 14 | g.23425343T>C | CA389048576 | MYH7 | c.2362A>G (p.Ile788Val) n.2468A>G | |
| 14 | g.23425343T>G | CA389048577 | MYH7 | c.2362A>C (p.Ile788Leu) n.2468A>C | |
| 14 | g.23425344A= | CA2123457511 | MYH7 | c.2361T= (p.Arg787=) n.2467T= | |
| 14 | g.23425344A>C | CA485622700 | MYH7 | c.2361T>G (p.Arg787=) n.2467T>G | |
| 14 | g.23425344A>G | CA485622701 | MYH7 | c.2361T>C (p.Arg787=) n.2467T>C | dbSNP gnomAD v2 |
| 14 | g.23425344A>T | CA485622702 | MYH7 | c.2361T>A (p.Arg787=) n.2467T>A | |
| 14 | g.23425345C>A | CA389048578 | MYH7 | c.2360G>T (p.Arg787Leu) n.2466G>T | |
| 14 | g.23425345C= | CA2123457518 | MYH7 | c.2360G= (p.Arg787=) n.2466G= | |
| 14 | g.23425345C>G | CA389048579 | MYH7 | c.2360G>C (p.Arg787Pro) n.2466G>C | ClinVar dbSNP |
| 14 | g.23425345C>T | CA012239 | MYH7 | c.2360G>A (p.Arg787His) n.2466G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23425346G>A | CA012232 | MYH7 | c.2359C>T (p.Arg787Cys) n.2465C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425346G>C | CA389048581 | MYH7 | c.2359C>G (p.Arg787Gly) n.2465C>G | gnomAD v4 |
| 14 | g.23425346G= | CA2123457529 | MYH7 | c.2359C= (p.Arg787=) n.2465C= | |
| 14 | g.23425346G>T | CA389048580 | MYH7 | c.2359C>A (p.Arg787Ser) n.2465C>A | gnomAD v4 |
| 14 | g.23425347C>A | CA012222 | MYH7 | c.2358G>T (p.Thr786=) n.2464G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425347C= | CA2123457537 | MYH7 | c.2358G= (p.Thr786=) n.2464G= | |
| 14 | g.23425347C>G | CA485622705 | MYH7 | c.2358G>C (p.Thr786=) n.2464G>C | gnomAD v4 |
| 14 | g.23425347C>T | CA012220 | MYH7 | c.2358G>A (p.Thr786=) n.2464G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425348G>A | CA032327 | MYH7 | c.2357C>T (p.Thr786Met) n.2463C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23425348G>C | CA389048582 | MYH7 | c.2357C>G (p.Thr786Arg) n.2463C>G | gnomAD v4 |
| 14 | g.23425348G= | CA2123457539 | MYH7 | c.2357C= (p.Thr786=) n.2463C= | |
| 14 | g.23425348G>T | CA389048583 | MYH7 | c.2357C>A (p.Thr786Lys) n.2463C>A | ClinVar |
| 14 | g.23425349T>A | CA389048584 | MYH7 | c.2356A>T (p.Thr786Ser) n.2462A>T | |
| 14 | g.23425349T>C | CA389048585 | MYH7 | c.2356A>G (p.Thr786Ala) n.2462A>G | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425349T>G | CA389048586 | MYH7 | c.2356A>C (p.Thr786Pro) n.2462A>C | |
| 14 | g.23425349T= | CA2123457543 | MYH7 | c.2356A= (p.Thr786=) n.2462A= | |
| 14 | g.23425350G>A | CA485622709 | MYH7 | c.2355C>T (p.Ile785=) n.2461C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23425350G>C | CA389048587 | MYH7 | c.2355C>G (p.Ile785Met) n.2461C>G | |
| 14 | g.23425350G= | CA2123457544 | MYH7 | c.2355C= (p.Ile785=) n.2461C= | |
| 14 | g.23425350G>T | CA485622711 | MYH7 | c.2355C>A (p.Ile785=) n.2461C>A | |
| 14 | g.23425351A>C | CA389048588 | MYH7 | c.2354T>G (p.Ile785Ser) n.2460T>G | |
| 14 | g.23425351A>G | CA389048589 | MYH7 | c.2354T>C (p.Ile785Thr) n.2460T>C | |
| 14 | g.23425351A>T | CA389048590 | MYH7 | c.2354T>A (p.Ile785Asn) n.2460T>A | ClinVar dbSNP |
| 14 | g.23425352T>A | CA389048593 | MYH7 | c.2353A>T (p.Ile785Phe) n.2459A>T | |
| 14 | g.23425352T>C | CA389048591 | MYH7 | c.2353A>G (p.Ile785Val) n.2459A>G | dbSNP |
| 14 | g.23425352T>G | CA389048592 | MYH7 | c.2353A>C (p.Ile785Leu) n.2459A>C | |
| 14 | g.23425352T= | CA2123457546 | MYH7 | c.2353A= (p.Ile785=) n.2459A= | |
| 14 | g.23425353G>A | CA012211 | MYH7 | c.2352C>T (p.Ile784=) n.2458C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425353G>C | CA389048594 | MYH7 | c.2352C>G (p.Ile784Met) n.2458C>G | |
| 14 | g.23425353G= | CA2123457551 | MYH7 | c.2352C= (p.Ile784=) n.2458C= | |
| 14 | g.23425353G>T | CA485622714 | MYH7 | c.2352C>A (p.Ile784=) n.2458C>A | |
| 14 | g.23425354A>C | CA389048595 | MYH7 | c.2351T>G (p.Ile784Ser) n.2457T>G | |
| 14 | g.23425354A>G | CA389048596 | MYH7 | c.2351T>C (p.Ile784Thr) n.2457T>C | |
| 14 | g.23425354A>T | CA389048597 | MYH7 | c.2351T>A (p.Ile784Asn) n.2457T>A | dbSNP gnomAD v4 |
| 14 | g.23425355T>A | CA389048598 | MYH7 | c.2350A>T (p.Ile784Phe) n.2456A>T | ClinVar |
| 14 | g.23425355T>C | CA389048599 | MYH7 | c.2350A>G (p.Ile784Val) n.2456A>G | |
| 14 | g.23425355T>G | CA389048600 | MYH7 | c.2350A>C (p.Ile784Leu) n.2456A>C | |
| 14 | g.23425356G>A | CA012206 | MYH7 | c.2349C>T (p.Arg783=) n.2455C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425356G>C | CA485622718 | MYH7 | c.2349C>G (p.Arg783=) n.2455C>G | |
| 14 | g.23425356G= | CA2123457555 | MYH7 | c.2349C= (p.Arg783=) n.2455C= | |
| 14 | g.23425356G>T | CA485622719 | MYH7 | c.2349C>A (p.Arg783=) n.2455C>A | |
| 14 | g.23425357C>A | CA389048601 | MYH7 | c.2348G>T (p.Arg783Leu) n.2454G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425357C= | CA2123457563 | MYH7 | c.2348G= (p.Arg783=) n.2454G= | |
| 14 | g.23425357C>G | CA012196 | MYH7 | c.2348G>C (p.Arg783Pro) n.2454G>C | ClinVar dbSNP |
| 14 | g.23425357C>T | CA012190 | MYH7 | c.2348G>A (p.Arg783His) n.2454G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23425358G>A | CA012184 | MYH7 | c.2347C>T (p.Arg783Cys) n.2453C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425358G>C | CA012174 | MYH7 | c.2347C>G (p.Arg783Gly) n.2453C>G | ClinVar dbSNP |
| 14 | g.23425358G= | CA2123457585 | MYH7 | c.2347C= (p.Arg783=) n.2453C= | |
| 14 | g.23425358G>T | CA389048602 | MYH7 | c.2347C>A (p.Arg783Ser) n.2453C>A | |
| 14 | g.23425359G>A | CA485622723 | MYH7 | c.2346C>T (p.Ser782=) n.2452C>T | gnomAD v4 |
| 14 | g.23425359G>C | CA389048603 | MYH7 | c.2346C>G (p.Ser782Arg) n.2452C>G | |
| 14 | g.23425359G= | CA2123457590 | MYH7 | c.2346C= (p.Ser782=) n.2452C= | |
| 14 | g.23425359G>T | CA012164 | MYH7 | c.2346C>A (p.Ser782Arg) n.2452C>A | ClinVar dbSNP |
| 14 | g.23425360C>A | CA389048604 | MYH7 | c.2345G>T (p.Ser782Ile) n.2451G>T | |
| 14 | g.23425360C= | CA2123457596 | MYH7 | c.2345G= (p.Ser782=) n.2451G= | |
| 14 | g.23425360C>G | CA389048605 | MYH7 | c.2345G>C (p.Ser782Thr) n.2451G>C | |
| 14 | g.23425360C>T | CA10587779 | MYH7 | c.2345G>A (p.Ser782Asn) n.2451G>A | ClinVar dbSNP |
| 14 | g.23425360_23425361delinsTC | CA2695219136 | MYH7 | c.2344_2345delinsGA (p.Ser782Asp) n.2450_2451delinsGA | |
| 14 | g.23425361T>A | CA389048606 | MYH7 | c.2344A>T (p.Ser782Cys) n.2450A>T | |
| 14 | g.23425361T>C | CA389048607 | MYH7 | c.2344A>G (p.Ser782Gly) n.2450A>G | |
| 14 | g.23425361T>G | CA389048608 | MYH7 | c.2344A>C (p.Ser782Arg) n.2450A>C | |
| 14 | g.23425362C>A | CA485622733 | MYH7 | c.2343G>T (p.Leu781=) n.2449G>T | |
| 14 | g.23425362C= | CA2123457607 | MYH7 | c.2343G= (p.Leu781=) n.2449G= | |
| 14 | g.23425362C>G | CA485622732 | MYH7 | c.2343G>C (p.Leu781=) n.2449G>C | |
| 14 | g.23425362C>T | CA032256 | MYH7 | c.2343G>A (p.Leu781=) n.2449G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425363A= | CA2123457614 | MYH7 | c.2342T= (p.Leu781=) n.2448T= | |
| 14 | g.23425363A>C | CA389048609 | MYH7 | c.2342T>G (p.Leu781Arg) n.2448T>G | |
| 14 | g.23425363A>G | CA012152 | MYH7 | c.2342T>C (p.Leu781Pro) n.2448T>C | ClinVar dbSNP |
| 14 | g.23425363A>T | CA389048610 | MYH7 | c.2342T>A (p.Leu781Gln) n.2448T>A | |
| 14 | g.23425364G>A | CA485622739 | MYH7 | c.2341C>T (p.Leu781=) n.2447C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425364G>C | CA389048611 | MYH7 | c.2341C>G (p.Leu781Val) n.2447C>G | |
| 14 | g.23425364G= | CA2123457623 | MYH7 | c.2341C= (p.Leu781=) n.2447C= | |
| 14 | g.23425364G>T | CA389048612 | MYH7 | c.2341C>A (p.Leu781Met) n.2447C>A | ClinVar dbSNP |
| 14 | g.23425365C>A | CA389048613 | MYH7 | c.2340G>T (p.Arg780Ser) n.2446G>T | ClinVar dbSNP |
| 14 | g.23425365C>G | CA389048614 | MYH7 | c.2340G>C (p.Arg780Ser) n.2446G>C | |
| 14 | g.23425365C>T | CA485622744 | MYH7 | c.2340G>A (p.Arg780=) n.2446G>A | ClinVar |
| 14 | g.23425366C>A | CA389048615 | MYH7 | c.2339G>T (p.Arg780Met) n.2445G>T | |
| 14 | g.23425366C>G | CA389048616 | MYH7 | c.2339G>C (p.Arg780Thr) n.2445G>C | |
| 14 | g.23425366C>T | CA389048617 | MYH7 | c.2339G>A (p.Arg780Lys) n.2445G>A | |
| 14 | g.23425367T>A | CA389048618 | MYH7 | c.2338A>T (p.Arg780Trp) n.2444A>T | |
| 14 | g.23425367T>C | CA389048619 | MYH7 | c.2338A>G (p.Arg780Gly) n.2444A>G | ClinVar |
| 14 | g.23425367T>G | CA485622749 | MYH7 | c.2338A>C (p.Arg780=) n.2444A>C | |
| 14 | g.23425368C>A | CA389048620 | MYH7 | c.2337G>T (p.Glu779Asp) n.2443G>T | |
| 14 | g.23425368C= | CA2123457627 | MYH7 | c.2337G= (p.Glu779=) n.2443G= | |
| 14 | g.23425368C>G | CA389048621 | MYH7 | c.2337G>C (p.Glu779Asp) n.2443G>C | |
| 14 | g.23425368C>T | CA485622753 | MYH7 | c.2337G>A (p.Glu779=) n.2443G>A | dbSNP |
| 14 | g.23425369T>A | CA389048622 | MYH7 | c.2336A>T (p.Glu779Val) n.2442A>T | |
| 14 | g.23425369T>C | CA389048623 | MYH7 | c.2336A>G (p.Glu779Gly) n.2442A>G | |
| 14 | g.23425369T>G | CA389048624 | MYH7 | c.2336A>C (p.Glu779Ala) n.2442A>C | |
| 14 | g.23425370C>A | CA389048625 | MYH7 | c.2335G>T (p.Glu779Ter) n.2441G>T | dbSNP |
| 14 | g.23425370C= | CA2123457632 | MYH7 | c.2335G= (p.Glu779=) n.2441G= | |
| 14 | g.23425370C>G | CA389048626 | MYH7 | c.2335G>C (p.Glu779Gln) n.2441G>C | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23425370C>T | CA389048627 | MYH7 | c.2335G>A (p.Glu779Lys) n.2441G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425371G>A | CA012146 | MYH7 | c.2334C>T (p.Asp778=) n.2440C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425371G>C | CA10588572 | MYH7 | c.2334C>G (p.Asp778Glu) n.2440C>G | ClinVar dbSNP |
| 14 | g.23425371G= | CA2123457650 | MYH7 | c.2334C= (p.Asp778=) n.2440C= | |
| 14 | g.23425371G>T | CA012141 | MYH7 | c.2334C>A (p.Asp778Glu) n.2440C>A | ClinVar dbSNP |
| 14 | g.23425372T>A | CA389048628 | MYH7 | c.2333A>T (p.Asp778Val) n.2439A>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425372T>C | CA012133 | MYH7 | c.2333A>G (p.Asp778Gly) n.2439A>G | ClinVar dbSNP |
| 14 | g.23425372T>G | CA389048629 | MYH7 | c.2333A>C (p.Asp778Ala) n.2439A>C | |
| 14 | g.23425372T= | CA2123457656 | MYH7 | c.2333A= (p.Asp778=) n.2439A= | |
| 14 | g.23425373C>A | CA389048630 | MYH7 | c.2332G>T (p.Asp778Tyr) n.2438G>T | |
| 14 | g.23425373C= | CA2123457671 | MYH7 | c.2332G= (p.Asp778=) n.2438G= | |
| 14 | g.23425373C>G | CA389048631 | MYH7 | c.2332G>C (p.Asp778His) n.2438G>C | ClinVar dbSNP |
| 14 | g.23425373C>T | CA012125 | MYH7 | c.2332G>A (p.Asp778Asn) n.2438G>A | ClinVar dbSNP |
| 14 | g.23425374C>A | CA389048632 | MYH7 | c.2331G>T (p.Arg777Ser) n.2437G>T | dbSNP gnomAD v2 |
| 14 | g.23425374C= | CA2123457677 | MYH7 | c.2331G= (p.Arg777=) n.2437G= | |
| 14 | g.23425374C>G | CA389048633 | MYH7 | c.2331G>C (p.Arg777Ser) n.2437G>C | |
| 14 | g.23425374C>T | CA485622776 | MYH7 | c.2331G>A (p.Arg777=) n.2437G>A | |
| 14 | g.23425375C>A | CA389048634 | MYH7 | c.2330G>T (p.Arg777Met) n.2436G>T | |
| 14 | g.23425375C>G | CA389048635 | MYH7 | c.2330G>C (p.Arg777Thr) n.2436G>C | ClinVar gnomAD v4 |
| 14 | g.23425375C>T | CA389048636 | MYH7 | c.2330G>A (p.Arg777Lys) n.2436G>A | ClinVar dbSNP |
| 14 | g.23425376T>A | CA389048637 | MYH7 | c.2329A>T (p.Arg777Trp) n.2435A>T | |
| 14 | g.23425376T>C | CA389048639 | MYH7 | c.2329A>G (p.Arg777Gly) n.2435A>G | |
| 14 | g.23425376T>G | CA485622781 | MYH7 | c.2329A>C (p.Arg777=) n.2435A>C | |
| 14 | g.23425377C>A | CA389048643 | MYH7 | c.2328G>T (p.Met776Ile) n.2434G>T | |
| 14 | g.23425377C>G | CA389048640 | MYH7 | c.2328G>C (p.Met776Ile) n.2434G>C | |
| 14 | g.23425377C>T | CA389048642 | MYH7 | c.2328G>A (p.Met776Ile) n.2434G>A | |
| 14 | g.23425378A>C | CA389048644 | MYH7 | c.2327T>G (p.Met776Arg) n.2433T>G | |
| 14 | g.23425378A>G | CA389048645 | MYH7 | c.2327T>C (p.Met776Thr) n.2433T>C | COSMIC |
| 14 | g.23425378A>T | CA389048646 | MYH7 | c.2327T>A (p.Met776Lys) n.2433T>A | |
| 14 | g.23425379T>A | CA389048647 | MYH7 | c.2326A>T (p.Met776Leu) n.2432A>T | |
| 14 | g.23425379T>C | CA389048648 | MYH7 | c.2326A>G (p.Met776Val) n.2432A>G | |
| 14 | g.23425379T>G | CA389048649 | MYH7 | c.2326A>C (p.Met776Leu) n.2432A>C | |
| 14 | g.23425381del | CA2580087927 | MYH7 | c.2326del (p.Met776Ter) n.2432del | ClinVar |
| 14 | g.23425380T>A | CA389048650 | MYH7 | c.2325A>T (p.Glu775Asp) n.2431A>T | |
| 14 | g.23425380T>C | CA485622794 | MYH7 | c.2325A>G (p.Glu775=) n.2431A>G | |
| 14 | g.23425380T>G | CA389048651 | MYH7 | c.2325A>C (p.Glu775Asp) n.2431A>C | |
| 14 | g.23425381T>A | CA389048652 | MYH7 | c.2324A>T (p.Glu775Val) n.2430A>T | |
| 14 | g.23425381T>C | CA389048653 | MYH7 | c.2324A>G (p.Glu775Gly) n.2430A>G | |
| 14 | g.23425381T>G | CA389048654 | MYH7 | c.2324A>C (p.Glu775Ala) n.2430A>C |