| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23416122A= | CA2123465389 | MHRT,MYH7 | c.4835T= (p.Leu1612=) n.383A= | |
| 14 | g.23416122A>C | CA389037544 | MHRT,MYH7 | c.4835T>G (p.Leu1612Arg) n.383A>C | |
| 14 | g.23416122A>G | CA015395 | MHRT,MYH7 | c.4835T>C (p.Leu1612Pro) n.383A>G | ClinVar dbSNP |
| 14 | g.23416122A>T | CA389037545 | MHRT,MYH7 | c.4835T>A (p.Leu1612Gln) n.383A>T | |
| 14 | g.23416123G>A | CA044032 | MHRT,MYH7 | c.4834C>T (p.Leu1612=) n.384G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416123G>C | CA015389 | MHRT,MYH7 | c.4834C>G (p.Leu1612Val) n.384G>C | ClinVar dbSNP |
| 14 | g.23416123G= | CA2123465403 | MHRT,MYH7 | c.4834C= (p.Leu1612=) n.384G= | |
| 14 | g.23416123G>T | CA389037546 | MHRT,MYH7 | c.4834C>A (p.Leu1612Met) n.384G>T | |
| 14 | g.23416124G>A | CA485766518 | MHRT,MYH7 | c.4833C>T (p.Ala1611=) n.385G>A | gnomAD v4 |
| 14 | g.23416124G>C | CA485766519 | MHRT,MYH7 | c.4833C>G (p.Ala1611=) n.385G>C | |
| 14 | g.23416124G>T | CA485766520 | MHRT,MYH7 | c.4833C>A (p.Ala1611=) n.385G>T | |
| 14 | g.23416125G>A | CA044022 | MHRT,MYH7 | c.4832C>T (p.Ala1611Val) n.386G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416125G>C | CA389037548 | MHRT,MYH7 | c.4832C>G (p.Ala1611Gly) n.386G>C | |
| 14 | g.23416125G= | CA2123465413 | MHRT,MYH7 | c.4832C= (p.Ala1611=) n.386G= | |
| 14 | g.23416125G>T | CA389037547 | MHRT,MYH7 | c.4832C>A (p.Ala1611Asp) n.386G>T | |
| 14 | g.23416126C>A | CA015382 | MHRT,MYH7 | c.4831G>T (p.Ala1611Ser) n.387C>A | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 14 | g.23416126C= | CA2123465419 | MHRT,MYH7 | c.4831G= (p.Ala1611=) n.387C= | |
| 14 | g.23416126C>G | CA389037549 | MHRT,MYH7 | c.4831G>C (p.Ala1611Pro) n.387C>G | |
| 14 | g.23416126C>T | CA389037550 | MHRT,MYH7 | c.4831G>A (p.Ala1611Thr) n.387C>T | ClinVar |
| 14 | g.23416127C>A | CA389037551 | MHRT,MYH7 | c.4830G>T (p.Glu1610Asp) n.388C>A | |
| 14 | g.23416127C>G | CA389037552 | MHRT,MYH7 | c.4830G>C (p.Glu1610Asp) n.388C>G | |
| 14 | g.23416127C>T | CA485766521 | MHRT,MYH7 | c.4830G>A (p.Glu1610=) n.388C>T | |
| 14 | g.23416128T>A | CA389037553 | MHRT,MYH7 | c.4829A>T (p.Glu1610Val) n.389T>A | |
| 14 | g.23416128T>C | CA389037554 | MHRT,MYH7 | c.4829A>G (p.Glu1610Gly) n.389T>C | |
| 14 | g.23416128T>G | CA389037555 | MHRT,MYH7 | c.4829A>C (p.Glu1610Ala) n.389T>G | |
| 14 | g.23416128_23416131delinsTCGT | CA2123465429 | MHRT,MYH7 | c.4826_4829delinsACGA (p.Asn1609=) n.389_392delinsTCGT | |
| 14 | g.23416129C>A | CA389037556 | MHRT,MYH7 | c.4828G>T (p.Glu1610Ter) n.390C>A | |
| 14 | g.23416129C= | CA2123465441 | MHRT,MYH7 | c.4828G= (p.Glu1610=) n.390C= | |
| 14 | g.23416129C>G | CA015373 | MHRT,MYH7 | c.4828G>C (p.Glu1610Gln) n.390C>G | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416129C>T | CA10645050 | MHRT,MYH7 | c.4828G>A (p.Glu1610Lys) n.390C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416129_23416131delinsGGTTGCGGC | CA658658243 | MHRT,MYH7 | c.4826_4828delinsGCCGCAACC (p.Asn1609_Glu1610delinsSerArgAsnGln) n.390_392delinsGGTTGCGGC | ClinVar dbSNP |
| 14 | g.23416130G>A | CA015366 | MHRT,MYH7 | c.4827C>T (p.Asn1609=) n.391G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416130G>C | CA389037558 | MHRT,MYH7 | c.4827C>G (p.Asn1609Lys) n.391G>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416130G= | CA2123465452 | MHRT,MYH7 | c.4827C= (p.Asn1609=) n.391G= | |
| 14 | g.23416130G>T | CA389037557 | MHRT,MYH7 | c.4827C>A (p.Asn1609Lys) n.391G>T | gnomAD v4 |
| 14 | g.23416131T>A | CA389037559 | MHRT,MYH7 | c.4826A>T (p.Asn1609Ile) n.392T>A | |
| 14 | g.23416131T>C | CA389037560 | MHRT,MYH7 | c.4826A>G (p.Asn1609Ser) n.392T>C | |
| 14 | g.23416131T>G | CA389037561 | MHRT,MYH7 | c.4826A>C (p.Asn1609Thr) n.392T>G | |
| 14 | g.23416132T>A | CA389037562 | MHRT,MYH7 | c.4825A>T (p.Asn1609Tyr) n.393T>A | |
| 14 | g.23416132T>C | CA389037563 | MHRT,MYH7 | c.4825A>G (p.Asn1609Asp) n.393T>C | |
| 14 | g.23416132T>G | CA389037564 | MHRT,MYH7 | c.4825A>C (p.Asn1609His) n.393T>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416132T= | CA2123465459 | MHRT,MYH7 | c.4825A= (p.Asn1609=) n.393T= | |
| 14 | g.23416133G>A | CA485766522 | MHRT,MYH7 | c.4824C>T (p.Arg1608=) n.394G>A | |
| 14 | g.23416133G>C | CA485766523 | MHRT,MYH7 | c.4824C>G (p.Arg1608=) n.394G>C | |
| 14 | g.23416133G>T | CA485766524 | MHRT,MYH7 | c.4824C>A (p.Arg1608=) n.394G>T | |
| 14 | g.23416134C>A | CA043989 | MHRT,MYH7 | c.4823G>T (p.Arg1608Leu) n.395C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416134C= | CA2123465468 | MHRT,MYH7 | c.4823G= (p.Arg1608=) n.395C= | |
| 14 | g.23416134C>G | CA015359 | MHRT,MYH7 | c.4823G>C (p.Arg1608Pro) n.395C>G | ClinVar dbSNP |
| 14 | g.23416134C>T | CA043977 | MHRT,MYH7 | c.4823G>A (p.Arg1608His) n.395C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416135G>A | CA043961 | MHRT,MYH7 | c.4822C>T (p.Arg1608Cys) n.396G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416135G>C | CA389037565 | MHRT,MYH7 | c.4822C>G (p.Arg1608Gly) n.396G>C | |
| 14 | g.23416135G= | CA2123465475 | MHRT,MYH7 | c.4822C= (p.Arg1608=) n.396G= | |
| 14 | g.23416135G>T | CA389037566 | MHRT,MYH7 | c.4822C>A (p.Arg1608Ser) n.396G>T | |
| 14 | g.23416136G>A | CA485766525 | MHRT,MYH7 | c.4821C>T (p.Ser1607=) n.397G>A | COSMIC |
| 14 | g.23416136G>C | CA389037567 | MHRT,MYH7 | c.4821C>G (p.Ser1607Arg) n.397G>C | gnomAD v4 |
| 14 | g.23416136G= | CA2123465483 | MHRT,MYH7 | c.4821C= (p.Ser1607=) n.397G= | |
| 14 | g.23416136G>T | CA043942 | MHRT,MYH7 | c.4821C>A (p.Ser1607Arg) n.397G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416137C>A | CA389037568 | MHRT,MYH7 | c.4820G>T (p.Ser1607Ile) n.398C>A | |
| 14 | g.23416137C= | CA2123465485 | MHRT,MYH7 | c.4820G= (p.Ser1607=) n.398C= | |
| 14 | g.23416137C>G | CA257810583 | MHRT,MYH7 | c.4820G>C (p.Ser1607Thr) n.398C>G | dbSNP |
| 14 | g.23416137C>T | CA389037569 | MHRT,MYH7 | c.4820G>A (p.Ser1607Asn) n.398C>T | ClinVar |
| 14 | g.23416138T>A | CA389037570 | MHRT,MYH7 | c.4819A>T (p.Ser1607Cys) n.399T>A | |
| 14 | g.23416138T>C | CA389037571 | MHRT,MYH7 | c.4819A>G (p.Ser1607Gly) n.399T>C | ClinVar dbSNP |
| 14 | g.23416138T>G | CA389037572 | MHRT,MYH7 | c.4819A>C (p.Ser1607Arg) n.399T>G | |
| 14 | g.23416138T= | CA2123465487 | MHRT,MYH7 | c.4819A= (p.Ser1607=) n.399T= | |
| 14 | g.23416139G>A | CA485766526 | MHRT,MYH7 | c.4818C>T (p.Arg1606=) n.400G>A | |
| 14 | g.23416139G>C | CA485766527 | MHRT,MYH7 | c.4818C>G (p.Arg1606=) n.400G>C | |
| 14 | g.23416139G= | CA2123465490 | MHRT,MYH7 | c.4818C= (p.Arg1606=) n.400G= | |
| 14 | g.23416139G>T | CA043912 | MHRT,MYH7 | c.4818C>A (p.Arg1606=) n.400G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416140C>A | CA389037573 | MHRT,MYH7 | c.4817G>T (p.Arg1606Leu) n.401C>A | |
| 14 | g.23416140C= | CA2123465495 | MHRT,MYH7 | c.4817G= (p.Arg1606=) n.401C= | |
| 14 | g.23416140C>G | CA389037574 | MHRT,MYH7 | c.4817G>C (p.Arg1606Pro) n.401C>G | ClinVar dbSNP |
| 14 | g.23416140C>T | CA015352 | MHRT,MYH7 | c.4817G>A (p.Arg1606His) n.401C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416140_23416142delinsCGT | CA2123465501 | MHRT,MYH7 | c.4815_4817delinsACG (p.Thr1605=) n.401_403delinsCGT | |
| 14 | g.23416141G>A | CA015344 | MHRT,MYH7 | c.4816C>T (p.Arg1606Cys) n.402G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416141G>C | CA389037575 | MHRT,MYH7 | c.4816C>G (p.Arg1606Gly) n.402G>C | ClinVar gnomAD v4 |
| 14 | g.23416141G= | CA2123465525 | MHRT,MYH7 | c.4816C= (p.Arg1606=) n.402G= | |
| 14 | g.23416141G>T | CA389037576 | MHRT,MYH7 | c.4816C>A (p.Arg1606Ser) n.402G>T | |
| 14 | g.23416143_23416144del | CA2123465517 | MHRT,MYH7 | c.4815_4816del (p.Arg1606GlnfsTer18) n.404_405del | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416142T>A | CA485766528 | MHRT,MYH7 | c.4815A>T (p.Thr1605=) n.403T>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416142T>C | CA043888 | MHRT,MYH7 | c.4815A>G (p.Thr1605=) n.403T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416142T>G | CA485766529 | MHRT,MYH7 | c.4815A>C (p.Thr1605=) n.403T>G | |
| 14 | g.23416142T= | CA2123465532 | MHRT,MYH7 | c.4815A= (p.Thr1605=) n.403T= | |
| 14 | g.23416143G>A | CA389037579 | MHRT,MYH7 | c.4814C>T (p.Thr1605Ile) n.404G>A | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416143G>C | CA389037578 | MHRT,MYH7 | c.4814C>G (p.Thr1605Arg) n.404G>C | dbSNP |
| 14 | g.23416143G= | CA2123465539 | MHRT,MYH7 | c.4814C= (p.Thr1605=) n.404G= | |
| 14 | g.23416143G>T | CA389037577 | MHRT,MYH7 | c.4814C>A (p.Thr1605Lys) n.404G>T | |
| 14 | g.23416144T>A | CA389037580 | MHRT,MYH7 | c.4813A>T (p.Thr1605Ser) n.405T>A | dbSNP |
| 14 | g.23416144T>C | CA389037581 | MHRT,MYH7 | c.4813A>G (p.Thr1605Ala) n.405T>C | |
| 14 | g.23416144T>G | CA389037582 | MHRT,MYH7 | c.4813A>C (p.Thr1605Pro) n.405T>G | |
| 14 | g.23416144T= | CA2123465542 | MHRT,MYH7 | c.4813A= (p.Thr1605=) n.405T= | |
| 14 | g.23416147_23416148del | CA2624234337 | MHRT,MYH7 | c.4812_4813del (p.Glu1604AspfsTer20) n.408_409del | gnomAD v4 |
| 14 | g.23416145C>A | CA389037583 | MHRT,MYH7 | c.4812G>T (p.Glu1604Asp) n.406C>A | |
| 14 | g.23416145C>G | CA389037584 | MHRT,MYH7 | c.4812G>C (p.Glu1604Asp) n.406C>G | |
| 14 | g.23416145C>T | CA485766530 | MHRT,MYH7 | c.4812G>A (p.Glu1604=) n.406C>T | |
| 14 | g.23416146T>A | CA389037585 | MHRT,MYH7 | c.4811A>T (p.Glu1604Val) n.407T>A | |
| 14 | g.23416146T>C | CA389037586 | MHRT,MYH7 | c.4811A>G (p.Glu1604Gly) n.407T>C | |
| 14 | g.23416146T>G | CA389037587 | MHRT,MYH7 | c.4811A>C (p.Glu1604Ala) n.407T>G | |
| 14 | g.23416147C>A | CA389037588 | MHRT,MYH7 | c.4810G>T (p.Glu1604Ter) n.408C>A | |
| 14 | g.23416147C>G | CA389037589 | MHRT,MYH7 | c.4810G>C (p.Glu1604Gln) n.408C>G | |
| 14 | g.23416147C>T | CA389037590 | MHRT,MYH7 | c.4810G>A (p.Glu1604Lys) n.408C>T | |
| 14 | g.23416148T>A | CA485766531 | MHRT,MYH7 | c.4809A>T (p.Ala1603=) n.409T>A | |
| 14 | g.23416148T>C | CA485766532 | MHRT,MYH7 | c.4809A>G (p.Ala1603=) n.409T>C | ClinVar dbSNP |
| 14 | g.23416148T>G | CA485766533 | MHRT,MYH7 | c.4809A>C (p.Ala1603=) n.409T>G | dbSNP |
| 14 | g.23416148T= | CA2123465546 | MHRT,MYH7 | c.4809A= (p.Ala1603=) n.409T= | |
| 14 | g.23416149G>A | CA389037593 | MHRT,MYH7 | c.4808C>T (p.Ala1603Val) n.410G>A | ClinVar dbSNP |
| 14 | g.23416149G>C | CA389037592 | MHRT,MYH7 | c.4808C>G (p.Ala1603Gly) n.410G>C | |
| 14 | g.23416149G= | CA2123465550 | MHRT,MYH7 | c.4808C= (p.Ala1603=) n.410G= | |
| 14 | g.23416149G>T | CA389037591 | MHRT,MYH7 | c.4808C>A (p.Ala1603Glu) n.410G>T | |
| 14 | g.23416150C>A | CA389037594 | MHRT,MYH7 | c.4807G>T (p.Ala1603Ser) n.411C>A | gnomAD v4 |
| 14 | g.23416150C= | CA2123465555 | MHRT,MYH7 | c.4807G= (p.Ala1603=) n.411C= | |
| 14 | g.23416150C>G | CA347265 | MHRT,MYH7 | c.4807G>C (p.Ala1603Pro) n.411C>G | ClinVar dbSNP |
| 14 | g.23416150C>T | CA015331 | MHRT,MYH7 | c.4807G>A (p.Ala1603Thr) n.411C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416150_23416154del | CA2800863124 | MHRT,MYH7 | c.4803_4807del (p.Asp1602ArgfsTer21) n.411_415del | |
| 14 | g.23416151G>A | CA015322 | MHRT,MYH7 | c.4806C>T (p.Asp1602=) n.412G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416151G>C | CA389037595 | MHRT,MYH7 | c.4806C>G (p.Asp1602Glu) n.412G>C | |
| 14 | g.23416151G= | CA2123465568 | MHRT,MYH7 | c.4806C= (p.Asp1602=) n.412G= | |
| 14 | g.23416151G>T | CA389037596 | MHRT,MYH7 | c.4806C>A (p.Asp1602Glu) n.412G>T | ClinVar gnomAD v4 |
| 14 | g.23416152T>A | CA389037597 | MHRT,MYH7 | c.4805A>T (p.Asp1602Val) n.413T>A | |
| 14 | g.23416152T>C | CA389037598 | MHRT,MYH7 | c.4805A>G (p.Asp1602Gly) n.413T>C | |
| 14 | g.23416152T>G | CA389037599 | MHRT,MYH7 | c.4805A>C (p.Asp1602Ala) n.413T>G | |
| 14 | g.23416153C>A | CA389037600 | MHRT,MYH7 | c.4804G>T (p.Asp1602Tyr) n.414C>A | |
| 14 | g.23416153C>G | CA389037601 | MHRT,MYH7 | c.4804G>C (p.Asp1602His) n.414C>G | |
| 14 | g.23416153C>T | CA389037602 | MHRT,MYH7 | c.4804G>A (p.Asp1602Asn) n.414C>T | |
| 14 | g.23416154C>A | CA485766534 | MHRT,MYH7 | c.4803G>T (p.Leu1601=) n.415C>A | |
| 14 | g.23416154C= | CA2123465574 | MHRT,MYH7 | c.4803G= (p.Leu1601=) n.415C= | |
| 14 | g.23416154C>G | CA485766535 | MHRT,MYH7 | c.4803G>C (p.Leu1601=) n.415C>G | |
| 14 | g.23416154C>T | CA015317 | MHRT,MYH7 | c.4803G>A (p.Leu1601=) n.415C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416155A>C | CA389037605 | MHRT,MYH7 | c.4802T>G (p.Leu1601Arg) n.416A>C | |
| 14 | g.23416155A>G | CA389037603 | MHRT,MYH7 | c.4802T>C (p.Leu1601Pro) n.416A>G | ClinVar dbSNP |
| 14 | g.23416155A>T | CA389037604 | MHRT,MYH7 | c.4802T>A (p.Leu1601Gln) n.416A>T | |
| 14 | g.23416156G>A | CA485766536 | MHRT,MYH7 | c.4801C>T (p.Leu1601=) n.417G>A | |
| 14 | g.23416156G>C | CA389037606 | MHRT,MYH7 | c.4801C>G (p.Leu1601Val) n.417G>C | ClinVar |
| 14 | g.23416156G>T | CA389037607 | MHRT,MYH7 | c.4801C>A (p.Leu1601Met) n.417G>T | |
| 14 | g.23416158del | CA2624234372 | MHRT,MYH7 | c.4801del (p.Leu1601TrpfsTer12) n.419del | gnomAD v4 |
| 14 | g.23416157G>A | CA16606527 | MHRT,MYH7 | c.4800C>T (p.Ser1600=) n.418G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416157G>C | CA485766537 | MHRT,MYH7 | c.4800C>G (p.Ser1600=) n.418G>C | |
| 14 | g.23416157G= | CA2123465585 | MHRT,MYH7 | c.4800C= (p.Ser1600=) n.418G= | |
| 14 | g.23416157G>T | CA485766538 | MHRT,MYH7 | c.4800C>A (p.Ser1600=) n.418G>T | |
| 14 | g.23416158G>A | CA389037608 | MHRT,MYH7 | c.4799C>T (p.Ser1600Phe) n.419G>A | ClinVar |
| 14 | g.23416158G>C | CA389037609 | MHRT,MYH7 | c.4799C>G (p.Ser1600Cys) n.419G>C | |
| 14 | g.23416158G>T | CA389037610 | MHRT,MYH7 | c.4799C>A (p.Ser1600Tyr) n.419G>T | |
| 14 | g.23416158_23416159delinsGA | CA2123465590 | MHRT,MYH7 | c.4798_4799delinsTC (p.Ser1600=) n.419_420delinsGA | |
| 14 | g.23416159del | CA961068778 | MHRT,MYH7 | c.4798del (p.Ser1600ProfsTer13) n.420del | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416159A>C | CA389037611 | MHRT,MYH7 | c.4798T>G (p.Ser1600Ala) n.420A>C | |
| 14 | g.23416159A>G | CA389037612 | MHRT,MYH7 | c.4798T>C (p.Ser1600Pro) n.420A>G | ClinVar |
| 14 | g.23416159A>T | CA389037613 | MHRT,MYH7 | c.4798T>A (p.Ser1600Thr) n.420A>T | |
| 14 | g.23416160G>A | CA257810607 | MHRT,MYH7 | c.4797C>T (p.Thr1599=) n.421G>A | dbSNP gnomAD v4 |
| 14 | g.23416160G>C | CA485766539 | MHRT,MYH7 | c.4797C>G (p.Thr1599=) n.421G>C | |
| 14 | g.23416160G= | CA2123465594 | MHRT,MYH7 | c.4797C= (p.Thr1599=) n.421G= | |
| 14 | g.23416160G>T | CA485766540 | MHRT,MYH7 | c.4797C>A (p.Thr1599=) n.421G>T | |
| 14 | g.23416161G>A | CA389037614 | MHRT,MYH7 | c.4796C>T (p.Thr1599Ile) n.422G>A | |
| 14 | g.23416161G>C | CA389037615 | MHRT,MYH7 | c.4796C>G (p.Thr1599Ser) n.422G>C | |
| 14 | g.23416161G>T | CA389037616 | MHRT,MYH7 | c.4796C>A (p.Thr1599Asn) n.422G>T | |
| 14 | g.23416162T>A | CA389037618 | MHRT,MYH7 | c.4795A>T (p.Thr1599Ser) n.423T>A | gnomAD v4 |
| 14 | g.23416162T>C | CA389037617 | MHRT,MYH7 | c.4795A>G (p.Thr1599Ala) n.423T>C | |
| 14 | g.23416162T>G | CA015308 | MHRT,MYH7 | c.4795A>C (p.Thr1599Pro) n.423T>G | ClinVar dbSNP |
| 14 | g.23416162T= | CA2123465601 | MHRT,MYH7 | c.4795A= (p.Thr1599=) n.423T= | |
| 14 | g.23416163C>A | CA389037619 | MHRT,MYH7 | c.4794G>T (p.Gln1598His) n.424C>A | |
| 14 | g.23416163C>G | CA389037620 | MHRT,MYH7 | c.4794G>C (p.Gln1598His) n.424C>G | |
| 14 | g.23416163C>T | CA485766541 | MHRT,MYH7 | c.4794G>A (p.Gln1598=) n.424C>T | |
| 14 | g.23416164T>A | CA389037621 | MHRT,MYH7 | c.4793A>T (p.Gln1598Leu) n.425T>A | |
| 14 | g.23416164T>C | CA389037622 | MHRT,MYH7 | c.4793A>G (p.Gln1598Arg) n.425T>C | |
| 14 | g.23416164T>G | CA389037623 | MHRT,MYH7 | c.4793A>C (p.Gln1598Pro) n.425T>G | ClinVar dbSNP |
| 14 | g.23416165G>A | CA389037624 | MHRT,MYH7 | c.4792C>T (p.Gln1598Ter) n.426G>A | |
| 14 | g.23416165G>C | CA389037625 | MHRT,MYH7 | c.4792C>G (p.Gln1598Glu) n.426G>C | |
| 14 | g.23416165G>T | CA389037626 | MHRT,MYH7 | c.4792C>A (p.Gln1598Lys) n.426G>T | |
| 14 | g.23416166C>A | CA485766542 | MHRT,MYH7 | c.4791G>T (p.Leu1597=) n.427C>A | |
| 14 | g.23416166C>G | CA485766543 | MHRT,MYH7 | c.4791G>C (p.Leu1597=) n.427C>G | |
| 14 | g.23416166C>T | CA485766544 | MHRT,MYH7 | c.4791G>A (p.Leu1597=) n.427C>T | |
| 14 | g.23416167A>C | CA389037627 | MHRT,MYH7 | c.4790T>G (p.Leu1597Arg) n.428A>C | |
| 14 | g.23416167A>G | CA389037628 | MHRT,MYH7 | c.4790T>C (p.Leu1597Pro) n.428A>G | ClinVar dbSNP |
| 14 | g.23416167A>T | CA389037629 | MHRT,MYH7 | c.4790T>A (p.Leu1597Gln) n.428A>T | |
| 14 | g.23416168G>A | CA485766545 | MHRT,MYH7 | c.4789C>T (p.Leu1597=) n.429G>A | ClinVar dbSNP |
| 14 | g.23416168G>C | CA389037630 | MHRT,MYH7 | c.4789C>G (p.Leu1597Val) n.429G>C | |
| 14 | g.23416168G= | CA2123465611 | MHRT,MYH7 | c.4789C= (p.Leu1597=) n.429G= | |
| 14 | g.23416168G>T | CA389037631 | MHRT,MYH7 | c.4789C>A (p.Leu1597Met) n.429G>T | |
| 14 | g.23416169C>A | CA485766546 | MHRT,MYH7 | c.4788G>T (p.Ser1596=) n.430C>A | ClinVar |
| 14 | g.23416169C= | CA2123465619 | MHRT,MYH7 | c.4788G= (p.Ser1596=) n.430C= | |
| 14 | g.23416169C>G | CA485766547 | MHRT,MYH7 | c.4788G>C (p.Ser1596=) n.430C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416169C>T | CA015299 | MHRT,MYH7 | c.4788G>A (p.Ser1596=) n.430C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416170G>A | CA043848 | MHRT,MYH7 | c.4787C>T (p.Ser1596Leu) n.431G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416170G>C | CA389037633 | MHRT,MYH7 | c.4787C>G (p.Ser1596Trp) n.431G>C | |
| 14 | g.23416170G= | CA2123465623 | MHRT,MYH7 | c.4787C= (p.Ser1596=) n.431G= | |
| 14 | g.23416170G>T | CA389037632 | MHRT,MYH7 | c.4787C>A (p.Ser1596Ter) n.431G>T | |
| 14 | g.23416171A= | CA2123465630 | MHRT,MYH7 | c.4786T= (p.Ser1596=) n.432A= | |
| 14 | g.23416171A>C | CA389037634 | MHRT,MYH7 | c.4786T>G (p.Ser1596Ala) n.432A>C | |
| 14 | g.23416171A>G | CA043838 | MHRT,MYH7 | c.4786T>C (p.Ser1596Pro) n.432A>G | dbSNP ExAC gnomAD v2 |
| 14 | g.23416171A>T | CA389037635 | MHRT,MYH7 | c.4786T>A (p.Ser1596Thr) n.432A>T | |
| 14 | g.23416172G>A | CA485766548 | MHRT,MYH7 | c.4785C>T (p.Asp1595=) n.433G>A | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416172G>C | CA389037636 | MHRT,MYH7 | c.4785C>G (p.Asp1595Glu) n.433G>C | |
| 14 | g.23416172G= | CA2123465633 | MHRT,MYH7 | c.4785C= (p.Asp1595=) n.433G= | |
| 14 | g.23416172G>T | CA389037637 | MHRT,MYH7 | c.4785C>A (p.Asp1595Glu) n.433G>T | |
| 14 | g.23416173T>A | CA389037638 | MHRT,MYH7 | c.4784A>T (p.Asp1595Val) n.434T>A | |
| 14 | g.23416173T>C | CA389037639 | MHRT,MYH7 | c.4784A>G (p.Asp1595Gly) n.434T>C | |
| 14 | g.23416173T>G | CA389037640 | MHRT,MYH7 | c.4784A>C (p.Asp1595Ala) n.434T>G | |
| 14 | g.23416174C>A | CA389037641 | MHRT,MYH7 | c.4783G>T (p.Asp1595Tyr) n.435C>A | |
| 14 | g.23416174C= | CA2123465636 | MHRT,MYH7 | c.4783G= (p.Asp1595=) n.435C= | |
| 14 | g.23416174C>G | CA389037642 | MHRT,MYH7 | c.4783G>C (p.Asp1595His) n.435C>G | |
| 14 | g.23416174C>T | CA389037643 | MHRT,MYH7 | c.4783G>A (p.Asp1595Asn) n.435C>T | ClinVar dbSNP |
| 14 | g.23416175C>A | CA485766549 | MHRT,MYH7 | c.4782G>T (p.Val1594=) n.436C>A | |
| 14 | g.23416175C>G | CA485766550 | MHRT,MYH7 | c.4782G>C (p.Val1594=) n.436C>G | |
| 14 | g.23416175C>T | CA485766551 | MHRT,MYH7 | c.4782G>A (p.Val1594=) n.436C>T | |
| 14 | g.23416176A= | CA2123465652 | MHRT,MYH7 | c.4781T= (p.Val1594=) n.437A= | |
| 14 | g.23416176A>C | CA389037644 | MHRT,MYH7 | c.4781T>G (p.Val1594Gly) n.437A>C | dbSNP |
| 14 | g.23416176A>G | CA389037645 | MHRT,MYH7 | c.4781T>C (p.Val1594Ala) n.437A>G | |
| 14 | g.23416176A>T | CA389037646 | MHRT,MYH7 | c.4781T>A (p.Val1594Glu) n.437A>T | |
| 14 | g.23416177C>A | CA389037648 | MHRT,MYH7 | c.4780G>T (p.Val1594Leu) n.438C>A | gnomAD v4 |
| 14 | g.23416177C= | CA2123465657 | MHRT,MYH7 | c.4780G= (p.Val1594=) n.438C= | |
| 14 | g.23416177C>G | CA043815 | MHRT,MYH7 | c.4780G>C (p.Val1594Leu) n.438C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416177C>T | CA389037647 | MHRT,MYH7 | c.4780G>A (p.Val1594Met) n.438C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416178C>A | CA485766552 | MHRT,MYH7 | c.4779G>T (p.Val1593=) n.439C>A | gnomAD v4 |
| 14 | g.23416178C= | CA2123465662 | MHRT,MYH7 | c.4779G= (p.Val1593=) n.439C= | |
| 14 | g.23416178C>G | CA485766553 | MHRT,MYH7 | c.4779G>C (p.Val1593=) n.439C>G | dbSNP |
| 14 | g.23416178C>T | CA485766554 | MHRT,MYH7 | c.4779G>A (p.Val1593=) n.439C>T | |
| 14 | g.23416179A>C | CA389037649 | MHRT,MYH7 | c.4778T>G (p.Val1593Gly) n.440A>C | |
| 14 | g.23416179A>G | CA389037650 | MHRT,MYH7 | c.4778T>C (p.Val1593Ala) n.440A>G | |
| 14 | g.23416179A>T | CA389037651 | MHRT,MYH7 | c.4778T>A (p.Val1593Glu) n.440A>T | |
| 14 | g.23416180C>A | CA389037652 | MHRT,MYH7 | c.4777G>T (p.Val1593Leu) n.441C>A | ClinVar |
| 14 | g.23416180C>G | CA389037653 | MHRT,MYH7 | c.4777G>C (p.Val1593Leu) n.441C>G | |
| 14 | g.23416180C>T | CA389037654 | MHRT,MYH7 | c.4777G>A (p.Val1593Met) n.441C>T | gnomAD v4 |
| 14 | g.23416181C>A | CA485766555 | MHRT,MYH7 | c.4776G>T (p.Arg1592=) n.442C>A | COSMIC |
| 14 | g.23416181C= | CA2123465669 | MHRT,MYH7 | c.4776G= (p.Arg1592=) n.442C= | |
| 14 | g.23416181C>G | CA485766556 | MHRT,MYH7 | c.4776G>C (p.Arg1592=) n.442C>G | dbSNP |
| 14 | g.23416181C>T | CA485766557 | MHRT,MYH7 | c.4776G>A (p.Arg1592=) n.442C>T | |
| 14 | g.23416182C>A | CA389037655 | MHRT,MYH7 | c.4775G>T (p.Arg1592Leu) n.443C>A | dbSNP gnomAD v4 |
| 14 | g.23416182C= | CA2123465676 | MHRT,MYH7 | c.4775G= (p.Arg1592=) n.443C= | |
| 14 | g.23416182C>G | CA389037656 | MHRT,MYH7 | c.4775G>C (p.Arg1592Pro) n.443C>G | |
| 14 | g.23416182C>T | CA389037657 | MHRT,MYH7 | c.4775G>A (p.Arg1592Gln) n.443C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416183G>A | CA389037658 | MHRT,MYH7 | c.4774C>T (p.Arg1592Trp) n.444G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23416183G>C | CA389037659 | MHRT,MYH7 | c.4774C>G (p.Arg1592Gly) n.444G>C | |
| 14 | g.23416183G= | CA2123465685 | MHRT,MYH7 | c.4774C= (p.Arg1592=) n.444G= | |
| 14 | g.23416183G>T | CA485766558 | MHRT,MYH7 | c.4774C>A (p.Arg1592=) n.444G>T | |
| 14 | g.23416184C>A | CA485766559 | MHRT,MYH7 | c.4773G>T (p.Leu1591=) n.445C>A | |
| 14 | g.23416184C= | CA2123465692 | MHRT,MYH7 | c.4773G= (p.Leu1591=) n.445C= | |
| 14 | g.23416184C>G | CA485766561 | MHRT,MYH7 | c.4773G>C (p.Leu1591=) n.445C>G | |
| 14 | g.23416184C>T | CA485766560 | MHRT,MYH7 | c.4773G>A (p.Leu1591=) n.445C>T | dbSNP |
| 14 | g.23416185A= | CA2123465700 | MHRT,MYH7 | c.4772T= (p.Leu1591=) n.446A= | |
| 14 | g.23416185A>C | CA389037660 | MHRT,MYH7 | c.4772T>G (p.Leu1591Arg) n.446A>C | |
| 14 | g.23416185A>G | CA347262 | MHRT,MYH7 | c.4772T>C (p.Leu1591Pro) n.446A>G | ClinVar dbSNP |
| 14 | g.23416185A>T | CA015292 | MHRT,MYH7 | c.4772T>A (p.Leu1591Gln) n.446A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416186G>A | CA485766562 | MHRT,MYH7 | c.4771C>T (p.Leu1591=) n.447G>A | |
| 14 | g.23416186G>C | CA389037661 | MHRT,MYH7 | c.4771C>G (p.Leu1591Val) n.447G>C | |
| 14 | g.23416186G>T | CA389037662 | MHRT,MYH7 | c.4771C>A (p.Leu1591Met) n.447G>T | |
| 14 | g.23416189_23416191del | CA2624234448 | MHRT,MYH7 | c.4769_4771del (p.His1590del) n.450_452del | gnomAD v4 |
| 14 | g.23416187G>A | CA043793 | MHRT,MYH7 | c.4770C>T (p.His1590=) n.448G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23416187G>C | CA389037663 | MHRT,MYH7 | c.4770C>G (p.His1590Gln) n.448G>C | |
| 14 | g.23416187G= | CA2123465703 | MHRT,MYH7 | c.4770C= (p.His1590=) n.448G= | |
| 14 | g.23416187G>T | CA389037664 | MHRT,MYH7 | c.4770C>A (p.His1590Gln) n.448G>T | gnomAD v4 |
| 14 | g.23416188T>A | CA389037665 | MHRT,MYH7 | c.4769A>T (p.His1590Leu) n.449T>A | |
| 14 | g.23416188T>C | CA389037666 | MHRT,MYH7 | c.4769A>G (p.His1590Arg) n.449T>C | |
| 14 | g.23416188T>G | CA389037667 | MHRT,MYH7 | c.4769A>C (p.His1590Pro) n.449T>G | |
| 14 | g.23416189G>A | CA389037668 | MHRT,MYH7 | c.4768C>T (p.His1590Tyr) n.450G>A | |
| 14 | g.23416189G>C | CA389037669 | MHRT,MYH7 | c.4768C>G (p.His1590Asp) n.450G>C | |
| 14 | g.23416189G>T | CA389037670 | MHRT,MYH7 | c.4768C>A (p.His1590Asn) n.450G>T | |
| 14 | g.23416190G>A | CA485766563 | MHRT,MYH7 | c.4767C>T (p.Asn1589=) n.451G>A | ClinVar |
| 14 | g.23416190G>C | CA389037671 | MHRT,MYH7 | c.4767C>G (p.Asn1589Lys) n.451G>C | dbSNP |
| 14 | g.23416190G>T | CA389037672 | MHRT,MYH7 | c.4767C>A (p.Asn1589Lys) n.451G>T | COSMIC |
| 14 | g.23416191T>A | CA389037673 | MHRT,MYH7 | c.4766A>T (p.Asn1589Ile) n.452T>A | |
| 14 | g.23416191T>C | CA389037675 | MHRT,MYH7 | c.4766A>G (p.Asn1589Ser) n.452T>C | |
| 14 | g.23416191T>G | CA389037674 | MHRT,MYH7 | c.4766A>C (p.Asn1589Thr) n.452T>G | |
| 14 | g.23416192del | CA2575486617 | MHRT,MYH7 | c.4766del (p.Asn1589ThrfsTer24) n.453del | |
| 14 | g.23416192T>A | CA389037676 | MHRT,MYH7 | c.4765A>T (p.Asn1589Tyr) n.453T>A | |
| 14 | g.23416192T>C | CA389037678 | MHRT,MYH7 | c.4765A>G (p.Asn1589Asp) n.453T>C | |
| 14 | g.23416192T>G | CA389037677 | MHRT,MYH7 | c.4765A>C (p.Asn1589His) n.453T>G | gnomAD v4 |
| 14 | g.23416193G>A | CA485766564 | MHRT,MYH7 | c.4764C>T (p.Arg1588=) n.454G>A | ClinVar dbSNP |
| 14 | g.23416193G>C | CA485766565 | MHRT,MYH7 | c.4764C>G (p.Arg1588=) n.454G>C | |
| 14 | g.23416193G= | CA2123465708 | MHRT,MYH7 | c.4764C= (p.Arg1588=) n.454G= | |
| 14 | g.23416193G>T | CA485766566 | MHRT,MYH7 | c.4764C>A (p.Arg1588=) n.454G>T | |
| 14 | g.23416194C>A | CA389037679 | MHRT,MYH7 | c.4763G>T (p.Arg1588Leu) n.455C>A | |
| 14 | g.23416194C= | CA2123465723 | MHRT,MYH7 | c.4763G= (p.Arg1588=) n.455C= | |
| 14 | g.23416194C>G | CA347259 | MHRT,MYH7 | c.4763G>C (p.Arg1588Pro) n.455C>G | dbSNP |
| 14 | g.23416194C>T | CA389037680 | MHRT,MYH7 | c.4763G>A (p.Arg1588His) n.455C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23416195G>A | CA389037681 | MHRT,MYH7 | c.4762C>T (p.Arg1588Cys) n.456G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23416195G>C | CA389037682 | MHRT,MYH7 | c.4762C>G (p.Arg1588Gly) n.456G>C | gnomAD v4 |
| 14 | g.23416195G= | CA2123465732 | MHRT,MYH7 | c.4762C= (p.Arg1588=) n.456G= | |
| 14 | g.23416195G>T | CA389037683 | MHRT,MYH7 | c.4762C>A (p.Arg1588Ser) n.456G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416196C>A | CA389037684 | MHRT,MYH7 | c.4761G>T (p.Lys1587Asn) n.457C>A | |
| 14 | g.23416196C>G | CA389037685 | MHRT,MYH7 | c.4761G>C (p.Lys1587Asn) n.457C>G | |
| 14 | g.23416196C>T | CA485766567 | MHRT,MYH7 | c.4761G>A (p.Lys1587=) n.457C>T | |
| 14 | g.23416197T>A | CA389037686 | MHRT,MYH7 | c.4760A>T (p.Lys1587Met) n.458T>A | |
| 14 | g.23416197T>C | CA389037687 | MHRT,MYH7 | c.4760A>G (p.Lys1587Arg) n.458T>C | COSMIC |
| 14 | g.23416197T>G | CA389037688 | MHRT,MYH7 | c.4760A>C (p.Lys1587Thr) n.458T>G | |
| 14 | g.23416198T>A | CA389037691 | MHRT,MYH7 | c.4759A>T (p.Lys1587Ter) n.459T>A | |
| 14 | g.23416198T>C | CA389037690 | MHRT,MYH7 | c.4759A>G (p.Lys1587Glu) n.459T>C | |
| 14 | g.23416198T>G | CA389037689 | MHRT,MYH7 | c.4759A>C (p.Lys1587Gln) n.459T>G | |
| 14 | g.23416199G>A | CA485766568 | MHRT,MYH7 | c.4758C>T (p.Ala1586=) n.460G>A | |
| 14 | g.23416199G>C | CA485766569 | MHRT,MYH7 | c.4758C>G (p.Ala1586=) n.460G>C | |
| 14 | g.23416199G>T | CA485766570 | MHRT,MYH7 | c.4758C>A (p.Ala1586=) n.460G>T | |
| 14 | g.23416200G>A | CA389037692 | MHRT,MYH7 | c.4757C>T (p.Ala1586Val) n.461G>A | |
| 14 | g.23416200G>C | CA389037693 | MHRT,MYH7 | c.4757C>G (p.Ala1586Gly) n.461G>C | ClinVar dbSNP |
| 14 | g.23416200G= | CA2123465743 | MHRT,MYH7 | c.4757C= (p.Ala1586=) n.461G= | |
| 14 | g.23416200G>T | CA389037694 | MHRT,MYH7 | c.4757C>A (p.Ala1586Asp) n.461G>T | |
| 14 | g.23416201C>A | CA389037695 | MHRT,MYH7 | c.4756G>T (p.Ala1586Ser) n.462C>A | |
| 14 | g.23416201C= | CA2123465750 | MHRT,MYH7 | c.4756G= (p.Ala1586=) n.462C= | |
| 14 | g.23416201C>G | CA389037696 | MHRT,MYH7 | c.4756G>C (p.Ala1586Pro) n.462C>G | |
| 14 | g.23416201C>T | CA389037697 | MHRT,MYH7 | c.4756G>A (p.Ala1586Thr) n.462C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23416202C>A | CA389037698 | MHRT,MYH7 | c.4755G>T (p.Gln1585His) n.463C>A | |
| 14 | g.23416202C>G | CA389037699 | MHRT,MYH7 | c.4755G>C (p.Gln1585His) n.463C>G | gnomAD v4 |
| 14 | g.23416202C>T | CA485766571 | MHRT,MYH7 | c.4755G>A (p.Gln1585=) n.463C>T | |
| 14 | g.23416203T>A | CA389037700 | MHRT,MYH7 | c.4754A>T (p.Gln1585Leu) n.464T>A | |
| 14 | g.23416203T>C | CA389037701 | MHRT,MYH7 | c.4754A>G (p.Gln1585Arg) n.464T>C | |
| 14 | g.23416203T>G | CA389037702 | MHRT,MYH7 | c.4754A>C (p.Gln1585Pro) n.464T>G | |
| 14 | g.23416204G>A | CA389037705 | MHRT,MYH7 | c.4753C>T (p.Gln1585Ter) n.465G>A | gnomAD v4 |
| 14 | g.23416204G>C | CA389037704 | MHRT,MYH7 | c.4753C>G (p.Gln1585Glu) n.465G>C | |
| 14 | g.23416204G>T | CA389037703 | MHRT,MYH7 | c.4753C>A (p.Gln1585Lys) n.465G>T | |
| 14 | g.23416205T>A | CA389037706 | MHRT,MYH7 | c.4752A>T (p.Glu1584Asp) n.466T>A | |
| 14 | g.23416205T>C | CA485766572 | MHRT,MYH7 | c.4752A>G (p.Glu1584=) n.466T>C | ClinVar dbSNP |
| 14 | g.23416205T>G | CA389037707 | MHRT,MYH7 | c.4752A>C (p.Glu1584Asp) n.466T>G | |
| 14 | g.23416205T= | CA2123465758 | MHRT,MYH7 | c.4752A= (p.Glu1584=) n.466T= | |
| 14 | g.23416206T>A | CA389037708 | MHRT,MYH7 | c.4751A>T (p.Glu1584Val) n.467T>A | |
| 14 | g.23416206T>C | CA043766 | MHRT,MYH7 | c.4751A>G (p.Glu1584Gly) n.467T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416206T>G | CA389037709 | MHRT,MYH7 | c.4751A>C (p.Glu1584Ala) n.467T>G | |
| 14 | g.23416206T= | CA2123465762 | MHRT,MYH7 | c.4751A= (p.Glu1584=) n.467T= | |
| 14 | g.23416207C>A | CA389037710 | MHRT,MYH7 | c.4750G>T (p.Glu1584Ter) n.468C>A | |
| 14 | g.23416207C>G | CA389037711 | MHRT,MYH7 | c.4750G>C (p.Glu1584Gln) n.468C>G | |
| 14 | g.23416207C>T | CA389037712 | MHRT,MYH7 | c.4750G>A (p.Glu1584Lys) n.468C>T | |
| 14 | g.23416208C>A | CA389037713 | MHRT,MYH7 | c.4749G>T (p.Met1583Ile) n.469C>A | ClinVar dbSNP |
| 14 | g.23416208C= | CA2123465770 | MHRT,MYH7 | c.4749G= (p.Met1583=) n.469C= | |
| 14 | g.23416208C>G | CA389037714 | MHRT,MYH7 | c.4749G>C (p.Met1583Ile) n.469C>G | |
| 14 | g.23416208C>T | CA389037715 | MHRT,MYH7 | c.4749G>A (p.Met1583Ile) n.469C>T | gnomAD v4 |
| 14 | g.23416209A= | CA2123465776 | MHRT,MYH7 | c.4748T= (p.Met1583=) n.470A= | |
| 14 | g.23416209A>C | CA389037718 | MHRT,MYH7 | c.4748T>G (p.Met1583Arg) n.470A>C | |
| 14 | g.23416209A>G | CA389037717 | MHRT,MYH7 | c.4748T>C (p.Met1583Thr) n.470A>G | dbSNP |
| 14 | g.23416209A>T | CA389037716 | MHRT,MYH7 | c.4748T>A (p.Met1583Lys) n.470A>T | |
| 14 | g.23416210T>A | CA389037719 | MHRT,MYH7 | c.4747A>T (p.Met1583Leu) n.471T>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416210T>C | CA389037720 | MHRT,MYH7 | c.4747A>G (p.Met1583Val) n.471T>C | |
| 14 | g.23416210T>G | CA389037721 | MHRT,MYH7 | c.4747A>C (p.Met1583Leu) n.471T>G | |
| 14 | g.23416210T= | CA2123465782 | MHRT,MYH7 | c.4747A= (p.Met1583=) n.471T= | |
| 14 | g.23416210_23416213delinsTCTC | CA2123465788 | MHRT,MYH7 | c.4744_4747delinsGAGA (p.Glu1582=) n.471_474delinsTCTC | |
| 14 | g.23416211C>A | CA389037722 | MHRT,MYH7 | c.4746G>T (p.Glu1582Asp) n.472C>A | |
| 14 | g.23416211C= | CA2123465797 | MHRT,MYH7 | c.4746G= (p.Glu1582=) n.472C= | |
| 14 | g.23416211C>G | CA389037723 | MHRT,MYH7 | c.4746G>C (p.Glu1582Asp) n.472C>G | ClinVar dbSNP |
| 14 | g.23416211C>T | CA485766573 | MHRT,MYH7 | c.4746G>A (p.Glu1582=) n.472C>T | |
| 14 | g.23416214_23416216del | CA658658244 | MHRT,MYH7 | c.4744_4746del (p.Glu1582del) n.475_477del | ClinVar dbSNP |
| 14 | g.23416212T>A | CA389037724 | MHRT,MYH7 | c.4745A>T (p.Glu1582Val) n.473T>A | |
| 14 | g.23416212T>C | CA389037725 | MHRT,MYH7 | c.4745A>G (p.Glu1582Gly) n.473T>C | |
| 14 | g.23416212T>G | CA389037726 | MHRT,MYH7 | c.4745A>C (p.Glu1582Ala) n.473T>G | |
| 14 | g.23416213C>A | CA389037727 | MHRT,MYH7 | c.4744G>T (p.Glu1582Ter) n.474C>A | COSMIC |
| 14 | g.23416213C= | CA2123465804 | MHRT,MYH7 | c.4744G= (p.Glu1582=) n.474C= | |
| 14 | g.23416213C>G | CA389037728 | MHRT,MYH7 | c.4744G>C (p.Glu1582Gln) n.474C>G | |
| 14 | g.23416213C>T | CA389037729 | MHRT,MYH7 | c.4744G>A (p.Glu1582Lys) n.474C>T | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23416214C>A | CA389037730 | MHRT,MYH7 | c.4743G>T (p.Glu1581Asp) n.475C>A | |
| 14 | g.23416214C>G | CA389037731 | MHRT,MYH7 | c.4743G>C (p.Glu1581Asp) n.475C>G | |
| 14 | g.23416214C>T | CA485766574 | MHRT,MYH7 | c.4743G>A (p.Glu1581=) n.475C>T | gnomAD v4 |
| 14 | g.23416215T>A | CA389037733 | MHRT,MYH7 | c.4742A>T (p.Glu1581Val) n.476T>A | |
| 14 | g.23416215T>C | CA389037734 | MHRT,MYH7 | c.4742A>G (p.Glu1581Gly) n.476T>C | |
| 14 | g.23416215T>G | CA389037732 | MHRT,MYH7 | c.4742A>C (p.Glu1581Ala) n.476T>G | |
| 14 | g.23416216C>A | CA389037737 | MHRT,MYH7 | c.4741G>T (p.Glu1581Ter) n.477C>A | |
| 14 | g.23416216C= | CA2123465811 | MHRT,MYH7 | c.4741G= (p.Glu1581=) n.477C= | |
| 14 | g.23416216C>G | CA389037735 | MHRT,MYH7 | c.4741G>C (p.Glu1581Gln) n.477C>G | |
| 14 | g.23416216C>T | CA389037736 | MHRT,MYH7 | c.4741G>A (p.Glu1581Lys) n.477C>T | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.23416217G>A | CA043734 | MHRT,MYH7 | c.4740C>T (p.Asp1580=) n.478G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23416217G>C | CA389037738 | MHRT,MYH7 | c.4740C>G (p.Asp1580Glu) n.478G>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23416217G= | CA2123465820 | MHRT,MYH7 | c.4740C= (p.Asp1580=) n.478G= | |
| 14 | g.23416217G>T | CA389037739 | MHRT,MYH7 | c.4740C>A (p.Asp1580Glu) n.478G>T | gnomAD v4 |
| 14 | g.23416218T>A | CA389037740 | MHRT,MYH7 | c.4739A>T (p.Asp1580Val) n.479T>A | |
| 14 | g.23416218T>C | CA389037741 | MHRT,MYH7 | c.4739A>G (p.Asp1580Gly) n.479T>C | |
| 14 | g.23416218T>G | CA389037742 | MHRT,MYH7 | c.4739A>C (p.Asp1580Ala) n.479T>G | |
| 14 | g.23416219C>A | CA389037743 | MHRT,MYH7 | c.4738G>T (p.Asp1580Tyr) n.480C>A | |
| 14 | g.23416219C>G | CA389037744 | MHRT,MYH7 | c.4738G>C (p.Asp1580His) n.480C>G | |
| 14 | g.23416219C>T | CA389037745 | MHRT,MYH7 | c.4738G>A (p.Asp1580Asn) n.480C>T | COSMIC |
| 14 | g.23416220C>A | CA389037746 | MHRT,MYH7 | c.4737G>T (p.Lys1579Asn) n.481C>A | |
| 14 | g.23416220C>G | CA389037747 | MHRT,MYH7 | c.4737G>C (p.Lys1579Asn) n.481C>G | |
| 14 | g.23416220C>T | CA485766360 | MHRT,MYH7 | c.4737G>A (p.Lys1579=) n.481C>T | |
| 14 | g.23416222_23416224del | CA2580087877 | MHRT,MYH7 | c.4735_4737del (p.Lys1579del) n.483_485del | ClinVar |
| 14 | g.23416221T>A | CA389037750 | MHRT,MYH7 | c.4736A>T (p.Lys1579Met) n.482T>A | |
| 14 | g.23416221T>C | CA389037749 | MHRT,MYH7 | c.4736A>G (p.Lys1579Arg) n.482T>C | |
| 14 | g.23416221T>G | CA389037748 | MHRT,MYH7 | c.4736A>C (p.Lys1579Thr) n.482T>G | |
| 14 | g.23416222T>A | CA389037751 | MHRT,MYH7 | c.4735A>T (p.Lys1579Ter) n.483T>A | gnomAD v4 |
| 14 | g.23416222T>C | CA389037752 | MHRT,MYH7 | c.4735A>G (p.Lys1579Glu) n.483T>C | |
| 14 | g.23416222T>G | CA389037753 | MHRT,MYH7 | c.4735A>C (p.Lys1579Gln) n.483T>G |