Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23418135C>TCA2575504205MYH7c.4169+75G>A (n.4169+75G>A)
gnomAD v4
14g.23418136T>GCA2575504206MYH7c.4169+74A>C (n.4169+74A>C)
14g.23418137G>ACA704287663MYH7c.4169+73C>T (n.4169+73C>T)
dbSNP gnomAD v3 gnomAD v4
14g.23418137G>CCA2575504207MYH7c.4169+73C>G (n.4169+73C>G)
14g.23418137G=CA2123442325MYH7c.4169+73C= (n.4169+73C=)
14g.23418140G>ACA913896085MYH7c.4169+70C>T (n.4169+70C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418140G=CA2123442327MYH7c.4169+70C= (n.4169+70C=)
14g.23418141A>TCA2575504208MYH7c.4169+69T>A (n.4169+69T>A)
14g.23418142G>ACA613318022MYH7c.4169+68C>T (n.4169+68C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418142G=CA2123442328MYH7c.4169+68C= (n.4169+68C=)
14g.23418142G>TCA2575504209MYH7c.4169+68C>A (n.4169+68C>A)
14g.23418143G>ACA2624239922MYH7c.4169+67C>T (n.4169+67C>T)
gnomAD v4
14g.23418144C=CA2123442330MYH7c.4169+66G= (n.4169+66G=)
14g.23418144C>GCA257813640MYH7c.4169+66G>C (n.4169+66G>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418145T>GCA2575504210MYH7c.4169+65A>C (n.4169+65A>C)
14g.23418146_23418150dupCA2624239926MYH7c.4169+60_4169+64dup (n.4169+60_4169+64dup)
gnomAD v4
14g.23418147G>ACA2624239927MYH7c.4169+63C>T (n.4169+63C>T)
gnomAD v4
14g.23418147G>CCA2624239931MYH7c.4169+63C>G (n.4169+63C>G)
gnomAD v4
14g.23418147G>TCA2575504211MYH7c.4169+63C>A (n.4169+63C>A)
14g.23418148G>ACA2624239933MYH7c.4169+62C>T (n.4169+62C>T)
gnomAD v4
14g.23418149G>CCA2624239937MYH7c.4169+61C>G (n.4169+61C>G)
gnomAD v4
14g.23418150C=CA2123442332MYH7c.4169+60G= (n.4169+60G=)
14g.23418150C>TCA961070139MYH7c.4169+60G>A (n.4169+60G>A)
dbSNP gnomAD v3 gnomAD v4
14g.23418151T>CCA2624239941MYH7c.4169+59A>G (n.4169+59A>G)
gnomAD v4
14g.23418152G>ACA2800863418MYH7c.4169+58C>T (n.4169+58C>T)
14g.23418152G=CA2123442333MYH7c.4169+58C= (n.4169+58C=)
14g.23418152G>TCA2123442334MYH7c.4169+58C>A (n.4169+58C>A)
dbSNP gnomAD v4
14g.23418154delCA2624239943MYH7c.4169+58del (n.4169+58del)
gnomAD v4
14g.23418155C>TCA2624239944MYH7c.4169+55G>A (n.4169+55G>A)
gnomAD v4
14g.23418156T>CCA2624239946MYH7c.4169+54A>G (n.4169+54A>G)
gnomAD v4
14g.23418156T>GCA2624239947MYH7c.4169+54A>C (n.4169+54A>C)
gnomAD v4
14g.23418158A=CA2123442336MYH7c.4169+52T= (n.4169+52T=)
14g.23418158A>GCA2123442337MYH7c.4169+52T>C (n.4169+52T>C)
dbSNP gnomAD v4
14g.23418159G>ACA2624239949MYH7c.4169+51C>T (n.4169+51C>T)
gnomAD v4
14g.23418160T>CCA2624239951MYH7c.4169+50A>G (n.4169+50A>G)
gnomAD v4
14g.23418160T>GCA2123442339MYH7c.4169+50A>C (n.4169+50A>C)
dbSNP
14g.23418160T=CA2123442338MYH7c.4169+50A= (n.4169+50A=)
14g.23418161C=CA2123442340MYH7c.4169+49G= (n.4169+49G=)
14g.23418161C>GCA2728941060MYH7c.4169+49G>C (n.4169+49G>C)
dbSNP
14g.23418161C>TCA613318023MYH7c.4169+49G>A (n.4169+49G>A)
dbSNP gnomAD v2
14g.23418164G>ACA2123442342MYH7c.4169+46C>T (n.4169+46C>T)
dbSNP gnomAD v4
14g.23418164G=CA2123442343MYH7c.4169+46C= (n.4169+46C=)
14g.23418167T>CCA040943MYH7c.4169+43A>G (n.4169+43A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418167T=CA2123442344MYH7c.4169+43A= (n.4169+43A=)
14g.23418168G>ACA613318024MYH7c.4169+42C>T (n.4169+42C>T)
dbSNP gnomAD v2 gnomAD v4
14g.23418168G=CA2123442346MYH7c.4169+42C= (n.4169+42C=)
14g.23418169C>ACA2624239966MYH7c.4169+41G>T (n.4169+41G>T)
gnomAD v4
14g.23418173G>CCA257813646MYH7c.4169+37C>G (n.4169+37C>G)
dbSNP gnomAD v2 gnomAD v4
14g.23418173G=CA2123442351MYH7c.4169+37C= (n.4169+37C=)
14g.23418175G>ACA2624239971MYH7c.4169+35C>T (n.4169+35C>T)
gnomAD v4
14g.23418176G>ACA2123442356MYH7c.4169+34C>T (n.4169+34C>T)
dbSNP gnomAD v3 gnomAD v4
14g.23418176G>CCA2123442357MYH7c.4169+34C>G (n.4169+34C>G)
dbSNP
14g.23418176G=CA2123442355MYH7c.4169+34C= (n.4169+34C=)
14g.23418176G>TCA2624239998MYH7c.4169+34C>A (n.4169+34C>A)
gnomAD v4
14g.23418177C>ACA257813647MYH7c.4169+33G>T (n.4169+33G>T)
dbSNP gnomAD v2 gnomAD v4
14g.23418177C=CA2123442360MYH7c.4169+33G= (n.4169+33G=)
14g.23418177C>GCA2624240002MYH7c.4169+33G>C (n.4169+33G>C)
gnomAD v4
14g.23418178C>TCA2575504212MYH7c.4169+32G>A (n.4169+32G>A)
14g.23418180C>TCA2624240004MYH7c.4169+30G>A (n.4169+30G>A)
gnomAD v4
14g.23418180_23418193delCA2800863422MYH7c.4169+17_4169+30del (n.4169+17_4169+30del)
14g.23418181A=CA2123442361MYH7c.4169+29T= (n.4169+29T=)
14g.23418181A>CCA257813652MYH7c.4169+29T>G (n.4169+29T>G)
dbSNP
14g.23418182G>ACA613318025MYH7c.4169+28C>T (n.4169+28C>T)
dbSNP gnomAD v2 gnomAD v4
14g.23418182G=CA2123442363MYH7c.4169+28C= (n.4169+28C=)
14g.23418183C>ACA2800863425MYH7c.4169+27G>T (n.4169+27G>T)
14g.23418185A=CA2123442364MYH7c.4169+25T= (n.4169+25T=)
14g.23418185A>GCA613318026MYH7c.4169+25T>C (n.4169+25T>C)
dbSNP gnomAD v2 gnomAD v4
14g.23418188A=CA2123442367MYH7c.4169+22T= (n.4169+22T=)
14g.23418188A>TCA257813670MYH7c.4169+22T>A (n.4169+22T>A)
dbSNP
14g.23418189G>ACA2575504213MYH7c.4169+21C>T (n.4169+21C>T)
14g.23418193G>ACA2575504214MYH7c.4169+17C>T (n.4169+17C>T)
14g.23418193G>CCA257813673MYH7c.4169+17C>G (n.4169+17C>G)
dbSNP
14g.23418193G=CA2123442370MYH7c.4169+17C= (n.4169+17C=)
14g.23418196T>ACA2624240008MYH7c.4169+14A>T (n.4169+14A>T)
gnomAD v4
14g.23418197G>ACA2624240009MYH7c.4169+13C>T (n.4169+13C>T)
gnomAD v4
14g.23418197G>CCA2624240010MYH7c.4169+13C>G (n.4169+13C>G)
gnomAD v4
14g.23418197G>TCA2624240012MYH7c.4169+13C>A (n.4169+13C>A)
gnomAD v4
14g.23418198C=CA2123442374MYH7c.4169+12G= (n.4169+12G=)
14g.23418198C>TCA613318027MYH7c.4169+12G>A (n.4169+12G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23418200C=CA2123442376MYH7c.4169+10G= (n.4169+10G=)
14g.23418200C>TCA613318028MYH7c.4169+10G>A (n.4169+10G>A)
dbSNP gnomAD v2 gnomAD v4
14g.23418202G>ACA613318029MYH7c.4169+8C>T (n.4169+8C>T)
dbSNP gnomAD v2 gnomAD v4
14g.23418202G=CA2123442378MYH7c.4169+8C= (n.4169+8C=)
14g.23418203A=CA2123442382MYH7c.4169+7T= (n.4169+7T=)
14g.23418203A>GCA704287707MYH7c.4169+7T>C (n.4169+7T>C)
ClinVar dbSNP gnomAD v4
14g.23418204A=CA2123442385MYH7c.4169+6T= (n.4169+6T=)
14g.23418204A>CCA10639968MYH7c.4169+6T>G (n.4169+6T>G)
ClinVar dbSNP gnomAD v4
14g.23418208A>CCA389040685MYH7c.4169+2T>G (n.4169+2T>G)
14g.23418208A>GCA389040686MYH7c.4169+2T>C (n.4169+2T>C)
14g.23418208A>TCA389040688MYH7c.4169+2T>A (n.4169+2T>A)
14g.23418209C>ACA389040689MYH7c.4169+1G>T (n.4169+1G>T)
14g.23418209C>GCA389040691MYH7c.4169+1G>C (n.4169+1G>C)
14g.23418209C>TCA389040692MYH7c.4169+1G>A (n.4169+1G>A)
14g.23418210T>ACA389040694MYH7c.4169A>T (p.Lys1390Met)
14g.23418210T>CCA389040696MYH7c.4169A>G (p.Lys1390Arg)
ClinVar dbSNP
14g.23418210T>GCA389040698MYH7c.4169A>C (p.Lys1390Thr)
14g.23418210T=CA2123442390MYH7c.4169A= (p.Lys1390=)
14g.23418211T>ACA389040699MYH7c.4168A>T (p.Lys1390Ter)
14g.23418211T>CCA389040700MYH7c.4168A>G (p.Lys1390Glu)
14g.23418211T>GCA389040702MYH7c.4168A>C (p.Lys1390Gln)
14g.23418212G>ACA485618255MYH7c.4167C>T (p.Ala1389=)
gnomAD v4
14g.23418212G>CCA485618256MYH7c.4167C>G (p.Ala1389=)
14g.23418212G>TCA485618258MYH7c.4167C>A (p.Ala1389=)
14g.23418213delCA2729049331MYH7c.4167del (p.Lys1390ArgfsTer?)
dbSNP
14g.23418213G>ACA389040707MYH7c.4166C>T (p.Ala1389Val)
14g.23418213G>CCA389040706MYH7c.4166C>G (p.Ala1389Gly)
14g.23418213G>TCA389040704MYH7c.4166C>A (p.Ala1389Asp)
14g.23418214C>ACA389040708MYH7c.4165G>T (p.Ala1389Ser)
14g.23418214C>GCA389040710MYH7c.4165G>C (p.Ala1389Pro)
14g.23418214C>TCA389040712MYH7c.4165G>A (p.Ala1389Thr)
14g.23418215C>ACA389040713MYH7c.4164G>T (p.Glu1388Asp)
ClinVar dbSNP gnomAD v4
14g.23418215C=CA2123442394MYH7c.4164G= (p.Glu1388=)
14g.23418215C>GCA389040715MYH7c.4164G>C (p.Glu1388Asp)
14g.23418215C>TCA485618259MYH7c.4164G>A (p.Glu1388=)
ClinVar dbSNP
14g.23418216T>ACA389040717MYH7c.4163A>T (p.Glu1388Val)
14g.23418216T>CCA389040722MYH7c.4163A>G (p.Glu1388Gly)
14g.23418216T>GCA389040723MYH7c.4163A>C (p.Glu1388Ala)
14g.23418217C>ACA389040726MYH7c.4162G>T (p.Glu1388Ter)
14g.23418217C>GCA389040729MYH7c.4162G>C (p.Glu1388Gln)
ClinVar
14g.23418217C>TCA389040727MYH7c.4162G>A (p.Glu1388Lys)
14g.23418218C>ACA389040730MYH7c.4161G>T (p.Glu1387Asp)
COSMIC
14g.23418218C=CA2123442397MYH7c.4161G= (p.Glu1387=)
14g.23418218C>GCA389040732MYH7c.4161G>C (p.Glu1387Asp)
14g.23418218C>TCA485618262MYH7c.4161G>A (p.Glu1387=)
dbSNP gnomAD v4
14g.23418219T>ACA389040733MYH7c.4160A>T (p.Glu1387Val)
14g.23418219T>CCA389040734MYH7c.4160A>G (p.Glu1387Gly)
14g.23418219T>GCA389040736MYH7c.4160A>C (p.Glu1387Ala)
14g.23418220C>ACA389040737MYH7c.4159G>T (p.Glu1387Ter)
14g.23418220C=CA2123442400MYH7c.4159G= (p.Glu1387=)
14g.23418220C>GCA040548MYH7c.4159G>C (p.Glu1387Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23418220C>TCA014551MYH7c.4159G>A (p.Glu1387Lys)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
14g.23418221G>ACA10634753MYH7c.4158C>T (p.Leu1386=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418221G>CCA485618265MYH7c.4158C>G (p.Leu1386=)
dbSNP
14g.23418221G=CA2123442405MYH7c.4158C= (p.Leu1386=)
14g.23418221G>TCA485618266MYH7c.4158C>A (p.Leu1386=)
14g.23418222A>CCA389040741MYH7c.4157T>G (p.Leu1386Arg)
14g.23418222A>GCA389040742MYH7c.4157T>C (p.Leu1386Pro)
14g.23418222A>TCA389040744MYH7c.4157T>A (p.Leu1386His)
14g.23418223G>ACA014542MYH7c.4156C>T (p.Leu1386Phe)
ClinVar dbSNP gnomAD v4
14g.23418223G>CCA389040746MYH7c.4156C>G (p.Leu1386Val)
ClinVar dbSNP
14g.23418223G=CA2123442419MYH7c.4156C= (p.Leu1386=)
14g.23418223G>TCA389040747MYH7c.4156C>A (p.Leu1386Ile)
14g.23418224C>ACA389040749MYH7c.4155G>T (p.Glu1385Asp)
14g.23418224C>GCA389040750MYH7c.4155G>C (p.Glu1385Asp)
14g.23418224C>TCA485618267MYH7c.4155G>A (p.Glu1385=)
gnomAD v4
14g.23418225T>ACA389040752MYH7c.4154A>T (p.Glu1385Val)
14g.23418225T>CCA389040754MYH7c.4154A>G (p.Glu1385Gly)
14g.23418225T>GCA389040755MYH7c.4154A>C (p.Glu1385Ala)
14g.23418226C>ACA389040757MYH7c.4153G>T (p.Glu1385Ter)
gnomAD v4 COSMIC
14g.23418226C>GCA389040760MYH7c.4153G>C (p.Glu1385Gln)
14g.23418226C>TCA389040758MYH7c.4153G>A (p.Glu1385Lys)
COSMIC
14g.23418227C>ACA389040762MYH7c.4152G>T (p.Glu1384Asp)
14g.23418227C>GCA389040763MYH7c.4152G>C (p.Glu1384Asp)
14g.23418227C>TCA485618270MYH7c.4152G>A (p.Glu1384=)
14g.23418228T>ACA389040766MYH7c.4151A>T (p.Glu1384Val)
14g.23418228T>CCA389040767MYH7c.4151A>G (p.Glu1384Gly)
14g.23418228T>GCA389040768MYH7c.4151A>C (p.Glu1384Ala)
14g.23418229C>ACA389040771MYH7c.4150G>T (p.Glu1384Ter)
14g.23418229C>GCA389040770MYH7c.4150G>C (p.Glu1384Gln)
14g.23418229C>TCA389040769MYH7c.4150G>A (p.Glu1384Lys)
14g.23418230A=CA2123442426MYH7c.4149T= (p.Thr1383=)
14g.23418230A>CCA485618273MYH7c.4149T>G (p.Thr1383=)
ClinVar dbSNP
14g.23418230A>GCA485618274MYH7c.4149T>C (p.Thr1383=)
14g.23418230A>TCA485618275MYH7c.4149T>A (p.Thr1383=)
14g.23418231G>ACA389040772MYH7c.4148C>T (p.Thr1383Ile)
14g.23418231G>CCA389040774MYH7c.4148C>G (p.Thr1383Ser)
14g.23418231G>TCA389040776MYH7c.4148C>A (p.Thr1383Asn)
14g.23418232T>ACA389040777MYH7c.4147A>T (p.Thr1383Ser)
14g.23418232T>CCA389040779MYH7c.4147A>G (p.Thr1383Ala)
14g.23418232T>GCA389040780MYH7c.4147A>C (p.Thr1383Pro)
14g.23418233C>ACA485618277MYH7c.4146G>T (p.Arg1382=)
14g.23418233C>GCA485618278MYH7c.4146G>C (p.Arg1382=)
14g.23418233C>TCA485618279MYH7c.4146G>A (p.Arg1382=)
14g.23418234C>ACA389040781MYH7c.4145G>T (p.Arg1382Leu)
ClinVar dbSNP
14g.23418234C=CA2123442432MYH7c.4145G= (p.Arg1382=)
14g.23418234C>GCA389040783MYH7c.4145G>C (p.Arg1382Pro)
14g.23418234C>TCA014533MYH7c.4145G>A (p.Arg1382Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23418235G>ACA014527MYH7c.4144C>T (p.Arg1382Trp)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
14g.23418235G>CCA389040786MYH7c.4144C>G (p.Arg1382Gly)
14g.23418235G=CA2123442439MYH7c.4144C= (p.Arg1382=)
14g.23418235G>TCA257813695MYH7c.4144C>A (p.Arg1382=)
ClinVar dbSNP gnomAD v4

Number of alleles fetched