Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23418244C>A | CA389040813 | MYH7 | c.4135G>T (p.Ala1379Ser) | ClinVar dbSNP |
14 | g.23418244C= | CA2123442472 | MYH7 | c.4135G= (p.Ala1379=) | |
14 | g.23418244C>G | CA389040814 | MYH7 | c.4135G>C (p.Ala1379Pro) | |
14 | g.23418244C>T | CA014503 | MYH7 | c.4135G>A (p.Ala1379Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23418245G>A | CA040474 | MYH7 | c.4134C>T (p.Asp1378=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23418245G>C | CA389040818 | MYH7 | c.4134C>G (p.Asp1378Glu) | |
14 | g.23418245G= | CA2123442480 | MYH7 | c.4134C= (p.Asp1378=) | |
14 | g.23418245G>T | CA389040819 | MYH7 | c.4134C>A (p.Asp1378Glu) | |
14 | g.23418246T>A | CA389040824 | MYH7 | c.4133A>T (p.Asp1378Val) | |
14 | g.23418246T>C | CA389040822 | MYH7 | c.4133A>G (p.Asp1378Gly) | ClinVar |
14 | g.23418246T>G | CA389040821 | MYH7 | c.4133A>C (p.Asp1378Ala) | |
14 | g.23418247C>A | CA389040828 | MYH7 | c.4132G>T (p.Asp1378Tyr) | |
14 | g.23418247C= | CA2123442485 | MYH7 | c.4132G= (p.Asp1378=) | |
14 | g.23418247C>G | CA389040830 | MYH7 | c.4132G>C (p.Asp1378His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.23418247C>T | CA389040831 | MYH7 | c.4132G>A (p.Asp1378Asn) | |
14 | g.23418248C>A | CA040456 | MYH7 | c.4131G>T (p.Thr1377=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23418248C= | CA2123442496 | MYH7 | c.4131G= (p.Thr1377=) | |
14 | g.23418248C>G | CA485618306 | MYH7 | c.4131G>C (p.Thr1377=) | |
14 | g.23418248C>T | CA040443 | MYH7 | c.4131G>A (p.Thr1377=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23418249G>A | CA014494 | MYH7 | c.4130C>T (p.Thr1377Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23418249G>C | CA389040835 | MYH7 | c.4130C>G (p.Thr1377Arg) | |
14 | g.23418249G= | CA2123442503 | MYH7 | c.4130C= (p.Thr1377=) | |
14 | g.23418249G>T | CA389040836 | MYH7 | c.4130C>A (p.Thr1377Lys) | |
14 | g.23418250T>A | CA389040838 | MYH7 | c.4129A>T (p.Thr1377Ser) | |
14 | g.23418250T>C | CA389040840 | MYH7 | c.4129A>G (p.Thr1377Ala) | |
14 | g.23418250T>G | CA389040841 | MYH7 | c.4129A>C (p.Thr1377Pro) | |
14 | g.23418251C>A | CA389040843 | MYH7 | c.4128G>T (p.Glu1376Asp) | |
14 | g.23418251C= | CA2123442505 | MYH7 | c.4128G= (p.Glu1376=) | |
14 | g.23418251C>G | CA389040844 | MYH7 | c.4128G>C (p.Glu1376Asp) | dbSNP gnomAD v4 |
14 | g.23418251C>T | CA485618308 | MYH7 | c.4128G>A (p.Glu1376=) | |
14 | g.23418252T>A | CA389040847 | MYH7 | c.4127A>T (p.Glu1376Val) | |
14 | g.23418252T>C | CA389040848 | MYH7 | c.4127A>G (p.Glu1376Gly) | |
14 | g.23418252T>G | CA389040846 | MYH7 | c.4127A>C (p.Glu1376Ala) | |
14 | g.23418253C>A | CA389040849 | MYH7 | c.4126G>T (p.Glu1376Ter) | |
14 | g.23418253C= | CA2123442508 | MYH7 | c.4126G= (p.Glu1376=) | |
14 | g.23418253C>G | CA389040851 | MYH7 | c.4126G>C (p.Glu1376Gln) | |
14 | g.23418253C>T | CA014488 | MYH7 | c.4126G>A (p.Glu1376Lys) | ClinVar dbSNP |
14 | g.23418254A= | CA2123442513 | MYH7 | c.4125T= (p.Tyr1375=) | |
14 | g.23418254A>C | CA389040853 | MYH7 | c.4125T>G (p.Tyr1375Ter) | |
14 | g.23418254A>G | CA485618310 | MYH7 | c.4125T>C (p.Tyr1375=) | |
14 | g.23418254A>T | CA389040855 | MYH7 | c.4125T>A (p.Tyr1375Ter) | ClinVar dbSNP gnomAD v4 |
14 | g.23418255T>A | CA389040857 | MYH7 | c.4124A>T (p.Tyr1375Phe) | |
14 | g.23418255T>C | CA014482 | MYH7 | c.4124A>G (p.Tyr1375Cys) | ClinVar dbSNP |
14 | g.23418255T>G | CA389040859 | MYH7 | c.4124A>C (p.Tyr1375Ser) | |
14 | g.23418255T= | CA2123442520 | MYH7 | c.4124A= (p.Tyr1375=) | |
14 | g.23418256A= | CA2123442526 | MYH7 | c.4123T= (p.Tyr1375=) | |
14 | g.23418256A>C | CA389040861 | MYH7 | c.4123T>G (p.Tyr1375Asp) | |
14 | g.23418256A>G | CA014472 | MYH7 | c.4123T>C (p.Tyr1375His) | ClinVar dbSNP COSMIC |
14 | g.23418256A>T | CA389040863 | MYH7 | c.4123T>A (p.Tyr1375Asn) | |
14 | g.23418257C>A | CA389040865 | MYH7 | c.4122G>T (p.Lys1374Asn) |