Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23415155G>A | CA016070 | MYH7 | c.5399C>T (p.Ala1800Val) | ClinVar dbSNP |
14 | g.23415155G>C | CA389035594 | MYH7 | c.5399C>G (p.Ala1800Gly) | |
14 | g.23415155G= | CA2123462210 | MYH7 | c.5399C= (p.Ala1800=) | |
14 | g.23415155G>T | CA389035596 | MYH7 | c.5399C>A (p.Ala1800Asp) | gnomAD v4 |
14 | g.23415156C>A | CA389035598 | MYH7 | c.5398G>T (p.Ala1800Ser) | |
14 | g.23415156C= | CA2123462230 | MYH7 | c.5398G= (p.Ala1800=) | |
14 | g.23415156C>G | CA016063 | MYH7 | c.5398G>C (p.Ala1800Pro) | ClinVar dbSNP |
14 | g.23415156C>T | CA389035600 | MYH7 | c.5398G>A (p.Ala1800Thr) | |
14 | g.23415157T>A | CA389035602 | MYH7 | c.5397A>T (p.Glu1799Asp) | |
14 | g.23415157T>C | CA016055 | MYH7 | c.5397A>G (p.Glu1799=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415157T>G | CA389035605 | MYH7 | c.5397A>C (p.Glu1799Asp) | |
14 | g.23415157T= | CA2123462238 | MYH7 | c.5397A= (p.Glu1799=) | |
14 | g.23415158T>A | CA389035608 | MYH7 | c.5396A>T (p.Glu1799Val) | |
14 | g.23415158T>C | CA389035610 | MYH7 | c.5396A>G (p.Glu1799Gly) | |
14 | g.23415158T>G | CA389035611 | MYH7 | c.5396A>C (p.Glu1799Ala) | |
14 | g.23415159C>A | CA389035613 | MYH7 | c.5395G>T (p.Glu1799Ter) | |
14 | g.23415159C= | CA2123462251 | MYH7 | c.5395G= (p.Glu1799=) | |
14 | g.23415159C>G | CA389035614 | MYH7 | c.5395G>C (p.Glu1799Gln) | |
14 | g.23415159C>T | CA016046 | MYH7 | c.5395G>A (p.Glu1799Lys) | ClinVar dbSNP COSMIC |
14 | g.23415160G>A | CA046635 | MYH7 | c.5394C>T (p.Asp1798=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23415160G>C | CA389035621 | MYH7 | c.5394C>G (p.Asp1798Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415160G= | CA2123462266 | MYH7 | c.5394C= (p.Asp1798=) | |
14 | g.23415160G>T | CA389035619 | MYH7 | c.5394C>A (p.Asp1798Glu) | gnomAD v4 |
14 | g.23415161T>A | CA389035632 | MYH7 | c.5393A>T (p.Asp1798Val) | |
14 | g.23415161T>C | CA389035625 | MYH7 | c.5393A>G (p.Asp1798Gly) | |
14 | g.23415161T>G | CA389035634 | MYH7 | c.5393A>C (p.Asp1798Ala) | |
14 | g.23415162C>A | CA389035636 | MYH7 | c.5392G>T (p.Asp1798Tyr) | ClinVar |
14 | g.23415162C>G | CA389035638 | MYH7 | c.5392G>C (p.Asp1798His) | |
14 | g.23415162C>T | CA389035640 | MYH7 | c.5392G>A (p.Asp1798Asn) | |
14 | g.23415163C>A | CA485766214 | MYH7 | c.5391G>T (p.Leu1797=) | |
14 | g.23415163C= | CA2123462271 | MYH7 | c.5391G= (p.Leu1797=) | |
14 | g.23415163C>G | CA485766215 | MYH7 | c.5391G>C (p.Leu1797=) | |
14 | g.23415163C>T | CA485766216 | MYH7 | c.5391G>A (p.Leu1797=) | dbSNP gnomAD v4 |
14 | g.23415164A= | CA2123462277 | MYH7 | c.5390T= (p.Leu1797=) | |
14 | g.23415164A>C | CA389035642 | MYH7 | c.5390T>G (p.Leu1797Arg) | |
14 | g.23415164A>G | CA389035644 | MYH7 | c.5390T>C (p.Leu1797Pro) | ClinVar dbSNP gnomAD v4 |
14 | g.23415164A>T | CA389035646 | MYH7 | c.5390T>A (p.Leu1797Gln) | |
14 | g.23415165G>A | CA485766221 | MYH7 | c.5389C>T (p.Leu1797=) | |
14 | g.23415165G>C | CA389035648 | MYH7 | c.5389C>G (p.Leu1797Val) | |
14 | g.23415165G>T | CA389035650 | MYH7 | c.5389C>A (p.Leu1797Met) | ClinVar gnomAD v4 |
14 | g.23415166C>A | CA485766225 | MYH7 | c.5388G>T (p.Arg1796=) | |
14 | g.23415166C>G | CA485766223 | MYH7 | c.5388G>C (p.Arg1796=) | |
14 | g.23415166C>T | CA485766222 | MYH7 | c.5388G>A (p.Arg1796=) | COSMIC |
14 | g.23415167C>A | CA389035652 | MYH7 | c.5387G>T (p.Arg1796Leu) | gnomAD v4 COSMIC |
14 | g.23415167C= | CA2123462289 | MYH7 | c.5387G= (p.Arg1796=) | |
14 | g.23415167C>G | CA389035654 | MYH7 | c.5387G>C (p.Arg1796Pro) | |
14 | g.23415167C>T | CA389035656 | MYH7 | c.5387G>A (p.Arg1796Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415168G>A | CA046625 | MYH7 | c.5386C>T (p.Arg1796Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415168G>C | CA389035659 | MYH7 | c.5386C>G (p.Arg1796Gly) | |
14 | g.23415168G= | CA2123462296 | MYH7 | c.5386C= (p.Arg1796=) |