Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23415082_23415093del | CA2624231769 | MYH7 | c.5470_5481del (p.Asn1824_Glu1827del) | gnomAD v4 |
14 | g.23415089_23415101del | CA2580610817 | MYH7 | c.5455_5467del (p.Val1819ArgfsTer15) | |
14 | g.23415088C>A | CA485765953 | MYH7 | c.5466G>T (p.Leu1822=) | |
14 | g.23415088C>G | CA485765954 | MYH7 | c.5466G>C (p.Leu1822=) | |
14 | g.23415088C>T | CA485765956 | MYH7 | c.5466G>A (p.Leu1822=) | |
14 | g.23415089A>C | CA389035277 | MYH7 | c.5465T>G (p.Leu1822Arg) | |
14 | g.23415089A>G | CA389035282 | MYH7 | c.5465T>C (p.Leu1822Pro) | |
14 | g.23415089A>T | CA389035280 | MYH7 | c.5465T>A (p.Leu1822Gln) | |
14 | g.23415090del | CA2624231812 | MYH7 | c.5464del (p.Leu1822TrpfsTer16) | gnomAD v4 |
14 | g.23415090G>A | CA485765959 | MYH7 | c.5464C>T (p.Leu1822=) | |
14 | g.23415090G>C | CA389035285 | MYH7 | c.5464C>G (p.Leu1822Val) | |
14 | g.23415090G>T | CA389035287 | MYH7 | c.5464C>A (p.Leu1822Met) | |
14 | g.23415091C>A | CA389035290 | MYH7 | c.5463G>T (p.Glu1821Asp) | |
14 | g.23415091C>G | CA389035291 | MYH7 | c.5463G>C (p.Glu1821Asp) | |
14 | g.23415091C>T | CA485765965 | MYH7 | c.5463G>A (p.Glu1821=) | |
14 | g.23415092_23415093dup | CA2624231820 | MYH7 | c.5462_5463dup (p.Leu1822SerfsTer17) | gnomAD v4 |
14 | g.23415092T>A | CA389035294 | MYH7 | c.5462A>T (p.Glu1821Val) | |
14 | g.23415092T>C | CA389035296 | MYH7 | c.5462A>G (p.Glu1821Gly) | |
14 | g.23415092T>G | CA389035298 | MYH7 | c.5462A>C (p.Glu1821Ala) | |
14 | g.23415093C>A | CA389035301 | MYH7 | c.5461G>T (p.Glu1821Ter) | |
14 | g.23415093C>G | CA389035303 | MYH7 | c.5461G>C (p.Glu1821Gln) | |
14 | g.23415093C>T | CA389035305 | MYH7 | c.5461G>A (p.Glu1821Lys) | gnomAD v4 |
14 | g.23415094C>A | CA485765972 | MYH7 | c.5460G>T (p.Arg1820=) | |
14 | g.23415094C>G | CA485765973 | MYH7 | c.5460G>C (p.Arg1820=) | ClinVar |
14 | g.23415094C>T | CA485765976 | MYH7 | c.5460G>A (p.Arg1820=) | gnomAD v4 |
14 | g.23415095C>A | CA389035311 | MYH7 | c.5459G>T (p.Arg1820Leu) | |
14 | g.23415095C= | CA2123461914 | MYH7 | c.5459G= (p.Arg1820=) | |
14 | g.23415095C>G | CA389035309 | MYH7 | c.5459G>C (p.Arg1820Pro) | |
14 | g.23415095C>T | CA046848 | MYH7 | c.5459G>A (p.Arg1820Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23415096G>A | CA016126 | MYH7 | c.5458C>T (p.Arg1820Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415096G>C | CA046829 | MYH7 | c.5458C>G (p.Arg1820Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23415096G= | CA2123461925 | MYH7 | c.5458C= (p.Arg1820=) | |
14 | g.23415096G>T | CA485765981 | MYH7 | c.5458C>A (p.Arg1820=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.23415097C>A | CA485765983 | MYH7 | c.5457G>T (p.Val1819=) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23415097C= | CA2123461938 | MYH7 | c.5457G= (p.Val1819=) | |
14 | g.23415097C>G | CA485765985 | MYH7 | c.5457G>C (p.Val1819=) | dbSNP |
14 | g.23415097C>T | CA485765986 | MYH7 | c.5457G>A (p.Val1819=) | |
14 | g.23415098A= | CA2123461943 | MYH7 | c.5456T= (p.Val1819=) | |
14 | g.23415098A>C | CA389035316 | MYH7 | c.5456T>G (p.Val1819Gly) | ClinVar dbSNP gnomAD v4 |
14 | g.23415098A>G | CA389035318 | MYH7 | c.5456T>C (p.Val1819Ala) | |
14 | g.23415098A>T | CA389035319 | MYH7 | c.5456T>A (p.Val1819Glu) | |
14 | g.23415099C>A | CA389035322 | MYH7 | c.5455G>T (p.Val1819Leu) | gnomAD v4 |
14 | g.23415099C>G | CA389035324 | MYH7 | c.5455G>C (p.Val1819Leu) | gnomAD v4 |
14 | g.23415099C>T | CA389035326 | MYH7 | c.5455G>A (p.Val1819Met) | |
14 | g.23415100C>A | CA485765993 | MYH7 | c.5454G>T (p.Arg1818=) | |
14 | g.23415100C>G | CA485765995 | MYH7 | c.5454G>C (p.Arg1818=) | |
14 | g.23415100C>T | CA485765997 | MYH7 | c.5454G>A (p.Arg1818=) | gnomAD v4 |
14 | g.23415101C>A | CA389035328 | MYH7 | c.5453G>T (p.Arg1818Leu) | |
14 | g.23415101C= | CA2123461956 | MYH7 | c.5453G= (p.Arg1818=) | |
14 | g.23415101C>G | CA389035329 | MYH7 | c.5453G>C (p.Arg1818Pro) |