Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23419950G>ACA013881MYH7c.3621C>T (p.Ile1207=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.23419950G>CCA038128MYH7c.3621C>G (p.Ile1207Met)
ClinVar dbSNP ExAC gnomAD v4
14g.23419950G=CA2123446245MYH7c.3621C= (p.Ile1207=)
14g.23419950G>TCA038110MYH7c.3621C>A (p.Ile1207=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419951A=CA2123446264MYH7c.3620T= (p.Ile1207=)
14g.23419951A>CCA389043265MYH7c.3620T>G (p.Ile1207Ser)
14g.23419951A>GCA389043267MYH7c.3620T>C (p.Ile1207Thr)
14g.23419951A>TCA013873MYH7c.3620T>A (p.Ile1207Asn)
ClinVar dbSNP gnomAD v4
14g.23419952T>ACA389043270MYH7c.3619A>T (p.Ile1207Phe)
gnomAD v4
14g.23419952T>CCA389043271MYH7c.3619A>G (p.Ile1207Val)
14g.23419952T>GCA389043272MYH7c.3619A>C (p.Ile1207Leu)
14g.23419953C>ACA389043273MYH7c.3618G>T (p.Gln1206His)
14g.23419953C=CA2123446269MYH7c.3618G= (p.Gln1206=)
14g.23419953C>GCA389043275MYH7c.3618G>C (p.Gln1206His)
14g.23419953C>TCA485766678MYH7c.3618G>A (p.Gln1206=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.23419954T>ACA389043277MYH7c.3617A>T (p.Gln1206Leu)
14g.23419954T>CCA038093MYH7c.3617A>G (p.Gln1206Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23419954T>GCA389043281MYH7c.3617A>C (p.Gln1206Pro)
14g.23419954T=CA2123446271MYH7c.3617A= (p.Gln1206=)
14g.23419955G>ACA389043283MYH7c.3616C>T (p.Gln1206Ter)
gnomAD v4
14g.23419955G>CCA389043285MYH7c.3616C>G (p.Gln1206Glu)
14g.23419955G>TCA389043287MYH7c.3616C>A (p.Gln1206Lys)
14g.23419956C>ACA389043288MYH7c.3615G>T (p.Glu1205Asp)
14g.23419956C>GCA389043289MYH7c.3615G>C (p.Glu1205Asp)
14g.23419956C>TCA485766679MYH7c.3615G>A (p.Glu1205=)
14g.23419957T>ACA389043290MYH7c.3614A>T (p.Glu1205Val)
14g.23419957T>CCA16619847MYH7c.3614A>G (p.Glu1205Gly)
ClinVar dbSNP
14g.23419957T>GCA389043292MYH7c.3614A>C (p.Glu1205Ala)
14g.23419957T=CA2123446276MYH7c.3614A= (p.Glu1205=)
14g.23419958C>ACA389043294MYH7c.3613G>T (p.Glu1205Ter)
14g.23419958C=CA2123446285MYH7c.3613G= (p.Glu1205=)
14g.23419958C>GCA389043296MYH7c.3613G>C (p.Glu1205Gln)
14g.23419958C>TCA013863MYH7c.3613G>A (p.Glu1205Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419959G>ACA013856MYH7c.3612C>T (p.Gly1204=)
ClinVar dbSNP
14g.23419959G>CCA485766680MYH7c.3612C>G (p.Gly1204=)
gnomAD v4
14g.23419959G=CA2123446292MYH7c.3612C= (p.Gly1204=)
14g.23419959G>TCA485766681MYH7c.3612C>A (p.Gly1204=)
14g.23419960C>ACA389043298MYH7c.3611G>T (p.Gly1204Val)
14g.23419960C=CA2123446295MYH7c.3611G= (p.Gly1204=)
14g.23419960C>GCA389043300MYH7c.3611G>C (p.Gly1204Ala)
14g.23419960C>TCA038065MYH7c.3611G>A (p.Gly1204Asp)
dbSNP ExAC gnomAD v2
14g.23419961C>ACA389043302MYH7c.3610G>T (p.Gly1204Cys)
14g.23419961C=CA2123446298MYH7c.3610G= (p.Gly1204=)
14g.23419961C>GCA013846MYH7c.3610G>C (p.Gly1204Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.23419961C>TCA038038MYH7c.3610G>A (p.Gly1204Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.23419962C>ACA485766682MYH7c.3609G>T (p.Leu1203=)
ClinVar dbSNP
14g.23419962C=CA2123446304MYH7c.3609G= (p.Leu1203=)
14g.23419962C>GCA485766683MYH7c.3609G>C (p.Leu1203=)
14g.23419962C>TCA485766684MYH7c.3609G>A (p.Leu1203=)
14g.23419963A>CCA389043305MYH7c.3608T>G (p.Leu1203Arg)

Number of alleles fetched