Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.23417576T>ACA014757MHRT,MYH7c.4280A>T (p.Asp1427Val)
n.857T>A
dbSNP
14g.23417576T>CCA389040247MHRT,MYH7c.4280A>G (p.Asp1427Gly)
n.857T>C
14g.23417576T>GCA389040245MHRT,MYH7c.4280A>C (p.Asp1427Ala)
n.857T>G
14g.23417576T=CA2123469571MHRT,MYH7c.4280A= (p.Asp1427=)
n.857T=
14g.23417577C>ACA389040248MHRT,MYH7c.4279G>T (p.Asp1427Tyr)
n.858C>A
ClinVar
14g.23417577C>GCA389040249MHRT,MYH7c.4279G>C (p.Asp1427His)
n.858C>G
14g.23417577C>TCA389040251MHRT,MYH7c.4279G>A (p.Asp1427Asn)
n.858C>T
ClinVar
14g.23417578C>ACA389040252MHRT,MYH7c.4278G>T (p.Glu1426Asp)
n.859C>A
14g.23417578C=CA2123469577MHRT,MYH7c.4278G= (p.Glu1426=)
n.859C=
14g.23417578C>GCA389040254MHRT,MYH7c.4278G>C (p.Glu1426Asp)
n.859C>G
14g.23417578C>TCA041463MHRT,MYH7c.4278G>A (p.Glu1426=)
n.859C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.23417579T>ACA389040256MHRT,MYH7c.4277A>T (p.Glu1426Val)
n.860T>A
14g.23417579T>CCA389040257MHRT,MYH7c.4277A>G (p.Glu1426Gly)
n.860T>C
14g.23417579T>GCA389040259MHRT,MYH7c.4277A>C (p.Glu1426Ala)
n.860T>G
14g.23417580C>ACA389040261MHRT,MYH7c.4276G>T (p.Glu1426Ter)
n.861C>A
gnomAD v4
14g.23417580C=CA2123469586MHRT,MYH7c.4276G= (p.Glu1426=)
n.861C=
14g.23417580C>GCA389040263MHRT,MYH7c.4276G>C (p.Glu1426Gln)
n.861C>G
14g.23417580C>TCA014743MHRT,MYH7c.4276G>A (p.Glu1426Lys)
n.861C>T
ClinVar dbSNP COSMIC
14g.23417581G>ACA041447MHRT,MYH7c.4275C>T (p.Ile1425=)
n.862G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417581G>CCA389040265MHRT,MYH7c.4275C>G (p.Ile1425Met)
n.862G>C
14g.23417581G=CA2123469597MHRT,MYH7c.4275C= (p.Ile1425=)
n.862G=
14g.23417581G>TCA041432MHRT,MYH7c.4275C>A (p.Ile1425=)
n.862G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.23417582A>CCA389040266MHRT,MYH7c.4274T>G (p.Ile1425Ser)
n.863A>C
14g.23417582A>GCA389040268MHRT,MYH7c.4274T>C (p.Ile1425Thr)
n.863A>G
14g.23417582A>TCA389040269MHRT,MYH7c.4274T>A (p.Ile1425Asn)
n.863A>T
14g.23417583T>ACA389040271MHRT,MYH7c.4273A>T (p.Ile1425Phe)
n.864T>A
gnomAD v4
14g.23417583T>CCA389040272MHRT,MYH7c.4273A>G (p.Ile1425Val)
n.864T>C
14g.23417583T>GCA389040273MHRT,MYH7c.4273A>C (p.Ile1425Leu)
n.864T>G
14g.23417584C>ACA389040274MHRT,MYH7c.4272G>T (p.Glu1424Asp)
n.865C>A
14g.23417584C>GCA389040275MHRT,MYH7c.4272G>C (p.Glu1424Asp)
n.865C>G
14g.23417584C>TCA485617815MHRT,MYH7c.4272G>A (p.Glu1424=)
n.865C>T
14g.23417585T>ACA389040277MHRT,MYH7c.4271A>T (p.Glu1424Val)
n.866T>A
ClinVar
14g.23417585T>CCA389040278MHRT,MYH7c.4271A>G (p.Glu1424Gly)
n.866T>C
14g.23417585T>GCA389040279MHRT,MYH7c.4271A>C (p.Glu1424Ala)
n.866T>G
14g.23417586C>ACA389040281MHRT,MYH7c.4270G>T (p.Glu1424Ter)
n.867C>A
14g.23417586C=CA2123469604MHRT,MYH7c.4270G= (p.Glu1424=)
n.867C=
14g.23417586C>GCA389040283MHRT,MYH7c.4270G>C (p.Glu1424Gln)
n.867C>G
14g.23417586C>TCA014734MHRT,MYH7c.4270G>A (p.Glu1424Lys)
n.867C>T
ClinVar dbSNP COSMIC
14g.23417587A=CA2123469610MHRT,MYH7c.4269T= (p.Asn1423=)
n.868A=
14g.23417587A>CCA389040285MHRT,MYH7c.4269T>G (p.Asn1423Lys)
n.868A>C
dbSNP gnomAD v4
14g.23417587A>GCA485617819MHRT,MYH7c.4269T>C (p.Asn1423=)
n.868A>G
dbSNP
14g.23417587A>TCA389040286MHRT,MYH7c.4269T>A (p.Asn1423Lys)
n.868A>T
14g.23417588T>ACA389040288MHRT,MYH7c.4268A>T (p.Asn1423Ile)
n.869T>A
14g.23417588T>CCA389040290MHRT,MYH7c.4268A>G (p.Asn1423Ser)
n.869T>C
14g.23417588T>GCA389040291MHRT,MYH7c.4268A>C (p.Asn1423Thr)
n.869T>G
14g.23417589T>ACA389040293MHRT,MYH7c.4267A>T (p.Asn1423Tyr)
n.870T>A
14g.23417589T>CCA389040294MHRT,MYH7c.4267A>G (p.Asn1423Asp)
n.870T>C
14g.23417589T>GCA389040296MHRT,MYH7c.4267A>C (p.Asn1423His)
n.870T>G
14g.23417590C>ACA389040297MHRT,MYH7c.4266G>T (p.Gln1422His)
n.871C>A
14g.23417590C>GCA389040299MHRT,MYH7c.4266G>C (p.Gln1422His)
n.871C>G

Number of alleles fetched