Variant "MYH7:c.767G>A(p.Gly256Glu)"
Search result: 1 record
Variant information
Gene:
Variant:
MYH7:c.767G>A(p.Gly256Glu)
Genomic location:
chr14:23900656(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000257.3:c.767G>A(p.Gly256Glu) |
protein_coding | 4DB1:A_200-A_256:NM_000257.3:c.767G>A |
protein_coding | NM_000257.3:c.767G>A |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Altered incidence(1)
Detail: