Variant "MYH7:c.1207C>G(p.Arg403Gly)"
Search result: 1 record
Variant information
Gene:
Variant:
MYH7:c.1207C>G(p.Arg403Gly)
Genomic location:
chr14:23898488(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000257.3:c.1207C>G(p.Arg403Gly) |
protein_coding | 4DB1:A_403-A_604:NM_000257.3:c.1207C>G |
protein_coding | 4DB1:B_403-B_604:NM_000257.3:c.1207C>G |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Altered life span(1)
Detail: