Variant "MYH7:c.1357C>A(p.Arg453Ser)"
Search result: 1 record
Variant information
Gene:
Variant:
MYH7:c.1357C>A(p.Arg453Ser)
Genomic location:
chr14:23898214(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000257.3:c.1357C>A(p.Arg453Ser) |
protein_coding | 4DB1:A_260-A_453:NM_000257.3:c.1357C>A |
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: