Variant "SRGAP1:c.447A>C(p.Gln149His)"
Search result: 1 record
Variant information
Gene:
Variant:
SRGAP1:c.447A>C(p.Gln149His)
Genomic location:
chr12:64410750(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_020762.2:c.447A>C(p.Gln149His) |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Altered incidence(1)
Detail: