Variant "FSIP1:c.1204T>C(p.Cys402Arg)"
Search result: 1 record
Variant information
Gene:
Variant:
FSIP1:c.1204T>C(p.Cys402Arg)
Genomic location:
chr15:39910431(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001324338.1:c.1204T>C(p.Cys402Arg) |
protein_coding | NM_152597.4:c.1204T>C(p.Cys402Arg) |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: