Variant "BRCA2:c.1389_1390del(p.Val464fs)"
Search results: 2 records
Variant information
Gene:
Variant:
BRCA2:c.1389_1390del(p.Val464fs)
Genomic location:
chr13:32907004-32907005(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000059.3:c.1389_1390del(p.Val464fs) |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
2
Disorder:
2
Reference:
1
Effect type:
Expressivity(2)
Modifier effect:
Risk factor(2)
Details: