Variant "BICD2:c.2080C>T(p.Arg694Cys)"
Search result: 1 record
Variant information
Gene:
Variant:
BICD2:c.2080C>T(p.Arg694Cys)
Genomic location:
chr9:95480847(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_001003800.1:c.2080C>T(p.Arg694Cys) |
protein_coding | NM_015250.3:c.2080C>T(p.Arg694Cys) |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Altered incidence(1)
Detail: