Variant "MC1R:c.332C>T(p.Ala111Val)"
Search result: 1 record
Variant information
Gene:
Variant:
MC1R:c.332C>T(p.Ala111Val)
Genomic location:
chr16:89985998(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_002386.3:c.332C>T(p.Ala111Val) |
protein_coding | NM_006086.3:c.-3812C>T |
protein_coding | NM_001197181.1:c.-13928C>T |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Altered incidence(1)
Detail: