Variant "TYK2:c.2783C>T(p.Ala928Val)"
Search results: 6 records
Variant information
Gene:
Variant:
TYK2:c.2783C>T(p.Ala928Val)
Genomic location:
chr19:10464843(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_003331.4:c.2783C>T(p.Ala928Val) |
protein_coding | 3LXN:A_928-A_978:NM_003331.4:c.2783C>T |
protein_coding | 3LXP:A_928-A_978:NM_003331.4:c.2783C>T |
protein_coding | 3NYX:A_928-A_978:NM_003331.4:c.2783C>T |
protein_coding | 3NZ0:A_928-A_978:NM_003331.4:c.2783C>T |
show all |
Alias:
TYK2:A928V
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
6
Disorder:
6
Reference:
1
Effect type:
Expressivity(6)
Modifier effect:
Risk factor(6)
Details: