Variant "RARG:c.1280C>T(p.Ser427Leu)"
Search result: 1 record
Variant information
Gene:
Variant:
RARG:c.1280C>T(p.Ser427Leu)
Genomic location:
chr12:53605545(hg19)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000966.5:c.1280C>T(p.Ser427Leu) |
protein_coding | NM_001042728.2:c.1247C>T(p.Ser416Leu) |
protein_coding | NM_001243732.1:c.1214C>T(p.Ser405Leu) |
protein_coding | NM_001243730.1:c.1064C>T(p.Ser355Leu) |
protein_coding | NM_001243731.1:c.917C>T(p.Ser306Leu) |
show all |
dbSNP ID:
GWAS trait:
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Expressivity(1)
Modifier effect:
Risk factor(1)
Detail: