Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.33 (C)
Location

Chromosome 4:154586438 (forward strand) | View in location tab

Co-located

with COSMIC COSM1131211 (T/C) ; HGMD-PUBLIC CM994632

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

4:g.154586438T>C
ENST00000302053.5:c.991A>G
ENSP00000306361.3:p.Thr331Ala
ENST00000403106.5:c.991A>G
ENSP00000385981.3:p.Thr331Ala
ENST00000622532.1:c.643+348A>G
LRG_557:g.9308A>G
LRG_557t2.1:c.991A>G
LRG_557p2.1:p.Thr331Ala
LRG_557t1.1:c.991A>G
LRG_557p1.1:p.Thr331Ala

This variation has assays on 5 chips - click the plus to show

Variation displays