Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 4:155507590 (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 5 HGVS names - click the plus to show

4:g.155507590T>C
ENST00000302053.3:c.991A>G
ENSP00000306361.3:p.Thr331Ala
ENST00000403106.3:c.991A>G
ENSP00000385981.3:p.Thr331Ala

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

Variation displays