Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 12:6355286 (forward strand) | View in location tab

Co-located

with COSMIC COSM1179185 (T/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_001038.5:c.1129A>G

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays