Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.14 (C)
Location

Chromosome 2:47795976 (forward strand) | View in location tab

Co-located

with COSMIC COSM3758252 (T/C) ; PhenCode MMR_c.540T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

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

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 16 transcripts, has 4003 individual genotypes, is associated with 2 phenotypes and is mentioned in 7 citations.

Variation displays