Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A/C | Ancestral: G | Ambiguity code: V | MAF: < 0.01 (A)

Chromosome 5:147828053 (forward strand) | View in location tab


with COSMIC COSM223032 (G/A) ; HGMD-PUBLIC CM014100

Most severe consequence
Missense variant
Evidence status


LSDB SPINK1_163C_T_081111

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays