Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Clinical significance


LSDB SPINK1_163C_T_081111

This variation has 12 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 1092 individual genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variation displays