Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 8:142875290 (forward strand) | View in location tab

Co-located

with COSMIC COSM749822 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays