This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

T/A/C/G | Ancestral: T | Ambiguity code: N | MAF: 0.12 (C)

Chromosome 15:74720644 (forward strand) | View in location tab


with COSMIC COSM3999600 (T/C) ; HGMD-PUBLIC CM940327

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 39 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 30 transcripts, has 2276 individual genotypes and is mentioned in 91 citations.

Variation displays