This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: < 0.01 (T)
Location

Chromosome 1:158685289 (forward strand) | View in location tab

Co-located

with COSMIC COSM3399856 (C/T) ; HGMD-PUBLIC CM910357, CM900201

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2504 individual genotypes and is associated with 5 phenotypes.

Variation displays