Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 18:23536736 (forward strand) | View in location tab

Co-located

with COSMIC COSM3524491 (A/G) ; HGMD-PUBLIC CM990946

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15113, NM_000271.3:c.3182T>C

This variation has 6 HGVS names - click the plus to show

18:g.23536736A>G
ENST00000269228.8:c.3182T>C
ENSP00000269228.4:p.Ile1061Thr
ENST00000591051.1:c.2260T>C
ENSP00000467636.1:p.Ile754Thr
ENST00000591955.1:n.525T>C

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 20 transcripts, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays