Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 17:48728343 (forward strand) | View in location tab

Co-located

with COSMIC COSM3889825 (C/T)

Most severe consequence
Evidence status

Clinical significance

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

17:g.48728343C>T
ENST00000290295.7:c.251G>A
ENSP00000290295.7:p.Gly84Glu
LRG_771:g.5407G>A
LRG_771t1:c.251G>A
LRG_771p1:p.Gly84Glu

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 8 transcripts, has 2504 individual genotypes and is mentioned in 8 citations.

Variation displays