Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 17:39715897 (forward strand) | View in location tab

Co-located

with COSMIC COSM107183 (C/T) ; ESP TMP_ESP_17_37872150_37872150 (C/G)

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB NC_000017.9:g.35125676C>T

This variant has 56 HGVS names - click the plus to show

About this variant

This variant overlaps 42 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Somatic mutation displays