Original source

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

Alleles
-/G
Location

Chromosome 18: between 51058149 and 51058150 (forward strand) | View in location tab

Co-located

with COSMIC COSM85615 (-/G), COSM1158484 (-/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB SCV000042357, SCV000042358

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and is mentioned in 2 citations.

Variation displays