This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/A/G/T | Ancestral: C | Ambiguity code: N

Chromosome 18:51065548 (forward strand) | View in location tab


with COSMIC COSM1158192 (C/G), COSM14151 (C/A), COSM14140 (C/T) ; HGMD-PUBLIC CM041789, CM040450, CM981228

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 42 HGVS names - click the plus to show

About this variant

This variant overlaps 27 transcripts, is associated with 8 phenotypes and is mentioned in 6 citations.

Variation displays