Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 19:18594338 (forward strand) | View in location tab

Co-located

with COSMIC COSM3822365 (A/T) ; HGMD-PUBLIC CM030431

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_022_CRLF1_604237_0002, NM_004750.4:c.1121T>G

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, 2 regulatory features and is associated with 3 phenotypes.

Variant displays