Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variants

COSMIC COSM3822365 ; 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

HGVS names

This variant has 4 HGVS names - Show

About this variant

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

Variant displays