Original source

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

Alleles
T/A/G|Ancestral: T|Ambiguity code: D|MAF: 0.45 (G)
Location

Chromosome 19:41761981 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 8 HGVS names - Hide

Variant allele A
19:g.41761981T>A
ENST00000601409.1:n.384-3900A>T
ENST00000199764.6:c.716T>A
ENSP00000199764.6:p.Val239Asp

Variant allele G
19:g.41761981T>G
ENST00000601409.1:n.384-3900A>C
ENST00000199764.6:c.716T>G
ENSP00000199764.6:p.Val239Gly

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 6 transcripts, has 2796 sample genotypes and is mentioned in 1 citation.

Variant displays