Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 11:71438975 (forward strand) | View in location tab


with HGMD-PUBLIC CD982593

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays