Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:2164339 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001359

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

11:g.2164339G>A
ENST00000352909.4:c.1388C>T
ENSP00000325951.3:p.Thr463Met
ENST00000381178.2:c.1481C>T
ENSP00000370571.1:p.Thr494Met
ENST00000333684.6:c.1118C>T
ENSP00000328814.5:p.Thr373Met
ENST00000381175.2:c.1469C>T
ENSP00000370567.1:p.Thr490Met

Variation displays