Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.10 (T)
Location

Chromosome 11:69078931 (forward strand) | View in location tab

Co-located

with COSMIC COSM4146228 (A/T) ; HGMD-PUBLIC CM083199

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

11:g.69078931A>T
ENST00000542467.1:c.1450A>T
ENSP00000445551.1:p.Met484Leu
ENST00000442692.2:n.1043A>T
ENST00000294309.5:c.1450A>T
ENSP00000294309.3:p.Met484Leu
ENST00000535009.3:n.1259A>T

This variation has assays on 7 chips - click the plus to show

Variation displays