Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 22:19763273 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033031

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

22:g.19763273T>A
ENST00000332710.6:c.443T>A
ENSP00000331791.4:p.Phe148Tyr
ENST00000475303.1:n.117T>A
ENST00000329705.9:c.443T>A
ENSP00000331176.7:p.Phe148Tyr
ENST00000359500.5:c.443T>A
ENSP00000352483.3:p.Phe148Tyr
ENST00000621939.1:c.443T>A
ENSP00000477982.1:p.Phe148Tyr
LRG_226:g.11571T>A
LRG_226t1.1:c.443T>A
LRG_226p1.1:p.Phe148Tyr

Variation displays