Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.22 (A)
Location

Chromosome 14:20940606 (forward strand) | View in location tab

Co-located

with COSMIC COSM147733 (G/A) ; HGMD-PUBLIC CM073244

Most severe consequence
Evidence status

Clinical significance

This variation has 10 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

14:g.20940606G>A
ENST00000557229.1:n.270G>A
ENST00000553591.1:c.268G>A
ENSP00000452421.1:p.Gly90Ser
ENST00000556293.1:n.270G>A
ENST00000554065.1:c.-87G>A
ENST00000553418.1:c.151G>A
ENSP00000450663.1:p.Gly51Ser
ENST00000361505.5:c.151G>A
ENSP00000354532.5:p.Gly51Ser
ENST00000554056.1:n.262G>A
LRG_91:g.8065G>A
LRG_91t1.1:c.151G>A
LRG_91p1.1:p.Gly51Ser

This variation has assays on 8 chips - click the plus to show

Variation displays