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 | MAF: 0.22 (A)
Location

Chromosome 15:73927241 (forward strand) | View in location tab

Co-located

with COSMIC COSM3754463 (G/A) ; HGMD-PUBLIC CM074330

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

15:g.73927241G>A
ENST00000564963.1:n.42+413C>T
ENST00000565756.3:n.183+536C>T
ENST00000562965.1:n.184+536C>T
ENST00000566011.3:c.458G>A
ENSP00000457827.1:p.Gly153Asp
ENST00000564194.3:n.184+824C>T
ENST00000565416.1:n.164+536C>T
ENST00000568087.3:n.166+536C>T
ENST00000566675.3:n.139+824C>T
ENST00000261921.7:c.458G>A
ENSP00000261921.7:p.Gly153Asp
ENST00000567257.3:n.133+413C>T
ENST00000562739.3:n.42+413C>T

This variation has assays on 5 chips - click the plus to show

Variation displays