Original source

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

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

Chromosome 15:34528920 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM022673 ; PhenCode IPNMDB_646 (G/A)

Most severe consequence
Clinical significance

Synonyms

LSDB 12860

This variation has 29 HGVS names - click the plus to show

15:g.34528920G>A
ENST00000560611.1:c.3031C>T
ENSP00000454168.1:p.Arg1011Ter
ENST00000558589.1:c.3004C>T
ENSP00000452776.1:p.Arg1002Ter
ENST00000559664.1:c.*240C>T
ENST00000397702.2:c.2854C>T
ENSP00000380814.2:p.Arg952Ter
ENST00000560164.1:c.2467C>T
ENSP00000452705.1:p.Arg823Ter
ENST00000354181.3:c.3031C>T
ENSP00000346112.3:p.Arg1011Ter
ENST00000458406.2:c.2854C>T
ENSP00000387725.2:p.Arg952Ter
ENST00000561080.1:c.*269C>T
ENST00000397707.2:c.2986C>T
ENSP00000380819.2:p.Arg996Ter
ENST00000290209.5:c.2878C>T
ENSP00000290209.5:p.Arg960Ter
ENST00000451844.2:c.2467C>T
ENSP00000390199.2:p.Arg823Ter
ENST00000559523.1:c.*54C>T
ENST00000558667.1:c.3031C>T
ENSP00000453473.1:p.Arg1011Ter
LRG_270:g.106346C>T
LRG_270t1.1:c.2878C>T
LRG_270p1.1:p.Arg960Ter
LRG_270t2.1:c.3031C>T
LRG_270p2.1:p.Arg1011Ter

Variation displays