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
Location

Chromosome 15:34257713 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061195

Most severe consequence
Clinical significance

Synonyms

LSDB 12865

This variation has 32 HGVS names - click the plus to show

15:g.34257713G>A
ENST00000560611.3:c.619C>T
ENSP00000454168.1:p.Arg207Cys
ENST00000558589.3:c.592C>T
ENSP00000452776.1:p.Arg198Cys
ENST00000559664.3:c.619C>T
ENSP00000453702.1:p.Arg207Cys
ENST00000397702.4:c.442C>T
ENSP00000380814.2:p.Arg148Cys
ENST00000559867.1:n.268G>A
ENST00000560164.3:c.126+1100C>T
ENST00000354181.5:c.619C>T
ENSP00000346112.3:p.Arg207Cys
ENST00000458406.4:c.442C>T
ENSP00000387725.2:p.Arg148Cys
ENST00000561080.3:c.619C>T
ENSP00000454069.1:p.Arg207Cys
ENST00000397707.4:c.574C>T
ENSP00000380819.2:p.Arg192Cys
ENST00000290209.7:c.466C>T
ENSP00000290209.5:p.Arg156Cys
ENST00000559523.3:c.442C>T
ENSP00000452904.1:p.Arg148Cys
ENST00000560332.1:c.202C>T
ENSP00000454037.1:p.Arg68Cys
ENST00000558667.3:c.619C>T
ENSP00000453473.1:p.Arg207Cys
LRG_270:g.85352C>T
LRG_270t1.1:c.466C>T
LRG_270p1.1:p.Arg156Cys
LRG_270t2.1:c.619C>T
LRG_270p2.1:p.Arg207Cys

Variation displays