Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 16:11553576 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030678 ; PhenCode IPNMDB_640 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12169, NM_004862.3:c.334G>A, 2010_April_001_058_LITAF_603795_0001

This variation has 35 HGVS names - click the plus to show

16:g.11553576C>T
ENST00000339430.7:c.334G>A
ENSP00000340118.5:p.Gly112Ser
ENST00000571459.3:c.220+2935G>A
ENST00000620789.2:c.334G>A
ENSP00000481589.1:p.Gly112Ser
ENST00000570798.3:c.334G>A
ENSP00000458871.1:p.Gly112Ser
ENST00000573332.3:c.*147G>A
ENST00000381810.5:c.334G>A
ENSP00000371231.3:p.Gly112Ser
ENST00000570904.3:c.334G>A
ENSP00000459138.1:p.Gly112Ser
ENST00000574701.3:c.334G>A
ENSP00000458981.1:p.Gly112Ser
ENST00000576036.3:c.334G>A
ENSP00000461667.1:p.Gly112Ser
ENST00000413364.4:c.334G>A
ENSP00000397958.2:p.Gly112Ser
ENST00000622633.2:c.334G>A
ENSP00000483114.1:p.Gly112Ser
ENST00000574763.3:c.334G>A
ENSP00000461813.1:p.Gly112Ser
ENST00000571688.3:c.334G>A
ENSP00000459533.1:p.Gly112Ser
ENST00000575426.1:c.*121G>A
ENST00000571976.1:c.334G>A
ENSP00000460133.1:p.Gly112Ser
ENST00000571627.3:c.334G>A
ENSP00000460743.1:p.Gly112Ser
ENST00000572255.3:c.55G>A
ENSP00000458836.1:p.Gly19Ser
LRG_253:g.38375G>A
LRG_253t1:c.334G>A
LRG_253p1:p.Gly112Ser

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays