Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 16:3254567 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981241

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 23 HGVS names - click the plus to show

16:g.3254567C>G
ENST00000538326.4:c.501G>C
ENSP00000437486.1:p.Glu167Asp
ENST00000621655.1:c.277+1744G>C
ENST00000219596.4:c.501G>C
ENSP00000219596.1:p.Glu167Asp
ENST00000576315.4:c.277+1744G>C
ENST00000536980.4:c.277+1744G>C
ENST00000536379.4:c.277+1744G>C
ENST00000339854.7:c.277+1744G>C
ENST00000541159.4:c.277+1744G>C
ENST00000570511.4:c.501G>C
ENSP00000458312.1:p.Glu167Asp
ENST00000574583.4:c.277+1744G>C
ENST00000542898.4:c.501G>C
ENSP00000444615.1:p.Glu167Asp
ENST00000572244.4:c.277+1744G>C
ENST00000537682.4:c.501G>C
ENSP00000438611.1:p.Glu167Asp
ENST00000539145.4:c.277+1744G>C
LRG_190:g.7061G>C
LRG_190t1:c.501G>C
LRG_190p1:p.Glu167Asp

About this variant

This variant overlaps 15 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays