Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.41 (T)
Location

Chromosome 14:33241581 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386567094

This variant has 11 HGVS names - click the plus to show

14:g.33241581T>C
ENST00000549770.1:n.245+26155T>C
ENST00000551492.5:c.406+26155T>C
ENST00000548645.5:c.295+26155T>C
ENST00000357798.9:c.346+25994T>C
ENST00000356141.8:c.385+26155T>C
ENST00000546849.1:c.115+26155T>C
ENST00000551008.5:c.79+26155T>C
ENST00000547068.5:c.79+26155T>C
ENST00000551634.5:c.316+26155T>C
ENST00000346562.6:c.295+26155T>C

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

About this variant

This variant overlaps 10 transcripts and has 5801 sample genotypes.

Variant displays