Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.48 (C)
Location

Chromosome 7:34742415 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 16 HGVS names - click the plus to show

7:g.34742415C>T
ENST00000419766.5:n.162-13599G>A
ENST00000359791.5:c.281-36047C>T
ENST00000381544.6:c.280+57731C>T
ENST00000436945.4:n.268-13599G>A
ENST00000531252.5:c.281-36080C>T
ENST00000431669.5:n.165-13599G>A
ENST00000381539.3:c.281-36047C>T
ENST00000381553.7:c.281-36047C>T
ENST00000396095.6:c.281-36047C>T
ENST00000381542.5:c.280+57731C>T
ENST00000439852.5:n.200-13599G>A
ENST00000428922.5:n.81-13599G>A
ENST00000360581.5:c.281-36047C>T
ENST00000358772.8:n.200-13599G>A
ENST00000539747.5:n.81-13599G>A

About this variant

This variant overlaps 15 transcripts, has 2576 sample genotypes and is mentioned in 4 citations.

Variant displays