Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.13 (G)
Location

Chromosome 1:113812320 (forward strand) | View in location tab

Co-located

with COSMIC COSM1560090 (T/G) ; HGMD-PUBLIC CR053507

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 3 HGVS names - click the plus to show

1:g.113812320T>G
ENST00000261441.9:c.93A>C
ENST00000612242.4:c.93A>C

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 2756 sample genotypes and is mentioned in 23 citations.

Variant displays