Original source

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

Alleles
TTAGAG/GC
Location

Chromosome 5:159333192-159333197 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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

5:g.159333192_159333197delTTAGAGinsGC
ENST00000515337.1:n.745+189_745+194delTTAGAGinsGC
LRG_71:g.2277_2282delCTCTAAinsGC

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and is mentioned in 24 citations.

Variant displays