Original source

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

Alleles
TGA/-
Location

Chromosome 1:25812789-25812791 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB 13655

This variation has 9 HGVS names - click the plus to show

1:g.25812789_25812791delTGA
ENST00000630065.1:c.-189_-187delTGA
ENST00000361547.5:c.1384_1386delTGA
ENSP00000355141.2:p.Sec462del
ENST00000494537.1:n.62_64delTGA
ENST00000354177.7:c.1274+8_1274+10delTGA
ENST00000374315.1:c.1282_1284delTGA
ENSP00000363434.1:p.Sec428del
ENST00000559265.1:n.255+910_255+912delTGA

About this variant

This variant overlaps 9 transcripts and is associated with 1 phenotype.

Variation displays