Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
TGA/-
Location

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

Most severe consequence
Clinical significance

Synonyms

LSDB 13655

This variation has 8 HGVS names - click the plus to show

1:g.25812789_25812791delTGA
ENST00000361547.4:c.1384_1386delTGA
ENSP00000355141.2:p.Sec462del
ENST00000494537.1:n.62_64delTGA
ENST00000354177.6:c.1274+8_1274+10delTGA
ENST00000374315.1:c.1282_1284delTGA
ENSP00000363434.1:p.Sec428del
ENST00000559265.1:n.255+910_255+912delTGA

Variation displays