Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
TGA/-
Location

Chromosome 4:998179-998181 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 6454

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

4:g.998179_998181delTGA
ENST00000514224.1:c.1564_1566delTGA
ENSP00000425081.1:p.Ter522delextTer?
ENST00000514698.1:n.2071_2073delTGA
ENST00000453894.1:c.2026_2028delTGA
ENSP00000396458.1:p.Ter676delextTer?
ENST00000247933.4:c.1960_1962delTGA
ENSP00000247933.4:p.Ter654delextTer?

Variation displays