Original source

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

Alleles
CATC/-
Location

Chromosome 1:173909681-173909684 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 364

This variation has 4 HGVS names - click the plus to show

1:g.173909681_173909684delCATC
ENST00000367698.3:c.1021_1024delGATG
ENSP00000356671.3:p.Asp341AsnfsTer5
ENST00000617423.2:c.559+2180_559+2183delGATG

Variation displays