Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 1:173910861 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD952113, CM910057

Most severe consequence
Clinical significance

Synonyms

LSDB 378

This variation has 5 HGVS names - click the plus to show

1:g.173910861T>C
ENST00000487183.1:n.330-24A>G
ENST00000367698.3:c.655A>G
ENSP00000356671.3:p.Asn219Asp
ENST00000617423.2:c.559+1003A>G

Variation displays