Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 8:96144951 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM0910799

Most severe consequence
Clinical significance

Synonyms

LSDB 9958

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

8:g.96144951G>T
ENST00000287020.6:c.980C>A
ENSP00000287020.4:p.Pro327His
ENST00000620978.1:c.793+125C>A
ENST00000621429.1:c.874+106C>A

Variation displays