Original source

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

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

Chromosome 1:45013928 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981990

Most severe consequence
Clinical significance

Synonyms

LSDB 4806

This variation has 18 HGVS names - click the plus to show

1:g.45013928T>G
ENST00000462688.4:n.621T>G
ENST00000491773.4:n.648T>G
ENST00000428106.1:c.454+137T>G
ENST00000494399.4:n.634T>G
ENST00000469548.4:n.690T>G
ENST00000478467.4:n.497T>G
ENST00000486699.4:n.614T>G
ENST00000434478.4:c.431T>G
ENSP00000404489.1:p.Met144Arg
ENST00000490385.4:n.568T>G
ENST00000460334.4:n.521T>G
ENST00000496439.1:n.590T>G
ENST00000491300.4:n.613T>G
ENST00000473012.1:n.541T>G
ENST00000246337.7:c.494T>G
ENSP00000246337.4:p.Met165Arg
ENST00000460906.4:n.628T>G

About this variant

This variant overlaps 22 transcripts and is associated with 2 phenotypes.

Variation displays