Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 7:30974052 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010308

Most severe consequence
Clinical significance

Synonyms

LSDB 2345

This variation has 12 HGVS names - click the plus to show

7:g.30974052C>A
ENST00000409904.6:c.473C>A
ENSP00000387113.3:p.Ala158Glu
ENST00000489974.4:n.438C>A
ENST00000337750.8:c.175-377C>A
ENST00000409316.4:c.51-377C>A
ENST00000461390.1:n.133C>A
ENST00000611037.1:c.111C>A
ENST00000396227.5:c.406-377C>A
ENST00000461424.4:n.241C>A
ENST00000326139.5:c.665C>A
ENSP00000320180.2:p.Ala222Glu

About this variant

This variant overlaps 10 transcripts and is associated with 2 phenotypes.

Variation displays