Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 9:129455868 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981225

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11278, 2010_April_001_040_LMX1B_602575_0001

This variation has 11 HGVS names - click the plus to show

9:g.129455868C>A
ENST00000373474.4:c.807C>A
ENSP00000362573.3:p.Asn269Lys
ENST00000425646.2:c.738C>A
ENSP00000390923.2:p.Asn246Lys
ENST00000526117.1:c.807C>A
ENSP00000436930.1:p.Asn269Lys
ENST00000561065.1:c.738C>A
ENSP00000453580.1:p.Asn246Lys
ENST00000355497.5:c.807C>A
ENSP00000347684.5:p.Asn269Lys

Variation displays