RGD:9586915 Rat Genome Database

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Variant: RGD:9586915 -  Homo sapiens

RGD ID: 9586915
RS ID: rs260631
ClinVar ID: CV165618
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EDAR  RANBP2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 109,527,087
GRCh38 2 108,910,631
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008257.1:g.83742C>T
NC_000002.12:g.108910631G>A
NC_000002.11:g.109527087G>A
NM_022336.3:c.731-99C>T
More...
05/03/2020 intron variant benign|uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:RANBP2
Accession:NM_006267
Location:INTRON

Gene Symbol:EDAR
Accession:NM_022336
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_005264002
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_005264007
Location:INTRON

Gene Symbol:EDAR
Accession:XM_006712204
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_011511576
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_011511575
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_011511578
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_017004625
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_017004624
Location:INTRON

Gene Symbol:RANBP2
Accession:XM_047445367
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:RANBP2
Accession:NM_001415871
Location:INTRON

Gene Symbol:RANBP2
Accession:NM_001415873
Location:INTRON

Gene Symbol:RANBP2
Accession:NM_001415872
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000143986 CLINVAR
dbSNP (RS) rs260631 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EDAR CLINVAR
  RANBP2 CLINVAR
OMIM 601181 CLINVAR
  604095 CLINVAR