RGD:15149772 Rat Genome Database

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Variant: RGD:15149772 -  Homo sapiens

RGD ID: 15149772
RS ID: rs993647773
ClinVar ID: CV743760
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC9A1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 27,428,626
GRCh38 1 27,102,135
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003047.5:c.1821-5C>T
NG_030006.1:g.57826C>T
NC_000001.11:g.27102135G>A
NC_000001.10:g.27428626G>A
More... 		02/09/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC9A1
Accession:XM_011542021
Location:INTRON

Gene Symbol:SLC9A1
Accession:XM_047428769
Location:INTRON

Gene Symbol:SLC9A1
Accession:NM_003047
Location:INTRON

Gene Symbol:SLC9A1
Accession:NR_046474
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000901007 CLINVAR
dbSNP (RS) rs993647773 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC9A1 CLINVAR
OMIM 107310 CLINVAR