RGD:10398319 Rat Genome Database

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Variant: RGD:10398319 -  Homo sapiens

RGD ID: 10398319
RS ID: rs796053284
ClinVar ID: CV203990
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC9A6  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 135,080,722
GRCh38 X 135,998,563
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006359.2:c.584+5G>A
NG_017160.1:g.18137G>A
NC_000023.11:g.135998563G>A
NC_000023.10:g.135080722G>A
More... 		10/17/2016 intron variant pathogenic|likely pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC9A6
Accession:NM_001379110
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001400909
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001330652
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001177651
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001400910
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001400913
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001042537
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001400912
Location:INTRON

Gene Symbol:SLC9A6
Accession:XM_047441765
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_006359
Location:INTRON

Gene Symbol:SLC9A6
Accession:NM_001400911
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000595933 CLINVAR
dbSNP (RS) rs796053284 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene SLC9A6 CLINVAR
OMIM 300231 CLINVAR