RGD:156371286 Rat Genome Database

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Variant: RGD:156371286 -  Homo sapiens

RGD ID: 156371286
ClinVar ID: CV2048874
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNX10  SNX10-AS1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 26,412,107
GRCh38 7 26,372,487
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001199838.2:c.273-4C>G
NM_001199837.3:c.516-4C>G
NM_001199835.1:c.525-4C>G
NM_001318199.3:c.525-4C>G
More... 		08/17/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SNX10-AS1
Accession:NR_136270
Location:EXON;NON-CODING

Gene Symbol:SNX10-AS1
Accession:NR_136272
Location:EXON;NON-CODING

Gene Symbol:SNX10-AS1
Accession:NR_136271
Location:EXON;NON-CODING

Gene Symbol:SNX10
Accession:NM_001318199
Location:INTRON

Gene Symbol:SNX10
Accession:NM_001362754
Location:INTRON

Gene Symbol:SNX10
Accession:NM_001199835
Location:INTRON

Gene Symbol:SNX10
Accession:NM_001318198
Location:INTRON

Gene Symbol:SNX10
Accession:XM_047420283
Location:INTRON

Gene Symbol:SNX10
Accession:NM_001199838
Location:INTRON

Gene Symbol:SNX10
Accession:NM_013322
Location:INTRON

Gene Symbol:SNX10
Accession:XM_006715712
Location:INTRON

Gene Symbol:SNX10
Accession:NM_001199837
Location:INTRON

Gene Symbol:SNX10
Accession:NM_001362753
Location:INTRON

Gene Symbol:SNX10
Accession:XM_047420282
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002814298 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNX10 CLINVAR
  SNX10-AS1 CLINVAR
OMIM 614780 CLINVAR