RGD:11659404 Rat Genome Database

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Variant: RGD:11659404 -  Homo sapiens

RGD ID: 11659404
RS ID: rs886062166
ClinVar ID: CV310669
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  CRPPA-AS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 16,298,535
GRCh38 7 16,258,910
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.16258910A>G
NC_000007.13:g.16298535A>G
NM_001101426.4:c.1026+10T>C
NM_001101417.4:c.876+10T>C
More... 		06/14/2016 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CRPPA
Accession:NM_001368197
Location:INTRON

Gene Symbol:CRPPA
Accession:NM_001101417
Location:INTRON

Gene Symbol:CRPPA
Accession:NM_001101426
Location:INTRON

Gene Symbol:CRPPA-AS1
Accession:NR_038947
Location:INTRON;NON-CODING

Gene Symbol:CRPPA
Accession:NR_160656
Location:INTRON;NON-CODING

Gene Symbol:CRPPA-AS1
Accession:NR_038946
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000357657 CLINVAR
dbSNP (RS) rs886062166 CLINVAR
MedGen CN239202 CLINVAR
NCBI Gene ISPD CLINVAR
  ISPD-AS1 CLINVAR
OMIM 614631 CLINVAR