RGD:14743331 Rat Genome Database

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Variant: RGD:14743331 -  Homo sapiens

RGD ID: 14743331
RS ID: rs7799150
ClinVar ID: CV662363
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  CRPPA-AS1  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 16,298,438
GRCh38 7 16,258,813
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001101426.4:c.1026+107A>C
NM_001101417.4:c.876+107A>C
NM_001368197.1:c.921+107A>C
NG_032690.2:g.167510A>C
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CRPPA
Accession:NM_001101426
Location:INTRON

Gene Symbol:CRPPA
Accession:NM_001368197
Location:INTRON

Gene Symbol:CRPPA
Accession:NM_001101417
Location:INTRON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000841981 CLINVAR
dbSNP (RS) rs7799150 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CRPPA CLINVAR
  CRPPA-AS1 CLINVAR
OMIM 614631 CLINVAR