RGD:28910042 Rat Genome Database

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Variant: RGD:28910042 -  Homo sapiens

RGD ID: 28910042
RS ID: rs1384388053
ClinVar ID: CV897826
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 16,131,244
GRCh38 7 16,091,619
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001101417.4:c.*76G>A
NM_001101426.4:c.*76G>A
NM_001368197.1:c.*76G>A
NG_032690.2:g.334704G>A
More... 		03/30/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CRPPA
Accession:NM_001101417
Location:3UTRS;EXON

Gene Symbol:CRPPA
Accession:NM_001368197
Location:3UTRS;EXON

Gene Symbol:CRPPA
Accession:NM_001101426
Location:3UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001161095 CLINVAR
dbSNP (RS) rs1384388053 CLINVAR
MedGen CN239202 CLINVAR
NCBI Gene CRPPA CLINVAR
OMIM 614631 CLINVAR