RGD:28907188 Rat Genome Database

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Variant: RGD:28907188 -  Homo sapiens

RGD ID: 28907188
RS ID: rs1274968540
ClinVar ID: CV897778
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 16,128,801
GRCh38 7 16,089,176
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.*2519T>A
NM_001101426.4:c.*2519T>A
NM_001368197.1:c.*2519T>A
NG_032690.2:g.337147T>A
More... 		01/12/2018 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_001101426
Location:3UTRS;EXON

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001159372 CLINVAR
dbSNP (RS) rs1274968540 CLINVAR
MedGen CN239202 CLINVAR
NCBI Gene CRPPA CLINVAR
OMIM 614631 CLINVAR