RGD:11606564 Rat Genome Database

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Variant: RGD:11606564 -  Homo sapiens

RGD ID: 11606564
RS ID: rs76015838
ClinVar ID: CV305580
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 16,128,754
GRCh38 7 16,089,129
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.*2566A>G
NM_001101426.4:c.*2566A>G
NM_001368197.1:c.*2566A>G
NG_032690.2:g.337194A>G
More... 		06/14/2016 3 prime utr variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CRPPA
Accession:NM_001101426
Location:3UTRS;EXON

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

Gene Symbol:CRPPA
Accession:NM_001101417
Location:3UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000332893 CLINVAR
dbSNP (RS) rs76015838 CLINVAR
MedGen CN239202 CLINVAR
NCBI Gene ISPD CLINVAR
OMIM 614631 CLINVAR