RGD:11604649 Rat Genome Database

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Variant: RGD:11604649 -  Homo sapiens

RGD ID: 11604649
RS ID: rs114572844
ClinVar ID: CV310557
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 16,128,969
GRCh38 7 16,089,344
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.16089344G>A
NC_000007.13:g.16128969G>A
NM_001101417.4:c.*2351C>T
NM_001101426.4:c.*2351C>T
More... 		06/14/2016 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CRPPA
Accession:NM_001368197
Location:3UTRS;EXON

Gene Symbol:CRPPA
Accession:NM_001101426
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 RCV000311300 CLINVAR
dbSNP (RS) rs114572844 CLINVAR
MedGen CN239202 CLINVAR
NCBI Gene ISPD CLINVAR
OMIM 614631 CLINVAR