RGD:11655997 Rat Genome Database

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Variant: RGD:11655997 -  Homo sapiens

RGD ID: 11655997
RS ID: rs886062163
ClinVar ID: CV310451
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 16,130,811
GRCh38 7 16,091,186
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001368197.1:c.*509A>G
NR_160656.1:n.1930A>G
NM_001101426.3:c.*509A>G
NC_000007.14:g.16091186T>C
More... 		06/14/2016 3 prime utr variant uncertain significance
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 RCV000329915 CLINVAR
dbSNP (RS) rs886062163 CLINVAR
MedGen CN239202 CLINVAR
NCBI Gene ISPD CLINVAR
OMIM 614631 CLINVAR