RGD:28868218 Rat Genome Database

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Variant: RGD:28868218 -  Homo sapiens

RGD ID: 28868218
RS ID: rs201756228
ClinVar ID: CV897787
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRPPA  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 16,128,987
GRCh38 7 16,089,362
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_032690.2:g.336961T>C
NC_000007.14:g.16089362A>G
NC_000007.13:g.16128987A>G
NR_160656.1:n.3754T>C
More... 		01/13/2018 3 prime utr variant benign
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 RCV001162358 CLINVAR
dbSNP (RS) rs201756228 CLINVAR
MedGen CN239202 CLINVAR
NCBI Gene CRPPA CLINVAR
OMIM 614631 CLINVAR