RGD:405207506 Rat Genome Database

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Variant: RGD:405207506 -  Homo sapiens

RGD ID: 405207506
ClinVar ID: CV2873997
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CEP97  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 101,476,561
GRCh38 3 101,757,717
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001410784.1:c.1009T>C
NM_001303401.2:c.1028-94T>C
NM_024548.4:c.1111T>C
NM_001410785.1:c.926-94T>C
More... 		01/07/2024 intron variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003552040 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CEP97 CLINVAR
OMIM 615864 CLINVAR