RGD:14722328 Rat Genome Database

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Variant: RGD:14722328 -  Homo sapiens

RGD ID: 14722328
RS ID: rs77092091
ClinVar ID: CV666451
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TECPR2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 14 102,874,740
GRCh38 14 102,408,403
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001172631.3:c.349-85T>C
NM_014844.5:c.349-85T>C
NG_042851.1:g.50492T>C
NC_000014.9:g.102408403T>C
More... 		06/14/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TECPR2
Accession:NM_001172631
Location:INTRON

Gene Symbol:TECPR2
Accession:NM_014844
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000832054 CLINVAR
dbSNP (RS) rs77092091 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TECPR2 CLINVAR
OMIM 615000 CLINVAR