RGD:14722261 Rat Genome Database

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Variant: RGD:14722261 -  Homo sapiens

RGD ID: 14722261
RS ID: rs17588387
ClinVar ID: CV667317
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124903389  TECPR2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 14 102,842,776
GRCh38 14 102,376,439
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.-72-211A>G
NM_014844.5:c.-72-211A>G
NG_042851.1:g.18528A>G
NC_000014.9:g.102376439A>G
More...
06/14/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TECPR2
Accession:NM_014844
Location:5UTRS;INTRON

Gene Symbol:TECPR2
Accession:NM_001172631
Location:5UTRS;INTRON

Gene Symbol:LOC124903389
Accession:XR_007064350
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000832026 CLINVAR
dbSNP (RS) rs17588387 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TECPR2 CLINVAR
OMIM 615000 CLINVAR