RGD:14746381 Rat Genome Database

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Variant: RGD:14746381 -  Homo sapiens

RGD ID: 14746381
RS ID: rs10763537
ClinVar ID: CV664966
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TFAM  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 60,147,784
GRCh38 10 58,388,024
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001270782.2:c.221-166G>A
NM_003201.3:c.221-166G>A
NG_053006.1:g.7882G>A
NC_000010.11:g.58388024G>A
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TFAM
Accession:XM_047425697
Location:INTRON

Gene Symbol:TFAM
Accession:XM_011540121
Location:INTRON

Gene Symbol:TFAM
Accession:NM_003201
Location:INTRON

Gene Symbol:TFAM
Accession:NM_001270782
Location:INTRON

Gene Symbol:TFAM
Accession:NR_073073
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000844388 CLINVAR
dbSNP (RS) rs10763537 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TFAM CLINVAR
OMIM 600438 CLINVAR