RGD:14730888 Rat Genome Database

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Variant: RGD:14730888 -  Homo sapiens

RGD ID: 14730888
RS ID: rs7759182
ClinVar ID: CV662119
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: UQCC2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 33,679,239
GRCh38 6 33,711,462
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_032340.4:c.138+87G>T
NG_034147.1:g.5290G>T
NC_000006.12:g.33711462C>A
NC_000006.11:g.33679239C>A
More... 		06/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:UQCC2
Accession:NM_032340
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000835879 CLINVAR
dbSNP (RS) rs7759182 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene UQCC2 CLINVAR
OMIM 614461 CLINVAR