RGD:8582400 Rat Genome Database

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Variant: RGD:8582400 -  Homo sapiens

RGD ID: 8582400
ClinVar ID: CV116871
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COG5  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 107,187,777
GRCh38 7 107,547,332
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006348.3:c.510+779A>T
NG_028095.1:g.22183A>T
NC_000007.14:g.107547332T>A
NC_000007.13:g.107187777T>A
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:COG5
Accession:NM_181733
Location:INTRON

Gene Symbol:COG5
Accession:NM_006348
Location:INTRON

Gene Symbol:COG5
Accession:NM_001161520
Location:INTRON

Gene Symbol:COG5
Accession:XM_024446634
Location:INTRON

Gene Symbol:COG5
Accession:NM_001379516
Location:INTRON

Gene Symbol:COG5
Accession:NM_001379515
Location:INTRON

Gene Symbol:COG5
Accession:NM_001379511
Location:INTRON

Gene Symbol:COG5
Accession:NM_001379512
Location:INTRON

Gene Symbol:COG5
Accession:NM_001379514
Location:INTRON

Gene Symbol:COG5
Accession:NM_001379513
Location:INTRON

Variant Samples