RGD:8584355 Rat Genome Database

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Variant: RGD:8584355 -  Homo sapiens

RGD ID: 8584355
ClinVar ID: CV118928
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RYR3  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 33,946,308
GRCh38 15 33,654,107
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.10:g.33654107G>T
NC_000015.9:g.33946308G>T
NM_001036.4:c.4308+1224G>T
NM_001036.3:c.4308+1224G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:RYR3
Accession:XM_017022477
Location:INTRON

Gene Symbol:RYR3
Accession:XM_011521880
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022468
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022475
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022476
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022471
Location:INTRON

Gene Symbol:RYR3
Accession:NM_001243996
Location:INTRON

Gene Symbol:RYR3
Accession:XM_047432931
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022472
Location:INTRON

Gene Symbol:RYR3
Accession:NM_001036
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022474
Location:INTRON

Gene Symbol:RYR3
Accession:XM_047432933
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022473
Location:INTRON

Gene Symbol:RYR3
Accession:XM_024450016
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022469
Location:INTRON

Gene Symbol:RYR3
Accession:XM_017022470
Location:INTRON

Gene Symbol:RYR3
Accession:XM_024450015
Location:INTRON

Gene Symbol:RYR3
Accession:XM_047432932
Location:INTRON

Gene Symbol:RYR3
Accession:XR_001751371
Location:INTRON;NON-CODING

Gene Symbol:RYR3
Accession:XR_001751370
Location:INTRON;NON-CODING

Variant Samples