RGD:8649799 Rat Genome Database

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Variant: RGD:8649799 -  Homo sapiens

RGD ID: 8649799
ClinVar ID: CV126373
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CSMD3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 113,264,425
GRCh38 8 112,252,196
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.112252196G>A
NC_000008.10:g.113264425G>A
NM_052900.2:c.9603+2057C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CSMD3
Accession:XM_011516815
Location:INTRON

Gene Symbol:CSMD3
Accession:XM_017013009
Location:INTRON

Gene Symbol:CSMD3
Accession:NM_001363185
Location:INTRON

Gene Symbol:CSMD3
Accession:NM_198124
Location:INTRON

Gene Symbol:CSMD3
Accession:XM_011516816
Location:INTRON

Gene Symbol:CSMD3
Accession:XM_047421314
Location:INTRON

Gene Symbol:CSMD3
Accession:XM_017013010
Location:INTRON

Gene Symbol:CSMD3
Accession:XM_017013008
Location:INTRON

Gene Symbol:CSMD3
Accession:NM_052900
Location:INTRON

Gene Symbol:CSMD3
Accession:NM_198123
Location:INTRON

Variant Samples