RGD:8587480 Rat Genome Database

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Variant: RGD:8587480 -  Homo sapiens

RGD ID: 8587480
ClinVar ID: CV122111
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SHROOM4  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 50,461,050
GRCh38 X 50,718,050
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_020717.3:c.118-22113G>T
NG_011882.1:g.100995G>T
NC_000023.11:g.50718050C>A
NC_000023.10:g.50461050C>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SHROOM4
Accession:NM_020717
Location:INTRON

Gene Symbol:SHROOM4
Accession:XM_017029683
Location:INTRON

Gene Symbol:SHROOM4
Accession:XM_047442279
Location:INTRON

Gene Symbol:SHROOM4
Accession:XM_017029684
Location:INTRON

Gene Symbol:SHROOM4
Accession:XM_017029685
Location:INTRON

Gene Symbol:SHROOM4
Accession:XM_017029682
Location:INTRON

Gene Symbol:SHROOM4
Accession:XM_017029687
Location:INTRON

Gene Symbol:SHROOM4
Accession:XM_047442280
Location:INTRON

Gene Symbol:SHROOM4
Accession:XR_001755717
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:NR_172070
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:XR_001755718
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:NR_172068
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:NR_172069
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:XR_007068196
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:NR_027121
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:XR_001755716
Location:INTRON;NON-CODING

Gene Symbol:SHROOM4
Accession:XR_007068197
Location:INTRON;NON-CODING

Variant Samples