RGD:8577758 Rat Genome Database

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Variant: RGD:8577758 -  Homo sapiens

RGD ID: 8577758
ClinVar ID: CV112135
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MORC1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 108,710,591
GRCh38 3 108,991,744
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.12:g.108991744C>A
NC_000003.11:g.108710591C>A
NM_014429.3:c.2188-4795G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:MORC1
Accession:XM_011512694
Location:INTRON

Gene Symbol:MORC1
Accession:XM_011512691
Location:INTRON

Gene Symbol:MORC1
Accession:XM_005247362
Location:INTRON

Gene Symbol:MORC1
Accession:XM_011512693
Location:INTRON

Gene Symbol:MORC1
Accession:NM_014429
Location:INTRON

Gene Symbol:MORC1
Accession:XM_011512696
Location:INTRON

Gene Symbol:MORC1
Accession:XM_011512697
Location:INTRON

Gene Symbol:MORC1
Accession:XM_047447970
Location:INTRON

Gene Symbol:MORC1
Accession:XM_017006169
Location:INTRON

Gene Symbol:MORC1
Accession:XM_011512692
Location:INTRON

Gene Symbol:MORC1
Accession:XM_047447968
Location:INTRON

Variant Samples