RGD:8649423 Rat Genome Database

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Variant: RGD:8649423 -  Homo sapiens

RGD ID: 8649423
ClinVar ID: CV125997
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: UMAD1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 7,816,751
GRCh38 7 7,777,120
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.7777120G>C
NC_000007.13:g.7816751G>C
NR_034084.1:n.257-24550G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:UMAD1
Accession:NM_001302350
Location:5UTRS;INTRON

Gene Symbol:UMAD1
Accession:NM_001302349
Location:INTRON

Gene Symbol:UMAD1
Accession:NM_001302348
Location:INTRON

Variant Samples