RGD:8649950 Rat Genome Database

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Variant: RGD:8649950 -  Homo sapiens

RGD ID: 8649950
ClinVar ID: CV126524
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WASHC5  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 126,075,735
GRCh38 8 125,063,493
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_014846.3:c.1408+29G>A
NG_012636.1:g.33327G>A
NC_000008.11:g.125063493C>T
NC_000008.10:g.126075735C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:WASHC5
Accession:NM_001330609
Location:INTRON

Gene Symbol:WASHC5
Accession:XM_047422502
Location:INTRON

Gene Symbol:WASHC5
Accession:NM_014846
Location:INTRON

Gene Symbol:WASHC5
Accession:XM_047422503
Location:INTRON

Gene Symbol:WASHC5
Accession:XM_011517409
Location:INTRON

Variant Samples