RGD:8579414 Rat Genome Database

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Variant: RGD:8579414 -  Homo sapiens

RGD ID: 8579414
ClinVar ID: CV113815
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GALNTL6  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 172,943,231
GRCh38 4 172,022,080
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.172022080T>C
NC_000004.11:g.172943231T>C
NM_001034845.2:c.138+207362T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:GALNTL6
Accession:XM_011531993
Location:INTRON

Gene Symbol:GALNTL6
Accession:XM_011531997
Location:INTRON

Gene Symbol:GALNTL6
Accession:XM_017008243
Location:INTRON

Gene Symbol:GALNTL6
Accession:XM_017008244
Location:INTRON

Gene Symbol:GALNTL6
Accession:XM_011531996
Location:INTRON

Gene Symbol:GALNTL6
Accession:XM_011531994
Location:INTRON

Gene Symbol:GALNTL6
Accession:NM_001034845
Location:INTRON

Gene Symbol:GALNTL6
Accession:XM_011531995
Location:INTRON

Variant Samples