RGD:8582193 Rat Genome Database

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Variant: RGD:8582193 -  Homo sapiens

RGD ID: 8582193
ClinVar ID: CV116662
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BMP6  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 7,879,021
GRCh38 6 7,878,788
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.12:g.7878788T>C
NC_000006.11:g.7879021T>C
NM_001718.4:c.1205-286T>C
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:BMP6
Accession:NM_001718
Location:INTRON

Variant Samples