RGD:8590726 Rat Genome Database

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Variant: RGD:8590726 -  Homo sapiens

RGD ID: 8590726
ClinVar ID: CV125435
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STEAP1B  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 22,514,110
GRCh38 7 22,474,491
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.22474491C>G
NC_000007.13:g.22514110C>G
NM_001164460.1:c.762+18074G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:STEAP1B
Accession:XM_047420103
Location:3UTRS;EXON

Gene Symbol:STEAP1B
Accession:XM_047420104
Location:3UTRS;EXON

Gene Symbol:STEAP1B
Accession:XM_047420106
Location:INTRON

Gene Symbol:STEAP1B
Accession:XM_047420107
Location:INTRON

Gene Symbol:STEAP1B
Accession:NM_001382447
Location:INTRON

Gene Symbol:STEAP1B
Accession:XM_047420111
Location:INTRON

Gene Symbol:STEAP1B
Accession:XM_047420109
Location:INTRON

Gene Symbol:STEAP1B
Accession:XM_047420110
Location:INTRON

Gene Symbol:STEAP1B
Accession:NM_001164460
Location:INTRON

Gene Symbol:STEAP1B
Accession:XM_047420108
Location:INTRON

Gene Symbol:STEAP1B
Accession:NM_207342
Location:INTRON

Variant Samples