RGD:8650691 Rat Genome Database

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Variant: RGD:8650691 -  Homo sapiens

RGD ID: 8650691
ClinVar ID: CV127266
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNX16  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 82,744,225
GRCh38 8 81,831,990
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.81831990G>A
NC_000008.10:g.82744225G>A
NM_022133.3:c.376-2474C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SNX16
Accession:XM_005251282
Location:INTRON

Gene Symbol:SNX16
Accession:NM_001348189
Location:INTRON

Gene Symbol:SNX16
Accession:NM_152837
Location:INTRON

Gene Symbol:SNX16
Accession:NM_152836
Location:INTRON

Gene Symbol:SNX16
Accession:XM_047422087
Location:INTRON

Gene Symbol:SNX16
Accession:XM_047422086
Location:INTRON

Gene Symbol:SNX16
Accession:XM_047422085
Location:INTRON

Gene Symbol:SNX16
Accession:NM_022133
Location:INTRON

Gene Symbol:SNX16
Accession:XM_011517574
Location:INTRON

Gene Symbol:SNX16
Accession:NR_145475
Location:INTRON;NON-CODING

Gene Symbol:SNX16
Accession:NR_145472
Location:INTRON;NON-CODING

Gene Symbol:SNX16
Accession:NR_145474
Location:INTRON;NON-CODING

Gene Symbol:SNX16
Accession:NR_145473
Location:INTRON;NON-CODING

Variant Samples