RGD:8650379 Rat Genome Database

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Variant: RGD:8650379 -  Homo sapiens

RGD ID: 8650379
ClinVar ID: CV126954
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNTG1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 50,973,225
GRCh38 8 50,060,665
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.50060665G>T
NC_000008.10:g.50973225G>T
NM_001287813.1:c.-102-111896G>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SNTG1
Accession:NM_018967
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:NM_001321775
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:NM_001321773
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:NM_001321777
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:NM_001287813
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_024447183
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_017013579
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_017013580
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:NM_001287814
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_017013582
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_047421898
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_047421896
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:NM_001321776
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_017013581
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:XM_047421897
Location:5UTRS;INTRON

Gene Symbol:SNTG1
Accession:NM_001321778
Location:INTRON

Gene Symbol:SNTG1
Accession:NR_135794
Location:INTRON;NON-CODING

Gene Symbol:SNTG1
Accession:NR_135796
Location:INTRON;NON-CODING

Gene Symbol:SNTG1
Accession:NR_135795
Location:INTRON;NON-CODING

Gene Symbol:SNTG1
Accession:NR_135798
Location:INTRON;NON-CODING

Gene Symbol:SNTG1
Accession:NR_135797
Location:INTRON;NON-CODING

Variant Samples