RGD:8651259 Rat Genome Database

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Variant: RGD:8651259 -  Homo sapiens

RGD ID: 8651259
ClinVar ID: CV127834
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RNF38  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 36,337,964
GRCh38 9 36,337,967
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.36337967C>T
NC_000009.11:g.36337964C>T
NM_022781.4:c.*1785G>A
 utr-3|3 prime utr variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:RNF38
Accession:XM_047422796
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422802
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422800
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:NM_022781
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422805
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_005251367
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422801
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422804
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422797
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422799
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422798
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:NM_194330
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_011517712
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:NM_194332
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422794
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_017014297
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_006716721
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422803
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_017014296
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422795
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_047422806
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:NM_194328
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:NM_194329
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_011517713
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_017014294
Location:3UTRS;EXON

Gene Symbol:RNF38
Accession:XM_005251366
Location:3UTRS;EXON

Variant Samples