RGD:15112001 Rat Genome Database

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Variant: RGD:15112001 -  Homo sapiens

RGD ID: 15112001
RS ID: rs370918986
ClinVar ID: CV787818
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NANS  TRIM14  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 100,845,124
GRCh38 9 98,082,842
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018946.4:c.871-4A>G
NG_052789.1:g.31166A>G
NC_000009.12:g.98082842A>G
NC_000009.11:g.100845124A>G
More... 		11/08/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TRIM14
Accession:XM_005252320
Location:3UTRS;EXON

Gene Symbol:TRIM14
Accession:XM_047424163
Location:3UTRS;EXON

Gene Symbol:TRIM14
Accession:XM_017015353
Location:3UTRS;INTRON

Gene Symbol:TRIM14
Accession:XM_047424160
Location:3UTRS;INTRON

Gene Symbol:TRIM14
Accession:XM_047424162
Location:3UTRS;INTRON

Gene Symbol:TRIM14
Accession:XM_047424161
Location:3UTRS;INTRON

Gene Symbol:TRIM14
Accession:XR_929880
Location:EXON;NON-CODING

Gene Symbol:TRIM14
Accession:NM_014788
Location:INTRON

Gene Symbol:NANS
Accession:NM_018946
Location:INTRON

Gene Symbol:NANS
Accession:XM_011518788
Location:INTRON

Gene Symbol:NANS
Accession:XM_047423476
Location:INTRON

Gene Symbol:TRIM14
Accession:XM_011519244
Location:INTRON

Gene Symbol:NANS
Accession:XM_011518787
Location:INTRON

Gene Symbol:TRIM14
Accession:NM_033219
Location:INTRON

Gene Symbol:TRIM14
Accession:XM_047424164
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000977744 CLINVAR
dbSNP (RS) rs370918986 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene NANS CLINVAR
  TRIM14 CLINVAR
OMIM 605202 CLINVAR
  606556 CLINVAR