RGD:28874217 Rat Genome Database

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Variant: RGD:28874217 -  Homo sapiens

RGD ID: 28874217
RS ID: rs190739281
ClinVar ID: CV897311
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MET  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 116,438,278
GRCh38 7 116,798,224
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001324402.2:c.*2100C>T
LRG_662:g.130820C>T
NG_008996.1:g.130820C>T
NC_000007.14:g.116798224C>T
More... 		01/13/2018 3 prime utr variant benign Renal adenocarcinoma; Renal cell carcinoma 1; RENAL CELL CARCINOMA, PAPILLARY, 1, SOMATIC; Renal cell carcinoma, somatic
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:MET
Accession:NM_001127500
Location:3UTRS;EXON

Gene Symbol:MET
Accession:NM_000245
Location:3UTRS;EXON

Gene Symbol:MET
Accession:XM_011516223
Location:3UTRS;EXON

Gene Symbol:MET
Accession:NM_001324402
Location:3UTRS;EXON

Gene Symbol:MET
Accession:NM_001324401
Location:INTRON

Gene Symbol:MET
Accession:XM_047420400
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001165257 CLINVAR
dbSNP (RS) rs190739281 CLINVAR
MedGen C1336839 CLINVAR
NCBI Gene MET CLINVAR
OMIM 164860 CLINVAR
  605074 CLINVAR