RGD:11659154 Rat Genome Database

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Variant: RGD:11659154 -  Homo sapiens

RGD ID: 11659154
RS ID: rs59399612
ClinVar ID: CV309613
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MET  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 116,436,409
GRCh38 7 116,796,355
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
LRG_662:g.128951T>G
NG_008996.1:g.128951T>G
NC_000007.14:g.116796355T>G
NC_000007.13:g.116436409T>G
More... 		01/13/2018 3 prime utr variant benign|likely benign adult 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_000245
Location:3UTRS;EXON

Gene Symbol:MET
Accession:NM_001127500
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:XM_047420400
Location:INTRON

Gene Symbol:MET
Accession:NM_001324401
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000355291 CLINVAR
dbSNP (RS) rs59399612 CLINVAR
MedGen C1336839 CLINVAR
NCBI Gene MET CLINVAR
OMIM 164860 CLINVAR
  605074 CLINVAR