rs907740769 Rat Genome Database

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Variant: rs907740769 -  Homo sapiens

RGD ID: 150482742
RS ID: rs907740769
ClinVar ID: CV1280051
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MVK  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 110,034,550
GRCh38 12 109,596,745
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000431.4:c.*168C>T
NM_001114185.3:c.*168C>T
NM_001301182.2:c.*168C>T
LRG_156:g.28051C>T
More... 		03/03/2015 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MVK
Accession:XM_017019314
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:XM_047428873
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_001301182
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_001414511
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:XM_017019313
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_001114185
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_001414515
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_001414514
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_001414513
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_000431
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NM_001414512
Location:3UTRS;EXON

Gene Symbol:MVK
Accession:NR_182760
Location:EXON;NON-CODING

Gene Symbol:MVK
Accession:NR_182762
Location:EXON;NON-CODING

Gene Symbol:MVK
Accession:NR_182758
Location:EXON;NON-CODING

Gene Symbol:MVK
Accession:NR_182759
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001715071 CLINVAR
dbSNP (RS) rs907740769 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MVK CLINVAR
OMIM 251170 CLINVAR