rs886046258 Rat Genome Database

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Variant: rs886046258 -  Homo sapiens

RGD ID: 11644644
RS ID: rs886046258
ClinVar ID: CV279936
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTR  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 237,067,045
GRCh38 1 236,903,745
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000254.3:c.*6101A>C
NG_008959.1:g.113465A>C
NC_000001.11:g.236903745A>C
NC_000001.10:g.237067045A>C
More... 		01/13/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MTR
Accession:XM_017001330
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:NM_001291939
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_017001329
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_011544194
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_047421183
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_047421185
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_047421187
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:NM_001410942
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_005273141
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:NM_000254
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_047421186
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:XM_047421182
Location:3UTRS;EXON

Gene Symbol:MTR
Accession:NM_001291940
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000261269 CLINVAR
dbSNP (RS) rs886046258 CLINVAR
MedGen CN043592 CLINVAR
NCBI Gene MTR CLINVAR
OMIM 156570 CLINVAR