RGD:11597360 Rat Genome Database

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Variant: RGD:11597360 -  Homo sapiens

RGD ID: 11597360
RS ID: rs533161726
ClinVar ID: CV279845
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTR  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 237,062,091
GRCh38 1 236,898,791
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000254.2:c.*1147T>G
NG_008959.1:g.108511T>G
NC_000001.11:g.236898791T>G
NC_000001.10:g.237062091T>G
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:NM_000254
Location:3UTRS;EXON

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

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

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

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

Gene Symbol:
Accession:
Location:3UTRS;EXON

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

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

Gene Symbol:MTR
Accession:XM_017001330
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_001410942
Location:3UTRS;EXON

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000393426 CLINVAR
dbSNP (RS) rs533161726 CLINVAR
MedGen CN043592 CLINVAR
NCBI Gene MTR CLINVAR
OMIM 156570 CLINVAR