RGD:13836617 Rat Genome Database

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Variant: RGD:13836617 -  Homo sapiens

RGD ID: 13836617
RS ID: rs1406614136
ClinVar ID: CV587894
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127896767  TRMU  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 46,731,653
GRCh38 22 46,335,756
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018006.5:c.-9G>A
NG_012173.1:g.5356G>A
NC_000022.11:g.46335756G>A
NC_000022.10:g.46731653G>A
More... 		04/09/2018 5 prime utr variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:TRMU
Accession:NM_001282783
Location:5UTRS;EXON

Gene Symbol:TRMU
Accession:NM_018006
Location:5UTRS;EXON

Gene Symbol:TRMU
Accession:NM_001282784
Location:5UTRS;EXON

Gene Symbol:TRMU
Accession:XM_011530272
Location:5UTRS;EXON

Gene Symbol:TRMU
Accession:XM_011530273
Location:5UTRS;EXON

Gene Symbol:TRMU
Accession:NM_001282785
Location:5UTRS;EXON

Gene Symbol:TRMU
Accession:NM_001282782
Location:5UTRS;EXON

Gene Symbol:TRMU
Accession:NR_104241
Location:EXON;NON-CODING

Gene Symbol:TRMU
Accession:NR_104240
Location:EXON;NON-CODING

Gene Symbol:TRMU
Accession:XM_047441446
Location:INTRON

Gene Symbol:TRMU
Accession:XM_047441444
Location:INTRON

Gene Symbol:TRMU
Accession:XM_047441445
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000732792 CLINVAR
dbSNP (RS) rs1406614136 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene TRMU CLINVAR
OMIM 610230 CLINVAR