RGD:150441001 Rat Genome Database

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Variant: RGD:150441001 -  Homo sapiens

RGD ID: 150441001
RS ID: rs142795512
ClinVar ID: CV1204486
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRMU  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 22 46,747,802
GRCh38 22 46,351,905
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282783.2:c.232-216C>T
NM_001282784.2:c.232-216C>T
NM_001282782.2:c.310-216C>T
NM_001282785.2:c.652-216C>T
More... 		07/15/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TRMU
Accession:NM_001282785
Location:INTRON

Gene Symbol:TRMU
Accession:XM_011530272
Location:INTRON

Gene Symbol:TRMU
Accession:NM_001282782
Location:INTRON

Gene Symbol:TRMU
Accession:XM_047441445
Location:INTRON

Gene Symbol:TRMU
Accession:NM_001282783
Location:INTRON

Gene Symbol:TRMU
Accession:XM_047441444
Location:INTRON

Gene Symbol:TRMU
Accession:XM_011530273
Location:INTRON

Gene Symbol:TRMU
Accession:XM_047441446
Location:INTRON

Gene Symbol:TRMU
Accession:NM_001282784
Location:INTRON

Gene Symbol:TRMU
Accession:NM_018006
Location:INTRON

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001583592 CLINVAR
dbSNP (RS) rs142795512 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TRMU CLINVAR
OMIM 610230 CLINVAR