RGD:150494633 Rat Genome Database

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Variant: RGD:150494633 -  Homo sapiens

RGD ID: 150494633
RS ID: rs2234532
ClinVar ID: CV1238899
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WARS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 100,801,423
GRCh38 14 100,335,086
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_213645.2:c.1132-50A>G
NM_213646.2:c.1132-50A>G
NM_004184.4:c.1255-50A>G
NM_173701.2:c.1255-50A>G
More... 		05/16/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WARS1
Accession:NM_173701
Location:INTRON

Gene Symbol:WARS1
Accession:XM_017021627
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431757
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431763
Location:INTRON

Gene Symbol:WARS1
Accession:NM_213645
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431759
Location:INTRON

Gene Symbol:WARS1
Accession:NM_213646
Location:INTRON

Gene Symbol:WARS1
Accession:NM_004184
Location:INTRON

Gene Symbol:WARS1
Accession:XM_011537136
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431764
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431761
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431758
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431762
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431765
Location:INTRON

Gene Symbol:WARS1
Accession:XM_047431760
Location:INTRON

Gene Symbol:WARS1
Accession:XM_024449707
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001655443 CLINVAR
dbSNP (RS) rs2234532 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WARS1 CLINVAR
OMIM 191050 CLINVAR