RGD:28897738 Rat Genome Database

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Variant: RGD:28897738 -  Homo sapiens

RGD ID: 28897738
RS ID: rs1038982726
ClinVar ID: CV895933
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MOCS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 39,872,826
GRCh38 6 39,905,050
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005943.6:c.*2075A>G
NG_009297.1:g.34429A>G
NC_000006.11:g.39872826T>C
NM_001358533.2:c.*2075A>G
More... 		01/13/2018 3 prime utr variant uncertain significance Molybdenum Cofactor Deficiency A; Molybdenum cofactor deficiency, complementation group A
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MOCS1
Accession:NM_001358533
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:NM_001358534
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:XM_047418828
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:NM_001358529
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:NM_001358531
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:NM_001358530
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:NM_001075098
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:NM_005943
Location:3UTRS;EXON

Gene Symbol:MOCS1
Accession:NR_033233
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001155154 CLINVAR
dbSNP (RS) rs1038982726 CLINVAR
MedGen C1854988 CLINVAR
NCBI Gene MOCS1 CLINVAR
OMIM 252150 CLINVAR
  603707 CLINVAR