RGD:11661581 Rat Genome Database

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Variant: RGD:11661581 -  Homo sapiens

RGD ID: 11661581
RS ID: rs886061378
ClinVar ID: CV302724
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DAAM2  MOCS1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 39,872,255
GRCh38 6 39,904,479
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009297.1:g.35000G>A
NC_000006.12:g.39904479C>T
NC_000006.11:g.39872255C>T
NM_015345.4:c.*2442C>T
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:DAAM2
Accession:NM_015345
Location:3UTRS;EXON

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

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

Gene Symbol:DAAM2
Accession:NM_001201427
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_006715043
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_006715046
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_006715039
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_006715040
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_006715045
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_017010630
Location:3UTRS;EXON

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

Gene Symbol:MOCS1
Accession:NM_001358533
Location:3UTRS;EXON

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

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

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

Gene Symbol:DAAM2
Accession:XM_047418533
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418534
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418537
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418535
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418538
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418531
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418532
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418541
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418536
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418539
Location:3UTRS;EXON

Gene Symbol:DAAM2
Accession:XM_047418540
Location:3UTRS;EXON

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000378094 CLINVAR
dbSNP (RS) rs886061378 CLINVAR
MedGen C1854988 CLINVAR
NCBI Gene DAAM2 CLINVAR
  MOCS1 CLINVAR
OMIM 252150 CLINVAR
  603707 CLINVAR
  606627 CLINVAR