RGD:401924404 Rat Genome Database

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Variant: RGD:401924404 -  Homo sapiens

RGD ID: 401924404
ClinVar ID: CV2828818
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOCAD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 20,986,463
GRCh38 9 20,986,464
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_017794.5:c.4905G>A
NC_000009.12:g.20986464G>A
NC_000009.11:g.20986463G>A
NP_001362497.1:p.Thr1600=
More... 		01/01/2023 synonymous variant likely benign FOCAD-related condition; none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FOCAD
Accession:XM_024447586
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423532
Location:EXON

Gene Symbol:FOCAD
Accession:NM_001375570
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423539
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423535
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423534
Location:EXON

Gene Symbol:FOCAD
Accession:XM_017014856
Location:EXON

Gene Symbol:FOCAD
Accession:XM_017014852
Location:EXON

Gene Symbol:FOCAD
Accession:XM_017014859
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423536
Location:EXON

Gene Symbol:FOCAD
Accession:XM_017014855
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423538
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423537
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423533
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423540
Location:EXON

Gene Symbol:FOCAD
Accession:NM_017794
Location:EXON

Gene Symbol:FOCAD
Accession:NM_001375567
Location:EXON

Gene Symbol:FOCAD
Accession:NM_001375568
Location:EXON

Gene Symbol:FOCAD
Accession:XM_047423531
Location:EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003435739 CLINVAR
  RCV003946616 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FOCAD CLINVAR
OMIM 614606 CLINVAR