RGD:11630785 Rat Genome Database

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Variant: RGD:11630785 -  Homo sapiens

RGD ID: 11630785
RS ID: rs10485703
ClinVar ID: CV344733
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDYN  PDYN-AS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 20 1,960,313
GRCh38 20 1,979,667
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_028027.1:g.19579T>C
NC_000020.11:g.1979667A>G
NC_000020.10:g.1960313A>G
NM_001190900.1:c.*656T>C
More... 		01/13/2018 3 prime utr variant benign|likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:PDYN
Accession:NM_001190900
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_011529246
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:NM_001190892
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_011529249
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_011529248
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:NM_024411
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_011529247
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_011529245
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:NM_001190898
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_011529250
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:NM_001190899
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_011529244
Location:3UTRS;EXON

Gene Symbol:PDYN
Accession:XM_017027878
Location:3UTRS;EXON

Gene Symbol:PDYN-AS1
Accession:NR_134520
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000359519 CLINVAR
dbSNP (RS) rs10485703 CLINVAR
MedGen C1853250 CLINVAR
NCBI Gene 727993 CLINVAR
  PDYN CLINVAR
OMIM 131340 CLINVAR
  610245 CLINVAR