rs3830265 Rat Genome Database

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Variant: rs3830265 -  Homo sapiens

RGD ID: 150331430
RS ID: rs3830265
ClinVar ID: CV1169002
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: PRKCD  
Reference Nucleotide: CTCAGAGC
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 3 53,220,765 - 53,220,773
GRCh38 3 53,186,749 - 53,186,757
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001354678.2:c.1400+54_1400+61del
NM_001354676.2:c.1409+54_1409+61del
LRG_1327:g.35741_35748del
NG_033864.2:g.35741_35748del
More... 		05/17/2021 intron variant benign AllHighlyPenetrant; none provided

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001536473 CLINVAR
  RCV003394119 CLINVAR
dbSNP (RS) rs3830265 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene PRKCD CLINVAR
OMIM 176977 CLINVAR