rs181410965 Rat Genome Database

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Variant: rs181410965 -  Homo sapiens

RGD ID: 150466306
RS ID: rs181410965
ClinVar ID: CV1201223
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DIAPH1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 140,909,149
GRCh38 5 141,529,582
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1117t1:c.2649+21G>A
LRG_1117t2:c.2676+21G>A
NM_001079812.3:c.2649+21G>A
NM_001314007.2:c.2676+21G>A
More... 		08/07/2018 intron variant likely benign none provided

Gene Symbol:DIAPH1
Accession:NM_001079812
Location:INTRON

Gene Symbol:DIAPH1
Accession:NM_005219
Location:INTRON

Gene Symbol:DIAPH1
Accession:NM_001314007
Location:INTRON

Gene Symbol:DIAPH1
Accession:XM_047416885
Location:INTRON

Gene Symbol:DIAPH1
Accession:XM_047416884
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001587703 CLINVAR
dbSNP (RS) rs181410965 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DIAPH1 CLINVAR
OMIM 602121 CLINVAR