rs368869644 Rat Genome Database

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Variant: rs368869644 -  Homo sapiens

RGD ID: 150504936
RS ID: rs368869644
ClinVar ID: CV1222768
Genic Status: GENIC
Type: insertion (SO:0000667) 
Associated Genes: DIAPH1  
Reference Nucleotide: -
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 140,968,041
GRCh38 5 141,588,474
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1117t1:c.118-1293dup
LRG_1117t2:c.118-240dup
NM_001079812.3:c.118-1293dup
NM_001314007.2:c.118-240dup
More... 		08/10/2019 intron variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001621702 CLINVAR
dbSNP (RS) rs368869644 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DIAPH1 CLINVAR
OMIM 602121 CLINVAR