RGD:14737524 Rat Genome Database

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Variant: RGD:14737524 -  Homo sapiens

RGD ID: 14737524
RS ID: rs114589854
ClinVar ID: CV669678
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNM2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 10,935,552
GRCh38 19 10,824,876
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004945.4:c.1882-181G>A
NM_001005360.3:c.1894-181G>A
NM_001005361.3:c.1894-181G>A
NM_001190716.2:c.1894-181G>A
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DNM2
Accession:NM_001190716
Location:INTRON

Gene Symbol:DNM2
Accession:NM_001005360
Location:INTRON

Gene Symbol:DNM2
Accession:NM_001005362
Location:INTRON

Gene Symbol:DNM2
Accession:NM_001005361
Location:INTRON

Gene Symbol:DNM2
Accession:NM_004945
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000838964 CLINVAR
dbSNP (RS) rs114589854 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNM2 CLINVAR
OMIM 602378 CLINVAR