RGD:155970727 Rat Genome Database

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Variant: RGD:155970727 -  Homo sapiens

RGD ID: 155970727
ClinVar ID: CV2158065
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNA2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 70,206,038
GRCh38 10 68,446,281
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001080449.3:c.1057+15T>C
NG_034247.1:g.30693T>C
NC_000010.11:g.68446281A>G
NC_000010.10:g.70206038A>G
 08/23/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DNA2
Accession:XM_011539417
Location:5UTRS;INTRON

Gene Symbol:DNA2
Accession:NM_001080449
Location:INTRON

Gene Symbol:DNA2
Accession:XM_017015799
Location:INTRON

Gene Symbol:DNA2
Accession:XM_006717680
Location:INTRON

Gene Symbol:DNA2
Accession:NR_102264
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003033423 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNA2 CLINVAR
OMIM 601810 CLINVAR