rs56408197 Rat Genome Database

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Variant: rs56408197 -  Homo sapiens

RGD ID: 150421007
RS ID: rs56408197
ClinVar ID: CV1196850
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DIS3L2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 233,074,739
GRCh38 2 232,210,029
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001257281.2:c.1125-297C>G
NM_152383.5:c.1125-297C>G
LRG_534:g.253447C>G
NG_032572.1:g.253447C>G
More... 		02/28/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DIS3L2
Accession:NM_001257281
Location:INTRON

Gene Symbol:DIS3L2
Accession:NM_001257282
Location:INTRON

Gene Symbol:DIS3L2
Accession:NM_152383
Location:INTRON

Gene Symbol:DIS3L2
Accession:NR_046476
Location:INTRON;NON-CODING

Gene Symbol:DIS3L2
Accession:NR_046477
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001577858 CLINVAR
dbSNP (RS) rs56408197 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DIS3L2 CLINVAR
OMIM 614184 CLINVAR