rs16828636 Rat Genome Database

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Variant: rs16828636 -  Homo sapiens

RGD ID: 150450371
RS ID: rs16828636
ClinVar ID: CV1260950
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DIS3L2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 233,001,119
GRCh38 2 232,136,409
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.703-63C>T
LRG_534:g.179827C>T
NG_032572.1:g.179827C>T
NC_000002.12:g.232136409C>T
More... 		06/12/2019 intron variant benign none provided

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

Gene Symbol:DIS3L2
Accession:NM_152383
Location:INTRON

Gene Symbol:DIS3L2
Accession:NM_001257282
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 References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001680619 CLINVAR
dbSNP (RS) rs16828636 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DIS3L2 CLINVAR
OMIM 614184 CLINVAR