rs1115570 Rat Genome Database

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Variant: rs1115570 -  Homo sapiens

RGD ID: 150473665
RS ID: rs1115570
ClinVar ID: CV1252444
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DDR2  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 162,725,655
GRCh38 1 162,755,865
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001354982.2:c.671+96A>C
NM_001354983.2:c.671+96A>C
NM_006182.4:c.671+96A>C
LRG_1390:g.129653A>C
More... 		10/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:DDR2
Accession:NM_006182
Location:INTRON

Gene Symbol:DDR2
Accession:XM_047421565
Location:INTRON

Gene Symbol:DDR2
Accession:XM_011509587
Location:INTRON

Gene Symbol:DDR2
Accession:NM_001354982
Location:INTRON

Gene Symbol:DDR2
Accession:NM_001354983
Location:INTRON

Gene Symbol:DDR2
Accession:XM_011509588
Location:INTRON

Gene Symbol:DDR2
Accession:XM_047421554
Location:INTRON

Gene Symbol:DDR2
Accession:NM_001014796
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001671646 CLINVAR
dbSNP (RS) rs1115570 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DDR2 CLINVAR
OMIM 191311 CLINVAR