RGD:8686688 Rat Genome Database

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Variant: RGD:8686688 -  Homo sapiens

RGD ID: 8686688
RS ID: rs17085310
ClinVar ID: CV139290
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KDR  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 55,970,782
GRCh38 4 55,104,615
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012004.1:g.25981C>T
NC_000004.12:g.55104615G>A
NC_000004.11:g.55970782G>A
LRG_1198:g.25981C>T
More... 		09/19/2013 intron variant not provided AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:KDR
Accession:NM_002253
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:24728327  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000122411 CLINVAR
dbSNP (RS) rs17085310 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene KDR CLINVAR
OMIM 191306 CLINVAR