RGD:11549478 Rat Genome Database

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Variant: RGD:11549478 -  Homo sapiens

RGD ID: 11549478
RS ID: rs2242219
ClinVar ID: CV251885
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FLT4  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 180,036,871
GRCh38 5 180,609,871
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011536.1:g.44754G>C
NC_000005.10:g.180609871C>G
NC_000005.9:g.180036871C>G
NM_001354989.2:c.3807+34G>C
More... 		11/11/2018 intron variant benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:FLT4
Accession:XM_047417002
Location:INTRON

Gene Symbol:FLT4
Accession:NM_002020
Location:INTRON

Gene Symbol:FLT4
Accession:XM_017009266
Location:INTRON

Gene Symbol:FLT4
Accession:NM_182925
Location:INTRON

Gene Symbol:FLT4
Accession:XM_011534478
Location:INTRON

Gene Symbol:FLT4
Accession:XM_011534484
Location:INTRON

Gene Symbol:FLT4
Accession:XM_017009268
Location:INTRON

Gene Symbol:FLT4
Accession:XM_017009263
Location:INTRON

Gene Symbol:FLT4
Accession:XM_047417003
Location:INTRON

Gene Symbol:FLT4
Accession:NM_001354989
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000250477 CLINVAR
  RCV001651287 CLINVAR
dbSNP (RS) rs2242219 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene FLT4 CLINVAR
OMIM 136352 CLINVAR