Overview

Variant ID 8382
Entrez Gene ID 2324
Gene FLT4 (GeneCards)
Location hg19 5:180120085-180120085
hg38 5:180693085-180693085
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000005.9:g.180120085 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.0153
SNP ID (dbSNP ID version 137) rs57118750
EIGEN score -0.4946
CADD Raw score (version 1.3) 0.001045 (Deleterious)
FATHMM raw prediction score 0.03996 (Tolerated)
Deleterious probability by DeFine 0.7082 (Deleterious)
Entrez Gene ID 2324 (NCBI Gene)
Official Gene Symbol FLT4 (GeneCards)
Number of variants in FLT4 in this database 2 (view all the variants)
Full name fms related tyrosine kinase 4
Band 5q35.3
Other IDs Vega: OTTHUMG00000130931
OMIM: 136352
HGNC: HGNC:3767
Ensembl: ENSG00000037280
Other names PCL, FLT-4, FLT41, LMPH1A, VEGFR3, VEGFR-3
Summary This gene encodes a tyrosine kinase receptor for vascular endothelial growth factors C and D. The protein is thought to be involved in lymphangiogenesis and maintenance of the lymphatic endothelium. Mutations in this gene cause hereditary lymphedema type IA. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.13 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;