Variant #0000525441 (NC_000005.9:g.180030376C>G, NM_182925.4:c.3908G>C (FLT4))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.180030376C>G
DNA change (hg38) g.180603376C>G
Published as FLT4(NM_182925.5):c.3908G>C (p.G1303A, p.(Gly1303Ala))
ISCN -
DB-ID FLT4_000068 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00328 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLT4 NM_182925.4 -/. - c.3908G>C r.(?) p.(Gly1303Ala)


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