Variant #0000521538 (NC_000004.11:g.126238865C>G, NM_024582.4:c.1299C>G (FAT4))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.126238865C>G
DNA change (hg38) g.125317710C>G
Published as FAT4(NM_001291303.1):c.1299C>G (p.S433=), FAT4(NM_001291303.3):c.1299C>G (p.(Ser433=)), FAT4(NM_024582.5):c.1299C>G (p.S433=)
ISCN -
DB-ID FAT4_000137 See all 3 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) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAT4 NM_024582.4 -?/. - c.1299C>G r.(?) p.(Ser433=)


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