Variant #0000287186 (NC_000004.11:g.126238090G>T, NM_024582.4:c.524G>T (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.126238090G>T
DNA change (hg38) g.125316935G>T
Published as FAT4(NM_001291303.1):c.524G>T (p.R175L), FAT4(NM_024582.4):c.524G>T (p.R175L), FAT4(NM_024582.5):c.524G>T (p.R175L), FAT4(NM_024582.6):c.524G>T (p...)
ISCN -
DB-ID FAT4_000009 See all 5 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) 0.00291 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.524G>T r.(?) p.(Arg175Leu)


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