Variant #0000719879 (NC_000004.11:g.187557782G>A, NM_005245.3:c.3929C>T (FAT1))

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.187557782G>A
DNA change (hg38) -
Published as FAT1(NM_005245.3):c.3929C>T (p.S1310L), FAT1(NM_005245.4):c.3929C>T (p.(Ser1310Leu), p.S1310L)
ISCN -
DB-ID FAT1_000079 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) 0.00043 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAT1 NM_005245.3 -?/. - c.3929C>T r.(?) p.(Ser1310Leu)


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