Variant #0000850854 (NC_000005.9:g.150924538_150924539del, NM_001447.2:c.6150_6151del (FAT2))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.150924538_150924539del
DNA change (hg38) -
Published as FAT2(NM_001447.2):c.6150_6151delGG (p.V2051Gfs*10)
ISCN -
DB-ID FAT2_000104
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAT2 NM_001447.2 +/. - c.6150_6151del r.(?) p.(Val2051Glyfs*10)


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