Variant #0000979949 (NC_000011.9:g.94349659G>A, NM_002033.3:c.*70767G>A (FUT4))

Chromosome 11
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.94349659G>A
DNA change (hg38) -
Published as PIWIL4(NM_152431.3):c.1944G>A (p.(Arg648=))
ISCN -
DB-ID FUT4_000003
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) 0.00049 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
FUT4 NM_002033.3 -?/. - c.*70767G>A r.(=) p.(=)
PIWIL4 NM_152431.2 -?/. - c.1944G>A r.(?) p.(=)


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