Variant #0000613509 (NC_000011.9:g.63994399G>T, NM_031471.5:c.*3435G>T (FERMT3))

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.63994399G>T
DNA change (hg38) g.64226927G>T
Published as NUDT22(NM_001128612.2):c.275G>T (p.(Gly92Val))
ISCN -
DB-ID NUDT22_000006
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) 0.0005 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-09-27 17:32:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAJC4 NM_005528.3 -?/. - c.-3816G>T r.(?) p.(=)
FERMT3 NM_031471.5 -?/. - c.*3435G>T r.(=) p.(=)
TRPT1 NM_031472.3 -?/. - c.-950C>A r.(?) p.(=)
NUDT22 NM_032344.2 -?/. - c.275G>T r.(?) p.(Gly92Val)


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