Variant #0000807452 (NC_000016.9:g.56481876C>T, NM_018233.3:c.-3649C>T (OGFOD1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56481876C>T
DNA change (hg38) -
Published as NUDT21(NM_007006.3):c.142G>A (p.G48S)
ISCN -
DB-ID OGFOD1_000030
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUDT21 NM_007006.2 ?/. - c.142G>A r.(?) p.(Gly48Ser)
OGFOD1 NM_018233.3 ?/. - c.-3649C>T r.(?) p.(=)


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