Variant #0001006255 (NC_000022.10:g.50962264C>T, NM_001257988.1:c.*1935G>A (TYMP))

Chromosome 22
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.50962264C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID NCAPH2_000008
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) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +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     
TYMP NM_001257988.1 +/. - c.*1935G>A r.(=) p.(=)
SCO2 NM_005138.2 +/. - c.577G>A r.(?) p.(Gly193Ser)
NCAPH2 NM_152299.3 +/. - c.*460C>T r.(=) p.(=)


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