Variant #0001046830 (NC_000022.10:g.50965067T>G, NM_001257988.1:c.866A>C (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.50965067T>G
DNA change (hg38) -
Published as TYMP(NM_001113755.2):c.866A>C (p.(Glu289Ala))
ISCN -
DB-ID TYMP_000014 See all 2 reported entries
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) 5.0E-5 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 2025-07-08 13:22:38 +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     
ODF3B NM_001014440.3 +/. - c.*3842A>C r.(=) p.(=)
TYMP NM_001257988.1 +/. - c.866A>C r.(?) p.(Glu289Ala)
SCO2 NM_005138.2 +/. - c.-1180A>C r.(?) p.(=)
NCAPH2 NM_152299.3 +/. - c.*3263T>G r.(=) p.(=)


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