Variant #0000951640 (NC_000022.10:g.50965683C>T, NM_001257988.1:c.676G>A (TYMP))

Chromosome 22
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.50965683C>T
DNA change (hg38) -
Published as TYMP(NM_001113755.2):c.676G>A (p.(Gly226Arg)), TYMP(NM_001113756.2):c.676G>A (p.G226R)
ISCN -
DB-ID NCAPH2_000023 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) 0.00015 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 2023-11-27 17:35:39 +01:00 (CET)
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.*3226G>A r.(=) p.(=)
TYMP NM_001257988.1 -?/. - c.676G>A r.(?) p.(Gly226Arg)
SCO2 NM_005138.2 -?/. - c.-1796G>A r.(?) p.(=)
NCAPH2 NM_152299.3 -?/. - c.*3879C>T r.(=) p.(=)


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