Variant #0000572393 (NC_000022.10:g.50962078G>T, NM_001257988.1:c.*2121C>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.50962078G>T
DNA change (hg38) g.50523649G>T
Published as NCAPH2(NM_001185011.2):c.*274G>T, SCO2(NM_001169109.1):c.763C>A (p.(Arg255=)), SCO2(NM_001169109.2):c.763C>A (p.R255=)
ISCN -
DB-ID NCAPH2_000003 See all 3 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) 0.00564 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYMP NM_001257988.1 -?/. - c.*2121C>A r.(=) p.(=)
SCO2 NM_005138.2 -?/. - c.763C>A r.(?) p.(Arg255=)
NCAPH2 NM_152299.3 -?/. - c.*274G>T r.(=) p.(=)


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