Variant #0000895818 (NC_000022.10:g.50962462A>G, NM_001257988.1:c.*1737T>C (TYMP))

Chromosome 22
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.50962462A>G
DNA change (hg38) -
Published as SCO2(NM_005138.3):c.379T>C (p.Y127H)
ISCN -
DB-ID NCAPH2_000042
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYMP NM_001257988.1 ?/. - c.*1737T>C r.(=) p.(=)
SCO2 NM_005138.2 ?/. - c.379T>C r.(?) p.(Tyr127His)
NCAPH2 NM_152299.3 ?/. - c.*658A>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.