Variant #0000728227 (NC_000022.10:g.50962699C>T, NM_001257988.1:c.*1500G>A (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.50962699C>T
DNA change (hg38) -
Published as SCO2(NM_001169109.1):c.142G>A (p.G48R)
ISCN -
DB-ID NCAPH2_000031
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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     
TYMP NM_001257988.1 ?/. - c.*1500G>A r.(=) p.(=)
SCO2 NM_005138.2 ?/. - c.142G>A r.(?) p.(Gly48Arg)
NCAPH2 NM_152299.3 ?/. - c.*895C>T r.(=) p.(=)


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