Variant #0001015959 (NC_000022.10:g.50962077C>T, NM_001257988.1:c.*2122G>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.50962077C>T
DNA change (hg38) -
Published as SCO2(NM_001169109.1):c.764G>A (p.(Arg255Gln))
ISCN -
DB-ID NCAPH2_000062
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) 3.0E-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 2024-10-29 21:08:56 +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.*2122G>A r.(=) p.(=)
SCO2 NM_005138.2 ?/. - c.764G>A r.(?) p.(Arg255Gln)
NCAPH2 NM_152299.3 ?/. - c.*273C>T r.(=) p.(=)


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