Variant #0001057278 (NC_000023.10:g.16672630T>C, NC_000023.10(NM_019857.3):c.1296+13007A>G (CTPS2))

Chromosome X
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.16672630T>C
DNA change (hg38) -
Published as S100G(NM_004057.3):c.238T>C (p.(*80Argext*31))
ISCN -
DB-ID CTPS2_000048
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) 1.0E-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 2025-11-01 13:22:20 +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     
S100G NM_004057.2 ?/. - c.238T>C r.(?) p.(*80Argext*31)
CTPS2 NM_019857.3 ?/. - c.1296+13007A>G r.(=) p.(=)


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