Variant #0000856486 (NC_000023.10:g.16627738C>T, NM_019857.3:c.1617G>A (CTPS2))

Chromosome X
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.16627738C>T
DNA change (hg38) -
Published as CTPS2(NM_001144002.1):c.1617G>A (p.P539=)
ISCN -
DB-ID CTPS2_000045
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) 0.00012 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 2022-05-09 15:47:41 +02:00 (CEST)
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.-40597C>T r.(?) p.(=)
CTPS2 NM_019857.3 -?/. - c.1617G>A r.(?) p.(Pro539=)


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