Variant #0000682306 (NC_000023.10:g.16707711T>C, NM_019857.3:c.734A>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.16707711T>C
DNA change (hg38) -
Published as CTPS2(NM_001144002.1):c.734A>G (p.H245R)
ISCN -
DB-ID CTPS2_000043
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
S100G NM_004057.2 ?/. - c.*35079T>C r.(=) p.(=)
CTPS2 NM_019857.3 ?/. - c.734A>G r.(?) p.(His245Arg)


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