Variant #0000984829 (NC_000023.10:g.70328185C>T, NM_001025265.2:c.-1779G>A (CXorf65))

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.70328185C>T
DNA change (hg38) -
Published as IL2RG(NM_000206.3):c.866G>A (p.R289Q)
ISCN -
DB-ID IL2RG_000033
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +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     
IL2RG NM_000206.2 ?/. - c.866G>A r.(?) p.(Arg289Gln)
CXorf65 NM_001025265.2 ?/. - c.-1779G>A r.(?) p.(=)
FOXO4 NM_005938.3 ?/. - c.*6251C>T r.(=) p.(=)


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