Variant #0001057357 (NC_000023.10:g.70327620del, NM_001025265.2:c.-1208del (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.70327620del
DNA change (hg38) -
Published as IL2RG(NM_000206.3):c.1082del (p.(Pro361Hisfs*5))
ISCN -
DB-ID IL2RG_000037
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) Retrieve
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL2RG NM_000206.2 ?/. - c.1082del r.(?) p.(Pro361Hisfs*5)
CXorf65 NM_001025265.2 ?/. - c.-1208del r.(?) p.(=)
FOXO4 NM_005938.3 ?/. - c.*5686del r.(?) p.(=)


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