Variant #0001006930 (NC_000023.10:g.70329090_70329091del, NM_001025265.2:c.-2685_-2684del (CXorf65))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70329090_70329091del
DNA change (hg38) -
Published as IL2RG(NM_000206.2):c.744_745delCA (p.(Ser248fs))
ISCN -
DB-ID IL2RG_000034
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 2024-08-28 13:16:32 +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.744_745del r.(?) p.(Ser248Argfs*54)
CXorf65 NM_001025265.2 +?/. - c.-2685_-2684del r.(?) p.(=)


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