Variant #0000951791 (NC_000023.10:g.70329235T>G, NM_001025265.2:c.-2829A>C (CXorf65))

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.70329235T>G
DNA change (hg38) -
Published as IL2RG(NM_000206.2):c.600A>C (p.Q200H)
ISCN -
DB-ID IL2RG_000026 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.600A>C r.(?) p.(Gln200His)
CXorf65 NM_001025265.2 -?/. - c.-2829A>C r.(?) p.(=)


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