Variant #0000693708 (NC_000023.10:g.70330483C>T, NM_001025265.2:c.-4077G>A (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.70330483C>T
DNA change (hg38) -
Published as IL2RG(NM_000206.2):c.325G>A (p.E109K)
ISCN -
DB-ID IL2RG_000020 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) 0.00094 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 2020-09-15 15:50:26 +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.325G>A r.(?) p.(Glu109Lys)
CXorf65 NM_001025265.2 -?/. - c.-4077G>A r.(?) p.(=)


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