Variant #0000285270 (NC_000023.10:g.70330480C>A, NM_001025265.2:c.-4074G>T (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.70330480C>A
DNA change (hg38) g.71110630C>A
Published as IL2RG(NM_000206.2):c.328G>T (p.E110*)
ISCN -
DB-ID IL2RG_000007
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-20 14:44:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL2RG NM_000206.2 ?/. - c.328G>T r.(?) p.(Glu110Ter)
CXorf65 NM_001025265.2 ?/. - c.-4074G>T r.(?) p.(=)


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