Variant #0000659431 (NC_000023.10:g.70328488_70328491del, NM_001025265.2:c.-2081_-2078del (CXorf65))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.70328488_70328491del
DNA change (hg38) g.71108638_71108641del
Published as IL2RG(NM_000206.2):c.816_819delGATT (p.I273Sfs*20), IL2RG(NM_000206.3):c.816_819delGATT (p.I273Sfs*20)
ISCN -
DB-ID IL2RG_000023 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL2RG NM_000206.2 +/. - c.816_819del r.(?) p.(Ile273SerfsTer20)
CXorf65 NM_001025265.2 +/. - c.-2081_-2078del r.(?) p.(=)


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