Variant #0001044013 (NC_000023.10:g.104464841T>C, NC_000023.10(NM_017416.1):c.357-13661T>C (IL1RAPL2))

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.104464841T>C
DNA change (hg38) -
Published as TEX13A(NM_031274.5):c.241A>G (p.(Arg81Gly))
ISCN -
DB-ID IL1RAPL2_000023
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
IL1RAPL2 NM_017416.1 ?/. - c.357-13661T>C r.(=) p.(=)
TEX13A NM_031274.3 ?/. - c.241A>G r.(?) p.?


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