Variant #0000335044 (NC_000023.10:g.104464066G>C, NC_000023.10(NM_017416.1):c.357-14436G>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.104464066G>C
DNA change (hg38) -
Published as TEX13A(NM_031274.3):c.812C>G (p.(Ser271Trp))
ISCN -
DB-ID IL1RAPL2_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-20 19:02:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL1RAPL2 NM_017416.1 ?/. - c.357-14436G>C r.(=) p.(=)
TEX13A NM_031274.3 ?/. - c.810C>G r.(?) p.(Val270=)


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