Variant #0000053091 (NC_000023.10:g.29959810_29959816del, NM_014271.3:c.1100_1106del (IL1RAPL1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.29959810_29959816del
DNA change (hg38) g.29941693_29941699del
Published as -
ISCN -
DB-ID IL1RAPL1_000015 See all 2 reported entries
Variant remarks cDNA expression cloning HEK293 shows mislocalized protein (cytoplasm in cell surface), no rescue increased number/length neurite outgrowths
Reference PubMed: Piton 2008, Journal: Piton 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-01-25 16:26:23 +01:00 (CET)
Date last edited 2020-07-17 21:27:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL1RAPL1 NM_014271.3 +/. 9 c.1100_1106del r.(?) p.Ile367Serfs*7


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