Variant #0000966570 (NC_000011.9:g.71951178_71951193del, NM_001567.3:c.*1781_*1796del (INPPL1))

Chromosome 11
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.71951178_71951193del
DNA change (hg38) -
Published as PHOX2A(NM_005169.3):c.455_470del (p.(Ala152GlyfsTer49))
ISCN -
DB-ID INPPL1_000043
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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPPL1 NM_001567.3 ?/. - c.*1781_*1796del r.(=) p.(=)
PHOX2A NM_005169.3 ?/. - c.455_470del r.(?) p.(Ala152Glyfs*49)


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