Variant #0000890166 (NC_000011.9:g.71941254G>A, NM_001567.3:c.1029G>A (INPPL1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71941254G>A
DNA change (hg38) -
Published as INPPL1(NM_001567.4):c.1029G>A (p.L343=)
ISCN -
DB-ID INPPL1_000034
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) 0.00046 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +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     
INPPL1 NM_001567.3 -?/. - c.1029G>A r.(?) p.(Leu343=)
PHOX2A NM_005169.3 -?/. - c.*9539C>T r.(=) p.(=)


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