Variant #0000545669 (NC_000011.9:g.71945332A>G, NM_001567.3:c.2220A>G (INPPL1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71945332A>G
DNA change (hg38) g.72234288A>G
Published as INPPL1(NM_001567.4):c.2220A>G (p.S740=)
ISCN -
DB-ID INPPL1_000012
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) 0.09641 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 2019-07-18 18:22:55 +02:00 (CEST)
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.2220A>G r.(?) p.(Ser740=)
PHOX2A NM_005169.3 -/. - c.*5461T>C r.(=) p.(=)


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