Variant #0000560318 (NC_000017.10:g.1412566T>C, NM_001135642.1:c.232A>G (INPP5K))

Chromosome 17
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.1412566T>C
DNA change (hg38) g.1509272T>C
Published as INPP5K(NM_001135642.1):c.232A>G (p.(Ile78Val))
ISCN -
DB-ID INPP5K_000003
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP5K NM_001135642.1 -?/. - c.232A>G r.(?) p.(Ile78Val)
INPP5K NM_016532.3 -?/. - c.460A>G r.(?) p.(Ile154Val)


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