Variant #0000616347 (NC_000017.10:g.1410357C>T, NM_001135642.1:c.465G>A (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.1410357C>T
DNA change (hg38) g.1507063C>T
Published as INPP5K(NM_001135642.1):c.465G>A (p.P155=), INPP5K(NM_001135642.2):c.465G>A (p.P155=)
ISCN -
DB-ID INPP5K_000007 See all 2 reported entries
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) 0.00078 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP5K NM_001135642.1 -?/. - c.465G>A r.(?) p.(Pro155=)
INPP5K NM_016532.3 -?/. - c.693G>A r.(?) p.(Pro231=)


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