Variant #0000680781 (NC_000017.10:g.1417158A>T, NC_000017.10(NM_001135642.1):c.-77+8T>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.1417158A>T
DNA change (hg38) -
Published as INPP5K(NM_001135642.1):c.-77+8T>A
ISCN -
DB-ID INPP5K_000008
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) 0.00649 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 2020-08-06 14:59:34 +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.-77+8T>A r.(=) p.(=)
PITPNA NM_006224.3 -?/. - c.*6697T>A r.(=) p.(=)
INPP5K NM_016532.3 -?/. - c.152+8T>A r.(=) p.(=)


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