Variant #0000914741 (NC_000017.10:g.1417232G>C, NM_001135642.1:c.-143C>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.1417232G>C
DNA change (hg38) -
Published as INPP5K(NM_001135642.1):c.-143C>G (p.(=)), INPP5K(NM_016532.4):c.86C>G (p.P29R)
ISCN -
DB-ID INPP5K_000004 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) 0.00041 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP5K NM_001135642.1 -?/. - c.-143C>G r.(?) p.(=)
PITPNA NM_006224.3 -?/. - c.*6623C>G r.(=) p.(=)
INPP5K NM_016532.3 -?/. - c.86C>G r.(?) p.(Pro29Arg)


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