Variant #0000289638 (NC_000009.11:g.139327599G>A, NC_000009.11(NM_019892.4):c.1159+8C>T (INPP5E))

Chromosome 9
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.139327599G>A
DNA change (hg38) g.136433147G>A
Published as INPP5E(NM_019892.5):c.1159+8C>T, INPP5E(NM_019892.6):c.1159+8C>T
ISCN -
DB-ID INPP5E_000025 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INPP5E NM_019892.4 -/. - c.1159+8C>T r.(=) p.(=)


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