Variant #0000611993 (NC_000009.11:g.139327590_139327607dup, NC_000009.11(NM_019892.4):c.1159+16_1159+33dup (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.139327590_139327607dup
DNA change (hg38) g.136433138_136433155dup
Published as INPP5E(NM_019892.6):c.1159+16_1159+33dupGGGGTGGGCGCGGCTGGA
ISCN -
DB-ID INPP5E_000060
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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+16_1159+33dup r.(=) p.(=)


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