Variant #0000611994 (NC_000009.11:g.139333646dup, NM_019892.4:c.226dup (INPP5E))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.139333646dup
DNA change (hg38) g.136439194dup
Published as INPP5E(NM_019892.5):c.226dupG (p.A76Gfs*75)
ISCN -
DB-ID C9orf163_000014
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 12:04:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEC16A NM_014866.1 +/. - c.*2561dup r.(?) p.(=)
INPP5E NM_019892.4 +/. - c.226dup r.(?) p.(Ala76GlyfsTer75)
C9orf163 NM_152571.2 +/. - c.-45255dup r.(?) p.(=)


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