Variant #0000281548 (NC_000009.11:g.139333054_139333057del, NC_000009.11(NM_019892.4):c.812+7_812+10del (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.139333054_139333057del
DNA change (hg38) g.136438602_136438605del
Published as INPP5E(NM_019892.5):c.812+7_812+10delAGGG, INPP5E(NM_019892.6):c.812+7_812+10delAGGG
ISCN -
DB-ID INPP5E_000032
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*3154_*3157del r.(=) p.(=)
INPP5E NM_019892.4 -/. - c.812+7_812+10del r.(=) p.(=)
C9orf163 NM_152571.2 -/. - c.-45847_-45844del r.(?) p.(=)


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