Variant #0000656293 (NC_000009.11:g.139333473C>G, NM_019892.4:c.399G>C (INPP5E))

Chromosome 9
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.139333473C>G
DNA change (hg38) g.136439021C>G
Published as INPP5E(NM_019892.5):c.399G>C (p.L133=)
ISCN -
DB-ID C9orf163_000015
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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-26 12:03:28 +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.*2734G>C r.(=) p.(=)
INPP5E NM_019892.4 -?/. - c.399G>C r.(?) p.(Leu133=)
C9orf163 NM_152571.2 -?/. - c.-45428C>G r.(?) p.(=)


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