Variant #0000722386 (NC_000009.11:g.139333231G>T, NM_019892.4:c.641C>A (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.139333231G>T
DNA change (hg38) -
Published as INPP5E(NM_019892.5):c.641C>A (p.S214*)
ISCN -
DB-ID C9orf163_000020
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEC16A NM_014866.1 +/. - c.*2976C>A r.(=) p.(=)
INPP5E NM_019892.4 +/. - c.641C>A r.(?) p.(Ser214*)
C9orf163 NM_152571.2 +/. - c.-45670G>T r.(?) p.(=)


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