Variant #0000285314 (NC_000009.11:g.139333839G>C, NM_019892.4:c.33C>G (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.139333839G>C
DNA change (hg38) g.136439387G>C
Published as INPP5E(NM_019892.5):c.33C>G (p.S11=), INPP5E(NM_019892.6):c.33C>G (p.S11=)
ISCN -
DB-ID INPP5E_000036 See all 2 reported entries
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) 0.00234 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.*2368C>G r.(=) p.(=)
INPP5E NM_019892.4 -/. - c.33C>G r.(?) p.(Ser11=)
C9orf163 NM_152571.2 -/. - c.-45062G>C r.(?) p.(=)


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