Variant #0000888735 (NC_000009.11:g.139333249G>A, NM_019892.4:c.623C>T (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.139333249G>A
DNA change (hg38) -
Published as INPP5E(NM_019892.5):c.623C>T (p.T208I), INPP5E(NM_019892.6):c.623C>T (p.T208I)
ISCN -
DB-ID C9orf163_000002 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) 0.00032 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEC16A NM_014866.1 -?/. - c.*2958C>T r.(=) p.(=)
INPP5E NM_019892.4 -?/. - c.623C>T r.(?) p.(Thr208Ile)
C9orf163 NM_152571.2 -?/. - c.-45652G>A r.(?) p.(=)


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