Variant #0000330193 (NC_000004.11:g.184605123C>T, NC_000004.11(NM_021942.5):c.1208-5C>T (TRAPPC11))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.184605123C>T
DNA change (hg38) g.183683970C>T
Published as TRAPPC11(NM_021942.5):c.1208-5C>T (p.?)
ISCN -
DB-ID TRAPPC11_000016
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) 0.00022 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 16:45:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC11 NM_021942.5 ?/. - c.1208-5C>T r.spl? p.?


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