Variant #0000317069 (NC_000022.10:g.38119756_38119758del, NM_001039141.2:c.1193_1195del (TRIOBP))

Chromosome 22
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.38119756_38119758del
DNA change (hg38) g.37723749_37723751del
Published as TRIOBP(NM_001039141.2):c.1193_1195delAAC (p.Q398del)
ISCN -
DB-ID TRIOBP_000021
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIOBP NM_001039141.2 -/. - c.1193_1195del r.(?) p.(Gln398del)


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