Variant #0000608225 (NC_000003.11:g.121491436_121491440dup, NM_001023570.2:c.1532_1536dup (IQCB1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.121491436_121491440dup
DNA change (hg38) g.121772589_121772593dup
Published as IQCB1(NM_001023570.3):c.1532_1536dupTAGCA (p.Q513*)
ISCN -
DB-ID IQCB1_000055 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) 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-15 12:51:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IQCB1 NM_001023570.2 +?/. - c.1532_1536dup r.(?) p.(Gln513Ter)


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