Variant #0000892221 (NC_000015.9:g.67529155del, NM_001031715.2:c.-18080del (IQCH))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.67529155del
DNA change (hg38) -
Published as -
ISCN -
DB-ID IQCH_000004
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 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IQCH NM_001031715.2 +/. - c.-18080del r.(?) p.(=)
AAGAB NM_024666.3 +/. - c.77del r.(?) p.(Ile26Thrfs*11)


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