Variant #0001068157 (NC_000011.9:g.32994968_32994971del, NM_001076786.1:c.5231_5234del (QSER1))

Chromosome 11
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.32994968_32994971del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr11_008633
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-09 09:54:02 +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     
QSER1 NM_001076786.1 ?/. - c.5231_5234del r.(?) p.(Leu1744GlnfsTer2)


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