Variant #0000807586 (NC_000016.9:g.732080_732082del, NC_000016.9(NM_005861.2):c.669+4_669+6del (STUB1))

Chromosome 16
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.732080_732082del
DNA change (hg38) -
Published as STUB1(NM_001293197.1):c.453+4_453+6delAGT
ISCN -
DB-ID JMJD8_000022
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JMJD8 NM_001005920.2 ?/. - c.*712_*714del r.(=) p.(=)
STUB1 NM_005861.2 ?/. - c.669+4_669+6del r.spl? p.?
WDR24 NM_032259.2 ?/. - c.*2652_*2654del r.(=) p.(=)


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