Variant #0001035401 (NC_000006.11:g.109763466_109763469del, NM_014797.2:c.*23586_*23589del (ZBTB24))

Chromosome 6
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.109763466_109763469del
DNA change (hg38) -
Published as SMPD2(NM_003080.3):c.372_375del (p.(His124Glnfs*10))
ISCN -
DB-ID MICAL1_000015
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
PPIL6 NM_001111298.2 ?/. - c.-1675_-1672del r.(?) p.(=)
SMPD2 NM_003080.2 ?/. - c.372_375del r.(?) p.(His124Glnfs*10)
ZBTB24 NM_014797.2 ?/. - c.*23586_*23589del r.(=) p.(=)
MICAL1 NM_022765.3 ?/. - c.*1926_*1929del r.(=) p.(=)


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