Variant #0000677588 (NC_000006.11:g.109788960_109788965del, NC_000006.11(NM_014797.2):c.1289-11_1289-6del (ZBTB24))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.109788960_109788965del
DNA change (hg38) -
Published as ZBTB24(NM_014797.2):c.1289-11_1289-6delGTTTTT
ISCN -
DB-ID MICAL1_000010
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB24 NM_014797.2 -?/. - c.1289-11_1289-6del r.(=) p.(=)
MICAL1 NM_022765.3 -?/. - c.-12070_-12065del r.(?) p.(=)


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