Variant #0000526639 (NC_000006.11:g.109787647G>A, NM_014797.2:c.1501C>T (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.109787647G>A
DNA change (hg38) g.109466444G>A
Published as ZBTB24(NM_014797.2):c.1501C>T (p.R501C)
ISCN -
DB-ID MICAL1_000005
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB24 NM_014797.2 ?/. - c.1501C>T r.(?) p.(Arg501Cys)
MICAL1 NM_022765.3 ?/. - c.-10769C>T r.(?) p.(=)


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