Variant #0000976920 (NC_000006.11:g.109774960C>T, NM_014797.2:c.*12094G>A (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.109774960C>T
DNA change (hg38) -
Published as MICAL1(NM_022765.4):c.347G>A (p.(Arg116His))
ISCN -
DB-ID MICAL1_000012
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) 0.00148 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
ZBTB24 NM_014797.2 -?/. - c.*12094G>A r.(=) p.(=)
MICAL1 NM_022765.3 -?/. - c.347G>A r.(?) p.(Arg116His)


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