Variant #0000331158 (NC_000006.11:g.109771215C>T, NM_014797.2:c.*15839G>A (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.109771215C>T
DNA change (hg38) g.109450012C>T
Published as MICAL1(NM_001159291.1):c.1007G>A (p.(Arg336Gln))
ISCN -
DB-ID MICAL1_000002
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) 0.00021 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 2018-01-15 20:58:59 +01:00 (CET)
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.*15839G>A r.(=) p.(=)
MICAL1 NM_022765.3 ?/. - c.1265G>A r.(?) p.(Arg422Gln)


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