Variant #0000331157 (NC_000006.11:g.109766147A>G, NM_014797.2:c.*20907T>C (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.109766147A>G
DNA change (hg38) g.109444944A>G
Published as MICAL1(NM_001159291.1):c.2675T>C (p.(Val892Ala))
ISCN -
DB-ID MICAL1_000001
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 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     
PPIL6 NM_001111298.2 ?/. - c.-4354T>C r.(?) p.(=)
SMPD2 NM_003080.2 ?/. - c.*1039A>G r.(=) p.(=)
ZBTB24 NM_014797.2 ?/. - c.*20907T>C r.(=) p.(=)
MICAL1 NM_022765.3 ?/. - c.2933T>C r.(?) p.(Val978Ala)


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