Variant #0001005877 (NC_000022.10:g.18314666_18314668del, NM_001122731.1:c.*2562_*2564del (MICAL3))

Chromosome 22
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.18314666_18314668del
DNA change (hg38) -
Published as MICAL3(NM_015241.2):c.3021_3023delGGA (p.(Glu1007del))
ISCN -
DB-ID MICAL3_000019
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 2024-08-28 13:16:32 +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     
MICAL3 NM_001122731.1 -?/. - c.*2562_*2564del r.(=) p.(=)


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