Variant #0000095155 (NC_000010.10:g.74267928_74267929del, NM_001195518.2:c.638_639del (MICU1))

Chromosome 10
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74267928_74267929del
DNA change (hg38) g.72508170_72508171del
Published as NM_006077.3:c.644_645del
ISCN -
DB-ID MICU1_000010
Variant remarks found 19x in European Americans, 13x in African Americans
Reference Exome Variant Server
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency 32/11324 controls
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-03-01 15:49:21 +01:00 (CET)
Date last edited 2025-09-08 12:53:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MICU1 NM_001195518.2 +?/. 7 c.638_639del r.spl p.(Thr213AsnfsTer11)


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