Variant #0000622425 (NC_000010.10:g.74267957_74267958dup, NM_001195518.2:c.608_609dup (MICU1))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74267957_74267958dup
DNA change (hg38) g.72508199_72508200dup
Published as MICU1(NM_006077.4):c.614_615dupTC (p.I206Sfs*30)
ISCN -
DB-ID MICU1_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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2025-09-08 12:54:02 +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 +/. - c.608_609dup r.(?) p.(Ile204SerfsTer30)


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