Variant #0000095149 (NC_000010.10:g.74236931C>T, NC_000010.10(NM_001195518.2):c.735+1G>A (MICU1))

Chromosome 10
Allele Parent #1
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.74236931C>T
DNA change (hg38) g.72477173C>T
Published as NM_006077.3:c.741+1G>A
ISCN -
DB-ID MICU1_000001 See all 11 reported entries
Variant remarks found once in 7119 European Americans, not in 3114 African Americans
Reference Exome Variant Server
ClinVar ID -
dbSNP ID rs369915689
Origin Unknown
Segregation -
Frequency 1/10233 controls
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
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 ?/. 8i c.735+1G>A r.spl? p.?


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