Variant #0000095150 (NC_000010.10:g.74326390C>T, NC_000010.10(NM_001195518.2):c.161+1G>A (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.74326390C>T
DNA change (hg38) g.72566632C>T
Published as -
ISCN -
DB-ID MICU1_000007 See all 4 reported entries
Variant remarks -
Reference Exome Variant Server
ClinVar ID -
dbSNP ID rs375502236
Origin Unknown
Segregation -
Frequency 1/12179 controls
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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 +?/. 2i c.161+1G>A r.spl p.?


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