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 International |
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) |

Variant on transcripts
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