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 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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