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 International |
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) |

Variant on transcripts
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