Variant #0000722313 (NC_000009.11:g.134381543G>C, NM_007171.3:c.165G>C (POMT1))
Chromosome |
9 |
Allele |
Unknown |
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.134381543G>C |
DNA change (hg38) |
- |
Published as |
POMT1(NM_001353198.1):c.3G>C (p.M1?) |
ISCN |
- |
DB-ID |
UCK1_000029 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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