Variant #0000861350 (NC_000009.11:g.113457722T>C, NM_005592.3:c.398T>C (MUSK))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.113457722T>C |
| DNA change (hg38) |
- |
| Published as |
MUSK(NM_001166280.1):c.398T>C (p.(Ile133Thr)), MUSK(NM_005592.4):c.398T>C (p.I133T) |
| ISCN |
- |
| DB-ID |
MUSK_000035 See all 2 reported entries |
| 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) |
0.00449 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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