Variant #0000012298 (NC_000006.11:-, PLN(NM_002667.3):c.116T>G)
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
PLN_00003 See all 5 reported entries |
Frequency |
- |
Variant remarks |
Mutations in PLN, such as the L39X, are rare among
patients with HCM. However, despite the low yield of
PLN-associated HCM genetic testing, the small size of
PLN and the paucity of genetic variation in PLN
among healthy subjects warrant consideration for its
inclusion in clinically available HCM gene test panels. |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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