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MT-TS1
A7451T
A7472C
A7472C-F4
A7472C-F3
A7472C-F2
A7474G
A7484G
A7484G-F1
C7462T
C7462T-F3
C7462T-F2
C7462T-F1
C7492T
G7453A
G7458A
G7486A
G7497A
G7497A-F3
G7497A-F2
G7497A-F1
G7506A
T7480G
T7496C
T7501A
T7505C
T7505C-F2
T7505C-F1
T7510C
T7510C-F5
T7510C-F4
T7510C-F3
T7510C-F2
T7510C-F1
T7511C
T7511C-F10
T7511C-F9
T7511C-F8
T7511C-F7
T7511C-F5
T7511C-F4
T7511C-F2
T7511C-F1
T7511C-F3
T7512C
T7512C-F4
T7512C-F3
T7512C-F2
T7512C-F1
T7501C
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G7486A
# **General Information** | **Position** | **7486** | **Variant** | **m.7486G\>A** | **Locus** | **MT\-TS1** | **RNA** | **tRNA Ser (UCN)** | | --- | --- | --- | --- | --- | --- | --- | --- | | **Homoplasmy** | \- | **Heteroplasmy** | \+ | **mitoTIP** | 50\.50% | **Pathogenicity** | Reported | "Pathogenicity" status is derived from published literature or predictions from bioinformatics tools. Researchers and clinicians are cautioned that additional data and/or analysis may still be necessary to confirm the pathological significance of these variants. For more information, please see [Mitofam Info](https://mitofam.com/doc/385/). # **Pedigree Information** The **m.7486G\>A** variant in MT\-TS1 has been reported in 1 pedigree. To date, 1 carrier has been reported. Reported mutation loads ranged from 4% to 50%, with a median of 11% overall; affected carriers showed mutation loads from 4% to 50%, with a median of 11%. In one affected carrier, a marked tissue\-specific difference was observed, with higher mutation loads in muscle (50%) and fibroblasts (11%) than in blood (4%). The main clinical manifestations among affected carriers included CPEO. | **No.** | **Position** | **Variant** | **Family ID** | **Nationality** | **Diseases** | **Unaffected Maternal Relatives** | **Affected Maternal Relatives** | **Publication Year** | **PMID/Ref** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 7486 | m.7486G\>A | G7486A\-F1 | Portugal | CPEO | ND | ND | 2018 | [29398297](https://pubmed.ncbi.nlm.nih.gov/29398297/) | | # **Carrier Information** | **No.** | **Position** | **Variant** | **Family ID** | **Carrier ID** | **Type (Fam/De novo/Uninf)** | **Gender (F/M)** | **Proband (Y/N)** | **Affected (Y/N)** | **Die/Alive(D/A)** | **Age** | **Blood Mutant Level** | **Muscle Mutant level** | **Urine Mutant level** | **Other Mutant level** | **Clinical Features** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 7486 | m.7486G\>A | G7486A\-F1 | G7486A\-F1\-P1 | Uninf | F | Y | Y | A | 62 | 4% | 50% | / | 11% (F) | CPEO | | For abbreviations and other usage instructions, please see [Mitofam Info](https://mitofam.com/doc/385/).
Haoying Chen
2026年6月22日 18:41
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