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MT-TI
A4263G
A4263G-F1
A4263G-F2
A4267G
A4269G
A4279G
A4281G
A4295G
A4295G-F4
A4295G-F3
A4295G-F2
A4295G-F1
A4300G
A4300G-F4
A4300G-F3
A4300G-F2
A4300G-F1
A4302G
A4316G
A4316G-F1
A4317G
A4317G-F5
A4317G-F4
A4317G-F3
C4320T
G4282A
G4284A
G4284A-F2
G4284A-F1
G4296A
G4296A-F4
G4296A-F3
G4296A-F2
G4296A-F1
G4298A
G4298A-F2
G4298A-F1
G4308A
G4309A
G4309A-F2
T4268C
T4268C-F1
T4274C
T4277C
T4277C-F1
T4285C
T4289C
T4289C-F1
T4290C
T4290C-F1
T4291C
T4291C-F2
T4291C-F1
T4327C
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A4281G
# **General Information** | **Position** | **4281** | **Variant** | **m.4281A\>G** | **Locus** | **MT\-TI** | **RNA** | **tRNA Ile** | | --- | --- | --- | --- | --- | --- | --- | --- | | **Homoplasmy** | \- | **Heteroplasmy** | \+ | **mitoTIP** | 87\.90% | **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.4281A\>G** variant in MT\-TI has been reported in 1 pedigree. To date, 1 carrier has been reported. Reported mutation loads ranged from 0% to 46%, with a median of 0% overall; affected carriers showed mutation loads from 0% to 46%, with a median of 0%. In one affected carrier, the mutation was undetectable in blood (0%) and urine (0%) but exceeded 20% in muscle (46%). The main clinical manifestations among affected carriers included myalgia and exercise\-related recurrent myoglobinuria. | **No.** | **Position** | **Variant** | **Family ID** | **Nationality** | **Diseases** | **Unaffected Maternal Relatives** | **Affected Maternal Relatives** | **Publication Year** | **PMID/Ref** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 4281 | m.4281A\>G | A4281G\-F1 | USA | Myalgia, exercise\-related recurrent myoglobinuria | 0 | 0 | 2011 | [21324494](https://pubmed.ncbi.nlm.nih.gov/21324494/) | | # **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 | 4281 | m.4281A\>G | A4281G\-F1 | A4281G\-F1\-P1 | De novo | F | Y | Y | A | 39 | 0 | 46% | 0 | / | Myalgia, exercise\-related recurrent myoglobinuria | | For abbreviations and other usage instructions, please see [Mitofam Info](https://mitofam.com/doc/385/).
Haoying Chen
2026年7月2日 20:36
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