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MT-TD
A7526G
A7530G
A7543G
A7543G-F1
A7551G
A7551G-F1
C7539T
C7539T-F1
G7554A
T7560C
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G7554A
# **General Information** | **Position** | **7554** | **Variant** | **m.7554G\>A** | **Locus** | **MT\-TD** | **RNA** | **tRNA Asp** | | --- | --- | --- | --- | --- | --- | --- | --- | | **Homoplasmy** | \- | **Heteroplasmy** | \+ | **mitoTIP** | 71\.20% | **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.7554G\>A** variant in MT\-TD has been reported in 1 pedigree. To date, 1 carrier has been reported. Reported mutation loads ranged from 6% to 87%, with a median of 16% overall; affected carriers showed mutation loads from 6% to 87%, with a median of 16%. In one affected carrier, a marked tissue\-specific difference was observed, with higher mutation loads in muscle (87%) and urine (22%) than in blood (6%). The main clinical manifestations among affected carriers included myopathy, ataxia, lactic acidosis, migraines, and nystagmus. | **No.** | **Position** | **Variant** | **Family ID** | **Nationality** | **Diseases** | **Unaffected Maternal Relatives** | **Affected Maternal Relatives** | **Publication Year** | **PMID/Ref** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 7554 | m.7554G\>A | G7554A\-F1 | UK | Myopathy, ataxia, nystagmus, migraines, lactic acidosis | 0 | 0 | 2013 | [23696415](https://pubmed.ncbi.nlm.nih.gov/23696415/) | | # **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 | 7554 | m.7554G\>A | G7554A\-F1 | G7554A\-F1\-II2 | De novo | M | Y | Y | A | 7 | 6% | 87% | 22% | 10% (BM) | Myopathy, ataxia, nystagmus, migraines, lactic acidosis | | For abbreviations and other usage instructions, please see [Mitofam Info](https://mitofam.com/doc/385/).
Haoying Chen
2026年6月22日 14:01
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