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MT-TC
A5816G
A5816G-F2
A5816G-F1
C5820A
G5780A
G5780A-F1
G5783A
G5783A-F1
G5783A-F7
G5783A-F8
G5821A
G5821A-F4
G5821A-F3
G5821A-F2
G5821A-F1
T5789C
T5789C-F1
T5794C
T5802C
T5802C-F3
T5802C-F2
T5802C-F1
T5814C
T5814C-F5
T5814C-F4
T5814C-F3
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G5780A
# **General Information** | **Position** | **5780** | **Variant** | **m.5780G\>A** | **Locus** | **MT\-TC** | **RNA** | **tRNA Cys** | | --- | --- | --- | --- | --- | --- | --- | --- | | **Homoplasmy** | \- | **Heteroplasmy** | \+ | **mitoTIP** | 35\.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.5780G\>A** variant in MT\-TC has been reported in 1 pedigree. To date, 3 carriers have been reported. Reported mutation loads ranged from 56% to 96%, with a median of 92% overall; affected carriers showed mutation loads from 56% to 96%, with a median of 92%; unaffected carriers showed mutation loads from 95%, with a median of 95%. The main clinical manifestations among affected carriers included sensorineural hearing impairment. | **No.** | **Position** | **Variant** | **Family ID** | **Nationality** | **Diseases** | **Unaffected Maternal Relatives** | **Affected Maternal Relatives** | **Publication Year** | **PMID/Ref** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 5780 | m.5780G\>A | [G5780A\-F1](https://mitofam.com/doc/540/) | Finland | Sensorineural hearing impairment | 1 | 1 | 2003 | [12802679](https://pubmed.ncbi.nlm.nih.gov/12802679/) | | # **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 | 5780 | m.5780G\>A | G5780A\-F1 | G5780A\-F1\-I2 | Uninf | F | N | Y | A | ND | 92% | / | / | / | Sensorineural hearing impairment | | | 2 | 5780 | m.5780G\>A | G5780A\-F1 | G5780A\-F1\-II1 | Fam | F | N | N | A | 36 | 95% | / | / | / | Healthy | | | 3 | 5780 | m.5780G\>A | G5780A\-F1 | G5780A\-F1\-II2 | Fam | F | Y | Y | A | ND | 56% | 92% | / | 96%(BM) | Sensorineural hearing impairment | | For abbreviations and other usage instructions, please see [Mitofam Info](https://mitofam.com/doc/385/).
Haoying Chen
2026年6月22日 01:00
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