A747G

# **General Information**

| **Position** | **747** | **Variant** | **m.747A\>G** | **Locus** | **MT\-RNR1** | **RNA** | **12S rRNA** |
| --- | --- | --- | --- | --- | --- | --- | --- |
| **Homoplasmy** | \+ | **Heteroplasmy** | \- | **mitoTIP** | N/A | **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.747A\>G** variant in MT\-RNR1 has been reported in 1 pedigree. To date, 1 carrier has been reported. Homoplasmy was reported in 1/1 carriers (100%), and 1/1 carriers (100%) were affected. The main clinical manifestations among affected carriers included 80 dB, L 100, PTA R, and profound.

| **No.** | **Position** | **Variant** | **Family ID** | **Nationality** | **Diseases** | **Unaffected Maternal Relatives** | **Affected Maternal Relatives** | **Publication Year** | **PMID/Ref** | **Note** |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| 1 | 747 | m.747A\>G | A747G\-F1 | China | five pedigrees with aminoglycoside\-induced and nonsyndromic hearing impairment | ND | ND | 2011 | [21205314](https://pubmed.ncbi.nlm.nih.gov/21205314/) |  |

# **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 | 747 | m.747A\>G | A747G\-F1 | A747G\-F1\-III4 | Fam | M | Y | Y | ND | 1 | Homo | / | / | / | PTA R/L 100/80 dB; profound | Original carrier ID: NS016\-III\-4; flat; no other affected person in NS016 pedigree besides proband per text; aminoglycoside: Yes |

For abbreviations and other usage instructions, please see [Mitofam Info](https://mitofam.com/doc/385/).