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MT-RNR1&2
A2755G
A2755G-F1
C2639A
C3093G
C3093G-F1
G2492A
G2647A
G3010A
G3054A
G3090A
T2336C
T2336C-F1
T2648C
T2806A
T3098C
A735G
A735G-F2
A735G-F1
A745G
A747G
A801G
A856G
A1027G
A1331G
A1374G
A1453G
A1517C
A1555G
A1555G-F9
A1555G-F10
A1555G-F11
A1555G-F353
A1555G-F323
A1555G-F302
A1555G-F228
A1555G-F227
A1555G-F186
A1555G-F185
A1555G-F226
A1555G-F183
A1555G-F112
A1555G-F182
A1555G-F225
A1555G-F111
A1555G-F66
A1555G-F181
A1555G-F110
A1555G-F65
A1555G-F136
A1555G-F222
A1555G-F109
A1555G-F63
A1555G-F120
A1555G-F133
A1555G-F102
A1555G-F108
A1555G-F61
A1555G-F119
A1555G-F125
A1555G-F70
A1555G-F2
A1555G-F221
A1555G-F58
A1555G-F100
A1555G-F107
A1555G-F1
A1555G-F24
A1555G-F118
A1555G-F124
A1555G-F56
A1555G-F69
A1555G-F23
A1555G-F81
A1555G-F55
A1555G-F99
A1555G-F106
A1555G-F22
A1555G-F7
A1555G-F116
A1555G-F123
A1555G-F53
A1555G-F21
A1555G-F68
A1555G-F80
A1555G-F4
A1555G-F220
A1555G-F83
A1555G-F95
A1555G-F32
A1555G-F98
A1555G-F104
A1555G-F20
A1555G-F31
A1555G-F12
A1555G-F114
A1555G-F27
A1555G-F122
A1555G-F29
A1555G-F26
A1555G-F67
A1555G-F28
A1555G-F71
A1555G-F82
A1555G-F92
A1555G-F93
A1555G-F96
A1555G-F97
A1555G-F103
A1555G-F113
A1555G-F121
C792T
C869T
C1192A
C1192T
C1226G
C1310T
C1494T
C1494T-F11
C1494T-F10
C1494T-F9
C1494T-F8
C1494T-F7
C1494T-F6
C1494T-F5
C1494T-F4
C1494T-F3
C1494T-F2
C1494T-F1
C1537T
C1556T
G988A
T669C
T669C-F2
T721C
T850C
T921C
T961G
T961G-F2
T990C
T1180G
T1391C
T1413C
T1452C
A839G
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T3098C
# **General Information** | **Position** | **3098** | **Variant** | **m.3098T\>C** | **Locus** | **MT\-RNR2** | **RNA** | **16S 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.3098T\>C** variant in MT\-RNR2 has been reported in 1 pedigree. To date, 1 carrier has been reported. Reported mutation loads ranged from 5\.1%, with a median of 5\.1% overall; affected carriers showed mutation loads from 5\.1%, with a median of 5\.1%. The main clinical manifestations among affected carriers included k. pneumoniae, pediatric septic shock, acute respiratory distress syndrome, and secondary hemophagocytic lymphohistiocytosis. | **No.** | **Position** | **Variant** | **Family ID** | **Nationality** | **Diseases** | **Unaffected Maternal Relatives** | **Affected Maternal Relatives** | **Publication Year** | **PMID/Ref** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 3098 | m.3098T\>C | T3098C\-F1 | South Korea | Pediatric septic shock | 0 | 0 | 2021 | [33504965](https://pubmed.ncbi.nlm.nih.gov/33504965/) | Patient 6; Co\-reported m.2492G\>A, m.2647G\>A, m.2806T\>A, m.7065G\>A, m.7943T\>C, m.15350G\>A. | # **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 | 3098 | m.3098T\>C | T3098C\-F1 | T3098C\-F1\-P6 | Uninf | ND | Y | Y | A | 1\.5 | 5\.08% | / | / | / | Pediatric septic shock; acute respiratory distress syndrome; secondary hemophagocytic lymphohistiocytosis; K. pneumoniae | PMID 33504965 Table 1 patient 6 and Table 2 m.3098T\>C in PBMCs. Co\-reported m.2492G\>A, m.2647G\>A, m.2806T\>A, m.7065G\>A, m.7943T\>C, m.15350G\>A. | For abbreviations and other usage instructions, please see [Mitofam Info](https://mitofam.com/doc/385/).
Haoying Chen
2026年6月30日 04:29
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