| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.5460_5488del | CA2740098124 | MT-ND2 | c.991_1019del (p.Ala331ProfsTer?) | |
| MT | m.5460G>A | CA337097146 | MT-ND2 | c.991G>A (p.Ala331Thr) | ClinVar dbSNP |
| MT | m.5460G>C | CA414780440 | MT-ND2 | c.991G>C (p.Ala331Pro) | |
| MT | m.5460G= | CA2499564325 | MT-ND2 | c.991G= (p.Ala331=) | |
| MT | m.5460G>T | CA414780438 | MT-ND2 | c.991G>T (p.Ala331Ser) | |
| MT | m.5461C>A | CA337097148 | MT-ND2 | c.992C>A (p.Ala331Asp) | |
| MT | m.5461C= | CA2499564326 | MT-ND2 | c.992C= (p.Ala331=) | |
| MT | m.5461C>G | CA337097150 | MT-ND2 | c.992C>G (p.Ala331Gly) | |
| MT | m.5461C>T | CA414780443 | MT-ND2 | c.992C>T (p.Ala331Val) | dbSNP |
| MT | m.5462C>A | CA913179641 | MT-ND2 | c.993C>A (p.Ala331=) | |
| MT | m.5462C= | CA2573331229 | MT-ND2 | c.993C= (p.Ala331=) | |
| MT | m.5462C>G | CA913179642 | MT-ND2 | c.993C>G (p.Ala331=) | |
| MT | m.5462C>T | CA913179639 | MT-ND2 | c.993C>T (p.Ala331=) | |
| MT | m.5463C>A | CA414780447 | MT-ND2 | c.994C>A (p.Leu332Ile) | |
| MT | m.5463C= | CA2499564327 | MT-ND2 | c.994C= (p.Leu332=) | |
| MT | m.5463C>G | CA414780449 | MT-ND2 | c.994C>G (p.Leu332Val) | |
| MT | m.5463C>T | CA414780451 | MT-ND2 | c.994C>T (p.Leu332Phe) | ClinVar dbSNP |
| MT | m.5464T>A | CA414780453 | MT-ND2 | c.995T>A (p.Leu332His) | |
| MT | m.5464T>C | CA414780454 | MT-ND2 | c.995T>C (p.Leu332Pro) | |
| MT | m.5464T>G | CA414780456 | MT-ND2 | c.995T>G (p.Leu332Arg) | |
| MT | m.5464T= | CA2573331230 | MT-ND2 | c.995T= (p.Leu332=) | |
| MT | m.5465T>A | CA913179643 | MT-ND2 | c.996T>A (p.Leu332=) | |
| MT | m.5465T>C | CA10581417 | MT-ND2 | c.996T>C (p.Leu332=) | ClinVar dbSNP |
| MT | m.5465T>G | CA913179644 | MT-ND2 | c.996T>G (p.Leu332=) | |
| MT | m.5465T= | CA2499564328 | MT-ND2 | c.996T= (p.Leu332=) | |
| MT | m.5466A= | CA2499564329 | MT-ND2 | c.997A= (p.Thr333=) | |
| MT | m.5466A>C | CA414780459 | MT-ND2 | c.997A>C (p.Thr333Pro) | |
| MT | m.5466A>G | CA414780461 | MT-ND2 | c.997A>G (p.Thr333Ala) | ClinVar dbSNP |
| MT | m.5466A>T | CA414780463 | MT-ND2 | c.997A>T (p.Thr333Ser) | |
| MT | m.5467C>A | CA414780469 | MT-ND2 | c.998C>A (p.Thr333Asn) | |
| MT | m.5467C= | CA2573331231 | MT-ND2 | c.998C= (p.Thr333=) | |
| MT | m.5467C>G | CA414780465 | MT-ND2 | c.998C>G (p.Thr333Ser) | |
| MT | m.5467C>T | CA414780467 | MT-ND2 | c.998C>T (p.Thr333Ile) | |
| MT | m.5468C>A | CA913179645 | MT-ND2 | c.999C>A (p.Thr333=) | |
| MT | m.5468C= | CA2573331232 | MT-ND2 | c.999C= (p.Thr333=) | |
| MT | m.5468C>G | CA913179647 | MT-ND2 | c.999C>G (p.Thr333=) | |
| MT | m.5468C>T | CA913179646 | MT-ND2 | c.999C>T (p.Thr333=) | |
| MT | m.5469A= | CA2573331233 | MT-ND2 | c.1000A= (p.Thr334=) | |
| MT | m.5469A>C | CA414780471 | MT-ND2 | c.1000A>C (p.Thr334Pro) | |
| MT | m.5469A>G | CA414780473 | MT-ND2 | c.1000A>G (p.Thr334Ala) | |
| MT | m.5469A>T | CA414780475 | MT-ND2 | c.1000A>T (p.Thr334Ser) | |
| MT | m.5470C>A | CA414780477 | MT-ND2 | c.1001C>A (p.Thr334Lys) | |
| MT | m.5470C= | CA2573331234 | MT-ND2 | c.1001C= (p.Thr334=) | |
| MT | m.5470C>G | CA414780479 | MT-ND2 | c.1001C>G (p.Thr334Arg) | |
| MT | m.5470C>T | CA414780481 | MT-ND2 | c.1001C>T (p.Thr334Met) | |
| MT | m.5471G>A | CA337097152 | MT-ND2 | c.1002G>A (p.Thr334=) | dbSNP |
| MT | m.5471G>C | CA913179652 | MT-ND2 | c.1002G>C (p.Thr334=) | dbSNP |
| MT | m.5471G= | CA2499564330 | MT-ND2 | c.1002G= (p.Thr334=) | |
| MT | m.5471G>T | CA913179651 | MT-ND2 | c.1002G>T (p.Thr334=) | |
| MT | m.5472C>A | CA414780484 | MT-ND2 | c.1003C>A (p.Leu335Ile) |