UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.5441A= | CA2499564313 | MT-ND2 | c.972A= (p.Pro324=) | |
| MT | m.5441A>C | CA913179620 | MT-ND2 | c.972A>C (p.Pro324=) | dbSNP |
| MT | m.5441A>G | CA913179619 | MT-ND2 | c.972A>G (p.Pro324=) | dbSNP |
| MT | m.5441A>T | CA913179618 | MT-ND2 | c.972A>T (p.Pro324=) | dbSNP |
| MT | m.5442T>A | CA414780365 | MT-ND2 | c.973T>A (p.Phe325Ile) | |
| MT | m.5442T>C | CA337097142 | MT-ND2 | c.973T>C (p.Phe325Leu) | ClinVar dbSNP |
| MT | m.5442T>G | CA414780367 | MT-ND2 | c.973T>G (p.Phe325Val) | |
| MT | m.5442T= | CA2499564314 | MT-ND2 | c.973T= (p.Phe325=) | |
| MT | m.5443T>A | CA414780370 | MT-ND2 | c.974T>A (p.Phe325Tyr) | |
| MT | m.5443T>C | CA337097144 | MT-ND2 | c.974T>C (p.Phe325Ser) | dbSNP |
| MT | m.5443T>G | CA414780372 | MT-ND2 | c.974T>G (p.Phe325Cys) | |
| MT | m.5443T= | CA2499564315 | MT-ND2 | c.974T= (p.Phe325=) | |
| MT | m.5444C>A | CA414780374 | MT-ND2 | c.975C>A (p.Phe325Leu) | ClinVar dbSNP |
| MT | m.5444C= | CA2499564316 | MT-ND2 | c.975C= (p.Phe325=) | |
| MT | m.5444C>G | CA414780376 | MT-ND2 | c.975C>G (p.Phe325Leu) | |
| MT | m.5444C>T | CA913179622 | MT-ND2 | c.975C>T (p.Phe325=) | dbSNP |
| MT | m.5445C>A | CA414780378 | MT-ND2 | c.976C>A (p.Leu326Ile) | |
| MT | m.5445C= | CA2573331222 | MT-ND2 | c.976C= (p.Leu326=) | |
| MT | m.5445C>G | CA414780380 | MT-ND2 | c.976C>G (p.Leu326Val) | |
| MT | m.5445C>T | CA414780382 | MT-ND2 | c.976C>T (p.Leu326Phe) | |
| MT | m.5446T>A | CA414780384 | MT-ND2 | c.977T>A (p.Leu326His) | |
| MT | m.5446T>C | CA414780387 | MT-ND2 | c.977T>C (p.Leu326Pro) | dbSNP |
| MT | m.5446T>G | CA414780386 | MT-ND2 | c.977T>G (p.Leu326Arg) | |
| MT | m.5446T= | CA2499564317 | MT-ND2 | c.977T= (p.Leu326=) | |
| MT | m.5447C>A | CA913179625 | MT-ND2 | c.978C>A (p.Leu326=) | dbSNP |
| MT | m.5447C= | CA2499564318 | MT-ND2 | c.978C= (p.Leu326=) | |
| MT | m.5447C>G | CA913179624 | MT-ND2 | c.978C>G (p.Leu326=) | |
| MT | m.5447C>T | CA913179626 | MT-ND2 | c.978C>T (p.Leu326=) | |
| MT | m.5448C>A | CA414780390 | MT-ND2 | c.979C>A (p.Pro327Thr) | |
| MT | m.5448C= | CA2573331223 | MT-ND2 | c.979C= (p.Pro327=) | |
| MT | m.5448C>G | CA414780391 | MT-ND2 | c.979C>G (p.Pro327Ala) | |
| MT | m.5448C>T | CA414780393 | MT-ND2 | c.979C>T (p.Pro327Ser) | |
| MT | m.5449C>A | CA414780395 | MT-ND2 | c.980C>A (p.Pro327His) | |
| MT | m.5449C= | CA2573331224 | MT-ND2 | c.980C= (p.Pro327=) | |
| MT | m.5449C>G | CA414780397 | MT-ND2 | c.980C>G (p.Pro327Arg) | |
| MT | m.5449C>T | CA414780399 | MT-ND2 | c.980C>T (p.Pro327Leu) | |
| MT | m.5450C>A | CA913179629 | MT-ND2 | c.981C>A (p.Pro327=) | |
| MT | m.5450C= | CA2499564319 | MT-ND2 | c.981C= (p.Pro327=) | |
| MT | m.5450C>G | CA913179628 | MT-ND2 | c.981C>G (p.Pro327=) | |
| MT | m.5450C>T | CA913179627 | MT-ND2 | c.981C>T (p.Pro327=) | dbSNP |
| MT | m.5451A= | CA2499564320 | MT-ND2 | c.982A= (p.Thr328=) | |
| MT | m.5451A>C | CA414780401 | MT-ND2 | c.982A>C (p.Thr328Pro) | |
| MT | m.5451A>G | CA414780403 | MT-ND2 | c.982A>G (p.Thr328Ala) | ClinVar dbSNP |
| MT | m.5451A>T | CA414780404 | MT-ND2 | c.982A>T (p.Thr328Ser) | |
| MT | m.5452C>A | CA414780407 | MT-ND2 | c.983C>A (p.Thr328Lys) | |
| MT | m.5452C= | CA2499564321 | MT-ND2 | c.983C= (p.Thr328=) | |
| MT | m.5452C>G | CA414780409 | MT-ND2 | c.983C>G (p.Thr328Arg) | |
| MT | m.5452C>T | CA414780410 | MT-ND2 | c.983C>T (p.Thr328Ile) | ClinVar dbSNP |
| MT | m.5453A= | CA2499564322 | MT-ND2 | c.984A= (p.Thr328=) | |
| MT | m.5453A>C | CA913179632 | MT-ND2 | c.984A>C (p.Thr328=) | |
| MT | m.5453A>G | CA913179631 | MT-ND2 | c.984A>G (p.Thr328=) | dbSNP |
| MT | m.5453A>T | CA913179630 | MT-ND2 | c.984A>T (p.Thr328=) | |
| MT | m.5454C>A | CA414780416 | MT-ND2 | c.985C>A (p.Leu329Ile) | |
| MT | m.5454C= | CA2573331225 | MT-ND2 | c.985C= (p.Leu329=) | |
| MT | m.5454C>G | CA414780413 | MT-ND2 | c.985C>G (p.Leu329Val) | |
| MT | m.5454C>T | CA414780415 | MT-ND2 | c.985C>T (p.Leu329Phe) | |
| MT | m.5455T>A | CA414780419 | MT-ND2 | c.986T>A (p.Leu329His) | |
| MT | m.5455T>C | CA414780421 | MT-ND2 | c.986T>C (p.Leu329Pro) | |
| MT | m.5455T>G | CA414780422 | MT-ND2 | c.986T>G (p.Leu329Arg) | |
| MT | m.5455T= | CA2573331226 | MT-ND2 | c.986T= (p.Leu329=) | |
| MT | m.5456C>A | CA913179635 | MT-ND2 | c.987C>A (p.Leu329=) | |
| MT | m.5456C= | CA2573331227 | MT-ND2 | c.987C= (p.Leu329=) | |
| MT | m.5456C>G | CA913179633 | MT-ND2 | c.987C>G (p.Leu329=) | |
| MT | m.5456C>T | CA913179634 | MT-ND2 | c.987C>T (p.Leu329=) | |
| MT | m.5457A= | CA2499564323 | MT-ND2 | c.988A= (p.Ile330=) | |
| MT | m.5457A>C | CA414780425 | MT-ND2 | c.988A>C (p.Ile330Leu) | dbSNP |
| MT | m.5457A>G | CA414780426 | MT-ND2 | c.988A>G (p.Ile330Val) | dbSNP |
| MT | m.5457A>T | CA414780428 | MT-ND2 | c.988A>T (p.Ile330Phe) | |
| MT | m.5458T>A | CA414780430 | MT-ND2 | c.989T>A (p.Ile330Asn) | |
| MT | m.5458T>C | CA414780432 | MT-ND2 | c.989T>C (p.Ile330Thr) | |
| MT | m.5458T>G | CA414780433 | MT-ND2 | c.989T>G (p.Ile330Ser) | |
| MT | m.5458T= | CA2573331228 | MT-ND2 | c.989T= (p.Ile330=) | |
| MT | m.5460_5488del | CA2740098124 | MT-ND2 | c.991_1019del (p.Ala331ProfsTer?) | |
| MT | m.5459C>A | CA913179636 | MT-ND2 | c.990C>A (p.Ile330=) | |
| MT | m.5459C= | CA2499564324 | MT-ND2 | c.990C= (p.Ile330=) | |
| MT | m.5459C>G | CA414780435 | MT-ND2 | c.990C>G (p.Ile330Met) | |
| MT | m.5459C>T | CA913179637 | MT-ND2 | c.990C>T (p.Ile330=) | dbSNP |
| 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) | |
| MT | m.5472C= | CA2573331235 | MT-ND2 | c.1003C= (p.Leu335=) | |
| MT | m.5472C>G | CA414780486 | MT-ND2 | c.1003C>G (p.Leu335Val) | |
| MT | m.5472C>T | CA913179653 | MT-ND2 | c.1003C>T (p.Leu335=) | |
| MT | m.5473T>A | CA414780490 | MT-ND2 | c.1004T>A (p.Leu335Gln) | |
| MT | m.5473T>C | CA414780492 | MT-ND2 | c.1004T>C (p.Leu335Pro) | |
| MT | m.5473T>G | CA414780489 | MT-ND2 | c.1004T>G (p.Leu335Arg) | |
| MT | m.5473T= | CA2573331236 | MT-ND2 | c.1004T= (p.Leu335=) | |
| MT | m.5474A= | CA2499564331 | MT-ND2 | c.1005A= (p.Leu335=) | |
| MT | m.5474A>C | CA913179657 | MT-ND2 | c.1005A>C (p.Leu335=) | |
| MT | m.5474A>G | CA913179655 | MT-ND2 | c.1005A>G (p.Leu335=) | dbSNP |
| MT | m.5474A>T | CA913179654 | MT-ND2 | c.1005A>T (p.Leu335=) | |
| MT | m.5475C>A | CA414780495 | MT-ND2 | c.1006C>A (p.Leu336Ile) | |
| MT | m.5475C= | CA2573331237 | MT-ND2 | c.1006C= (p.Leu336=) | |
| MT | m.5475C>G | CA414780496 | MT-ND2 | c.1006C>G (p.Leu336Val) | |
| MT | m.5475C>T | CA414780497 | MT-ND2 | c.1006C>T (p.Leu336Phe) | |
| MT | m.5476T>A | CA414780500 | MT-ND2 | c.1007T>A (p.Leu336His) | |
| MT | m.5476T>C | CA414780502 | MT-ND2 | c.1007T>C (p.Leu336Pro) | |
| MT | m.5476T>G | CA414780503 | MT-ND2 | c.1007T>G (p.Leu336Arg) | |
| MT | m.5476T= | CA2573331238 | MT-ND2 | c.1007T= (p.Leu336=) | |
| MT | m.5477C>A | CA913179660 | MT-ND2 | c.1008C>A (p.Leu336=) | |
| MT | m.5477C= | CA2573331239 | MT-ND2 | c.1008C= (p.Leu336=) | |
| MT | m.5477C>G | CA913179661 | MT-ND2 | c.1008C>G (p.Leu336=) | |
| MT | m.5477C>T | CA913179659 | MT-ND2 | c.1008C>T (p.Leu336=) | |
| MT | m.5478C>A | CA414780506 | MT-ND2 | c.1009C>A (p.Leu337Ile) | |
| MT | m.5478C= | CA2499564332 | MT-ND2 | c.1009C= (p.Leu337=) | |
| MT | m.5478C>G | CA414780507 | MT-ND2 | c.1009C>G (p.Leu337Val) | |
| MT | m.5478C>T | CA913179663 | MT-ND2 | c.1009C>T (p.Leu337=) | dbSNP |
| MT | m.5479T>A | CA414780509 | MT-ND2 | c.1010T>A (p.Leu337Gln) | |
| MT | m.5479T>C | CA414780511 | MT-ND2 | c.1010T>C (p.Leu337Pro) | |
| MT | m.5479T>G | CA414780513 | MT-ND2 | c.1010T>G (p.Leu337Arg) | |
| MT | m.5479T= | CA2573331240 | MT-ND2 | c.1010T= (p.Leu337=) | |
| MT | m.5480A= | CA2499564333 | MT-ND2 | c.1011A= (p.Leu337=) | |
| MT | m.5480A>C | CA913179664 | MT-ND2 | c.1011A>C (p.Leu337=) | |
| MT | m.5480A>G | CA913179665 | MT-ND2 | c.1011A>G (p.Leu337=) | dbSNP |
| MT | m.5480A>T | CA913179666 | MT-ND2 | c.1011A>T (p.Leu337=) | |
| MT | m.5481C>A | CA414780519 | MT-ND2 | c.1012C>A (p.Pro338Thr) | |
| MT | m.5481C= | CA2573331241 | MT-ND2 | c.1012C= (p.Pro338=) | |
| MT | m.5481C>G | CA414780517 | MT-ND2 | c.1012C>G (p.Pro338Ala) | |
| MT | m.5481C>T | CA414780515 | MT-ND2 | c.1012C>T (p.Pro338Ser) | |
| MT | m.5482C>A | CA414780521 | MT-ND2 | c.1013C>A (p.Pro338His) | |
| MT | m.5482C= | CA2513156647 | MT-ND2 | c.1013C= (p.Pro338=) | |
| MT | m.5482C>G | CA414780523 | MT-ND2 | c.1013C>G (p.Pro338Arg) | |
| MT | m.5482C>T | CA414780525 | MT-ND2 | c.1013C>T (p.Pro338Leu) | |
| MT | m.5483T>A | CA913179670 | MT-ND2 | c.1014T>A (p.Pro338=) | |
| MT | m.5483T>C | CA913179669 | MT-ND2 | c.1014T>C (p.Pro338=) | dbSNP |
| MT | m.5483T>G | CA913179668 | MT-ND2 | c.1014T>G (p.Pro338=) | |
| MT | m.5483T= | CA2499564334 | MT-ND2 | c.1014T= (p.Pro338=) | |
| MT | m.5484A= | CA2499564335 | MT-ND2 | c.1015A= (p.Ile339=) | |
| MT | m.5484A>C | CA414780528 | MT-ND2 | c.1015A>C (p.Ile339Leu) | |
| MT | m.5484A>G | CA414780529 | MT-ND2 | c.1015A>G (p.Ile339Val) | ClinVar dbSNP |
| MT | m.5484A>T | CA414780530 | MT-ND2 | c.1015A>T (p.Ile339Phe) | |
| MT | m.5485T>A | CA414780533 | MT-ND2 | c.1016T>A (p.Ile339Asn) | |
| MT | m.5485T>C | CA414780535 | MT-ND2 | c.1016T>C (p.Ile339Thr) | |
| MT | m.5485T>G | CA414780537 | MT-ND2 | c.1016T>G (p.Ile339Ser) | |
| MT | m.5485T= | CA2573331242 | MT-ND2 | c.1016T= (p.Ile339=) | |
| MT | m.5486C>A | CA913179672 | MT-ND2 | c.1017C>A (p.Ile339=) | |
| MT | m.5486C= | CA2499564336 | MT-ND2 | c.1017C= (p.Ile339=) | |
| MT | m.5486C>G | CA414780539 | MT-ND2 | c.1017C>G (p.Ile339Met) | |
| MT | m.5486C>T | CA913179671 | MT-ND2 | c.1017C>T (p.Ile339=) | dbSNP |
| MT | m.5487T>A | CA414780540 | MT-ND2 | c.1018T>A (p.Ser340Thr) | |
| MT | m.5487T>C | CA414780542 | MT-ND2 | c.1018T>C (p.Ser340Pro) | |
| MT | m.5487T>G | CA414780544 | MT-ND2 | c.1018T>G (p.Ser340Ala) | |
| MT | m.5487T= | CA2573331243 | MT-ND2 | c.1018T= (p.Ser340=) | |
| MT | m.5488C>A | CA414780547 | MT-ND2 | c.1019C>A (p.Ser340Tyr) | |
| MT | m.5488C= | CA2573331244 | MT-ND2 | c.1019C= (p.Ser340=) | |
| MT | m.5488C>G | CA414780549 | MT-ND2 | c.1019C>G (p.Ser340Cys) | |
| MT | m.5488C>T | CA414780546 | MT-ND2 | c.1019C>T (p.Ser340Phe) | |
| MT | m.5489C>A | CA913179676 | MT-ND2 | c.1020C>A (p.Ser340=) | |
| MT | m.5489C= | CA2573331245 | MT-ND2 | c.1020C= (p.Ser340=) | |
| MT | m.5489C>G | CA913179675 | MT-ND2 | c.1020C>G (p.Ser340=) | |
| MT | m.5489C>T | CA913179673 | MT-ND2 | c.1020C>T (p.Ser340=) | |
| MT | m.5490C>A | CA414780552 | MT-ND2 | c.1021C>A (p.Pro341Thr) | |
| MT | m.5490C= | CA2573331246 | MT-ND2 | c.1021C= (p.Pro341=) | |
| MT | m.5490C>G | CA414780555 | MT-ND2 | c.1021C>G (p.Pro341Ala) | |
| MT | m.5490C>T | CA414780553 | MT-ND2 | c.1021C>T (p.Pro341Ser) | |
| MT | m.5491C>A | CA414780557 | MT-ND2 | c.1022C>A (p.Pro341His) | |
| MT | m.5491C= | CA2513084297 | MT-ND2 | c.1022C= (p.Pro341=) | |
| MT | m.5491C>G | CA414780561 | MT-ND2 | c.1022C>G (p.Pro341Arg) | |
| MT | m.5491C>T | CA414780558 | MT-ND2 | c.1022C>T (p.Pro341Leu) | |
| MT | m.5492T>A | CA913179679 | MT-ND2 | c.1023T>A (p.Pro341=) | |
| MT | m.5492T>C | CA337097154 | MT-ND2 | c.1023T>C (p.Pro341=) | dbSNP |
| MT | m.5492T>G | CA913179680 | MT-ND2 | c.1023T>G (p.Pro341=) | |
| MT | m.5492T= | CA2499564337 | MT-ND2 | c.1023T= (p.Pro341=) | |
| MT | m.5493T>A | CA414780566 | MT-ND2 | c.1024T>A (p.Phe342Ile) | |
| MT | m.5493T>C | CA414780564 | MT-ND2 | c.1024T>C (p.Phe342Leu) | ClinVar dbSNP |
| MT | m.5493T>G | CA414780568 | MT-ND2 | c.1024T>G (p.Phe342Val) | |
| MT | m.5493T= | CA2499564338 | MT-ND2 | c.1024T= (p.Phe342=) | |
| MT | m.5494T>A | CA414780570 | MT-ND2 | c.1025T>A (p.Phe342Tyr) | |
| MT | m.5494T>C | CA414780573 | MT-ND2 | c.1025T>C (p.Phe342Ser) | dbSNP |
| MT | m.5494T>G | CA414780571 | MT-ND2 | c.1025T>G (p.Phe342Cys) | ClinVar dbSNP |
| MT | m.5494T= | CA2499564339 | MT-ND2 | c.1025T= (p.Phe342=) | |
| MT | m.5495T>A | CA414780575 | MT-ND2 | c.1026T>A (p.Phe342Leu) | |
| MT | m.5495T>C | CA337097156 | MT-ND2 | c.1026T>C (p.Phe342=) | dbSNP |
| MT | m.5495T>G | CA414780578 | MT-ND2 | c.1026T>G (p.Phe342Leu) | |
| MT | m.5495T= | CA2499564340 | MT-ND2 | c.1026T= (p.Phe342=) | |
| MT | m.5496A= | CA2499564341 | MT-ND2 | c.1027A= (p.Ile343=) | |
| MT | m.5496A>C | CA414780580 | MT-ND2 | c.1027A>C (p.Ile343Leu) | |
| MT | m.5496A>G | CA337097158 | MT-ND2 | c.1027A>G (p.Ile343Val) | ClinVar dbSNP |
| MT | m.5496A>T | CA414780583 | MT-ND2 | c.1027A>T (p.Ile343Leu) | |
| MT | m.5497T>A | CA414780585 | MT-ND2 | c.1028T>A (p.Ile343Lys) | |
| MT | m.5497T>C | CA414780587 | MT-ND2 | c.1028T>C (p.Ile343Thr) | |
| MT | m.5497T>G | CA414780589 | MT-ND2 | c.1028T>G (p.Ile343Arg) | |
| MT | m.5497T= | CA2573331247 | MT-ND2 | c.1028T= (p.Ile343=) | |
| MT | m.5498A= | CA2499564342 | MT-ND2 | c.1029A= (p.Ile343=) | |
| MT | m.5498A>C | CA913179682 | MT-ND2 | c.1029A>C (p.Ile343=) | |
| MT | m.5498A>G | CA337097160 | MT-ND2 | c.1029A>G (p.Ile343Met) | dbSNP |
| MT | m.5498A>T | CA913179683 | MT-ND2 | c.1029A>T (p.Ile343=) | |
| MT | m.5499C>A | CA414780594 | MT-ND2 | c.1030C>A (p.Leu344Ile) | |
| MT | m.5499C= | CA2573331248 | MT-ND2 | c.1030C= (p.Leu344=) | |
| MT | m.5499C>G | CA414780592 | MT-ND2 | c.1030C>G (p.Leu344Val) | |
| MT | m.5499C>T | CA913179684 | MT-ND2 | c.1030C>T (p.Leu344=) | |
| MT | m.5500T>A | CA414780595 | MT-ND2 | c.1031T>A (p.Leu344Gln) | |
| MT | m.5500T>C | CA414780598 | MT-ND2 | c.1031T>C (p.Leu344Pro) | |
| MT | m.5500T>G | CA414780600 | MT-ND2 | c.1031T>G (p.Leu344Arg) | |
| MT | m.5500T= | CA2573331249 | MT-ND2 | c.1031T= (p.Leu344=) | |
| MT | m.5501A= | CA2499564343 | MT-ND2 | c.1032A= (p.Leu344=) | |
| MT | m.5501A>C | CA913179689 | MT-ND2 | c.1032A>C (p.Leu344=) | |
| MT | m.5501A>G | CA913179686 | MT-ND2 | c.1032A>G (p.Leu344=) | dbSNP |
| MT | m.5501A>T | CA913179685 | MT-ND2 | c.1032A>T (p.Leu344=) | |
| MT | m.5502A= | CA2499564344 | MT-ND2 | c.1033A= (p.Ile345=) | |
| MT | m.5502A>C | CA414780601 | MT-ND2 | c.1033A>C (p.Ile345Leu) | |
| MT | m.5502A>G | CA414780603 | MT-ND2 | c.1033A>G (p.Ile345Val) | dbSNP |
| MT | m.5502A>T | CA414780605 | MT-ND2 | c.1033A>T (p.Ile345Leu) | |
| MT | m.5503T>A | CA414780607 | MT-ND2 | c.1034T>A (p.Ile345Lys) | |
| MT | m.5503T>C | CA414780609 | MT-ND2 | c.1034T>C (p.Ile345Thr) | dbSNP |
| MT | m.5503T>G | CA414780611 | MT-ND2 | c.1034T>G (p.Ile345Arg) | |
| MT | m.5503T= | CA2499564345 | MT-ND2 | c.1034T= (p.Ile345=) | |
| MT | m.5504A= | CA2573331250 | MT-ND2 | c.1035A= (p.Ile345=) | |
| MT | m.5504A>C | CA913179692 | MT-ND2 | c.1035A>C (p.Ile345=) | |
| MT | m.5504A>G | CA414780613 | MT-ND2 | c.1035A>G (p.Ile345Met) | |
| MT | m.5504A>T | CA913179691 | MT-ND2 | c.1035A>T (p.Ile345=) | |
| MT | m.5505A= | CA2499564346 | MT-ND2 | c.1036A= (p.Ile346=) | |
| MT | m.5505A>C | CA414780617 | MT-ND2 | c.1036A>C (p.Ile346Leu) | |
| MT | m.5505A>G | CA414780619 | MT-ND2 | c.1036A>G (p.Ile346Val) | ClinVar dbSNP |
| MT | m.5505A>T | CA414780615 | MT-ND2 | c.1036A>T (p.Ile346Phe) | |
| MT | m.5506T>A | CA414780622 | MT-ND2 | c.1037T>A (p.Ile346Asn) | |
| MT | m.5506T>C | CA414780623 | MT-ND2 | c.1037T>C (p.Ile346Thr) | |
| MT | m.5506T>G | CA414780625 | MT-ND2 | c.1037T>G (p.Ile346Ser) | |
| MT | m.5506T= | CA2573331251 | MT-ND2 | c.1037T= (p.Ile346=) | |
| MT | m.5507C>A | CA913179697 | MT-ND2 | c.1038C>A (p.Ile346=) | |
| MT | m.5507C= | CA2499564347 | MT-ND2 | c.1038C= (p.Ile346=) | |
| MT | m.5507C>G | CA414780627 | MT-ND2 | c.1038C>G (p.Ile346Met) | |
| MT | m.5507C>T | CA337097162 | MT-ND2 | c.1038C>T (p.Ile346=) | dbSNP |
| MT | m.5508T>A | CA414780630 | MT-ND2 | c.1039T>A (p.Leu347Ile) | |
| MT | m.5508T>C | CA913179698 | MT-ND2 | c.1039T>C (p.Leu347=) | dbSNP |
| MT | m.5508T>G | CA414780632 | MT-ND2 | c.1039T>G (p.Leu347Val) | |
| MT | m.5508T= | CA2499564348 | MT-ND2 | c.1039T= (p.Leu347=) | |
| MT | m.5509T>A | CA414780634 | MT-ND2 | c.1040T>A (p.Leu347Ter) | |
| MT | m.5509T>C | CA414780637 | MT-ND2 | c.1040T>C (p.Leu347Ser) | dbSNP |
| MT | m.5509T>G | CA414780638 | MT-ND2 | c.1040T>G (p.Leu347Ter) | |
| MT | m.5509T= | CA2499564349 | MT-ND2 | c.1040T= (p.Leu347=) | |
| MT | m.5510A= | CA2499564350 | MT-ND2 | c.1041A= (p.Leu347=) | |
| MT | m.5510A>C | CA414780641 | MT-ND2 | c.1041A>C (p.Leu347Phe) | |
| MT | m.5510A>G | CA337097164 | MT-ND2 | c.1041A>G (p.Leu347=) | dbSNP |
| MT | m.5510A>T | CA414780643 | MT-ND2 | c.1041A>T (p.Leu347Phe) | |
| MT | m.5511T>A | CA913179699 | MT-ND2 | c.1042T>A | |
| MT | m.5511T>C | CA913179700 | MT-ND2 | c.1042T>C | |
| MT | m.5511T>G | CA913179703 | MT-ND2 | c.1042T>G | |
| MT | m.5511T= | CA2573331252 | MT-ND2 | c.1042T= | |
| MT | m.5512A= | CA2573331253 | |||
| MT | m.5512A>C | CA913179707 | |||
| MT | m.5512A>G | CA913179706 | |||
| MT | m.5512A>T | CA913179705 | |||
| MT | m.5513G>A | CA913179710 | dbSNP | ||
| MT | m.5513G>C | CA913179709 | |||
| MT | m.5513G= | CA2573331254 | |||
| MT | m.5513G>T | CA913179708 | |||
| MT | m.5514A= | CA2499564351 | |||
| MT | m.5514A>C | CA913179713 | |||
| MT | m.5514A>G | CA913179712 | ClinVar dbSNP | ||
| MT | m.5514A>T | CA913179711 | |||
| MT | m.5515A= | CA2499564352 | |||
| MT | m.5515A>C | CA913179716 | |||
| MT | m.5515A>G | CA913179715 | ClinVar dbSNP | ||
| MT | m.5515A>T | CA913179714 | |||
| MT | m.5516A= | CA2499564354 | |||
| MT | m.5516A>C | CA913179719 | |||
| MT | m.5516A>G | CA913179718 | ClinVar dbSNP | ||
| MT | m.5516A>T | CA913179717 | |||
| MT | m.5517T>A | CA913179723 | |||
| MT | m.5517T>C | CA913179722 | |||
| MT | m.5517T>G | CA913179720 | |||
| MT | m.5517T= | CA2573331255 | |||
| MT | m.5518T>A | CA913179725 | |||
| MT | m.5518T>C | CA913179726 | |||
| MT | m.5518T>G | CA913179724 | |||
| MT | m.5518T= | CA2573331256 | |||
| MT | m.5519T>A | CA913179729 | |||
| MT | m.5519T>C | CA913179728 | |||
| MT | m.5519T>G | CA913179730 | |||
| MT | m.5519T= | CA2573331257 | |||
| MT | m.5520A= | CA2499564356 | |||
| MT | m.5520A>C | CA913179733 | |||
| MT | m.5520A>G | CA337097166 | dbSNP | ||
| MT | m.5520A>T | CA913179732 | |||
| MT | m.5521G>A | CA254831 | ClinVar dbSNP | ||
| MT | m.5521G>C | CA913179735 | |||
| MT | m.5521G= | CA2499564358 | |||
| MT | m.5521G>T | CA913179734 | |||
| MT | m.5522G>A | CA913179740 | dbSNP | ||
| MT | m.5522G>C | CA913179739 | |||
| MT | m.5522G= | CA2573331258 | |||
| MT | m.5522G>T | CA913179738 | |||
| MT | m.5523T>A | CA913179742 | |||
| MT | m.5523T>C | CA913179741 | |||
| MT | m.5523T>G | CA345912 | ClinVar dbSNP | ||
| MT | m.5523T= | CA2499564360 | |||
| MT | m.5524T>A | CA913179743 | |||
| MT | m.5524T>C | CA913179744 | ClinVar dbSNP | ||
| MT | m.5524T>G | CA913179745 | |||
| MT | m.5524T= | CA2499564361 | |||
| MT | m.5525A= | CA2573331259 | |||
| MT | m.5525A>C | CA913179746 | |||
| MT | m.5525A>G | CA913179747 | |||
| MT | m.5525A>T | CA913179748 | |||
| MT | m.5526A= | CA2573331260 | |||
| MT | m.5526A>C | CA913179749 | |||
| MT | m.5526A>G | CA913179752 | |||
| MT | m.5526A>T | CA913179750 | |||
| MT | m.5527A= | CA2499564362 | |||
| MT | m.5527A>C | CA913179757 | |||
| MT | m.5527A>G | CA913179755 | ClinVar dbSNP | ||
| MT | m.5527A>T | CA913179753 | |||
| MT | m.5528T>A | CA913179758 | |||
| MT | m.5528T>C | CA913179759 | ClinVar dbSNP | ||
| MT | m.5528T>G | CA913179760 | |||
| MT | m.5528T= | CA2499564364 | |||
| MT | m.5529A= | CA2499564367 | |||
| MT | m.5529A>C | CA913179763 | |||
| MT | m.5529A>G | CA913179762 | dbSNP | ||
| MT | m.5529A>T | CA913179761 | |||
| MT | m.5530C>A | CA913179765 | |||
| MT | m.5530C= | CA2499564369 | |||
| MT | m.5530C>G | CA913179764 | |||
| MT | m.5530C>T | CA913179766 | ClinVar dbSNP | ||
| MT | m.5531A= | CA2573320866 | |||
| MT | m.5531A>C | CA913179771 | |||
| MT | m.5531A>G | CA913179770 | |||
| MT | m.5531A>T | CA913179768 | |||
| MT | m.5532G>A | CA120542 | ClinVar dbSNP | ||
| MT | m.5532G>C | CA913179773 | |||
| MT | m.5532G= | CA2499564372 | |||
| MT | m.5532G>T | CA913179772 | |||
| MT | m.5533A= | CA2573320897 | |||
| MT | m.5533A>C | CA913179777 | |||
| MT | m.5533A>G | CA913179775 | |||
| MT | m.5533A>T | CA913179776 | |||
| MT | m.5534C>A | CA913179780 | |||
| MT | m.5534C= | CA2573320901 | |||
| MT | m.5534C>G | CA913179779 | |||
| MT | m.5534C>T | CA913179778 | |||
| MT | m.5535C>A | CA913179783 | |||
| MT | m.5535C= | CA2573320906 | |||
| MT | m.5535C>G | CA913179782 | |||
| MT | m.5535C>T | CA913179781 | |||
| MT | m.5536A= | CA2499564375 | |||
| MT | m.5536A>C | CA913179784 | |||
| MT | m.5536A>G | CA913179786 | |||
| MT | m.5536A>T | CA913179787 | |||
| MT | m.5536_5537insT | CA915952206 | ClinVar dbSNP | ||
| MT | m.5537A= | CA2499564378 | |||
| MT | m.5537A>C | CA913179788 | |||
| MT | m.5537A>G | CA913179790 | |||
| MT | m.5537A>T | CA913179791 | |||
| MT | m.5537_5538insT | CA120541 | ClinVar dbSNP | ||
| MT | m.5538G>A | CA913179793 | ClinVar dbSNP | ||
| MT | m.5538G>C | CA913179795 | |||
| MT | m.5538G= | CA2499564382 | |||
| MT | m.5538G>T | CA913179794 | |||
| MT | m.5539A= | CA2499564384 | |||
| MT | m.5539A>C | CA913179798 | |||
| MT | m.5539A>G | CA913179797 | ClinVar dbSNP | ||
| MT | m.5539A>T | CA913179796 | ClinVar dbSNP | ||
| MT | m.5540G>A | CA913179801 | ClinVar dbSNP | ||
| MT | m.5540G>C | CA913179799 | |||
| MT | m.5540G= | CA2499564387 | |||
| MT | m.5540G>T | CA913179800 | |||
| MT | m.5541C>A | CA913179804 | |||
| MT | m.5541C= | CA2573320946 | |||
| MT | m.5541C>G | CA913179803 | |||
| MT | m.5541C>T | CA913179802 |