| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| MT | m.4409T>A | CA913178047 | |||
| MT | m.4409T>C | CA254835 | ClinVar dbSNP | ||
| MT | m.4409T>G | CA913178046 | |||
| MT | m.4409T= | CA2499563868 | |||
| MT | m.4410C>A | CA913178048 | |||
| MT | m.4410C= | CA2573329823 | |||
| MT | m.4410C>G | CA913178049 | |||
| MT | m.4410C>T | CA913178050 | |||
| MT | m.4411A= | CA2573329824 | |||
| MT | m.4411A>C | CA913178051 | |||
| MT | m.4411A>G | CA913178052 | |||
| MT | m.4411A>T | CA913178053 | |||
| MT | m.4412G>A | CA658475630 | dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC COSMIC | ||
| MT | m.4412G>C | CA913178058 | |||
| MT | m.4412G= | CA2573329825 | |||
| MT | m.4412G>T | CA913178055 | |||
| MT | m.4413C>A | CA913178064 | |||
| MT | m.4413C= | CA2573329827 | |||
| MT | m.4413C>G | CA913178063 | |||
| MT | m.4413C>T | CA913178062 | |||
| MT | m.4414T>A | CA913178065 | |||
| MT | m.4414T>C | CA913178066 | |||
| MT | m.4414T>G | CA913178067 | |||
| MT | m.4414T= | CA2573329828 | |||
| MT | m.4415A= | CA2573329829 | |||
| MT | m.4415A>C | CA913178070 | |||
| MT | m.4415A>G | CA913178071 | |||
| MT | m.4415A>T | CA913178068 | |||
| MT | m.4416A= | CA2573329831 | |||
| MT | m.4416A>C | CA913178077 | |||
| MT | m.4416A>G | CA913178076 | |||
| MT | m.4416A>T | CA913178075 | |||
| MT | m.4417A= | CA2499563869 | |||
| MT | m.4417A>C | CA913178080 | |||
| MT | m.4417A>G | CA913178082 | ClinVar dbSNP | ||
| MT | m.4417A>T | CA913178083 | |||
| MT | m.4418T>A | CA913178086 | |||
| MT | m.4418T>C | CA913178085 | ClinVar dbSNP | ||
| MT | m.4418T>G | CA913178084 | |||
| MT | m.4418T= | CA2499563870 | |||
| MT | m.4419A= | CA2573329837 | |||
| MT | m.4419A>C | CA913178089 | |||
| MT | m.4419A>G | CA913178088 | |||
| MT | m.4419A>T | CA913178087 | |||
| MT | m.4420A= | CA2573329840 | |||
| MT | m.4420A>C | CA913178092 | |||
| MT | m.4420A>G | CA913178091 | |||
| MT | m.4420A>T | CA913178090 | |||
| MT | m.4421G>A | CA913178093 | |||
| MT | m.4421G>C | CA913178094 |