Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
MT | m.3739A= | CA2573328443 | MT-ND1 | c.433A= (p.Thr145=) | |
MT | m.3739A>C | CA414773412 | MT-ND1 | c.433A>C (p.Thr145Pro) | |
MT | m.3739A>G | CA414773413 | MT-ND1 | c.433A>G (p.Thr145Ala) | |
MT | m.3739A>T | CA414773411 | MT-ND1 | c.433A>T (p.Thr145Ser) | |
MT | m.3740C>A | CA414773416 | MT-ND1 | c.434C>A (p.Thr145Asn) | |
MT | m.3740C= | CA2573328445 | MT-ND1 | c.434C= (p.Thr145=) | |
MT | m.3740C>G | CA414773414 | MT-ND1 | c.434C>G (p.Thr145Ser) | |
MT | m.3740C>T | CA414773415 | MT-ND1 | c.434C>T (p.Thr145Ile) | |
MT | m.3741C>A | CA913170235 | MT-ND1 | c.435C>A (p.Thr145=) | |
MT | m.3741C= | CA2499563580 | MT-ND1 | c.435C= (p.Thr145=) | |
MT | m.3741C>G | CA913170236 | MT-ND1 | c.435C>G (p.Thr145=) | |
MT | m.3741C>T | CA337096662 | MT-ND1 | c.435C>T (p.Thr145=) | dbSNP |
MT | m.3742C>A | CA414773417 | MT-ND1 | c.436C>A (p.Leu146Ile) | |
MT | m.3742C= | CA2573328451 | MT-ND1 | c.436C= (p.Leu146=) | |
MT | m.3742C>G | CA414773418 | MT-ND1 | c.436C>G (p.Leu146Val) | |
MT | m.3742C>T | CA913170237 | MT-ND1 | c.436C>T (p.Leu146=) | |
MT | m.3743T>A | CA414773419 | MT-ND1 | c.437T>A (p.Leu146Gln) | |
MT | m.3743T>C | CA414773420 | MT-ND1 | c.437T>C (p.Leu146Pro) | |
MT | m.3743T>G | CA414773421 | MT-ND1 | c.437T>G (p.Leu146Arg) | |
MT | m.3743T= | CA2573328455 | MT-ND1 | c.437T= (p.Leu146=) | |
MT | m.3744A= | CA2499563581 | MT-ND1 | c.438A= (p.Leu146=) | |
MT | m.3744A>C | CA913170242 | MT-ND1 | c.438A>C (p.Leu146=) | |
MT | m.3744A>G | CA913170243 | MT-ND1 | c.438A>G (p.Leu146=) | dbSNP |
MT | m.3744A>T | CA913170238 | MT-ND1 | c.438A>T (p.Leu146=) | |
MT | m.3745G>A | CA414773422 | MT-ND1 | c.439G>A (p.Ala147Thr) | ClinVar dbSNP |
MT | m.3745G>C | CA414773423 | MT-ND1 | c.439G>C (p.Ala147Pro) | |
MT | m.3745G= | CA2499563582 | MT-ND1 | c.439G= (p.Ala147=) | |
MT | m.3745G>T | CA414773424 | MT-ND1 | c.439G>T (p.Ala147Ser) | dbSNP |
MT | m.3746C>A | CA414773426 | MT-ND1 | c.440C>A (p.Ala147Asp) | |
MT | m.3746C= | CA2499563583 | MT-ND1 | c.440C= (p.Ala147=) | |
MT | m.3746C>G | CA414773425 | MT-ND1 | c.440C>G (p.Ala147Gly) | |
MT | m.3746C>T | CA337096664 | MT-ND1 | c.440C>T (p.Ala147Val) | ClinVar dbSNP |
MT | m.3747C>A | CA913170249 | MT-ND1 | c.441C>A (p.Ala147=) | |
MT | m.3747C= | CA2499563584 | MT-ND1 | c.441C= (p.Ala147=) | |
MT | m.3747C>G | CA913170247 | MT-ND1 | c.441C>G (p.Ala147=) | |
MT | m.3747C>T | CA913170248 | MT-ND1 | c.441C>T (p.Ala147=) | dbSNP |
MT | m.3748A= | CA2573328470 | MT-ND1 | c.442A= (p.Ile148=) | |
MT | m.3748A>C | CA414773427 | MT-ND1 | c.442A>C (p.Ile148Leu) | |
MT | m.3748A>G | CA414773428 | MT-ND1 | c.442A>G (p.Ile148Val) | |
MT | m.3748A>T | CA414773429 | MT-ND1 | c.442A>T (p.Ile148Phe) | |
MT | m.3749T>A | CA414773430 | MT-ND1 | c.443T>A (p.Ile148Asn) | |
MT | m.3749T>C | CA414773431 | MT-ND1 | c.443T>C (p.Ile148Thr) | ClinVar dbSNP |
MT | m.3749T>G | CA414773432 | MT-ND1 | c.443T>G (p.Ile148Ser) | |
MT | m.3749T= | CA2499563585 | MT-ND1 | c.443T= (p.Ile148=) | |
MT | m.3750C>A | CA913170251 | MT-ND1 | c.444C>A (p.Ile148=) | |
MT | m.3750C= | CA2499563586 | MT-ND1 | c.444C= (p.Ile148=) | |
MT | m.3750C>G | CA414773433 | MT-ND1 | c.444C>G (p.Ile148Met) | |
MT | m.3750C>T | CA337096666 | MT-ND1 | c.444C>T (p.Ile148=) | dbSNP |
MT | m.3751A= | CA2499563587 | MT-ND1 | c.445A= (p.Ile149=) | |
MT | m.3751A>C | CA414773434 | MT-ND1 | c.445A>C (p.Ile149Leu) |