Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49457877A= | CA1627395283 | MMUT | c.567T= (p.Asn189=) | |
6 | g.49457877A>C | CA364404447 | MMUT | c.567T>G (p.Asn189Lys) | ClinVar dbSNP |
6 | g.49457877A>G | CA450608591 | MMUT | c.567T>C (p.Asn189=) | dbSNP |
6 | g.49457877A>T | CA364404448 | MMUT | c.567T>A (p.Asn189Lys) | |
6 | g.49457877dup | CA2695206686 | MMUT | c.567dup (p.Gly190TrpfsTer21) | |
6 | g.49457878T>A | CA3847091 | MMUT | c.566A>T (p.Asn189Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457878T>C | CA3847090 | MMUT | c.566A>G (p.Asn189Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457878T>G | CA364404449 | MMUT | c.566A>C (p.Asn189Thr) | |
6 | g.49457878T= | CA1627395284 | MMUT | c.566A= (p.Asn189=) | |
6 | g.49457879T>A | CA364404450 | MMUT | c.565A>T (p.Asn189Tyr) | |
6 | g.49457879T>C | CA364404451 | MMUT | c.565A>G (p.Asn189Asp) | |
6 | g.49457879T>G | CA364404452 | MMUT | c.565A>C (p.Asn189His) | |
6 | g.49457880C>A | CA364404453 | MMUT | c.564G>T (p.Met188Ile) | |
6 | g.49457880C>G | CA364404454 | MMUT | c.564G>C (p.Met188Ile) | gnomAD v4 |
6 | g.49457880C>T | CA364404455 | MMUT | c.564G>A (p.Met188Ile) | |
6 | g.49457881A>C | CA364404458 | MMUT | c.563T>G (p.Met188Arg) | gnomAD v4 |
6 | g.49457881A>G | CA364404456 | MMUT | c.563T>C (p.Met188Thr) | |
6 | g.49457881A>T | CA364404457 | MMUT | c.563T>A (p.Met188Lys) | |
6 | g.49457882T>A | CA364404459 | MMUT | c.562A>T (p.Met188Leu) | |
6 | g.49457882T>C | CA364404460 | MMUT | c.562A>G (p.Met188Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457882T>G | CA364404461 | MMUT | c.562A>C (p.Met188Leu) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49457882T= | CA1627395285 | MMUT | c.562A= (p.Met188=) | |
6 | g.49457883A= | CA1627395286 | MMUT | c.561T= (p.Thr187=) | |
6 | g.49457883A>C | CA3847092 | MMUT | c.561T>G (p.Thr187=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457883A>G | CA450608592 | MMUT | c.561T>C (p.Thr187=) | |
6 | g.49457883A>T | CA450608593 | MMUT | c.561T>A (p.Thr187=) | |
6 | g.49457884G>A | CA364404462 | MMUT | c.560C>T (p.Thr187Ile) | |
6 | g.49457884G>C | CA10575881 | MMUT | c.560C>G (p.Thr187Ser) | ClinVar dbSNP |
6 | g.49457884G= | CA1627395287 | MMUT | c.560C= (p.Thr187=) | |
6 | g.49457884G>T | CA364404463 | MMUT | c.560C>A (p.Thr187Asn) | |
6 | g.49457885T>A | CA364404464 | MMUT | c.559A>T (p.Thr187Ser) | |
6 | g.49457885T>C | CA364404465 | MMUT | c.559A>G (p.Thr187Ala) | |
6 | g.49457885T>G | CA364404466 | MMUT | c.559A>C (p.Thr187Pro) | |
6 | g.49457886C>A | CA364404467 | MMUT | c.558G>T (p.Met186Ile) | |
6 | g.49457886C>G | CA364404468 | MMUT | c.558G>C (p.Met186Ile) | |
6 | g.49457886C>T | CA364404469 | MMUT | c.558G>A (p.Met186Ile) | |
6 | g.49457887A>C | CA364404470 | MMUT | c.557T>G (p.Met186Arg) | |
6 | g.49457887A>G | CA364404472 | MMUT | c.557T>C (p.Met186Thr) | COSMIC |
6 | g.49457887A>T | CA364404471 | MMUT | c.557T>A (p.Met186Lys) | |
6 | g.49457888T>A | CA364404473 | MMUT | c.556A>T (p.Met186Leu) | gnomAD v4 |
6 | g.49457888T>C | CA3847093 | MMUT | c.556A>G (p.Met186Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457888T>G | CA364404474 | MMUT | c.556A>C (p.Met186Leu) | |
6 | g.49457888T= | CA1627395292 | MMUT | c.556A= (p.Met186=) | |
6 | g.49457889G>A | CA450608595 | MMUT | c.555C>T (p.Ser185=) | |
6 | g.49457889G>C | CA450608596 | MMUT | c.555C>G (p.Ser185=) | |
6 | g.49457889G>T | CA450608594 | MMUT | c.555C>A (p.Ser185=) | |
6 | g.49457890G>A | CA364404475 | MMUT | c.554C>T (p.Ser185Phe) | |
6 | g.49457890G>C | CA364404476 | MMUT | c.554C>G (p.Ser185Cys) | |
6 | g.49457890G>T | CA364404477 | MMUT | c.554C>A (p.Ser185Tyr) | |
6 | g.49457891A>C | CA364404478 | MMUT | c.553T>G (p.Ser185Ala) |