Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.132873146_132873147del | CA584913901 | TG | c.563_564del (p.Glu188ValfsTer18) c.*414_*415del (n.*414_*415del) c.302_303del (p.Glu101ValfsTer18) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873147del | CA2688647983 | TG | c.564del (p.Glu188AspfsTer15) c.*415del (n.*415del) c.303del (p.Glu101AspfsTer15) | gnomAD v4 |
8 | g.132873147G>A | CA463013919 | TG | c.564G>A (p.Glu188=) c.*415G>A (n.*415G>A) c.303G>A (p.Glu101=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873147G>C | CA372247339 | TG | c.564G>C (p.Glu188Asp) c.*415G>C (n.*415G>C) c.303G>C (p.Glu101Asp) | |
8 | g.132873147G= | CA1820984248 | TG | c.564G= (p.Glu188=) c.*415G= (n.*415G=) c.303G= (p.Glu101=) | |
8 | g.132873147G>T | CA372247343 | TG | c.564G>T (p.Glu188Asp) c.*415G>T (n.*415G>T) c.303G>T (p.Glu101Asp) | |
8 | g.132873148T>A | CA4882954 | TG | c.565T>A (p.Phe189Ile) c.*416T>A (n.*416T>A) c.304T>A (p.Phe102Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132873148T>C | CA372247347 | TG | c.565T>C (p.Phe189Leu) c.*416T>C (n.*416T>C) c.304T>C (p.Phe102Leu) | dbSNP gnomAD v2 |
8 | g.132873148T>G | CA372247348 | TG | c.565T>G (p.Phe189Val) c.*416T>G (n.*416T>G) c.304T>G (p.Phe102Val) | dbSNP |
8 | g.132873148T= | CA1820984249 | TG | c.565T= (p.Phe189=) c.*416T= (n.*416T=) c.304T= (p.Phe102=) | |
8 | g.132873149T>A | CA372247349 | TG | c.566T>A (p.Phe189Tyr) c.*417T>A (n.*417T>A) c.305T>A (p.Phe102Tyr) | |
8 | g.132873149T>C | CA372247350 | TG | c.566T>C (p.Phe189Ser) c.*417T>C (n.*417T>C) c.305T>C (p.Phe102Ser) | |
8 | g.132873149T>G | CA372247351 | TG | c.566T>G (p.Phe189Cys) c.*417T>G (n.*417T>G) c.305T>G (p.Phe102Cys) | |
8 | g.132873150T>A | CA372247352 | TG | c.567T>A (p.Phe189Leu) c.*418T>A (n.*418T>A) c.306T>A (p.Phe102Leu) | |
8 | g.132873150T>C | CA463013920 | TG | c.567T>C (p.Phe189=) c.*418T>C (n.*418T>C) c.306T>C (p.Phe102=) | |
8 | g.132873150T>G | CA372247353 | TG | c.567T>G (p.Phe189Leu) c.*418T>G (n.*418T>G) c.306T>G (p.Phe102Leu) | |
8 | g.132873151A>C | CA372247354 | TG | c.568A>C (p.Met190Leu) c.*419A>C (n.*419A>C) c.307A>C (p.Met103Leu) | gnomAD v4 |
8 | g.132873151A>G | CA372247357 | TG | c.568A>G (p.Met190Val) c.*419A>G (n.*419A>G) c.307A>G (p.Met103Val) | |
8 | g.132873151A>T | CA372247360 | TG | c.568A>T (p.Met190Leu) c.*419A>T (n.*419A>T) c.307A>T (p.Met103Leu) | |
8 | g.132873152T>A | CA372247362 | TG | c.569T>A (p.Met190Lys) c.*420T>A (n.*420T>A) c.308T>A (p.Met103Lys) | |
8 | g.132873152T>C | CA4882955 | TG | c.569T>C (p.Met190Thr) c.*420T>C (n.*420T>C) c.308T>C (p.Met103Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873152T>G | CA372247363 | TG | c.569T>G (p.Met190Arg) c.*420T>G (n.*420T>G) c.308T>G (p.Met103Arg) | |
8 | g.132873152T= | CA1820984250 | TG | c.569T= (p.Met190=) c.*420T= (n.*420T=) c.308T= (p.Met103=) | |
8 | g.132873153G>A | CA372247364 | TG | c.570G>A (p.Met190Ile) c.*421G>A (n.*421G>A) c.309G>A (p.Met103Ile) | |
8 | g.132873153G>C | CA372247365 | TG | c.570G>C (p.Met190Ile) c.*421G>C (n.*421G>C) c.309G>C (p.Met103Ile) | |
8 | g.132873153G>T | CA372247366 | TG | c.570G>T (p.Met190Ile) c.*421G>T (n.*421G>T) c.309G>T (p.Met103Ile) | gnomAD v4 |
8 | g.132873154C>A | CA372247367 | TG | c.571C>A (p.Pro191Thr) c.*422C>A (n.*422C>A) c.310C>A (p.Pro104Thr) | gnomAD v4 |
8 | g.132873154C= | CA1820984251 | TG | c.571C= (p.Pro191=) c.*422C= (n.*422C=) c.310C= (p.Pro104=) | |
8 | g.132873154C>G | CA372247368 | TG | c.571C>G (p.Pro191Ala) c.*422C>G (n.*422C>G) c.310C>G (p.Pro104Ala) | |
8 | g.132873154C>T | CA4882956 | TG | c.571C>T (p.Pro191Ser) c.*422C>T (n.*422C>T) c.310C>T (p.Pro104Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132873155C>A | CA372247369 | TG | c.572C>A (p.Pro191His) c.*423C>A (n.*423C>A) c.311C>A (p.Pro104His) | |
8 | g.132873155C>G | CA372247370 | TG | c.572C>G (p.Pro191Arg) c.*423C>G (n.*423C>G) c.311C>G (p.Pro104Arg) | |
8 | g.132873155C>T | CA372247371 | TG | c.572C>T (p.Pro191Leu) c.*423C>T (n.*423C>T) c.311C>T (p.Pro104Leu) | |
8 | g.132873156T>A | CA463013921 | TG | c.573T>A (p.Pro191=) c.*424T>A (n.*424T>A) c.312T>A (p.Pro104=) | |
8 | g.132873156T>C | CA463013922 | TG | c.573T>C (p.Pro191=) c.*424T>C (n.*424T>C) c.312T>C (p.Pro104=) | |
8 | g.132873156T>G | CA463013923 | TG | c.573T>G (p.Pro191=) c.*424T>G (n.*424T>G) c.312T>G (p.Pro104=) | |
8 | g.132873157G>A | CA372247372 | TG | c.574G>A (p.Val192Ile) c.*425G>A (n.*425G>A) c.313G>A (p.Val105Ile) | gnomAD v4 |
8 | g.132873157G>C | CA372247373 | TG | c.574G>C (p.Val192Leu) c.*425G>C (n.*425G>C) c.313G>C (p.Val105Leu) | |
8 | g.132873157G>T | CA372247375 | TG | c.574G>T (p.Val192Phe) c.*425G>T (n.*425G>T) c.313G>T (p.Val105Phe) | |
8 | g.132873158T>A | CA372247390 | TG | c.575T>A (p.Val192Asp) c.*426T>A (n.*426T>A) c.314T>A (p.Val105Asp) | dbSNP |
8 | g.132873158T>C | CA372247388 | TG | c.575T>C (p.Val192Ala) c.*426T>C (n.*426T>C) c.314T>C (p.Val105Ala) | |
8 | g.132873158T>G | CA372247389 | TG | c.575T>G (p.Val192Gly) c.*426T>G (n.*426T>G) c.314T>G (p.Val105Gly) | |
8 | g.132873158T= | CA1820984252 | TG | c.575T= (p.Val192=) c.*426T= (n.*426T=) c.314T= (p.Val105=) | |
8 | g.132873159C>A | CA463013924 | TG | c.576C>A (p.Val192=) c.*427C>A (n.*427C>A) c.315C>A (p.Val105=) | |
8 | g.132873159C= | CA1820984253 | TG | c.576C= (p.Val192=) c.*427C= (n.*427C=) c.315C= (p.Val105=) | |
8 | g.132873159C>G | CA463013925 | TG | c.576C>G (p.Val192=) c.*427C>G (n.*427C>G) c.315C>G (p.Val105=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873159C>T | CA463013926 | TG | c.576C>T (p.Val192=) c.*427C>T (n.*427C>T) c.315C>T (p.Val105=) | gnomAD v4 |
8 | g.132873160dup | CA2841422307 | TG | c.577dup (p.Gln193ProfsTer14) c.*428dup (n.*428dup) c.316dup (p.Gln106ProfsTer14) | |
8 | g.132873160C>A | CA372247397 | TG | c.577C>A (p.Gln193Lys) c.*428C>A (n.*428C>A) c.316C>A (p.Gln106Lys) | |
8 | g.132873160C>G | CA372247398 | TG | c.577C>G (p.Gln193Glu) c.*428C>G (n.*428C>G) c.316C>G (p.Gln106Glu) | |
8 | g.132873160C>T | CA372247401 | TG | c.577C>T (p.Gln193Ter) c.*428C>T (n.*428C>T) c.316C>T (p.Gln106Ter) | gnomAD v4 |
8 | g.132873161A>C | CA372247402 | TG | c.578A>C (p.Gln193Pro) c.*429A>C (n.*429A>C) c.317A>C (p.Gln106Pro) | |
8 | g.132873161A>G | CA372247404 | TG | c.578A>G (p.Gln193Arg) c.*429A>G (n.*429A>G) c.317A>G (p.Gln106Arg) | gnomAD v4 |
8 | g.132873161A>T | CA372247405 | TG | c.578A>T (p.Gln193Leu) c.*429A>T (n.*429A>T) c.317A>T (p.Gln106Leu) | |
8 | g.132873162G>A | CA463013927 | TG | c.579G>A (p.Gln193=) c.*430G>A (n.*430G>A) c.318G>A (p.Gln106=) | gnomAD v4 |
8 | g.132873162G>C | CA372247414 | TG | c.579G>C (p.Gln193His) c.*430G>C (n.*430G>C) c.318G>C (p.Gln106His) | |
8 | g.132873162G>T | CA372247417 | TG | c.579G>T (p.Gln193His) c.*430G>T (n.*430G>T) c.318G>T (p.Gln106His) | |
8 | g.132873163T>A | CA372247420 | TG | c.580T>A (p.Cys194Ser) c.*431T>A (n.*431T>A) c.319T>A (p.Cys107Ser) | |
8 | g.132873163T>C | CA372247422 | TG | c.580T>C (p.Cys194Arg) c.*431T>C (n.*431T>C) c.319T>C (p.Cys107Arg) | |
8 | g.132873163T>G | CA372247423 | TG | c.580T>G (p.Cys194Gly) c.*431T>G (n.*431T>G) c.319T>G (p.Cys107Gly) | |
8 | g.132873164G>A | CA372247429 | TG | c.581G>A (p.Cys194Tyr) c.*432G>A (n.*432G>A) c.320G>A (p.Cys107Tyr) | COSMIC |
8 | g.132873164G>C | CA372247428 | TG | c.581G>C (p.Cys194Ser) c.*432G>C (n.*432G>C) c.320G>C (p.Cys107Ser) | |
8 | g.132873164G>T | CA372247426 | TG | c.581G>T (p.Cys194Phe) c.*432G>T (n.*432G>T) c.320G>T (p.Cys107Phe) | |
8 | g.132873165C>A | CA372247442 | TG | c.582C>A (p.Cys194Ter) c.*433C>A (n.*433C>A) c.321C>A (p.Cys107Ter) | dbSNP gnomAD v4 |
8 | g.132873165C= | CA1820984254 | TG | c.582C= (p.Cys194=) c.*433C= (n.*433C=) c.321C= (p.Cys107=) | |
8 | g.132873165C>G | CA372247444 | TG | c.582C>G (p.Cys194Trp) c.*433C>G (n.*433C>G) c.321C>G (p.Cys107Trp) | |
8 | g.132873165C>T | CA4882957 | TG | c.582C>T (p.Cys194=) c.*433C>T (n.*433C>T) c.321C>T (p.Cys107=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873166A= | CA1820984255 | TG | c.583A= (p.Lys195=) c.*434A= (n.*434A=) c.322A= (p.Lys108=) | |
8 | g.132873166A>C | CA372247457 | TG | c.583A>C (p.Lys195Gln) c.*434A>C (n.*434A>C) c.322A>C (p.Lys108Gln) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873166A>G | CA186328611 | TG | c.583A>G (p.Lys195Glu) c.*434A>G (n.*434A>G) c.322A>G (p.Lys108Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873166A>T | CA372247448 | TG | c.583A>T (p.Lys195Ter) c.*434A>T (n.*434A>T) c.322A>T (p.Lys108Ter) | |
8 | g.132873168dup | CA186328603 | TG | c.585dup (p.Phe196IlefsTer11) c.*436dup (n.*436dup) c.324dup (p.Phe109IlefsTer11) | dbSNP |
8 | g.132873167A>C | CA372247466 | TG | c.584A>C (p.Lys195Thr) c.*435A>C (n.*435A>C) c.323A>C (p.Lys108Thr) | |
8 | g.132873167A>G | CA372247461 | TG | c.584A>G (p.Lys195Arg) c.*435A>G (n.*435A>G) c.323A>G (p.Lys108Arg) | |
8 | g.132873167A>T | CA372247463 | TG | c.584A>T (p.Lys195Ile) c.*435A>T (n.*435A>T) c.323A>T (p.Lys108Ile) | |
8 | g.132873168A>C | CA372247471 | TG | c.585A>C (p.Lys195Asn) c.*436A>C (n.*436A>C) c.324A>C (p.Lys108Asn) | |
8 | g.132873168A>G | CA463013928 | TG | c.585A>G (p.Lys195=) c.*436A>G (n.*436A>G) c.324A>G (p.Lys108=) | |
8 | g.132873168A>T | CA372247473 | TG | c.585A>T (p.Lys195Asn) c.*436A>T (n.*436A>T) c.324A>T (p.Lys108Asn) | |
8 | g.132873169T>A | CA372247478 | TG | c.586T>A (p.Phe196Ile) c.*437T>A (n.*437T>A) c.325T>A (p.Phe109Ile) | |
8 | g.132873169T>C | CA372247480 | TG | c.586T>C (p.Phe196Leu) c.*437T>C (n.*437T>C) c.325T>C (p.Phe109Leu) | |
8 | g.132873169T>G | CA372247482 | TG | c.586T>G (p.Phe196Val) c.*437T>G (n.*437T>G) c.325T>G (p.Phe109Val) | |
8 | g.132873170T>A | CA372247486 | TG | c.587T>A (p.Phe196Tyr) c.*438T>A (n.*438T>A) c.326T>A (p.Phe109Tyr) | |
8 | g.132873170T>C | CA372247487 | TG | c.587T>C (p.Phe196Ser) c.*438T>C (n.*438T>C) c.326T>C (p.Phe109Ser) | gnomAD v4 |
8 | g.132873170T>G | CA372247489 | TG | c.587T>G (p.Phe196Cys) c.*438T>G (n.*438T>G) c.326T>G (p.Phe109Cys) | |
8 | g.132873171T>A | CA372247492 | TG | c.588T>A (p.Phe196Leu) c.*439T>A (n.*439T>A) c.327T>A (p.Phe109Leu) | gnomAD v4 |
8 | g.132873171T>C | CA4882958 | TG | c.588T>C (p.Phe196=) c.*439T>C (n.*439T>C) c.327T>C (p.Phe109=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132873171T>G | CA372247494 | TG | c.588T>G (p.Phe196Leu) c.*439T>G (n.*439T>G) c.327T>G (p.Phe109Leu) | |
8 | g.132873171T= | CA1820984256 | TG | c.588T= (p.Phe196=) c.*439T= (n.*439T=) c.327T= (p.Phe109=) | |
8 | g.132873172G>A | CA372247495 | TG | c.589G>A (p.Val197Ile) c.*440G>A (n.*440G>A) c.328G>A (p.Val110Ile) | |
8 | g.132873172G>C | CA372247499 | TG | c.589G>C (p.Val197Leu) c.*440G>C (n.*440G>C) c.328G>C (p.Val110Leu) | |
8 | g.132873172G>T | CA372247497 | TG | c.589G>T (p.Val197Phe) c.*440G>T (n.*440G>T) c.328G>T (p.Val110Phe) | gnomAD v4 |
8 | g.132873173T>A | CA372247500 | TG | c.590T>A (p.Val197Asp) c.*441T>A (n.*441T>A) c.329T>A (p.Val110Asp) | |
8 | g.132873173T>C | CA372247501 | TG | c.590T>C (p.Val197Ala) c.*441T>C (n.*441T>C) c.329T>C (p.Val110Ala) | |
8 | g.132873173T>G | CA372247502 | TG | c.590T>G (p.Val197Gly) c.*441T>G (n.*441T>G) c.329T>G (p.Val110Gly) | |
8 | g.132873174_132873194dup | CA2688648019 | TG | c.591_611dup (p.Ile204_Phe205insAsnThrThrAspMetMetIle) c.*442_*462dup (n.*442_*462dup) c.330_350dup (p.Ile117_Phe118insAsnThrThrAspMetMetIle) | gnomAD v4 |
8 | g.132873174C>A | CA463013930 | TG | c.591C>A (p.Val197=) c.*442C>A (n.*442C>A) c.330C>A (p.Val110=) | |
8 | g.132873174C>G | CA463013931 | TG | c.591C>G (p.Val197=) c.*442C>G (n.*442C>G) c.330C>G (p.Val110=) | |
8 | g.132873174C>T | CA463013932 | TG | c.591C>T (p.Val197=) c.*442C>T (n.*442C>T) c.330C>T (p.Val110=) | ClinVar gnomAD v4 |
8 | g.132873175A>C | CA372247503 | TG | c.592A>C (p.Asn198His) c.*443A>C (n.*443A>C) c.331A>C (p.Asn111His) | |
8 | g.132873175A>G | CA372247505 | TG | c.592A>G (p.Asn198Asp) c.*443A>G (n.*443A>G) c.331A>G (p.Asn111Asp) | |
8 | g.132873175A>T | CA372247507 | TG | c.592A>T (p.Asn198Tyr) c.*443A>T (n.*443A>T) c.331A>T (p.Asn111Tyr) | |
8 | g.132873176A= | CA1820984257 | TG | c.593A= (p.Asn198=) c.*444A= (n.*444A=) c.332A= (p.Asn111=) | |
8 | g.132873176A>C | CA372247509 | TG | c.593A>C (p.Asn198Thr) c.*444A>C (n.*444A>C) c.332A>C (p.Asn111Thr) | |
8 | g.132873176A>G | CA4882959 | TG | c.593A>G (p.Asn198Ser) c.*444A>G (n.*444A>G) c.332A>G (p.Asn111Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
8 | g.132873176A>T | CA372247511 | TG | c.593A>T (p.Asn198Ile) c.*444A>T (n.*444A>T) c.332A>T (p.Asn111Ile) | |
8 | g.132873177C>A | CA372247513 | TG | c.594C>A (p.Asn198Lys) c.*445C>A (n.*445C>A) c.333C>A (p.Asn111Lys) | |
8 | g.132873177C>G | CA372247514 | TG | c.594C>G (p.Asn198Lys) c.*445C>G (n.*445C>G) c.333C>G (p.Asn111Lys) | |
8 | g.132873177C>T | CA463013933 | TG | c.594C>T (p.Asn198=) c.*445C>T (n.*445C>T) c.333C>T (p.Asn111=) | gnomAD v4 |
8 | g.132873178A>C | CA372247518 | TG | c.595A>C (p.Thr199Pro) c.*446A>C (n.*446A>C) c.334A>C (p.Thr112Pro) | |
8 | g.132873178A>G | CA372247516 | TG | c.595A>G (p.Thr199Ala) c.*446A>G (n.*446A>G) c.334A>G (p.Thr112Ala) | |
8 | g.132873178A>T | CA372247515 | TG | c.595A>T (p.Thr199Ser) c.*446A>T (n.*446A>T) c.334A>T (p.Thr112Ser) | |
8 | g.132873179C>A | CA372247526 | TG | c.596C>A (p.Thr199Asn) c.*447C>A (n.*447C>A) c.335C>A (p.Thr112Asn) | |
8 | g.132873179C= | CA1820984258 | TG | c.596C= (p.Thr199=) c.*447C= (n.*447C=) c.335C= (p.Thr112=) | |
8 | g.132873179C>G | CA372247521 | TG | c.596C>G (p.Thr199Ser) c.*447C>G (n.*447C>G) c.335C>G (p.Thr112Ser) | |
8 | g.132873179C>T | CA4882960 | TG | c.596C>T (p.Thr199Ile) c.*447C>T (n.*447C>T) c.335C>T (p.Thr112Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
8 | g.132873180C>A | CA463013934 | TG | c.597C>A (p.Thr199=) c.*448C>A (n.*448C>A) c.336C>A (p.Thr112=) | |
8 | g.132873180C>G | CA463013935 | TG | c.597C>G (p.Thr199=) c.*448C>G (n.*448C>G) c.336C>G (p.Thr112=) | |
8 | g.132873180C>T | CA463013936 | TG | c.597C>T (p.Thr199=) c.*448C>T (n.*448C>T) c.336C>T (p.Thr112=) | gnomAD v4 COSMIC |
8 | g.132873181A>C | CA372247529 | TG | c.598A>C (p.Thr200Pro) c.*449A>C (n.*449A>C) c.337A>C (p.Thr113Pro) | |
8 | g.132873181A>G | CA372247531 | TG | c.598A>G (p.Thr200Ala) c.*449A>G (n.*449A>G) c.337A>G (p.Thr113Ala) | |
8 | g.132873181A>T | CA372247536 | TG | c.598A>T (p.Thr200Ser) c.*449A>T (n.*449A>T) c.337A>T (p.Thr113Ser) | |
8 | g.132873182C>A | CA372247539 | TG | c.599C>A (p.Thr200Lys) c.*450C>A (n.*450C>A) c.338C>A (p.Thr113Lys) | |
8 | g.132873182C>G | CA372247541 | TG | c.599C>G (p.Thr200Arg) c.*450C>G (n.*450C>G) c.338C>G (p.Thr113Arg) | |
8 | g.132873182C>T | CA372247544 | TG | c.599C>T (p.Thr200Ile) c.*450C>T (n.*450C>T) c.338C>T (p.Thr113Ile) | |
8 | g.132873183A>C | CA463013937 | TG | c.600A>C (p.Thr200=) c.*451A>C (n.*451A>C) c.339A>C (p.Thr113=) | |
8 | g.132873183A>G | CA463013938 | TG | c.600A>G (p.Thr200=) c.*451A>G (n.*451A>G) c.339A>G (p.Thr113=) | |
8 | g.132873183A>T | CA463013939 | TG | c.600A>T (p.Thr200=) c.*451A>T (n.*451A>T) c.339A>T (p.Thr113=) | |
8 | g.132873184G>A | CA372247546 | TG | c.601G>A (p.Asp201Asn) c.*452G>A (n.*452G>A) c.340G>A (p.Asp114Asn) | |
8 | g.132873184G>C | CA186328642 | TG | c.601G>C (p.Asp201His) c.*452G>C (n.*452G>C) c.340G>C (p.Asp114His) | dbSNP |
8 | g.132873184G= | CA1820984259 | TG | c.601G= (p.Asp201=) c.*452G= (n.*452G=) c.340G= (p.Asp114=) | |
8 | g.132873184G>T | CA372247549 | TG | c.601G>T (p.Asp201Tyr) c.*452G>T (n.*452G>T) c.340G>T (p.Asp114Tyr) | |
8 | g.132873185A>C | CA372247553 | TG | c.602A>C (p.Asp201Ala) c.*453A>C (n.*453A>C) c.341A>C (p.Asp114Ala) | |
8 | g.132873185A>G | CA372247555 | TG | c.602A>G (p.Asp201Gly) c.*453A>G (n.*453A>G) c.341A>G (p.Asp114Gly) | |
8 | g.132873185A>T | CA372247557 | TG | c.602A>T (p.Asp201Val) c.*453A>T (n.*453A>T) c.341A>T (p.Asp114Val) | |
8 | g.132873186C>A | CA372247560 | TG | c.603C>A (p.Asp201Glu) c.*454C>A (n.*454C>A) c.342C>A (p.Asp114Glu) | |
8 | g.132873186C>G | CA372247562 | TG | c.603C>G (p.Asp201Glu) c.*454C>G (n.*454C>G) c.342C>G (p.Asp114Glu) | |
8 | g.132873186C>T | CA463013940 | TG | c.603C>T (p.Asp201=) c.*454C>T (n.*454C>T) c.342C>T (p.Asp114=) | |
8 | g.132873186_132873189delinsCATG | CA1820984260 | TG | c.603_606delinsCATG (p.Asp201=) c.*454_*457delinsCATG (n.*454_*457delinsCATG) c.342_345delinsCATG (p.Asp114=) | |
8 | g.132873187A>C | CA372247566 | TG | c.604A>C (p.Met202Leu) c.*455A>C (n.*455A>C) c.343A>C (p.Met115Leu) | |
8 | g.132873187A>G | CA372247568 | TG | c.604A>G (p.Met202Val) c.*455A>G (n.*455A>G) c.343A>G (p.Met115Val) | |
8 | g.132873187A>T | CA372247570 | TG | c.604A>T (p.Met202Leu) c.*455A>T (n.*455A>T) c.343A>T (p.Met115Leu) | |
8 | g.132873192_132873194del | CA584914002 | TG | c.609_611del (p.Met203del) c.*460_*462del (n.*460_*462del) c.348_350del (p.Met116del) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873188T>A | CA372247572 | TG | c.605T>A (p.Met202Lys) c.*456T>A (n.*456T>A) c.344T>A (p.Met115Lys) | |
8 | g.132873188T>C | CA372247574 | TG | c.605T>C (p.Met202Thr) c.*456T>C (n.*456T>C) c.344T>C (p.Met115Thr) | gnomAD v4 |
8 | g.132873188T>G | CA372247577 | TG | c.605T>G (p.Met202Arg) c.*456T>G (n.*456T>G) c.344T>G (p.Met115Arg) | |
8 | g.132873189G>A | CA372247580 | TG | c.606G>A (p.Met202Ile) c.*457G>A (n.*457G>A) c.345G>A (p.Met115Ile) | gnomAD v4 |
8 | g.132873189G>C | CA372247581 | TG | c.606G>C (p.Met202Ile) c.*457G>C (n.*457G>C) c.345G>C (p.Met115Ile) | |
8 | g.132873189G>T | CA372247583 | TG | c.606G>T (p.Met202Ile) c.*457G>T (n.*457G>T) c.345G>T (p.Met115Ile) | |
8 | g.132873190A>C | CA372247585 | TG | c.607A>C (p.Met203Leu) c.*458A>C (n.*458A>C) c.346A>C (p.Met116Leu) | |
8 | g.132873190A>G | CA372247588 | TG | c.607A>G (p.Met203Val) c.*458A>G (n.*458A>G) c.346A>G (p.Met116Val) | gnomAD v4 |
8 | g.132873190A>T | CA372247590 | TG | c.607A>T (p.Met203Leu) c.*458A>T (n.*458A>T) c.346A>T (p.Met116Leu) | |
8 | g.132873191T>A | CA4882961 | TG | c.608T>A (p.Met203Lys) c.*459T>A (n.*459T>A) c.347T>A (p.Met116Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132873191T>C | CA372247596 | TG | c.608T>C (p.Met203Thr) c.*459T>C (n.*459T>C) c.347T>C (p.Met116Thr) | gnomAD v4 |
8 | g.132873191T>G | CA372247593 | TG | c.608T>G (p.Met203Arg) c.*459T>G (n.*459T>G) c.347T>G (p.Met116Arg) | |
8 | g.132873191T= | CA1820984261 | TG | c.608T= (p.Met203=) c.*459T= (n.*459T=) c.347T= (p.Met116=) | |
8 | g.132873192G>A | CA372247599 | TG | c.609G>A (p.Met203Ile) c.*460G>A (n.*460G>A) c.348G>A (p.Met116Ile) | COSMIC |
8 | g.132873192G>C | CA372247601 | TG | c.609G>C (p.Met203Ile) c.*460G>C (n.*460G>C) c.348G>C (p.Met116Ile) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132873192G= | CA1820984262 | TG | c.609G= (p.Met203=) c.*460G= (n.*460G=) c.348G= (p.Met116=) | |
8 | g.132873192G>T | CA372247603 | TG | c.609G>T (p.Met203Ile) c.*460G>T (n.*460G>T) c.348G>T (p.Met116Ile) | |
8 | g.132873193A>C | CA372247606 | TG | c.610A>C (p.Ile204Leu) c.*461A>C (n.*461A>C) c.349A>C (p.Ile117Leu) | |
8 | g.132873193A>G | CA372247607 | TG | c.610A>G (p.Ile204Val) c.*461A>G (n.*461A>G) c.349A>G (p.Ile117Val) | |
8 | g.132873193A>T | CA372247610 | TG | c.610A>T (p.Ile204Phe) c.*461A>T (n.*461A>T) c.349A>T (p.Ile117Phe) | COSMIC |
8 | g.132873194T>A | CA372247613 | TG | c.611T>A (p.Ile204Asn) c.*462T>A (n.*462T>A) c.350T>A (p.Ile117Asn) | |
8 | g.132873194T>C | CA372247616 | TG | c.611T>C (p.Ile204Thr) c.*462T>C (n.*462T>C) c.350T>C (p.Ile117Thr) | |
8 | g.132873194T>G | CA372247618 | TG | c.611T>G (p.Ile204Ser) c.*462T>G (n.*462T>G) c.350T>G (p.Ile117Ser) | |
8 | g.132873195T>A | CA463013941 | TG | c.612T>A (p.Ile204=) c.*463T>A (n.*463T>A) c.351T>A (p.Ile117=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873195T>C | CA463013942 | TG | c.612T>C (p.Ile204=) c.*463T>C (n.*463T>C) c.351T>C (p.Ile117=) | |
8 | g.132873195T>G | CA372247619 | TG | c.612T>G (p.Ile204Met) c.*463T>G (n.*463T>G) c.351T>G (p.Ile117Met) | |
8 | g.132873195T= | CA1820984263 | TG | c.612T= (p.Ile204=) c.*463T= (n.*463T=) c.351T= (p.Ile117=) | |
8 | g.132873196T>A | CA372247621 | TG | c.613T>A (p.Phe205Ile) c.*464T>A (n.*464T>A) c.352T>A (p.Phe118Ile) | |
8 | g.132873196T>C | CA372247622 | TG | c.613T>C (p.Phe205Leu) c.*464T>C (n.*464T>C) c.352T>C (p.Phe118Leu) | |
8 | g.132873196T>G | CA372247625 | TG | c.613T>G (p.Phe205Val) c.*464T>G (n.*464T>G) c.352T>G (p.Phe118Val) | |
8 | g.132873197T>A | CA372247632 | TG | c.614T>A (p.Phe205Tyr) c.*465T>A (n.*465T>A) c.353T>A (p.Phe118Tyr) | |
8 | g.132873197T>C | CA372247630 | TG | c.614T>C (p.Phe205Ser) c.*465T>C (n.*465T>C) c.353T>C (p.Phe118Ser) | COSMIC |
8 | g.132873197T>G | CA372247627 | TG | c.614T>G (p.Phe205Cys) c.*465T>G (n.*465T>G) c.353T>G (p.Phe118Cys) | gnomAD v4 |
8 | g.132873198T>A | CA372247634 | TG | c.615T>A (p.Phe205Leu) c.*466T>A (n.*466T>A) c.354T>A (p.Phe118Leu) | |
8 | g.132873198T>C | CA463013945 | TG | c.615T>C (p.Phe205=) c.*466T>C (n.*466T>C) c.354T>C (p.Phe118=) | |
8 | g.132873198T>G | CA372247636 | TG | c.615T>G (p.Phe205Leu) c.*466T>G (n.*466T>G) c.354T>G (p.Phe118Leu) | |
8 | g.132873199G>A | CA372247638 | TG | c.616G>A (p.Asp206Asn) c.*467G>A (n.*467G>A) c.355G>A (p.Asp119Asn) | |
8 | g.132873199G>C | CA372247640 | TG | c.616G>C (p.Asp206His) c.*467G>C (n.*467G>C) c.355G>C (p.Asp119His) | |
8 | g.132873199G= | CA1820984264 | TG | c.616G= (p.Asp206=) c.*467G= (n.*467G=) c.355G= (p.Asp119=) | |
8 | g.132873199G>T | CA186328644 | TG | c.616G>T (p.Asp206Tyr) c.*467G>T (n.*467G>T) c.355G>T (p.Asp119Tyr) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873200A>C | CA372247644 | TG | c.617A>C (p.Asp206Ala) c.*468A>C (n.*468A>C) c.356A>C (p.Asp119Ala) | |
8 | g.132873200A>G | CA372247646 | TG | c.617A>G (p.Asp206Gly) c.*468A>G (n.*468A>G) c.356A>G (p.Asp119Gly) | gnomAD v4 |
8 | g.132873200A>T | CA372247647 | TG | c.617A>T (p.Asp206Val) c.*468A>T (n.*468A>T) c.356A>T (p.Asp119Val) | |
8 | g.132873201T>A | CA372247648 | TG | c.618T>A (p.Asp206Glu) c.*469T>A (n.*469T>A) c.357T>A (p.Asp119Glu) | |
8 | g.132873201T>C | CA186328648 | TG | c.618T>C (p.Asp206=) c.*469T>C (n.*469T>C) c.357T>C (p.Asp119=) | dbSNP |
8 | g.132873201T>G | CA372247649 | TG | c.618T>G (p.Asp206Glu) c.*469T>G (n.*469T>G) c.357T>G (p.Asp119Glu) | |
8 | g.132873201T= | CA1820984265 | TG | c.618T= (p.Asp206=) c.*469T= (n.*469T=) c.357T= (p.Asp119=) | |
8 | g.132873202C>A | CA372247652 | TG | c.619C>A (p.Leu207Met) c.*470C>A (n.*470C>A) c.358C>A (p.Leu120Met) | dbSNP |
8 | g.132873202C= | CA1820984266 | TG | c.619C= (p.Leu207=) c.*470C= (n.*470C=) c.358C= (p.Leu120=) | |
8 | g.132873202C>G | CA372247654 | TG | c.619C>G (p.Leu207Val) c.*470C>G (n.*470C>G) c.358C>G (p.Leu120Val) | gnomAD v4 |
8 | g.132873202C>T | CA4882962 | TG | c.619C>T (p.Leu207=) c.*470C>T (n.*470C>T) c.358C>T (p.Leu120=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873203T>A | CA372247661 | TG | c.620T>A (p.Leu207Gln) c.*471T>A (n.*471T>A) c.359T>A (p.Leu120Gln) | |
8 | g.132873203T>C | CA372247662 | TG | c.620T>C (p.Leu207Pro) c.*471T>C (n.*471T>C) c.359T>C (p.Leu120Pro) | |
8 | g.132873203T>G | CA372247658 | TG | c.620T>G (p.Leu207Arg) c.*471T>G (n.*471T>G) c.359T>G (p.Leu120Arg) | |
8 | g.132873204G>A | CA463013950 | TG | c.621G>A (p.Leu207=) c.*472G>A (n.*472G>A) c.360G>A (p.Leu120=) | gnomAD v4 |
8 | g.132873204G>C | CA463013951 | TG | c.621G>C (p.Leu207=) c.*472G>C (n.*472G>C) c.360G>C (p.Leu120=) | |
8 | g.132873204G>T | CA463013952 | TG | c.621G>T (p.Leu207=) c.*472G>T (n.*472G>T) c.360G>T (p.Leu120=) | |
8 | g.132873205G>A | CA372247664 | TG | c.622G>A (p.Val208Ile) c.*473G>A (n.*473G>A) c.361G>A (p.Val121Ile) | gnomAD v4 |
8 | g.132873205G>C | CA372247666 | TG | c.622G>C (p.Val208Leu) c.*473G>C (n.*473G>C) c.361G>C (p.Val121Leu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873205G= | CA1820984267 | TG | c.622G= (p.Val208=) c.*473G= (n.*473G=) c.361G= (p.Val121=) | |
8 | g.132873205G>T | CA372247667 | TG | c.622G>T (p.Val208Phe) c.*473G>T (n.*473G>T) c.361G>T (p.Val121Phe) | COSMIC |
8 | g.132873206T>A | CA372247669 | TG | c.623T>A (p.Val208Asp) c.*474T>A (n.*474T>A) c.362T>A (p.Val121Asp) | |
8 | g.132873206T>C | CA372247673 | TG | c.623T>C (p.Val208Ala) c.*474T>C (n.*474T>C) c.362T>C (p.Val121Ala) | gnomAD v4 |
8 | g.132873206T>G | CA4882963 | TG | c.623T>G (p.Val208Gly) c.*474T>G (n.*474T>G) c.362T>G (p.Val121Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873206T= | CA1820984268 | TG | c.623T= (p.Val208=) c.*474T= (n.*474T=) c.362T= (p.Val121=) | |
8 | g.132873207C>A | CA463013958 | TG | c.624C>A (p.Val208=) c.*475C>A (n.*475C>A) c.363C>A (p.Val121=) | |
8 | g.132873207C>G | CA463013959 | TG | c.624C>G (p.Val208=) c.*475C>G (n.*475C>G) c.363C>G (p.Val121=) | |
8 | g.132873207C>T | CA463013960 | TG | c.624C>T (p.Val208=) c.*475C>T (n.*475C>T) c.363C>T (p.Val121=) | |
8 | g.132873208C>A | CA372247677 | TG | c.625C>A (p.His209Asn) c.*476C>A (n.*476C>A) c.364C>A (p.His122Asn) | |
8 | g.132873208C>G | CA372247679 | TG | c.625C>G (p.His209Asp) c.*476C>G (n.*476C>G) c.364C>G (p.His122Asp) | |
8 | g.132873208C>T | CA372247681 | TG | c.625C>T (p.His209Tyr) c.*476C>T (n.*476C>T) c.364C>T (p.His122Tyr) | |
8 | g.132873209del | CA2688648038 | TG | c.626del (p.His209ProfsTer11) c.*477del (n.*477del) c.365del (p.His122ProfsTer11) | gnomAD v4 |
8 | g.132873209A>C | CA372247682 | TG | c.626A>C (p.His209Pro) c.*477A>C (n.*477A>C) c.365A>C (p.His122Pro) | |
8 | g.132873209A>G | CA372247685 | TG | c.626A>G (p.His209Arg) c.*477A>G (n.*477A>G) c.365A>G (p.His122Arg) | |
8 | g.132873209A>T | CA372247687 | TG | c.626A>T (p.His209Leu) c.*477A>T (n.*477A>T) c.365A>T (p.His122Leu) | |
8 | g.132873210C>A | CA372247692 | TG | c.627C>A (p.His209Gln) c.*478C>A (n.*478C>A) c.366C>A (p.His122Gln) | |
8 | g.132873210C>G | CA372247690 | TG | c.627C>G (p.His209Gln) c.*478C>G (n.*478C>G) c.366C>G (p.His122Gln) | |
8 | g.132873210C>T | CA463013966 | TG | c.627C>T (p.His209=) c.*478C>T (n.*478C>T) c.366C>T (p.His122=) | |
8 | g.132873211A>C | CA372247696 | TG | c.628A>C (p.Ser210Arg) c.*479A>C (n.*479A>C) c.367A>C (p.Ser123Arg) | |
8 | g.132873211A>G | CA372247697 | TG | c.628A>G (p.Ser210Gly) c.*479A>G (n.*479A>G) c.367A>G (p.Ser123Gly) | gnomAD v4 |
8 | g.132873211A>T | CA372247700 | TG | c.628A>T (p.Ser210Cys) c.*479A>T (n.*479A>T) c.367A>T (p.Ser123Cys) | |
8 | g.132873212_132873215del | CA2688648039 | TG | c.629_632del (p.Ser210ThrfsTer9) c.*480_*483del (n.*480_*483del) c.368_371del (p.Ser123ThrfsTer9) | gnomAD v4 |
8 | g.132873212G>A | CA372247702 | TG | c.629G>A (p.Ser210Asn) c.*480G>A (n.*480G>A) c.368G>A (p.Ser123Asn) | |
8 | g.132873212G>C | CA372247715 | TG | c.629G>C (p.Ser210Thr) c.*480G>C (n.*480G>C) c.368G>C (p.Ser123Thr) | |
8 | g.132873212G>T | CA372247716 | TG | c.629G>T (p.Ser210Ile) c.*480G>T (n.*480G>T) c.368G>T (p.Ser123Ile) | |
8 | g.132873213C>A | CA372247717 | TG | c.630C>A (p.Ser210Arg) c.*481C>A (n.*481C>A) c.369C>A (p.Ser123Arg) | dbSNP gnomAD v4 |
8 | g.132873213C= | CA1820984269 | TG | c.630C= (p.Ser210=) c.*481C= (n.*481C=) c.369C= (p.Ser123=) | |
8 | g.132873213C>G | CA372247718 | TG | c.630C>G (p.Ser210Arg) c.*481C>G (n.*481C>G) c.369C>G (p.Ser123Arg) | |
8 | g.132873213C>T | CA463013970 | TG | c.630C>T (p.Ser210=) c.*481C>T (n.*481C>T) c.369C>T (p.Ser123=) | dbSNP gnomAD v2 |
8 | g.132873214T>A | CA372247721 | TG | c.631T>A (p.Tyr211Asn) c.*482T>A (n.*482T>A) c.370T>A (p.Tyr124Asn) | |
8 | g.132873214T>C | CA372247722 | TG | c.631T>C (p.Tyr211His) c.*482T>C (n.*482T>C) c.370T>C (p.Tyr124His) | |
8 | g.132873214T>G | CA372247723 | TG | c.631T>G (p.Tyr211Asp) c.*482T>G (n.*482T>G) c.370T>G (p.Tyr124Asp) | |
8 | g.132873215A>C | CA372247731 | TG | c.632A>C (p.Tyr211Ser) c.*483A>C (n.*483A>C) c.371A>C (p.Tyr124Ser) | |
8 | g.132873215A>G | CA372247728 | TG | c.632A>G (p.Tyr211Cys) c.*483A>G (n.*483A>G) c.371A>G (p.Tyr124Cys) | gnomAD v4 |
8 | g.132873215A>T | CA372247726 | TG | c.632A>T (p.Tyr211Phe) c.*483A>T (n.*483A>T) c.371A>T (p.Tyr124Phe) | |
8 | g.132873216C>A | CA372247734 | TG | c.633C>A (p.Tyr211Ter) c.*484C>A (n.*484C>A) c.372C>A (p.Tyr124Ter) | |
8 | g.132873216C= | CA1820984270 | TG | c.633C= (p.Tyr211=) c.*484C= (n.*484C=) c.372C= (p.Tyr124=) | |
8 | g.132873216C>G | CA372247735 | TG | c.633C>G (p.Tyr211Ter) c.*484C>G (n.*484C>G) c.372C>G (p.Tyr124Ter) | dbSNP |
8 | g.132873216C>T | CA463013973 | TG | c.633C>T (p.Tyr211=) c.*484C>T (n.*484C>T) c.372C>T (p.Tyr124=) | dbSNP |
8 | g.132873217A>C | CA372247738 | TG | c.634A>C (p.Asn212His) c.*485A>C (n.*485A>C) c.373A>C (p.Asn125His) | |
8 | g.132873217A>G | CA372247742 | TG | c.634A>G (p.Asn212Asp) c.*485A>G (n.*485A>G) c.373A>G (p.Asn125Asp) | |
8 | g.132873217A>T | CA372247740 | TG | c.634A>T (p.Asn212Tyr) c.*485A>T (n.*485A>T) c.373A>T (p.Asn125Tyr) | |
8 | g.132873218A= | CA1820984271 | TG | c.635A= (p.Asn212=) c.*486A= (n.*486A=) c.374A= (p.Asn125=) | |
8 | g.132873218A>C | CA372247745 | TG | c.635A>C (p.Asn212Thr) c.*486A>C (n.*486A>C) c.374A>C (p.Asn125Thr) | |
8 | g.132873218A>G | CA4882964 | TG | c.635A>G (p.Asn212Ser) c.*486A>G (n.*486A>G) c.374A>G (p.Asn125Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873218A>T | CA372247750 | TG | c.635A>T (p.Asn212Ile) c.*486A>T (n.*486A>T) c.374A>T (p.Asn125Ile) | |
8 | g.132873219C>A | CA372247752 | TG | c.636C>A (p.Asn212Lys) c.*487C>A (n.*487C>A) c.375C>A (p.Asn125Lys) | |
8 | g.132873219C= | CA1820984272 | TG | c.636C= (p.Asn212=) c.*487C= (n.*487C=) c.375C= (p.Asn125=) | |
8 | g.132873219C>G | CA372247755 | TG | c.636C>G (p.Asn212Lys) c.*487C>G (n.*487C>G) c.375C>G (p.Asn125Lys) | |
8 | g.132873219C>T | CA4882965 | TG | c.636C>T (p.Asn212=) c.*487C>T (n.*487C>T) c.375C>T (p.Asn125=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873220A= | CA1820984273 | TG | c.637A= (p.Arg213=) c.*488A= (n.*488A=) c.376A= (p.Arg126=) | |
8 | g.132873220A>C | CA463013977 | TG | c.637A>C (p.Arg213=) c.*488A>C (n.*488A>C) c.376A>C (p.Arg126=) | |
8 | g.132873220A>G | CA372247760 | TG | c.637A>G (p.Arg213Gly) c.*488A>G (n.*488A>G) c.376A>G (p.Arg126Gly) | dbSNP |
8 | g.132873220A>T | CA372247762 | TG | c.637A>T (p.Arg213Trp) c.*488A>T (n.*488A>T) c.376A>T (p.Arg126Trp) | |
8 | g.132873221G>A | CA372247765 | TG | c.638G>A (p.Arg213Lys) c.*489G>A (n.*489G>A) c.377G>A (p.Arg126Lys) | |
8 | g.132873221G>C | CA372247767 | TG | c.638G>C (p.Arg213Thr) c.*489G>C (n.*489G>C) c.377G>C (p.Arg126Thr) | dbSNP |
8 | g.132873221G= | CA1820984274 | TG | c.638G= (p.Arg213=) c.*489G= (n.*489G=) c.377G= (p.Arg126=) | |
8 | g.132873221G>T | CA372247769 | TG | c.638G>T (p.Arg213Met) c.*489G>T (n.*489G>T) c.377G>T (p.Arg126Met) | |
8 | g.132873222G>A | CA372247777 | TG | c.638+1G>A (n.638+1G>A) c.*489+1G>A (n.*489+1G>A) c.377+1G>A (n.377+1G>A) | ClinVar dbSNP |
8 | g.132873222G>C | CA372247774 | TG | c.638+1G>C (n.638+1G>C) c.*489+1G>C (n.*489+1G>C) c.377+1G>C (n.377+1G>C) | |
8 | g.132873222G= | CA1820984275 | TG | c.638+1G= (n.638+1G=) c.*489+1G= (n.*489+1G=) c.377+1G= (n.377+1G=) | |
8 | g.132873222G>T | CA372247771 | TG | c.638+1G>T (n.638+1G>T) c.*489+1G>T (n.*489+1G>T) c.377+1G>T (n.377+1G>T) | |
8 | g.132873223T>A | CA372247780 | TG | c.638+2T>A (n.638+2T>A) c.*489+2T>A (n.*489+2T>A) c.377+2T>A (n.377+2T>A) | |
8 | g.132873223T>C | CA372247782 | TG | c.638+2T>C (n.638+2T>C) c.*489+2T>C (n.*489+2T>C) c.377+2T>C (n.377+2T>C) | |
8 | g.132873223T>G | CA372247785 | TG | c.638+2T>G (n.638+2T>G) c.*489+2T>G (n.*489+2T>G) c.377+2T>G (n.377+2T>G) | |
8 | g.132873225A>T | CA2718409245 | TG | c.638+4A>T (n.638+4A>T) c.*489+4A>T (n.*489+4A>T) c.377+4A>T (n.377+4A>T) | dbSNP |
8 | g.132873226G>A | CA353884 | TG | c.638+5G>A (n.638+5G>A) c.*489+5G>A (n.*489+5G>A) c.377+5G>A (n.377+5G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873226G= | CA1820984276 | TG | c.638+5G= (n.638+5G=) c.*489+5G= (n.*489+5G=) c.377+5G= (n.377+5G=) | |
8 | g.132873227G>A | CA4882967 | TG | c.638+6G>A (n.638+6G>A) c.*489+6G>A (n.*489+6G>A) c.377+6G>A (n.377+6G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873227G>C | CA4882966 | TG | c.638+6G>C (n.638+6G>C) c.*489+6G>C (n.*489+6G>C) c.377+6G>C (n.377+6G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873227G= | CA1820984277 | TG | c.638+6G= (n.638+6G=) c.*489+6G= (n.*489+6G=) c.377+6G= (n.377+6G=) | |
8 | g.132873228G>A | CA2688648040 | TG | c.638+7G>A (n.638+7G>A) c.*489+7G>A (n.*489+7G>A) c.377+7G>A (n.377+7G>A) | gnomAD v4 |
8 | g.132873229G>A | CA2688648041 | TG | c.638+8G>A (n.638+8G>A) c.*489+8G>A (n.*489+8G>A) c.377+8G>A (n.377+8G>A) | ClinVar gnomAD v4 |
8 | g.132873231G>A | CA2688648043 | TG | c.638+10G>A (n.638+10G>A) c.*489+10G>A (n.*489+10G>A) c.377+10G>A (n.377+10G>A) | gnomAD v4 |
8 | g.132873233_132873242del | CA2688648042 | TG | c.638+12_638+21del (n.638+12_638+21del) c.*489+12_*489+21del (n.*489+12_*489+21del) c.377+12_377+21del (n.377+12_377+21del) | ClinVar gnomAD v4 |
8 | g.132873232C>G | CA2688648044 | TG | c.638+11C>G (n.638+11C>G) c.*489+11C>G (n.*489+11C>G) c.377+11C>G (n.377+11C>G) | gnomAD v4 |
8 | g.132873233_132873234delinsAG | CA1820984278 | TG | c.638+12_638+13delinsAG (n.638+12_638+13delinsAG) c.*489+12_*489+13delinsAG (n.*489+12_*489+13delinsAG) c.377+12_377+13delinsAG (n.377+12_377+13delinsAG) | |
8 | g.132873234G>A | CA186328664 | TG | c.638+13G>A (n.638+13G>A) c.*489+13G>A (n.*489+13G>A) c.377+13G>A (n.377+13G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
8 | g.132873234G= | CA1820984280 | TG | c.638+13G= (n.638+13G=) c.*489+13G= (n.*489+13G=) c.377+13G= (n.377+13G=) | |
8 | g.132873237del | CA1820984279 | TG | c.638+16del (n.638+16del) c.*489+16del (n.*489+16del) c.377+16del (n.377+16del) | dbSNP gnomAD v4 |
8 | g.132873235G>A | CA4882968 | TG | c.638+14G>A (n.638+14G>A) c.*489+14G>A (n.*489+14G>A) c.377+14G>A (n.377+14G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873235G= | CA1820984281 | TG | c.638+14G= (n.638+14G=) c.*489+14G= (n.*489+14G=) c.377+14G= (n.377+14G=) | |
8 | g.132873235G>T | CA2688648045 | TG | c.638+14G>T (n.638+14G>T) c.*489+14G>T (n.*489+14G>T) c.377+14G>T (n.377+14G>T) | gnomAD v4 |
8 | g.132873236G>C | CA4882969 | TG | c.638+15G>C (n.638+15G>C) c.*489+15G>C (n.*489+15G>C) c.377+15G>C (n.377+15G>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873236G= | CA1820984282 | TG | c.638+15G= (n.638+15G=) c.*489+15G= (n.*489+15G=) c.377+15G= (n.377+15G=) | |
8 | g.132873236G>T | CA2841422308 | TG | c.638+15G>T (n.638+15G>T) c.*489+15G>T (n.*489+15G>T) c.377+15G>T (n.377+15G>T) | |
8 | g.132873237G>A | CA2688648046 | TG | c.638+16G>A (n.638+16G>A) c.*489+16G>A (n.*489+16G>A) c.377+16G>A (n.377+16G>A) | gnomAD v4 |
8 | g.132873237G>T | CA2688648047 | TG | c.638+16G>T (n.638+16G>T) c.*489+16G>T (n.*489+16G>T) c.377+16G>T (n.377+16G>T) | gnomAD v4 |
8 | g.132873238T>C | CA584914003 | TG | c.638+17T>C (n.638+17T>C) c.*489+17T>C (n.*489+17T>C) c.377+17T>C (n.377+17T>C) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873238T= | CA1820984283 | TG | c.638+17T= (n.638+17T=) c.*489+17T= (n.*489+17T=) c.377+17T= (n.377+17T=) | |
8 | g.132873239G>A | CA2579253658 | TG | c.638+18G>A (n.638+18G>A) c.*489+18G>A (n.*489+18G>A) c.377+18G>A (n.377+18G>A) | gnomAD v4 |
8 | g.132873239G>C | CA1820984284 | TG | c.638+18G>C (n.638+18G>C) c.*489+18G>C (n.*489+18G>C) c.377+18G>C (n.377+18G>C) | ClinVar dbSNP |
8 | g.132873239G= | CA1820984285 | TG | c.638+18G= (n.638+18G=) c.*489+18G= (n.*489+18G=) c.377+18G= (n.377+18G=) | |
8 | g.132873239G>T | CA2841422309 | TG | c.638+18G>T (n.638+18G>T) c.*489+18G>T (n.*489+18G>T) c.377+18G>T (n.377+18G>T) | |
8 | g.132873240dup | CA2688648048 | TG | c.638+19dup (n.638+19dup) c.*489+19dup (n.*489+19dup) c.377+19dup (n.377+19dup) | gnomAD v4 |
8 | g.132873241G>A | CA1820984287 | TG | c.638+20G>A (n.638+20G>A) c.*489+20G>A (n.*489+20G>A) c.377+20G>A (n.377+20G>A) | dbSNP gnomAD v4 |
8 | g.132873241G= | CA1820984286 | TG | c.638+20G= (n.638+20G=) c.*489+20G= (n.*489+20G=) c.377+20G= (n.377+20G=) | |
8 | g.132873243del | CA2688648050 | TG | c.638+22del (n.638+22del) c.*489+22del (n.*489+22del) c.377+22del (n.377+22del) | gnomAD v4 |
8 | g.132873244A= | CA1820984288 | TG | c.638+23A= (n.638+23A=) c.*489+23A= (n.*489+23A=) c.377+23A= (n.377+23A=) | |
8 | g.132873244A>G | CA2688648051 | TG | c.638+23A>G (n.638+23A>G) c.*489+23A>G (n.*489+23A>G) c.377+23A>G (n.377+23A>G) | gnomAD v4 |
8 | g.132873244A>T | CA4882970 | TG | c.638+23A>T (n.638+23A>T) c.*489+23A>T (n.*489+23A>T) c.377+23A>T (n.377+23A>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132873245G= | CA1820984289 | TG | c.638+24G= (n.638+24G=) c.*489+24G= (n.*489+24G=) c.377+24G= (n.377+24G=) | |
8 | g.132873245G>T | CA584914004 | TG | c.638+24G>T (n.638+24G>T) c.*489+24G>T (n.*489+24G>T) c.377+24G>T (n.377+24G>T) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132873246T>C | CA2530916621 | TG | c.638+25T>C (n.638+25T>C) c.*489+25T>C (n.*489+25T>C) c.377+25T>C (n.377+25T>C) | gnomAD v4 |
8 | g.132873247C= | CA1820984290 | TG | c.638+26C= (n.638+26C=) c.*489+26C= (n.*489+26C=) c.377+26C= (n.377+26C=) | |
8 | g.132873247C>T | CA4882971 | TG | c.638+26C>T (n.638+26C>T) c.*489+26C>T (n.*489+26C>T) c.377+26C>T (n.377+26C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |