| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.4862779_4862850del | CA2760244033 | MSX1 | c.548_619del (p.Gln183_Ser207delinsArg) n.260_331del | |
| 4 | g.4862850A>C | CA356138488 | MSX1 | c.619A>C (p.Ser207Arg) n.331A>C | |
| 4 | g.4862850A>G | CA356138489 | MSX1 | c.619A>G (p.Ser207Gly) n.331A>G | gnomAD v4 |
| 4 | g.4862850A>T | CA356138490 | MSX1 | c.619A>T (p.Ser207Cys) n.331A>T | |
| 4 | g.4862851G>A | CA356138491 | MSX1 | c.620G>A (p.Ser207Asn) n.332G>A | |
| 4 | g.4862851G>C | CA356138492 | MSX1 | c.620G>C (p.Ser207Thr) n.332G>C | |
| 4 | g.4862851G>T | CA356138493 | MSX1 | c.620G>T (p.Ser207Ile) n.332G>T | |
| 4 | g.4862852C>A | CA356138494 | MSX1 | c.621C>A (p.Ser207Arg) n.333C>A | |
| 4 | g.4862852C>G | CA356138495 | MSX1 | c.621C>G (p.Ser207Arg) n.333C>G | |
| 4 | g.4862852C>T | CA438366162 | MSX1 | c.621C>T (p.Ser207=) n.333C>T | |
| 4 | g.4862853T>A | CA356138496 | MSX1 | c.622T>A (p.Ser208Thr) n.334T>A | |
| 4 | g.4862853T>C | CA356138497 | MSX1 | c.622T>C (p.Ser208Pro) n.334T>C | |
| 4 | g.4862853T>G | CA356138498 | MSX1 | c.622T>G (p.Ser208Ala) n.334T>G | |
| 4 | g.4862854C>A | CA124428 | MSX1 | c.623C>A (p.Ser208Ter) n.335C>A | ClinVar dbSNP gnomAD v4 |
| 4 | g.4862854C= | CA1435013680 | MSX1 | c.623C= (p.Ser208=) n.335C= | |
| 4 | g.4862854C>G | CA2833087 | MSX1 | c.623C>G (p.Ser208Trp) n.335C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.4862854C>T | CA356138499 | MSX1 | c.623C>T (p.Ser208Leu) n.335C>T | gnomAD v4 COSMIC |
| 4 | g.4862855G>A | CA91672108 | MSX1 | c.624G>A (p.Ser208=) n.336G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 4 | g.4862855G>C | CA2833089 | MSX1 | c.624G>C (p.Ser208=) n.336G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.4862855G= | CA1435013681 | MSX1 | c.624G= (p.Ser208=) n.336G= | |
| 4 | g.4862855G>T | CA2833088 | MSX1 | c.624G>T (p.Ser208=) n.336G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.4862856C>A | CA356138500 | MSX1 | c.625C>A (p.Leu209Ile) n.337C>A | |
| 4 | g.4862856C>G | CA356138501 | MSX1 | c.625C>G (p.Leu209Val) n.337C>G | |
| 4 | g.4862856C>T | CA356138502 | MSX1 | c.625C>T (p.Leu209Phe) n.337C>T | |
| 4 | g.4862857T>A | CA356138503 | MSX1 | c.626T>A (p.Leu209His) n.338T>A | |
| 4 | g.4862857T>C | CA356138504 | MSX1 | c.626T>C (p.Leu209Pro) n.338T>C | |
| 4 | g.4862857T>G | CA356138505 | MSX1 | c.626T>G (p.Leu209Arg) n.338T>G | |
| 4 | g.4862858C>A | CA438366163 | MSX1 | c.627C>A (p.Leu209=) n.339C>A | |
| 4 | g.4862858C= | CA1435013682 | MSX1 | c.627C= (p.Leu209=) n.339C= | |
| 4 | g.4862858C>G | CA438366164 | MSX1 | c.627C>G (p.Leu209=) n.339C>G | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.4862858C>T | CA2833090 | MSX1 | c.627C>T (p.Leu209=) n.339C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.4862859A>C | CA356138506 | MSX1 | c.628A>C (p.Ser210Arg) n.340A>C | |
| 4 | g.4862859A>G | CA356138507 | MSX1 | c.628A>G (p.Ser210Gly) n.340A>G | |
| 4 | g.4862859A>T | CA356138508 | MSX1 | c.628A>T (p.Ser210Cys) n.340A>T | gnomAD v4 |
| 4 | g.4862860G>A | CA2833091 | MSX1 | c.629G>A (p.Ser210Asn) n.341G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.4862860G>C | CA356138510 | MSX1 | c.629G>C (p.Ser210Thr) n.341G>C | |
| 4 | g.4862860G= | CA1435013683 | MSX1 | c.629G= (p.Ser210=) n.341G= | |
| 4 | g.4862860G>T | CA356138509 | MSX1 | c.629G>T (p.Ser210Ile) n.341G>T | |
| 4 | g.4862861C>A | CA356138511 | MSX1 | c.630C>A (p.Ser210Arg) n.342C>A | |
| 4 | g.4862861C>G | CA356138512 | MSX1 | c.630C>G (p.Ser210Arg) n.342C>G | |
| 4 | g.4862861C>T | CA438366165 | MSX1 | c.630C>T (p.Ser210=) n.342C>T | |
| 4 | g.4862862C>A | CA356138513 | MSX1 | c.631C>A (p.Leu211Ile) n.343C>A | |
| 4 | g.4862862C>G | CA356138514 | MSX1 | c.631C>G (p.Leu211Val) n.343C>G | |
| 4 | g.4862862C>T | CA356138515 | MSX1 | c.631C>T (p.Leu211Phe) n.343C>T | |
| 4 | g.4862863T>A | CA356138516 | MSX1 | c.632T>A (p.Leu211His) n.344T>A | |
| 4 | g.4862863T>C | CA356138517 | MSX1 | c.632T>C (p.Leu211Pro) n.344T>C | |
| 4 | g.4862863T>G | CA356138518 | MSX1 | c.632T>G (p.Leu211Arg) n.344T>G | |
| 4 | g.4862864C>A | CA438366166 | MSX1 | c.633C>A (p.Leu211=) n.345C>A | |
| 4 | g.4862864C>G | CA438366167 | MSX1 | c.633C>G (p.Leu211=) n.345C>G | |
| 4 | g.4862864C>T | CA438366168 | MSX1 | c.633C>T (p.Leu211=) n.345C>T | |
| 4 | g.4862865A= | CA1435013684 | MSX1 | c.634A= (p.Thr212=) n.346A= | |
| 4 | g.4862865A>C | CA356138519 | MSX1 | c.634A>C (p.Thr212Pro) n.346A>C | |
| 4 | g.4862865A>G | CA356138520 | MSX1 | c.634A>G (p.Thr212Ala) n.346A>G | |
| 4 | g.4862865A>T | CA91672119 | MSX1 | c.634A>T (p.Thr212Ser) n.346A>T | dbSNP |
| 4 | g.4862866C>A | CA356138522 | MSX1 | c.635C>A (p.Thr212Asn) n.347C>A | |
| 4 | g.4862866C>G | CA356138523 | MSX1 | c.635C>G (p.Thr212Ser) n.347C>G | |
| 4 | g.4862866C>T | CA356138521 | MSX1 | c.635C>T (p.Thr212Ile) n.347C>T | |
| 4 | g.4862867T>A | CA438366169 | MSX1 | c.636T>A (p.Thr212=) n.348T>A | |
| 4 | g.4862867T>C | CA438366170 | MSX1 | c.636T>C (p.Thr212=) n.348T>C | dbSNP gnomAD v4 |
| 4 | g.4862867T>G | CA438366171 | MSX1 | c.636T>G (p.Thr212=) n.348T>G | |
| 4 | g.4862867T= | CA1435013685 | MSX1 | c.636T= (p.Thr212=) n.348T= | |
| 4 | g.4862868G>A | CA356138524 | MSX1 | c.637G>A (p.Glu213Lys) n.349G>A | |
| 4 | g.4862868G>C | CA356138525 | MSX1 | c.637G>C (p.Glu213Gln) n.349G>C | |
| 4 | g.4862868G>T | CA356138526 | MSX1 | c.637G>T (p.Glu213Ter) n.349G>T | |
| 4 | g.4862869A>C | CA356138527 | MSX1 | c.638A>C (p.Glu213Ala) n.350A>C | |
| 4 | g.4862869A>G | CA356138528 | MSX1 | c.638A>G (p.Glu213Gly) n.350A>G | |
| 4 | g.4862869A>T | CA356138529 | MSX1 | c.638A>T (p.Glu213Val) n.350A>T | |
| 4 | g.4862870G>A | CA438366172 | MSX1 | c.639G>A (p.Glu213=) n.351G>A | |
| 4 | g.4862870G>C | CA356138530 | MSX1 | c.639G>C (p.Glu213Asp) n.351G>C | |
| 4 | g.4862870G>T | CA356138531 | MSX1 | c.639G>T (p.Glu213Asp) n.351G>T | |
| 4 | g.4862871A>C | CA356138532 | MSX1 | c.640A>C (p.Thr214Pro) n.352A>C | |
| 4 | g.4862871A>G | CA356138533 | MSX1 | c.640A>G (p.Thr214Ala) n.352A>G | |
| 4 | g.4862871A>T | CA356138534 | MSX1 | c.640A>T (p.Thr214Ser) n.352A>T | |
| 4 | g.4862872C>A | CA356138535 | MSX1 | c.641C>A (p.Thr214Lys) n.353C>A | |
| 4 | g.4862872C= | CA1435013686 | MSX1 | c.641C= (p.Thr214=) n.353C= | |
| 4 | g.4862872C>G | CA356138536 | MSX1 | c.641C>G (p.Thr214Arg) n.353C>G | |
| 4 | g.4862872C>T | CA2833092 | MSX1 | c.641C>T (p.Thr214Met) n.353C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.4862873G>A | CA2833093 | MSX1 | c.642G>A (p.Thr214=) n.354G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.4862873G>C | CA438366173 | MSX1 | c.642G>C (p.Thr214=) n.354G>C | gnomAD v4 |
| 4 | g.4862873G= | CA1435013687 | MSX1 | c.642G= (p.Thr214=) n.354G= | |
| 4 | g.4862873G>T | CA438366174 | MSX1 | c.642G>T (p.Thr214=) n.354G>T | gnomAD v4 |
| 4 | g.4862874C>A | CA356138537 | MSX1 | c.643C>A (p.Gln215Lys) n.355C>A | |
| 4 | g.4862874C>G | CA356138538 | MSX1 | c.643C>G (p.Gln215Glu) n.355C>G | |
| 4 | g.4862874C>T | CA356138539 | MSX1 | c.643C>T (p.Gln215Ter) n.355C>T | |
| 4 | g.4862875A= | CA1435013688 | MSX1 | c.644A= (p.Gln215=) n.356A= | |
| 4 | g.4862875A>C | CA356138540 | MSX1 | c.644A>C (p.Gln215Pro) n.356A>C | |
| 4 | g.4862875A>G | CA356138541 | MSX1 | c.644A>G (p.Gln215Arg) n.356A>G | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.4862875A>T | CA356138542 | MSX1 | c.644A>T (p.Gln215Leu) n.356A>T | |
| 4 | g.4862875dup | CA2586973675 | MSX1 | c.644dup (p.Val216GlyfsTer?) n.356dup | |
| 4 | g.4862876G>A | CA438366175 | MSX1 | c.645G>A (p.Gln215=) n.357G>A | gnomAD v4 |
| 4 | g.4862876G>C | CA356138543 | MSX1 | c.645G>C (p.Gln215His) n.357G>C | |
| 4 | g.4862876G>T | CA356138544 | MSX1 | c.645G>T (p.Gln215His) n.357G>T | |
| 4 | g.4862877G>A | CA356138545 | MSX1 | c.646G>A (p.Val216Met) n.358G>A | |
| 4 | g.4862877G>C | CA356138546 | MSX1 | c.646G>C (p.Val216Leu) n.358G>C | |
| 4 | g.4862877G>T | CA356138547 | MSX1 | c.646G>T (p.Val216Leu) n.358G>T | |
| 4 | g.4862878T>A | CA356138548 | MSX1 | c.647T>A (p.Val216Glu) n.359T>A | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.4862878T>C | CA356138549 | MSX1 | c.647T>C (p.Val216Ala) n.359T>C | |
| 4 | g.4862878T>G | CA356138550 | MSX1 | c.647T>G (p.Val216Gly) n.359T>G | |
| 4 | g.4862878T= | CA1435013689 | MSX1 | c.647T= (p.Val216=) n.359T= | |
| 4 | g.4862879G>A | CA438366176 | MSX1 | c.648G>A (p.Val216=) n.360G>A | |
| 4 | g.4862879G>C | CA438366177 | MSX1 | c.648G>C (p.Val216=) n.360G>C | |
| 4 | g.4862879G>T | CA438366178 | MSX1 | c.648G>T (p.Val216=) n.360G>T | |
| 4 | g.4862880A>C | CA356138553 | MSX1 | c.649A>C (p.Lys217Gln) n.361A>C | |
| 4 | g.4862880A>G | CA356138552 | MSX1 | c.649A>G (p.Lys217Glu) n.361A>G | |
| 4 | g.4862880A>T | CA356138551 | MSX1 | c.649A>T (p.Lys217Ter) n.361A>T | |
| 4 | g.4862881A>C | CA356138556 | MSX1 | c.650A>C (p.Lys217Thr) n.362A>C | |
| 4 | g.4862881A>G | CA356138554 | MSX1 | c.650A>G (p.Lys217Arg) n.362A>G | ClinVar |
| 4 | g.4862881A>T | CA356138555 | MSX1 | c.650A>T (p.Lys217Met) n.362A>T | |
| 4 | g.4862882G>A | CA438366179 | MSX1 | c.651G>A (p.Lys217=) n.363G>A | dbSNP gnomAD v4 |
| 4 | g.4862882G>C | CA356138557 | MSX1 | c.651G>C (p.Lys217Asn) n.363G>C | |
| 4 | g.4862882G= | CA1435013690 | MSX1 | c.651G= (p.Lys217=) n.363G= | |
| 4 | g.4862882G>T | CA356138558 | MSX1 | c.651G>T (p.Lys217Asn) n.363G>T | |
| 4 | g.4862883A>C | CA356138559 | MSX1 | c.652A>C (p.Ile218Leu) n.364A>C | |
| 4 | g.4862883A>G | CA356138560 | MSX1 | c.652A>G (p.Ile218Val) n.364A>G | |
| 4 | g.4862883A>T | CA356138561 | MSX1 | c.652A>T (p.Ile218Leu) n.364A>T | |
| 4 | g.4862884T>A | CA356138562 | MSX1 | c.653T>A (p.Ile218Lys) n.365T>A | COSMIC |
| 4 | g.4862884T>C | CA356138563 | MSX1 | c.653T>C (p.Ile218Thr) n.365T>C | gnomAD v4 |
| 4 | g.4862884T>G | CA356138564 | MSX1 | c.653T>G (p.Ile218Arg) n.365T>G | |
| 4 | g.4862885A>C | CA438366180 | MSX1 | c.654A>C (p.Ile218=) n.366A>C | |
| 4 | g.4862885A>G | CA356138565 | MSX1 | c.654A>G (p.Ile218Met) n.366A>G | |
| 4 | g.4862885A>T | CA438366181 | MSX1 | c.654A>T (p.Ile218=) n.366A>T | |
| 4 | g.4862885_4862890delinsATGGTT | CA1435013691 | MSX1 | c.654_659delinsATGGTT (p.Ile218=) n.366_371delinsATGGTT | |
| 4 | g.4862886T>A | CA356138566 | MSX1 | c.655T>A (p.Trp219Arg) n.367T>A | |
| 4 | g.4862886T>C | CA356138567 | MSX1 | c.655T>C (p.Trp219Arg) n.367T>C | ClinVar dbSNP |
| 4 | g.4862886T>G | CA356138568 | MSX1 | c.655T>G (p.Trp219Gly) n.367T>G | gnomAD v4 |
| 4 | g.4862886T= | CA1435013692 | MSX1 | c.655T= (p.Trp219=) n.367T= | |
| 4 | g.4862886_4862890del | CA916082630 | MSX1 | c.655_659del (p.Trp219ProfsTer?) n.367_371del | ClinVar dbSNP |
| 4 | g.4862887G>A | CA356138571 | MSX1 | c.656G>A (p.Trp219Ter) n.368G>A | |
| 4 | g.4862887G>C | CA356138570 | MSX1 | c.656G>C (p.Trp219Ser) n.368G>C | |
| 4 | g.4862887G>T | CA356138569 | MSX1 | c.656G>T (p.Trp219Leu) n.368G>T | |
| 4 | g.4862888G>A | CA356138572 | MSX1 | c.657G>A (p.Trp219Ter) n.369G>A | |
| 4 | g.4862888G>C | CA356138573 | MSX1 | c.657G>C (p.Trp219Cys) n.369G>C | |
| 4 | g.4862888G>T | CA356138574 | MSX1 | c.657G>T (p.Trp219Cys) n.369G>T | |
| 4 | g.4862889T>A | CA356138575 | MSX1 | c.658T>A (p.Phe220Ile) n.370T>A | |
| 4 | g.4862889T>C | CA356138576 | MSX1 | c.658T>C (p.Phe220Leu) n.370T>C | |
| 4 | g.4862889T>G | CA356138577 | MSX1 | c.658T>G (p.Phe220Val) n.370T>G | |
| 4 | g.4862890T>A | CA356138578 | MSX1 | c.659T>A (p.Phe220Tyr) n.371T>A | |
| 4 | g.4862890T>C | CA356138579 | MSX1 | c.659T>C (p.Phe220Ser) n.371T>C | |
| 4 | g.4862890T>G | CA356138580 | MSX1 | c.659T>G (p.Phe220Cys) n.371T>G | |
| 4 | g.4862891C>A | CA356138581 | MSX1 | c.660C>A (p.Phe220Leu) n.372C>A | |
| 4 | g.4862891C>G | CA356138582 | MSX1 | c.660C>G (p.Phe220Leu) n.372C>G | |
| 4 | g.4862891C>T | CA438366182 | MSX1 | c.660C>T (p.Phe220=) n.372C>T | |
| 4 | g.4862892C>A | CA356138583 | MSX1 | c.661C>A (p.Gln221Lys) n.373C>A | |
| 4 | g.4862892C= | CA1435013693 | MSX1 | c.661C= (p.Gln221=) n.373C= | |
| 4 | g.4862892C>G | CA356138584 | MSX1 | c.661C>G (p.Gln221Glu) n.373C>G | |
| 4 | g.4862892C>T | CA356138585 | MSX1 | c.661C>T (p.Gln221Ter) n.373C>T | ClinVar dbSNP |
| 4 | g.4862893A>C | CA356138587 | MSX1 | c.662A>C (p.Gln221Pro) n.374A>C | |
| 4 | g.4862893A>G | CA356138588 | MSX1 | c.662A>G (p.Gln221Arg) n.374A>G | |
| 4 | g.4862893A>T | CA356138586 | MSX1 | c.662A>T (p.Gln221Leu) n.374A>T | |
| 4 | g.4862894G>A | CA438366183 | MSX1 | c.663G>A (p.Gln221=) n.375G>A | |
| 4 | g.4862894G>C | CA356138589 | MSX1 | c.663G>C (p.Gln221His) n.375G>C | |
| 4 | g.4862894G>T | CA356138590 | MSX1 | c.663G>T (p.Gln221His) n.375G>T | |
| 4 | g.4862895A>C | CA356138591 | MSX1 | c.664A>C (p.Asn222His) n.376A>C | |
| 4 | g.4862895A>G | CA356138592 | MSX1 | c.664A>G (p.Asn222Asp) n.376A>G | |
| 4 | g.4862895A>T | CA356138593 | MSX1 | c.664A>T (p.Asn222Tyr) n.376A>T | |
| 4 | g.4862896dup | CA2586973676 | MSX1 | c.665dup (p.Asn222LysfsTer?) n.377dup | |
| 4 | g.4862896A= | CA1435013694 | MSX1 | c.665A= (p.Asn222=) n.377A= | |
| 4 | g.4862896A>C | CA356138594 | MSX1 | c.665A>C (p.Asn222Thr) n.377A>C | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.4862896A>G | CA356138595 | MSX1 | c.665A>G (p.Asn222Ser) n.377A>G | |
| 4 | g.4862896A>T | CA356138596 | MSX1 | c.665A>T (p.Asn222Ile) n.377A>T | |
| 4 | g.4862897C>A | CA356138597 | MSX1 | c.666C>A (p.Asn222Lys) n.378C>A | |
| 4 | g.4862897C>G | CA356138598 | MSX1 | c.666C>G (p.Asn222Lys) n.378C>G | |
| 4 | g.4862897C>T | CA438366184 | MSX1 | c.666C>T (p.Asn222=) n.378C>T | |
| 4 | g.4862898C>A | CA356138599 | MSX1 | c.667C>A (p.Arg223Ser) n.379C>A | |
| 4 | g.4862898C>G | CA356138600 | MSX1 | c.667C>G (p.Arg223Gly) n.379C>G | |
| 4 | g.4862898C>T | CA356138601 | MSX1 | c.667C>T (p.Arg223Cys) n.379C>T | |
| 4 | g.4862899G>A | CA356138604 | MSX1 | c.668G>A (p.Arg223His) n.380G>A | |
| 4 | g.4862899G>C | CA356138602 | MSX1 | c.668G>C (p.Arg223Pro) n.380G>C | |
| 4 | g.4862899G>T | CA356138603 | MSX1 | c.668G>T (p.Arg223Leu) n.380G>T | |
| 4 | g.4862900C>A | CA438366185 | MSX1 | c.669C>A (p.Arg223=) n.381C>A | |
| 4 | g.4862900C= | CA1435013695 | MSX1 | c.669C= (p.Arg223=) n.381C= | |
| 4 | g.4862900C>G | CA438366186 | MSX1 | c.669C>G (p.Arg223=) n.381C>G | |
| 4 | g.4862900C>T | CA438366187 | MSX1 | c.669C>T (p.Arg223=) n.381C>T | dbSNP gnomAD v2 gnomAD v4 |
| 4 | g.4862901C>A | CA356138605 | MSX1 | c.670C>A (p.Arg224Ser) n.382C>A | |
| 4 | g.4862901C= | CA1435013696 | MSX1 | c.670C= (p.Arg224=) n.382C= | |
| 4 | g.4862901C>G | CA356138606 | MSX1 | c.670C>G (p.Arg224Gly) n.382C>G | |
| 4 | g.4862901C>T | CA356138607 | MSX1 | c.670C>T (p.Arg224Cys) n.382C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 4 | g.4862902G>A | CA356138608 | MSX1 | c.671G>A (p.Arg224His) n.383G>A | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.4862902G>C | CA356138609 | MSX1 | c.671G>C (p.Arg224Pro) n.383G>C | |
| 4 | g.4862902G>T | CA356138610 | MSX1 | c.671G>T (p.Arg224Leu) n.383G>T | |
| 4 | g.4862903C>A | CA438366190 | MSX1 | c.672C>A (p.Arg224=) n.384C>A | |
| 4 | g.4862903C= | CA1435013697 | MSX1 | c.672C= (p.Arg224=) n.384C= | |
| 4 | g.4862903C>G | CA438366188 | MSX1 | c.672C>G (p.Arg224=) n.384C>G | |
| 4 | g.4862903C>T | CA438366189 | MSX1 | c.672C>T (p.Arg224=) n.384C>T | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 4 | g.4862904G>A | CA356138611 | MSX1 | c.673G>A (p.Ala225Thr) n.385G>A | COSMIC |
| 4 | g.4862904G>C | CA2833094 | MSX1 | c.673G>C (p.Ala225Pro) n.385G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.4862904G= | CA1435013698 | MSX1 | c.673G= (p.Ala225=) n.385G= | |
| 4 | g.4862904G>T | CA356138612 | MSX1 | c.673G>T (p.Ala225Ser) n.385G>T | |
| 4 | g.4862905C>A | CA356138613 | MSX1 | c.674C>A (p.Ala225Asp) n.386C>A | |
| 4 | g.4862905C= | CA1435013699 | MSX1 | c.674C= (p.Ala225=) n.386C= | |
| 4 | g.4862905C>G | CA356138614 | MSX1 | c.674C>G (p.Ala225Gly) n.386C>G | |
| 4 | g.4862905C>T | CA2833095 | MSX1 | c.674C>T (p.Ala225Val) n.386C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.4862906C>A | CA438366191 | MSX1 | c.675C>A (p.Ala225=) n.387C>A | |
| 4 | g.4862906C>G | CA438366192 | MSX1 | c.675C>G (p.Ala225=) n.387C>G | |
| 4 | g.4862906C>T | CA438366193 | MSX1 | c.675C>T (p.Ala225=) n.387C>T | gnomAD v4 |
| 4 | g.4862906_4862907del | CA2760244049 | MSX1 | c.675_676del (p.Lys226GlyfsTer?) n.387_388del | |
| 4 | g.4862907A>C | CA356138615 | MSX1 | c.676A>C (p.Lys226Gln) n.388A>C | |
| 4 | g.4862907A>G | CA356138617 | MSX1 | c.676A>G (p.Lys226Glu) n.388A>G | |
| 4 | g.4862907A>T | CA356138616 | MSX1 | c.676A>T (p.Lys226Ter) n.388A>T | |
| 4 | g.4862908A>C | CA356138618 | MSX1 | c.677A>C (p.Lys226Thr) n.389A>C | |
| 4 | g.4862908A>G | CA356138620 | MSX1 | c.677A>G (p.Lys226Arg) n.389A>G | |
| 4 | g.4862908A>T | CA356138619 | MSX1 | c.677A>T (p.Lys226Met) n.389A>T | |
| 4 | g.4862909G>A | CA2833096 | MSX1 | c.678G>A (p.Lys226=) n.390G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.4862909G>C | CA356138622 | MSX1 | c.678G>C (p.Lys226Asn) n.390G>C | |
| 4 | g.4862909G= | CA1435013700 | MSX1 | c.678G= (p.Lys226=) n.390G= | |
| 4 | g.4862909G>T | CA356138623 | MSX1 | c.678G>T (p.Lys226Asn) n.390G>T | |
| 4 | g.4862910del | CA2669788568 | MSX1 | c.679del (p.Ala227GlnfsTer12) n.391del | gnomAD v4 |
| 4 | g.4862910G>A | CA356138624 | MSX1 | c.679G>A (p.Ala227Thr) n.391G>A | |
| 4 | g.4862910G>C | CA356138625 | MSX1 | c.679G>C (p.Ala227Pro) n.391G>C | dbSNP gnomAD v3 gnomAD v4 |
| 4 | g.4862910G= | CA1435013701 | MSX1 | c.679G= (p.Ala227=) n.391G= | |
| 4 | g.4862910G>T | CA356138626 | MSX1 | c.679G>T (p.Ala227Ser) n.391G>T | |
| 4 | g.4862911C>A | CA356138627 | MSX1 | c.680C>A (p.Ala227Glu) n.392C>A | |
| 4 | g.4862911C= | CA1435013702 | MSX1 | c.680C= (p.Ala227=) n.392C= | |
| 4 | g.4862911C>G | CA356138628 | MSX1 | c.680C>G (p.Ala227Gly) n.392C>G | |
| 4 | g.4862911C>T | CA356138629 | MSX1 | c.680C>T (p.Ala227Val) n.392C>T | dbSNP |
| 4 | g.4862911_4862913delinsCAA | CA1435013703 | MSX1 | c.680_682delinsCAA (p.Ala227=) n.392_394delinsCAA | |
| 4 | g.4862912A>C | CA438366194 | MSX1 | c.681A>C (p.Ala227=) n.393A>C | |
| 4 | g.4862912A>G | CA438366195 | MSX1 | c.681A>G (p.Ala227=) n.393A>G | gnomAD v4 |
| 4 | g.4862912A>T | CA438366196 | MSX1 | c.681A>T (p.Ala227=) n.393A>T | |
| 4 | g.4862914dup | CA2573137594 | MSX1 | c.683dup (p.Arg229GlufsTer?) n.395dup | ClinVar dbSNP |
| 4 | g.4862913_4862914del | CA916082631 | MSX1 | c.682_683del (p.Lys228GlufsTer?) n.394_395del | ClinVar dbSNP gnomAD v4 |
| 4 | g.4862913A>C | CA356138630 | MSX1 | c.682A>C (p.Lys228Gln) n.394A>C | |
| 4 | g.4862913A>G | CA356138631 | MSX1 | c.682A>G (p.Lys228Glu) n.394A>G | ClinVar |
| 4 | g.4862913A>T | CA356138632 | MSX1 | c.682A>T (p.Lys228Ter) n.394A>T | |
| 4 | g.4862914A>C | CA356138633 | MSX1 | c.683A>C (p.Lys228Thr) n.395A>C | |
| 4 | g.4862914A>G | CA356138635 | MSX1 | c.683A>G (p.Lys228Arg) n.395A>G | |
| 4 | g.4862914A>T | CA356138634 | MSX1 | c.683A>T (p.Lys228Met) n.395A>T | |
| 4 | g.4862915G>A | CA2833097 | MSX1 | c.684G>A (p.Lys228=) n.396G>A | dbSNP ExAC gnomAD v2 |
| 4 | g.4862915G>C | CA356138636 | MSX1 | c.684G>C (p.Lys228Asn) n.396G>C | |
| 4 | g.4862915G= | CA1435013704 | MSX1 | c.684G= (p.Lys228=) n.396G= | |
| 4 | g.4862915G>T | CA356138637 | MSX1 | c.684G>T (p.Lys228Asn) n.396G>T | |
| 4 | g.4862916A>C | CA438366197 | MSX1 | c.685A>C (p.Arg229=) n.397A>C | |
| 4 | g.4862916A>G | CA356138638 | MSX1 | c.685A>G (p.Arg229Gly) n.397A>G | |
| 4 | g.4862916A>T | CA356138639 | MSX1 | c.685A>T (p.Arg229Ter) n.397A>T | |
| 4 | g.4862917G>A | CA356138640 | MSX1 | c.686G>A (p.Arg229Lys) n.398G>A | |
| 4 | g.4862917G>C | CA356138641 | MSX1 | c.686G>C (p.Arg229Thr) n.398G>C | |
| 4 | g.4862917G>T | CA356138642 | MSX1 | c.686G>T (p.Arg229Ile) n.398G>T | |
| 4 | g.4862918A>C | CA356138643 | MSX1 | c.687A>C (p.Arg229Ser) n.399A>C | |
| 4 | g.4862918A>G | CA438366198 | MSX1 | c.687A>G (p.Arg229=) n.399A>G | |
| 4 | g.4862918A>T | CA356138644 | MSX1 | c.687A>T (p.Arg229Ser) n.399A>T | |
| 4 | g.4862919C>A | CA356138646 | MSX1 | c.688C>A (p.Leu230Ile) n.400C>A | |
| 4 | g.4862919C>G | CA356138645 | MSX1 | c.688C>G (p.Leu230Val) n.400C>G | |
| 4 | g.4862919C>T | CA438366199 | MSX1 | c.688C>T (p.Leu230=) n.400C>T | |
| 4 | g.4862920T>A | CA356138647 | MSX1 | c.689T>A (p.Leu230Gln) n.401T>A | |
| 4 | g.4862920T>C | CA356138648 | MSX1 | c.689T>C (p.Leu230Pro) n.401T>C | |
| 4 | g.4862920T>G | CA356138649 | MSX1 | c.689T>G (p.Leu230Arg) n.401T>G | dbSNP gnomAD v4 |
| 4 | g.4862920T= | CA1435013705 | MSX1 | c.689T= (p.Leu230=) n.401T= | |
| 4 | g.4862920dup | CA2669788569 | MSX1 | c.689dup (p.Gln231ThrfsTer?) n.401dup | gnomAD v4 |
| 4 | g.4862921A= | CA1435013706 | MSX1 | c.690A= (p.Leu230=) n.402A= | |
| 4 | g.4862921A>C | CA438366200 | MSX1 | c.690A>C (p.Leu230=) n.402A>C | |
| 4 | g.4862921A>G | CA2833098 | MSX1 | c.690A>G (p.Leu230=) n.402A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.4862921A>T | CA438366201 | MSX1 | c.690A>T (p.Leu230=) n.402A>T | |
| 4 | g.4862922C>A | CA356138650 | MSX1 | c.691C>A (p.Gln231Lys) n.403C>A | gnomAD v4 |
| 4 | g.4862922C>G | CA356138651 | MSX1 | c.691C>G (p.Gln231Glu) n.403C>G | |
| 4 | g.4862922C>T | CA356138652 | MSX1 | c.691C>T (p.Gln231Ter) n.403C>T | |
| 4 | g.4862923A>C | CA356138653 | MSX1 | c.692A>C (p.Gln231Pro) n.404A>C | |
| 4 | g.4862923A>G | CA356138654 | MSX1 | c.692A>G (p.Gln231Arg) n.404A>G | |
| 4 | g.4862923A>T | CA356138655 | MSX1 | c.692A>T (p.Gln231Leu) n.404A>T | |
| 4 | g.4862924A>C | CA356138656 | MSX1 | c.693A>C (p.Gln231His) n.405A>C | |
| 4 | g.4862924A>G | CA438366202 | MSX1 | c.693A>G (p.Gln231=) n.405A>G | |
| 4 | g.4862924A>T | CA356138657 | MSX1 | c.693A>T (p.Gln231His) n.405A>T | |
| 4 | g.4862925G>A | CA356138659 | MSX1 | c.694G>A (p.Glu232Lys) n.406G>A | |
| 4 | g.4862925G>C | CA356138660 | MSX1 | c.694G>C (p.Glu232Gln) n.406G>C | gnomAD v4 |
| 4 | g.4862925G>T | CA356138658 | MSX1 | c.694G>T (p.Glu232Ter) n.406G>T | gnomAD v4 |
| 4 | g.4862926A>C | CA356138661 | MSX1 | c.695A>C (p.Glu232Ala) n.407A>C | |
| 4 | g.4862926A>G | CA356138662 | MSX1 | c.695A>G (p.Glu232Gly) n.407A>G | |
| 4 | g.4862926A>T | CA356138663 | MSX1 | c.695A>T (p.Glu232Val) n.407A>T | gnomAD v4 |
| 4 | g.4862927G>A | CA438366203 | MSX1 | c.696G>A (p.Glu232=) n.408G>A | |
| 4 | g.4862927G>C | CA356138664 | MSX1 | c.696G>C (p.Glu232Asp) n.408G>C | |
| 4 | g.4862927G>T | CA356138665 | MSX1 | c.696G>T (p.Glu232Asp) n.408G>T | |
| 4 | g.4862928G>A | CA356138668 | MSX1 | c.697G>A (p.Ala233Thr) n.409G>A | gnomAD v4 |
| 4 | g.4862928G>C | CA356138666 | MSX1 | c.697G>C (p.Ala233Pro) n.409G>C | ClinVar |
| 4 | g.4862928G>T | CA356138667 | MSX1 | c.697G>T (p.Ala233Ser) n.409G>T | gnomAD v4 |
| 4 | g.4862929C>A | CA356138669 | MSX1 | c.698C>A (p.Ala233Glu) n.410C>A | gnomAD v4 |
| 4 | g.4862929C= | CA1435013707 | MSX1 | c.698C= (p.Ala233=) n.410C= | |
| 4 | g.4862929C>G | CA356138670 | MSX1 | c.698C>G (p.Ala233Gly) n.410C>G | |
| 4 | g.4862929C>T | CA356138671 | MSX1 | c.698C>T (p.Ala233Val) n.410C>T | dbSNP gnomAD v4 |
| 4 | g.4862930A>C | CA438366205 | MSX1 | c.699A>C (p.Ala233=) n.411A>C | gnomAD v4 |
| 4 | g.4862930A>G | CA438366206 | MSX1 | c.699A>G (p.Ala233=) n.411A>G | |
| 4 | g.4862930A>T | CA438366207 | MSX1 | c.699A>T (p.Ala233=) n.411A>T | |
| 4 | g.4862931G>A | CA356138672 | MSX1 | c.700G>A (p.Glu234Lys) n.412G>A | |
| 4 | g.4862931G>C | CA356138673 | MSX1 | c.700G>C (p.Glu234Gln) n.412G>C | |
| 4 | g.4862931G>T | CA356138674 | MSX1 | c.700G>T (p.Glu234Ter) n.412G>T | |
| 4 | g.4862932A>C | CA356138676 | MSX1 | c.701A>C (p.Glu234Ala) n.413A>C | |
| 4 | g.4862932A>G | CA356138677 | MSX1 | c.701A>G (p.Glu234Gly) n.413A>G | |
| 4 | g.4862932A>T | CA356138675 | MSX1 | c.701A>T (p.Glu234Val) n.413A>T | |
| 4 | g.4862933G>A | CA438366210 | MSX1 | c.702G>A (p.Glu234=) n.414G>A | |
| 4 | g.4862933G>C | CA356138678 | MSX1 | c.702G>C (p.Glu234Asp) n.414G>C | |
| 4 | g.4862933G>T | CA356138679 | MSX1 | c.702G>T (p.Glu234Asp) n.414G>T | |
| 4 | g.4862934C>A | CA356138680 | MSX1 | c.703C>A (p.Leu235Met) n.415C>A | |
| 4 | g.4862934C= | CA1435013708 | MSX1 | c.703C= (p.Leu235=) n.415C= | |
| 4 | g.4862934C>G | CA356138681 | MSX1 | c.703C>G (p.Leu235Val) n.415C>G | dbSNP |
| 4 | g.4862934C>T | CA438366211 | MSX1 | c.703C>T (p.Leu235=) n.415C>T | |
| 4 | g.4862935T>A | CA356138682 | MSX1 | c.704T>A (p.Leu235Gln) n.416T>A | |
| 4 | g.4862935T>C | CA356138683 | MSX1 | c.704T>C (p.Leu235Pro) n.416T>C | |
| 4 | g.4862935T>G | CA356138684 | MSX1 | c.704T>G (p.Leu235Arg) n.416T>G | |
| 4 | g.4862936G>A | CA438366214 | MSX1 | c.705G>A (p.Leu235=) n.417G>A | |
| 4 | g.4862936G>C | CA438366215 | MSX1 | c.705G>C (p.Leu235=) n.417G>C | |
| 4 | g.4862936G>T | CA438366216 | MSX1 | c.705G>T (p.Leu235=) n.417G>T | |
| 4 | g.4862937G>A | CA356138685 | MSX1 | c.706G>A (p.Glu236Lys) n.418G>A | |
| 4 | g.4862937G>C | CA356138686 | MSX1 | c.706G>C (p.Glu236Gln) n.418G>C | |
| 4 | g.4862937G>T | CA356138687 | MSX1 | c.706G>T (p.Glu236Ter) n.418G>T | |
| 4 | g.4862938A>C | CA356138690 | MSX1 | c.707A>C (p.Glu236Ala) n.419A>C | |
| 4 | g.4862938A>G | CA356138688 | MSX1 | c.707A>G (p.Glu236Gly) n.419A>G | dbSNP |
| 4 | g.4862938A>T | CA356138689 | MSX1 | c.707A>T (p.Glu236Val) n.419A>T | |
| 4 | g.4862939del | CA2586973677 | MSX1 | c.708del (p.Lys237SerfsTer2) n.420del | |
| 4 | g.4862939G>A | CA438366219 | MSX1 | c.708G>A (p.Glu236=) n.420G>A | |
| 4 | g.4862939G>C | CA356138691 | MSX1 | c.708G>C (p.Glu236Asp) n.420G>C | |
| 4 | g.4862939G>T | CA356138692 | MSX1 | c.708G>T (p.Glu236Asp) n.420G>T | |
| 4 | g.4862940A>C | CA356138693 | MSX1 | c.709A>C (p.Lys237Gln) n.421A>C | |
| 4 | g.4862940A>G | CA356138694 | MSX1 | c.709A>G (p.Lys237Glu) n.421A>G | |
| 4 | g.4862940A>T | CA356138695 | MSX1 | c.709A>T (p.Lys237Ter) n.421A>T | |
| 4 | g.4862941A>C | CA356138696 | MSX1 | c.710A>C (p.Lys237Thr) n.422A>C | |
| 4 | g.4862941A>G | CA356138698 | MSX1 | c.710A>G (p.Lys237Arg) n.422A>G | |
| 4 | g.4862941A>T | CA356138697 | MSX1 | c.710A>T (p.Lys237Met) n.422A>T | |
| 4 | g.4862942G>A | CA438366220 | MSX1 | c.711G>A (p.Lys237=) n.423G>A | |
| 4 | g.4862942G>C | CA356138699 | MSX1 | c.711G>C (p.Lys237Asn) n.423G>C | |
| 4 | g.4862942G>T | CA356138700 | MSX1 | c.711G>T (p.Lys237Asn) n.423G>T | |
| 4 | g.4862943C>A | CA356138701 | MSX1 | c.712C>A (p.Leu238Met) n.424C>A | |
| 4 | g.4862943C= | CA1435013709 | MSX1 | c.712C= (p.Leu238=) n.424C= | |
| 4 | g.4862943C>G | CA356138702 | MSX1 | c.712C>G (p.Leu238Val) n.424C>G | |
| 4 | g.4862943C>T | CA438366221 | MSX1 | c.712C>T (p.Leu238=) n.424C>T | dbSNP |
| 4 | g.4862944T>A | CA356138703 | MSX1 | c.713T>A (p.Leu238Gln) n.425T>A | gnomAD v4 |
| 4 | g.4862944T>C | CA356138704 | MSX1 | c.713T>C (p.Leu238Pro) n.425T>C | |
| 4 | g.4862944T>G | CA356138705 | MSX1 | c.713T>G (p.Leu238Arg) n.425T>G | |
| 4 | g.4862945G>A | CA438366222 | MSX1 | c.714G>A (p.Leu238=) n.426G>A | |
| 4 | g.4862945G>C | CA438366223 | MSX1 | c.714G>C (p.Leu238=) n.426G>C | |
| 4 | g.4862945G= | CA1435013710 | MSX1 | c.714G= (p.Leu238=) n.426G= | |
| 4 | g.4862945G>T | CA2833099 | MSX1 | c.714G>T (p.Leu238=) n.426G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 4 | g.4862946A= | CA1435013711 | MSX1 | c.715A= (p.Lys239=) n.427A= | |
| 4 | g.4862946A>C | CA356138706 | MSX1 | c.715A>C (p.Lys239Gln) n.427A>C | |
| 4 | g.4862946A>G | CA356138707 | MSX1 | c.715A>G (p.Lys239Glu) n.427A>G | |
| 4 | g.4862946A>T | CA91672150 | MSX1 | c.715A>T (p.Lys239Ter) n.427A>T | dbSNP |
| 4 | g.4862947A= | CA1435013712 | MSX1 | c.716A= (p.Lys239=) n.428A= | |
| 4 | g.4862947A>C | CA356138708 | MSX1 | c.716A>C (p.Lys239Thr) n.428A>C | |
| 4 | g.4862947A>G | CA2833100 | MSX1 | c.716A>G (p.Lys239Arg) n.428A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.4862947A>T | CA356138709 | MSX1 | c.716A>T (p.Lys239Met) n.428A>T | |
| 4 | g.4862948G>A | CA438366227 | MSX1 | c.717G>A (p.Lys239=) n.429G>A | |
| 4 | g.4862948G>C | CA356138710 | MSX1 | c.717G>C (p.Lys239Asn) n.429G>C | gnomAD v4 COSMIC |
| 4 | g.4862948G>T | CA356138711 | MSX1 | c.717G>T (p.Lys239Asn) n.429G>T | |
| 4 | g.4862949A>C | CA356138712 | MSX1 | c.718A>C (p.Met240Leu) n.430A>C | |
| 4 | g.4862949A>G | CA356138713 | MSX1 | c.718A>G (p.Met240Val) n.430A>G | |
| 4 | g.4862949A>T | CA356138714 | MSX1 | c.718A>T (p.Met240Leu) n.430A>T | |
| 4 | g.4862950T>A | CA356138715 | MSX1 | c.719T>A (p.Met240Lys) n.431T>A | |
| 4 | g.4862950T>C | CA356138716 | MSX1 | c.719T>C (p.Met240Thr) n.431T>C | |
| 4 | g.4862950T>G | CA356138717 | MSX1 | c.719T>G (p.Met240Arg) n.431T>G |