| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.136674754_136674756del | CA5342892 | AGPAT2 | c.646_648del (p.Lys216del) c.550_552del (p.Lys184del) n.574_576del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136674753T>A | CA277949 | AGPAT2 | c.643A>T (p.Lys215Ter) c.547A>T (p.Lys183Ter) n.571A>T | ClinVar dbSNP |
| 9 | g.136674753T>C | CA375578333 | AGPAT2 | c.643A>G (p.Lys215Glu) c.547A>G (p.Lys183Glu) n.571A>G | gnomAD v4 |
| 9 | g.136674753T>G | CA375578339 | AGPAT2 | c.643A>C (p.Lys215Gln) c.547A>C (p.Lys183Gln) n.571A>C | |
| 9 | g.136674754C>A | CA375578340 | AGPAT2 | c.642G>T (p.Lys214Asn) c.546G>T (p.Lys182Asn) n.570G>T | gnomAD v4 |
| 9 | g.136674754C>G | CA375578341 | AGPAT2 | c.642G>C (p.Lys214Asn) c.546G>C (p.Lys182Asn) n.570G>C | |
| 9 | g.136674754C>T | CA201627646 | AGPAT2 | c.642G>A (p.Lys214=) c.546G>A (p.Lys182=) n.570G>A | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136674755T>A | CA375578347 | AGPAT2 | c.641A>T (p.Lys214Met) c.545A>T (p.Lys182Met) n.569A>T | COSMIC |
| 9 | g.136674755T>C | CA375578359 | AGPAT2 | c.641A>G (p.Lys214Arg) c.545A>G (p.Lys182Arg) n.569A>G | gnomAD v4 |
| 9 | g.136674755T>G | CA375578372 | AGPAT2 | c.641A>C (p.Lys214Thr) c.545A>C (p.Lys182Thr) n.569A>C | |
| 9 | g.136674756T>A | CA375578373 | AGPAT2 | c.640A>T (p.Lys214Ter) c.544A>T (p.Lys182Ter) n.568A>T | |
| 9 | g.136674756T>C | CA5342897 | AGPAT2 | c.640A>G (p.Lys214Glu) c.544A>G (p.Lys182Glu) n.568A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136674756T>G | CA375578377 | AGPAT2 | c.640A>C (p.Lys214Gln) c.544A>C (p.Lys182Gln) n.568A>C | |
| 9 | g.136674757G>A | CA467738055 | AGPAT2 | c.639C>T (p.Thr213=) c.543C>T (p.Thr181=) n.567C>T | gnomAD v4 |
| 9 | g.136674757G>C | CA467738056 | AGPAT2 | c.639C>G (p.Thr213=) c.543C>G (p.Thr181=) n.567C>G | |
| 9 | g.136674757G>T | CA467738058 | AGPAT2 | c.639C>A (p.Thr213=) c.543C>A (p.Thr181=) n.567C>A | gnomAD v4 |
| 9 | g.136674758del | CA2692654221 | AGPAT2 | c.639del (p.Lys214ArgfsTer?) c.543del (p.Lys182ArgfsTer?) n.567del | gnomAD v4 |
| 9 | g.136674758G>A | CA5342898 | AGPAT2 | c.638C>T (p.Thr213Ile) c.542C>T (p.Thr181Ile) n.566C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136674758G>C | CA375578386 | AGPAT2 | c.638C>G (p.Thr213Ser) c.542C>G (p.Thr181Ser) n.566C>G | dbSNP gnomAD v4 |
| 9 | g.136674758G>T | CA375578392 | AGPAT2 | c.638C>A (p.Thr213Asn) c.542C>A (p.Thr181Asn) n.566C>A | gnomAD v4 |
| 9 | g.136674759T>A | CA375578404 | AGPAT2 | c.637A>T (p.Thr213Ser) c.541A>T (p.Thr181Ser) n.565A>T | |
| 9 | g.136674759T>C | CA375578407 | AGPAT2 | c.637A>G (p.Thr213Ala) c.541A>G (p.Thr181Ala) n.565A>G | gnomAD v4 |
| 9 | g.136674759T>G | CA375578421 | AGPAT2 | c.637A>C (p.Thr213Pro) c.541A>C (p.Thr181Pro) n.565A>C | |
| 9 | g.136674760G>A | CA467738083 | AGPAT2 | c.636C>T (p.Asn212=) c.540C>T (p.Asn180=) n.564C>T | gnomAD v4 |
| 9 | g.136674760G>C | CA375578426 | AGPAT2 | c.636C>G (p.Asn212Lys) c.540C>G (p.Asn180Lys) n.564C>G | |
| 9 | g.136674760G>T | CA375578444 | AGPAT2 | c.636C>A (p.Asn212Lys) c.540C>A (p.Asn180Lys) n.564C>A | |
| 9 | g.136674761T>A | CA375578457 | AGPAT2 | c.635A>T (p.Asn212Ile) c.539A>T (p.Asn180Ile) n.563A>T | gnomAD v4 |
| 9 | g.136674761T>C | CA375578460 | AGPAT2 | c.635A>G (p.Asn212Ser) c.539A>G (p.Asn180Ser) n.563A>G | gnomAD v4 |
| 9 | g.136674761T>G | CA5342899 | AGPAT2 | c.635A>C (p.Asn212Thr) c.539A>C (p.Asn180Thr) n.563A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136674762T>A | CA375578467 | AGPAT2 | c.634A>T (p.Asn212Tyr) c.538A>T (p.Asn180Tyr) n.562A>T | |
| 9 | g.136674762T>C | CA375578480 | AGPAT2 | c.634A>G (p.Asn212Asp) c.538A>G (p.Asn180Asp) n.562A>G | gnomAD v4 |
| 9 | g.136674762T>G | CA375578482 | AGPAT2 | c.634A>C (p.Asn212His) c.538A>C (p.Asn180His) n.562A>C | |
| 9 | g.136674763G>A | CA5342900 | AGPAT2 | c.633C>T (p.Tyr211=) c.537C>T (p.Tyr179=) n.561C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136674763G>C | CA375578488 | AGPAT2 | c.633C>G (p.Tyr211Ter) c.537C>G (p.Tyr179Ter) n.561C>G | |
| 9 | g.136674763G>T | CA375578501 | AGPAT2 | c.633C>A (p.Tyr211Ter) c.537C>A (p.Tyr179Ter) n.561C>A | |
| 9 | g.136674764T>A | CA375578503 | AGPAT2 | c.632A>T (p.Tyr211Phe) c.536A>T (p.Tyr179Phe) n.560A>T | |
| 9 | g.136674764T>C | CA375578504 | AGPAT2 | c.632A>G (p.Tyr211Cys) c.536A>G (p.Tyr179Cys) n.560A>G | gnomAD v4 |
| 9 | g.136674764T>G | CA375578506 | AGPAT2 | c.632A>C (p.Tyr211Ser) c.536A>C (p.Tyr179Ser) n.560A>C | |
| 9 | g.136674765A>C | CA375578511 | AGPAT2 | c.631T>G (p.Tyr211Asp) c.535T>G (p.Tyr179Asp) n.559T>G | |
| 9 | g.136674765A>G | CA375578517 | AGPAT2 | c.631T>C (p.Tyr211His) c.535T>C (p.Tyr179His) n.559T>C | gnomAD v4 |
| 9 | g.136674765A>T | CA375578533 | AGPAT2 | c.631T>A (p.Tyr211Asn) c.535T>A (p.Tyr179Asn) n.559T>A | gnomAD v4 |
| 9 | g.136674767_136674769del | CA2692654222 | AGPAT2 | c.629_631del (p.Phe210del) c.533_535del (p.Phe178del) n.557_559del | gnomAD v4 |
| 9 | g.136674766G>A | CA467738142 | AGPAT2 | c.630C>T (p.Phe210=) c.534C>T (p.Phe178=) n.558C>T | gnomAD v4 |
| 9 | g.136674766G>C | CA375578544 | AGPAT2 | c.630C>G (p.Phe210Leu) c.534C>G (p.Phe178Leu) n.558C>G | |
| 9 | g.136674766G>T | CA375578539 | AGPAT2 | c.630C>A (p.Phe210Leu) c.534C>A (p.Phe178Leu) n.558C>A | |
| 9 | g.136674767A>C | CA375578553 | AGPAT2 | c.629T>G (p.Phe210Cys) c.533T>G (p.Phe178Cys) n.557T>G | |
| 9 | g.136674767A>G | CA5342902 | AGPAT2 | c.629T>C (p.Phe210Ser) c.533T>C (p.Phe178Ser) n.557T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136674767A>T | CA375578557 | AGPAT2 | c.629T>A (p.Phe210Tyr) c.533T>A (p.Phe178Tyr) n.557T>A | |
| 9 | g.136674768dup | CA1130033743 | AGPAT2 | c.629dup (p.Tyr211LeufsTer?) c.533dup (p.Tyr179LeufsTer?) n.557dup | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136674768del | CA2692654223 | AGPAT2 | c.629del (p.Phe210SerfsTer?) c.533del (p.Phe178SerfsTer?) n.557del | gnomAD v4 |