| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.93104045_93104060del | CA2683736274 | SAMD9 | c.2042_2057del (p.Glu681ValfsTer?) | gnomAD v4 |
| 7 | g.93104044C>A | CA368193487 | SAMD9 | c.2054G>T (p.Arg685Leu) | |
| 7 | g.93104044C= | CA1726201426 | SAMD9 | c.2054G= (p.Arg685=) | |
| 7 | g.93104044C>G | CA368193490 | SAMD9 | c.2054G>C (p.Arg685Pro) | |
| 7 | g.93104044C>T | CA16618572 | SAMD9 | c.2054G>A (p.Arg685Gln) | ClinVar dbSNP |
| 7 | g.93104044_93104045insTTCT | CA1726201436 | SAMD9 | c.2053_2054insAGAA (p.Arg685GlnfsTer16) | dbSNP |
| 7 | g.93104045G>A | CA4342898 | SAMD9 | c.2053C>T (p.Arg685Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.93104045G>C | CA368193494 | SAMD9 | c.2053C>G (p.Arg685Gly) | |
| 7 | g.93104045G= | CA1726201439 | SAMD9 | c.2053C= (p.Arg685=) | |
| 7 | g.93104045G>T | CA456626297 | SAMD9 | c.2053C>A (p.Arg685=) | |
| 7 | g.93104046A= | CA1726201445 | SAMD9 | c.2052T= (p.Tyr684=) | |
| 7 | g.93104046A>C | CA368193497 | SAMD9 | c.2052T>G (p.Tyr684Ter) | |
| 7 | g.93104046A>G | CA456626298 | SAMD9 | c.2052T>C (p.Tyr684=) | |
| 7 | g.93104046A>T | CA368193499 | SAMD9 | c.2052T>A (p.Tyr684Ter) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.93104046_93104049delinsATAG | CA1726201447 | SAMD9 | c.2049_2052delinsCTAT (p.Phe683=) | |
| 7 | g.93104047T>A | CA368193502 | SAMD9 | c.2051A>T (p.Tyr684Phe) | |
| 7 | g.93104047T>C | CA368193507 | SAMD9 | c.2051A>G (p.Tyr684Cys) | |
| 7 | g.93104047T>G | CA368193505 | SAMD9 | c.2051A>C (p.Tyr684Ser) | |
| 7 | g.93104047_93104049del | CA1726201452 | SAMD9 | c.2049_2051del (p.Tyr684del) | dbSNP |
| 7 | g.93104048A>C | CA368193510 | SAMD9 | c.2050T>G (p.Tyr684Asp) | |
| 7 | g.93104048A>G | CA368193513 | SAMD9 | c.2050T>C (p.Tyr684His) | |
| 7 | g.93104048A>T | CA368193514 | SAMD9 | c.2050T>A (p.Tyr684Asn) | |
| 7 | g.93104050_93104052del | CA2683736275 | SAMD9 | c.2048_2050del (p.Phe683del) | gnomAD v4 |
| 7 | g.93104049G>A | CA456626300 | SAMD9 | c.2049C>T (p.Phe683=) | |
| 7 | g.93104049G>C | CA368193517 | SAMD9 | c.2049C>G (p.Phe683Leu) | |
| 7 | g.93104049G>T | CA368193519 | SAMD9 | c.2049C>A (p.Phe683Leu) | ClinVar |
| 7 | g.93104050A= | CA1726201455 | SAMD9 | c.2048T= (p.Phe683=) | |
| 7 | g.93104050A>C | CA368193522 | SAMD9 | c.2048T>G (p.Phe683Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.93104050A>G | CA368193523 | SAMD9 | c.2048T>C (p.Phe683Ser) | |
| 7 | g.93104050A>T | CA368193526 | SAMD9 | c.2048T>A (p.Phe683Tyr) | |
| 7 | g.93104051A>C | CA368193529 | SAMD9 | c.2047T>G (p.Phe683Val) | |
| 7 | g.93104051A>G | CA368193531 | SAMD9 | c.2047T>C (p.Phe683Leu) | |
| 7 | g.93104051A>T | CA368193532 | SAMD9 | c.2047T>A (p.Phe683Ile) | gnomAD v4 |
| 7 | g.93104052G>A | CA456626302 | SAMD9 | c.2046C>T (p.Asp682=) | |
| 7 | g.93104052G>C | CA368193535 | SAMD9 | c.2046C>G (p.Asp682Glu) | gnomAD v4 |
| 7 | g.93104052G= | CA1726201458 | SAMD9 | c.2046C= (p.Asp682=) | |
| 7 | g.93104052G>T | CA368193533 | SAMD9 | c.2046C>A (p.Asp682Glu) | |
| 7 | g.93104053T>A | CA368193540 | SAMD9 | c.2045A>T (p.Asp682Val) | |
| 7 | g.93104053T>C | CA368193543 | SAMD9 | c.2045A>G (p.Asp682Gly) | |
| 7 | g.93104053T>G | CA368193545 | SAMD9 | c.2045A>C (p.Asp682Ala) | |
| 7 | g.93104053_93104054insTATT | CA1726201462 | SAMD9 | c.2045_2046insATAA (p.Asp682GlufsTer2) | dbSNP |
| 7 | g.93104054C>A | CA368193548 | SAMD9 | c.2044G>T (p.Asp682Tyr) | gnomAD v4 |
| 7 | g.93104054C>G | CA368193550 | SAMD9 | c.2044G>C (p.Asp682His) | |
| 7 | g.93104054C>T | CA368193553 | SAMD9 | c.2044G>A (p.Asp682Asn) | |
| 7 | g.93104055T>A | CA368193555 | SAMD9 | c.2043A>T (p.Glu681Asp) | |
| 7 | g.93104055T>C | CA456626304 | SAMD9 | c.2043A>G (p.Glu681=) | |
| 7 | g.93104055T>G | CA368193557 | SAMD9 | c.2043A>C (p.Glu681Asp) | |
| 7 | g.93104056T>A | CA368193560 | SAMD9 | c.2042A>T (p.Glu681Val) | |
| 7 | g.93104056T>C | CA368193562 | SAMD9 | c.2042A>G (p.Glu681Gly) | |
| 7 | g.93104056T>G | CA161992228 | SAMD9 | c.2042A>C (p.Glu681Ala) | dbSNP gnomAD v4 |