| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.93101615T>A | CA368178538 | SAMD9 | c.4483A>T (p.Lys1495Ter) | |
| 7 | g.93101615T>C | CA114859 | SAMD9 | c.4483A>G (p.Lys1495Glu) | ClinVar dbSNP |
| 7 | g.93101615T>G | CA368178540 | SAMD9 | c.4483A>C (p.Lys1495Gln) | |
| 7 | g.93101615T= | CA1726196688 | SAMD9 | c.4483A= (p.Lys1495=) | |
| 7 | g.93101616G>A | CA456624897 | SAMD9 | c.4482C>T (p.His1494=) | ClinVar |
| 7 | g.93101616G>C | CA368178543 | SAMD9 | c.4482C>G (p.His1494Gln) | |
| 7 | g.93101616G= | CA1726196696 | SAMD9 | c.4482C= (p.His1494=) | |
| 7 | g.93101616G>T | CA368178546 | SAMD9 | c.4482C>A (p.His1494Gln) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.93101617T>A | CA368178555 | SAMD9 | c.4481A>T (p.His1494Leu) | |
| 7 | g.93101617T>C | CA368178558 | SAMD9 | c.4481A>G (p.His1494Arg) | |
| 7 | g.93101617T>G | CA368178561 | SAMD9 | c.4481A>C (p.His1494Pro) | |
| 7 | g.93101618G>A | CA368178569 | SAMD9 | c.4480C>T (p.His1494Tyr) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.93101618G>C | CA368178573 | SAMD9 | c.4480C>G (p.His1494Asp) | |
| 7 | g.93101618G= | CA1726196701 | SAMD9 | c.4480C= (p.His1494=) | |
| 7 | g.93101618G>T | CA368178565 | SAMD9 | c.4480C>A (p.His1494Asn) | |
| 7 | g.93101619A>C | CA456624901 | SAMD9 | c.4479T>G (p.Val1493=) | |
| 7 | g.93101619A>G | CA456624902 | SAMD9 | c.4479T>C (p.Val1493=) | |
| 7 | g.93101619A>T | CA456624903 | SAMD9 | c.4479T>A (p.Val1493=) | |
| 7 | g.93101620A>C | CA368178587 | SAMD9 | c.4478T>G (p.Val1493Gly) | |
| 7 | g.93101620A>G | CA368178593 | SAMD9 | c.4478T>C (p.Val1493Ala) | gnomAD v4 |
| 7 | g.93101620A>T | CA368178595 | SAMD9 | c.4478T>A (p.Val1493Asp) | |
| 7 | g.93101621C>A | CA368178601 | SAMD9 | c.4477G>T (p.Val1493Phe) | |
| 7 | g.93101621C>G | CA368178602 | SAMD9 | c.4477G>C (p.Val1493Leu) | |
| 7 | g.93101621C>T | CA368178605 | SAMD9 | c.4477G>A (p.Val1493Ile) | |
| 7 | g.93101622A= | CA1726196714 | SAMD9 | c.4476T= (p.Leu1492=) | |
| 7 | g.93101622A>C | CA456624905 | SAMD9 | c.4476T>G (p.Leu1492=) | |
| 7 | g.93101622A>G | CA4342546 | SAMD9 | c.4476T>C (p.Leu1492=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.93101622A>T | CA456624906 | SAMD9 | c.4476T>A (p.Leu1492=) | |
| 7 | g.93101623A= | CA1726196716 | SAMD9 | c.4475T= (p.Leu1492=) | |
| 7 | g.93101623A>C | CA161989323 | SAMD9 | c.4475T>G (p.Leu1492Arg) | dbSNP |
| 7 | g.93101623A>G | CA368178613 | SAMD9 | c.4475T>C (p.Leu1492Pro) | |
| 7 | g.93101623A>T | CA368178615 | SAMD9 | c.4475T>A (p.Leu1492His) | |
| 7 | g.93101624G>A | CA368178618 | SAMD9 | c.4474C>T (p.Leu1492Phe) | gnomAD v4 |
| 7 | g.93101624G>C | CA368178619 | SAMD9 | c.4474C>G (p.Leu1492Val) | |
| 7 | g.93101624G>T | CA368178621 | SAMD9 | c.4474C>A (p.Leu1492Ile) | |
| 7 | g.93101625T>A | CA368178627 | SAMD9 | c.4473A>T (p.Arg1491Ser) | |
| 7 | g.93101625T>C | CA456624907 | SAMD9 | c.4473A>G (p.Arg1491=) | |
| 7 | g.93101625T>G | CA368178623 | SAMD9 | c.4473A>C (p.Arg1491Ser) | |
| 7 | g.93101626C>A | CA368178630 | SAMD9 | c.4472G>T (p.Arg1491Ile) | gnomAD v4 |
| 7 | g.93101626C>G | CA368178631 | SAMD9 | c.4472G>C (p.Arg1491Thr) | COSMIC |
| 7 | g.93101626C>T | CA368178635 | SAMD9 | c.4472G>A (p.Arg1491Lys) | |
| 7 | g.93101627T>A | CA368178638 | SAMD9 | c.4471A>T (p.Arg1491Ter) | |
| 7 | g.93101627T>C | CA368178643 | SAMD9 | c.4471A>G (p.Arg1491Gly) | |
| 7 | g.93101627T>G | CA456624909 | SAMD9 | c.4471A>C (p.Arg1491=) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.93101628T>A | CA368178646 | SAMD9 | c.4470A>T (p.Glu1490Asp) | |
| 7 | g.93101628T>C | CA456624910 | SAMD9 | c.4470A>G (p.Glu1490=) | ClinVar dbSNP |
| 7 | g.93101628T>G | CA368178647 | SAMD9 | c.4470A>C (p.Glu1490Asp) | |
| 7 | g.93101628T= | CA1726196720 | SAMD9 | c.4470A= (p.Glu1490=) | |
| 7 | g.93101629T>A | CA368178648 | SAMD9 | c.4469A>T (p.Glu1490Val) | |
| 7 | g.93101629T>C | CA368178649 | SAMD9 | c.4469A>G (p.Glu1490Gly) |