Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.93101422C>A | CA368176448 | SAMD9 | c.4676G>T (p.Gly1559Val) | |
7 | g.93101422C>G | CA368176449 | SAMD9 | c.4676G>C (p.Gly1559Ala) | |
7 | g.93101422C>T | CA368176453 | SAMD9 | c.4676G>A (p.Gly1559Asp) | |
7 | g.93101423C>A | CA368176499 | SAMD9 | c.4675G>T (p.Gly1559Cys) | |
7 | g.93101423C>G | CA368176492 | SAMD9 | c.4675G>C (p.Gly1559Arg) | |
7 | g.93101423C>T | CA368176474 | SAMD9 | c.4675G>A (p.Gly1559Ser) | |
7 | g.93101424T>A | CA368176512 | SAMD9 | c.4674A>T (p.Leu1558Phe) | |
7 | g.93101424T>C | CA456624809 | SAMD9 | c.4674A>G (p.Leu1558=) | |
7 | g.93101424T>G | CA368176514 | SAMD9 | c.4674A>C (p.Leu1558Phe) | |
7 | g.93101424T= | CA1726196319 | SAMD9 | c.4674A= (p.Leu1558=) | |
7 | g.93101425A= | CA1726196328 | SAMD9 | c.4673T= (p.Leu1558=) | |
7 | g.93101425A>C | CA368176515 | SAMD9 | c.4673T>G (p.Leu1558Ter) | |
7 | g.93101425A>G | CA368176523 | SAMD9 | c.4673T>C (p.Leu1558Ser) | |
7 | g.93101425A>T | CA4342510 | SAMD9 | c.4673T>A (p.Leu1558Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101430dup | CA161989056 | SAMD9 | c.4673dup (p.Leu1558PhefsTer5) | dbSNP gnomAD v4 |
7 | g.93101426A>C | CA368176532 | SAMD9 | c.4672T>G (p.Leu1558Val) | |
7 | g.93101426A>G | CA456624810 | SAMD9 | c.4672T>C (p.Leu1558=) | |
7 | g.93101426A>T | CA368176537 | SAMD9 | c.4672T>A (p.Leu1558Ile) | |
7 | g.93101427A= | CA1726196333 | SAMD9 | c.4671T= (p.Phe1557=) | |
7 | g.93101427A>C | CA368176549 | SAMD9 | c.4671T>G (p.Phe1557Leu) | |
7 | g.93101427A>G | CA4342511 | SAMD9 | c.4671T>C (p.Phe1557=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101427A>T | CA368176570 | SAMD9 | c.4671T>A (p.Phe1557Leu) | |
7 | g.93101428A>C | CA368176574 | SAMD9 | c.4670T>G (p.Phe1557Cys) | |
7 | g.93101428A>G | CA368176579 | SAMD9 | c.4670T>C (p.Phe1557Ser) | |
7 | g.93101428A>T | CA368176583 | SAMD9 | c.4670T>A (p.Phe1557Tyr) | |
7 | g.93101429A>C | CA368176590 | SAMD9 | c.4669T>G (p.Phe1557Val) | |
7 | g.93101429A>G | CA368176592 | SAMD9 | c.4669T>C (p.Phe1557Leu) | |
7 | g.93101429A>T | CA368176595 | SAMD9 | c.4669T>A (p.Phe1557Ile) | |
7 | g.93101430A= | CA1726196342 | SAMD9 | c.4668T= (p.Ala1556=) | |
7 | g.93101430A>C | CA4342512 | SAMD9 | c.4668T>G (p.Ala1556=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101430A>G | CA456624811 | SAMD9 | c.4668T>C (p.Ala1556=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.93101430A>T | CA456624812 | SAMD9 | c.4668T>A (p.Ala1556=) | |
7 | g.93101431G>A | CA368176606 | SAMD9 | c.4667C>T (p.Ala1556Val) | |
7 | g.93101431G>C | CA368176616 | SAMD9 | c.4667C>G (p.Ala1556Gly) | |
7 | g.93101431G>T | CA368176615 | SAMD9 | c.4667C>A (p.Ala1556Asp) | |
7 | g.93101432C>A | CA368176619 | SAMD9 | c.4666G>T (p.Ala1556Ser) | |
7 | g.93101432C= | CA1726196353 | SAMD9 | c.4666G= (p.Ala1556=) | |
7 | g.93101432C>G | CA368176621 | SAMD9 | c.4666G>C (p.Ala1556Pro) | |
7 | g.93101432C>T | CA4342513 | SAMD9 | c.4666G>A (p.Ala1556Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101433G>A | CA4342514 | SAMD9 | c.4665C>T (p.Pro1555=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101433G>C | CA456624813 | SAMD9 | c.4665C>G (p.Pro1555=) | |
7 | g.93101433G= | CA1726196359 | SAMD9 | c.4665C= (p.Pro1555=) | |
7 | g.93101433G>T | CA456624814 | SAMD9 | c.4665C>A (p.Pro1555=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.93101434G>A | CA368176623 | SAMD9 | c.4664C>T (p.Pro1555Leu) | |
7 | g.93101434G>C | CA368176626 | SAMD9 | c.4664C>G (p.Pro1555Arg) | ClinVar |
7 | g.93101434G>T | CA368176631 | SAMD9 | c.4664C>A (p.Pro1555His) | |
7 | g.93101435G>A | CA368176636 | SAMD9 | c.4663C>T (p.Pro1555Ser) | ClinVar dbSNP |
7 | g.93101435G>C | CA368176661 | SAMD9 | c.4663C>G (p.Pro1555Ala) | |
7 | g.93101435G= | CA1726196364 | SAMD9 | c.4663C= (p.Pro1555=) | |
7 | g.93101435G>T | CA368176666 | SAMD9 | c.4663C>A (p.Pro1555Thr) |