Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.93101430dup | CA161989056 | SAMD9 | c.4673dup (p.Leu1558PhefsTer5) | dbSNP gnomAD v4 |
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) | |
7 | g.93101436A>C | CA456624817 | SAMD9 | c.4662T>G (p.Thr1554=) | |
7 | g.93101436A>G | CA456624815 | SAMD9 | c.4662T>C (p.Thr1554=) | gnomAD v4 |
7 | g.93101436A>T | CA456624816 | SAMD9 | c.4662T>A (p.Thr1554=) | |
7 | g.93101437G>A | CA368176676 | SAMD9 | c.4661C>T (p.Thr1554Ile) | gnomAD v4 |
7 | g.93101437G>C | CA368176677 | SAMD9 | c.4661C>G (p.Thr1554Ser) | |
7 | g.93101437G>T | CA368176670 | SAMD9 | c.4661C>A (p.Thr1554Asn) | |
7 | g.93101438T>A | CA368176681 | SAMD9 | c.4660A>T (p.Thr1554Ser) | |
7 | g.93101438T>C | CA368176683 | SAMD9 | c.4660A>G (p.Thr1554Ala) | |
7 | g.93101438T>G | CA368176684 | SAMD9 | c.4660A>C (p.Thr1554Pro) | |
7 | g.93101439G>A | CA456624818 | SAMD9 | c.4659C>T (p.Ile1553=) | |
7 | g.93101439G>C | CA368176685 | SAMD9 | c.4659C>G (p.Ile1553Met) | |
7 | g.93101439G>T | CA456624819 | SAMD9 | c.4659C>A (p.Ile1553=) | |
7 | g.93101440A= | CA1726196372 | SAMD9 | c.4658T= (p.Ile1553=) | |
7 | g.93101440A>C | CA368176688 | SAMD9 | c.4658T>G (p.Ile1553Ser) | |
7 | g.93101440A>G | CA4342515 | SAMD9 | c.4658T>C (p.Ile1553Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101440A>T | CA368176693 | SAMD9 | c.4658T>A (p.Ile1553Asn) | |
7 | g.93101441T>A | CA368176698 | SAMD9 | c.4657A>T (p.Ile1553Phe) | |
7 | g.93101441T>C | CA4342516 | SAMD9 | c.4657A>G (p.Ile1553Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101441T>G | CA368176700 | SAMD9 | c.4657A>C (p.Ile1553Leu) | |
7 | g.93101441T= | CA1726196376 | SAMD9 | c.4657A= (p.Ile1553=) | |
7 | g.93101442G>A | CA456624820 | SAMD9 | c.4656C>T (p.Pro1552=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.93101442G>C | CA456624821 | SAMD9 | c.4656C>G (p.Pro1552=) | |
7 | g.93101442G= | CA1726196380 | SAMD9 | c.4656C= (p.Pro1552=) | |
7 | g.93101442G>T | CA456624822 | SAMD9 | c.4656C>A (p.Pro1552=) |