Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.93101415A= | CA1726196300 | SAMD9 | c.4683T= (p.Leu1561=) | |
7 | g.93101415A>C | CA456624804 | SAMD9 | c.4683T>G (p.Leu1561=) | |
7 | g.93101415A>G | CA456624802 | SAMD9 | c.4683T>C (p.Leu1561=) | |
7 | g.93101415A>T | CA456624803 | SAMD9 | c.4683T>A (p.Leu1561=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.93101416A>C | CA368176393 | SAMD9 | c.4682T>G (p.Leu1561Arg) | |
7 | g.93101416A>G | CA368176397 | SAMD9 | c.4682T>C (p.Leu1561Pro) | |
7 | g.93101416A>T | CA368176389 | SAMD9 | c.4682T>A (p.Leu1561His) | |
7 | g.93101417G>A | CA368176401 | SAMD9 | c.4681C>T (p.Leu1561Phe) | |
7 | g.93101417G>C | CA368176405 | SAMD9 | c.4681C>G (p.Leu1561Val) | |
7 | g.93101417G>T | CA368176424 | SAMD9 | c.4681C>A (p.Leu1561Ile) | |
7 | g.93101418T>A | CA368176426 | SAMD9 | c.4680A>T (p.Gln1560His) | |
7 | g.93101418T>C | CA456624805 | SAMD9 | c.4680A>G (p.Gln1560=) | |
7 | g.93101418T>G | CA368176430 | SAMD9 | c.4680A>C (p.Gln1560His) | |
7 | g.93101419T>A | CA368176441 | SAMD9 | c.4679A>T (p.Gln1560Leu) | |
7 | g.93101419T>C | CA4342509 | SAMD9 | c.4679A>G (p.Gln1560Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.93101419T>G | CA368176431 | SAMD9 | c.4679A>C (p.Gln1560Pro) | |
7 | g.93101419T= | CA1726196306 | SAMD9 | c.4679A= (p.Gln1560=) | |
7 | g.93101420G>A | CA368176444 | SAMD9 | c.4678C>T (p.Gln1560Ter) | gnomAD v4 |
7 | g.93101420G>C | CA368176445 | SAMD9 | c.4678C>G (p.Gln1560Glu) | |
7 | g.93101420G>T | CA368176446 | SAMD9 | c.4678C>A (p.Gln1560Lys) | gnomAD v4 |
7 | g.93101421A= | CA1726196311 | SAMD9 | c.4677T= (p.Gly1559=) | |
7 | g.93101421A>C | CA456624808 | SAMD9 | c.4677T>G (p.Gly1559=) | |
7 | g.93101421A>G | CA456624806 | SAMD9 | c.4677T>C (p.Gly1559=) | |
7 | g.93101421A>T | CA456624807 | SAMD9 | c.4677T>A (p.Gly1559=) | ClinVar dbSNP |
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) |