Chr Mutation (hg38) CAid Gene Transcript Linkouts
Yg.12812834T>ACA414991529USP9Yc.4391T>A (p.Leu1464Ter)
n.4403T>A
c.4157T>A (p.Leu1386Ter)
c.4406T>A (p.Leu1469Ter)
Yg.12812834T>CCA414991532USP9Yc.4391T>C (p.Leu1464Ser)
n.4403T>C
c.4157T>C (p.Leu1386Ser)
c.4406T>C (p.Leu1469Ser)
Yg.12812834T>GCA414991535USP9Yc.4391T>G (p.Leu1464Ter)
n.4403T>G
c.4157T>G (p.Leu1386Ter)
c.4406T>G (p.Leu1469Ter)
Yg.12812835A>CCA414991540USP9Yc.4392A>C (p.Leu1464Phe)
n.4404A>C
c.4158A>C (p.Leu1386Phe)
c.4407A>C (p.Leu1469Phe)
Yg.12812835A>GCA519895090USP9Yc.4392A>G (p.Leu1464=)
n.4404A>G
c.4158A>G (p.Leu1386=)
c.4407A>G (p.Leu1469=)
Yg.12812835A>TCA414991538USP9Yc.4392A>T (p.Leu1464Phe)
n.4404A>T
c.4158A>T (p.Leu1386Phe)
c.4407A>T (p.Leu1469Phe)
Yg.12812836A>CCA414991543USP9Yc.4393A>C (p.Ile1465Leu)
n.4405A>C
c.4159A>C (p.Ile1387Leu)
c.4408A>C (p.Ile1470Leu)
Yg.12812836A>GCA414991546USP9Yc.4393A>G (p.Ile1465Val)
n.4405A>G
c.4159A>G (p.Ile1387Val)
c.4408A>G (p.Ile1470Val)
Yg.12812836A>TCA414991549USP9Yc.4393A>T (p.Ile1465Phe)
n.4405A>T
c.4159A>T (p.Ile1387Phe)
c.4408A>T (p.Ile1470Phe)
Yg.12812837T>ACA414991552USP9Yc.4394T>A (p.Ile1465Asn)
n.4406T>A
c.4160T>A (p.Ile1387Asn)
c.4409T>A (p.Ile1470Asn)
Yg.12812837T>CCA414991555USP9Yc.4394T>C (p.Ile1465Thr)
n.4406T>C
c.4160T>C (p.Ile1387Thr)
c.4409T>C (p.Ile1470Thr)
Yg.12812837T>GCA414991562USP9Yc.4394T>G (p.Ile1465Ser)
n.4406T>G
c.4160T>G (p.Ile1387Ser)
c.4409T>G (p.Ile1470Ser)
Yg.12812838T>ACA519895111USP9Yc.4395T>A (p.Ile1465=)
n.4407T>A
c.4161T>A (p.Ile1387=)
c.4410T>A (p.Ile1470=)
Yg.12812838T>CCA519895113USP9Yc.4395T>C (p.Ile1465=)
n.4407T>C
c.4161T>C (p.Ile1387=)
c.4410T>C (p.Ile1470=)
Yg.12812838T>GCA414991564USP9Yc.4395T>G (p.Ile1465Met)
n.4407T>G
c.4161T>G (p.Ile1387Met)
c.4410T>G (p.Ile1470Met)
Yg.12812839G>ACA414991579USP9Yc.4396G>A (p.Asp1466Asn)
n.4408G>A
c.4162G>A (p.Asp1388Asn)
c.4411G>A (p.Asp1471Asn)
Yg.12812839G>CCA414991581USP9Yc.4396G>C (p.Asp1466His)
n.4408G>C
c.4162G>C (p.Asp1388His)
c.4411G>C (p.Asp1471His)
Yg.12812839G>TCA414991584USP9Yc.4396G>T (p.Asp1466Tyr)
n.4408G>T
c.4162G>T (p.Asp1388Tyr)
c.4411G>T (p.Asp1471Tyr)
Yg.12812840A>CCA414991593USP9Yc.4397A>C (p.Asp1466Ala)
n.4409A>C
c.4163A>C (p.Asp1388Ala)
c.4412A>C (p.Asp1471Ala)
Yg.12812840A>GCA414991594USP9Yc.4397A>G (p.Asp1466Gly)
n.4409A>G
c.4163A>G (p.Asp1388Gly)
c.4412A>G (p.Asp1471Gly)
Yg.12812840A>TCA414991595USP9Yc.4397A>T (p.Asp1466Val)
n.4409A>T
c.4163A>T (p.Asp1388Val)
c.4412A>T (p.Asp1471Val)
Yg.12812841T>ACA414991596USP9Yc.4398T>A (p.Asp1466Glu)
n.4410T>A
c.4164T>A (p.Asp1388Glu)
c.4413T>A (p.Asp1471Glu)
Yg.12812841T>CCA519895134USP9Yc.4398T>C (p.Asp1466=)
n.4410T>C
c.4164T>C (p.Asp1388=)
c.4413T>C (p.Asp1471=)
Yg.12812841T>GCA414991597USP9Yc.4398T>G (p.Asp1466Glu)
n.4410T>G
c.4164T>G (p.Asp1388Glu)
c.4413T>G (p.Asp1471Glu)
Yg.12812842G>ACA414991599USP9Yc.4399G>A (p.Asp1467Asn)
n.4411G>A
c.4165G>A (p.Asp1389Asn)
c.4414G>A (p.Asp1472Asn)
Yg.12812842G>CCA414991601USP9Yc.4399G>C (p.Asp1467His)
n.4411G>C
c.4165G>C (p.Asp1389His)
c.4414G>C (p.Asp1472His)
Yg.12812842G>TCA414991604USP9Yc.4399G>T (p.Asp1467Tyr)
n.4411G>T
c.4165G>T (p.Asp1389Tyr)
c.4414G>T (p.Asp1472Tyr)
Yg.12812843A>CCA414991607USP9Yc.4400A>C (p.Asp1467Ala)
n.4412A>C
c.4166A>C (p.Asp1389Ala)
c.4415A>C (p.Asp1472Ala)
Yg.12812843A>GCA414991609USP9Yc.4400A>G (p.Asp1467Gly)
n.4412A>G
c.4166A>G (p.Asp1389Gly)
c.4415A>G (p.Asp1472Gly)
Yg.12812843A>TCA414991612USP9Yc.4400A>T (p.Asp1467Val)
n.4412A>T
c.4166A>T (p.Asp1389Val)
c.4415A>T (p.Asp1472Val)
Yg.12812844T>ACA414991626USP9Yc.4401T>A (p.Asp1467Glu)
n.4413T>A
c.4167T>A (p.Asp1389Glu)
c.4416T>A (p.Asp1472Glu)
Yg.12812844T>CCA519895143USP9Yc.4401T>C (p.Asp1467=)
n.4413T>C
c.4167T>C (p.Asp1389=)
c.4416T>C (p.Asp1472=)
Yg.12812844T>GCA414991629USP9Yc.4401T>G (p.Asp1467Glu)
n.4413T>G
c.4167T>G (p.Asp1389Glu)
c.4416T>G (p.Asp1472Glu)
Yg.12812845T>ACA414991632USP9Yc.4402T>A (p.Phe1468Ile)
n.4414T>A
c.4168T>A (p.Phe1390Ile)
c.4417T>A (p.Phe1473Ile)
Yg.12812845T>CCA414991635USP9Yc.4402T>C (p.Phe1468Leu)
n.4414T>C
c.4168T>C (p.Phe1390Leu)
c.4417T>C (p.Phe1473Leu)
Yg.12812845T>GCA414991638USP9Yc.4402T>G (p.Phe1468Val)
n.4414T>G
c.4168T>G (p.Phe1390Val)
c.4417T>G (p.Phe1473Val)
Yg.12812846T>ACA414991643USP9Yc.4403T>A (p.Phe1468Tyr)
n.4415T>A
c.4169T>A (p.Phe1390Tyr)
c.4418T>A (p.Phe1473Tyr)
Yg.12812846T>CCA414991645USP9Yc.4403T>C (p.Phe1468Ser)
n.4415T>C
c.4169T>C (p.Phe1390Ser)
c.4418T>C (p.Phe1473Ser)
Yg.12812846T>GCA414991642USP9Yc.4403T>G (p.Phe1468Cys)
n.4415T>G
c.4169T>G (p.Phe1390Cys)
c.4418T>G (p.Phe1473Cys)
Yg.12812847C>ACA414991650USP9Yc.4404C>A (p.Phe1468Leu)
n.4416C>A
c.4170C>A (p.Phe1390Leu)
c.4419C>A (p.Phe1473Leu)
Yg.12812847C>GCA414991647USP9Yc.4404C>G (p.Phe1468Leu)
n.4416C>G
c.4170C>G (p.Phe1390Leu)
c.4419C>G (p.Phe1473Leu)
Yg.12812847C>TCA519895173USP9Yc.4404C>T (p.Phe1468=)
n.4416C>T
c.4170C>T (p.Phe1390=)
c.4419C>T (p.Phe1473=)
COSMIC
Yg.12812848A>CCA414991659USP9Yc.4405A>C (p.Ile1469Leu)
n.4417A>C
c.4171A>C (p.Ile1391Leu)
c.4420A>C (p.Ile1474Leu)
Yg.12812848A>GCA414991654USP9Yc.4405A>G (p.Ile1469Val)
n.4417A>G
c.4171A>G (p.Ile1391Val)
c.4420A>G (p.Ile1474Val)
Yg.12812848A>TCA414991657USP9Yc.4405A>T (p.Ile1469Phe)
n.4417A>T
c.4171A>T (p.Ile1391Phe)
c.4420A>T (p.Ile1474Phe)
Yg.12812849T>ACA414991663USP9Yc.4406T>A (p.Ile1469Asn)
n.4418T>A
c.4172T>A (p.Ile1391Asn)
c.4421T>A (p.Ile1474Asn)
Yg.12812849T>CCA414991666USP9Yc.4406T>C (p.Ile1469Thr)
n.4418T>C
c.4172T>C (p.Ile1391Thr)
c.4421T>C (p.Ile1474Thr)
Yg.12812849T>GCA414991668USP9Yc.4406T>G (p.Ile1469Ser)
n.4418T>G
c.4172T>G (p.Ile1391Ser)
c.4421T>G (p.Ile1474Ser)
Yg.12812850C>ACA519895200USP9Yc.4407C>A (p.Ile1469=)
n.4419C>A
c.4173C>A (p.Ile1391=)
c.4422C>A (p.Ile1474=)
Yg.12812850C>GCA414991672USP9Yc.4407C>G (p.Ile1469Met)
n.4419C>G
c.4173C>G (p.Ile1391Met)
c.4422C>G (p.Ile1474Met)

Number of alleles fetched