Chr Mutation (hg38) CAid Gene Transcript Linkouts
Yg.12833793G>ACA10573383USP9Yc.5127G>A (p.Pro1709=)
n.5139G>A
c.4893G>A (p.Pro1631=)
c.5142G>A (p.Pro1714=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Yg.12833793G>CCA519901826USP9Yc.5127G>C (p.Pro1709=)
n.5139G>C
c.4893G>C (p.Pro1631=)
c.5142G>C (p.Pro1714=)
Yg.12833793G=CA2470560455USP9Yc.5127G= (p.Pro1709=)
n.5139G=
c.4893G= (p.Pro1631=)
c.5142G= (p.Pro1714=)
Yg.12833793G>TCA519901828USP9Yc.5127G>T (p.Pro1709=)
n.5139G>T
c.4893G>T (p.Pro1631=)
c.5142G>T (p.Pro1714=)
Yg.12833794G>ACA414999060USP9Yc.5128G>A (p.Ala1710Thr)
n.5140G>A
c.4894G>A (p.Ala1632Thr)
c.5143G>A (p.Ala1715Thr)
Yg.12833794G>CCA414999062USP9Yc.5128G>C (p.Ala1710Pro)
n.5140G>C
c.4894G>C (p.Ala1632Pro)
c.5143G>C (p.Ala1715Pro)
Yg.12833794G=CA2470560456USP9Yc.5128G= (p.Ala1710=)
n.5140G=
c.4894G= (p.Ala1632=)
c.5143G= (p.Ala1715=)
Yg.12833794G>TCA414999063USP9Yc.5128G>T (p.Ala1710Ser)
n.5140G>T
c.4894G>T (p.Ala1632Ser)
c.5143G>T (p.Ala1715Ser)
dbSNP gnomAD v2
Yg.12833795C>ACA414999065USP9Yc.5129C>A (p.Ala1710Asp)
n.5141C>A
c.4895C>A (p.Ala1632Asp)
c.5144C>A (p.Ala1715Asp)
Yg.12833795C>GCA414999068USP9Yc.5129C>G (p.Ala1710Gly)
n.5141C>G
c.4895C>G (p.Ala1632Gly)
c.5144C>G (p.Ala1715Gly)
Yg.12833795C>TCA414999067USP9Yc.5129C>T (p.Ala1710Val)
n.5141C>T
c.4895C>T (p.Ala1632Val)
c.5144C>T (p.Ala1715Val)
Yg.12833796T>ACA519901837USP9Yc.5130T>A (p.Ala1710=)
n.5142T>A
c.4896T>A (p.Ala1632=)
c.5145T>A (p.Ala1715=)
Yg.12833796T>CCA519901840USP9Yc.5130T>C (p.Ala1710=)
n.5142T>C
c.4896T>C (p.Ala1632=)
c.5145T>C (p.Ala1715=)
Yg.12833796T>GCA519901838USP9Yc.5130T>G (p.Ala1710=)
n.5142T>G
c.4896T>G (p.Ala1632=)
c.5145T>G (p.Ala1715=)
Yg.12833797A>CCA414999070USP9Yc.5131A>C (p.Ile1711Leu)
n.5143A>C
c.4897A>C (p.Ile1633Leu)
c.5146A>C (p.Ile1716Leu)
Yg.12833797A>GCA414999074USP9Yc.5131A>G (p.Ile1711Val)
n.5143A>G
c.4897A>G (p.Ile1633Val)
c.5146A>G (p.Ile1716Val)
Yg.12833797A>TCA414999072USP9Yc.5131A>T (p.Ile1711Leu)
n.5143A>T
c.4897A>T (p.Ile1633Leu)
c.5146A>T (p.Ile1716Leu)
Yg.12833798T>ACA414999075USP9Yc.5132T>A (p.Ile1711Lys)
n.5144T>A
c.4898T>A (p.Ile1633Lys)
c.5147T>A (p.Ile1716Lys)
Yg.12833798T>CCA414999077USP9Yc.5132T>C (p.Ile1711Thr)
n.5144T>C
c.4898T>C (p.Ile1633Thr)
c.5147T>C (p.Ile1716Thr)
Yg.12833798T>GCA414999079USP9Yc.5132T>G (p.Ile1711Arg)
n.5144T>G
c.4898T>G (p.Ile1633Arg)
c.5147T>G (p.Ile1716Arg)
Yg.12833799A=CA2470560457USP9Yc.5133A= (p.Ile1711=)
n.5145A=
c.4899A= (p.Ile1633=)
c.5148A= (p.Ile1716=)
Yg.12833799A>CCA519901847USP9Yc.5133A>C (p.Ile1711=)
n.5145A>C
c.4899A>C (p.Ile1633=)
c.5148A>C (p.Ile1716=)
Yg.12833799A>GCA414999081USP9Yc.5133A>G (p.Ile1711Met)
n.5145A>G
c.4899A>G (p.Ile1633Met)
c.5148A>G (p.Ile1716Met)
dbSNP gnomAD v2
Yg.12833799A>TCA519901850USP9Yc.5133A>T (p.Ile1711=)
n.5145A>T
c.4899A>T (p.Ile1633=)
c.5148A>T (p.Ile1716=)
Yg.12833800C>ACA414999082USP9Yc.5134C>A (p.Leu1712Ile)
n.5146C>A
c.4900C>A (p.Leu1634Ile)
c.5149C>A (p.Leu1717Ile)
Yg.12833800C>GCA414999084USP9Yc.5134C>G (p.Leu1712Val)
n.5146C>G
c.4900C>G (p.Leu1634Val)
c.5149C>G (p.Leu1717Val)
Yg.12833800C>TCA519901854USP9Yc.5134C>T (p.Leu1712=)
n.5146C>T
c.4900C>T (p.Leu1634=)
c.5149C>T (p.Leu1717=)
Yg.12833801T>ACA414999086USP9Yc.5135T>A (p.Leu1712Gln)
n.5147T>A
c.4901T>A (p.Leu1634Gln)
c.5150T>A (p.Leu1717Gln)
Yg.12833801T>CCA414999088USP9Yc.5135T>C (p.Leu1712Pro)
n.5147T>C
c.4901T>C (p.Leu1634Pro)
c.5150T>C (p.Leu1717Pro)
Yg.12833801T>GCA414999089USP9Yc.5135T>G (p.Leu1712Arg)
n.5147T>G
c.4901T>G (p.Leu1634Arg)
c.5150T>G (p.Leu1717Arg)
Yg.12833802A>CCA519901861USP9Yc.5136A>C (p.Leu1712=)
n.5148A>C
c.4902A>C (p.Leu1634=)
c.5151A>C (p.Leu1717=)
Yg.12833802A>GCA519901866USP9Yc.5136A>G (p.Leu1712=)
n.5148A>G
c.4902A>G (p.Leu1634=)
c.5151A>G (p.Leu1717=)
Yg.12833802A>TCA519901864USP9Yc.5136A>T (p.Leu1712=)
n.5148A>T
c.4902A>T (p.Leu1634=)
c.5151A>T (p.Leu1717=)
Yg.12833803A>CCA414999094USP9Yc.5137A>C (p.Ser1713Arg)
n.5149A>C
c.4903A>C (p.Ser1635Arg)
c.5152A>C (p.Ser1718Arg)
Yg.12833803A>GCA414999093USP9Yc.5137A>G (p.Ser1713Gly)
n.5149A>G
c.4903A>G (p.Ser1635Gly)
c.5152A>G (p.Ser1718Gly)
Yg.12833803A>TCA414999092USP9Yc.5137A>T (p.Ser1713Cys)
n.5149A>T
c.4903A>T (p.Ser1635Cys)
c.5152A>T (p.Ser1718Cys)
Yg.12833804G>ACA10573384USP9Yc.5138G>A (p.Ser1713Asn)
n.5150G>A
c.4904G>A (p.Ser1635Asn)
c.5153G>A (p.Ser1718Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Yg.12833804G>CCA414999097USP9Yc.5138G>C (p.Ser1713Thr)
n.5150G>C
c.4904G>C (p.Ser1635Thr)
c.5153G>C (p.Ser1718Thr)
Yg.12833804G=CA2470560458USP9Yc.5138G= (p.Ser1713=)
n.5150G=
c.4904G= (p.Ser1635=)
c.5153G= (p.Ser1718=)
Yg.12833804G>TCA414999099USP9Yc.5138G>T (p.Ser1713Ile)
n.5150G>T
c.4904G>T (p.Ser1635Ile)
c.5153G>T (p.Ser1718Ile)
Yg.12833805T>ACA414999101USP9Yc.5139T>A (p.Ser1713Arg)
n.5151T>A
c.4905T>A (p.Ser1635Arg)
c.5154T>A (p.Ser1718Arg)
Yg.12833805T>CCA519901873USP9Yc.5139T>C (p.Ser1713=)
n.5151T>C
c.4905T>C (p.Ser1635=)
c.5154T>C (p.Ser1718=)
Yg.12833805T>GCA414999102USP9Yc.5139T>G (p.Ser1713Arg)
n.5151T>G
c.4905T>G (p.Ser1635Arg)
c.5154T>G (p.Ser1718Arg)
Yg.12833806A>CCA414999104USP9Yc.5140A>C (p.Lys1714Gln)
n.5152A>C
c.4906A>C (p.Lys1636Gln)
c.5155A>C (p.Lys1719Gln)
Yg.12833806A>GCA414999105USP9Yc.5140A>G (p.Lys1714Glu)
n.5152A>G
c.4906A>G (p.Lys1636Glu)
c.5155A>G (p.Lys1719Glu)
Yg.12833806A>TCA414999107USP9Yc.5140A>T (p.Lys1714Ter)
n.5152A>T
c.4906A>T (p.Lys1636Ter)
c.5155A>T (p.Lys1719Ter)
Yg.12833807A>CCA414999109USP9Yc.5141A>C (p.Lys1714Thr)
n.5153A>C
c.4907A>C (p.Lys1636Thr)
c.5156A>C (p.Lys1719Thr)
Yg.12833807A>GCA414999110USP9Yc.5141A>G (p.Lys1714Arg)
n.5153A>G
c.4907A>G (p.Lys1636Arg)
c.5156A>G (p.Lys1719Arg)
Yg.12833807A>TCA414999112USP9Yc.5141A>T (p.Lys1714Ile)
n.5153A>T
c.4907A>T (p.Lys1636Ile)
c.5156A>T (p.Lys1719Ile)
Yg.12833808A>CCA414999116USP9Yc.5142A>C (p.Lys1714Asn)
n.5154A>C
c.4908A>C (p.Lys1636Asn)
c.5157A>C (p.Lys1719Asn)

Number of alleles fetched