Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.91724524C>ACA373796769ROR2c.1970G>T (p.Arg657Leu)
c.1550G>T (p.Arg517Leu)
n.2438G>T
c.767G>T (p.Arg256Leu)
c.1961G>T (p.Arg654Leu)
gnomAD v4
9g.91724524C=CA1863922889ROR2c.1970G= (p.Arg657=)
c.1550G= (p.Arg517=)
n.2438G=
c.767G= (p.Arg256=)
c.1961G= (p.Arg654=)
9g.91724524C>GCA373796771ROR2c.1970G>C (p.Arg657Pro)
c.1550G>C (p.Arg517Pro)
n.2438G>C
c.767G>C (p.Arg256Pro)
c.1961G>C (p.Arg654Pro)
9g.91724524C>TCA173318ROR2c.1970G>A (p.Arg657His)
c.1550G>A (p.Arg517His)
n.2438G>A
c.767G>A (p.Arg256His)
c.1961G>A (p.Arg654His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.91724524_91724525insCTCA1863922894ROR2c.1969_1970insAG (p.Arg657GlnfsTer?)
c.1549_1550insAG (p.Arg517GlnfsTer?)
n.2437_2438insAG
c.766_767insAG (p.Arg256GlnfsTer?)
c.1960_1961insAG (p.Arg654GlnfsTer?)
dbSNP
9g.91724525G>ACA5120517ROR2c.1969C>T (p.Arg657Cys)
c.1549C>T (p.Arg517Cys)
n.2437C>T
c.766C>T (p.Arg256Cys)
c.1960C>T (p.Arg654Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
9g.91724525G>CCA373796777ROR2c.1969C>G (p.Arg657Gly)
c.1549C>G (p.Arg517Gly)
n.2437C>G
c.766C>G (p.Arg256Gly)
c.1960C>G (p.Arg654Gly)
9g.91724525G=CA1863922895ROR2c.1969C= (p.Arg657=)
c.1549C= (p.Arg517=)
n.2437C=
c.766C= (p.Arg256=)
c.1960C= (p.Arg654=)
9g.91724525G>TCA373796779ROR2c.1969C>A (p.Arg657Ser)
c.1549C>A (p.Arg517Ser)
n.2437C>A
c.766C>A (p.Arg256Ser)
c.1960C>A (p.Arg654Ser)
9g.91724526G>ACA466339130ROR2c.1968C>T (p.Ile656=)
c.1548C>T (p.Ile516=)
n.2436C>T
c.765C>T (p.Ile255=)
c.1959C>T (p.Ile653=)
gnomAD v4
9g.91724526G>CCA373796782ROR2c.1968C>G (p.Ile656Met)
c.1548C>G (p.Ile516Met)
n.2436C>G
c.765C>G (p.Ile255Met)
c.1959C>G (p.Ile653Met)
9g.91724526G=CA1863922898ROR2c.1968C= (p.Ile656=)
c.1548C= (p.Ile516=)
n.2436C=
c.765C= (p.Ile255=)
c.1959C= (p.Ile653=)
9g.91724526G>TCA466339131ROR2c.1968C>A (p.Ile656=)
c.1548C>A (p.Ile516=)
n.2436C>A
c.765C>A (p.Ile255=)
c.1959C>A (p.Ile653=)
dbSNP gnomAD v4
9g.91724527A>CCA373796785ROR2c.1967T>G (p.Ile656Ser)
c.1547T>G (p.Ile516Ser)
n.2435T>G
c.764T>G (p.Ile255Ser)
c.1958T>G (p.Ile653Ser)
9g.91724527A>GCA373796786ROR2c.1967T>C (p.Ile656Thr)
c.1547T>C (p.Ile516Thr)
n.2435T>C
c.764T>C (p.Ile255Thr)
c.1958T>C (p.Ile653Thr)
9g.91724527A>TCA373796789ROR2c.1967T>A (p.Ile656Asn)
c.1547T>A (p.Ile516Asn)
n.2435T>A
c.764T>A (p.Ile255Asn)
c.1958T>A (p.Ile653Asn)
9g.91724528T>ACA373796796ROR2c.1966A>T (p.Ile656Phe)
c.1546A>T (p.Ile516Phe)
n.2434A>T
c.763A>T (p.Ile255Phe)
c.1957A>T (p.Ile653Phe)
9g.91724528T>CCA373796794ROR2c.1966A>G (p.Ile656Val)
c.1546A>G (p.Ile516Val)
n.2434A>G
c.763A>G (p.Ile255Val)
c.1957A>G (p.Ile653Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
9g.91724528T>GCA373796792ROR2c.1966A>C (p.Ile656Leu)
c.1546A>C (p.Ile516Leu)
n.2434A>C
c.763A>C (p.Ile255Leu)
c.1957A>C (p.Ile653Leu)
9g.91724528T=CA1863922900ROR2c.1966A= (p.Ile656=)
c.1546A= (p.Ile516=)
n.2434A=
c.763A= (p.Ile255=)
c.1957A= (p.Ile653=)
9g.91724529A>CCA466339212ROR2c.1965T>G (p.Pro655=)
c.1545T>G (p.Pro515=)
n.2433T>G
c.762T>G (p.Pro254=)
c.1956T>G (p.Pro652=)
9g.91724529A>GCA466339213ROR2c.1965T>C (p.Pro655=)
c.1545T>C (p.Pro515=)
n.2433T>C
c.762T>C (p.Pro254=)
c.1956T>C (p.Pro652=)
9g.91724529A>TCA466339214ROR2c.1965T>A (p.Pro655=)
c.1545T>A (p.Pro515=)
n.2433T>A
c.762T>A (p.Pro254=)
c.1956T>A (p.Pro652=)
9g.91724530G>ACA5120518ROR2c.1964C>T (p.Pro655Leu)
c.1544C>T (p.Pro515Leu)
n.2432C>T
c.761C>T (p.Pro254Leu)
c.1955C>T (p.Pro652Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.91724530G>CCA373796798ROR2c.1964C>G (p.Pro655Arg)
c.1544C>G (p.Pro515Arg)
n.2432C>G
c.761C>G (p.Pro254Arg)
c.1955C>G (p.Pro652Arg)
9g.91724530G=CA1863922904ROR2c.1964C= (p.Pro655=)
c.1544C= (p.Pro515=)
n.2432C=
c.761C= (p.Pro254=)
c.1955C= (p.Pro652=)
9g.91724530G>TCA373796801ROR2c.1964C>A (p.Pro655His)
c.1544C>A (p.Pro515His)
n.2432C>A
c.761C>A (p.Pro254His)
c.1955C>A (p.Pro652His)
9g.91724531G>ACA5120519ROR2c.1963C>T (p.Pro655Ser)
c.1543C>T (p.Pro515Ser)
n.2431C>T
c.760C>T (p.Pro254Ser)
c.1954C>T (p.Pro652Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.91724531G>CCA373796804ROR2c.1963C>G (p.Pro655Ala)
c.1543C>G (p.Pro515Ala)
n.2431C>G
c.760C>G (p.Pro254Ala)
c.1954C>G (p.Pro652Ala)
9g.91724531G=CA1863922906ROR2c.1963C= (p.Pro655=)
c.1543C= (p.Pro515=)
n.2431C=
c.760C= (p.Pro254=)
c.1954C= (p.Pro652=)
9g.91724531G>TCA373796806ROR2c.1963C>A (p.Pro655Thr)
c.1543C>A (p.Pro515Thr)
n.2431C>A
c.760C>A (p.Pro254Thr)
c.1954C>A (p.Pro652Thr)
9g.91724531_91724545dupCA2690632374ROR2c.1949_1963dup (p.Leu654_Pro655insArgAsnSerLeuLeu)
c.1529_1543dup (p.Leu514_Pro515insArgAsnSerLeuLeu)
n.2417_2431dup
c.746_760dup (p.Leu253_Pro254insArgAsnSerLeuLeu)
c.1940_1954dup (p.Leu651_Pro652insArgAsnSerLeuLeu)
gnomAD v4
9g.91724532C>ACA466339218ROR2c.1962G>T (p.Leu654=)
c.1542G>T (p.Leu514=)
n.2430G>T
c.759G>T (p.Leu253=)
c.1953G>T (p.Leu651=)
9g.91724532C=CA1863922908ROR2c.1962G= (p.Leu654=)
c.1542G= (p.Leu514=)
n.2430G=
c.759G= (p.Leu253=)
c.1953G= (p.Leu651=)
9g.91724532C>GCA466339219ROR2c.1962G>C (p.Leu654=)
c.1542G>C (p.Leu514=)
n.2430G>C
c.759G>C (p.Leu253=)
c.1953G>C (p.Leu651=)
9g.91724532C>TCA5120520ROR2c.1962G>A (p.Leu654=)
c.1542G>A (p.Leu514=)
n.2430G>A
c.759G>A (p.Leu253=)
c.1953G>A (p.Leu651=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.91724539_91724553delCA2690632375ROR2c.1948_1962del (p.Gly650_Leu654del)
c.1528_1542del (p.Gly510_Leu514del)
n.2416_2430del
c.745_759del (p.Gly249_Leu253del)
c.1939_1953del (p.Gly647_Leu651del)
gnomAD v4
9g.91724533A>CCA373796810ROR2c.1961T>G (p.Leu654Arg)
c.1541T>G (p.Leu514Arg)
n.2429T>G
c.758T>G (p.Leu253Arg)
c.1952T>G (p.Leu651Arg)
9g.91724533A>GCA373796813ROR2c.1961T>C (p.Leu654Pro)
c.1541T>C (p.Leu514Pro)
n.2429T>C
c.758T>C (p.Leu253Pro)
c.1952T>C (p.Leu651Pro)
9g.91724533A>TCA373796816ROR2c.1961T>A (p.Leu654Gln)
c.1541T>A (p.Leu514Gln)
n.2429T>A
c.758T>A (p.Leu253Gln)
c.1952T>A (p.Leu651Gln)
9g.91724534G>ACA466339221ROR2c.1960C>T (p.Leu654=)
c.1540C>T (p.Leu514=)
n.2428C>T
c.757C>T (p.Leu253=)
c.1951C>T (p.Leu651=)
9g.91724534G>CCA373796818ROR2c.1960C>G (p.Leu654Val)
c.1540C>G (p.Leu514Val)
n.2428C>G
c.757C>G (p.Leu253Val)
c.1951C>G (p.Leu651Val)
9g.91724534G>TCA373796819ROR2c.1960C>A (p.Leu654Met)
c.1540C>A (p.Leu514Met)
n.2428C>A
c.757C>A (p.Leu253Met)
c.1951C>A (p.Leu651Met)
9g.91724535C>ACA466339222ROR2c.1959G>T (p.Leu653=)
c.1539G>T (p.Leu513=)
n.2427G>T
c.756G>T (p.Leu252=)
c.1950G>T (p.Leu650=)
9g.91724535C=CA1863922914ROR2c.1959G= (p.Leu653=)
c.1539G= (p.Leu513=)
n.2427G=
c.756G= (p.Leu252=)
c.1950G= (p.Leu650=)
9g.91724535C>GCA466339223ROR2c.1959G>C (p.Leu653=)
c.1539G>C (p.Leu513=)
n.2427G>C
c.756G>C (p.Leu252=)
c.1950G>C (p.Leu650=)
9g.91724535C>TCA272467ROR2c.1959G>A (p.Leu653=)
c.1539G>A (p.Leu513=)
n.2427G>A
c.756G>A (p.Leu252=)
c.1950G>A (p.Leu650=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.91724536A>CCA373796823ROR2c.1958T>G (p.Leu653Arg)
c.1538T>G (p.Leu513Arg)
n.2426T>G
c.755T>G (p.Leu252Arg)
c.1949T>G (p.Leu650Arg)
9g.91724536A>GCA373796825ROR2c.1958T>C (p.Leu653Pro)
c.1538T>C (p.Leu513Pro)
n.2426T>C
c.755T>C (p.Leu252Pro)
c.1949T>C (p.Leu650Pro)
9g.91724536A>TCA373796822ROR2c.1958T>A (p.Leu653Gln)
c.1538T>A (p.Leu513Gln)
n.2426T>A
c.755T>A (p.Leu252Gln)
c.1949T>A (p.Leu650Gln)

Number of alleles fetched