Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122257060T>CCA2569443CASRc.186-21T>C (p.=)
c.9+2686T>C (p.=)
n.45-21T>C
dbSNP ExAC gnomAD
3g.122257062C>TCA2569444CASRc.186-19C>T (p.=)
c.9+2688C>T (p.=)
n.45-19C>T
dbSNP ExAC gnomAD
3g.122257063A>CCA1052951305CASRc.186-18A>C (p.=)
c.9+2689A>C (p.=)
n.45-18A>C
3g.122257064_122257066delCA2569445CASRc.186-17_186-15del (p.=)
c.9+2690_9+2692del (p.=)
n.45-17_45-15del
dbSNP ExAC gnomAD
3g.122257067C>ACA82609836CASRc.186-14C>A (p.=)
c.9+2693C>A (p.=)
n.45-14C>A
dbSNP
3g.122257070C>GCA2569446CASRc.186-11C>G (p.=)
c.9+2696C>G (p.=)
n.45-11C>G
dbSNP ExAC gnomAD
3g.122257074C>ACA2569447CASRc.186-7C>A (p.=)
c.9+2700C>A (p.=)
n.45-7C>A
dbSNP ExAC gnomAD
3g.122257078C>TCA545964947CASRc.186-3C>T (p.=)
c.9+2704C>T (p.=)
n.45-3C>T
gnomAD
3g.122257079A>CCA354362329CASRc.186-2A>C (p.=)
c.9+2705A>C (p.=)
n.45-2A>C
3g.122257079A>GCA354362330CASRc.186-2A>G (p.=)
c.9+2705A>G (p.=)
n.45-2A>G
gnomAD
3g.122257079A>TCA354362331CASRc.186-2A>T (p.=)
c.9+2705A>T (p.=)
n.45-2A>T
3g.122257080G>ACA354362332CASRc.186-1G>A (p.=)
c.9+2706G>A (p.=)
n.45-1G>A
COSMIC
3g.122257080G>CCA354362333CASRc.186-1G>C (p.=)
c.9+2706G>C (p.=)
n.45-1G>C
3g.122257080G>TCA212893CASRc.186-1G>T (p.=)
c.9+2706G>T (p.=)
n.45-1G>T
ClinVar dbSNP
3g.122257081G>ACA435403984CASRc.186G>A (p.Arg62=)
c.9+2707G>A (p.=)
n.45G>A
3g.122257081G>CCA354362334CASRc.186G>C (p.Arg62Ser)
c.9+2707G>C (p.=)
n.45G>C
3g.122257081G>TCA354362335CASRc.186G>T (p.Arg62Ser)
c.9+2707G>T (p.=)
n.45G>T
gnomAD
3g.122257082T>ACA354362336CASRc.187T>A (p.Tyr63Asn)
c.9+2708T>A (p.=)
n.46T>A
3g.122257082T>CCA354362337CASRc.187T>C (p.Tyr63His)
c.9+2708T>C (p.=)
n.46T>C
3g.122257082T>GCA354362338CASRc.187T>G (p.Tyr63Asp)
c.9+2708T>G (p.=)
n.46T>G
3g.122257083A>CCA354362339CASRc.188A>C (p.Tyr63Ser)
c.9+2709A>C (p.=)
n.47A>C
3g.122257083A>GCA354362340CASRc.188A>G (p.Tyr63Cys)
c.9+2709A>G (p.=)
n.47A>G
gnomAD
3g.122257083A>TCA354362341CASRc.188A>T (p.Tyr63Phe)
c.9+2709A>T (p.=)
n.47A>T
3g.122257084T>ACA354362342CASRc.189T>A (p.Tyr63Ter)
c.9+2710T>A (p.=)
n.48T>A
3g.122257084T>CCA435403985CASRc.189T>C (p.Tyr63=)
c.9+2710T>C (p.=)
n.48T>C
3g.122257084T>GCA354362343CASRc.189T>G (p.Tyr63Ter)
c.9+2710T>G (p.=)
n.48T>G
3g.122257085A>CCA354362344CASRc.190A>C (p.Asn64His)
c.9+2711A>C (p.=)
n.49A>C
3g.122257085A>GCA354362345CASRc.190A>G (p.Asn64Asp)
c.9+2711A>G (p.=)
n.49A>G
3g.122257085A>TCA354362346CASRc.190A>T (p.Asn64Tyr)
c.9+2711A>T (p.=)
n.49A>T
3g.122257086A>CCA354362347CASRc.191A>C (p.Asn64Thr)
c.9+2712A>C (p.=)
n.50A>C
3g.122257086A>GCA354362348CASRc.191A>G (p.Asn64Ser)
c.9+2712A>G (p.=)
n.50A>G
3g.122257086A>TCA354362349CASRc.191A>T (p.Asn64Ile)
c.9+2712A>T (p.=)
n.50A>T
3g.122257087T>ACA354362350CASRc.192T>A (p.Asn64Lys)
c.9+2713T>A (p.=)
n.51T>A
3g.122257087T>CCA435403986CASRc.192T>C (p.Asn64=)
c.9+2713T>C (p.=)
n.51T>C
3g.122257087T>GCA354362351CASRc.192T>G (p.Asn64Lys)
c.9+2713T>G (p.=)
n.51T>G
3g.122257088T>ACA354362352CASRc.193T>A (p.Phe65Ile)
c.9+2714T>A (p.=)
n.52T>A
3g.122257088T>CCA354362353CASRc.193T>C (p.Phe65Leu)
c.9+2714T>C (p.=)
n.52T>C
3g.122257088T>GCA354362354CASRc.193T>G (p.Phe65Val)
c.9+2714T>G (p.=)
n.52T>G
3g.122257089T>ACA354362355CASRc.194T>A (p.Phe65Tyr)
c.9+2715T>A (p.=)
n.53T>A
3g.122257089T>CCA354362356CASRc.194T>C (p.Phe65Ser)
c.9+2715T>C (p.=)
n.53T>C
3g.122257089T>GCA354362357CASRc.194T>G (p.Phe65Cys)
c.9+2715T>G (p.=)
n.53T>G
3g.122257090C>ACA354362358CASRc.195C>A (p.Phe65Leu)
c.9+2716C>A (p.=)
n.54C>A
3g.122257090C>GCA354362359CASRc.195C>G (p.Phe65Leu)
c.9+2716C>G (p.=)
n.54C>G
3g.122257090C>TCA435403987CASRc.195C>T (p.Phe65=)
c.9+2716C>T (p.=)
n.54C>T
COSMIC
3g.122257091C>ACA354362360CASRc.196C>A (p.Arg66Ser)
c.9+2717C>A (p.=)
n.55C>A
3g.122257091C>GCA354362361CASRc.196C>G (p.Arg66Gly)
c.9+2717C>G (p.=)
n.55C>G
3g.122257091C>TCA119507CASRc.196C>T (p.Arg66Cys)
c.9+2717C>T (p.=)
n.55C>T
ClinVar dbSNP
3g.122257092G>ACA354362364CASRc.197G>A (p.Arg66His)
c.9+2718G>A (p.=)
n.56G>A
ClinVar COSMIC
3g.122257092G>CCA354362363CASRc.197G>C (p.Arg66Pro)
c.9+2718G>C (p.=)
n.56G>C
3g.122257092G>TCA354362362CASRc.197G>T (p.Arg66Leu)
c.9+2718G>T (p.=)
n.56G>T
ClinVar COSMIC

Number of alleles fetched