Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.38349380A=CA2170811784SPRED1c.583-42A= (n.583-42A=)
c.619-42A= (n.619-42A=)
c.361-42A= (n.361-42A=)
c.520-42A= (n.520-42A=)
15g.38349380A>GCA7470127SPRED1c.583-42A>G (n.583-42A>G)
c.619-42A>G (n.619-42A>G)
c.361-42A>G (n.361-42A>G)
c.520-42A>G (n.520-42A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349383delCA2627716018SPRED1c.583-39del (n.583-39del)
c.619-39del (n.619-39del)
c.361-39del (n.361-39del)
c.520-39del (n.520-39del)
 gnomAD v4
15g.38349380_38349381insCAAACAACCCCA2512594323SPRED1c.583-42_583-41insCAAACAACCC (n.583-42_583-41insCAAACAACCC)
c.619-42_619-41insCAAACAACCC (n.619-42_619-41insCAAACAACCC)
c.361-42_361-41insCAAACAACCC (n.361-42_361-41insCAAACAACCC)
c.520-42_520-41insCAAACAACCC (n.520-42_520-41insCAAACAACCC)
15g.38349382A=CA2170811785SPRED1c.583-40A= (n.583-40A=)
c.619-40A= (n.619-40A=)
c.361-40A= (n.361-40A=)
c.520-40A= (n.520-40A=)
15g.38349382A>CCA2170811786SPRED1c.583-40A>C (n.583-40A>C)
c.619-40A>C (n.619-40A>C)
c.361-40A>C (n.361-40A>C)
c.520-40A>C (n.520-40A>C)
 dbSNP
15g.38349385T>CCA7470128SPRED1c.583-37T>C (n.583-37T>C)
c.619-37T>C (n.619-37T>C)
c.361-37T>C (n.361-37T>C)
c.520-37T>C (n.520-37T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38349385T=CA2170811787SPRED1c.583-37T= (n.583-37T=)
c.619-37T= (n.619-37T=)
c.361-37T= (n.361-37T=)
c.520-37T= (n.520-37T=)
15g.38349385_38349393delinsTCTTGTGTCCA2170811788SPRED1c.583-37_583-29delinsTCTTGTGTC (n.583-37_583-29delinsTCTTGTGTC)
c.619-37_619-29delinsTCTTGTGTC (n.619-37_619-29delinsTCTTGTGTC)
c.361-37_361-29delinsTCTTGTGTC (n.361-37_361-29delinsTCTTGTGTC)
c.520-37_520-29delinsTCTTGTGTC (n.520-37_520-29delinsTCTTGTGTC)
15g.38349386C>ACA655988844SPRED1c.583-36C>A (n.583-36C>A)
c.619-36C>A (n.619-36C>A)
c.361-36C>A (n.361-36C>A)
c.520-36C>A (n.520-36C>A)
 dbSNP gnomAD v4 COSMIC COSMIC
15g.38349386_38349393delCA2170811789SPRED1c.583-36_583-29del (n.583-36_583-29del)
c.619-36_619-29del (n.619-36_619-29del)
c.361-36_361-29del (n.361-36_361-29del)
c.520-36_520-29del (n.520-36_520-29del)
 dbSNP
15g.38349387T>CCA617505698SPRED1c.583-35T>C (n.583-35T>C)
c.619-35T>C (n.619-35T>C)
c.361-35T>C (n.361-35T>C)
c.520-35T>C (n.520-35T>C)
 dbSNP gnomAD v2 gnomAD v4
15g.38349387T=CA2170811790SPRED1c.583-35T= (n.583-35T=)
c.619-35T= (n.619-35T=)
c.361-35T= (n.361-35T=)
c.520-35T= (n.520-35T=)
15g.38349388delCA2803806043SPRED1c.583-34del (n.583-34del)
c.619-34del (n.619-34del)
c.361-34del (n.361-34del)
c.520-34del (n.520-34del)
15g.38349389G>ACA7470129SPRED1c.583-33G>A (n.583-33G>A)
c.619-33G>A (n.619-33G>A)
c.361-33G>A (n.361-33G>A)
c.520-33G>A (n.520-33G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38349389G=CA2170811791SPRED1c.583-33G= (n.583-33G=)
c.619-33G= (n.619-33G=)
c.361-33G= (n.361-33G=)
c.520-33G= (n.520-33G=)
15g.38349389G>TCA269293275SPRED1c.583-33G>T (n.583-33G>T)
c.619-33G>T (n.619-33G>T)
c.361-33G>T (n.361-33G>T)
c.520-33G>T (n.520-33G>T)
 dbSNP gnomAD v4
15g.38349390T>CCA2575673283SPRED1c.583-32T>C (n.583-32T>C)
c.619-32T>C (n.619-32T>C)
c.361-32T>C (n.361-32T>C)
c.520-32T>C (n.520-32T>C)
15g.38349390T>GCA2575673284SPRED1c.583-32T>G (n.583-32T>G)
c.619-32T>G (n.619-32T>G)
c.361-32T>G (n.361-32T>G)
c.520-32T>G (n.520-32T>G)
15g.38349391G>TCA655988845SPRED1c.583-31G>T (n.583-31G>T)
c.619-31G>T (n.619-31G>T)
c.361-31G>T (n.361-31G>T)
c.520-31G>T (n.520-31G>T)
 COSMIC
15g.38349392T>GCA2170811793SPRED1c.583-30T>G (n.583-30T>G)
c.619-30T>G (n.619-30T>G)
c.361-30T>G (n.361-30T>G)
c.520-30T>G (n.520-30T>G)
 dbSNP
15g.38349392T=CA2170811792SPRED1c.583-30T= (n.583-30T=)
c.619-30T= (n.619-30T=)
c.361-30T= (n.361-30T=)
c.520-30T= (n.520-30T=)
15g.38349393C>ACA2627716019SPRED1c.583-29C>A (n.583-29C>A)
c.619-29C>A (n.619-29C>A)
c.361-29C>A (n.361-29C>A)
c.520-29C>A (n.520-29C>A)
 gnomAD v4
15g.38349395T>CCA2170811795SPRED1c.583-27T>C (n.583-27T>C)
c.619-27T>C (n.619-27T>C)
c.361-27T>C (n.361-27T>C)
c.520-27T>C (n.520-27T>C)
 dbSNP
15g.38349395T=CA2170811794SPRED1c.583-27T= (n.583-27T=)
c.619-27T= (n.619-27T=)
c.361-27T= (n.361-27T=)
c.520-27T= (n.520-27T=)
15g.38349397T>GCA2803806044SPRED1c.583-25T>G (n.583-25T>G)
c.619-25T>G (n.619-25T>G)
c.361-25T>G (n.361-25T>G)
c.520-25T>G (n.520-25T>G)
15g.38349398A=CA2170811796SPRED1c.583-24A= (n.583-24A=)
c.619-24A= (n.619-24A=)
c.361-24A= (n.361-24A=)
c.520-24A= (n.520-24A=)
15g.38349398A>GCA617505699SPRED1c.583-24A>G (n.583-24A>G)
c.619-24A>G (n.619-24A>G)
c.361-24A>G (n.361-24A>G)
c.520-24A>G (n.520-24A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38349398A>TCA2575673285SPRED1c.583-24A>T (n.583-24A>T)
c.619-24A>T (n.619-24A>T)
c.361-24A>T (n.361-24A>T)
c.520-24A>T (n.520-24A>T)
15g.38349399delCA2627716020SPRED1c.583-23del (n.583-23del)
c.619-23del (n.619-23del)
c.361-23del (n.361-23del)
c.520-23del (n.520-23del)
 gnomAD v4
15g.38349398_38349413delinsAAGTAGAAATTGTTTGCA2170811797SPRED1c.583-24_583-9delinsAAGTAGAAATTGTTTG (n.583-24_583-9delinsAAGTAGAAATTGTTTG)
c.619-24_619-9delinsAAGTAGAAATTGTTTG (n.619-24_619-9delinsAAGTAGAAATTGTTTG)
c.361-24_361-9delinsAAGTAGAAATTGTTTG (n.361-24_361-9delinsAAGTAGAAATTGTTTG)
c.520-24_520-9delinsAAGTAGAAATTGTTTG (n.520-24_520-9delinsAAGTAGAAATTGTTTG)
15g.38349399A>GCA2627716021SPRED1c.583-23A>G (n.583-23A>G)
c.619-23A>G (n.619-23A>G)
c.361-23A>G (n.361-23A>G)
c.520-23A>G (n.520-23A>G)
 gnomAD v4
15g.38349399_38349413delCA2170811798SPRED1c.583-23_583-9del (n.583-23_583-9del)
c.619-23_619-9del (n.619-23_619-9del)
c.361-23_361-9del (n.361-23_361-9del)
c.520-23_520-9del (n.520-23_520-9del)
 dbSNP
15g.38349400G>ACA617505700SPRED1c.583-22G>A (n.583-22G>A)
c.619-22G>A (n.619-22G>A)
c.361-22G>A (n.361-22G>A)
c.520-22G>A (n.520-22G>A)
 dbSNP gnomAD v2 gnomAD v4
15g.38349400G=CA2170811799SPRED1c.583-22G= (n.583-22G=)
c.619-22G= (n.619-22G=)
c.361-22G= (n.361-22G=)
c.520-22G= (n.520-22G=)
15g.38349402A>GCA2627716022SPRED1c.583-20A>G (n.583-20A>G)
c.619-20A>G (n.619-20A>G)
c.361-20A>G (n.361-20A>G)
c.520-20A>G (n.520-20A>G)
 gnomAD v4
15g.38349404A>CCA2573150668SPRED1c.583-18A>C (n.583-18A>C)
c.619-18A>C (n.619-18A>C)
c.361-18A>C (n.361-18A>C)
c.520-18A>C (n.520-18A>C)
 ClinVar dbSNP
15g.38349404A>GCA2627716023SPRED1c.583-18A>G (n.583-18A>G)
c.619-18A>G (n.619-18A>G)
c.361-18A>G (n.361-18A>G)
c.520-18A>G (n.520-18A>G)
 gnomAD v4
15g.38349405A>GCA2627716024SPRED1c.583-17A>G (n.583-17A>G)
c.619-17A>G (n.619-17A>G)
c.361-17A>G (n.361-17A>G)
c.520-17A>G (n.520-17A>G)
 gnomAD v4
15g.38349406A=CA2170811800SPRED1c.583-16A= (n.583-16A=)
c.619-16A= (n.619-16A=)
c.361-16A= (n.361-16A=)
c.520-16A= (n.520-16A=)
15g.38349406A>GCA7470130SPRED1c.583-16A>G (n.583-16A>G)
c.619-16A>G (n.619-16A>G)
c.361-16A>G (n.361-16A>G)
c.520-16A>G (n.520-16A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349407T>CCA7470131SPRED1c.583-15T>C (n.583-15T>C)
c.619-15T>C (n.619-15T>C)
c.361-15T>C (n.361-15T>C)
c.520-15T>C (n.520-15T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38349407T=CA2170811801SPRED1c.583-15T= (n.583-15T=)
c.619-15T= (n.619-15T=)
c.361-15T= (n.361-15T=)
c.520-15T= (n.520-15T=)
15g.38349411_38349414delCA2580613791SPRED1c.583-11_583-8del (n.583-11_583-8del)
c.619-11_619-8del (n.619-11_619-8del)
c.361-11_361-8del (n.361-11_361-8del)
c.520-11_520-8del (n.520-11_520-8del)
 ClinVar gnomAD v4
15g.38349409G>CCA968817096SPRED1c.583-13G>C (n.583-13G>C)
c.619-13G>C (n.619-13G>C)
c.361-13G>C (n.361-13G>C)
c.520-13G>C (n.520-13G>C)
 dbSNP gnomAD v3 gnomAD v4
15g.38349409G=CA2170811802SPRED1c.583-13G= (n.583-13G=)
c.619-13G= (n.619-13G=)
c.361-13G= (n.361-13G=)
c.520-13G= (n.520-13G=)
15g.38349410T>CCA7470132SPRED1c.583-12T>C (n.583-12T>C)
c.619-12T>C (n.619-12T>C)
c.361-12T>C (n.361-12T>C)
c.520-12T>C (n.520-12T>C)
 dbSNP ExAC gnomAD v2
15g.38349410T=CA2170811803SPRED1c.583-12T= (n.583-12T=)
c.619-12T= (n.619-12T=)
c.361-12T= (n.361-12T=)
c.520-12T= (n.520-12T=)
15g.38349412T>CCA2627716025SPRED1c.583-10T>C (n.583-10T>C)
c.619-10T>C (n.619-10T>C)
c.361-10T>C (n.361-10T>C)
c.520-10T>C (n.520-10T>C)
 gnomAD v4
15g.38349413G>ACA2575673286SPRED1c.583-9G>A (n.583-9G>A)
c.619-9G>A (n.619-9G>A)
c.361-9G>A (n.361-9G>A)
c.520-9G>A (n.520-9G>A)
15g.38349413G=CA2170811804SPRED1c.583-9G= (n.583-9G=)
c.619-9G= (n.619-9G=)
c.361-9G= (n.361-9G=)
c.520-9G= (n.520-9G=)
15g.38349413G>TCA617505701SPRED1c.583-9G>T (n.583-9G>T)
c.619-9G>T (n.619-9G>T)
c.361-9G>T (n.361-9G>T)
c.520-9G>T (n.520-9G>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38349413_38349414insCCCCA2170811805SPRED1c.583-9_583-8insCCC (n.583-9_583-8insCCC)
c.619-9_619-8insCCC (n.619-9_619-8insCCC)
c.361-9_361-8insCCC (n.361-9_361-8insCCC)
c.520-9_520-8insCCC (n.520-9_520-8insCCC)
 dbSNP
15g.38349414T>CCA7470133SPRED1c.583-8T>C (n.583-8T>C)
c.619-8T>C (n.619-8T>C)
c.361-8T>C (n.361-8T>C)
c.520-8T>C (n.520-8T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349414T=CA2170811806SPRED1c.583-8T= (n.583-8T=)
c.619-8T= (n.619-8T=)
c.361-8T= (n.361-8T=)
c.520-8T= (n.520-8T=)
15g.38349415A=CA2170811807SPRED1c.583-7A= (n.583-7A=)
c.619-7A= (n.619-7A=)
c.361-7A= (n.361-7A=)
c.520-7A= (n.520-7A=)
15g.38349415A>GCA142280SPRED1c.583-7A>G (n.583-7A>G)
c.619-7A>G (n.619-7A>G)
c.361-7A>G (n.361-7A>G)
c.520-7A>G (n.520-7A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38349420A>CCA391932762SPRED1c.583-2A>C (n.583-2A>C)
c.619-2A>C (n.619-2A>C)
c.361-2A>C (n.361-2A>C)
c.520-2A>C (n.520-2A>C)
15g.38349420A>GCA391932760SPRED1c.583-2A>G (n.583-2A>G)
c.619-2A>G (n.619-2A>G)
c.361-2A>G (n.361-2A>G)
c.520-2A>G (n.520-2A>G)
15g.38349420A>TCA391932761SPRED1c.583-2A>T (n.583-2A>T)
c.619-2A>T (n.619-2A>T)
c.361-2A>T (n.361-2A>T)
c.520-2A>T (n.520-2A>T)
15g.38349421G>ACA391932763SPRED1c.583-1G>A (n.583-1G>A)
c.619-1G>A (n.619-1G>A)
c.361-1G>A (n.361-1G>A)
c.520-1G>A (n.520-1G>A)
15g.38349421G>CCA391932764SPRED1c.583-1G>C (n.583-1G>C)
c.619-1G>C (n.619-1G>C)
c.361-1G>C (n.361-1G>C)
c.520-1G>C (n.520-1G>C)
15g.38349421G>TCA391932765SPRED1c.583-1G>T (n.583-1G>T)
c.619-1G>T (n.619-1G>T)
c.361-1G>T (n.361-1G>T)
c.520-1G>T (n.520-1G>T)
15g.38349422A=CA2170811808SPRED1c.583A= (p.Ile195=)
c.619A= (p.Ile207=)
c.361A= (p.Ile121=)
c.520A= (p.Ile174=)
15g.38349422A>CCA391932766SPRED1c.583A>C (p.Ile195Leu)
c.619A>C (p.Ile207Leu)
c.361A>C (p.Ile121Leu)
c.520A>C (p.Ile174Leu)
15g.38349422A>GCA391932767SPRED1c.583A>G (p.Ile195Val)
c.619A>G (p.Ile207Val)
c.361A>G (p.Ile121Val)
c.520A>G (p.Ile174Val)
 dbSNP gnomAD v2 gnomAD v4
15g.38349422A>TCA391932768SPRED1c.583A>T (p.Ile195Leu)
c.619A>T (p.Ile207Leu)
c.361A>T (p.Ile121Leu)
c.520A>T (p.Ile174Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.38349423T>ACA391932769SPRED1c.584T>A (p.Ile195Lys)
c.620T>A (p.Ile207Lys)
c.362T>A (p.Ile121Lys)
c.521T>A (p.Ile174Lys)
 ClinVar dbSNP gnomAD v4
15g.38349423T>CCA391932770SPRED1c.584T>C (p.Ile195Thr)
c.620T>C (p.Ile207Thr)
c.362T>C (p.Ile121Thr)
c.521T>C (p.Ile174Thr)
 dbSNP gnomAD v2 gnomAD v4
15g.38349423T>GCA391932771SPRED1c.584T>G (p.Ile195Arg)
c.620T>G (p.Ile207Arg)
c.362T>G (p.Ile121Arg)
c.521T>G (p.Ile174Arg)
15g.38349423T=CA2170811809SPRED1c.584T= (p.Ile195=)
c.620T= (p.Ile207=)
c.362T= (p.Ile121=)
c.521T= (p.Ile174=)
15g.38349424A>CCA489922822SPRED1c.585A>C (p.Ile195=)
c.621A>C (p.Ile207=)
c.363A>C (p.Ile121=)
c.522A>C (p.Ile174=)
15g.38349424A>GCA391932772SPRED1c.585A>G (p.Ile195Met)
c.621A>G (p.Ile207Met)
c.363A>G (p.Ile121Met)
c.522A>G (p.Ile174Met)
15g.38349424A>TCA489922823SPRED1c.585A>T (p.Ile195=)
c.621A>T (p.Ile207=)
c.363A>T (p.Ile121=)
c.522A>T (p.Ile174=)
15g.38349425A>CCA391932773SPRED1c.586A>C (p.Thr196Pro)
c.622A>C (p.Thr208Pro)
c.364A>C (p.Thr122Pro)
c.523A>C (p.Thr175Pro)
15g.38349425A>GCA391932774SPRED1c.586A>G (p.Thr196Ala)
c.622A>G (p.Thr208Ala)
c.364A>G (p.Thr122Ala)
c.523A>G (p.Thr175Ala)
15g.38349425A>TCA391932775SPRED1c.586A>T (p.Thr196Ser)
c.622A>T (p.Thr208Ser)
c.364A>T (p.Thr122Ser)
c.523A>T (p.Thr175Ser)
15g.38349426C>ACA391932776SPRED1c.587C>A (p.Thr196Lys)
c.623C>A (p.Thr208Lys)
c.365C>A (p.Thr122Lys)
c.524C>A (p.Thr175Lys)
 gnomAD v4
15g.38349426C=CA2170811810SPRED1c.587C= (p.Thr196=)
c.623C= (p.Thr208=)
c.365C= (p.Thr122=)
c.524C= (p.Thr175=)
15g.38349426C>GCA391932777SPRED1c.587C>G (p.Thr196Arg)
c.623C>G (p.Thr208Arg)
c.365C>G (p.Thr122Arg)
c.524C>G (p.Thr175Arg)
15g.38349426C>TCA501231SPRED1c.587C>T (p.Thr196Ile)
c.623C>T (p.Thr208Ile)
c.365C>T (p.Thr122Ile)
c.524C>T (p.Thr175Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38349427A>CCA489922826SPRED1c.588A>C (p.Thr196=)
c.624A>C (p.Thr208=)
c.366A>C (p.Thr122=)
c.525A>C (p.Thr175=)
15g.38349427A>GCA489922825SPRED1c.588A>G (p.Thr196=)
c.624A>G (p.Thr208=)
c.366A>G (p.Thr122=)
c.525A>G (p.Thr175=)
15g.38349427A>TCA489922824SPRED1c.588A>T (p.Thr196=)
c.624A>T (p.Thr208=)
c.366A>T (p.Thr122=)
c.525A>T (p.Thr175=)
 ClinVar gnomAD v4
15g.38349428T>ACA391932779SPRED1c.589T>A (p.Phe197Ile)
c.625T>A (p.Phe209Ile)
c.367T>A (p.Phe123Ile)
c.526T>A (p.Phe176Ile)
15g.38349428T>CCA391932778SPRED1c.589T>C (p.Phe197Leu)
c.625T>C (p.Phe209Leu)
c.367T>C (p.Phe123Leu)
c.526T>C (p.Phe176Leu)
 gnomAD v4
15g.38349428T>GCA391932780SPRED1c.589T>G (p.Phe197Val)
c.625T>G (p.Phe209Val)
c.367T>G (p.Phe123Val)
c.526T>G (p.Phe176Val)
15g.38349429T>ACA391932781SPRED1c.590T>A (p.Phe197Tyr)
c.626T>A (p.Phe209Tyr)
c.368T>A (p.Phe123Tyr)
c.527T>A (p.Phe176Tyr)
15g.38349429T>CCA391932782SPRED1c.590T>C (p.Phe197Ser)
c.626T>C (p.Phe209Ser)
c.368T>C (p.Phe123Ser)
c.527T>C (p.Phe176Ser)
15g.38349429T>GCA391932783SPRED1c.590T>G (p.Phe197Cys)
c.626T>G (p.Phe209Cys)
c.368T>G (p.Phe123Cys)
c.527T>G (p.Phe176Cys)
15g.38349430T>ACA391932784SPRED1c.591T>A (p.Phe197Leu)
c.627T>A (p.Phe209Leu)
c.369T>A (p.Phe123Leu)
c.528T>A (p.Phe176Leu)
15g.38349430T>CCA489922827SPRED1c.591T>C (p.Phe197=)
c.627T>C (p.Phe209=)
c.369T>C (p.Phe123=)
c.528T>C (p.Phe176=)
 COSMIC
15g.38349430T>GCA391932785SPRED1c.591T>G (p.Phe197Leu)
c.627T>G (p.Phe209Leu)
c.369T>G (p.Phe123Leu)
c.528T>G (p.Phe176Leu)
15g.38349431G>ACA391932786SPRED1c.592G>A (p.Gly198Ser)
c.628G>A (p.Gly210Ser)
c.370G>A (p.Gly124Ser)
c.529G>A (p.Gly177Ser)
15g.38349431G>CCA391932787SPRED1c.592G>C (p.Gly198Arg)
c.628G>C (p.Gly210Arg)
c.370G>C (p.Gly124Arg)
c.529G>C (p.Gly177Arg)
15g.38349431G=CA2170811811SPRED1c.592G= (p.Gly198=)
c.628G= (p.Gly210=)
c.370G= (p.Gly124=)
c.529G= (p.Gly177=)
15g.38349431G>TCA391932788SPRED1c.592G>T (p.Gly198Cys)
c.628G>T (p.Gly210Cys)
c.370G>T (p.Gly124Cys)
c.529G>T (p.Gly177Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38349432G>ACA391932789SPRED1c.593G>A (p.Gly198Asp)
c.629G>A (p.Gly210Asp)
c.371G>A (p.Gly124Asp)
c.530G>A (p.Gly177Asp)
15g.38349432G>CCA391932790SPRED1c.593G>C (p.Gly198Ala)
c.629G>C (p.Gly210Ala)
c.371G>C (p.Gly124Ala)
c.530G>C (p.Gly177Ala)
 ClinVar dbSNP gnomAD v4
15g.38349432G=CA2170811812SPRED1c.593G= (p.Gly198=)
c.629G= (p.Gly210=)
c.371G= (p.Gly124=)
c.530G= (p.Gly177=)
15g.38349432G>TCA391932791SPRED1c.593G>T (p.Gly198Val)
c.629G>T (p.Gly210Val)
c.371G>T (p.Gly124Val)
c.530G>T (p.Gly177Val)
15g.38349433T>ACA489922828SPRED1c.594T>A (p.Gly198=)
c.630T>A (p.Gly210=)
c.372T>A (p.Gly124=)
c.531T>A (p.Gly177=)
15g.38349433T>CCA7470134SPRED1c.594T>C (p.Gly198=)
c.630T>C (p.Gly210=)
c.372T>C (p.Gly124=)
c.531T>C (p.Gly177=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38349433T>GCA489922829SPRED1c.594T>G (p.Gly198=)
c.630T>G (p.Gly210=)
c.372T>G (p.Gly124=)
c.531T>G (p.Gly177=)
 gnomAD v4
15g.38349433T=CA2170811813SPRED1c.594T= (p.Gly198=)
c.630T= (p.Gly210=)
c.372T= (p.Gly124=)
c.531T= (p.Gly177=)
15g.38349434C>ACA391932794SPRED1c.595C>A (p.Gln199Lys)
c.631C>A (p.Gln211Lys)
c.373C>A (p.Gln125Lys)
c.532C>A (p.Gln178Lys)
 gnomAD v4
15g.38349434C>GCA391932792SPRED1c.595C>G (p.Gln199Glu)
c.631C>G (p.Gln211Glu)
c.373C>G (p.Gln125Glu)
c.532C>G (p.Gln178Glu)
15g.38349434C>TCA391932793SPRED1c.595C>T (p.Gln199Ter)
c.631C>T (p.Gln211Ter)
c.373C>T (p.Gln125Ter)
c.532C>T (p.Gln178Ter)
15g.38349435A>CCA391932795SPRED1c.596A>C (p.Gln199Pro)
c.632A>C (p.Gln211Pro)
c.374A>C (p.Gln125Pro)
c.533A>C (p.Gln178Pro)
15g.38349435A>GCA391932796SPRED1c.596A>G (p.Gln199Arg)
c.632A>G (p.Gln211Arg)
c.374A>G (p.Gln125Arg)
c.533A>G (p.Gln178Arg)
15g.38349435A>TCA391932797SPRED1c.596A>T (p.Gln199Leu)
c.632A>T (p.Gln211Leu)
c.374A>T (p.Gln125Leu)
c.533A>T (p.Gln178Leu)
15g.38349436G>ACA489922830SPRED1c.597G>A (p.Gln199=)
c.633G>A (p.Gln211=)
c.375G>A (p.Gln125=)
c.534G>A (p.Gln178=)
 dbSNP
15g.38349436G>CCA391932798SPRED1c.597G>C (p.Gln199His)
c.633G>C (p.Gln211His)
c.375G>C (p.Gln125His)
c.534G>C (p.Gln178His)
15g.38349436G=CA2170811814SPRED1c.597G= (p.Gln199=)
c.633G= (p.Gln211=)
c.375G= (p.Gln125=)
c.534G= (p.Gln178=)
15g.38349436G>TCA391932799SPRED1c.597G>T (p.Gln199His)
c.633G>T (p.Gln211His)
c.375G>T (p.Gln125His)
c.534G>T (p.Gln178His)
 gnomAD v4
15g.38349437C>ACA391932800SPRED1c.598C>A (p.Pro200Thr)
c.634C>A (p.Pro212Thr)
c.376C>A (p.Pro126Thr)
c.535C>A (p.Pro179Thr)
15g.38349437C>GCA391932801SPRED1c.598C>G (p.Pro200Ala)
c.634C>G (p.Pro212Ala)
c.376C>G (p.Pro126Ala)
c.535C>G (p.Pro179Ala)
15g.38349437C>TCA391932802SPRED1c.598C>T (p.Pro200Ser)
c.634C>T (p.Pro212Ser)
c.376C>T (p.Pro126Ser)
c.535C>T (p.Pro179Ser)
15g.38349438C>ACA391932803SPRED1c.599C>A (p.Pro200Gln)
c.635C>A (p.Pro212Gln)
c.377C>A (p.Pro126Gln)
c.536C>A (p.Pro179Gln)
15g.38349438C=CA2170811815SPRED1c.599C= (p.Pro200=)
c.635C= (p.Pro212=)
c.377C= (p.Pro126=)
c.536C= (p.Pro179=)
15g.38349438C>GCA391932804SPRED1c.599C>G (p.Pro200Arg)
c.635C>G (p.Pro212Arg)
c.377C>G (p.Pro126Arg)
c.536C>G (p.Pro179Arg)
15g.38349438C>TCA7470135SPRED1c.599C>T (p.Pro200Leu)
c.635C>T (p.Pro212Leu)
c.377C>T (p.Pro126Leu)
c.536C>T (p.Pro179Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349439A>CCA489922833SPRED1c.600A>C (p.Pro200=)
c.636A>C (p.Pro212=)
c.378A>C (p.Pro126=)
c.537A>C (p.Pro179=)
15g.38349439A>GCA489922831SPRED1c.600A>G (p.Pro200=)
c.636A>G (p.Pro212=)
c.378A>G (p.Pro126=)
c.537A>G (p.Pro179=)
 gnomAD v4
15g.38349439A>TCA489922832SPRED1c.600A>T (p.Pro200=)
c.636A>T (p.Pro212=)
c.378A>T (p.Pro126=)
c.537A>T (p.Pro179=)
15g.38349440G>ACA391932807SPRED1c.601G>A (p.Gly201Ser)
c.637G>A (p.Gly213Ser)
c.379G>A (p.Gly127Ser)
c.538G>A (p.Gly180Ser)
15g.38349440G>CCA391932806SPRED1c.601G>C (p.Gly201Arg)
c.637G>C (p.Gly213Arg)
c.379G>C (p.Gly127Arg)
c.538G>C (p.Gly180Arg)
15g.38349440G>TCA391932805SPRED1c.601G>T (p.Gly201Cys)
c.637G>T (p.Gly213Cys)
c.379G>T (p.Gly127Cys)
c.538G>T (p.Gly180Cys)
15g.38349441G>ACA391932808SPRED1c.602G>A (p.Gly201Asp)
c.638G>A (p.Gly213Asp)
c.380G>A (p.Gly127Asp)
c.539G>A (p.Gly180Asp)
15g.38349441G>CCA391932809SPRED1c.602G>C (p.Gly201Ala)
c.638G>C (p.Gly213Ala)
c.380G>C (p.Gly127Ala)
c.539G>C (p.Gly180Ala)
 gnomAD v4
15g.38349441G=CA2170811816SPRED1c.602G= (p.Gly201=)
c.638G= (p.Gly213=)
c.380G= (p.Gly127=)
c.539G= (p.Gly180=)
15g.38349441G>TCA391932810SPRED1c.602G>T (p.Gly201Val)
c.638G>T (p.Gly213Val)
c.380G>T (p.Gly127Val)
c.539G>T (p.Gly180Val)
 ClinVar dbSNP
15g.38349442C>ACA489922834SPRED1c.603C>A (p.Gly201=)
c.639C>A (p.Gly213=)
c.381C>A (p.Gly127=)
c.540C>A (p.Gly180=)
15g.38349442C=CA2170811817SPRED1c.603C= (p.Gly201=)
c.639C= (p.Gly213=)
c.381C= (p.Gly127=)
c.540C= (p.Gly180=)
15g.38349442C>GCA489922835SPRED1c.603C>G (p.Gly201=)
c.639C>G (p.Gly213=)
c.381C>G (p.Gly127=)
c.540C>G (p.Gly180=)
 dbSNP gnomAD v3 gnomAD v4
15g.38349442C>TCA489922836SPRED1c.603C>T (p.Gly201=)
c.639C>T (p.Gly213=)
c.381C>T (p.Gly127=)
c.540C>T (p.Gly180=)
15g.38349443T>ACA391932811SPRED1c.604T>A (p.Leu202Met)
c.640T>A (p.Leu214Met)
c.382T>A (p.Leu128Met)
c.541T>A (p.Leu181Met)
15g.38349443T>CCA489922837SPRED1c.604T>C (p.Leu202=)
c.640T>C (p.Leu214=)
c.382T>C (p.Leu128=)
c.541T>C (p.Leu181=)
 dbSNP
15g.38349443T>GCA391932812SPRED1c.604T>G (p.Leu202Val)
c.640T>G (p.Leu214Val)
c.382T>G (p.Leu128Val)
c.541T>G (p.Leu181Val)
 dbSNP gnomAD v4
15g.38349443T=CA2170811818SPRED1c.604T= (p.Leu202=)
c.640T= (p.Leu214=)
c.382T= (p.Leu128=)
c.541T= (p.Leu181=)
15g.38349444T>ACA391932813SPRED1c.605T>A (p.Leu202Ter)
c.641T>A (p.Leu214Ter)
c.383T>A (p.Leu128Ter)
c.542T>A (p.Leu181Ter)
15g.38349444T>CCA391932814SPRED1c.605T>C (p.Leu202Ser)
c.641T>C (p.Leu214Ser)
c.383T>C (p.Leu128Ser)
c.542T>C (p.Leu181Ser)
 ClinVar dbSNP
15g.38349444T>GCA391932815SPRED1c.605T>G (p.Leu202Trp)
c.641T>G (p.Leu214Trp)
c.383T>G (p.Leu128Trp)
c.542T>G (p.Leu181Trp)
15g.38349444T=CA2170811819SPRED1c.605T= (p.Leu202=)
c.641T= (p.Leu214=)
c.383T= (p.Leu128=)
c.542T= (p.Leu181=)
15g.38349445G>ACA489922838SPRED1c.606G>A (p.Leu202=)
c.642G>A (p.Leu214=)
c.384G>A (p.Leu128=)
c.543G>A (p.Leu181=)
 dbSNP
15g.38349445G>CCA391932816SPRED1c.606G>C (p.Leu202Phe)
c.642G>C (p.Leu214Phe)
c.384G>C (p.Leu128Phe)
c.543G>C (p.Leu181Phe)
15g.38349445G=CA2170811820SPRED1c.606G= (p.Leu202=)
c.642G= (p.Leu214=)
c.384G= (p.Leu128=)
c.543G= (p.Leu181=)
15g.38349445G>TCA391932817SPRED1c.606G>T (p.Leu202Phe)
c.642G>T (p.Leu214Phe)
c.384G>T (p.Leu128Phe)
c.543G>T (p.Leu181Phe)
15g.38349446G>ACA7470136SPRED1c.607G>A (p.Asp203Asn)
c.643G>A (p.Asp215Asn)
c.385G>A (p.Asp129Asn)
c.544G>A (p.Asp182Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349446G>CCA391932818SPRED1c.607G>C (p.Asp203His)
c.643G>C (p.Asp215His)
c.385G>C (p.Asp129His)
c.544G>C (p.Asp182His)
15g.38349446G=CA2170811821SPRED1c.607G= (p.Asp203=)
c.643G= (p.Asp215=)
c.385G= (p.Asp129=)
c.544G= (p.Asp182=)
15g.38349446G>TCA391932819SPRED1c.607G>T (p.Asp203Tyr)
c.643G>T (p.Asp215Tyr)
c.385G>T (p.Asp129Tyr)
c.544G>T (p.Asp182Tyr)
15g.38349447A>CCA391932822SPRED1c.608A>C (p.Asp203Ala)
c.644A>C (p.Asp215Ala)
c.386A>C (p.Asp129Ala)
c.545A>C (p.Asp182Ala)
15g.38349447A>GCA391932820SPRED1c.608A>G (p.Asp203Gly)
c.644A>G (p.Asp215Gly)
c.386A>G (p.Asp129Gly)
c.545A>G (p.Asp182Gly)
 gnomAD v4
15g.38349447A>TCA391932821SPRED1c.608A>T (p.Asp203Val)
c.644A>T (p.Asp215Val)
c.386A>T (p.Asp129Val)
c.545A>T (p.Asp182Val)
15g.38349448C>ACA391932823SPRED1c.609C>A (p.Asp203Glu)
c.645C>A (p.Asp215Glu)
c.387C>A (p.Asp129Glu)
c.546C>A (p.Asp182Glu)
15g.38349448C>GCA391932824SPRED1c.609C>G (p.Asp203Glu)
c.645C>G (p.Asp215Glu)
c.387C>G (p.Asp129Glu)
c.546C>G (p.Asp182Glu)
15g.38349448C>TCA489922839SPRED1c.609C>T (p.Asp203=)
c.645C>T (p.Asp215=)
c.387C>T (p.Asp129=)
c.546C>T (p.Asp182=)
15g.38349449A=CA2170811822SPRED1c.610A= (p.Ile204=)
c.646A= (p.Ile216=)
c.388A= (p.Ile130=)
c.547A= (p.Ile183=)
15g.38349449A>CCA391932825SPRED1c.610A>C (p.Ile204Leu)
c.646A>C (p.Ile216Leu)
c.388A>C (p.Ile130Leu)
c.547A>C (p.Ile183Leu)
15g.38349449A>GCA7470137SPRED1c.610A>G (p.Ile204Val)
c.646A>G (p.Ile216Val)
c.388A>G (p.Ile130Val)
c.547A>G (p.Ile183Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349449A>TCA391932826SPRED1c.610A>T (p.Ile204Phe)
c.646A>T (p.Ile216Phe)
c.388A>T (p.Ile130Phe)
c.547A>T (p.Ile183Phe)
 gnomAD v4
15g.38349450T>ACA391932827SPRED1c.611T>A (p.Ile204Asn)
c.647T>A (p.Ile216Asn)
c.389T>A (p.Ile130Asn)
c.548T>A (p.Ile183Asn)
15g.38349450T>CCA391932828SPRED1c.611T>C (p.Ile204Thr)
c.647T>C (p.Ile216Thr)
c.389T>C (p.Ile130Thr)
c.548T>C (p.Ile183Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38349450T>GCA391932829SPRED1c.611T>G (p.Ile204Ser)
c.647T>G (p.Ile216Ser)
c.389T>G (p.Ile130Ser)
c.548T>G (p.Ile183Ser)
15g.38349450T=CA2170811823SPRED1c.611T= (p.Ile204=)
c.647T= (p.Ile216=)
c.389T= (p.Ile130=)
c.548T= (p.Ile183=)
15g.38349451T>ACA489922840SPRED1c.612T>A (p.Ile204=)
c.648T>A (p.Ile216=)
c.390T>A (p.Ile130=)
c.549T>A (p.Ile183=)
15g.38349451T>CCA489922841SPRED1c.612T>C (p.Ile204=)
c.648T>C (p.Ile216=)
c.390T>C (p.Ile130=)
c.549T>C (p.Ile183=)
15g.38349451T>GCA391932830SPRED1c.612T>G (p.Ile204Met)
c.648T>G (p.Ile216Met)
c.390T>G (p.Ile130Met)
c.549T>G (p.Ile183Met)
15g.38349452C>ACA391932831SPRED1c.613C>A (p.Gln205Lys)
c.649C>A (p.Gln217Lys)
c.391C>A (p.Gln131Lys)
c.550C>A (p.Gln184Lys)
15g.38349452C>GCA391932832SPRED1c.613C>G (p.Gln205Glu)
c.649C>G (p.Gln217Glu)
c.391C>G (p.Gln131Glu)
c.550C>G (p.Gln184Glu)
 dbSNP gnomAD v3
15g.38349452C>TCA391932833SPRED1c.613C>T (p.Gln205Ter)
c.649C>T (p.Gln217Ter)
c.391C>T (p.Gln131Ter)
c.550C>T (p.Gln184Ter)
 ClinVar dbSNP COSMIC
15g.38349453A=CA2170811824SPRED1c.614A= (p.Gln205=)
c.650A= (p.Gln217=)
c.392A= (p.Gln131=)
c.551A= (p.Gln184=)
15g.38349453A>CCA391932835SPRED1c.614A>C (p.Gln205Pro)
c.650A>C (p.Gln217Pro)
c.392A>C (p.Gln131Pro)
c.551A>C (p.Gln184Pro)
15g.38349453A>GCA7470138SPRED1c.614A>G (p.Gln205Arg)
c.650A>G (p.Gln217Arg)
c.392A>G (p.Gln131Arg)
c.551A>G (p.Gln184Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349453A>TCA391932834SPRED1c.614A>T (p.Gln205Leu)
c.650A>T (p.Gln217Leu)
c.392A>T (p.Gln131Leu)
c.551A>T (p.Gln184Leu)
15g.38349454G>ACA489922842SPRED1c.615G>A (p.Gln205=)
c.651G>A (p.Gln217=)
c.393G>A (p.Gln131=)
c.552G>A (p.Gln184=)
15g.38349454G>CCA391932836SPRED1c.615G>C (p.Gln205His)
c.651G>C (p.Gln217His)
c.393G>C (p.Gln131His)
c.552G>C (p.Gln184His)
15g.38349454G>TCA391932837SPRED1c.615G>T (p.Gln205His)
c.651G>T (p.Gln217His)
c.393G>T (p.Gln131His)
c.552G>T (p.Gln184His)
15g.38349455A>CCA391932838SPRED1c.616A>C (p.Ser206Arg)
c.652A>C (p.Ser218Arg)
c.394A>C (p.Ser132Arg)
c.553A>C (p.Ser185Arg)
15g.38349455A>GCA391932839SPRED1c.616A>G (p.Ser206Gly)
c.652A>G (p.Ser218Gly)
c.394A>G (p.Ser132Gly)
c.553A>G (p.Ser185Gly)
15g.38349455A>TCA391932840SPRED1c.616A>T (p.Ser206Cys)
c.652A>T (p.Ser218Cys)
c.394A>T (p.Ser132Cys)
c.553A>T (p.Ser185Cys)
15g.38349456G>ACA391932841SPRED1c.617G>A (p.Ser206Asn)
c.653G>A (p.Ser218Asn)
c.395G>A (p.Ser132Asn)
c.554G>A (p.Ser185Asn)
 gnomAD v4
15g.38349456G>CCA391932842SPRED1c.617G>C (p.Ser206Thr)
c.653G>C (p.Ser218Thr)
c.395G>C (p.Ser132Thr)
c.554G>C (p.Ser185Thr)
15g.38349456G>TCA391932843SPRED1c.617G>T (p.Ser206Ile)
c.653G>T (p.Ser218Ile)
c.395G>T (p.Ser132Ile)
c.554G>T (p.Ser185Ile)
15g.38349457C>ACA391932844SPRED1c.618C>A (p.Ser206Arg)
c.654C>A (p.Ser218Arg)
c.396C>A (p.Ser132Arg)
c.555C>A (p.Ser185Arg)
15g.38349457C=CA2170811825SPRED1c.618C= (p.Ser206=)
c.654C= (p.Ser218=)
c.396C= (p.Ser132=)
c.555C= (p.Ser185=)
15g.38349457C>GCA7470139SPRED1c.618C>G (p.Ser206Arg)
c.654C>G (p.Ser218Arg)
c.396C>G (p.Ser132Arg)
c.555C>G (p.Ser185Arg)
 dbSNP ExAC gnomAD v2
15g.38349457C>TCA489922843SPRED1c.618C>T (p.Ser206=)
c.654C>T (p.Ser218=)
c.396C>T (p.Ser132=)
c.555C>T (p.Ser185=)
 COSMIC
15g.38349458A=CA2170811826SPRED1c.619A= (p.Arg207=)
c.655A= (p.Arg219=)
c.397A= (p.Arg133=)
c.556A= (p.Arg186=)
15g.38349458A>CCA7470140SPRED1c.619A>C (p.Arg207=)
c.655A>C (p.Arg219=)
c.397A>C (p.Arg133=)
c.556A>C (p.Arg186=)
 ClinVar dbSNP ExAC gnomAD v2
15g.38349458A>GCA391932845SPRED1c.619A>G (p.Arg207Gly)
c.655A>G (p.Arg219Gly)
c.397A>G (p.Arg133Gly)
c.556A>G (p.Arg186Gly)
15g.38349458A>TCA391932846SPRED1c.619A>T (p.Arg207Ter)
c.655A>T (p.Arg219Ter)
c.397A>T (p.Arg133Ter)
c.556A>T (p.Arg186Ter)
 ClinVar dbSNP
15g.38349459G>ACA391932849SPRED1c.620G>A (p.Arg207Lys)
c.656G>A (p.Arg219Lys)
c.398G>A (p.Arg133Lys)
c.557G>A (p.Arg186Lys)
15g.38349459G>CCA391932848SPRED1c.620G>C (p.Arg207Thr)
c.656G>C (p.Arg219Thr)
c.398G>C (p.Arg133Thr)
c.557G>C (p.Arg186Thr)
 ClinVar dbSNP gnomAD v4
15g.38349459G>TCA391932847SPRED1c.620G>T (p.Arg207Ile)
c.656G>T (p.Arg219Ile)
c.398G>T (p.Arg133Ile)
c.557G>T (p.Arg186Ile)
15g.38349460A>CCA391932850SPRED1c.621A>C (p.Arg207Ser)
c.657A>C (p.Arg219Ser)
c.399A>C (p.Arg133Ser)
c.558A>C (p.Arg186Ser)
15g.38349460A>GCA489922844SPRED1c.621A>G (p.Arg207=)
c.657A>G (p.Arg219=)
c.399A>G (p.Arg133=)
c.558A>G (p.Arg186=)
15g.38349460A>TCA391932851SPRED1c.621A>T (p.Arg207Ser)
c.657A>T (p.Arg219Ser)
c.399A>T (p.Arg133Ser)
c.558A>T (p.Arg186Ser)
15g.38349461A>CCA391932852SPRED1c.622A>C (p.Ser208Arg)
c.658A>C (p.Ser220Arg)
c.400A>C (p.Ser134Arg)
c.559A>C (p.Ser187Arg)
15g.38349461A>GCA391932853SPRED1c.622A>G (p.Ser208Gly)
c.658A>G (p.Ser220Gly)
c.400A>G (p.Ser134Gly)
c.559A>G (p.Ser187Gly)
15g.38349461A>TCA391932854SPRED1c.622A>T (p.Ser208Cys)
c.658A>T (p.Ser220Cys)
c.400A>T (p.Ser134Cys)
c.559A>T (p.Ser187Cys)
15g.38349462G>ACA391932855SPRED1c.623G>A (p.Ser208Asn)
c.659G>A (p.Ser220Asn)
c.401G>A (p.Ser134Asn)
c.560G>A (p.Ser187Asn)
15g.38349462G>CCA391932856SPRED1c.623G>C (p.Ser208Thr)
c.659G>C (p.Ser220Thr)
c.401G>C (p.Ser134Thr)
c.560G>C (p.Ser187Thr)
15g.38349462G>TCA391932857SPRED1c.623G>T (p.Ser208Ile)
c.659G>T (p.Ser220Ile)
c.401G>T (p.Ser134Ile)
c.560G>T (p.Ser187Ile)
15g.38349465_38349475delCA2695197208SPRED1c.626_636del (p.Met209ThrfsTer16)
c.662_672del (p.Met221ThrfsTer16)
c.404_414del (p.Met135ThrfsTer16)
c.563_573del (p.Met188ThrfsTer16)
 ClinVar
15g.38349463T>ACA391932858SPRED1c.624T>A (p.Ser208Arg)
c.660T>A (p.Ser220Arg)
c.402T>A (p.Ser134Arg)
c.561T>A (p.Ser187Arg)
15g.38349463T>CCA7470141SPRED1c.624T>C (p.Ser208=)
c.660T>C (p.Ser220=)
c.402T>C (p.Ser134=)
c.561T>C (p.Ser187=)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38349463T>GCA391932859SPRED1c.624T>G (p.Ser208Arg)
c.660T>G (p.Ser220Arg)
c.402T>G (p.Ser134Arg)
c.561T>G (p.Ser187Arg)
15g.38349463T=CA2170811827SPRED1c.624T= (p.Ser208=)
c.660T= (p.Ser220=)
c.402T= (p.Ser134=)
c.561T= (p.Ser187=)
15g.38349464A>CCA391932860SPRED1c.625A>C (p.Met209Leu)
c.661A>C (p.Met221Leu)
c.403A>C (p.Met135Leu)
c.562A>C (p.Met188Leu)
15g.38349464A>GCA391932861SPRED1c.625A>G (p.Met209Val)
c.661A>G (p.Met221Val)
c.403A>G (p.Met135Val)
c.562A>G (p.Met188Val)
15g.38349464A>TCA391932862SPRED1c.625A>T (p.Met209Leu)
c.661A>T (p.Met221Leu)
c.403A>T (p.Met135Leu)
c.562A>T (p.Met188Leu)
15g.38349465T>ACA391932864SPRED1c.626T>A (p.Met209Lys)
c.662T>A (p.Met221Lys)
c.404T>A (p.Met135Lys)
c.563T>A (p.Met188Lys)
15g.38349465T>CCA391932865SPRED1c.626T>C (p.Met209Thr)
c.662T>C (p.Met221Thr)
c.404T>C (p.Met135Thr)
c.563T>C (p.Met188Thr)
15g.38349465T>GCA391932863SPRED1c.626T>G (p.Met209Arg)
c.662T>G (p.Met221Arg)
c.404T>G (p.Met135Arg)
c.563T>G (p.Met188Arg)
15g.38349466G>ACA391932866SPRED1c.627G>A (p.Met209Ile)
c.663G>A (p.Met221Ile)
c.405G>A (p.Met135Ile)
c.564G>A (p.Met188Ile)
15g.38349466G>CCA391932867SPRED1c.627G>C (p.Met209Ile)
c.663G>C (p.Met221Ile)
c.405G>C (p.Met135Ile)
c.564G>C (p.Met188Ile)
15g.38349466G>TCA391932868SPRED1c.627G>T (p.Met209Ile)
c.663G>T (p.Met221Ile)
c.405G>T (p.Met135Ile)
c.564G>T (p.Met188Ile)
15g.38349467G>ACA391932869SPRED1c.628G>A (p.Glu210Lys)
c.664G>A (p.Glu222Lys)
c.406G>A (p.Glu136Lys)
c.565G>A (p.Glu189Lys)
15g.38349467G>CCA391932870SPRED1c.628G>C (p.Glu210Gln)
c.664G>C (p.Glu222Gln)
c.406G>C (p.Glu136Gln)
c.565G>C (p.Glu189Gln)
15g.38349467G>TCA391932871SPRED1c.628G>T (p.Glu210Ter)
c.664G>T (p.Glu222Ter)
c.406G>T (p.Glu136Ter)
c.565G>T (p.Glu189Ter)
15g.38349468A>CCA391932874SPRED1c.629A>C (p.Glu210Ala)
c.665A>C (p.Glu222Ala)
c.407A>C (p.Glu136Ala)
c.566A>C (p.Glu189Ala)
15g.38349468A>GCA391932872SPRED1c.629A>G (p.Glu210Gly)
c.665A>G (p.Glu222Gly)
c.407A>G (p.Glu136Gly)
c.566A>G (p.Glu189Gly)
15g.38349468A>TCA391932873SPRED1c.629A>T (p.Glu210Val)
c.665A>T (p.Glu222Val)
c.407A>T (p.Glu136Val)
c.566A>T (p.Glu189Val)
15g.38349469A>CCA391932875SPRED1c.630A>C (p.Glu210Asp)
c.666A>C (p.Glu222Asp)
c.408A>C (p.Glu136Asp)
c.567A>C (p.Glu189Asp)
15g.38349469A>GCA489922845SPRED1c.630A>G (p.Glu210=)
c.666A>G (p.Glu222=)
c.408A>G (p.Glu136=)
c.567A>G (p.Glu189=)
 gnomAD v4
15g.38349469A>TCA391932876SPRED1c.630A>T (p.Glu210Asp)
c.666A>T (p.Glu222Asp)
c.408A>T (p.Glu136Asp)
c.567A>T (p.Glu189Asp)
 ClinVar dbSNP
15g.38349470T>ACA391932877SPRED1c.631T>A (p.Tyr211Asn)
c.667T>A (p.Tyr223Asn)
c.409T>A (p.Tyr137Asn)
c.568T>A (p.Tyr190Asn)
 dbSNP
15g.38349470T>CCA391932878SPRED1c.631T>C (p.Tyr211His)
c.667T>C (p.Tyr223His)
c.409T>C (p.Tyr137His)
c.568T>C (p.Tyr190His)
 ClinVar
15g.38349470T>GCA391932879SPRED1c.631T>G (p.Tyr211Asp)
c.667T>G (p.Tyr223Asp)
c.409T>G (p.Tyr137Asp)
c.568T>G (p.Tyr190Asp)
15g.38349470T=CA2170811828SPRED1c.631T= (p.Tyr211=)
c.667T= (p.Tyr223=)
c.409T= (p.Tyr137=)
c.568T= (p.Tyr190=)
15g.38349471A>CCA391932880SPRED1c.632A>C (p.Tyr211Ser)
c.668A>C (p.Tyr223Ser)
c.410A>C (p.Tyr137Ser)
c.569A>C (p.Tyr190Ser)
15g.38349471A>GCA391932882SPRED1c.632A>G (p.Tyr211Cys)
c.668A>G (p.Tyr223Cys)
c.410A>G (p.Tyr137Cys)
c.569A>G (p.Tyr190Cys)
15g.38349471A>TCA391932881SPRED1c.632A>T (p.Tyr211Phe)
c.668A>T (p.Tyr223Phe)
c.410A>T (p.Tyr137Phe)
c.569A>T (p.Tyr190Phe)
15g.38349472C>ACA391932883SPRED1c.633C>A (p.Tyr211Ter)
c.669C>A (p.Tyr223Ter)
c.411C>A (p.Tyr137Ter)
c.570C>A (p.Tyr190Ter)
15g.38349472C=CA2170811829SPRED1c.633C= (p.Tyr211=)
c.669C= (p.Tyr223=)
c.411C= (p.Tyr137=)
c.570C= (p.Tyr190=)
15g.38349472C>GCA391932884SPRED1c.633C>G (p.Tyr211Ter)
c.669C>G (p.Tyr223Ter)
c.411C>G (p.Tyr137Ter)
c.570C>G (p.Tyr190Ter)
15g.38349472C>TCA7470142SPRED1c.633C>T (p.Tyr211=)
c.669C>T (p.Tyr223=)
c.411C>T (p.Tyr137=)
c.570C>T (p.Tyr190=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.38349473G>ACA7470143SPRED1c.634G>A (p.Val212Ile)
c.670G>A (p.Val224Ile)
c.412G>A (p.Val138Ile)
c.571G>A (p.Val191Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.38349473G>CCA391932885SPRED1c.634G>C (p.Val212Leu)
c.670G>C (p.Val224Leu)
c.412G>C (p.Val138Leu)
c.571G>C (p.Val191Leu)
15g.38349473G=CA2170811830SPRED1c.634G= (p.Val212=)
c.670G= (p.Val224=)
c.412G= (p.Val138=)
c.571G= (p.Val191=)
15g.38349473G>TCA391932886SPRED1c.634G>T (p.Val212Leu)
c.670G>T (p.Val224Leu)
c.412G>T (p.Val138Leu)
c.571G>T (p.Val191Leu)
15g.38349474T>ACA391932887SPRED1c.635T>A (p.Val212Glu)
c.671T>A (p.Val224Glu)
c.413T>A (p.Val138Glu)
c.572T>A (p.Val191Glu)
15g.38349474T>CCA391932888SPRED1c.635T>C (p.Val212Ala)
c.671T>C (p.Val224Ala)
c.413T>C (p.Val138Ala)
c.572T>C (p.Val191Ala)
15g.38349474T>GCA391932889SPRED1c.635T>G (p.Val212Gly)
c.671T>G (p.Val224Gly)
c.413T>G (p.Val138Gly)
c.572T>G (p.Val191Gly)
15g.38349475A=CA2170811831SPRED1c.636A= (p.Val212=)
c.672A= (p.Val224=)
c.414A= (p.Val138=)
c.573A= (p.Val191=)
15g.38349475A>CCA16606923SPRED1c.636A>C (p.Val212=)
c.672A>C (p.Val224=)
c.414A>C (p.Val138=)
c.573A>C (p.Val191=)
 ClinVar dbSNP
15g.38349475A>GCA489922846SPRED1c.636A>G (p.Val212=)
c.672A>G (p.Val224=)
c.414A>G (p.Val138=)
c.573A>G (p.Val191=)
15g.38349475A>TCA489922847SPRED1c.636A>T (p.Val212=)
c.672A>T (p.Val224=)
c.414A>T (p.Val138=)
c.573A>T (p.Val191=)
15g.38349476C>ACA391932890SPRED1c.637C>A (p.Gln213Lys)
c.673C>A (p.Gln225Lys)
c.415C>A (p.Gln139Lys)
c.574C>A (p.Gln192Lys)
15g.38349476C=CA2170811832SPRED1c.637C= (p.Gln213=)
c.673C= (p.Gln225=)
c.415C= (p.Gln139=)
c.574C= (p.Gln192=)
15g.38349476C>GCA391932891SPRED1c.637C>G (p.Gln213Glu)
c.673C>G (p.Gln225Glu)
c.415C>G (p.Gln139Glu)
c.574C>G (p.Gln192Glu)
15g.38349476C>TCA251957SPRED1c.637C>T (p.Gln213Ter)
c.673C>T (p.Gln225Ter)
c.415C>T (p.Gln139Ter)
c.574C>T (p.Gln192Ter)
 ClinVar dbSNP gnomAD v4
15g.38349477A>CCA391932893SPRED1c.638A>C (p.Gln213Pro)
c.674A>C (p.Gln225Pro)
c.416A>C (p.Gln139Pro)
c.575A>C (p.Gln192Pro)
 gnomAD v4
15g.38349477A>GCA391932894SPRED1c.638A>G (p.Gln213Arg)
c.674A>G (p.Gln225Arg)
c.416A>G (p.Gln139Arg)
c.575A>G (p.Gln192Arg)
15g.38349477A>TCA391932892SPRED1c.638A>T (p.Gln213Leu)
c.674A>T (p.Gln225Leu)
c.416A>T (p.Gln139Leu)
c.575A>T (p.Gln192Leu)
15g.38349478G>ACA489922848SPRED1c.639G>A (p.Gln213=)
c.675G>A (p.Gln225=)
c.417G>A (p.Gln139=)
c.576G>A (p.Gln192=)
 gnomAD v4
15g.38349478G>CCA391932896SPRED1c.639G>C (p.Gln213His)
c.675G>C (p.Gln225His)
c.417G>C (p.Gln139His)
c.576G>C (p.Gln192His)
15g.38349478G>TCA391932895SPRED1c.639G>T (p.Gln213His)
c.675G>T (p.Gln225His)
c.417G>T (p.Gln139His)
c.576G>T (p.Gln192His)
15g.38349479C>ACA269293276SPRED1c.640C>A (p.Arg214=)
c.676C>A (p.Arg226=)
c.418C>A (p.Arg140=)
c.577C>A (p.Arg193=)
 dbSNP
15g.38349479C=CA2170811833SPRED1c.640C= (p.Arg214=)
c.676C= (p.Arg226=)
c.418C= (p.Arg140=)
c.577C= (p.Arg193=)
15g.38349479C>GCA391932897SPRED1c.640C>G (p.Arg214Gly)
c.676C>G (p.Arg226Gly)
c.418C>G (p.Arg140Gly)
c.577C>G (p.Arg193Gly)
15g.38349479C>TCA7470144SPRED1c.640C>T (p.Arg214Trp)
c.676C>T (p.Arg226Trp)
c.418C>T (p.Arg140Trp)
c.577C>T (p.Arg193Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38349480G>ACA269293277SPRED1c.641G>A (p.Arg214Gln)
c.677G>A (p.Arg226Gln)
c.419G>A (p.Arg140Gln)
c.578G>A (p.Arg193Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38349480G>CCA391932899SPRED1c.641G>C (p.Arg214Pro)
c.677G>C (p.Arg226Pro)
c.419G>C (p.Arg140Pro)
c.578G>C (p.Arg193Pro)
15g.38349480G=CA2170811834SPRED1c.641G= (p.Arg214=)
c.677G= (p.Arg226=)
c.419G= (p.Arg140=)
c.578G= (p.Arg193=)
15g.38349480G>TCA391932898SPRED1c.641G>T (p.Arg214Leu)
c.677G>T (p.Arg226Leu)
c.419G>T (p.Arg140Leu)
c.578G>T (p.Arg193Leu)

Number of alleles fetched