Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.44953170A>CCA402325274SETBP1c.3830A>C (p.Asn1277Thr)
c.3908A>C (p.Asn1303Thr)
c.3353A>C (p.Asn1118Thr)
 gnomAD v4
18g.44953170A>GCA402325275SETBP1c.3830A>G (p.Asn1277Ser)
c.3908A>G (p.Asn1303Ser)
c.3353A>G (p.Asn1118Ser)
 ClinVar
18g.44953170A>TCA402325276SETBP1c.3830A>T (p.Asn1277Ile)
c.3908A>T (p.Asn1303Ile)
c.3353A>T (p.Asn1118Ile)
18g.44953171C>ACA402325277SETBP1c.3831C>A (p.Asn1277Lys)
c.3909C>A (p.Asn1303Lys)
c.3354C>A (p.Asn1118Lys)
18g.44953171C=CA2300141294SETBP1c.3831C= (p.Asn1277=)
c.3909C= (p.Asn1303=)
c.3354C= (p.Asn1118=)
18g.44953171C>GCA402325278SETBP1c.3831C>G (p.Asn1277Lys)
c.3909C>G (p.Asn1303Lys)
c.3354C>G (p.Asn1118Lys)
18g.44953171C>TCA503983032SETBP1c.3831C>T (p.Asn1277=)
c.3909C>T (p.Asn1303=)
c.3354C>T (p.Asn1118=)
 dbSNP gnomAD v4
18g.44953172C>ACA402325279SETBP1c.3832C>A (p.Leu1278Met)
c.3910C>A (p.Leu1304Met)
c.3355C>A (p.Leu1119Met)
18g.44953172C=CA2300141295SETBP1c.3832C= (p.Leu1278=)
c.3910C= (p.Leu1304=)
c.3355C= (p.Leu1119=)
18g.44953172C>GCA8945995SETBP1c.3832C>G (p.Leu1278Val)
c.3910C>G (p.Leu1304Val)
c.3355C>G (p.Leu1119Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953172C>TCA503983034SETBP1c.3832C>T (p.Leu1278=)
c.3910C>T (p.Leu1304=)
c.3355C>T (p.Leu1119=)
 ClinVar gnomAD v4
18g.44953173T>ACA402325280SETBP1c.3833T>A (p.Leu1278Gln)
c.3911T>A (p.Leu1304Gln)
c.3356T>A (p.Leu1119Gln)
18g.44953173T>CCA402325281SETBP1c.3833T>C (p.Leu1278Pro)
c.3911T>C (p.Leu1304Pro)
c.3356T>C (p.Leu1119Pro)
 gnomAD v4
18g.44953173T>GCA402325282SETBP1c.3833T>G (p.Leu1278Arg)
c.3911T>G (p.Leu1304Arg)
c.3356T>G (p.Leu1119Arg)
18g.44953174G>ACA503982788SETBP1c.3834G>A (p.Leu1278=)
c.3912G>A (p.Leu1304=)
c.3357G>A (p.Leu1119=)
18g.44953174G>CCA8945996SETBP1c.3834G>C (p.Leu1278=)
c.3912G>C (p.Leu1304=)
c.3357G>C (p.Leu1119=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953174G=CA2300141296SETBP1c.3834G= (p.Leu1278=)
c.3912G= (p.Leu1304=)
c.3357G= (p.Leu1119=)
18g.44953174G>TCA8945997SETBP1c.3834G>T (p.Leu1278=)
c.3912G>T (p.Leu1304=)
c.3357G>T (p.Leu1119=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953175G>ACA402325285SETBP1c.3835G>A (p.Asp1279Asn)
c.3913G>A (p.Asp1305Asn)
c.3358G>A (p.Asp1120Asn)
 ClinVar
18g.44953175G>CCA402325284SETBP1c.3835G>C (p.Asp1279His)
c.3913G>C (p.Asp1305His)
c.3358G>C (p.Asp1120His)
18g.44953175G>TCA402325283SETBP1c.3835G>T (p.Asp1279Tyr)
c.3913G>T (p.Asp1305Tyr)
c.3358G>T (p.Asp1120Tyr)
 gnomAD v4
18g.44953176A>CCA402325286SETBP1c.3836A>C (p.Asp1279Ala)
c.3914A>C (p.Asp1305Ala)
c.3359A>C (p.Asp1120Ala)
18g.44953176A>GCA402325287SETBP1c.3836A>G (p.Asp1279Gly)
c.3914A>G (p.Asp1305Gly)
c.3359A>G (p.Asp1120Gly)
18g.44953176A>TCA402325288SETBP1c.3836A>T (p.Asp1279Val)
c.3914A>T (p.Asp1305Val)
c.3359A>T (p.Asp1120Val)
18g.44953177C>ACA402325289SETBP1c.3837C>A (p.Asp1279Glu)
c.3915C>A (p.Asp1305Glu)
c.3360C>A (p.Asp1120Glu)
 dbSNP gnomAD v2 gnomAD v4
18g.44953177C=CA2300141297SETBP1c.3837C= (p.Asp1279=)
c.3915C= (p.Asp1305=)
c.3360C= (p.Asp1120=)
18g.44953177C>GCA402325290SETBP1c.3837C>G (p.Asp1279Glu)
c.3915C>G (p.Asp1305Glu)
c.3360C>G (p.Asp1120Glu)
18g.44953177C>TCA8945998SETBP1c.3837C>T (p.Asp1279=)
c.3915C>T (p.Asp1305=)
c.3360C>T (p.Asp1120=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953178G>ACA8945999SETBP1c.3838G>A (p.Val1280Met)
c.3916G>A (p.Val1306Met)
c.3361G>A (p.Val1121Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953178G>CCA402325291SETBP1c.3838G>C (p.Val1280Leu)
c.3916G>C (p.Val1306Leu)
c.3361G>C (p.Val1121Leu)
18g.44953178G=CA2300141298SETBP1c.3838G= (p.Val1280=)
c.3916G= (p.Val1306=)
c.3361G= (p.Val1121=)
18g.44953178G>TCA8946000SETBP1c.3838G>T (p.Val1280Leu)
c.3916G>T (p.Val1306Leu)
c.3361G>T (p.Val1121Leu)
 dbSNP ExAC gnomAD v4 COSMIC
18g.44953179T>ACA402325292SETBP1c.3839T>A (p.Val1280Glu)
c.3917T>A (p.Val1306Glu)
c.3362T>A (p.Val1121Glu)
 gnomAD v4
18g.44953179T>CCA402325293SETBP1c.3839T>C (p.Val1280Ala)
c.3917T>C (p.Val1306Ala)
c.3362T>C (p.Val1121Ala)
18g.44953179T>GCA402325294SETBP1c.3839T>G (p.Val1280Gly)
c.3917T>G (p.Val1306Gly)
c.3362T>G (p.Val1121Gly)
18g.44953180G>ACA503982816SETBP1c.3840G>A (p.Val1280=)
c.3918G>A (p.Val1306=)
c.3363G>A (p.Val1121=)
18g.44953180G>CCA503982814SETBP1c.3840G>C (p.Val1280=)
c.3918G>C (p.Val1306=)
c.3363G>C (p.Val1121=)
18g.44953180G>TCA503982812SETBP1c.3840G>T (p.Val1280=)
c.3918G>T (p.Val1306=)
c.3363G>T (p.Val1121=)
18g.44953181T>ACA402325296SETBP1c.3841T>A (p.Phe1281Ile)
c.3919T>A (p.Phe1307Ile)
c.3364T>A (p.Phe1122Ile)
18g.44953181T>CCA402325297SETBP1c.3841T>C (p.Phe1281Leu)
c.3919T>C (p.Phe1307Leu)
c.3364T>C (p.Phe1122Leu)
18g.44953181T>GCA402325295SETBP1c.3841T>G (p.Phe1281Val)
c.3919T>G (p.Phe1307Val)
c.3364T>G (p.Phe1122Val)
 gnomAD v4
18g.44953182T>ACA402325298SETBP1c.3842T>A (p.Phe1281Tyr)
c.3920T>A (p.Phe1307Tyr)
c.3365T>A (p.Phe1122Tyr)
18g.44953182T>CCA402325299SETBP1c.3842T>C (p.Phe1281Ser)
c.3920T>C (p.Phe1307Ser)
c.3365T>C (p.Phe1122Ser)
18g.44953182T>GCA402325300SETBP1c.3842T>G (p.Phe1281Cys)
c.3920T>G (p.Phe1307Cys)
c.3365T>G (p.Phe1122Cys)
18g.44953183C>ACA402325301SETBP1c.3843C>A (p.Phe1281Leu)
c.3921C>A (p.Phe1307Leu)
c.3366C>A (p.Phe1122Leu)
18g.44953183C>GCA402325302SETBP1c.3843C>G (p.Phe1281Leu)
c.3921C>G (p.Phe1307Leu)
c.3366C>G (p.Phe1122Leu)
18g.44953183C>TCA503982822SETBP1c.3843C>T (p.Phe1281=)
c.3921C>T (p.Phe1307=)
c.3366C>T (p.Phe1122=)
18g.44953184A>CCA402325305SETBP1c.3844A>C (p.Ser1282Arg)
c.3922A>C (p.Ser1308Arg)
c.3367A>C (p.Ser1123Arg)
18g.44953184A>GCA402325303SETBP1c.3844A>G (p.Ser1282Gly)
c.3922A>G (p.Ser1308Gly)
c.3367A>G (p.Ser1123Gly)
 gnomAD v4
18g.44953184A>TCA402325304SETBP1c.3844A>T (p.Ser1282Cys)
c.3922A>T (p.Ser1308Cys)
c.3367A>T (p.Ser1123Cys)
18g.44953185G>ACA402325306SETBP1c.3845G>A (p.Ser1282Asn)
c.3923G>A (p.Ser1308Asn)
c.3368G>A (p.Ser1123Asn)
18g.44953185G>CCA402325307SETBP1c.3845G>C (p.Ser1282Thr)
c.3923G>C (p.Ser1308Thr)
c.3368G>C (p.Ser1123Thr)
18g.44953185G>TCA402325308SETBP1c.3845G>T (p.Ser1282Ile)
c.3923G>T (p.Ser1308Ile)
c.3368G>T (p.Ser1123Ile)
18g.44953186T>ACA8946001SETBP1c.3846T>A (p.Ser1282Arg)
c.3924T>A (p.Ser1308Arg)
c.3369T>A (p.Ser1123Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953186T>CCA503982832SETBP1c.3846T>C (p.Ser1282=)
c.3924T>C (p.Ser1308=)
c.3369T>C (p.Ser1123=)
18g.44953186T>GCA402325309SETBP1c.3846T>G (p.Ser1282Arg)
c.3924T>G (p.Ser1308Arg)
c.3369T>G (p.Ser1123Arg)
18g.44953186T=CA2300141299SETBP1c.3846T= (p.Ser1282=)
c.3924T= (p.Ser1308=)
c.3369T= (p.Ser1123=)
18g.44953187G>ACA402325311SETBP1c.3847G>A (p.Glu1283Lys)
c.3925G>A (p.Glu1309Lys)
c.3370G>A (p.Glu1124Lys)
18g.44953187G>CCA8946002SETBP1c.3847G>C (p.Glu1283Gln)
c.3925G>C (p.Glu1309Gln)
c.3370G>C (p.Glu1124Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953187G=CA2300141300SETBP1c.3847G= (p.Glu1283=)
c.3925G= (p.Glu1309=)
c.3370G= (p.Glu1124=)
18g.44953187G>TCA402325310SETBP1c.3847G>T (p.Glu1283Ter)
c.3925G>T (p.Glu1309Ter)
c.3370G>T (p.Glu1124Ter)
18g.44953188A=CA2300141301SETBP1c.3848A= (p.Glu1283=)
c.3926A= (p.Glu1309=)
c.3371A= (p.Glu1124=)
18g.44953188A>CCA402325312SETBP1c.3848A>C (p.Glu1283Ala)
c.3926A>C (p.Glu1309Ala)
c.3371A>C (p.Glu1124Ala)
 dbSNP gnomAD v2 gnomAD v4
18g.44953188A>GCA402325314SETBP1c.3848A>G (p.Glu1283Gly)
c.3926A>G (p.Glu1309Gly)
c.3371A>G (p.Glu1124Gly)
18g.44953188A>TCA402325313SETBP1c.3848A>T (p.Glu1283Val)
c.3926A>T (p.Glu1309Val)
c.3371A>T (p.Glu1124Val)
18g.44953189A>CCA402325315SETBP1c.3849A>C (p.Glu1283Asp)
c.3927A>C (p.Glu1309Asp)
c.3372A>C (p.Glu1124Asp)
18g.44953189A>GCA503982837SETBP1c.3849A>G (p.Glu1283=)
c.3927A>G (p.Glu1309=)
c.3372A>G (p.Glu1124=)
18g.44953189A>TCA402325316SETBP1c.3849A>T (p.Glu1283Asp)
c.3927A>T (p.Glu1309Asp)
c.3372A>T (p.Glu1124Asp)
18g.44953190A>CCA402325317SETBP1c.3850A>C (p.Met1284Leu)
c.3928A>C (p.Met1310Leu)
c.3373A>C (p.Met1125Leu)
18g.44953190A>GCA402325319SETBP1c.3850A>G (p.Met1284Val)
c.3928A>G (p.Met1310Val)
c.3373A>G (p.Met1125Val)
18g.44953190A>TCA402325318SETBP1c.3850A>T (p.Met1284Leu)
c.3928A>T (p.Met1310Leu)
c.3373A>T (p.Met1125Leu)
18g.44953191T>ACA402325320SETBP1c.3851T>A (p.Met1284Lys)
c.3929T>A (p.Met1310Lys)
c.3374T>A (p.Met1125Lys)
18g.44953191T>CCA402325321SETBP1c.3851T>C (p.Met1284Thr)
c.3929T>C (p.Met1310Thr)
c.3374T>C (p.Met1125Thr)
 ClinVar dbSNP gnomAD v4
18g.44953191T>GCA402325322SETBP1c.3851T>G (p.Met1284Arg)
c.3929T>G (p.Met1310Arg)
c.3374T>G (p.Met1125Arg)
18g.44953192G>ACA402325323SETBP1c.3852G>A (p.Met1284Ile)
c.3930G>A (p.Met1310Ile)
c.3375G>A (p.Met1125Ile)
18g.44953192G>CCA402325324SETBP1c.3852G>C (p.Met1284Ile)
c.3930G>C (p.Met1310Ile)
c.3375G>C (p.Met1125Ile)
18g.44953192G=CA2300141302SETBP1c.3852G= (p.Met1284=)
c.3930G= (p.Met1310=)
c.3375G= (p.Met1125=)
18g.44953192G>TCA8946003SETBP1c.3852G>T (p.Met1284Ile)
c.3930G>T (p.Met1310Ile)
c.3375G>T (p.Met1125Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953193A=CA2300141303SETBP1c.3853A= (p.Asn1285=)
c.3931A= (p.Asn1311=)
c.3376A= (p.Asn1126=)
18g.44953193A>CCA402325327SETBP1c.3853A>C (p.Asn1285His)
c.3931A>C (p.Asn1311His)
c.3376A>C (p.Asn1126His)
18g.44953193A>GCA402325325SETBP1c.3853A>G (p.Asn1285Asp)
c.3931A>G (p.Asn1311Asp)
c.3376A>G (p.Asn1126Asp)
 dbSNP gnomAD v3 gnomAD v4
18g.44953193A>TCA402325326SETBP1c.3853A>T (p.Asn1285Tyr)
c.3931A>T (p.Asn1311Tyr)
c.3376A>T (p.Asn1126Tyr)
18g.44953194A=CA2300141304SETBP1c.3854A= (p.Asn1285=)
c.3932A= (p.Asn1311=)
c.3377A= (p.Asn1126=)
18g.44953194A>CCA402325328SETBP1c.3854A>C (p.Asn1285Thr)
c.3932A>C (p.Asn1311Thr)
c.3377A>C (p.Asn1126Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953194A>GCA402325329SETBP1c.3854A>G (p.Asn1285Ser)
c.3932A>G (p.Asn1311Ser)
c.3377A>G (p.Asn1126Ser)
 gnomAD v4
18g.44953194A>TCA402325330SETBP1c.3854A>T (p.Asn1285Ile)
c.3932A>T (p.Asn1311Ile)
c.3377A>T (p.Asn1126Ile)
18g.44953195C>ACA402325331SETBP1c.3855C>A (p.Asn1285Lys)
c.3933C>A (p.Asn1311Lys)
c.3378C>A (p.Asn1126Lys)
18g.44953195C=CA2300141305SETBP1c.3855C= (p.Asn1285=)
c.3933C= (p.Asn1311=)
c.3378C= (p.Asn1126=)
18g.44953195C>GCA402325332SETBP1c.3855C>G (p.Asn1285Lys)
c.3933C>G (p.Asn1311Lys)
c.3378C>G (p.Asn1126Lys)
18g.44953195C>TCA503982846SETBP1c.3855C>T (p.Asn1285=)
c.3933C>T (p.Asn1311=)
c.3378C>T (p.Asn1126=)
 dbSNP gnomAD v4
18g.44953196C>ACA402325333SETBP1c.3856C>A (p.Pro1286Thr)
c.3934C>A (p.Pro1312Thr)
c.3379C>A (p.Pro1127Thr)
18g.44953196C=CA2300141306SETBP1c.3856C= (p.Pro1286=)
c.3934C= (p.Pro1312=)
c.3379C= (p.Pro1127=)
18g.44953196C>GCA402325334SETBP1c.3856C>G (p.Pro1286Ala)
c.3934C>G (p.Pro1312Ala)
c.3379C>G (p.Pro1127Ala)
18g.44953196C>TCA8946004SETBP1c.3856C>T (p.Pro1286Ser)
c.3934C>T (p.Pro1312Ser)
c.3379C>T (p.Pro1127Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
18g.44953197C>ACA402325335SETBP1c.3857C>A (p.Pro1286His)
c.3935C>A (p.Pro1312His)
c.3380C>A (p.Pro1127His)
18g.44953197C>GCA402325336SETBP1c.3857C>G (p.Pro1286Arg)
c.3935C>G (p.Pro1312Arg)
c.3380C>G (p.Pro1127Arg)
18g.44953197C>TCA402325337SETBP1c.3857C>T (p.Pro1286Leu)
c.3935C>T (p.Pro1312Leu)
c.3380C>T (p.Pro1127Leu)
18g.44953198T>ACA503982853SETBP1c.3858T>A (p.Pro1286=)
c.3936T>A (p.Pro1312=)
c.3381T>A (p.Pro1127=)
18g.44953198T>CCA503982854SETBP1c.3858T>C (p.Pro1286=)
c.3936T>C (p.Pro1312=)
c.3381T>C (p.Pro1127=)
18g.44953198T>GCA503982855SETBP1c.3858T>G (p.Pro1286=)
c.3936T>G (p.Pro1312=)
c.3381T>G (p.Pro1127=)
 dbSNP
18g.44953198T=CA2300141307SETBP1c.3858T= (p.Pro1286=)
c.3936T= (p.Pro1312=)
c.3381T= (p.Pro1127=)
18g.44953199T>ACA402325338SETBP1c.3859T>A (p.Ser1287Thr)
c.3937T>A (p.Ser1313Thr)
c.3382T>A (p.Ser1128Thr)
18g.44953199T>CCA402325339SETBP1c.3859T>C (p.Ser1287Pro)
c.3937T>C (p.Ser1313Pro)
c.3382T>C (p.Ser1128Pro)
18g.44953199T>GCA402325340SETBP1c.3859T>G (p.Ser1287Ala)
c.3937T>G (p.Ser1313Ala)
c.3382T>G (p.Ser1128Ala)
18g.44953200C>ACA402325341SETBP1c.3860C>A (p.Ser1287Ter)
c.3938C>A (p.Ser1313Ter)
c.3383C>A (p.Ser1128Ter)
18g.44953200C=CA2300141308SETBP1c.3860C= (p.Ser1287=)
c.3938C= (p.Ser1313=)
c.3383C= (p.Ser1128=)
18g.44953200C>GCA402325342SETBP1c.3860C>G (p.Ser1287Trp)
c.3938C>G (p.Ser1313Trp)
c.3383C>G (p.Ser1128Trp)
18g.44953200C>TCA8946005SETBP1c.3860C>T (p.Ser1287Leu)
c.3938C>T (p.Ser1313Leu)
c.3383C>T (p.Ser1128Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
18g.44953201G>ACA8946006SETBP1c.3861G>A (p.Ser1287=)
c.3939G>A (p.Ser1313=)
c.3384G>A (p.Ser1128=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953201G>CCA503982859SETBP1c.3861G>C (p.Ser1287=)
c.3939G>C (p.Ser1313=)
c.3384G>C (p.Ser1128=)
18g.44953201G=CA2300141309SETBP1c.3861G= (p.Ser1287=)
c.3939G= (p.Ser1313=)
c.3384G= (p.Ser1128=)
18g.44953201G>TCA299699912SETBP1c.3861G>T (p.Ser1287=)
c.3939G>T (p.Ser1313=)
c.3384G>T (p.Ser1128=)
 dbSNP gnomAD v4
18g.44953202A>CCA402325343SETBP1c.3862A>C (p.Asn1288His)
c.3940A>C (p.Asn1314His)
c.3385A>C (p.Asn1129His)
18g.44953202A>GCA402325345SETBP1c.3862A>G (p.Asn1288Asp)
c.3940A>G (p.Asn1314Asp)
c.3385A>G (p.Asn1129Asp)
18g.44953202A>TCA402325344SETBP1c.3862A>T (p.Asn1288Tyr)
c.3940A>T (p.Asn1314Tyr)
c.3385A>T (p.Asn1129Tyr)
18g.44953203A=CA2300141310SETBP1c.3863A= (p.Asn1288=)
c.3941A= (p.Asn1314=)
c.3386A= (p.Asn1129=)
18g.44953203A>CCA402325346SETBP1c.3863A>C (p.Asn1288Thr)
c.3941A>C (p.Asn1314Thr)
c.3386A>C (p.Asn1129Thr)
18g.44953203A>GCA402325347SETBP1c.3863A>G (p.Asn1288Ser)
c.3941A>G (p.Asn1314Ser)
c.3386A>G (p.Asn1129Ser)
 dbSNP gnomAD v2 gnomAD v4
18g.44953203A>TCA402325348SETBP1c.3863A>T (p.Asn1288Ile)
c.3941A>T (p.Asn1314Ile)
c.3386A>T (p.Asn1129Ile)
18g.44953204T>ACA402325349SETBP1c.3864T>A (p.Asn1288Lys)
c.3942T>A (p.Asn1314Lys)
c.3387T>A (p.Asn1129Lys)
18g.44953204T>CCA503982869SETBP1c.3864T>C (p.Asn1288=)
c.3942T>C (p.Asn1314=)
c.3387T>C (p.Asn1129=)
18g.44953204T>GCA402325350SETBP1c.3864T>G (p.Asn1288Lys)
c.3942T>G (p.Asn1314Lys)
c.3387T>G (p.Asn1129Lys)
18g.44953205G>ACA402325351SETBP1c.3865G>A (p.Asp1289Asn)
c.3943G>A (p.Asp1315Asn)
c.3388G>A (p.Asp1130Asn)
18g.44953205G>CCA402325352SETBP1c.3865G>C (p.Asp1289His)
c.3943G>C (p.Asp1315His)
c.3388G>C (p.Asp1130His)
18g.44953205G>TCA402325353SETBP1c.3865G>T (p.Asp1289Tyr)
c.3943G>T (p.Asp1315Tyr)
c.3388G>T (p.Asp1130Tyr)
18g.44953206A>CCA402325354SETBP1c.3866A>C (p.Asp1289Ala)
c.3944A>C (p.Asp1315Ala)
c.3389A>C (p.Asp1130Ala)
18g.44953206A>GCA402325355SETBP1c.3866A>G (p.Asp1289Gly)
c.3944A>G (p.Asp1315Gly)
c.3389A>G (p.Asp1130Gly)
 gnomAD v4
18g.44953206A>TCA402325356SETBP1c.3866A>T (p.Asp1289Val)
c.3944A>T (p.Asp1315Val)
c.3389A>T (p.Asp1130Val)
 ClinVar gnomAD v4
18g.44953207C>ACA402325358SETBP1c.3867C>A (p.Asp1289Glu)
c.3945C>A (p.Asp1315Glu)
c.3390C>A (p.Asp1130Glu)
18g.44953207C=CA2300141311SETBP1c.3867C= (p.Asp1289=)
c.3945C= (p.Asp1315=)
c.3390C= (p.Asp1130=)
18g.44953207C>GCA402325357SETBP1c.3867C>G (p.Asp1289Glu)
c.3945C>G (p.Asp1315Glu)
c.3390C>G (p.Asp1130Glu)
18g.44953207C>TCA8946007SETBP1c.3867C>T (p.Asp1289=)
c.3945C>T (p.Asp1315=)
c.3390C>T (p.Asp1130=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953208A>CCA402325359SETBP1c.3868A>C (p.Lys1290Gln)
c.3946A>C (p.Lys1316Gln)
c.3391A>C (p.Lys1131Gln)
18g.44953208A>GCA402325360SETBP1c.3868A>G (p.Lys1290Glu)
c.3946A>G (p.Lys1316Glu)
c.3391A>G (p.Lys1131Glu)
18g.44953208A>TCA402325361SETBP1c.3868A>T (p.Lys1290Ter)
c.3946A>T (p.Lys1316Ter)
c.3391A>T (p.Lys1131Ter)
18g.44953209A=CA2300141312SETBP1c.3869A= (p.Lys1290=)
c.3947A= (p.Lys1316=)
c.3392A= (p.Lys1131=)
18g.44953209A>CCA402325362SETBP1c.3869A>C (p.Lys1290Thr)
c.3947A>C (p.Lys1316Thr)
c.3392A>C (p.Lys1131Thr)
18g.44953209A>GCA402325363SETBP1c.3869A>G (p.Lys1290Arg)
c.3947A>G (p.Lys1316Arg)
c.3392A>G (p.Lys1131Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953209A>TCA402325364SETBP1c.3869A>T (p.Lys1290Met)
c.3947A>T (p.Lys1316Met)
c.3392A>T (p.Lys1131Met)
18g.44953210G>ACA299699914SETBP1c.3870G>A (p.Lys1290=)
c.3948G>A (p.Lys1316=)
c.3393G>A (p.Lys1131=)
 ClinVar dbSNP gnomAD v4
18g.44953210G>CCA8946008SETBP1c.3870G>C (p.Lys1290Asn)
c.3948G>C (p.Lys1316Asn)
c.3393G>C (p.Lys1131Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953210G=CA2300141313SETBP1c.3870G= (p.Lys1290=)
c.3948G= (p.Lys1316=)
c.3393G= (p.Lys1131=)
18g.44953210G>TCA402325365SETBP1c.3870G>T (p.Lys1290Asn)
c.3948G>T (p.Lys1316Asn)
c.3393G>T (p.Lys1131Asn)
18g.44953211T>ACA402325366SETBP1c.3871T>A (p.Trp1291Arg)
c.3949T>A (p.Trp1317Arg)
c.3394T>A (p.Trp1132Arg)
18g.44953211T>CCA402325367SETBP1c.3871T>C (p.Trp1291Arg)
c.3949T>C (p.Trp1317Arg)
c.3394T>C (p.Trp1132Arg)
18g.44953211T>GCA402325368SETBP1c.3871T>G (p.Trp1291Gly)
c.3949T>G (p.Trp1317Gly)
c.3394T>G (p.Trp1132Gly)
18g.44953212G>ACA402325370SETBP1c.3872G>A (p.Trp1291Ter)
c.3950G>A (p.Trp1317Ter)
c.3395G>A (p.Trp1132Ter)
18g.44953212G>CCA402325371SETBP1c.3872G>C (p.Trp1291Ser)
c.3950G>C (p.Trp1317Ser)
c.3395G>C (p.Trp1132Ser)
 dbSNP
18g.44953212G=CA2300141314SETBP1c.3872G= (p.Trp1291=)
c.3950G= (p.Trp1317=)
c.3395G= (p.Trp1132=)
18g.44953212G>TCA402325369SETBP1c.3872G>T (p.Trp1291Leu)
c.3950G>T (p.Trp1317Leu)
c.3395G>T (p.Trp1132Leu)
18g.44953213G>ACA402325374SETBP1c.3873G>A (p.Trp1291Ter)
c.3951G>A (p.Trp1317Ter)
c.3396G>A (p.Trp1132Ter)
18g.44953213G>CCA402325372SETBP1c.3873G>C (p.Trp1291Cys)
c.3951G>C (p.Trp1317Cys)
c.3396G>C (p.Trp1132Cys)
18g.44953213G>TCA402325373SETBP1c.3873G>T (p.Trp1291Cys)
c.3951G>T (p.Trp1317Cys)
c.3396G>T (p.Trp1132Cys)
18g.44953214G>ACA402325375SETBP1c.3874G>A (p.Asp1292Asn)
c.3952G>A (p.Asp1318Asn)
c.3397G>A (p.Asp1133Asn)
 gnomAD v4
18g.44953214G>CCA402325376SETBP1c.3874G>C (p.Asp1292His)
c.3952G>C (p.Asp1318His)
c.3397G>C (p.Asp1133His)
 ClinVar
18g.44953214G>TCA402325377SETBP1c.3874G>T (p.Asp1292Tyr)
c.3952G>T (p.Asp1318Tyr)
c.3397G>T (p.Asp1133Tyr)
18g.44953215A>CCA402325378SETBP1c.3875A>C (p.Asp1292Ala)
c.3953A>C (p.Asp1318Ala)
c.3398A>C (p.Asp1133Ala)
18g.44953215A>GCA402325379SETBP1c.3875A>G (p.Asp1292Gly)
c.3953A>G (p.Asp1318Gly)
c.3398A>G (p.Asp1133Gly)
18g.44953215A>TCA402325380SETBP1c.3875A>T (p.Asp1292Val)
c.3953A>T (p.Asp1318Val)
c.3398A>T (p.Asp1133Val)
 ClinVar dbSNP
18g.44953216C>ACA402325381SETBP1c.3876C>A (p.Asp1292Glu)
c.3954C>A (p.Asp1318Glu)
c.3399C>A (p.Asp1133Glu)
18g.44953216C=CA2300141315SETBP1c.3876C= (p.Asp1292=)
c.3954C= (p.Asp1318=)
c.3399C= (p.Asp1133=)
18g.44953216C>GCA8946009SETBP1c.3876C>G (p.Asp1292Glu)
c.3954C>G (p.Asp1318Glu)
c.3399C>G (p.Asp1133Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953216C>TCA503982903SETBP1c.3876C>T (p.Asp1292=)
c.3954C>T (p.Asp1318=)
c.3399C>T (p.Asp1133=)
18g.44953217A=CA2300141316SETBP1c.3877A= (p.Ser1293=)
c.3955A= (p.Ser1319=)
c.3400A= (p.Ser1134=)
18g.44953217A>CCA402325382SETBP1c.3877A>C (p.Ser1293Arg)
c.3955A>C (p.Ser1319Arg)
c.3400A>C (p.Ser1134Arg)
18g.44953217A>GCA402325383SETBP1c.3877A>G (p.Ser1293Gly)
c.3955A>G (p.Ser1319Gly)
c.3400A>G (p.Ser1134Gly)
 ClinVar dbSNP gnomAD v4
18g.44953217A>TCA402325384SETBP1c.3877A>T (p.Ser1293Cys)
c.3955A>T (p.Ser1319Cys)
c.3400A>T (p.Ser1134Cys)
18g.44953218G>ACA402325385SETBP1c.3878G>A (p.Ser1293Asn)
c.3956G>A (p.Ser1319Asn)
c.3401G>A (p.Ser1134Asn)
18g.44953218G>CCA402325387SETBP1c.3878G>C (p.Ser1293Thr)
c.3956G>C (p.Ser1319Thr)
c.3401G>C (p.Ser1134Thr)
18g.44953218G>TCA402325386SETBP1c.3878G>T (p.Ser1293Ile)
c.3956G>T (p.Ser1319Ile)
c.3401G>T (p.Ser1134Ile)
18g.44953219T>ACA402325388SETBP1c.3879T>A (p.Ser1293Arg)
c.3957T>A (p.Ser1319Arg)
c.3402T>A (p.Ser1134Arg)
18g.44953219T>CCA503982910SETBP1c.3879T>C (p.Ser1293=)
c.3957T>C (p.Ser1319=)
c.3402T>C (p.Ser1134=)
18g.44953219T>GCA402325389SETBP1c.3879T>G (p.Ser1293Arg)
c.3957T>G (p.Ser1319Arg)
c.3402T>G (p.Ser1134Arg)
 ClinVar
18g.44953220G>ACA402325390SETBP1c.3880G>A (p.Asp1294Asn)
c.3958G>A (p.Asp1320Asn)
c.3403G>A (p.Asp1135Asn)
18g.44953220G>CCA402325391SETBP1c.3880G>C (p.Asp1294His)
c.3958G>C (p.Asp1320His)
c.3403G>C (p.Asp1135His)
 gnomAD v4 COSMIC
18g.44953220G>TCA402325392SETBP1c.3880G>T (p.Asp1294Tyr)
c.3958G>T (p.Asp1320Tyr)
c.3403G>T (p.Asp1135Tyr)
18g.44953221A>CCA402325393SETBP1c.3881A>C (p.Asp1294Ala)
c.3959A>C (p.Asp1320Ala)
c.3404A>C (p.Asp1135Ala)
18g.44953221A>GCA402325394SETBP1c.3881A>G (p.Asp1294Gly)
c.3959A>G (p.Asp1320Gly)
c.3404A>G (p.Asp1135Gly)
18g.44953221A>TCA402325395SETBP1c.3881A>T (p.Asp1294Val)
c.3959A>T (p.Asp1320Val)
c.3404A>T (p.Asp1135Val)
18g.44953222C>ACA402325396SETBP1c.3882C>A (p.Asp1294Glu)
c.3960C>A (p.Asp1320Glu)
c.3405C>A (p.Asp1135Glu)
 gnomAD v4
18g.44953222C=CA2300141317SETBP1c.3882C= (p.Asp1294=)
c.3960C= (p.Asp1320=)
c.3405C= (p.Asp1135=)
18g.44953222C>GCA402325397SETBP1c.3882C>G (p.Asp1294Glu)
c.3960C>G (p.Asp1320Glu)
c.3405C>G (p.Asp1135Glu)
18g.44953222C>TCA8946010SETBP1c.3882C>T (p.Asp1294=)
c.3960C>T (p.Asp1320=)
c.3405C>T (p.Asp1135=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953223G>ACA8946011SETBP1c.3883G>A (p.Val1295Met)
c.3961G>A (p.Val1321Met)
c.3406G>A (p.Val1136Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.44953223G>CCA402325399SETBP1c.3883G>C (p.Val1295Leu)
c.3961G>C (p.Val1321Leu)
c.3406G>C (p.Val1136Leu)
 gnomAD v4
18g.44953223G=CA2300141318SETBP1c.3883G= (p.Val1295=)
c.3961G= (p.Val1321=)
c.3406G= (p.Val1136=)
18g.44953223G>TCA402325398SETBP1c.3883G>T (p.Val1295Leu)
c.3961G>T (p.Val1321Leu)
c.3406G>T (p.Val1136Leu)
18g.44953224T>ACA402325400SETBP1c.3884T>A (p.Val1295Glu)
c.3962T>A (p.Val1321Glu)
c.3407T>A (p.Val1136Glu)
18g.44953224T>CCA402325401SETBP1c.3884T>C (p.Val1295Ala)
c.3962T>C (p.Val1321Ala)
c.3407T>C (p.Val1136Ala)
18g.44953224T>GCA402325402SETBP1c.3884T>G (p.Val1295Gly)
c.3962T>G (p.Val1321Gly)
c.3407T>G (p.Val1136Gly)
 gnomAD v4
18g.44953225G>ACA503982918SETBP1c.3885G>A (p.Val1295=)
c.3963G>A (p.Val1321=)
c.3408G>A (p.Val1136=)
 gnomAD v4
18g.44953225G>CCA503982919SETBP1c.3885G>C (p.Val1295=)
c.3963G>C (p.Val1321=)
c.3408G>C (p.Val1136=)
18g.44953225G>TCA503982923SETBP1c.3885G>T (p.Val1295=)
c.3963G>T (p.Val1321=)
c.3408G>T (p.Val1136=)
18g.44953226A>CCA402325403SETBP1c.3886A>C (p.Ser1296Arg)
c.3964A>C (p.Ser1322Arg)
c.3409A>C (p.Ser1137Arg)
18g.44953226A>GCA402325404SETBP1c.3886A>G (p.Ser1296Gly)
c.3964A>G (p.Ser1322Gly)
c.3409A>G (p.Ser1137Gly)
18g.44953226A>TCA402325405SETBP1c.3886A>T (p.Ser1296Cys)
c.3964A>T (p.Ser1322Cys)
c.3409A>T (p.Ser1137Cys)
18g.44953227G>ACA8946012SETBP1c.3887G>A (p.Ser1296Asn)
c.3965G>A (p.Ser1322Asn)
c.3410G>A (p.Ser1137Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953227G>CCA402325406SETBP1c.3887G>C (p.Ser1296Thr)
c.3965G>C (p.Ser1322Thr)
c.3410G>C (p.Ser1137Thr)
 gnomAD v4
18g.44953227G=CA2300141319SETBP1c.3887G= (p.Ser1296=)
c.3965G= (p.Ser1322=)
c.3410G= (p.Ser1137=)
18g.44953227G>TCA402325407SETBP1c.3887G>T (p.Ser1296Ile)
c.3965G>T (p.Ser1322Ile)
c.3410G>T (p.Ser1137Ile)
18g.44953228T>ACA402325408SETBP1c.3888T>A (p.Ser1296Arg)
c.3966T>A (p.Ser1322Arg)
c.3411T>A (p.Ser1137Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
18g.44953228T>CCA503982926SETBP1c.3888T>C (p.Ser1296=)
c.3966T>C (p.Ser1322=)
c.3411T>C (p.Ser1137=)
18g.44953228T>GCA402325409SETBP1c.3888T>G (p.Ser1296Arg)
c.3966T>G (p.Ser1322Arg)
c.3411T>G (p.Ser1137Arg)
18g.44953228T=CA2300141320SETBP1c.3888T= (p.Ser1296=)
c.3966T= (p.Ser1322=)
c.3411T= (p.Ser1137=)
18g.44953229G>ACA402325410SETBP1c.3889G>A (p.Gly1297Arg)
c.3967G>A (p.Gly1323Arg)
c.3412G>A (p.Gly1138Arg)
18g.44953229G>CCA402325411SETBP1c.3889G>C (p.Gly1297Arg)
c.3967G>C (p.Gly1323Arg)
c.3412G>C (p.Gly1138Arg)
 gnomAD v4
18g.44953229G>TCA402325412SETBP1c.3889G>T (p.Gly1297Trp)
c.3967G>T (p.Gly1323Trp)
c.3412G>T (p.Gly1138Trp)
18g.44953230G>ACA402325413SETBP1c.3890G>A (p.Gly1297Glu)
c.3968G>A (p.Gly1323Glu)
c.3413G>A (p.Gly1138Glu)
18g.44953230G>CCA402325415SETBP1c.3890G>C (p.Gly1297Ala)
c.3968G>C (p.Gly1323Ala)
c.3413G>C (p.Gly1138Ala)
18g.44953230G>TCA402325414SETBP1c.3890G>T (p.Gly1297Val)
c.3968G>T (p.Gly1323Val)
c.3413G>T (p.Gly1138Val)
18g.44953231G>ACA8946013SETBP1c.3891G>A (p.Gly1297=)
c.3969G>A (p.Gly1323=)
c.3414G>A (p.Gly1138=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953231G>CCA503982931SETBP1c.3891G>C (p.Gly1297=)
c.3969G>C (p.Gly1323=)
c.3414G>C (p.Gly1138=)
18g.44953231G=CA2300141321SETBP1c.3891G= (p.Gly1297=)
c.3969G= (p.Gly1323=)
c.3414G= (p.Gly1138=)
18g.44953231G>TCA503982933SETBP1c.3891G>T (p.Gly1297=)
c.3969G>T (p.Gly1323=)
c.3414G>T (p.Gly1138=)
18g.44953232A>CCA402325416SETBP1c.3892A>C (p.Ser1298Arg)
c.3970A>C (p.Ser1324Arg)
c.3415A>C (p.Ser1139Arg)
18g.44953232A>GCA402325417SETBP1c.3892A>G (p.Ser1298Gly)
c.3970A>G (p.Ser1324Gly)
c.3415A>G (p.Ser1139Gly)
18g.44953232A>TCA402325418SETBP1c.3892A>T (p.Ser1298Cys)
c.3970A>T (p.Ser1324Cys)
c.3415A>T (p.Ser1139Cys)
18g.44953233G>ACA402325419SETBP1c.3893G>A (p.Ser1298Asn)
c.3971G>A (p.Ser1324Asn)
c.3416G>A (p.Ser1139Asn)
 dbSNP gnomAD v4
18g.44953233G>CCA402325420SETBP1c.3893G>C (p.Ser1298Thr)
c.3971G>C (p.Ser1324Thr)
c.3416G>C (p.Ser1139Thr)
18g.44953233G=CA2300141322SETBP1c.3893G= (p.Ser1298=)
c.3971G= (p.Ser1324=)
c.3416G= (p.Ser1139=)
18g.44953233G>TCA402325421SETBP1c.3893G>T (p.Ser1298Ile)
c.3971G>T (p.Ser1324Ile)
c.3416G>T (p.Ser1139Ile)
18g.44953234T>ACA402325422SETBP1c.3894T>A (p.Ser1298Arg)
c.3972T>A (p.Ser1324Arg)
c.3417T>A (p.Ser1139Arg)
18g.44953234T>CCA503982936SETBP1c.3894T>C (p.Ser1298=)
c.3972T>C (p.Ser1324=)
c.3417T>C (p.Ser1139=)
18g.44953234T>GCA402325423SETBP1c.3894T>G (p.Ser1298Arg)
c.3972T>G (p.Ser1324Arg)
c.3417T>G (p.Ser1139Arg)
18g.44953235A=CA2300141323SETBP1c.3895A= (p.Lys1299=)
c.3973A= (p.Lys1325=)
c.3418A= (p.Lys1140=)
18g.44953235A>CCA402325424SETBP1c.3895A>C (p.Lys1299Gln)
c.3973A>C (p.Lys1325Gln)
c.3418A>C (p.Lys1140Gln)
18g.44953235A>GCA402325425SETBP1c.3895A>G (p.Lys1299Glu)
c.3973A>G (p.Lys1325Glu)
c.3418A>G (p.Lys1140Glu)
 dbSNP gnomAD v4
18g.44953235A>TCA402325426SETBP1c.3895A>T (p.Lys1299Ter)
c.3973A>T (p.Lys1325Ter)
c.3418A>T (p.Lys1140Ter)
18g.44953236A>CCA402325429SETBP1c.3896A>C (p.Lys1299Thr)
c.3974A>C (p.Lys1325Thr)
c.3419A>C (p.Lys1140Thr)
18g.44953236A>GCA402325428SETBP1c.3896A>G (p.Lys1299Arg)
c.3974A>G (p.Lys1325Arg)
c.3419A>G (p.Lys1140Arg)
18g.44953236A>TCA402325427SETBP1c.3896A>T (p.Lys1299Ile)
c.3974A>T (p.Lys1325Ile)
c.3419A>T (p.Lys1140Ile)
18g.44953237A>CCA402325430SETBP1c.3897A>C (p.Lys1299Asn)
c.3975A>C (p.Lys1325Asn)
c.3420A>C (p.Lys1140Asn)
18g.44953237A>GCA503982939SETBP1c.3897A>G (p.Lys1299=)
c.3975A>G (p.Lys1325=)
c.3420A>G (p.Lys1140=)
18g.44953237A>TCA402325431SETBP1c.3897A>T (p.Lys1299Asn)
c.3975A>T (p.Lys1325Asn)
c.3420A>T (p.Lys1140Asn)
18g.44953237_44953240delinsAAGGCA2300141324SETBP1c.3897_3900delinsAAGG (p.Lys1299=)
c.3975_3978delinsAAGG (p.Lys1325=)
c.3420_3423delinsAAGG (p.Lys1140=)
18g.44953238A>CCA503982940SETBP1c.3898A>C (p.Arg1300=)
c.3976A>C (p.Arg1326=)
c.3421A>C (p.Arg1141=)
18g.44953238A>GCA402325432SETBP1c.3898A>G (p.Arg1300Gly)
c.3976A>G (p.Arg1326Gly)
c.3421A>G (p.Arg1141Gly)
 gnomAD v4
18g.44953238A>TCA402325433SETBP1c.3898A>T (p.Arg1300Trp)
c.3976A>T (p.Arg1326Trp)
c.3421A>T (p.Arg1141Trp)
18g.44953243_44953245delCA8946014SETBP1c.3903_3905del (p.Arg1301del)
c.3981_3983del (p.Arg1327del)
c.3426_3428del (p.Arg1142del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953239G>ACA402325434SETBP1c.3899G>A (p.Arg1300Lys)
c.3977G>A (p.Arg1326Lys)
c.3422G>A (p.Arg1141Lys)
18g.44953239G>CCA402325435SETBP1c.3899G>C (p.Arg1300Thr)
c.3977G>C (p.Arg1326Thr)
c.3422G>C (p.Arg1141Thr)
18g.44953239G>TCA402325436SETBP1c.3899G>T (p.Arg1300Met)
c.3977G>T (p.Arg1326Met)
c.3422G>T (p.Arg1141Met)
18g.44953240G>ACA503982942SETBP1c.3900G>A (p.Arg1300=)
c.3978G>A (p.Arg1326=)
c.3423G>A (p.Arg1141=)
18g.44953240G>CCA402325437SETBP1c.3900G>C (p.Arg1300Ser)
c.3978G>C (p.Arg1326Ser)
c.3423G>C (p.Arg1141Ser)
18g.44953240G>TCA402325438SETBP1c.3900G>T (p.Arg1300Ser)
c.3978G>T (p.Arg1326Ser)
c.3423G>T (p.Arg1141Ser)
18g.44953241A>CCA503982944SETBP1c.3901A>C (p.Arg1301=)
c.3979A>C (p.Arg1327=)
c.3424A>C (p.Arg1142=)
18g.44953241A>GCA402325439SETBP1c.3901A>G (p.Arg1301Gly)
c.3979A>G (p.Arg1327Gly)
c.3424A>G (p.Arg1142Gly)
18g.44953241A>TCA402325440SETBP1c.3901A>T (p.Arg1301Trp)
c.3979A>T (p.Arg1327Trp)
c.3424A>T (p.Arg1142Trp)
18g.44953242G>ACA402325441SETBP1c.3902G>A (p.Arg1301Lys)
c.3980G>A (p.Arg1327Lys)
c.3425G>A (p.Arg1142Lys)
18g.44953242G>CCA402325442SETBP1c.3902G>C (p.Arg1301Thr)
c.3980G>C (p.Arg1327Thr)
c.3425G>C (p.Arg1142Thr)
18g.44953242G>TCA402325443SETBP1c.3902G>T (p.Arg1301Met)
c.3980G>T (p.Arg1327Met)
c.3425G>T (p.Arg1142Met)
 dbSNP
18g.44953243G>ACA503982947SETBP1c.3903G>A (p.Arg1301=)
c.3981G>A (p.Arg1327=)
c.3426G>A (p.Arg1142=)
 gnomAD v4
18g.44953243G>CCA402325445SETBP1c.3903G>C (p.Arg1301Ser)
c.3981G>C (p.Arg1327Ser)
c.3426G>C (p.Arg1142Ser)
18g.44953243G=CA2300141325SETBP1c.3903G= (p.Arg1301=)
c.3981G= (p.Arg1327=)
c.3426G= (p.Arg1142=)
18g.44953243G>TCA402325444SETBP1c.3903G>T (p.Arg1301Ser)
c.3981G>T (p.Arg1327Ser)
c.3426G>T (p.Arg1142Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953244A>CCA402325446SETBP1c.3904A>C (p.Ser1302Arg)
c.3982A>C (p.Ser1328Arg)
c.3427A>C (p.Ser1143Arg)
18g.44953244A>GCA402325447SETBP1c.3904A>G (p.Ser1302Gly)
c.3982A>G (p.Ser1328Gly)
c.3427A>G (p.Ser1143Gly)
18g.44953244A>TCA402325448SETBP1c.3904A>T (p.Ser1302Cys)
c.3982A>T (p.Ser1328Cys)
c.3427A>T (p.Ser1143Cys)
18g.44953245G>ACA8946015SETBP1c.3905G>A (p.Ser1302Asn)
c.3983G>A (p.Ser1328Asn)
c.3428G>A (p.Ser1143Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953245G>CCA402325449SETBP1c.3905G>C (p.Ser1302Thr)
c.3983G>C (p.Ser1328Thr)
c.3428G>C (p.Ser1143Thr)
18g.44953245G=CA2300141326SETBP1c.3905G= (p.Ser1302=)
c.3983G= (p.Ser1328=)
c.3428G= (p.Ser1143=)
18g.44953245G>TCA402325450SETBP1c.3905G>T (p.Ser1302Ile)
c.3983G>T (p.Ser1328Ile)
c.3428G>T (p.Ser1143Ile)
 gnomAD v4
18g.44953246C>ACA402325451SETBP1c.3906C>A (p.Ser1302Arg)
c.3984C>A (p.Ser1328Arg)
c.3429C>A (p.Ser1143Arg)
18g.44953246C=CA2300141327SETBP1c.3906C= (p.Ser1302=)
c.3984C= (p.Ser1328=)
c.3429C= (p.Ser1143=)
18g.44953246C>GCA402325452SETBP1c.3906C>G (p.Ser1302Arg)
c.3984C>G (p.Ser1328Arg)
c.3429C>G (p.Ser1143Arg)
18g.44953246C>TCA503982952SETBP1c.3906C>T (p.Ser1302=)
c.3984C>T (p.Ser1328=)
c.3429C>T (p.Ser1143=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
18g.44953247T>ACA402325453SETBP1c.3907T>A (p.Tyr1303Asn)
c.3985T>A (p.Tyr1329Asn)
c.3430T>A (p.Tyr1144Asn)
18g.44953247T>CCA402325454SETBP1c.3907T>C (p.Tyr1303His)
c.3985T>C (p.Tyr1329His)
c.3430T>C (p.Tyr1144His)
18g.44953247T>GCA402325455SETBP1c.3907T>G (p.Tyr1303Asp)
c.3985T>G (p.Tyr1329Asp)
c.3430T>G (p.Tyr1144Asp)
18g.44953248A=CA2300141328SETBP1c.3908A= (p.Tyr1303=)
c.3986A= (p.Tyr1329=)
c.3431A= (p.Tyr1144=)
18g.44953248A>CCA8946016SETBP1c.3908A>C (p.Tyr1303Ser)
c.3986A>C (p.Tyr1329Ser)
c.3431A>C (p.Tyr1144Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953248A>GCA402325457SETBP1c.3908A>G (p.Tyr1303Cys)
c.3986A>G (p.Tyr1329Cys)
c.3431A>G (p.Tyr1144Cys)
 ClinVar
18g.44953248A>TCA402325456SETBP1c.3908A>T (p.Tyr1303Phe)
c.3986A>T (p.Tyr1329Phe)
c.3431A>T (p.Tyr1144Phe)
18g.44953249T>ACA402325458SETBP1c.3909T>A (p.Tyr1303Ter)
c.3987T>A (p.Tyr1329Ter)
c.3432T>A (p.Tyr1144Ter)
 ClinVar
18g.44953249T>CCA503982957SETBP1c.3909T>C (p.Tyr1303=)
c.3987T>C (p.Tyr1329=)
c.3432T>C (p.Tyr1144=)
18g.44953249T>GCA402325459SETBP1c.3909T>G (p.Tyr1303Ter)
c.3987T>G (p.Tyr1329Ter)
c.3432T>G (p.Tyr1144Ter)
18g.44953250G>ACA402325460SETBP1c.3910G>A (p.Glu1304Lys)
c.3988G>A (p.Glu1330Lys)
c.3433G>A (p.Glu1145Lys)
18g.44953250G>CCA402325461SETBP1c.3910G>C (p.Glu1304Gln)
c.3988G>C (p.Glu1330Gln)
c.3433G>C (p.Glu1145Gln)
18g.44953250G>TCA402325462SETBP1c.3910G>T (p.Glu1304Ter)
c.3988G>T (p.Glu1330Ter)
c.3433G>T (p.Glu1145Ter)
18g.44953251A>CCA402325465SETBP1c.3911A>C (p.Glu1304Ala)
c.3989A>C (p.Glu1330Ala)
c.3434A>C (p.Glu1145Ala)
18g.44953251A>GCA402325464SETBP1c.3911A>G (p.Glu1304Gly)
c.3989A>G (p.Glu1330Gly)
c.3434A>G (p.Glu1145Gly)
18g.44953251A>TCA402325463SETBP1c.3911A>T (p.Glu1304Val)
c.3989A>T (p.Glu1330Val)
c.3434A>T (p.Glu1145Val)
18g.44953252A=CA2300141329SETBP1c.3912A= (p.Glu1304=)
c.3990A= (p.Glu1330=)
c.3435A= (p.Glu1145=)
18g.44953252A>CCA402325466SETBP1c.3912A>C (p.Glu1304Asp)
c.3990A>C (p.Glu1330Asp)
c.3435A>C (p.Glu1145Asp)
 gnomAD v4
18g.44953252A>GCA8946017SETBP1c.3912A>G (p.Glu1304=)
c.3990A>G (p.Glu1330=)
c.3435A>G (p.Glu1145=)
 dbSNP ExAC gnomAD v2 gnomAD v4
18g.44953252A>TCA402325467SETBP1c.3912A>T (p.Glu1304Asp)
c.3990A>T (p.Glu1330Asp)
c.3435A>T (p.Glu1145Asp)
 dbSNP gnomAD v2 gnomAD v4
18g.44953253G>ACA402325468SETBP1c.3913G>A (p.Gly1305Ser)
c.3991G>A (p.Gly1331Ser)
c.3436G>A (p.Gly1146Ser)
18g.44953253G>CCA402325469SETBP1c.3913G>C (p.Gly1305Arg)
c.3991G>C (p.Gly1331Arg)
c.3436G>C (p.Gly1146Arg)
18g.44953253G>TCA402325470SETBP1c.3913G>T (p.Gly1305Cys)
c.3991G>T (p.Gly1331Cys)
c.3436G>T (p.Gly1146Cys)
18g.44953254G>ACA402325471SETBP1c.3914G>A (p.Gly1305Asp)
c.3992G>A (p.Gly1331Asp)
c.3437G>A (p.Gly1146Asp)
18g.44953254G>CCA402325472SETBP1c.3914G>C (p.Gly1305Ala)
c.3992G>C (p.Gly1331Ala)
c.3437G>C (p.Gly1146Ala)
 gnomAD v4
18g.44953254G=CA2300141330SETBP1c.3914G= (p.Gly1305=)
c.3992G= (p.Gly1331=)
c.3437G= (p.Gly1146=)
18g.44953254G>TCA8946018SETBP1c.3914G>T (p.Gly1305Val)
c.3992G>T (p.Gly1331Val)
c.3437G>T (p.Gly1146Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953255C>ACA503982964SETBP1c.3915C>A (p.Gly1305=)
c.3993C>A (p.Gly1331=)
c.3438C>A (p.Gly1146=)
18g.44953255C>GCA503982965SETBP1c.3915C>G (p.Gly1305=)
c.3993C>G (p.Gly1331=)
c.3438C>G (p.Gly1146=)
18g.44953255C>TCA503982966SETBP1c.3915C>T (p.Gly1305=)
c.3993C>T (p.Gly1331=)
c.3438C>T (p.Gly1146=)
18g.44953256T>ACA402325473SETBP1c.3916T>A (p.Phe1306Ile)
c.3994T>A (p.Phe1332Ile)
c.3439T>A (p.Phe1147Ile)
18g.44953256T>CCA402325474SETBP1c.3916T>C (p.Phe1306Leu)
c.3994T>C (p.Phe1332Leu)
c.3439T>C (p.Phe1147Leu)
18g.44953256T>GCA402325475SETBP1c.3916T>G (p.Phe1306Val)
c.3994T>G (p.Phe1332Val)
c.3439T>G (p.Phe1147Val)
18g.44953257T>ACA402325476SETBP1c.3917T>A (p.Phe1306Tyr)
c.3995T>A (p.Phe1332Tyr)
c.3440T>A (p.Phe1147Tyr)
18g.44953257T>CCA402325477SETBP1c.3917T>C (p.Phe1306Ser)
c.3995T>C (p.Phe1332Ser)
c.3440T>C (p.Phe1147Ser)
18g.44953257T>GCA402325478SETBP1c.3917T>G (p.Phe1306Cys)
c.3995T>G (p.Phe1332Cys)
c.3440T>G (p.Phe1147Cys)
18g.44953258T>ACA402325479SETBP1c.3918T>A (p.Phe1306Leu)
c.3996T>A (p.Phe1332Leu)
c.3441T>A (p.Phe1147Leu)
 gnomAD v4
18g.44953258T>CCA503982971SETBP1c.3918T>C (p.Phe1306=)
c.3996T>C (p.Phe1332=)
c.3441T>C (p.Phe1147=)
18g.44953258T>GCA402325480SETBP1c.3918T>G (p.Phe1306Leu)
c.3996T>G (p.Phe1332Leu)
c.3441T>G (p.Phe1147Leu)
18g.44953259G>ACA402325481SETBP1c.3919G>A (p.Gly1307Arg)
c.3997G>A (p.Gly1333Arg)
c.3442G>A (p.Gly1148Arg)
18g.44953259G>CCA402325482SETBP1c.3919G>C (p.Gly1307Arg)
c.3997G>C (p.Gly1333Arg)
c.3442G>C (p.Gly1148Arg)
18g.44953259G>TCA402325483SETBP1c.3919G>T (p.Gly1307Ter)
c.3997G>T (p.Gly1333Ter)
c.3442G>T (p.Gly1148Ter)
18g.44953260G>ACA402325486SETBP1c.3920G>A (p.Gly1307Glu)
c.3998G>A (p.Gly1333Glu)
c.3443G>A (p.Gly1148Glu)
18g.44953260G>CCA402325485SETBP1c.3920G>C (p.Gly1307Ala)
c.3998G>C (p.Gly1333Ala)
c.3443G>C (p.Gly1148Ala)
18g.44953260G>TCA402325484SETBP1c.3920G>T (p.Gly1307Val)
c.3998G>T (p.Gly1333Val)
c.3443G>T (p.Gly1148Val)
18g.44953261A=CA2300141331SETBP1c.3921A= (p.Gly1307=)
c.3999A= (p.Gly1333=)
c.3444A= (p.Gly1148=)
18g.44953261A>CCA503982977SETBP1c.3921A>C (p.Gly1307=)
c.3999A>C (p.Gly1333=)
c.3444A>C (p.Gly1148=)
18g.44953261A>GCA503982978SETBP1c.3921A>G (p.Gly1307=)
c.3999A>G (p.Gly1333=)
c.3444A>G (p.Gly1148=)
 dbSNP gnomAD v3 gnomAD v4
18g.44953261A>TCA503982979SETBP1c.3921A>T (p.Gly1307=)
c.3999A>T (p.Gly1333=)
c.3444A>T (p.Gly1148=)
18g.44953262A=CA2300141332SETBP1c.3922A= (p.Thr1308=)
c.4000A= (p.Thr1334=)
c.3445A= (p.Thr1149=)
18g.44953262A>CCA402325487SETBP1c.3922A>C (p.Thr1308Pro)
c.4000A>C (p.Thr1334Pro)
c.3445A>C (p.Thr1149Pro)
18g.44953262A>GCA402325489SETBP1c.3922A>G (p.Thr1308Ala)
c.4000A>G (p.Thr1334Ala)
c.3445A>G (p.Thr1149Ala)
 dbSNP gnomAD v4
18g.44953262A>TCA402325488SETBP1c.3922A>T (p.Thr1308Ser)
c.4000A>T (p.Thr1334Ser)
c.3445A>T (p.Thr1149Ser)
18g.44953263C>ACA402325490SETBP1c.3923C>A (p.Thr1308Lys)
c.4001C>A (p.Thr1334Lys)
c.3446C>A (p.Thr1149Lys)
 COSMIC
18g.44953263C=CA2300141333SETBP1c.3923C= (p.Thr1308=)
c.4001C= (p.Thr1334=)
c.3446C= (p.Thr1149=)
18g.44953263C>GCA402325491SETBP1c.3923C>G (p.Thr1308Arg)
c.4001C>G (p.Thr1334Arg)
c.3446C>G (p.Thr1149Arg)
 gnomAD v4
18g.44953263C>TCA299699955SETBP1c.3923C>T (p.Thr1308Met)
c.4001C>T (p.Thr1334Met)
c.3446C>T (p.Thr1149Met)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.44953264G>ACA8946019SETBP1c.3924G>A (p.Thr1308=)
c.4002G>A (p.Thr1334=)
c.3447G>A (p.Thr1149=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953264G>CCA8946020SETBP1c.3924G>C (p.Thr1308=)
c.4002G>C (p.Thr1334=)
c.3447G>C (p.Thr1149=)
 dbSNP ExAC gnomAD v2
18g.44953264G=CA2300141334SETBP1c.3924G= (p.Thr1308=)
c.4002G= (p.Thr1334=)
c.3447G= (p.Thr1149=)
18g.44953264G>TCA503982987SETBP1c.3924G>T (p.Thr1308=)
c.4002G>T (p.Thr1334=)
c.3447G>T (p.Thr1149=)
 gnomAD v4
18g.44953265T>ACA402325492SETBP1c.3925T>A (p.Tyr1309Asn)
c.4003T>A (p.Tyr1335Asn)
c.3448T>A (p.Tyr1150Asn)
18g.44953265T>CCA299699959SETBP1c.3925T>C (p.Tyr1309His)
c.4003T>C (p.Tyr1335His)
c.3448T>C (p.Tyr1150His)
 ClinVar dbSNP
18g.44953265T>GCA402325493SETBP1c.3925T>G (p.Tyr1309Asp)
c.4003T>G (p.Tyr1335Asp)
c.3448T>G (p.Tyr1150Asp)
18g.44953265T=CA2300141335SETBP1c.3925T= (p.Tyr1309=)
c.4003T= (p.Tyr1335=)
c.3448T= (p.Tyr1150=)
18g.44953266A=CA2300141336SETBP1c.3926A= (p.Tyr1309=)
c.4004A= (p.Tyr1335=)
c.3449A= (p.Tyr1150=)
18g.44953266A>CCA402325494SETBP1c.3926A>C (p.Tyr1309Ser)
c.4004A>C (p.Tyr1335Ser)
c.3449A>C (p.Tyr1150Ser)
18g.44953266A>GCA8946021SETBP1c.3926A>G (p.Tyr1309Cys)
c.4004A>G (p.Tyr1335Cys)
c.3449A>G (p.Tyr1150Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.44953266A>TCA402325495SETBP1c.3926A>T (p.Tyr1309Phe)
c.4004A>T (p.Tyr1335Phe)
c.3449A>T (p.Tyr1150Phe)
18g.44953267C>ACA402325496SETBP1c.3927C>A (p.Tyr1309Ter)
c.4005C>A (p.Tyr1335Ter)
c.3450C>A (p.Tyr1150Ter)
18g.44953267C>GCA402325497SETBP1c.3927C>G (p.Tyr1309Ter)
c.4005C>G (p.Tyr1335Ter)
c.3450C>G (p.Tyr1150Ter)
18g.44953267C>TCA503982993SETBP1c.3927C>T (p.Tyr1309=)
c.4005C>T (p.Tyr1335=)
c.3450C>T (p.Tyr1150=)
18g.44953268A=CA2300141337SETBP1c.3928A= (p.Arg1310=)
c.4006A= (p.Arg1336=)
c.3451A= (p.Arg1151=)
18g.44953268A>CCA503982994SETBP1c.3928A>C (p.Arg1310=)
c.4006A>C (p.Arg1336=)
c.3451A>C (p.Arg1151=)
18g.44953268A>GCA402325498SETBP1c.3928A>G (p.Arg1310Gly)
c.4006A>G (p.Arg1336Gly)
c.3451A>G (p.Arg1151Gly)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953268A>TCA402325499SETBP1c.3928A>T (p.Arg1310Trp)
c.4006A>T (p.Arg1336Trp)
c.3451A>T (p.Arg1151Trp)
18g.44953269G>ACA8946022SETBP1c.3929G>A (p.Arg1310Lys)
c.4007G>A (p.Arg1336Lys)
c.3452G>A (p.Arg1151Lys)
 dbSNP ExAC gnomAD v2
18g.44953269G>CCA402325500SETBP1c.3929G>C (p.Arg1310Thr)
c.4007G>C (p.Arg1336Thr)
c.3452G>C (p.Arg1151Thr)
18g.44953269G=CA2300141338SETBP1c.3929G= (p.Arg1310=)
c.4007G= (p.Arg1336=)
c.3452G= (p.Arg1151=)
18g.44953269G>TCA402325501SETBP1c.3929G>T (p.Arg1310Met)
c.4007G>T (p.Arg1336Met)
c.3452G>T (p.Arg1151Met)
18g.44953270G>ACA503983001SETBP1c.3930G>A (p.Arg1310=)
c.4008G>A (p.Arg1336=)
c.3453G>A (p.Arg1151=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.44953270G>CCA402325502SETBP1c.3930G>C (p.Arg1310Ser)
c.4008G>C (p.Arg1336Ser)
c.3453G>C (p.Arg1151Ser)
18g.44953270G=CA2300141339SETBP1c.3930G= (p.Arg1310=)
c.4008G= (p.Arg1336=)
c.3453G= (p.Arg1151=)
18g.44953270G>TCA402325503SETBP1c.3930G>T (p.Arg1310Ser)
c.4008G>T (p.Arg1336Ser)
c.3453G>T (p.Arg1151Ser)

Number of alleles fetched