Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50720430_50720459dupCA640358963SHANK3c.2198_2227dup (p.Ala742_Ala743insGlyAlaAlaGlyLeuTyrGluProGlyAla)
n.2782_2811dup
c.1250_1279dup (p.Ala426_Ala427insGlyAlaAlaGlyLeuTyrGluProGlyAla)
c.740_769dup (p.Ala256_Ala257insGlyAlaAlaGlyLeuTyrGluProGlyAla)
c.*1196_*1225dup (n.*1196_*1225dup)
c.2594_2623dup (p.Ala874_Ala875insGlyAlaAlaGlyLeuTyrGluProGlyAla)
c.2576_2605dup (p.Ala868_Ala869insGlyAlaAlaGlyLeuTyrGluProGlyAla)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50720430_50720459delCA2657583131SHANK3c.2198_2227del (p.Gly733_Ala742del)
n.2782_2811del
c.1250_1279del (p.Gly417_Ala426del)
c.740_769del (p.Gly247_Ala256del)
c.*1196_*1225del (n.*1196_*1225del)
c.2594_2623del (p.Gly865_Ala874del)
c.2576_2605del (p.Gly859_Ala868del)
gnomAD v4
22g.50720434_50720457dupCA2657583139SHANK3c.2202_2225dup (p.Ala742_Ala743insAlaGlyLeuTyrGluProGlyAla)
n.2786_2809dup
c.1254_1277dup (p.Ala426_Ala427insAlaGlyLeuTyrGluProGlyAla)
c.744_767dup (p.Ala256_Ala257insAlaGlyLeuTyrGluProGlyAla)
c.*1200_*1223dup (n.*1200_*1223dup)
c.2598_2621dup (p.Ala874_Ala875insAlaGlyLeuTyrGluProGlyAla)
c.2580_2603dup (p.Ala868_Ala869insAlaGlyLeuTyrGluProGlyAla)
gnomAD v4
22g.50720446C>ACA515259290SHANK3c.2214C>A (p.Tyr738Ter)
n.2798C>A
c.1266C>A (p.Tyr422Ter)
c.756C>A (p.Tyr252Ter)
c.*1212C>A (n.*1212C>A)
c.2610C>A (p.Tyr870Ter)
c.2592C>A (p.Tyr864Ter)
ClinVar dbSNP gnomAD v4
22g.50720446C=CA2411007620SHANK3c.2214C= (p.Tyr738=)
n.2798C=
c.1266C= (p.Tyr422=)
c.756C= (p.Tyr252=)
c.*1212C= (n.*1212C=)
c.2610C= (p.Tyr870=)
c.2592C= (p.Tyr864=)
22g.50720446C>GCA16043165SHANK3c.2214C>G (p.Tyr738Ter)
n.2798C>G
c.1266C>G (p.Tyr422Ter)
c.756C>G (p.Tyr252Ter)
c.*1212C>G (n.*1212C>G)
c.2610C>G (p.Tyr870Ter)
c.2592C>G (p.Tyr864Ter)
ClinVar dbSNP gnomAD v4
22g.50720446C>TCA325578103SHANK3c.2214C>T (p.Tyr738=)
n.2798C>T
c.1266C>T (p.Tyr422=)
c.756C>T (p.Tyr252=)
c.*1212C>T (n.*1212C>T)
c.2610C>T (p.Tyr870=)
c.2592C>T (p.Tyr864=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50720448_50720458delCA2657583149SHANK3c.2216_2226del (p.Glu739GlyfsTer?)
n.2800_2810del
c.1268_1278del (p.Glu423GlyfsTer?)
c.758_768del (p.Glu253GlyfsTer?)
c.*1214_*1224del (n.*1214_*1224del)
c.2612_2622del (p.Glu871GlyfsTer?)
c.2594_2604del (p.Glu865GlyfsTer?)
gnomAD v4
22g.50720447G>ACA515259291SHANK3c.2215G>A (p.Glu739Lys)
n.2799G>A
c.1267G>A (p.Glu423Lys)
c.757G>A (p.Glu253Lys)
c.*1213G>A (n.*1213G>A)
c.2611G>A (p.Glu871Lys)
c.2593G>A (p.Glu865Lys)
gnomAD v4
22g.50720447G>CCA515259292SHANK3c.2215G>C (p.Glu739Gln)
n.2799G>C
c.1267G>C (p.Glu423Gln)
c.757G>C (p.Glu253Gln)
c.*1213G>C (n.*1213G>C)
c.2611G>C (p.Glu871Gln)
c.2593G>C (p.Glu865Gln)
gnomAD v4
22g.50720447G>TCA515259293SHANK3c.2215G>T (p.Glu739Ter)
n.2799G>T
c.1267G>T (p.Glu423Ter)
c.757G>T (p.Glu253Ter)
c.*1213G>T (n.*1213G>T)
c.2611G>T (p.Glu871Ter)
c.2593G>T (p.Glu865Ter)
gnomAD v4
22g.50720448A>CCA515259294SHANK3c.2216A>C (p.Glu739Ala)
n.2800A>C
c.1268A>C (p.Glu423Ala)
c.758A>C (p.Glu253Ala)
c.*1214A>C (n.*1214A>C)
c.2612A>C (p.Glu871Ala)
c.2594A>C (p.Glu865Ala)
22g.50720448A>GCA515259295SHANK3c.2216A>G (p.Glu739Gly)
n.2800A>G
c.1268A>G (p.Glu423Gly)
c.758A>G (p.Glu253Gly)
c.*1214A>G (n.*1214A>G)
c.2612A>G (p.Glu871Gly)
c.2594A>G (p.Glu865Gly)
gnomAD v4
22g.50720448A>TCA515259296SHANK3c.2216A>T (p.Glu739Val)
n.2800A>T
c.1268A>T (p.Glu423Val)
c.758A>T (p.Glu253Val)
c.*1214A>T (n.*1214A>T)
c.2612A>T (p.Glu871Val)
c.2594A>T (p.Glu865Val)
22g.50720449G>ACA515259297SHANK3c.2217G>A (p.Glu739=)
n.2801G>A
c.1269G>A (p.Glu423=)
c.759G>A (p.Glu253=)
c.*1215G>A (n.*1215G>A)
c.2613G>A (p.Glu871=)
c.2595G>A (p.Glu865=)
gnomAD v4
22g.50720449G>CCA515259298SHANK3c.2217G>C (p.Glu739Asp)
n.2801G>C
c.1269G>C (p.Glu423Asp)
c.759G>C (p.Glu253Asp)
c.*1215G>C (n.*1215G>C)
c.2613G>C (p.Glu871Asp)
c.2595G>C (p.Glu865Asp)
gnomAD v4
22g.50720449G>TCA515259299SHANK3c.2217G>T (p.Glu739Asp)
n.2801G>T
c.1269G>T (p.Glu423Asp)
c.759G>T (p.Glu253Asp)
c.*1215G>T (n.*1215G>T)
c.2613G>T (p.Glu871Asp)
c.2595G>T (p.Glu865Asp)
gnomAD v4
22g.50720450C>ACA515259300SHANK3c.2218C>A (p.Pro740Thr)
n.2802C>A
c.1270C>A (p.Pro424Thr)
c.760C>A (p.Pro254Thr)
c.*1216C>A (n.*1216C>A)
c.2614C>A (p.Pro872Thr)
c.2596C>A (p.Pro866Thr)
gnomAD v4
22g.50720450C=CA2411007621SHANK3c.2218C= (p.Pro740=)
n.2802C=
c.1270C= (p.Pro424=)
c.760C= (p.Pro254=)
c.*1216C= (n.*1216C=)
c.2614C= (p.Pro872=)
c.2596C= (p.Pro866=)
22g.50720450C>GCA515259301SHANK3c.2218C>G (p.Pro740Ala)
n.2802C>G
c.1270C>G (p.Pro424Ala)
c.760C>G (p.Pro254Ala)
c.*1216C>G (n.*1216C>G)
c.2614C>G (p.Pro872Ala)
c.2596C>G (p.Pro866Ala)
dbSNP gnomAD v3 gnomAD v4
22g.50720450C>TCA515259302SHANK3c.2218C>T (p.Pro740Ser)
n.2802C>T
c.1270C>T (p.Pro424Ser)
c.760C>T (p.Pro254Ser)
c.*1216C>T (n.*1216C>T)
c.2614C>T (p.Pro872Ser)
c.2596C>T (p.Pro866Ser)
gnomAD v4
22g.50720451C>ACA515259304SHANK3c.2219C>A (p.Pro740Gln)
n.2803C>A
c.1271C>A (p.Pro424Gln)
c.761C>A (p.Pro254Gln)
c.*1217C>A (n.*1217C>A)
c.2615C>A (p.Pro872Gln)
c.2597C>A (p.Pro866Gln)
gnomAD v4
22g.50720451C=CA2411007622SHANK3c.2219C= (p.Pro740=)
n.2803C=
c.1271C= (p.Pro424=)
c.761C= (p.Pro254=)
c.*1217C= (n.*1217C=)
c.2615C= (p.Pro872=)
c.2597C= (p.Pro866=)
22g.50720451C>GCA515259303SHANK3c.2219C>G (p.Pro740Arg)
n.2803C>G
c.1271C>G (p.Pro424Arg)
c.761C>G (p.Pro254Arg)
c.*1217C>G (n.*1217C>G)
c.2615C>G (p.Pro872Arg)
c.2597C>G (p.Pro866Arg)
gnomAD v4
22g.50720451C>TCA325578107SHANK3c.2219C>T (p.Pro740Leu)
n.2803C>T
c.1271C>T (p.Pro424Leu)
c.761C>T (p.Pro254Leu)
c.*1217C>T (n.*1217C>T)
c.2615C>T (p.Pro872Leu)
c.2597C>T (p.Pro866Leu)
dbSNP gnomAD v2 gnomAD v4
22g.50720452G>ACA515259305SHANK3c.2220G>A (p.Pro740=)
n.2804G>A
c.1272G>A (p.Pro424=)
c.762G>A (p.Pro254=)
c.*1218G>A (n.*1218G>A)
c.2616G>A (p.Pro872=)
c.2598G>A (p.Pro866=)
dbSNP gnomAD v2 gnomAD v4
22g.50720452G>CCA515259306SHANK3c.2220G>C (p.Pro740=)
n.2804G>C
c.1272G>C (p.Pro424=)
c.762G>C (p.Pro254=)
c.*1218G>C (n.*1218G>C)
c.2616G>C (p.Pro872=)
c.2598G>C (p.Pro866=)
gnomAD v4
22g.50720452G=CA2411007623SHANK3c.2220G= (p.Pro740=)
n.2804G=
c.1272G= (p.Pro424=)
c.762G= (p.Pro254=)
c.*1218G= (n.*1218G=)
c.2616G= (p.Pro872=)
c.2598G= (p.Pro866=)
22g.50720452G>TCA515259307SHANK3c.2220G>T (p.Pro740=)
n.2804G>T
c.1272G>T (p.Pro424=)
c.762G>T (p.Pro254=)
c.*1218G>T (n.*1218G>T)
c.2616G>T (p.Pro872=)
c.2598G>T (p.Pro866=)
gnomAD v4
22g.50720454delCA2657583150SHANK3c.2222del (p.Gly741AlafsTer19)
n.2806del
c.1274del (p.Gly425AlafsTer19)
c.764del (p.Gly255AlafsTer19)
c.*1220del (n.*1220del)
c.2618del (p.Gly873AlafsTer19)
c.2600del (p.Gly867AlafsTer19)
gnomAD v4
22g.50720453G>ACA515259308SHANK3c.2221G>A (p.Gly741Ser)
n.2805G>A
c.1273G>A (p.Gly425Ser)
c.763G>A (p.Gly255Ser)
c.*1219G>A (n.*1219G>A)
c.2617G>A (p.Gly873Ser)
c.2599G>A (p.Gly867Ser)
gnomAD v4
22g.50720453G>CCA515259309SHANK3c.2221G>C (p.Gly741Arg)
n.2805G>C
c.1273G>C (p.Gly425Arg)
c.763G>C (p.Gly255Arg)
c.*1219G>C (n.*1219G>C)
c.2617G>C (p.Gly873Arg)
c.2599G>C (p.Gly867Arg)
gnomAD v4
22g.50720453G>TCA515259310SHANK3c.2221G>T (p.Gly741Cys)
n.2805G>T
c.1273G>T (p.Gly425Cys)
c.763G>T (p.Gly255Cys)
c.*1219G>T (n.*1219G>T)
c.2617G>T (p.Gly873Cys)
c.2599G>T (p.Gly867Cys)
gnomAD v4
22g.50720454G>ACA515259311SHANK3c.2222G>A (p.Gly741Asp)
n.2806G>A
c.1274G>A (p.Gly425Asp)
c.764G>A (p.Gly255Asp)
c.*1220G>A (n.*1220G>A)
c.2618G>A (p.Gly873Asp)
c.2600G>A (p.Gly867Asp)
gnomAD v4
22g.50720454G>CCA515259312SHANK3c.2222G>C (p.Gly741Ala)
n.2806G>C
c.1274G>C (p.Gly425Ala)
c.764G>C (p.Gly255Ala)
c.*1220G>C (n.*1220G>C)
c.2618G>C (p.Gly873Ala)
c.2600G>C (p.Gly867Ala)
gnomAD v4
22g.50720454G>TCA515259313SHANK3c.2222G>T (p.Gly741Val)
n.2806G>T
c.1274G>T (p.Gly425Val)
c.764G>T (p.Gly255Val)
c.*1220G>T (n.*1220G>T)
c.2618G>T (p.Gly873Val)
c.2600G>T (p.Gly867Val)
gnomAD v4
22g.50720455C>ACA515259314SHANK3c.2223C>A (p.Gly741=)
n.2807C>A
c.1275C>A (p.Gly425=)
c.765C>A (p.Gly255=)
c.*1221C>A (n.*1221C>A)
c.2619C>A (p.Gly873=)
c.2601C>A (p.Gly867=)
gnomAD v4
22g.50720455C=CA2411007624SHANK3c.2223C= (p.Gly741=)
n.2807C=
c.1275C= (p.Gly425=)
c.765C= (p.Gly255=)
c.*1221C= (n.*1221C=)
c.2619C= (p.Gly873=)
c.2601C= (p.Gly867=)
22g.50720455C>GCA515259315SHANK3c.2223C>G (p.Gly741=)
n.2807C>G
c.1275C>G (p.Gly425=)
c.765C>G (p.Gly255=)
c.*1221C>G (n.*1221C>G)
c.2619C>G (p.Gly873=)
c.2601C>G (p.Gly867=)
gnomAD v4
22g.50720455C>TCA515259316SHANK3c.2223C>T (p.Gly741=)
n.2807C>T
c.1275C>T (p.Gly425=)
c.765C>T (p.Gly255=)
c.*1221C>T (n.*1221C>T)
c.2619C>T (p.Gly873=)
c.2601C>T (p.Gly867=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50720456G>ACA515259319SHANK3c.2224G>A (p.Ala742Thr)
n.2808G>A
c.1276G>A (p.Ala426Thr)
c.766G>A (p.Ala256Thr)
c.*1222G>A (n.*1222G>A)
c.2620G>A (p.Ala874Thr)
c.2602G>A (p.Ala868Thr)
gnomAD v4
22g.50720456G>CCA515259318SHANK3c.2224G>C (p.Ala742Pro)
n.2808G>C
c.1276G>C (p.Ala426Pro)
c.766G>C (p.Ala256Pro)
c.*1222G>C (n.*1222G>C)
c.2620G>C (p.Ala874Pro)
c.2602G>C (p.Ala868Pro)
gnomAD v4
22g.50720456G>TCA515259317SHANK3c.2224G>T (p.Ala742Ser)
n.2808G>T
c.1276G>T (p.Ala426Ser)
c.766G>T (p.Ala256Ser)
c.*1222G>T (n.*1222G>T)
c.2620G>T (p.Ala874Ser)
c.2602G>T (p.Ala868Ser)
gnomAD v4
22g.50720457C>ACA515259320SHANK3c.2225C>A (p.Ala742Glu)
n.2809C>A
c.1277C>A (p.Ala426Glu)
c.767C>A (p.Ala256Glu)
c.*1223C>A (n.*1223C>A)
c.2621C>A (p.Ala874Glu)
c.2603C>A (p.Ala868Glu)
gnomAD v4
22g.50720457C=CA2411007625SHANK3c.2225C= (p.Ala742=)
n.2809C=
c.1277C= (p.Ala426=)
c.767C= (p.Ala256=)
c.*1223C= (n.*1223C=)
c.2621C= (p.Ala874=)
c.2603C= (p.Ala868=)
22g.50720457C>GCA515259321SHANK3c.2225C>G (p.Ala742Gly)
n.2809C>G
c.1277C>G (p.Ala426Gly)
c.767C>G (p.Ala256Gly)
c.*1223C>G (n.*1223C>G)
c.2621C>G (p.Ala874Gly)
c.2603C>G (p.Ala868Gly)
ClinVar dbSNP
22g.50720457C>TCA14963183SHANK3c.2225C>T (p.Ala742Val)
n.2809C>T
c.1277C>T (p.Ala426Val)
c.767C>T (p.Ala256Val)
c.*1223C>T (n.*1223C>T)
c.2621C>T (p.Ala874Val)
c.2603C>T (p.Ala868Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50720458G>ACA515259322SHANK3c.2226G>A (p.Ala742=)
n.2810G>A
c.1278G>A (p.Ala426=)
c.768G>A (p.Ala256=)
c.*1224G>A (n.*1224G>A)
c.2622G>A (p.Ala874=)
c.2604G>A (p.Ala868=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50720458G>CCA515259324SHANK3c.2226G>C (p.Ala742=)
n.2810G>C
c.1278G>C (p.Ala426=)
c.768G>C (p.Ala256=)
c.*1224G>C (n.*1224G>C)
c.2622G>C (p.Ala874=)
c.2604G>C (p.Ala868=)
dbSNP gnomAD v4
22g.50720458G=CA2411007626SHANK3c.2226G= (p.Ala742=)
n.2810G=
c.1278G= (p.Ala426=)
c.768G= (p.Ala256=)
c.*1224G= (n.*1224G=)
c.2622G= (p.Ala874=)
c.2604G= (p.Ala868=)

Number of alleles fetched