NM_001372044.2:c.1116C>T (p.Ser372=)
|
rs201282170
|
0.00386
|
NM_001372044.2(SHANK3):c.5185C>A (p.Pro1729Thr)
|
rs749130556
|
0.00319
|
NM_001372044.2(SHANK3):c.4104C>T (p.Ser1368=)
|
rs201793890
|
0.00221
|
NM_001372044.2(SHANK3):c.1190+7C>T
|
rs186106384
|
0.00149
|
NM_001372044.2(SHANK3):c.474G>T (p.Thr158=)
|
rs530240325
|
0.00137
|
NM_001372044.2(SHANK3):c.2436C>T (p.Ala812=)
|
rs61729465
|
0.00131
|
NM_001372044.2(SHANK3):c.3114G>C (p.Ala1038=)
|
rs772152761
|
0.00113
|
NM_001372044.2(SHANK3):c.1635C>T (p.Ala545=)
|
rs780922475
|
0.00111
|
NM_001372044.2(SHANK3):c.4410C>T (p.Thr1470=)
|
rs376136109
|
0.00094
|
NM_001372044.2(SHANK3):c.2220-36T>C
|
rs201640074
|
0.00092
|
NM_001372044.2(SHANK3):c.996-7C>G
|
rs371172305
|
0.00088
|
NM_001372044.2(SHANK3):c.2300+10G>A
|
rs202200715
|
0.00087
|
NM_001372044.2(SHANK3):c.4223T>G (p.Val1408Gly)
|
rs200087210
|
0.00064
|
NM_001372044.2(SHANK3):c.3257G>T (p.Gly1086Val)
|
rs767058690
|
0.00061
|
NM_001372044.2(SHANK3):c.3742G>A (p.Ala1248Thr)
|
rs139686326
|
0.00053
|
NM_001372044.2(SHANK3):c.4038C>T (p.Gly1346=)
|
rs367676023
|
0.00050
|
NM_001372044.2(SHANK3):c.4259C>T (p.Pro1420Leu)
|
rs73174429
|
0.00046
|
NM_001372044.2(SHANK3):c.708C>T (p.Asn236=)
|
rs79762996
|
0.00045
|
NM_001372044.2(SHANK3):c.2799C>T (p.Gly933=)
|
rs907713706
|
0.00033
|
NM_001372044.2(SHANK3):c.3876C>T (p.Asn1292=)
|
rs371876840
|
0.00028
|
NM_001372044.2(SHANK3):c.5043C>G (p.Pro1681=)
|
rs958460783
|
0.00020
|
NM_001372044.2(SHANK3):c.3938C>T (p.Ala1313Val)
|
rs188531567
|
0.00010
|
NM_001372044.2(SHANK3):c.2184T>C (p.Gly728=)
|
rs747708688
|
0.00005
|
NM_001372044.2(SHANK3):c.651C>T (p.Asn217=)
|
rs751998473
|
0.00005
|
NM_001372044.2(SHANK3):c.2745G>A (p.Pro915=)
|
rs1453397190
|
0.00004
|
NM_001372044.2(SHANK3):c.4083A>G (p.Pro1361=)
|
rs371543035
|
0.00004
|
NM_001372044.2(SHANK3):c.5160C>T (p.Pro1720=)
|
rs751652089
|
0.00003
|
NM_001372044.2(SHANK3):c.3547C>T (p.Leu1183=)
|
rs764710574
|
0.00002
|
NM_001372044.2(SHANK3):c.4365C>T (p.Ser1455=)
|
rs371175325
|
0.00002
|
NM_001372044.2(SHANK3):c.3675C>T (p.Asp1225=)
|
rs747936370
|
0.00001
|
NM_001372044.2(SHANK3):c.4600G>A (p.Gly1534Arg)
|
rs1440735830
|
0.00001
|
NM_001372044.2(SHANK3):c.4749G>A (p.Thr1583=)
|
rs751058928
|
0.00001
|
NC_000022.11:g.50697558T>C
|
|
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NM_001372044.2(SHANK3):c.1471G>A (p.Asp491Asn)
|
|
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NM_001372044.2(SHANK3):c.1482C>G (p.Ser494Arg)
|
|
|
NM_001372044.2(SHANK3):c.1530-280dup
|
rs745950788
|
|
NM_001372044.2(SHANK3):c.1688+21_1688+30del
|
|
|
NM_001372044.2(SHANK3):c.1689-3C>T
|
rs565420289
|
|
NM_001372044.2(SHANK3):c.16GCC[10] (p.Ala13_Pro14insAlaAla)
|
|
|
NM_001372044.2(SHANK3):c.16GCC[7] (p.Ala13del)
|
|
|
NM_001372044.2(SHANK3):c.2214T>C (p.Ser738=)
|
rs2146808552
|
|
NM_001372044.2(SHANK3):c.2220-134C>T
|
|
|
NM_001372044.2(SHANK3):c.2220-83G>A
|
|
|
NM_001372044.2(SHANK3):c.2416G>A (p.Ala806Thr)
|
|
|
NM_001372044.2(SHANK3):c.2421C>T (p.Asp807=)
|
|
|
NM_001372044.2(SHANK3):c.2664C>G (p.Ile888Met)
|
rs1603447099
|
|
NM_001372044.2(SHANK3):c.2673G>C (p.Pro891=)
|
rs1569114751
|
|
NM_001372044.2(SHANK3):c.2676G>C (p.Pro892=)
|
rs1173390690
|
|
NM_001372044.2(SHANK3):c.2697G>C (p.Pro899=)
|
|
|
NM_001372044.2(SHANK3):c.2703G>A (p.Ala901=)
|
|
|
NM_001372044.2(SHANK3):c.2712C>T (p.Tyr904=)
|
|
|
NM_001372044.2(SHANK3):c.2958G>C (p.Ala986=)
|
|
|
NM_001372044.2(SHANK3):c.2967G>A (p.Pro989=)
|
|
|
NM_001372044.2(SHANK3):c.3033C>G (p.Ala1011=)
|
|
|
NM_001372044.2(SHANK3):c.312C>A (p.Ala104=)
|
|
|
NM_001372044.2(SHANK3):c.3133G>T (p.Ala1045Ser)
|
rs530255181
|
|
NM_001372044.2(SHANK3):c.3216C>A (p.Leu1072=)
|
|
|
NM_001372044.2(SHANK3):c.3279G>C (p.Arg1093=)
|
rs2146830361
|
|
NM_001372044.2(SHANK3):c.3327C>A (p.Ala1109=)
|
|
|
NM_001372044.2(SHANK3):c.3339C>T (p.Ser1113=)
|
|
|
NM_001372044.2(SHANK3):c.3870C>T (p.Thr1290=)
|
|
|
NM_001372044.2(SHANK3):c.3941C>T (p.Pro1314Leu)
|
rs753314270
|
|
NM_001372044.2(SHANK3):c.399G>T (p.Pro133=)
|
|
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NM_001372044.2(SHANK3):c.4173G>A (p.Gly1391=)
|
|
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NM_001372044.2(SHANK3):c.4719C>T (p.Ser1573=)
|
|
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NM_001372044.2(SHANK3):c.5016A>C (p.Ala1672=)
|
|
|
NM_001372044.2(SHANK3):c.5097C>T (p.Arg1699=)
|
|
|
NM_001372044.2(SHANK3):c.5136C>G (p.Pro1712=)
|
|
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NM_001372044.2(SHANK3):c.5325C>T (p.Pro1775=)
|
|
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NM_001372044.2(SHANK3):c.813G>A (p.Ala271=)
|
|
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NM_001372044.2(SHANK3):c.996-5C>T
|
|
|
NM_033517.1(SHANK3):c.48G>A (p.Pro16=)
|
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