Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.51026311_51028334delCA1139657030NRXN1c.-59_772+1193del
c.-59_871+62del
ClinVar
2g.51026421T>ACA346823175NRXN1c.772+1081A>T (n.772+1081A>T)
c.329+1081A>T
n.66+1081A>T
c.821A>T (p.Asn274Ile)
c.297+1081A>T
c.251A>T (p.Asn84Ile)
2g.51026421T>CCA1655388NRXN1c.772+1081A>G (n.772+1081A>G)
c.329+1081A>G
n.66+1081A>G
c.821A>G (p.Asn274Ser)
c.297+1081A>G
c.251A>G (p.Asn84Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026421T>GCA346823177NRXN1c.772+1081A>C (n.772+1081A>C)
c.329+1081A>C
n.66+1081A>C
c.821A>C (p.Asn274Thr)
c.297+1081A>C
c.251A>C (p.Asn84Thr)
2g.51026421T=CA1249877832NRXN1c.772+1081A= (n.772+1081A=)
c.329+1081A=
n.66+1081A=
c.821A= (p.Asn274=)
c.297+1081A=
c.251A= (p.Asn84=)
2g.51026422T>ACA346823179NRXN1c.772+1080A>T (n.772+1080A>T)
c.329+1080A>T
n.66+1080A>T
c.820A>T (p.Asn274Tyr)
c.297+1080A>T
c.250A>T (p.Asn84Tyr)
2g.51026422T>CCA346823180NRXN1c.772+1080A>G (n.772+1080A>G)
c.329+1080A>G
n.66+1080A>G
c.820A>G (p.Asn274Asp)
c.297+1080A>G
c.250A>G (p.Asn84Asp)
dbSNP gnomAD v2
2g.51026422T>GCA346823182NRXN1c.772+1080A>C (n.772+1080A>C)
c.329+1080A>C
n.66+1080A>C
c.820A>C (p.Asn274His)
c.297+1080A>C
c.250A>C (p.Asn84His)
2g.51026422T=CA1249877833NRXN1c.772+1080A= (n.772+1080A=)
c.329+1080A=
n.66+1080A=
c.820A= (p.Asn274=)
c.297+1080A=
c.250A= (p.Asn84=)
2g.51026423G>ACA426106428NRXN1c.772+1079C>T (n.772+1079C>T)
c.329+1079C>T
n.66+1079C>T
c.819C>T (p.Asp273=)
c.297+1079C>T
c.249C>T (p.Asp83=)
gnomAD v4
2g.51026423G>CCA346823183NRXN1c.772+1079C>G (n.772+1079C>G)
c.329+1079C>G
n.66+1079C>G
c.819C>G (p.Asp273Glu)
c.297+1079C>G
c.249C>G (p.Asp83Glu)
2g.51026423G>TCA346823185NRXN1c.772+1079C>A (n.772+1079C>A)
c.329+1079C>A
n.66+1079C>A
c.819C>A (p.Asp273Glu)
c.297+1079C>A
c.249C>A (p.Asp83Glu)
gnomAD v4
2g.51026424T>ACA346823186NRXN1c.772+1078A>T (n.772+1078A>T)
c.329+1078A>T
n.66+1078A>T
c.818A>T (p.Asp273Val)
c.297+1078A>T
c.248A>T (p.Asp83Val)
gnomAD v4
2g.51026424T>CCA295629NRXN1c.772+1078A>G (n.772+1078A>G)
c.329+1078A>G
n.66+1078A>G
c.818A>G (p.Asp273Gly)
c.297+1078A>G
c.248A>G (p.Asp83Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026424T>GCA346823189NRXN1c.772+1078A>C (n.772+1078A>C)
c.329+1078A>C
n.66+1078A>C
c.818A>C (p.Asp273Ala)
c.297+1078A>C
c.248A>C (p.Asp83Ala)
2g.51026424T=CA1249877834NRXN1c.772+1078A= (n.772+1078A=)
c.329+1078A=
n.66+1078A=
c.818A= (p.Asp273=)
c.297+1078A=
c.248A= (p.Asp83=)
2g.51026425C>ACA346823190NRXN1c.772+1077G>T (n.772+1077G>T)
c.329+1077G>T
n.66+1077G>T
c.817G>T (p.Asp273Tyr)
c.297+1077G>T
c.247G>T (p.Asp83Tyr)
gnomAD v4
2g.51026425C>GCA346823192NRXN1c.772+1077G>C (n.772+1077G>C)
c.329+1077G>C
n.66+1077G>C
c.817G>C (p.Asp273His)
c.297+1077G>C
c.247G>C (p.Asp83His)
2g.51026425C>TCA346823193NRXN1c.772+1077G>A (n.772+1077G>A)
c.329+1077G>A
n.66+1077G>A
c.817G>A (p.Asp273Asn)
c.297+1077G>A
c.247G>A (p.Asp83Asn)
2g.51026426A=CA1249877835NRXN1c.772+1076T= (n.772+1076T=)
c.329+1076T=
n.66+1076T=
c.816T= (p.His272=)
c.297+1076T=
c.246T= (p.His82=)
2g.51026426A>CCA346823197NRXN1c.772+1076T>G (n.772+1076T>G)
c.329+1076T>G
n.66+1076T>G
c.816T>G (p.His272Gln)
c.297+1076T>G
c.246T>G (p.His82Gln)
2g.51026426A>GCA1655389NRXN1c.772+1076T>C (n.772+1076T>C)
c.329+1076T>C
n.66+1076T>C
c.816T>C (p.His272=)
c.297+1076T>C
c.246T>C (p.His82=)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.51026426A>TCA346823195NRXN1c.772+1076T>A (n.772+1076T>A)
c.329+1076T>A
n.66+1076T>A
c.816T>A (p.His272Gln)
c.297+1076T>A
c.246T>A (p.His82Gln)
2g.51026427T>ACA346823198NRXN1c.772+1075A>T (n.772+1075A>T)
c.329+1075A>T
n.66+1075A>T
c.815A>T (p.His272Leu)
c.297+1075A>T
c.245A>T (p.His82Leu)
ClinVar
2g.51026427T>CCA346823200NRXN1c.772+1075A>G (n.772+1075A>G)
c.329+1075A>G
n.66+1075A>G
c.815A>G (p.His272Arg)
c.297+1075A>G
c.245A>G (p.His82Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.51026427T>GCA346823201NRXN1c.772+1075A>C (n.772+1075A>C)
c.329+1075A>C
n.66+1075A>C
c.815A>C (p.His272Pro)
c.297+1075A>C
c.245A>C (p.His82Pro)
dbSNP gnomAD v2
2g.51026427T=CA1249877836NRXN1c.772+1075A= (n.772+1075A=)
c.329+1075A=
n.66+1075A=
c.815A= (p.His272=)
c.297+1075A=
c.245A= (p.His82=)
2g.51026428G>ACA346823203NRXN1c.772+1074C>T (n.772+1074C>T)
c.329+1074C>T
n.66+1074C>T
c.814C>T (p.His272Tyr)
c.297+1074C>T
c.244C>T (p.His82Tyr)
dbSNP gnomAD v3 gnomAD v4
2g.51026428G>CCA346823204NRXN1c.772+1074C>G (n.772+1074C>G)
c.329+1074C>G
n.66+1074C>G
c.814C>G (p.His272Asp)
c.297+1074C>G
c.244C>G (p.His82Asp)
2g.51026428G=CA1249877837NRXN1c.772+1074C= (n.772+1074C=)
c.329+1074C=
n.66+1074C=
c.814C= (p.His272=)
c.297+1074C=
c.244C= (p.His82=)
2g.51026428G>TCA48054733NRXN1c.772+1074C>A (n.772+1074C>A)
c.329+1074C>A
n.66+1074C>A
c.814C>A (p.His272Asn)
c.297+1074C>A
c.244C>A (p.His82Asn)
dbSNP gnomAD v2 gnomAD v4
2g.51026429T>ACA346823207NRXN1c.772+1073A>T (n.772+1073A>T)
c.329+1073A>T
n.66+1073A>T
c.813A>T (p.Leu271Phe)
c.297+1073A>T
c.243A>T (p.Leu81Phe)
2g.51026429T>CCA426106429NRXN1c.772+1073A>G (n.772+1073A>G)
c.329+1073A>G
n.66+1073A>G
c.813A>G (p.Leu271=)
c.297+1073A>G
c.243A>G (p.Leu81=)
dbSNP gnomAD v3 gnomAD v4
2g.51026429T>GCA346823208NRXN1c.772+1073A>C (n.772+1073A>C)
c.329+1073A>C
n.66+1073A>C
c.813A>C (p.Leu271Phe)
c.297+1073A>C
c.243A>C (p.Leu81Phe)
2g.51026429T=CA1249877838NRXN1c.772+1073A= (n.772+1073A=)
c.329+1073A=
n.66+1073A=
c.813A= (p.Leu271=)
c.297+1073A=
c.243A= (p.Leu81=)
2g.51026430A>CCA346823210NRXN1c.772+1072T>G (n.772+1072T>G)
c.329+1072T>G
n.66+1072T>G
c.812T>G (p.Leu271Ter)
c.297+1072T>G
c.242T>G (p.Leu81Ter)
2g.51026430A>GCA346823212NRXN1c.772+1072T>C (n.772+1072T>C)
c.329+1072T>C
n.66+1072T>C
c.812T>C (p.Leu271Ser)
c.297+1072T>C
c.242T>C (p.Leu81Ser)
ClinVar
2g.51026430A>TCA346823213NRXN1c.772+1072T>A (n.772+1072T>A)
c.329+1072T>A
n.66+1072T>A
c.812T>A (p.Leu271Ter)
c.297+1072T>A
c.242T>A (p.Leu81Ter)
2g.51026431A=CA1249877839NRXN1c.772+1071T= (n.772+1071T=)
c.329+1071T=
n.66+1071T=
c.811T= (p.Leu271=)
c.297+1071T=
c.241T= (p.Leu81=)
2g.51026431A>CCA346823215NRXN1c.772+1071T>G (n.772+1071T>G)
c.329+1071T>G
n.66+1071T>G
c.811T>G (p.Leu271Val)
c.297+1071T>G
c.241T>G (p.Leu81Val)
COSMIC COSMIC
2g.51026431A>GCA426106430NRXN1c.772+1071T>C (n.772+1071T>C)
c.329+1071T>C
n.66+1071T>C
c.811T>C (p.Leu271=)
c.297+1071T>C
c.241T>C (p.Leu81=)
dbSNP gnomAD v2 gnomAD v4
2g.51026431A>TCA346823216NRXN1c.772+1071T>A (n.772+1071T>A)
c.329+1071T>A
n.66+1071T>A
c.811T>A (p.Leu271Ile)
c.297+1071T>A
c.241T>A (p.Leu81Ile)
gnomAD v4
2g.51026432C>ACA426106431NRXN1c.772+1070G>T (n.772+1070G>T)
c.329+1070G>T
n.66+1070G>T
c.810G>T (p.Leu270=)
c.297+1070G>T
c.240G>T (p.Leu80=)
gnomAD v4
2g.51026432C=CA1249877840NRXN1c.772+1070G= (n.772+1070G=)
c.329+1070G=
n.66+1070G=
c.810G= (p.Leu270=)
c.297+1070G=
c.240G= (p.Leu80=)
2g.51026432C>GCA426106432NRXN1c.772+1070G>C (n.772+1070G>C)
c.329+1070G>C
n.66+1070G>C
c.810G>C (p.Leu270=)
c.297+1070G>C
c.240G>C (p.Leu80=)
dbSNP gnomAD v3 gnomAD v4
2g.51026432C>TCA426106433NRXN1c.772+1070G>A (n.772+1070G>A)
c.329+1070G>A
n.66+1070G>A
c.810G>A (p.Leu270=)
c.297+1070G>A
c.240G>A (p.Leu80=)
ClinVar dbSNP gnomAD v4
2g.51026433A>CCA346823221NRXN1c.772+1069T>G (n.772+1069T>G)
c.329+1069T>G
n.66+1069T>G
c.809T>G (p.Leu270Arg)
c.297+1069T>G
c.239T>G (p.Leu80Arg)
2g.51026433A>GCA346823220NRXN1c.772+1069T>C (n.772+1069T>C)
c.329+1069T>C
n.66+1069T>C
c.809T>C (p.Leu270Pro)
c.297+1069T>C
c.239T>C (p.Leu80Pro)
gnomAD v4
2g.51026433A>TCA346823218NRXN1c.772+1069T>A (n.772+1069T>A)
c.329+1069T>A
n.66+1069T>A
c.809T>A (p.Leu270Gln)
c.297+1069T>A
c.239T>A (p.Leu80Gln)
2g.51026434G>ACA426106434NRXN1c.772+1068C>T (n.772+1068C>T)
c.329+1068C>T
n.66+1068C>T
c.808C>T (p.Leu270=)
c.297+1068C>T
c.238C>T (p.Leu80=)
gnomAD v4
2g.51026434G>CCA1655390NRXN1c.772+1068C>G (n.772+1068C>G)
c.329+1068C>G
n.66+1068C>G
c.808C>G (p.Leu270Val)
c.297+1068C>G
c.238C>G (p.Leu80Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026434G=CA1249877841NRXN1c.772+1068C= (n.772+1068C=)
c.329+1068C=
n.66+1068C=
c.808C= (p.Leu270=)
c.297+1068C=
c.238C= (p.Leu80=)
2g.51026434G>TCA346823223NRXN1c.772+1068C>A (n.772+1068C>A)
c.329+1068C>A
n.66+1068C>A
c.808C>A (p.Leu270Met)
c.297+1068C>A
c.238C>A (p.Leu80Met)
gnomAD v4
2g.51026435C>ACA426106435NRXN1c.772+1067G>T (n.772+1067G>T)
c.329+1067G>T
n.66+1067G>T
c.807G>T (p.Val269=)
c.297+1067G>T
c.237G>T (p.Val79=)
gnomAD v4
2g.51026435C>GCA426106436NRXN1c.772+1067G>C (n.772+1067G>C)
c.329+1067G>C
n.66+1067G>C
c.807G>C (p.Val269=)
c.297+1067G>C
c.237G>C (p.Val79=)
2g.51026435C>TCA426106437NRXN1c.772+1067G>A (n.772+1067G>A)
c.329+1067G>A
n.66+1067G>A
c.807G>A (p.Val269=)
c.297+1067G>A
c.237G>A (p.Val79=)
2g.51026436A=CA1249877842NRXN1c.772+1066T= (n.772+1066T=)
c.329+1066T=
n.66+1066T=
c.806T= (p.Val269=)
c.297+1066T=
c.236T= (p.Val79=)
2g.51026436A>CCA346823224NRXN1c.772+1066T>G (n.772+1066T>G)
c.329+1066T>G
n.66+1066T>G
c.806T>G (p.Val269Gly)
c.297+1066T>G
c.236T>G (p.Val79Gly)
2g.51026436A>GCA346823225NRXN1c.772+1066T>C (n.772+1066T>C)
c.329+1066T>C
n.66+1066T>C
c.806T>C (p.Val269Ala)
c.297+1066T>C
c.236T>C (p.Val79Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.51026436A>TCA346823226NRXN1c.772+1066T>A (n.772+1066T>A)
c.329+1066T>A
n.66+1066T>A
c.806T>A (p.Val269Glu)
c.297+1066T>A
c.236T>A (p.Val79Glu)
gnomAD v4
2g.51026437C>ACA346823227NRXN1c.772+1065G>T (n.772+1065G>T)
c.329+1065G>T
n.66+1065G>T
c.805G>T (p.Val269Leu)
c.297+1065G>T
c.235G>T (p.Val79Leu)
dbSNP gnomAD v4
2g.51026437C=CA1249877843NRXN1c.772+1065G= (n.772+1065G=)
c.329+1065G=
n.66+1065G=
c.805G= (p.Val269=)
c.297+1065G=
c.235G= (p.Val79=)
2g.51026437C>GCA346823228NRXN1c.772+1065G>C (n.772+1065G>C)
c.329+1065G>C
n.66+1065G>C
c.805G>C (p.Val269Leu)
c.297+1065G>C
c.235G>C (p.Val79Leu)
2g.51026437C>TCA346823229NRXN1c.772+1065G>A (n.772+1065G>A)
c.329+1065G>A
n.66+1065G>A
c.805G>A (p.Val269Met)
c.297+1065G>A
c.235G>A (p.Val79Met)
2g.51026438C>ACA426106439NRXN1c.772+1064G>T (n.772+1064G>T)
c.329+1064G>T
n.66+1064G>T
c.804G>T (p.Pro268=)
c.297+1064G>T
c.234G>T (p.Pro78=)
gnomAD v4
2g.51026438C=CA1249877844NRXN1c.772+1064G= (n.772+1064G=)
c.329+1064G=
n.66+1064G=
c.804G= (p.Pro268=)
c.297+1064G=
c.234G= (p.Pro78=)
2g.51026438C>GCA1655391NRXN1c.772+1064G>C (n.772+1064G>C)
c.329+1064G>C
n.66+1064G>C
c.804G>C (p.Pro268=)
c.297+1064G>C
c.234G>C (p.Pro78=)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.51026438C>TCA48054734NRXN1c.772+1064G>A (n.772+1064G>A)
c.329+1064G>A
n.66+1064G>A
c.804G>A (p.Pro268=)
c.297+1064G>A
c.234G>A (p.Pro78=)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.51026439G>ACA1655392NRXN1c.772+1063C>T (n.772+1063C>T)
c.329+1063C>T
n.66+1063C>T
c.803C>T (p.Pro268Leu)
c.297+1063C>T
c.233C>T (p.Pro78Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026439G>CCA346823230NRXN1c.772+1063C>G (n.772+1063C>G)
c.329+1063C>G
n.66+1063C>G
c.803C>G (p.Pro268Arg)
c.297+1063C>G
c.233C>G (p.Pro78Arg)
2g.51026439G=CA1249877845NRXN1c.772+1063C= (n.772+1063C=)
c.329+1063C=
n.66+1063C=
c.803C= (p.Pro268=)
c.297+1063C=
c.233C= (p.Pro78=)
2g.51026439G>TCA346823231NRXN1c.772+1063C>A (n.772+1063C>A)
c.329+1063C>A
n.66+1063C>A
c.803C>A (p.Pro268Gln)
c.297+1063C>A
c.233C>A (p.Pro78Gln)
gnomAD v4
2g.51026440G>ACA346823233NRXN1c.772+1062C>T (n.772+1062C>T)
c.329+1062C>T
n.66+1062C>T
c.802C>T (p.Pro268Ser)
c.297+1062C>T
c.232C>T (p.Pro78Ser)
dbSNP gnomAD v4
2g.51026440G>CCA346823234NRXN1c.772+1062C>G (n.772+1062C>G)
c.329+1062C>G
n.66+1062C>G
c.802C>G (p.Pro268Ala)
c.297+1062C>G
c.232C>G (p.Pro78Ala)
2g.51026440G=CA1249877846NRXN1c.772+1062C= (n.772+1062C=)
c.329+1062C=
n.66+1062C=
c.802C= (p.Pro268=)
c.297+1062C=
c.232C= (p.Pro78=)
2g.51026440G>TCA346823232NRXN1c.772+1062C>A (n.772+1062C>A)
c.329+1062C>A
n.66+1062C>A
c.802C>A (p.Pro268Thr)
c.297+1062C>A
c.232C>A (p.Pro78Thr)
gnomAD v4
2g.51026441C>ACA346823235NRXN1c.772+1061G>T (n.772+1061G>T)
c.329+1061G>T
n.66+1061G>T
c.801G>T (p.Leu267Phe)
c.297+1061G>T
c.231G>T (p.Leu77Phe)
gnomAD v4
2g.51026441C>GCA346823236NRXN1c.772+1061G>C (n.772+1061G>C)
c.329+1061G>C
n.66+1061G>C
c.801G>C (p.Leu267Phe)
c.297+1061G>C
c.231G>C (p.Leu77Phe)
2g.51026441C>TCA426106440NRXN1c.772+1061G>A (n.772+1061G>A)
c.329+1061G>A
n.66+1061G>A
c.801G>A (p.Leu267=)
c.297+1061G>A
c.231G>A (p.Leu77=)
2g.51026442A>CCA346823237NRXN1c.772+1060T>G (n.772+1060T>G)
c.329+1060T>G
n.66+1060T>G
c.800T>G (p.Leu267Trp)
c.297+1060T>G
c.230T>G (p.Leu77Trp)
2g.51026442A>GCA346823238NRXN1c.772+1060T>C (n.772+1060T>C)
c.329+1060T>C
n.66+1060T>C
c.800T>C (p.Leu267Ser)
c.297+1060T>C
c.230T>C (p.Leu77Ser)
2g.51026442A>TCA346823239NRXN1c.772+1060T>A (n.772+1060T>A)
c.329+1060T>A
n.66+1060T>A
c.800T>A (p.Leu267Ter)
c.297+1060T>A
c.230T>A (p.Leu77Ter)
2g.51026445delCA2659012556NRXN1c.772+1060del (n.772+1060del)
c.329+1060del
n.66+1060del
c.800del (p.Leu267CysfsTer16)
c.297+1060del
c.230del (p.Leu77CysfsTer16)
gnomAD v4
2g.51026443A>CCA346823240NRXN1c.772+1059T>G (n.772+1059T>G)
c.329+1059T>G
n.66+1059T>G
c.799T>G (p.Leu267Val)
c.297+1059T>G
c.229T>G (p.Leu77Val)
2g.51026443A>GCA426106441NRXN1c.772+1059T>C (n.772+1059T>C)
c.329+1059T>C
n.66+1059T>C
c.799T>C (p.Leu267=)
c.297+1059T>C
c.229T>C (p.Leu77=)
2g.51026443A>TCA346823241NRXN1c.772+1059T>A (n.772+1059T>A)
c.329+1059T>A
n.66+1059T>A
c.799T>A (p.Leu267Met)
c.297+1059T>A
c.229T>A (p.Leu77Met)
2g.51026444A>CCA426106442NRXN1c.772+1058T>G (n.772+1058T>G)
c.329+1058T>G
n.66+1058T>G
c.798T>G (p.Val266=)
c.297+1058T>G
c.228T>G (p.Val76=)
2g.51026444A>GCA426106443NRXN1c.772+1058T>C (n.772+1058T>C)
c.329+1058T>C
n.66+1058T>C
c.798T>C (p.Val266=)
c.297+1058T>C
c.228T>C (p.Val76=)
2g.51026444A>TCA426106444NRXN1c.772+1058T>A (n.772+1058T>A)
c.329+1058T>A
n.66+1058T>A
c.798T>A (p.Val266=)
c.297+1058T>A
c.228T>A (p.Val76=)
2g.51026445A>CCA346823242NRXN1c.772+1057T>G (n.772+1057T>G)
c.329+1057T>G
n.66+1057T>G
c.797T>G (p.Val266Gly)
c.297+1057T>G
c.227T>G (p.Val76Gly)
2g.51026445A>GCA346823243NRXN1c.772+1057T>C (n.772+1057T>C)
c.329+1057T>C
n.66+1057T>C
c.797T>C (p.Val266Ala)
c.297+1057T>C
c.227T>C (p.Val76Ala)
2g.51026445A>TCA346823244NRXN1c.772+1057T>A (n.772+1057T>A)
c.329+1057T>A
n.66+1057T>A
c.797T>A (p.Val266Asp)
c.297+1057T>A
c.227T>A (p.Val76Asp)
2g.51026446C>ACA346823245NRXN1c.772+1056G>T (n.772+1056G>T)
c.329+1056G>T
n.66+1056G>T
c.796G>T (p.Val266Phe)
c.297+1056G>T
c.226G>T (p.Val76Phe)
dbSNP
2g.51026446C=CA1249877847NRXN1c.772+1056G= (n.772+1056G=)
c.329+1056G=
n.66+1056G=
c.796G= (p.Val266=)
c.297+1056G=
c.226G= (p.Val76=)
2g.51026446C>GCA346823246NRXN1c.772+1056G>C (n.772+1056G>C)
c.329+1056G>C
n.66+1056G>C
c.796G>C (p.Val266Leu)
c.297+1056G>C
c.226G>C (p.Val76Leu)
2g.51026446C>TCA346823247NRXN1c.772+1056G>A (n.772+1056G>A)
c.329+1056G>A
n.66+1056G>A
c.796G>A (p.Val266Ile)
c.297+1056G>A
c.226G>A (p.Val76Ile)
2g.51026447A>CCA346823248NRXN1c.772+1055T>G (n.772+1055T>G)
c.329+1055T>G
n.66+1055T>G
c.795T>G (p.Cys265Trp)
c.297+1055T>G
c.225T>G (p.Cys75Trp)
2g.51026447A>GCA426106445NRXN1c.772+1055T>C (n.772+1055T>C)
c.329+1055T>C
n.66+1055T>C
c.795T>C (p.Cys265=)
c.297+1055T>C
c.225T>C (p.Cys75=)
2g.51026447A>TCA346823249NRXN1c.772+1055T>A (n.772+1055T>A)
c.329+1055T>A
n.66+1055T>A
c.795T>A (p.Cys265Ter)
c.297+1055T>A
c.225T>A (p.Cys75Ter)
2g.51026448C>ACA346823252NRXN1c.772+1054G>T (n.772+1054G>T)
c.329+1054G>T
n.66+1054G>T
c.794G>T (p.Cys265Phe)
c.297+1054G>T
c.224G>T (p.Cys75Phe)
2g.51026448C=CA1249877848NRXN1c.772+1054G= (n.772+1054G=)
c.329+1054G=
n.66+1054G=
c.794G= (p.Cys265=)
c.297+1054G=
c.224G= (p.Cys75=)
2g.51026448C>GCA346823250NRXN1c.772+1054G>C (n.772+1054G>C)
c.329+1054G>C
n.66+1054G>C
c.794G>C (p.Cys265Ser)
c.297+1054G>C
c.224G>C (p.Cys75Ser)
2g.51026448C>TCA346823251NRXN1c.772+1054G>A (n.772+1054G>A)
c.329+1054G>A
n.66+1054G>A
c.794G>A (p.Cys265Tyr)
c.297+1054G>A
c.224G>A (p.Cys75Tyr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.51026449A=CA1249877849NRXN1c.772+1053T= (n.772+1053T=)
c.329+1053T=
n.66+1053T=
c.793T= (p.Cys265=)
c.297+1053T=
c.223T= (p.Cys75=)
2g.51026449A>CCA346823253NRXN1c.772+1053T>G (n.772+1053T>G)
c.329+1053T>G
n.66+1053T>G
c.793T>G (p.Cys265Gly)
c.297+1053T>G
c.223T>G (p.Cys75Gly)
2g.51026449A>GCA346823254NRXN1c.772+1053T>C (n.772+1053T>C)
c.329+1053T>C
n.66+1053T>C
c.793T>C (p.Cys265Arg)
c.297+1053T>C
c.223T>C (p.Cys75Arg)
ClinVar dbSNP
2g.51026449A>TCA1655393NRXN1c.772+1053T>A (n.772+1053T>A)
c.329+1053T>A
n.66+1053T>A
c.793T>A (p.Cys265Ser)
c.297+1053T>A
c.223T>A (p.Cys75Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026450C>ACA346823255NRXN1c.772+1052G>T (n.772+1052G>T)
c.329+1052G>T
n.66+1052G>T
c.792G>T (p.Gln264His)
c.297+1052G>T
c.222G>T (p.Gln74His)
gnomAD v4
2g.51026450C>GCA346823256NRXN1c.772+1052G>C (n.772+1052G>C)
c.329+1052G>C
n.66+1052G>C
c.792G>C (p.Gln264His)
c.297+1052G>C
c.222G>C (p.Gln74His)
2g.51026450C>TCA426106446NRXN1c.772+1052G>A (n.772+1052G>A)
c.329+1052G>A
n.66+1052G>A
c.792G>A (p.Gln264=)
c.297+1052G>A
c.222G>A (p.Gln74=)
gnomAD v4
2g.51026451T>ACA346823257NRXN1c.772+1051A>T (n.772+1051A>T)
c.329+1051A>T
n.66+1051A>T
c.791A>T (p.Gln264Leu)
c.297+1051A>T
c.221A>T (p.Gln74Leu)
2g.51026451T>CCA48054735NRXN1c.772+1051A>G (n.772+1051A>G)
c.329+1051A>G
n.66+1051A>G
c.791A>G (p.Gln264Arg)
c.297+1051A>G
c.221A>G (p.Gln74Arg)
dbSNP gnomAD v4
2g.51026451T>GCA346823258NRXN1c.772+1051A>C (n.772+1051A>C)
c.329+1051A>C
n.66+1051A>C
c.791A>C (p.Gln264Pro)
c.297+1051A>C
c.221A>C (p.Gln74Pro)
gnomAD v4
2g.51026451T=CA1249877850NRXN1c.772+1051A= (n.772+1051A=)
c.329+1051A=
n.66+1051A=
c.791A= (p.Gln264=)
c.297+1051A=
c.221A= (p.Gln74=)
2g.51026452G>ACA346823259NRXN1c.772+1050C>T (n.772+1050C>T)
c.329+1050C>T
n.66+1050C>T
c.790C>T (p.Gln264Ter)
c.297+1050C>T
c.220C>T (p.Gln74Ter)
dbSNP gnomAD v4 COSMIC COSMIC
2g.51026452G>CCA346823260NRXN1c.772+1050C>G (n.772+1050C>G)
c.329+1050C>G
n.66+1050C>G
c.790C>G (p.Gln264Glu)
c.297+1050C>G
c.220C>G (p.Gln74Glu)
2g.51026452G=CA1249877851NRXN1c.772+1050C= (n.772+1050C=)
c.329+1050C=
n.66+1050C=
c.790C= (p.Gln264=)
c.297+1050C=
c.220C= (p.Gln74=)
2g.51026452G>TCA231337NRXN1c.772+1050C>A (n.772+1050C>A)
c.329+1050C>A
n.66+1050C>A
c.790C>A (p.Gln264Lys)
c.297+1050C>A
c.220C>A (p.Gln74Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026453A>CCA426106447NRXN1c.772+1049T>G (n.772+1049T>G)
c.329+1049T>G
n.66+1049T>G
c.789T>G (p.Leu263=)
c.297+1049T>G
c.219T>G (p.Leu73=)
2g.51026453A>GCA426106448NRXN1c.772+1049T>C (n.772+1049T>C)
c.329+1049T>C
n.66+1049T>C
c.789T>C (p.Leu263=)
c.297+1049T>C
c.219T>C (p.Leu73=)
2g.51026453A>TCA426106449NRXN1c.772+1049T>A (n.772+1049T>A)
c.329+1049T>A
n.66+1049T>A
c.789T>A (p.Leu263=)
c.297+1049T>A
c.219T>A (p.Leu73=)
2g.51026454A>CCA346823263NRXN1c.772+1048T>G (n.772+1048T>G)
c.329+1048T>G
n.66+1048T>G
c.788T>G (p.Leu263Arg)
c.297+1048T>G
c.218T>G (p.Leu73Arg)
gnomAD v4
2g.51026454A>GCA346823262NRXN1c.772+1048T>C (n.772+1048T>C)
c.329+1048T>C
n.66+1048T>C
c.788T>C (p.Leu263Pro)
c.297+1048T>C
c.218T>C (p.Leu73Pro)
2g.51026454A>TCA346823261NRXN1c.772+1048T>A (n.772+1048T>A)
c.329+1048T>A
n.66+1048T>A
c.788T>A (p.Leu263His)
c.297+1048T>A
c.218T>A (p.Leu73His)
2g.51026455G>ACA346823264NRXN1c.772+1047C>T (n.772+1047C>T)
c.329+1047C>T
n.66+1047C>T
c.787C>T (p.Leu263Phe)
c.297+1047C>T
c.217C>T (p.Leu73Phe)
gnomAD v4
2g.51026455G>CCA346823265NRXN1c.772+1047C>G (n.772+1047C>G)
c.329+1047C>G
n.66+1047C>G
c.787C>G (p.Leu263Val)
c.297+1047C>G
c.217C>G (p.Leu73Val)
2g.51026455G=CA1249877852NRXN1c.772+1047C= (n.772+1047C=)
c.329+1047C=
n.66+1047C=
c.787C= (p.Leu263=)
c.297+1047C=
c.217C= (p.Leu73=)
2g.51026455G>TCA1655394NRXN1c.772+1047C>A (n.772+1047C>A)
c.329+1047C>A
n.66+1047C>A
c.787C>A (p.Leu263Ile)
c.297+1047C>A
c.217C>A (p.Leu73Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026456A>CCA426106450NRXN1c.772+1046T>G (n.772+1046T>G)
c.329+1046T>G
n.66+1046T>G
c.786T>G (p.Gly262=)
c.297+1046T>G
c.216T>G (p.Gly72=)
2g.51026456A>GCA426106451NRXN1c.772+1046T>C (n.772+1046T>C)
c.329+1046T>C
n.66+1046T>C
c.786T>C (p.Gly262=)
c.297+1046T>C
c.216T>C (p.Gly72=)
2g.51026456A>TCA426106452NRXN1c.772+1046T>A (n.772+1046T>A)
c.329+1046T>A
n.66+1046T>A
c.786T>A (p.Gly262=)
c.297+1046T>A
c.216T>A (p.Gly72=)
2g.51026457C>ACA346823266NRXN1c.772+1045G>T (n.772+1045G>T)
c.329+1045G>T
n.66+1045G>T
c.785G>T (p.Gly262Val)
c.297+1045G>T
c.215G>T (p.Gly72Val)
2g.51026457C=CA1249877853NRXN1c.772+1045G= (n.772+1045G=)
c.329+1045G=
n.66+1045G=
c.785G= (p.Gly262=)
c.297+1045G=
c.215G= (p.Gly72=)
2g.51026457C>GCA346823267NRXN1c.772+1045G>C (n.772+1045G>C)
c.329+1045G>C
n.66+1045G>C
c.785G>C (p.Gly262Ala)
c.297+1045G>C
c.215G>C (p.Gly72Ala)
2g.51026457C>TCA48054736NRXN1c.772+1045G>A (n.772+1045G>A)
c.329+1045G>A
n.66+1045G>A
c.785G>A (p.Gly262Asp)
c.297+1045G>A
c.215G>A (p.Gly72Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.51026458C>ACA1655395NRXN1c.772+1044G>T (n.772+1044G>T)
c.329+1044G>T
n.66+1044G>T
c.784G>T (p.Gly262Cys)
c.297+1044G>T
c.214G>T (p.Gly72Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.51026458C=CA1249877854NRXN1c.772+1044G= (n.772+1044G=)
c.329+1044G=
n.66+1044G=
c.784G= (p.Gly262=)
c.297+1044G=
c.214G= (p.Gly72=)
2g.51026458C>GCA346823268NRXN1c.772+1044G>C (n.772+1044G>C)
c.329+1044G>C
n.66+1044G>C
c.784G>C (p.Gly262Arg)
c.297+1044G>C
c.214G>C (p.Gly72Arg)
ClinVar dbSNP gnomAD v4
2g.51026458C>TCA346823269NRXN1c.772+1044G>A (n.772+1044G>A)
c.329+1044G>A
n.66+1044G>A
c.784G>A (p.Gly262Ser)
c.297+1044G>A
c.214G>A (p.Gly72Ser)
gnomAD v4
2g.51026459G>ACA426106453NRXN1c.772+1043C>T (n.772+1043C>T)
c.329+1043C>T
n.66+1043C>T
c.783C>T (p.Phe261=)
c.297+1043C>T
c.213C>T (p.Phe71=)
gnomAD v4
2g.51026459G>CCA346823270NRXN1c.772+1043C>G (n.772+1043C>G)
c.329+1043C>G
n.66+1043C>G
c.783C>G (p.Phe261Leu)
c.297+1043C>G
c.213C>G (p.Phe71Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.51026459G=CA1249877855NRXN1c.772+1043C= (n.772+1043C=)
c.329+1043C=
n.66+1043C=
c.783C= (p.Phe261=)
c.297+1043C=
c.213C= (p.Phe71=)
2g.51026459G>TCA346823271NRXN1c.772+1043C>A (n.772+1043C>A)
c.329+1043C>A
n.66+1043C>A
c.783C>A (p.Phe261Leu)
c.297+1043C>A
c.213C>A (p.Phe71Leu)
ClinVar gnomAD v4
2g.51026460A>CCA346823272NRXN1c.772+1042T>G (n.772+1042T>G)
c.329+1042T>G
n.66+1042T>G
c.782T>G (p.Phe261Cys)
c.297+1042T>G
c.212T>G (p.Phe71Cys)
2g.51026460A>GCA346823273NRXN1c.772+1042T>C (n.772+1042T>C)
c.329+1042T>C
n.66+1042T>C
c.782T>C (p.Phe261Ser)
c.297+1042T>C
c.212T>C (p.Phe71Ser)
2g.51026460A>TCA346823274NRXN1c.772+1042T>A (n.772+1042T>A)
c.329+1042T>A
n.66+1042T>A
c.782T>A (p.Phe261Tyr)
c.297+1042T>A
c.212T>A (p.Phe71Tyr)
2g.51026461A>CCA346823275NRXN1c.772+1041T>G (n.772+1041T>G)
c.329+1041T>G
n.66+1041T>G
c.781T>G (p.Phe261Val)
c.297+1041T>G
c.211T>G (p.Phe71Val)
2g.51026461A>GCA346823277NRXN1c.772+1041T>C (n.772+1041T>C)
c.329+1041T>C
n.66+1041T>C
c.781T>C (p.Phe261Leu)
c.297+1041T>C
c.211T>C (p.Phe71Leu)
2g.51026461A>TCA346823276NRXN1c.772+1041T>A (n.772+1041T>A)
c.329+1041T>A
n.66+1041T>A
c.781T>A (p.Phe261Ile)
c.297+1041T>A
c.211T>A (p.Phe71Ile)
2g.51026462T>ACA316169NRXN1c.772+1040A>T (n.772+1040A>T)
c.329+1040A>T
n.66+1040A>T
c.780A>T (p.Lys260Asn)
c.297+1040A>T
c.210A>T (p.Lys70Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026462T>CCA48054737NRXN1c.772+1040A>G (n.772+1040A>G)
c.329+1040A>G
n.66+1040A>G
c.780A>G (p.Lys260=)
c.297+1040A>G
c.210A>G (p.Lys70=)
dbSNP
2g.51026462T>GCA346823278NRXN1c.772+1040A>C (n.772+1040A>C)
c.329+1040A>C
n.66+1040A>C
c.780A>C (p.Lys260Asn)
c.297+1040A>C
c.210A>C (p.Lys70Asn)
2g.51026462T=CA1249877856NRXN1c.772+1040A= (n.772+1040A=)
c.329+1040A=
n.66+1040A=
c.780A= (p.Lys260=)
c.297+1040A=
c.210A= (p.Lys70=)
2g.51026465delCA2659012557NRXN1c.772+1040del (n.772+1040del)
c.329+1040del
n.66+1040del
c.780del (p.Lys260AsnfsTer23)
c.297+1040del
c.210del (p.Lys70AsnfsTer23)
gnomAD v4
2g.51026463T>ACA346823279NRXN1c.772+1039A>T (n.772+1039A>T)
c.329+1039A>T
n.66+1039A>T
c.779A>T (p.Lys260Ile)
c.297+1039A>T
c.209A>T (p.Lys70Ile)
2g.51026463T>CCA346823280NRXN1c.772+1039A>G (n.772+1039A>G)
c.329+1039A>G
n.66+1039A>G
c.779A>G (p.Lys260Arg)
c.297+1039A>G
c.209A>G (p.Lys70Arg)
2g.51026463T>GCA346823281NRXN1c.772+1039A>C (n.772+1039A>C)
c.329+1039A>C
n.66+1039A>C
c.779A>C (p.Lys260Thr)
c.297+1039A>C
c.209A>C (p.Lys70Thr)
gnomAD v4
2g.51026464T>ACA346823282NRXN1c.772+1038A>T (n.772+1038A>T)
c.329+1038A>T
n.66+1038A>T
c.778A>T (p.Lys260Ter)
c.297+1038A>T
c.208A>T (p.Lys70Ter)
2g.51026464T>CCA346823283NRXN1c.772+1038A>G (n.772+1038A>G)
c.329+1038A>G
n.66+1038A>G
c.778A>G (p.Lys260Glu)
c.297+1038A>G
c.208A>G (p.Lys70Glu)
2g.51026464T>GCA346823284NRXN1c.772+1038A>C (n.772+1038A>C)
c.329+1038A>C
n.66+1038A>C
c.778A>C (p.Lys260Gln)
c.297+1038A>C
c.208A>C (p.Lys70Gln)
2g.51026464_51026465insACA2659012558NRXN1c.772+1037_772+1038insT (n.772+1037_772+1038insT)
c.329+1037_329+1038insT
n.66+1037_66+1038insT
c.777_778insT (p.Lys260Ter)
c.297+1037_297+1038insT
c.207_208insT (p.Lys70Ter)
gnomAD v4
2g.51026465T>ACA426106454NRXN1c.772+1037A>T (n.772+1037A>T)
c.329+1037A>T
n.66+1037A>T
c.777A>T (p.Ile259=)
c.297+1037A>T
c.207A>T (p.Ile69=)
gnomAD v4
2g.51026465T>CCA346823285NRXN1c.772+1037A>G (n.772+1037A>G)
c.329+1037A>G
n.66+1037A>G
c.777A>G (p.Ile259Met)
c.297+1037A>G
c.207A>G (p.Ile69Met)
2g.51026465T>GCA426106455NRXN1c.772+1037A>C (n.772+1037A>C)
c.329+1037A>C
n.66+1037A>C
c.777A>C (p.Ile259=)
c.297+1037A>C
c.207A>C (p.Ile69=)
2g.51026466A>CCA346823286NRXN1c.772+1036T>G (n.772+1036T>G)
c.329+1036T>G
n.66+1036T>G
c.776T>G (p.Ile259Arg)
c.297+1036T>G
c.206T>G (p.Ile69Arg)
2g.51026466A>GCA346823288NRXN1c.772+1036T>C (n.772+1036T>C)
c.329+1036T>C
n.66+1036T>C
c.776T>C (p.Ile259Thr)
c.297+1036T>C
c.206T>C (p.Ile69Thr)
2g.51026466A>TCA346823287NRXN1c.772+1036T>A (n.772+1036T>A)
c.329+1036T>A
n.66+1036T>A
c.776T>A (p.Ile259Lys)
c.297+1036T>A
c.206T>A (p.Ile69Lys)
2g.51026467T>ACA346823289NRXN1c.772+1035A>T (n.772+1035A>T)
c.329+1035A>T
n.66+1035A>T
c.775A>T (p.Ile259Leu)
c.297+1035A>T
c.205A>T (p.Ile69Leu)
2g.51026467T>CCA346823291NRXN1c.772+1035A>G (n.772+1035A>G)
c.329+1035A>G
n.66+1035A>G
c.775A>G (p.Ile259Val)
c.297+1035A>G
c.205A>G (p.Ile69Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.51026467T>GCA346823290NRXN1c.772+1035A>C (n.772+1035A>C)
c.329+1035A>C
n.66+1035A>C
c.775A>C (p.Ile259Leu)
c.297+1035A>C
c.205A>C (p.Ile69Leu)
2g.51026467T=CA1249877857NRXN1c.772+1035A= (n.772+1035A=)
c.329+1035A=
n.66+1035A=
c.775A= (p.Ile259=)
c.297+1035A=
c.205A= (p.Ile69=)
2g.51026468T>ACA346823292NRXN1c.772+1034A>T (n.772+1034A>T)
c.329+1034A>T
n.66+1034A>T
c.774A>T (p.Glu258Asp)
c.297+1034A>T
c.204A>T (p.Glu68Asp)
2g.51026468T>CCA426106456NRXN1c.772+1034A>G (n.772+1034A>G)
c.329+1034A>G
n.66+1034A>G
c.774A>G (p.Glu258=)
c.297+1034A>G
c.204A>G (p.Glu68=)
dbSNP gnomAD v3 gnomAD v4
2g.51026468T>GCA346823293NRXN1c.772+1034A>C (n.772+1034A>C)
c.329+1034A>C
n.66+1034A>C
c.774A>C (p.Glu258Asp)
c.297+1034A>C
c.204A>C (p.Glu68Asp)
2g.51026468T=CA1249877858NRXN1c.772+1034A= (n.772+1034A=)
c.329+1034A=
n.66+1034A=
c.774A= (p.Glu258=)
c.297+1034A=
c.204A= (p.Glu68=)
2g.51026469T>ACA346823294NRXN1c.772+1033A>T (n.772+1033A>T)
c.329+1033A>T
n.66+1033A>T
c.773A>T (p.Glu258Val)
c.297+1033A>T
c.203A>T (p.Glu68Val)
2g.51026469T>CCA346823295NRXN1c.772+1033A>G (n.772+1033A>G)
c.329+1033A>G
n.66+1033A>G
c.773A>G (p.Glu258Gly)
c.297+1033A>G
c.203A>G (p.Glu68Gly)
ClinVar dbSNP gnomAD v4
2g.51026469T>GCA1655396NRXN1c.772+1033A>C (n.772+1033A>C)
c.329+1033A>C
n.66+1033A>C
c.773A>C (p.Glu258Ala)
c.297+1033A>C
c.203A>C (p.Glu68Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026469T=CA1249877859NRXN1c.772+1033A= (n.772+1033A=)
c.329+1033A=
n.66+1033A=
c.773A= (p.Glu258=)
c.297+1033A=
c.203A= (p.Glu68=)
2g.51026470C>ACA346823296NRXN1c.772+1032G>T (n.772+1032G>T)
c.329+1032G>T
n.66+1032G>T
c.773-1G>T (n.773-1G>T)
c.297+1032G>T
c.203-1G>T (n.203-1G>T)
gnomAD v4
2g.51026470C=CA1249877860NRXN1c.772+1032G= (n.772+1032G=)
c.329+1032G=
n.66+1032G=
c.773-1G= (n.773-1G=)
c.297+1032G=
c.203-1G= (n.203-1G=)
2g.51026470C>GCA346823297NRXN1c.772+1032G>C (n.772+1032G>C)
c.329+1032G>C
n.66+1032G>C
c.773-1G>C (n.773-1G>C)
c.297+1032G>C
c.203-1G>C (n.203-1G>C)
2g.51026470C>TCA1655397NRXN1c.772+1032G>A (n.772+1032G>A)
c.329+1032G>A
n.66+1032G>A
c.773-1G>A (n.773-1G>A)
c.297+1032G>A
c.203-1G>A (n.203-1G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026471T>ACA346823298NRXN1c.772+1031A>T (n.772+1031A>T)
c.329+1031A>T
n.66+1031A>T
c.773-2A>T (n.773-2A>T)
c.297+1031A>T
c.203-2A>T (n.203-2A>T)
2g.51026471T>CCA346823299NRXN1c.772+1031A>G (n.772+1031A>G)
c.329+1031A>G
n.66+1031A>G
c.773-2A>G (n.773-2A>G)
c.297+1031A>G
c.203-2A>G (n.203-2A>G)
gnomAD v4
2g.51026471T>GCA346823300NRXN1c.772+1031A>C (n.772+1031A>C)
c.329+1031A>C
n.66+1031A>C
c.773-2A>C (n.773-2A>C)
c.297+1031A>C
c.203-2A>C (n.203-2A>C)
2g.51026472A>GCA2659012559NRXN1c.772+1030T>C (n.772+1030T>C)
c.329+1030T>C
n.66+1030T>C
c.773-3T>C (n.773-3T>C)
c.297+1030T>C
c.203-3T>C (n.203-3T>C)
gnomAD v4
2g.51026474delCA2576965072NRXN1c.772+1030del (n.772+1030del)
c.329+1030del
n.66+1030del
c.773-3del (n.773-3del)
c.297+1030del
c.203-3del (n.203-3del)
2g.51026473A>GCA2659012560NRXN1c.772+1029T>C (n.772+1029T>C)
c.329+1029T>C
n.66+1029T>C
c.773-4T>C (n.773-4T>C)
c.297+1029T>C
c.203-4T>C (n.203-4T>C)
gnomAD v4
2g.51026474A=CA1249877861NRXN1c.772+1028T= (n.772+1028T=)
c.329+1028T=
n.66+1028T=
c.773-5T= (n.773-5T=)
c.297+1028T=
c.203-5T= (n.203-5T=)
2g.51026474A>GCA48054738NRXN1c.772+1028T>C (n.772+1028T>C)
c.329+1028T>C
n.66+1028T>C
c.773-5T>C (n.773-5T>C)
c.297+1028T>C
c.203-5T>C (n.203-5T>C)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.51026474A>TCA2659012561NRXN1c.772+1028T>A (n.772+1028T>A)
c.329+1028T>A
n.66+1028T>A
c.773-5T>A (n.773-5T>A)
c.297+1028T>A
c.203-5T>A (n.203-5T>A)
gnomAD v4
2g.51026475G>ACA2576965073NRXN1c.772+1027C>T (n.772+1027C>T)
c.329+1027C>T
n.66+1027C>T
c.773-6C>T (n.773-6C>T)
c.297+1027C>T
c.203-6C>T (n.203-6C>T)
2g.51026475G>TCA2659012562NRXN1c.772+1027C>A (n.772+1027C>A)
c.329+1027C>A
n.66+1027C>A
c.773-6C>A (n.773-6C>A)
c.297+1027C>A
c.203-6C>A (n.203-6C>A)
gnomAD v4
2g.51026477G>ACA2659012563NRXN1c.772+1025C>T (n.772+1025C>T)
c.329+1025C>T
n.66+1025C>T
c.773-8C>T (n.773-8C>T)
c.297+1025C>T
c.203-8C>T (n.203-8C>T)
gnomAD v4
2g.51026477G>TCA2659012564NRXN1c.772+1025C>A (n.772+1025C>A)
c.329+1025C>A
n.66+1025C>A
c.773-8C>A (n.773-8C>A)
c.297+1025C>A
c.203-8C>A (n.203-8C>A)
gnomAD v4
2g.51026478G>ACA532659847NRXN1c.772+1024C>T (n.772+1024C>T)
c.329+1024C>T
n.66+1024C>T
c.773-9C>T (n.773-9C>T)
c.297+1024C>T
c.203-9C>T (n.203-9C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.51026478G>CCA205964NRXN1c.772+1024C>G (n.772+1024C>G)
c.329+1024C>G
n.66+1024C>G
c.773-9C>G (n.773-9C>G)
c.297+1024C>G
c.203-9C>G (n.203-9C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026478G=CA1249877862NRXN1c.772+1024C= (n.772+1024C=)
c.329+1024C=
n.66+1024C=
c.773-9C= (n.773-9C=)
c.297+1024C=
c.203-9C= (n.203-9C=)
2g.51026478G>TCA2659012565NRXN1c.772+1024C>A (n.772+1024C>A)
c.329+1024C>A
n.66+1024C>A
c.773-9C>A (n.773-9C>A)
c.297+1024C>A
c.203-9C>A (n.203-9C>A)
gnomAD v4
2g.51026479delCA2659012566NRXN1c.772+1023del (n.772+1023del)
c.329+1023del
n.66+1023del
c.773-10del (n.773-10del)
c.297+1023del
c.203-10del (n.203-10del)
gnomAD v4
2g.51026479A>GCA2659012567NRXN1c.772+1023T>C (n.772+1023T>C)
c.329+1023T>C
n.66+1023T>C
c.773-10T>C (n.773-10T>C)
c.297+1023T>C
c.203-10T>C (n.203-10T>C)
gnomAD v4
2g.51026480G>ACA769808837NRXN1c.772+1022C>T (n.772+1022C>T)
c.329+1022C>T
n.66+1022C>T
c.773-11C>T (n.773-11C>T)
c.297+1022C>T
c.203-11C>T (n.203-11C>T)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.51026480G>CCA1030546961NRXN1c.772+1022C>G (n.772+1022C>G)
c.329+1022C>G
n.66+1022C>G
c.773-11C>G (n.773-11C>G)
c.297+1022C>G
c.203-11C>G (n.203-11C>G)
dbSNP gnomAD v3 gnomAD v4
2g.51026480G=CA1249877863NRXN1c.772+1022C= (n.772+1022C=)
c.329+1022C=
n.66+1022C=
c.773-11C= (n.773-11C=)
c.297+1022C=
c.203-11C= (n.203-11C=)
2g.51026480G>TCA2659012568NRXN1c.772+1022C>A (n.772+1022C>A)
c.329+1022C>A
n.66+1022C>A
c.773-11C>A (n.773-11C>A)
c.297+1022C>A
c.203-11C>A (n.203-11C>A)
gnomAD v4
2g.51026484A>GCA2659012569NRXN1c.772+1018T>C (n.772+1018T>C)
c.329+1018T>C
n.66+1018T>C
c.773-15T>C (n.773-15T>C)
c.297+1018T>C
c.203-15T>C (n.203-15T>C)
gnomAD v4
2g.51026484A>TCA2659012570NRXN1c.772+1018T>A (n.772+1018T>A)
c.329+1018T>A
n.66+1018T>A
c.773-15T>A (n.773-15T>A)
c.297+1018T>A
c.203-15T>A (n.203-15T>A)
gnomAD v4
2g.51026485G>CCA2573134993NRXN1c.772+1017C>G (n.772+1017C>G)
c.329+1017C>G
n.66+1017C>G
c.773-16C>G (n.773-16C>G)
c.297+1017C>G
c.203-16C>G (n.203-16C>G)
ClinVar dbSNP gnomAD v4
2g.51026486A>GCA2659012571NRXN1c.772+1016T>C (n.772+1016T>C)
c.329+1016T>C
n.66+1016T>C
c.773-17T>C (n.773-17T>C)
c.297+1016T>C
c.203-17T>C (n.203-17T>C)
gnomAD v4
2g.51026486A>TCA2659012572NRXN1c.772+1016T>A (n.772+1016T>A)
c.329+1016T>A
n.66+1016T>A
c.773-17T>A (n.773-17T>A)
c.297+1016T>A
c.203-17T>A (n.203-17T>A)
gnomAD v4
2g.51026487G>ACA2659012573NRXN1c.772+1015C>T (n.772+1015C>T)
c.329+1015C>T
n.66+1015C>T
c.773-18C>T (n.773-18C>T)
c.297+1015C>T
c.203-18C>T (n.203-18C>T)
gnomAD v4
2g.51026487G=CA1249877864NRXN1c.772+1015C= (n.772+1015C=)
c.329+1015C=
n.66+1015C=
c.773-18C= (n.773-18C=)
c.297+1015C=
c.203-18C= (n.203-18C=)
2g.51026487G>TCA1655398NRXN1c.772+1015C>A (n.772+1015C>A)
c.329+1015C>A
n.66+1015C>A
c.773-18C>A (n.773-18C>A)
c.297+1015C>A
c.203-18C>A (n.203-18C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026488A>TCA2659012574NRXN1c.772+1014T>A (n.772+1014T>A)
c.329+1014T>A
n.66+1014T>A
c.773-19T>A (n.773-19T>A)
c.297+1014T>A
c.203-19T>A (n.203-19T>A)
gnomAD v4
2g.51026490C>ACA2659012576NRXN1c.772+1012G>T (n.772+1012G>T)
c.329+1012G>T
n.66+1012G>T
c.773-21G>T (n.773-21G>T)
c.297+1012G>T
c.203-21G>T (n.203-21G>T)
gnomAD v4
2g.51026490C=CA1249877865NRXN1c.772+1012G= (n.772+1012G=)
c.329+1012G=
n.66+1012G=
c.773-21G= (n.773-21G=)
c.297+1012G=
c.203-21G= (n.203-21G=)
2g.51026490C>GCA1030546967NRXN1c.772+1012G>C (n.772+1012G>C)
c.329+1012G>C
n.66+1012G>C
c.773-21G>C (n.773-21G>C)
c.297+1012G>C
c.203-21G>C (n.203-21G>C)
dbSNP gnomAD v3 gnomAD v4
2g.51026490C>TCA2659012575NRXN1c.772+1012G>A (n.772+1012G>A)
c.329+1012G>A
n.66+1012G>A
c.773-21G>A (n.773-21G>A)
c.297+1012G>A
c.203-21G>A (n.203-21G>A)
gnomAD v4
2g.51026491T>CCA1655399NRXN1c.772+1011A>G (n.772+1011A>G)
c.329+1011A>G
n.66+1011A>G
c.773-22A>G (n.773-22A>G)
c.297+1011A>G
c.203-22A>G (n.203-22A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.51026491T=CA1249877866NRXN1c.772+1011A= (n.772+1011A=)
c.329+1011A=
n.66+1011A=
c.773-22A= (n.773-22A=)
c.297+1011A=
c.203-22A= (n.203-22A=)
2g.51026492T>ACA1655400NRXN1c.772+1010A>T (n.772+1010A>T)
c.329+1010A>T
n.66+1010A>T
c.773-23A>T (n.773-23A>T)
c.297+1010A>T
c.203-23A>T (n.203-23A>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026492T>CCA2659012577NRXN1c.772+1010A>G (n.772+1010A>G)
c.329+1010A>G
n.66+1010A>G
c.773-23A>G (n.773-23A>G)
c.297+1010A>G
c.203-23A>G (n.203-23A>G)
gnomAD v4
2g.51026492T=CA1249877867NRXN1c.772+1010A= (n.772+1010A=)
c.329+1010A=
n.66+1010A=
c.773-23A= (n.773-23A=)
c.297+1010A=
c.203-23A= (n.203-23A=)
2g.51026493A>GCA2576965074NRXN1c.772+1009T>C (n.772+1009T>C)
c.329+1009T>C
n.66+1009T>C
c.773-24T>C (n.773-24T>C)
c.297+1009T>C
c.203-24T>C (n.203-24T>C)
2g.51026494G>ACA532659848NRXN1c.772+1008C>T (n.772+1008C>T)
c.329+1008C>T
n.66+1008C>T
c.773-25C>T (n.773-25C>T)
c.297+1008C>T
c.203-25C>T (n.203-25C>T)
dbSNP gnomAD v2 gnomAD v4
2g.51026494G>CCA1249877868NRXN1c.772+1008C>G (n.772+1008C>G)
c.329+1008C>G
n.66+1008C>G
c.773-25C>G (n.773-25C>G)
c.297+1008C>G
c.203-25C>G (n.203-25C>G)
dbSNP gnomAD v4
2g.51026494G=CA1249877869NRXN1c.772+1008C= (n.772+1008C=)
c.329+1008C=
n.66+1008C=
c.773-25C= (n.773-25C=)
c.297+1008C=
c.203-25C= (n.203-25C=)
2g.51026494G>TCA914398286NRXN1c.772+1008C>A (n.772+1008C>A)
c.329+1008C>A
n.66+1008C>A
c.773-25C>A (n.773-25C>A)
c.297+1008C>A
c.203-25C>A (n.203-25C>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.51026495G>ACA532659849NRXN1c.772+1007C>T (n.772+1007C>T)
c.329+1007C>T
n.66+1007C>T
c.773-26C>T (n.773-26C>T)
c.297+1007C>T
c.203-26C>T (n.203-26C>T)
dbSNP gnomAD v2 gnomAD v4
2g.51026495G=CA1249877870NRXN1c.772+1007C= (n.772+1007C=)
c.329+1007C=
n.66+1007C=
c.773-26C= (n.773-26C=)
c.297+1007C=
c.203-26C= (n.203-26C=)
2g.51026495G>TCA2659012578NRXN1c.772+1007C>A (n.772+1007C>A)
c.329+1007C>A
n.66+1007C>A
c.773-26C>A (n.773-26C>A)
c.297+1007C>A
c.203-26C>A (n.203-26C>A)
gnomAD v4
2g.51026496T>CCA48054739NRXN1c.772+1006A>G (n.772+1006A>G)
c.329+1006A>G
n.66+1006A>G
c.773-27A>G (n.773-27A>G)
c.297+1006A>G
c.203-27A>G (n.203-27A>G)
dbSNP gnomAD v4
2g.51026496T=CA1249877871NRXN1c.772+1006A= (n.772+1006A=)
c.329+1006A=
n.66+1006A=
c.773-27A= (n.773-27A=)
c.297+1006A=
c.203-27A= (n.203-27A=)
2g.51026497A>GCA2659012579NRXN1c.772+1005T>C (n.772+1005T>C)
c.329+1005T>C
n.66+1005T>C
c.773-28T>C (n.773-28T>C)
c.297+1005T>C
c.203-28T>C (n.203-28T>C)
gnomAD v4
2g.51026498T>GCA2659012580NRXN1c.772+1004A>C (n.772+1004A>C)
c.329+1004A>C
n.66+1004A>C
c.773-29A>C (n.773-29A>C)
c.297+1004A>C
c.203-29A>C (n.203-29A>C)
gnomAD v4
2g.51026499G>ACA48054740NRXN1c.772+1003C>T (n.772+1003C>T)
c.329+1003C>T
n.66+1003C>T
c.773-30C>T (n.773-30C>T)
c.297+1003C>T
c.203-30C>T (n.203-30C>T)
dbSNP gnomAD v4
2g.51026499G=CA1249877872NRXN1c.772+1003C= (n.772+1003C=)
c.329+1003C=
n.66+1003C=
c.773-30C= (n.773-30C=)
c.297+1003C=
c.203-30C= (n.203-30C=)
2g.51026499G>TCA2659012581NRXN1c.772+1003C>A (n.772+1003C>A)
c.329+1003C>A
n.66+1003C>A
c.773-30C>A (n.773-30C>A)
c.297+1003C>A
c.203-30C>A (n.203-30C>A)
gnomAD v4
2g.51026500A=CA1249877873NRXN1c.772+1002T= (n.772+1002T=)
c.329+1002T=
n.66+1002T=
c.773-31T= (n.773-31T=)
c.297+1002T=
c.203-31T= (n.203-31T=)
2g.51026500A>CCA48054741NRXN1c.772+1002T>G (n.772+1002T>G)
c.329+1002T>G
n.66+1002T>G
c.773-31T>G (n.773-31T>G)
c.297+1002T>G
c.203-31T>G (n.203-31T>G)
dbSNP gnomAD v2 gnomAD v4
2g.51026501delCA2659012582NRXN1c.772+1001del (n.772+1001del)
c.329+1001del
n.66+1001del
c.773-32del (n.773-32del)
c.297+1001del
c.203-32del (n.203-32del)
gnomAD v4
2g.51026501C>ACA769809073NRXN1c.772+1001G>T (n.772+1001G>T)
c.329+1001G>T
n.66+1001G>T
c.773-32G>T (n.773-32G>T)
c.297+1001G>T
c.203-32G>T (n.203-32G>T)
dbSNP gnomAD v3 gnomAD v4
2g.51026501C=CA1249877874NRXN1c.772+1001G= (n.772+1001G=)
c.329+1001G=
n.66+1001G=
c.773-32G= (n.773-32G=)
c.297+1001G=
c.203-32G= (n.203-32G=)
2g.51026501C>TCA2659012583NRXN1c.772+1001G>A (n.772+1001G>A)
c.329+1001G>A
n.66+1001G>A
c.773-32G>A (n.773-32G>A)
c.297+1001G>A
c.203-32G>A (n.203-32G>A)
gnomAD v4
2g.51026505dupCA2659012584NRXN1c.772+1000dup (n.772+1000dup)
c.329+1000dup
n.66+1000dup
c.773-33dup (n.773-33dup)
c.297+1000dup
c.203-33dup (n.203-33dup)
gnomAD v4
2g.51026504T>CCA1655401NRXN1c.772+998A>G (n.772+998A>G)
c.329+998A>G
n.66+998A>G
c.773-35A>G (n.773-35A>G)
c.297+998A>G
c.203-35A>G (n.203-35A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.51026504T=CA1249877875NRXN1c.772+998A= (n.772+998A=)
c.329+998A=
n.66+998A=
c.773-35A= (n.773-35A=)
c.297+998A=
c.203-35A= (n.203-35A=)
2g.51026505T>CCA2659012585NRXN1c.772+997A>G (n.772+997A>G)
c.329+997A>G
n.66+997A>G
c.773-36A>G (n.773-36A>G)
c.297+997A>G
c.203-36A>G (n.203-36A>G)
gnomAD v4
2g.51026505T>GCA1249877877NRXN1c.772+997A>C (n.772+997A>C)
c.329+997A>C
n.66+997A>C
c.773-36A>C (n.773-36A>C)
c.297+997A>C
c.203-36A>C (n.203-36A>C)
dbSNP gnomAD v4
2g.51026505T=CA1249877876NRXN1c.772+997A= (n.772+997A=)
c.329+997A=
n.66+997A=
c.773-36A= (n.773-36A=)
c.297+997A=
c.203-36A= (n.203-36A=)
2g.51026506G>TCA2659012586NRXN1c.772+996C>A (n.772+996C>A)
c.329+996C>A
n.66+996C>A
c.773-37C>A (n.773-37C>A)
c.297+996C>A
c.203-37C>A (n.203-37C>A)
gnomAD v4
2g.51026507T>CCA48054742NRXN1c.772+995A>G (n.772+995A>G)
c.329+995A>G
n.66+995A>G
c.773-38A>G (n.773-38A>G)
c.297+995A>G
c.203-38A>G (n.203-38A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.51026507T=CA1249877878NRXN1c.772+995A= (n.772+995A=)
c.329+995A=
n.66+995A=
c.773-38A= (n.773-38A=)
c.297+995A=
c.203-38A= (n.203-38A=)
2g.51026508A>GCA2659012587NRXN1c.772+994T>C (n.772+994T>C)
c.329+994T>C
n.66+994T>C
c.773-39T>C (n.773-39T>C)
c.297+994T>C
c.203-39T>C (n.203-39T>C)
gnomAD v4
2g.51026509G>ACA2659012588NRXN1c.772+993C>T (n.772+993C>T)
c.329+993C>T
n.66+993C>T
c.773-40C>T (n.773-40C>T)
c.297+993C>T
c.203-40C>T (n.203-40C>T)
gnomAD v4
2g.51026509G>TCA2659012589NRXN1c.772+993C>A (n.772+993C>A)
c.329+993C>A
n.66+993C>A
c.773-40C>A (n.773-40C>A)
c.297+993C>A
c.203-40C>A (n.203-40C>A)
gnomAD v4
2g.51026511T>GCA1249877880NRXN1c.772+991A>C (n.772+991A>C)
c.329+991A>C
n.66+991A>C
c.773-42A>C (n.773-42A>C)
c.297+991A>C
c.203-42A>C (n.203-42A>C)
dbSNP
2g.51026511T=CA1249877879NRXN1c.772+991A= (n.772+991A=)
c.329+991A=
n.66+991A=
c.773-42A= (n.773-42A=)
c.297+991A=
c.203-42A= (n.203-42A=)
2g.51026512T>CCA1249877882NRXN1c.772+990A>G (n.772+990A>G)
c.329+990A>G
n.66+990A>G
c.773-43A>G (n.773-43A>G)
c.297+990A>G
c.203-43A>G (n.203-43A>G)
dbSNP
2g.51026512T=CA1249877881NRXN1c.772+990A= (n.772+990A=)
c.329+990A=
n.66+990A=
c.773-43A= (n.773-43A=)
c.297+990A=
c.203-43A= (n.203-43A=)
2g.51026515T>CCA1249877884NRXN1c.772+987A>G (n.772+987A>G)
c.329+987A>G
n.66+987A>G
c.773-46A>G (n.773-46A>G)
c.297+987A>G
c.203-46A>G (n.203-46A>G)
dbSNP
2g.51026515T=CA1249877883NRXN1c.772+987A= (n.772+987A=)
c.329+987A=
n.66+987A=
c.773-46A= (n.773-46A=)
c.297+987A=
c.203-46A= (n.203-46A=)
2g.51026516G>ACA2659012590NRXN1c.772+986C>T (n.772+986C>T)
c.329+986C>T
n.66+986C>T
c.773-47C>T (n.773-47C>T)
c.297+986C>T
c.203-47C>T (n.203-47C>T)
gnomAD v4
2g.51026516G>CCA532659850NRXN1c.772+986C>G (n.772+986C>G)
c.329+986C>G
n.66+986C>G
c.773-47C>G (n.773-47C>G)
c.297+986C>G
c.203-47C>G (n.203-47C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.51026516G=CA1249877885NRXN1c.772+986C= (n.772+986C=)
c.329+986C=
n.66+986C=
c.773-47C= (n.773-47C=)
c.297+986C=
c.203-47C= (n.203-47C=)
2g.51026516G>TCA2659012591NRXN1c.772+986C>A (n.772+986C>A)
c.329+986C>A
n.66+986C>A
c.773-47C>A (n.773-47C>A)
c.297+986C>A
c.203-47C>A (n.203-47C>A)
gnomAD v4
2g.51026517C>ACA2576965075NRXN1c.772+985G>T (n.772+985G>T)
c.329+985G>T
n.66+985G>T
c.773-48G>T (n.773-48G>T)
c.297+985G>T
c.203-48G>T (n.203-48G>T)
gnomAD v4
2g.51026517C=CA1249877886NRXN1c.772+985G= (n.772+985G=)
c.329+985G=
n.66+985G=
c.773-48G= (n.773-48G=)
c.297+985G=
c.203-48G= (n.203-48G=)
2g.51026517C>TCA48054743NRXN1c.772+985G>A (n.772+985G>A)
c.329+985G>A
n.66+985G>A
c.773-48G>A (n.773-48G>A)
c.297+985G>A
c.203-48G>A (n.203-48G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.51026518delCA2659012592NRXN1c.772+985del (n.772+985del)
c.329+985del
n.66+985del
c.773-48del (n.773-48del)
c.297+985del
c.203-48del (n.203-48del)
gnomAD v4
2g.51026518C>ACA2659012593NRXN1c.772+984G>T (n.772+984G>T)
c.329+984G>T
n.66+984G>T
c.773-49G>T (n.773-49G>T)
c.297+984G>T
c.203-49G>T (n.203-49G>T)
gnomAD v4
2g.51026519A=CA1249877887NRXN1c.772+983T= (n.772+983T=)
c.329+983T=
n.66+983T=
c.773-50T= (n.773-50T=)
c.297+983T=
c.203-50T= (n.203-50T=)
2g.51026519A>GCA48054744NRXN1c.772+983T>C (n.772+983T>C)
c.329+983T>C
n.66+983T>C
c.773-50T>C (n.773-50T>C)
c.297+983T>C
c.203-50T>C (n.203-50T>C)
dbSNP gnomAD v3 gnomAD v4
2g.51026520C>TCA2659012594NRXN1c.772+982G>A (n.772+982G>A)
c.329+982G>A
n.66+982G>A
c.773-51G>A (n.773-51G>A)
c.297+982G>A
c.203-51G>A (n.203-51G>A)
gnomAD v4
2g.51026521A>GCA2576965076NRXN1c.772+981T>C (n.772+981T>C)
c.329+981T>C
n.66+981T>C
c.773-52T>C (n.773-52T>C)
c.297+981T>C
c.203-52T>C (n.203-52T>C)

Number of alleles fetched