geneid | 9379 |
---|---|
ensemblid | ENSG00000110076.21 |
hgncid | 8009 |
symbol | NRXN2 |
name | neurexin 2 |
refseq_nuc | NM_015080.4 |
refseq_prot | NP_055895.1 |
ensembl_nuc | ENST00000265459.11 |
ensembl_prot | ENSP00000265459.5 |
mane_status | MANE Select |
chr | chr11 |
start | 64606174 |
end | 64723197 |
strand | - |
ver | v1.2 |
region | chr11:64606174-64723197 |
region5000 | chr11:64601174-64728197 |
regionname0 | NRXN2_chr11_64606174_64723197 |
regionname5000 | NRXN2_chr11_64601174_64728197 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1712 | 230 | 60 | 39 | 98 | 9 | 22 | 70 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002 | 0/0 | 1712 | 70 | 20 | 12 | 29 | 3 | 6 | 21 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0003 | 0/0 | 1712 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0004 | 0/0 | 1712 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0005 | 0/0 | 1712 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0006 | 0/0 | 1712 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0007 | 0/0 | 1712 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0008 | 0/0 | 1712 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0009 | 0/0 | 1712 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0010 | 0/0 | 1712 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 5139 | 87 | 36 | 13 | 29 | 3 | 5 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0002 | 0/1 | 5139 | 69 | 5 | 19 | 27 | 6 | 11 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0003 | 0/0 | 5139 | 57 | 17 | 6 | 29 | 0 | 5 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0004 | 0/0 | 5139 | 47 | 3 | 8 | 27 | 3 | 6 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0005 | 0/0 | 5139 | 10 | 8 | 1 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0006 | 0/0 | 5139 | 8 | 6 | 2 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0007 | 0/0 | 5139 | 8 | 0 | 1 | 7 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0008 | 0/0 | 5139 | 2 | 1 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0009 | 0/0 | 5139 | 2 | 0 | 0 | 2 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0010 | 0/0 | 5139 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0011 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0012 | 0/0 | 5139 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0013 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0014 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0015 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0016 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0017 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0018 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0019 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0020 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0021 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0022 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0023 | 0/0 | 5139 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0024 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0025 | 0/0 | 5139 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0026 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
c0027 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1494 | 208 | 38 | 40 | 94 | 10 | 24 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0002 | 0/0 | 1494 | 31 | 20 | 6 | 3 | 0 | 2 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0003 | 0/0 | 1494 | 29 | 1 | 1 | 27 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0004 | 0/0 | 1494 | 18 | 18 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0005 | 0/0 | 1494 | 5 | 0 | 1 | 0 | 1 | 3 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0006 | 0/0 | 1494 | 5 | 0 | 0 | 5 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0007 | 0/0 | 1494 | 3 | 2 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0008 | 0/0 | 1494 | 2 | 0 | 2 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0009 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0010 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0011 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0012 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0013 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0014 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
t0015 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5139 | 87 | 36 | 13 | 29 | 3 | 5 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0002 | 0/1 | 5139 | 69 | 5 | 19 | 27 | 6 | 11 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0003 | 0/0 | 5139 | 57 | 17 | 6 | 29 | 0 | 5 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0007 | 0/0 | 5139 | 8 | 0 | 1 | 7 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0009 | 0/0 | 5139 | 2 | 0 | 0 | 2 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0017 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0018 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0019 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0020 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0022 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0023 | 0/0 | 5139 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0024 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0004 | 0/0 | 5139 | 47 | 3 | 8 | 27 | 3 | 6 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0005 | 0/0 | 5139 | 10 | 8 | 1 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0006 | 0/0 | 5139 | 8 | 6 | 2 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0008 | 0/0 | 5139 | 2 | 1 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0011 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0013 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0015 | 0/0 | 5139 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0003c0027 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0004c0010 | 0/0 | 5139 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0005c0016 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0006c0021 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0007c0025 | 0/0 | 5139 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0008c0026 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0009c0012 | 0/0 | 5139 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0010c0014 | 0/0 | 5139 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6632 | 65 | 18 | 11 | 27 | 3 | 5 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0001t0004 | 0/0 | 6632 | 18 | 18 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0001t0008 | 0/0 | 6632 | 2 | 0 | 2 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0001t0012 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0001t0014 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0002t0001 | 0/1 | 6632 | 65 | 5 | 17 | 26 | 5 | 11 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0002t0005 | 0/0 | 6632 | 2 | 0 | 1 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0002t0010 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0002t0013 | 0/0 | 6632 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0003t0001 | 0/0 | 6632 | 5 | 4 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0003t0002 | 0/0 | 6632 | 22 | 12 | 5 | 3 | 0 | 2 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0003t0003 | 0/0 | 6632 | 22 | 1 | 1 | 20 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0003t0005 | 0/0 | 6632 | 3 | 0 | 0 | 0 | 0 | 3 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0003t0006 | 0/0 | 6632 | 5 | 0 | 0 | 5 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0007t0001 | 0/0 | 6632 | 7 | 0 | 0 | 7 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0007t0007 | 0/0 | 6632 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0009t0003 | 0/0 | 6632 | 2 | 0 | 0 | 2 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0017t0007 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0018t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0019t0001 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0020t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0022t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0023t0001 | 0/0 | 6632 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0001c0024t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0004t0001 | 0/0 | 6632 | 44 | 3 | 8 | 26 | 2 | 5 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0004t0003 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0004t0011 | 0/0 | 6632 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0004t0015 | 0/0 | 6632 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0005t0002 | 0/0 | 6632 | 8 | 7 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0005t0003 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0005t0009 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0006t0001 | 0/0 | 6632 | 8 | 6 | 2 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0008t0001 | 0/0 | 6632 | 2 | 1 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0011t0007 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0013t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0002c0015t0002 | 0/0 | 6632 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0003c0027t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0004c0010t0001 | 0/0 | 6632 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0005c0016t0003 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0006c0021t0003 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0007c0025t0001 | 0/0 | 6632 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0008c0026t0003 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0009c0012t0001 | 0/0 | 6632 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
a0010c0014t0001 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | copy fasta | chr11 | 64601174 | 64728197 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0008g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0001t0014g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0002t0013g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0003t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0007t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0009t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0017t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0018t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0019t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0020t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0022t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0023t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0001c0024t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0011g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0004t0015g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0005t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0006t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0008t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0011t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0013t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0002c0015t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0003c0027t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0004c0010t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0005c0016t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0006c0021t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0007c0025t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0008c0026t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0009c0012t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
a0010c0014t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0089 | EUR | GBR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00280 | hp1 | a0002 | c0004 | t0001 | g0113 | EUR | FIN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0069 | EUR | FIN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00438 | hp2 | a0002 | c0004 | t0001 | g0209 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00558 | hp1 | a0001 | c0020 | t0001 | g0041 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00597 | hp2 | a0001 | c0007 | t0001 | g0283 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00609 | hp1 | a0002 | c0004 | t0001 | g0278 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00609 | hp2 | a0006 | c0021 | t0003 | g0136 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00639 | hp2 | a0001 | c0003 | t0002 | g0299 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00673 | hp2 | a0001 | c0009 | t0003 | g0002 | EAS | CHS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0173 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00738 | hp1 | a0007 | c0025 | t0001 | g0201 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG00738 | hp2 | a0001 | c0003 | t0002 | g0141 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0026 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0285 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01106 | hp1 | a0002 | c0006 | t0001 | g0006 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01106 | hp2 | a0002 | c0004 | t0001 | g0207 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01109 | hp2 | a0001 | c0007 | t0007 | g0013 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01167 | hp1 | a0002 | c0004 | t0001 | g0155 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01168 | hp2 | a0001 | c0003 | t0002 | g0296 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01175 | hp1 | a0002 | c0004 | t0001 | g0114 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01243 | hp1 | a0002 | c0008 | t0001 | g0281 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01243 | hp2 | a0002 | c0005 | t0002 | g0277 | AMR | PUR | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0292 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0295 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01346 | hp1 | a0002 | c0004 | t0001 | g0216 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0055 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01358 | hp1 | a0002 | c0004 | t0001 | g0125 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01496 | hp2 | a0002 | c0004 | t0001 | g0217 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0062 | EUR | IBS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0073 | EUR | IBS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01891 | hp2 | a0001 | c0003 | t0002 | g0234 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01934 | hp2 | a0002 | c0006 | t0001 | g0163 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01978 | hp1 | a0001 | c0003 | t0003 | g0235 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02015 | hp1 | a0001 | c0003 | t0003 | g0142 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02027 | hp1 | a0001 | c0003 | t0003 | g0246 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02040 | hp2 | a0001 | c0003 | t0006 | g0304 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02055 | hp1 | a0001 | c0003 | t0002 | g0297 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02056 | hp1 | a0002 | c0004 | t0001 | g0279 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02056 | hp2 | a0001 | c0002 | t0010 | g0064 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02071 | hp1 | a0001 | c0003 | t0006 | g0305 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02071 | hp2 | a0002 | c0004 | t0001 | g0020 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02083 | hp1 | a0002 | c0004 | t0001 | g0167 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02083 | hp2 | a0001 | c0003 | t0003 | g0227 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02129 | hp1 | a0001 | c0001 | t0014 | g0039 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02129 | hp2 | a0002 | c0004 | t0001 | g0116 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02132 | hp1 | a0002 | c0004 | t0001 | g0168 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02132 | hp2 | a0001 | c0009 | t0003 | g0002 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02135 | hp2 | a0002 | c0004 | t0001 | g0214 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02145 | hp1 | a0002 | c0006 | t0001 | g0161 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02145 | hp2 | a0002 | c0015 | t0002 | g0275 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02165 | hp1 | a0008 | c0026 | t0003 | g0244 | EAS | CDX | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0063 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02280 | hp1 | a0001 | c0003 | t0003 | g0153 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02300 | hp2 | a0002 | c0004 | t0001 | g0110 | AMR | PEL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0107 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0151 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02523 | hp2 | a0001 | c0007 | t0001 | g0036 | EAS | KHV | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02630 | hp1 | a0001 | c0003 | t0002 | g0291 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02683 | hp2 | a0001 | c0003 | t0002 | g0147 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02698 | hp1 | a0004 | c0010 | t0001 | g0224 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02698 | hp2 | a0001 | c0003 | t0002 | g0294 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0287 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02809 | hp2 | a0002 | c0005 | t0002 | g0219 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0134 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02896 | hp1 | a0002 | c0004 | t0001 | g0222 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02897 | hp1 | a0002 | c0004 | t0001 | g0223 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02922 | hp2 | a0002 | c0005 | t0002 | g0170 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0104 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02976 | hp2 | a0001 | c0017 | t0007 | g0189 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0290 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03098 | hp2 | a0001 | c0003 | t0002 | g0289 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0133 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03139 | hp1 | a0002 | c0006 | t0001 | g0010 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03139 | hp2 | a0002 | c0005 | t0002 | g0276 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0233 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03225 | hp2 | a0001 | c0003 | t0002 | g0298 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03516 | hp1 | a0001 | c0003 | t0002 | g0226 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03516 | hp2 | a0002 | c0005 | t0002 | g0300 | AFR | ESN | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03540 | hp1 | a0002 | c0006 | t0001 | g0007 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03579 | hp2 | a0001 | c0003 | t0002 | g0140 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03654 | hp1 | a0002 | c0004 | t0011 | g0212 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03654 | hp2 | a0001 | c0023 | t0001 | g0192 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03669 | hp1 | a0002 | c0004 | t0001 | g0284 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0288 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03710 | hp2 | a0009 | c0012 | t0001 | g0112 | SAS | PJL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0245 | SAS | BEB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03831 | hp2 | a0002 | c0004 | t0001 | g0213 | SAS | BEB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03927 | hp1 | a0001 | c0003 | t0005 | g0203 | SAS | BEB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03927 | hp2 | a0002 | c0004 | t0001 | g0215 | SAS | BEB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04115 | hp2 | a0001 | c0003 | t0005 | g0105 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | BEB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04199 | hp1 | a0001 | c0003 | t0005 | g0106 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04204 | hp1 | a0002 | c0004 | t0001 | g0131 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | STU | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18522 | hp1 | a0002 | c0005 | t0009 | g0004 | AFR | YRI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18522 | hp2 | a0002 | c0006 | t0001 | g0162 | AFR | YRI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18747 | hp2 | a0001 | c0003 | t0003 | g0143 | EAS | CHB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18939 | hp1 | a0001 | c0001 | t0012 | g0048 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18939 | hp2 | a0002 | c0004 | t0001 | g0221 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18943 | hp1 | a0002 | c0004 | t0003 | g0115 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18943 | hp2 | a0001 | c0022 | t0001 | g0241 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18944 | hp1 | a0002 | c0013 | t0001 | g0191 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18944 | hp2 | a0001 | c0003 | t0003 | g0237 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18945 | hp1 | a0001 | c0007 | t0001 | g0043 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18947 | hp1 | a0002 | c0005 | t0003 | g0210 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18948 | hp1 | a0002 | c0004 | t0001 | g0169 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18948 | hp2 | a0001 | c0003 | t0006 | g0303 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18950 | hp1 | a0002 | c0004 | t0001 | g0019 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18951 | hp1 | a0002 | c0004 | t0001 | g0118 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18952 | hp1 | a0001 | c0003 | t0003 | g0240 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18954 | hp1 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18954 | hp2 | a0010 | c0014 | t0001 | g0127 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18956 | hp1 | a0001 | c0003 | t0003 | g0145 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18960 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18963 | hp2 | a0001 | c0003 | t0006 | g0302 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18964 | hp1 | a0002 | c0004 | t0001 | g0211 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18969 | hp2 | a0001 | c0003 | t0003 | g0229 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18971 | hp1 | a0002 | c0004 | t0001 | g0128 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18979 | hp1 | a0001 | c0003 | t0003 | g0236 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18980 | hp1 | a0001 | c0003 | t0003 | g0293 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18983 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18984 | hp1 | a0002 | c0004 | t0001 | g0123 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18987 | hp1 | a0005 | c0016 | t0003 | g0132 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18990 | hp1 | a0001 | c0007 | t0001 | g0044 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18990 | hp2 | a0002 | c0004 | t0001 | g0126 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA18995 | hp2 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19002 | hp2 | a0002 | c0004 | t0001 | g0129 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19003 | hp1 | a0001 | c0007 | t0001 | g0180 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0242 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0239 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19011 | hp2 | a0002 | c0004 | t0001 | g0208 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19030 | hp1 | a0002 | c0011 | t0007 | g0014 | AFR | LWK | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | LWK | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | LWK | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0135 | AFR | LWK | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19054 | hp1 | a0001 | c0003 | t0003 | g0103 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19055 | hp1 | a0001 | c0003 | t0003 | g0228 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19056 | hp1 | a0002 | c0004 | t0001 | g0166 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19056 | hp2 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19062 | hp2 | a0002 | c0004 | t0001 | g0111 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19063 | hp1 | a0001 | c0003 | t0002 | g0230 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19063 | hp2 | a0001 | c0024 | t0001 | g0100 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19064 | hp1 | a0003 | c0027 | t0001 | g0056 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19064 | hp2 | a0001 | c0007 | t0001 | g0042 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19065 | hp2 | a0002 | c0004 | t0001 | g0120 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19066 | hp2 | a0002 | c0004 | t0001 | g0121 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19068 | hp2 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19079 | hp2 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19081 | hp1 | a0001 | c0018 | t0001 | g0047 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19081 | hp2 | a0001 | c0003 | t0003 | g0238 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19084 | hp1 | a0002 | c0004 | t0001 | g0122 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19085 | hp1 | a0002 | c0004 | t0001 | g0156 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19087 | hp1 | a0001 | c0007 | t0001 | g0018 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19087 | hp2 | a0001 | c0003 | t0006 | g0301 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | YRI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA19240 | hp2 | a0001 | c0019 | t0001 | g0263 | AFR | YRI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ASW | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ASW | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20752 | hp1 | a0001 | c0002 | t0005 | g0204 | EUR | TSI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20752 | hp2 | a0002 | c0004 | t0015 | g0109 | EUR | TSI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0075 | EUR | TSI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20805 | hp2 | a0002 | c0004 | t0001 | g0119 | EUR | TSI | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | GIH | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20905 | hp2 | a0002 | c0004 | t0001 | g0117 | SAS | GIH | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01123 | hp1 | a0002 | c0004 | t0001 | g0218 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG01123 | hp2 | a0001 | c0002 | t0013 | g0061 | AMR | CLM | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02109 | hp1 | a0002 | c0004 | t0001 | g0124 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02109 | hp2 | a0002 | c0008 | t0001 | g0188 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02559 | hp1 | a0002 | c0006 | t0001 | g0009 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG03471 | hp2 | a0002 | c0005 | t0002 | g0274 | AFR | MSL | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
HG06807 | hp2 | a0002 | c0006 | t0001 | g0008 | AFR | USA | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20300 | hp1 | a0002 | c0005 | t0002 | g0220 | AFR | USA | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
NA20300 | hp2 | a0002 | c0005 | t0002 | g0280 | AFR | USA | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0093 | REF | REF | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0268 | REF | REF | NRXN2_chr11_64601174_64728197 | NRXN2 | chr11 | 64601174 | 64728197 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64622908
|
C | G | 1 | a0009 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.4018G>C | p.Val1340Leu | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/23 | 4489/6632 | 4018/5139 | 1340/1712 | chr11 | 64622908 | ||
chr11:64623027
|
C | T | 1 | a0004 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.3899G>A | p.Arg1300Gln | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/23 | 4370/6632 | 3899/5139 | 1300/1712 | chr11 | 64623027 | ||
chr11:64648842
|
G | C | 1 | a0007 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.3175C>G | p.Arg1059Gly | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 16/23 | 3646/6632 | 3175/5139 | 1059/1712 | chr11 | 64648842 | ||
chr11:64660767
|
C | T | 1 | a0006 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.2171G>A | p.Arg724Gln | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 10/23 | 2642/6632 | 2171/5139 | 724/1712 | chr11 | 64660767 | ||
chr11:64667534
|
G | A | 1 | a0010 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.1514C>T | p.Ala505Val | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/23 | 1985/6632 | 1514/5139 | 505/1712 | chr11 | 64667534 | ||
chr11:64713001
|
G | C | 1 | a0008 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.699C>G | p.His233Gln | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 1170/6632 | 699/5139 | 233/1712 | chr11 | 64713001 | ||
chr11:64713194
|
A | C | 1 | a0005 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.506T>G | p.Val169Gly | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 977/6632 | 506/5139 | 169/1712 | chr11 | 64713194 | ||
chr11:64713458
|
A | T | 4 | a0002a0003a0009others(1): Show | 73 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(70): Show |
missense_variant | MODERATE | c.242T>A | p.Leu81Gln | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 713/6632 | 242/5139 | 81/1712 | chr11 | 64713458 | ||
chr11:64713538
|
G | T | 1 | a0004 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.162C>A | p.Ser54Arg | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 633/6632 | 162/5139 | 54/1712 | chr11 | 64713538 | ||
chr11:64713539
|
C | T | 1 | a0004 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.161G>A | p.Ser54Asn | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 632/6632 | 161/5139 | 54/1712 | chr11 | 64713539 | ||
chr11:64713626
|
C | A | 1 | a0003 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.74G>T | p.Arg25Leu | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 545/6632 | 74/5139 | 25/1712 | chr11 | 64713626 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64607757
|
G | T | 1 | a0002c0013 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.4578C>A | p.Leu1526Leu | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 5049/6632 | 4578/5139 | 1526/1712 | chr11 | 64607757 | ||
chr11:64622891
|
G | A | 1 | a0001c0023 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.4035C>T | p.Ser1345Ser | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/23 | 4506/6632 | 4035/5139 | 1345/1712 | chr11 | 64622891 | ||
chr11:64622891
|
G | T | 1 | a0001c0018 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.4035C>A | p.Ser1345Ser | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/23 | 4506/6632 | 4035/5139 | 1345/1712 | chr11 | 64622891 | ||
chr11:64630508
|
G | A | 1 | a0001c0019 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.3651C>T | p.Asn1217Asn | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/23 | 4122/6632 | 3651/5139 | 1217/1712 | chr11 | 64630508 | ||
chr11:64648295
|
G | A | 6 | a0001c0022a0002c0004a0002c0013others(3): Show | 52 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
synonymous_variant | LOW | c.3327C>T | p.Gly1109Gly | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/23 | 3798/6632 | 3327/5139 | 1109/1712 | chr11 | 64648295 | ||
chr11:64648804
|
G | C | 1 | a0001c0024 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.3213C>G | p.Leu1071Leu | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 16/23 | 3684/6632 | 3213/5139 | 1071/1712 | chr11 | 64648804 | ||
chr11:64651428
|
G | A | 7 | a0001c0002a0001c0020a0001c0023others(4): Show | 76 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(73): Show |
synonymous_variant | LOW | c.2745C>T | p.Ile915Ile | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 14/23 | 3216/6632 | 2745/5139 | 915/1712 | chr11 | 64651428 | ||
chr11:64667368
|
G | A | 1 | a0001c0009 | 2 | HG00673.hp2 HG02132.hp2 |
synonymous_variant | LOW | c.1680C>T | p.Asp560Asp | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/23 | 2151/6632 | 1680/5139 | 560/1712 | chr11 | 64667368 | ||
chr11:64677032
|
T | C | 1 | a0002c0015 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1158A>G | p.Ala386Ala | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/23 | 1629/6632 | 1158/5139 | 386/1712 | chr11 | 64677032 | ||
chr11:64685796
|
G | A | 3 | a0001c0007a0001c0017a0002c0011 | 10 | HG00597.hp2 HG01109.hp2 HG02523.hp2 others(7): Show |
synonymous_variant | LOW | c.1002C>T | p.Ala334Ala | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/23 | 1473/6632 | 1002/5139 | 334/1712 | chr11 | 64685796 | ||
chr11:64685874
|
C | T | 1 | a0001c0017 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.924G>A | p.Gln308Gln | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/23 | 1395/6632 | 924/5139 | 308/1712 | chr11 | 64685874 | ||
chr11:64713169
|
G | A | 11 | a0001c0002a0001c0003a0001c0009others(8): Show | 136 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(133): Show |
synonymous_variant | LOW | c.531C>T | p.Gly177Gly | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 1002/6632 | 531/5139 | 177/1712 | chr11 | 64713169 | ||
chr11:64713193
|
G | A | 1 | a0005c0016 | 1 | NA18987.hp1 | synonymous_variant | LOW | c.507C>T | p.Val169Val | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 978/6632 | 507/5139 | 169/1712 | chr11 | 64713193 | ||
chr11:64713454
|
C | T | 2 | a0002c0006a0002c0011 | 9 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(6): Show |
synonymous_variant | LOW | c.246G>A | p.Leu82Leu | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 717/6632 | 246/5139 | 82/1712 | chr11 | 64713454 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64606184
|
G | C | 8 | a0001c0003t0003a0001c0003t0006a0001c0009t0003others(5): Show | 34 | HG00609.hp2 HG00673.hp2 HG01978.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1012C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 1012 | chr11 | 64606184 | |||||
chr11:64606217
|
C | T | 1 | a0001c0002t0013 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 979 | chr11 | 64606217 | |||||
chr11:64606224
|
G | T | 1 | a0001c0001t0012 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 972 | chr11 | 64606224 | |||||
chr11:64606427
|
T | G | 1 | a0001c0001t0004 | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*769A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 769 | chr11 | 64606427 | |||||
chr11:64606450
|
C | A | 1 | a0001c0001t0014 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 746 | chr11 | 64606450 | |||||
chr11:64606769
|
G | A | 12 | a0001c0003t0002a0001c0003t0003a0001c0003t0006others(9): Show | 66 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*427C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 427 | chr11 | 64606769 | |||||
chr11:64606840
|
C | T | 3 | a0001c0007t0007a0001c0017t0007a0002c0011t0007 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*356G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 356 | chr11 | 64606840 | |||||
chr11:64606930
|
C | T | 1 | a0002c0004t0011 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 266 | chr11 | 64606930 | |||||
chr11:64606955
|
T | G | 1 | a0001c0001t0008 | 2 | HG00735.hp1 HG01070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*241A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 241 | chr11 | 64606955 | |||||
chr11:64607126
|
G | A | 1 | a0002c0004t0015 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 23/23 | 70 | chr11 | 64607126 | |||||
chr11:64713732
|
G | C | 2 | a0001c0002t0005a0001c0003t0005 | 5 | HG01346.hp2 HG03927.hp1 HG04115.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 33 | chr11 | 64713732 | |||||
chr11:64713920
|
C | G | 1 | a0001c0002t0010 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-221G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/23 | 221 | chr11 | 64713920 | |||||
chr11:64722980
|
G | A | 1 | a0001c0003t0006 | 5 | HG02040.hp2 HG02071.hp1 NA18948.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-254C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/23 | chr11 | 64722980 | ||||||
chr11:64723152
|
G | T | 1 | a0002c0005t0009 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-426C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/23 | 9453 | chr11 | 64723152 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64608285
|
C | T | 1 | a0009c0012t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4253-203G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608285 | ||||||
chr11:64608300
|
T | C | 1 | a0001c0002t0001g0088 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4253-218A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608300 | ||||||
chr11:64608494
|
C | CT | 19 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 19 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.4253-413dupA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608494 | ||||||
chr11:64608494
|
CT | C | 67 | a0001c0001t0001g0108a0001c0002t0001g0286a0001c0003t0002g0133others(64): Show | 68 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.4253-413delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608494 | ||||||
chr11:64608494
|
CTT | C | 23 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(20): Show | 23 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.4253-414_4253-413d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608494 | ||||||
chr11:64608524
|
A | T | 1 | a0001c0003t0002g0292 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4253-442T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608524 | ||||||
chr11:64608579
|
G | A | 1 | a0001c0001t0004g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4253-497C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608579 | ||||||
chr11:64608725
|
G | A | 9 | a0001c0002t0001g0075a0002c0006t0001g0006a0002c0006t0001g0007others(6): Show | 9 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4253-643C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608725 | ||||||
chr11:64608811
|
A | G | 1 | a0002c0006t0001g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4253-729T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608811 | ||||||
chr11:64608835
|
C | T | 65 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(62): Show | 66 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.4253-753G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608835 | ||||||
chr11:64608888
|
A | G | 1 | a0001c0002t0001g0070 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4253-806T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608888 | ||||||
chr11:64608984
|
T | C | 1 | a0001c0003t0006g0304 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4253-902A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64608984 | ||||||
chr11:64609124
|
G | C | 1 | a0002c0004t0001g0166 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4253-1042C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609124 | ||||||
chr11:64609327
|
T | C | 5 | a0001c0003t0003g0143a0001c0003t0003g0150a0001c0003t0003g0242others(2): Show | 5 | NA18747.hp2 NA18947.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.4253-1245A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609327 | ||||||
chr11:64609350
|
C | T | 1 | a0001c0002t0001g0225 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4253-1268G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609350 | ||||||
chr11:64609680
|
T | C | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.4253-1598A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609680 | ||||||
chr11:64609708
|
T | C | 2 | a0001c0001t0004g0012a0001c0001t0004g0256 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4253-1626A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609708 | ||||||
chr11:64609830
|
G | A | 1 | a0001c0001t0014g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4253-1748C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609830 | ||||||
chr11:64609836
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.4253-1754G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609836 | ||||||
chr11:64609864
|
C | T | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.4253-1782G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609864 | ||||||
chr11:64609909
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4253-1827G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64609909 | ||||||
chr11:64610178
|
C | T | 65 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(62): Show | 66 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.4253-2096G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64610178 | ||||||
chr11:64610254
|
G | C | 79 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0002t0001g0058others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.4253-2172C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64610254 | ||||||
chr11:64610582
|
A | G | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4253-2500T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64610582 | ||||||
chr11:64610739
|
C | G | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4253-2657G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64610739 | ||||||
chr11:64610979
|
G | A | 2 | a0001c0003t0003g0143a0001c0003t0003g0293 | 2 | NA18747.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.4253-2897C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64610979 | ||||||
chr11:64610980
|
C | A | 77 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.4253-2898G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64610980 | ||||||
chr11:64611034
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4253-2952C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64611034 | ||||||
chr11:64611108
|
A | G | 1 | a0002c0005t0002g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4253-3026T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64611108 | ||||||
chr11:64611288
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4253-3206G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64611288 | ||||||
chr11:64611793
|
C | T | 1 | a0001c0007t0001g0180 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4253-3711G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64611793 | ||||||
chr11:64611869
|
G | A | 1 | a0001c0003t0003g0237 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4253-3787C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64611869 | ||||||
chr11:64612110
|
C | T | 2 | a0001c0002t0001g0197a0001c0002t0001g0285 | 2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.4253-4028G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612110 | ||||||
chr11:64612173
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4253-4091A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612173 | ||||||
chr11:64612197
|
T | C | 1 | a0001c0003t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4253-4115A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612197 | ||||||
chr11:64612394
|
C | T | 1 | a0002c0015t0002g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4253-4312G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612394 | ||||||
chr11:64612451
|
T | C | 304 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(301): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.4253-4369A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612451 | ||||||
chr11:64612577
|
TC | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4253-4496delG | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612577 | ||||||
chr11:64612580
|
T | G | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4253-4498A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612580 | ||||||
chr11:64612846
|
T | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0186 | 3 | HG02602.hp2 HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.4253-4764A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612846 | ||||||
chr11:64612933
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4253-4851C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612933 | ||||||
chr11:64612952
|
G | A | 1 | a0001c0023t0001g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4253-4870C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64612952 | ||||||
chr11:64613286
|
G | A | 3 | a0002c0004t0001g0218a0002c0008t0001g0188a0002c0008t0001g0281 | 3 | HG01123.hp1 HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4253-5204C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64613286 | ||||||
chr11:64613421
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4253-5339G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64613421 | ||||||
chr11:64613505
|
G | A | 1 | a0001c0003t0002g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4253-5423C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64613505 | ||||||
chr11:64613660
|
T | C | 145 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(142): Show | 147 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.4253-5578A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64613660 | ||||||
chr11:64613747
|
C | T | 1 | a0001c0002t0001g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4253-5665G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64613747 | ||||||
chr11:64613853
|
A | C | 1 | a0001c0007t0001g0180 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4253-5771T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64613853 | ||||||
chr11:64614159
|
G | A | 1 | a0001c0001t0012g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4253-6077C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614159 | ||||||
chr11:64614252
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0157 | 2 | HG01175.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4252+6042G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614252 | ||||||
chr11:64614315
|
G | C | 1 | a0002c0004t0001g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4252+5979C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614315 | ||||||
chr11:64614450
|
AAGG | A | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4252+5841_4252+584 others(7): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614450 | ||||||
chr11:64614457
|
A | G | 1 | a0001c0003t0002g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4252+5837T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614457 | ||||||
chr11:64614728
|
A | G | 1 | a0002c0004t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4252+5566T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614728 | ||||||
chr11:64614732
|
C | T | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.4252+5562G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614732 | ||||||
chr11:64614852
|
C | T | 1 | a0009c0012t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4252+5442G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64614852 | ||||||
chr11:64615075
|
C | T | 1 | a0002c0005t0002g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4252+5219G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615075 | ||||||
chr11:64615134
|
C | G | 1 | a0001c0007t0001g0043 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4252+5160G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615134 | ||||||
chr11:64615243
|
G | A | 1 | a0002c0004t0001g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4252+5051C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615243 | ||||||
chr11:64615297
|
G | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4252+4997C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615297 | ||||||
chr11:64615334
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.4252+4960T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615334 | ||||||
chr11:64615686
|
C | T | 1 | a0002c0004t0015g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4252+4608G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615686 | ||||||
chr11:64615829
|
CGT | C | 75 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.4252+4463_4252+446 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615829 | ||||||
chr11:64615829
|
CGTGT | C | 28 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(25): Show | 28 | HG01106.hp1 HG01109.hp2 HG01934.hp2 others(25): Show |
intron_variant | MODIFIER | c.4252+4461_4252+446 others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615829 | ||||||
chr11:64615829
|
CGTGTGTG others(17): Show |
C | 69 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(66): Show | 70 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.4252+4441_4252+446 others(28): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615829 | ||||||
chr11:64615830
|
G | A | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.4252+4464C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615830 | ||||||
chr11:64615834
|
G | A | 11 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0006t0001g0006others(8): Show | 11 | HG01106.hp1 HG01109.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.4252+4460C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615834 | ||||||
chr11:64615855
|
T | C | 115 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(112): Show | 117 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.4252+4439A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615855 | ||||||
chr11:64615856
|
G | A | 115 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(112): Show | 117 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.4252+4438C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615856 | ||||||
chr11:64615857
|
T | C | 30 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(27): Show | 30 | HG01106.hp1 HG01109.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.4252+4437A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615857 | ||||||
chr11:64615858
|
G | A | 30 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(27): Show | 30 | HG01106.hp1 HG01109.hp2 HG01934.hp2 others(27): Show |
intron_variant | MODIFIER | c.4252+4436C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615858 | ||||||
chr11:64615868
|
GTA | G | 115 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(112): Show | 117 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.4252+4424_4252+442 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615868 | ||||||
chr11:64615870
|
A | G | 1 | a0001c0003t0002g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4252+4424T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64615870 | ||||||
chr11:64616212
|
C | T | 1 | a0002c0004t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4252+4082G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64616212 | ||||||
chr11:64616422
|
C | T | 1 | a0001c0002t0005g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4252+3872G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64616422 | ||||||
chr11:64616428
|
G | A | 5 | a0002c0004t0001g0118a0002c0004t0001g0120a0002c0004t0001g0122others(2): Show | 5 | NA18951.hp1 NA18984.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.4252+3866C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64616428 | ||||||
chr11:64616505
|
A | G | 1 | a0001c0002t0005g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4252+3789T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64616505 | ||||||
chr11:64616728
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4252+3566A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64616728 | ||||||
chr11:64616797
|
G | A | 2 | a0002c0004t0001g0121a0002c0004t0001g0211 | 2 | NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.4252+3497C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64616797 | ||||||
chr11:64616829
|
CA | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(4): Show | 7 | HG00140.hp1 HG01433.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.4252+3464delT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64616829 | ||||||
chr11:64617006
|
G | A | 1 | a0001c0007t0001g0283 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4252+3288C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617006 | ||||||
chr11:64617107
|
G | A | 1 | a0002c0004t0001g0111 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4252+3187C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617107 | ||||||
chr11:64617136
|
T | C | 1 | a0001c0001t0012g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4252+3158A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617136 | ||||||
chr11:64617161
|
C | CGT | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4252+3131_4252+313 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617161 | ||||||
chr11:64617163
|
T | C | 1 | a0001c0007t0007g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4252+3131A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617163 | ||||||
chr11:64617491
|
G | A | 1 | a0001c0001t0004g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4252+2803C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617491 | ||||||
chr11:64617572
|
A | C | 1 | a0001c0007t0001g0180 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.4252+2722T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617572 | ||||||
chr11:64617609
|
G | C | 1 | a0002c0006t0001g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4252+2685C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617609 | ||||||
chr11:64617748
|
G | A | 4 | a0002c0005t0002g0219a0002c0005t0002g0220a0002c0005t0002g0277others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4252+2546C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617748 | ||||||
chr11:64617855
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4252+2439C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617855 | ||||||
chr11:64617997
|
G | A | 1 | a0001c0003t0003g0242 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4252+2297C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64617997 | ||||||
chr11:64618464
|
C | T | 1 | a0002c0005t0002g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4252+1830G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64618464 | ||||||
chr11:64618504
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4252+1790G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64618504 | ||||||
chr11:64619054
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(60): Show | 63 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.4252+1240A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64619054 | ||||||
chr11:64619196
|
A | G | 2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | NA18984.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.4252+1098T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64619196 | ||||||
chr11:64619245
|
C | T | 1 | a0001c0002t0001g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4252+1049G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64619245 | ||||||
chr11:64619327
|
A | T | 2 | a0002c0005t0002g0219a0002c0005t0002g0220 | 2 | HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4252+967T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64619327 | ||||||
chr11:64619875
|
G | A | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4252+419C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64619875 | ||||||
chr11:64619907
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4252+387C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64619907 | ||||||
chr11:64620276
|
G | C | 1 | a0002c0004t0001g0166 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4252+18C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 22/22 | chr11 | 64620276 | ||||||
chr11:64620390
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4174-18C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620390 | ||||||
chr11:64620460
|
G | A | 74 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.4174-88C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620460 | ||||||
chr11:64620660
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4174-288G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620660 | ||||||
chr11:64620719
|
C | T | 1 | a0001c0003t0002g0298 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4174-347G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620719 | ||||||
chr11:64620790
|
G | A | 59 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(56): Show | 60 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.4174-418C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620790 | ||||||
chr11:64620914
|
A | T | 294 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(291): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.4174-542T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620914 | ||||||
chr11:64620980
|
T | A | 1 | a0002c0004t0001g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4174-608A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620980 | ||||||
chr11:64620992
|
G | C | 1 | a0001c0003t0002g0147 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4174-620C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64620992 | ||||||
chr11:64621020
|
C | T | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4174-648G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64621020 | ||||||
chr11:64621207
|
C | T | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4174-835G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64621207 | ||||||
chr11:64621457
|
A | G | 51 | a0001c0003t0001g0144a0001c0022t0001g0241a0002c0004t0001g0001others(48): Show | 52 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.4174-1085T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64621457 | ||||||
chr11:64621490
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4174-1118C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64621490 | ||||||
chr11:64621566
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.4173+1187C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64621566 | ||||||
chr11:64621847
|
T | C | 1 | a0001c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4173+906A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64621847 | ||||||
chr11:64622065
|
G | A | 1 | a0001c0001t0004g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4173+688C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64622065 | ||||||
chr11:64622113
|
C | T | 1 | a0001c0002t0001g0093 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4173+640G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64622113 | ||||||
chr11:64622150
|
G | T | 1 | a0001c0001t0001g0037 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4173+603C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64622150 | ||||||
chr11:64622151
|
C | A | 1 | a0001c0001t0001g0037 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4173+602G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64622151 | ||||||
chr11:64622195
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4173+558C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64622195 | ||||||
chr11:64622293
|
C | T | 1 | a0001c0017t0007g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4173+460G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64622293 | ||||||
chr11:64622415
|
A | G | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4173+338T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 21/22 | chr11 | 64622415 | ||||||
chr11:64623593
|
G | A | 1 | a0002c0004t0001g0110 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3848-515C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64623593 | ||||||
chr11:64623685
|
G | C | 74 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.3848-607C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64623685 | ||||||
chr11:64623902
|
A | G | 2 | a0002c0004t0001g0222a0002c0004t0001g0223 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3848-824T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64623902 | ||||||
chr11:64623942
|
T | G | 2 | a0002c0008t0001g0188a0002c0008t0001g0281 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3848-864A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64623942 | ||||||
chr11:64624063
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3848-985C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624063 | ||||||
chr11:64624116
|
G | T | 10 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0166others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3848-1038C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624116 | ||||||
chr11:64624173
|
C | T | 1 | a0002c0005t0002g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3848-1095G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624173 | ||||||
chr11:64624174
|
G | A | 1 | a0001c0007t0007g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3848-1096C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624174 | ||||||
chr11:64624181
|
A | T | 1 | a0001c0002t0001g0288 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3848-1103T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624181 | ||||||
chr11:64624437
|
G | T | 117 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(114): Show | 119 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.3848-1359C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624437 | ||||||
chr11:64624438
|
C | T | 117 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(114): Show | 119 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.3848-1360G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624438 | ||||||
chr11:64624844
|
C | T | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3847+1619G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64624844 | ||||||
chr11:64625056
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3847+1407G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64625056 | ||||||
chr11:64625084
|
T | C | 2 | a0002c0005t0002g0219a0002c0005t0002g0220 | 2 | HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3847+1379A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64625084 | ||||||
chr11:64625185
|
A | G | 1 | a0002c0006t0001g0163 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3847+1278T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64625185 | ||||||
chr11:64625282
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3847+1181C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64625282 | ||||||
chr11:64625728
|
C | T | 1 | a0001c0002t0001g0087 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3847+735G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64625728 | ||||||
chr11:64625761
|
C | G | 1 | a0001c0002t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3847+702G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64625761 | ||||||
chr11:64626233
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0190 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.3847+230G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 20/22 | chr11 | 64626233 | ||||||
chr11:64627115
|
C | G | 1 | a0002c0004t0015g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3758-563G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64627115 | ||||||
chr11:64627212
|
C | T | 294 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(291): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.3758-660G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64627212 | ||||||
chr11:64627357
|
CT | C | 29 | a0001c0003t0003g0103a0001c0003t0003g0142a0001c0003t0003g0143others(26): Show | 30 | HG00609.hp2 HG00673.hp2 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.3758-806delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64627357 | ||||||
chr11:64627510
|
A | G | 1 | a0001c0002t0001g0070 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3758-958T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64627510 | ||||||
chr11:64627644
|
G | C | 1 | a0002c0004t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3758-1092C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64627644 | ||||||
chr11:64627780
|
G | C | 77 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.3758-1228C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64627780 | ||||||
chr11:64627926
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0024 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3758-1374G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64627926 | ||||||
chr11:64628283
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.3758-1731G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64628283 | ||||||
chr11:64628478
|
T | C | 1 | a0001c0003t0002g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3757+1924A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64628478 | ||||||
chr11:64628536
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3757+1866C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64628536 | ||||||
chr11:64628545
|
A | G | 1 | a0001c0003t0003g0142 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3757+1857T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64628545 | ||||||
chr11:64628937
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3757+1465C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64628937 | ||||||
chr11:64629004
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3757+1398C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64629004 | ||||||
chr11:64629096
|
T | C | 74 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.3757+1306A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64629096 | ||||||
chr11:64629097
|
A | T | 74 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.3757+1305T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64629097 | ||||||
chr11:64629191
|
C | T | 1 | a0002c0004t0001g0214 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3757+1211G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64629191 | ||||||
chr11:64629245
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3757+1157G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64629245 | ||||||
chr11:64629528
|
T | C | 1 | a0001c0002t0001g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3757+874A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64629528 | ||||||
chr11:64629767
|
C | A | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3757+635G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64629767 | ||||||
chr11:64630019
|
T | C | 12 | a0001c0002t0001g0065a0001c0002t0001g0072a0001c0002t0001g0078others(9): Show | 12 | HG00558.hp2 HG02027.hp2 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.3757+383A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64630019 | ||||||
chr11:64630195
|
C | T | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3757+207G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64630195 | ||||||
chr11:64630273
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3757+129A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64630273 | ||||||
chr11:64630393
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3757+9C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 19/22 | chr11 | 64630393 | ||||||
chr11:64630763
|
G | A | 1 | a0001c0002t0001g0199 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3586-190C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64630763 | ||||||
chr11:64631196
|
G | C | 1 | a0001c0002t0001g0098 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3586-623C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64631196 | ||||||
chr11:64631253
|
A | G | 2 | a0002c0008t0001g0188a0002c0008t0001g0281 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3586-680T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64631253 | ||||||
chr11:64631291
|
G | A | 1 | a0002c0004t0001g0113 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3586-718C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64631291 | ||||||
chr11:64631522
|
C | T | 1 | a0001c0002t0001g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3586-949G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64631522 | ||||||
chr11:64631613
|
T | C | 1 | a0002c0004t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3586-1040A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64631613 | ||||||
chr11:64631734
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3586-1161C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64631734 | ||||||
chr11:64632864
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3586-2291C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64632864 | ||||||
chr11:64632867
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3586-2294C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64632867 | ||||||
chr11:64633038
|
G | A | 2 | a0002c0008t0001g0188a0002c0008t0001g0281 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3585+2233C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64633038 | ||||||
chr11:64633247
|
A | G | 145 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(142): Show | 147 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.3585+2024T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64633247 | ||||||
chr11:64633354
|
T | G | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.3585+1917A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64633354 | ||||||
chr11:64633694
|
G | T | 1 | a0002c0005t0009g0004 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3585+1577C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64633694 | ||||||
chr11:64633869
|
G | A | 1 | a0001c0003t0003g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3585+1402C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64633869 | ||||||
chr11:64633869
|
G | T | 1 | a0001c0003t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3585+1402C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64633869 | ||||||
chr11:64634052
|
T | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3585+1219A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64634052 | ||||||
chr11:64634514
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3585+757C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64634514 | ||||||
chr11:64634555
|
T | C | 144 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(141): Show | 146 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.3585+716A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64634555 | ||||||
chr11:64634555
|
T | G | 1 | a0002c0004t0001g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3585+716A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64634555 | ||||||
chr11:64634661
|
CAA | C | 58 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(55): Show | 59 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.3585+608_3585+609d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64634661 | ||||||
chr11:64634946
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3585+325A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64634946 | ||||||
chr11:64635223
|
T | C | 127 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(124): Show | 129 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.3585+48A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 18/22 | chr11 | 64635223 | ||||||
chr11:64635475
|
A | G | 1 | a0001c0003t0003g0246 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3404-23T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64635475 | ||||||
chr11:64635951
|
G | A | 1 | a0001c0023t0001g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3404-499C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64635951 | ||||||
chr11:64636110
|
T | G | 1 | a0001c0003t0002g0230 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3404-658A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64636110 | ||||||
chr11:64636265
|
C | T | 2 | a0001c0003t0005g0105a0001c0003t0005g0203 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3404-813G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64636265 | ||||||
chr11:64636502
|
T | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.3404-1050A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64636502 | ||||||
chr11:64636742
|
G | A | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3404-1290C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64636742 | ||||||
chr11:64636890
|
T | C | 1 | a0002c0006t0001g0163 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3404-1438A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64636890 | ||||||
chr11:64636905
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3404-1453G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64636905 | ||||||
chr11:64637269
|
A | G | 2 | a0001c0003t0006g0303a0001c0003t0006g0305 | 2 | HG02071.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.3404-1817T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637269 | ||||||
chr11:64637320
|
C | A | 2 | a0001c0003t0003g0146a0001c0003t0003g0149 | 2 | NA18954.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3404-1868G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637320 | ||||||
chr11:64637332
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3404-1880G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637332 | ||||||
chr11:64637345
|
G | C | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3404-1893C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637345 | ||||||
chr11:64637379
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3404-1927G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637379 | ||||||
chr11:64637445
|
G | A | 1 | a0002c0004t0001g0114 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3404-1993C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637445 | ||||||
chr11:64637481
|
T | G | 1 | a0002c0004t0001g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3404-2029A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637481 | ||||||
chr11:64637491
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.3404-2039A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637491 | ||||||
chr11:64637937
|
G | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3404-2485C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64637937 | ||||||
chr11:64638476
|
G | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3404-3024C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64638476 | ||||||
chr11:64638806
|
T | C | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3404-3354A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64638806 | ||||||
chr11:64638953
|
C | A | 1 | a0001c0003t0005g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3404-3501G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64638953 | ||||||
chr11:64638957
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01496.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3404-3505G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64638957 | ||||||
chr11:64639362
|
CT | C | 5 | a0002c0004t0001g0124a0002c0004t0001g0125a0002c0004t0001g0216others(2): Show | 5 | HG01123.hp1 HG01346.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.3404-3911delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64639362 | ||||||
chr11:64639478
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3404-4026C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64639478 | ||||||
chr11:64639486
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3404-4034G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64639486 | ||||||
chr11:64639506
|
T | C | 1 | a0001c0001t0004g0260 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3404-4054A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64639506 | ||||||
chr11:64639681
|
G | A | 1 | a0001c0001t0004g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3404-4229C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64639681 | ||||||
chr11:64639913
|
C | A | 62 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(59): Show | 62 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.3404-4461G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64639913 | ||||||
chr11:64639947
|
G | A | 80 | a0001c0001t0001g0046a0001c0001t0001g0164a0001c0001t0001g0248others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.3404-4495C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64639947 | ||||||
chr11:64640370
|
C | T | 1 | a0002c0004t0015g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3404-4918G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64640370 | ||||||
chr11:64640484
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3404-5032C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64640484 | ||||||
chr11:64640627
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3404-5175T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64640627 | ||||||
chr11:64641244
|
C | T | 65 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(62): Show | 66 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.3404-5792G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64641244 | ||||||
chr11:64641642
|
G | A | 1 | a0002c0005t0009g0004 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3404-6190C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64641642 | ||||||
chr11:64641647
|
G | A | 1 | a0002c0005t0002g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3404-6195C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64641647 | ||||||
chr11:64641760
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3404-6308C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64641760 | ||||||
chr11:64641854
|
G | A | 1 | a0002c0004t0001g0221 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3403+6365C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64641854 | ||||||
chr11:64642239
|
T | C | 1 | a0002c0004t0001g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3403+5980A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64642239 | ||||||
chr11:64642333
|
T | A | 1 | a0001c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3403+5886A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64642333 | ||||||
chr11:64642360
|
G | C | 1 | a0001c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3403+5859C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64642360 | ||||||
chr11:64642466
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3403+5753G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64642466 | ||||||
chr11:64642724
|
G | A | 1 | a0001c0002t0001g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3403+5495C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64642724 | ||||||
chr11:64643179
|
G | A | 1 | a0001c0002t0001g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3403+5040C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643179 | ||||||
chr11:64643356
|
C | G | 1 | a0001c0003t0003g0228 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3403+4863G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643356 | ||||||
chr11:64643362
|
A | AG | 85 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0028others(82): Show | 85 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.3403+4856dupC | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643362 | ||||||
chr11:64643362
|
AG | A | 50 | a0001c0022t0001g0241a0002c0004t0001g0001a0002c0004t0001g0019others(47): Show | 51 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.3403+4856delC | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643362 | ||||||
chr11:64643365
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3403+4854C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643365 | ||||||
chr11:64643365
|
G | C | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3403+4854C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643365 | ||||||
chr11:64643366
|
G | A | 2 | a0002c0004t0001g0121a0002c0004t0001g0211 | 2 | NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.3403+4853C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643366 | ||||||
chr11:64643464
|
G | T | 2 | a0001c0003t0003g0145a0001c0003t0003g0239 | 2 | NA18956.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3403+4755C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643464 | ||||||
chr11:64643465
|
A | T | 2 | a0001c0003t0003g0145a0001c0003t0003g0239 | 2 | NA18956.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3403+4754T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643465 | ||||||
chr11:64643506
|
G | A | 1 | a0009c0012t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3403+4713C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643506 | ||||||
chr11:64643522
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3403+4697A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643522 | ||||||
chr11:64643556
|
GGAGGGAG others(1): Show |
G | 4 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0069others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.3403+4655_3403+466 others(12): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643556 | ||||||
chr11:64643710
|
C | A | 1 | a0002c0005t0002g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3403+4509G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643710 | ||||||
chr11:64643792
|
A | T | 1 | a0001c0002t0001g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3403+4427T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643792 | ||||||
chr11:64643826
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3403+4393A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643826 | ||||||
chr11:64643895
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.3403+4324G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64643895 | ||||||
chr11:64644279
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3403+3940T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644279 | ||||||
chr11:64644293
|
C | T | 11 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0006t0001g0006others(8): Show | 11 | HG01106.hp1 HG01109.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.3403+3926G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644293 | ||||||
chr11:64644437
|
G | A | 1 | a0001c0002t0001g0086 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3403+3782C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644437 | ||||||
chr11:64644490
|
G | C | 5 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(2): Show | 5 | HG02818.hp1 HG03130.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3403+3729C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644490 | ||||||
chr11:64644614
|
G | C | 144 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(141): Show | 146 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.3403+3605C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644614 | ||||||
chr11:64644636
|
C | T | 3 | a0001c0002t0001g0060a0001c0002t0001g0194a0001c0002t0001g0196 | 3 | HG01070.hp1 HG01978.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3403+3583G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644636 | ||||||
chr11:64644734
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3403+3485C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644734 | ||||||
chr11:64644888
|
C | T | 1 | a0001c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3403+3331G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64644888 | ||||||
chr11:64645253
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3403+2966G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645253 | ||||||
chr11:64645267
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3403+2952C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645267 | ||||||
chr11:64645405
|
A | G | 149 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(146): Show | 151 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.3403+2814T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645405 | ||||||
chr11:64645419
|
C | T | 59 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(56): Show | 60 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.3403+2800G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645419 | ||||||
chr11:64645487
|
A | G | 4 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(1): Show | 4 | HG00639.hp1 HG01517.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.3403+2732T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645487 | ||||||
chr11:64645604
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3403+2615A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645604 | ||||||
chr11:64645826
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3403+2393C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645826 | ||||||
chr11:64645846
|
G | T | 1 | a0002c0004t0001g0209 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3403+2373C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645846 | ||||||
chr11:64645954
|
G | C | 1 | a0001c0001t0004g0250 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3403+2265C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64645954 | ||||||
chr11:64646383
|
C | T | 10 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0166others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3403+1836G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64646383 | ||||||
chr11:64646496
|
C | A | 115 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(112): Show | 117 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.3403+1723G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64646496 | ||||||
chr11:64646592
|
TCTTA | T | 126 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(123): Show | 128 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.3403+1623_3403+162 others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64646592 | ||||||
chr11:64646812
|
A | AG | 296 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(293): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.3403+1406dupC | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64646812 | ||||||
chr11:64646848
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3403+1371G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64646848 | ||||||
chr11:64647157
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.3403+1062C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647157 | ||||||
chr11:64647200
|
C | T | 1 | a0002c0004t0001g0221 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3403+1019G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647200 | ||||||
chr11:64647207
|
T | TTG | 44 | a0001c0001t0001g0003a0001c0001t0001g0049a0001c0001t0001g0182others(41): Show | 46 | HG00280.hp1 HG00438.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.3403+1010_3403+101 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647207 | ||||||
chr11:64647207
|
T | TTGTG | 15 | a0001c0002t0005g0055a0002c0004t0001g0117a0002c0004t0001g0119others(12): Show | 15 | HG01346.hp1 HG01346.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.3403+1008_3403+101 others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647207 | ||||||
chr11:64647207
|
TTG | T | 76 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(73): Show | 77 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.3403+1010_3403+101 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647207 | ||||||
chr11:64647207
|
TTGTG | T | 5 | a0001c0003t0003g0153a0002c0005t0002g0219a0002c0005t0002g0220others(2): Show | 5 | HG01243.hp2 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3403+1008_3403+101 others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647207 | ||||||
chr11:64647207
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3403+1000_3403+101 others(16): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647207 | ||||||
chr11:64647424
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3403+795G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647424 | ||||||
chr11:64647574
|
G | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(4): Show | 7 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3403+645C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647574 | ||||||
chr11:64647639
|
C | T | 125 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(122): Show | 127 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.3403+580G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647639 | ||||||
chr11:64647674
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.3403+545C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647674 | ||||||
chr11:64647675
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3403+544C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647675 | ||||||
chr11:64647759
|
A | C | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3403+460T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647759 | ||||||
chr11:64647912
|
G | C | 1 | a0001c0007t0001g0042 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3403+307C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647912 | ||||||
chr11:64647937
|
A | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.3403+282T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 17/22 | chr11 | 64647937 | ||||||
chr11:64648431
|
C | T | 51 | a0001c0022t0001g0241a0002c0004t0001g0001a0002c0004t0001g0019others(48): Show | 52 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.3284-93G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 16/22 | chr11 | 64648431 | ||||||
chr11:64648559
|
C | A | 1 | a0009c0012t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3283+175G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 16/22 | chr11 | 64648559 | ||||||
chr11:64649066
|
C | T | 1 | a0002c0004t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3110-159G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 15/22 | chr11 | 64649066 | ||||||
chr11:64649234
|
A | T | 1 | a0001c0002t0001g0154 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3110-327T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 15/22 | chr11 | 64649234 | ||||||
chr11:64650092
|
C | T | 3 | a0001c0002t0001g0087a0001c0002t0001g0139a0001c0002t0001g0206 | 3 | NA18950.hp2 NA18979.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.3109+356G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 15/22 | chr11 | 64650092 | ||||||
chr11:64650223
|
C | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3109+225G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 15/22 | chr11 | 64650223 | ||||||
chr11:64650276
|
A | C | 3 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0273 | 3 | HG02723.hp2 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3109+172T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 15/22 | chr11 | 64650276 | ||||||
chr11:64650787
|
T | C | 77 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.2919-149A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 14/22 | chr11 | 64650787 | ||||||
chr11:64650833
|
G | A | 126 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(123): Show | 128 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.2919-195C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 14/22 | chr11 | 64650833 | ||||||
chr11:64651122
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2918+133C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 14/22 | chr11 | 64651122 | ||||||
chr11:64651745
|
T | G | 144 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(141): Show | 146 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.2537-109A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 13/22 | chr11 | 64651745 | ||||||
chr11:64651746
|
T | C | 144 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(141): Show | 146 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.2537-110A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 13/22 | chr11 | 64651746 | ||||||
chr11:64651778
|
G | C | 1 | a0001c0002t0001g0085 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2537-142C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 13/22 | chr11 | 64651778 | ||||||
chr11:64652405
|
G | C | 1 | a0001c0001t0012g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2417-251C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64652405 | ||||||
chr11:64652411
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2417-257G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64652411 | ||||||
chr11:64652733
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.2417-579C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64652733 | ||||||
chr11:64652911
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.2417-757A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64652911 | ||||||
chr11:64652931
|
C | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2416+765G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64652931 | ||||||
chr11:64653156
|
C | T | 1 | a0001c0003t0003g0149 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2416+540G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64653156 | ||||||
chr11:64653256
|
T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(293): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.2416+440A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64653256 | ||||||
chr11:64653538
|
C | A | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2416+158G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64653538 | ||||||
chr11:64653580
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.2416+116G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 12/22 | chr11 | 64653580 | ||||||
chr11:64653823
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2390-101C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64653823 | ||||||
chr11:64653873
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2390-151A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64653873 | ||||||
chr11:64653949
|
G | C | 2 | a0001c0002t0001g0197a0001c0002t0001g0285 | 2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2390-227C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64653949 | ||||||
chr11:64654068
|
G | A | 2 | a0001c0007t0007g0013a0002c0004t0001g0167 | 2 | HG01109.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.2390-346C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64654068 | ||||||
chr11:64654494
|
C | G | 2 | a0002c0004t0001g0222a0002c0004t0001g0223 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2390-772G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64654494 | ||||||
chr11:64654506
|
G | A | 1 | a0002c0006t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2390-784C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64654506 | ||||||
chr11:64654579
|
G | A | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2390-857C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64654579 | ||||||
chr11:64654583
|
G | C | 10 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0166others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2390-861C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64654583 | ||||||
chr11:64654712
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2390-990C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64654712 | ||||||
chr11:64655017
|
G | A | 1 | a0001c0002t0001g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2390-1295C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655017 | ||||||
chr11:64655048
|
C | T | 1 | a0002c0004t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2390-1326G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655048 | ||||||
chr11:64655212
|
G | A | 1 | a0001c0002t0001g0288 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2390-1490C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655212 | ||||||
chr11:64655257
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2390-1535C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655257 | ||||||
chr11:64655501
|
G | C | 1 | a0001c0003t0003g0103 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2390-1779C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655501 | ||||||
chr11:64655560
|
G | A | 41 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0065others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.2390-1838C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655560 | ||||||
chr11:64655592
|
T | C | 1 | a0001c0003t0003g0142 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2390-1870A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655592 | ||||||
chr11:64655700
|
C | A | 2 | a0002c0004t0001g0125a0002c0004t0001g0216 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.2390-1978G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655700 | ||||||
chr11:64655703
|
C | G | 1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2390-1981G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64655703 | ||||||
chr11:64656008
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2390-2286C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656008 | ||||||
chr11:64656122
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2390-2400C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656122 | ||||||
chr11:64656132
|
G | C | 1 | a0002c0004t0001g0169 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2390-2410C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656132 | ||||||
chr11:64656133
|
C | G | 1 | a0002c0004t0001g0169 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2390-2411G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656133 | ||||||
chr11:64656359
|
G | A | 115 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(112): Show | 117 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.2390-2637C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656359 | ||||||
chr11:64656370
|
A | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(301): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2390-2648T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656370 | ||||||
chr11:64656384
|
C | CGGGAATT others(11): Show |
141 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(138): Show | 143 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.2390-2680_2390-266 others(22): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656384 | ||||||
chr11:64656385
|
G | A | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2390-2663C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656385 | ||||||
chr11:64656567
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2390-2845G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656567 | ||||||
chr11:64656663
|
C | A | 1 | a0001c0003t0001g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2390-2941G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656663 | ||||||
chr11:64656834
|
G | C | 1 | a0001c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2390-3112C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656834 | ||||||
chr11:64656897
|
G | A | 115 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(112): Show | 117 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.2390-3175C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656897 | ||||||
chr11:64656941
|
T | C | 1 | a0002c0004t0001g0217 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2390-3219A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64656941 | ||||||
chr11:64657219
|
C | A | 77 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.2389+3113G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657219 | ||||||
chr11:64657284
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2389+3048C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657284 | ||||||
chr11:64657495
|
C | A | 11 | a0001c0002t0001g0065a0001c0002t0001g0072a0001c0002t0001g0078others(8): Show | 11 | HG00558.hp2 HG02027.hp2 NA18971.hp2 others(8): Show |
intron_variant | MODIFIER | c.2389+2837G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657495 | ||||||
chr11:64657552
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(66): Show | 70 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.2389+2780G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657552 | ||||||
chr11:64657553
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2389+2779T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657553 | ||||||
chr11:64657562
|
G | A | 1 | a0001c0002t0001g0088 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2389+2770C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657562 | ||||||
chr11:64657648
|
G | T | 123 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(120): Show | 125 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.2389+2684C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657648 | ||||||
chr11:64657687
|
G | A | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2389+2645C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657687 | ||||||
chr11:64657753
|
A | G | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2389+2579T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64657753 | ||||||
chr11:64658173
|
G | A | 145 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(142): Show | 147 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.2389+2159C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658173 | ||||||
chr11:64658381
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2389+1951A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658381 | ||||||
chr11:64658474
|
G | A | 1 | a0001c0002t0001g0085 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2389+1858C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658474 | ||||||
chr11:64658657
|
T | C | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.2389+1675A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658657 | ||||||
chr11:64658778
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2389+1554C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658778 | ||||||
chr11:64658779
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2389+1553G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658779 | ||||||
chr11:64658836
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2389+1496G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658836 | ||||||
chr11:64658885
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2389+1447G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658885 | ||||||
chr11:64658917
|
C | T | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2389+1415G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64658917 | ||||||
chr11:64659270
|
C | G | 1 | a0002c0005t0002g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2389+1062G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64659270 | ||||||
chr11:64659460
|
C | T | 8 | a0001c0003t0002g0140a0001c0003t0002g0233a0001c0003t0002g0234others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2389+872G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64659460 | ||||||
chr11:64659461
|
A | G | 145 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(142): Show | 147 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.2389+871T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64659461 | ||||||
chr11:64659561
|
G | A | 8 | a0001c0003t0002g0140a0001c0003t0002g0233a0001c0003t0002g0234others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2389+771C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64659561 | ||||||
chr11:64659711
|
A | T | 1 | a0001c0003t0002g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2389+621T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64659711 | ||||||
chr11:64660127
|
G | A | 1 | a0002c0004t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2389+205C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64660127 | ||||||
chr11:64660201
|
G | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.2389+131C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 11/22 | chr11 | 64660201 | ||||||
chr11:64661153
|
G | C | 1 | a0006c0021t0003g0136 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1799-14C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64661153 | ||||||
chr11:64661509
|
G | A | 1 | a0001c0002t0001g0093 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1799-370C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64661509 | ||||||
chr11:64661587
|
T | C | 79 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0002t0001g0058others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1799-448A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64661587 | ||||||
chr11:64661595
|
C | T | 1 | a0001c0017t0007g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1799-456G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64661595 | ||||||
chr11:64662090
|
T | TA | 78 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0164others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1799-952dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64662090 | ||||||
chr11:64662191
|
G | C | 1 | a0001c0002t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1799-1052C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64662191 | ||||||
chr11:64662625
|
A | T | 1 | a0001c0001t0004g0262 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1799-1486T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64662625 | ||||||
chr11:64662655
|
G | A | 1 | a0001c0002t0010g0064 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1799-1516C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64662655 | ||||||
chr11:64662789
|
A | T | 146 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(143): Show | 148 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.1799-1650T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64662789 | ||||||
chr11:64662793
|
T | A | 2 | a0001c0002t0001g0195a0001c0002t0001g0205 | 2 | HG02004.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1799-1654A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64662793 | ||||||
chr11:64662848
|
C | T | 3 | a0002c0005t0002g0170a0002c0005t0002g0280a0002c0005t0002g0300 | 3 | HG02922.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1799-1709G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64662848 | ||||||
chr11:64663092
|
G | A | 3 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0168 | 3 | HG02071.hp2 HG02132.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1799-1953C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64663092 | ||||||
chr11:64663109
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(4): Show | 8 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1799-1970G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64663109 | ||||||
chr11:64663312
|
A | G | 1 | a0002c0008t0001g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1799-2173T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64663312 | ||||||
chr11:64663375
|
C | CA | 17 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0049others(14): Show | 17 | HG00597.hp2 HG00673.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1799-2237dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64663375 | ||||||
chr11:64663402
|
A | C | 1 | a0002c0004t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1799-2263T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64663402 | ||||||
chr11:64663560
|
T | A | 1 | a0001c0001t0004g0250 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1799-2421A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64663560 | ||||||
chr11:64664091
|
A | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0080 | 2 | HG00639.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1799-2952T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664091 | ||||||
chr11:64664314
|
T | G | 1 | a0002c0005t0002g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1798+2936A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664314 | ||||||
chr11:64664478
|
C | CA | 139 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(136): Show | 141 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.1798+2771dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664478 | ||||||
chr11:64664478
|
C | CAA | 8 | a0001c0001t0004g0253a0001c0003t0003g0103a0001c0003t0003g0242others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1798+2770_1798+277 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664478 | ||||||
chr11:64664718
|
G | C | 2 | a0001c0002t0001g0197a0001c0002t0001g0285 | 2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1798+2532C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664718 | ||||||
chr11:64664721
|
G | A | 59 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(56): Show | 60 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.1798+2529C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664721 | ||||||
chr11:64664818
|
C | CTATTTTA | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1798+2431_1798+243 others(11): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664818 | ||||||
chr11:64664828
|
A | G | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1798+2422T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664828 | ||||||
chr11:64664840
|
A | T | 1 | a0001c0007t0007g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1798+2410T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664840 | ||||||
chr11:64664969
|
G | A | 2 | a0002c0008t0001g0188a0002c0008t0001g0281 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1798+2281C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664969 | ||||||
chr11:64664971
|
CAG | C | 7 | a0001c0003t0002g0141a0001c0003t0002g0147a0001c0003t0002g0292others(4): Show | 7 | HG00639.hp2 HG00738.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1798+2277_1798+227 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64664971 | ||||||
chr11:64665174
|
G | A | 1 | a0002c0004t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1798+2076C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665174 | ||||||
chr11:64665228
|
C | T | 1 | a0002c0004t0001g0279 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1798+2022G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665228 | ||||||
chr11:64665258
|
C | T | 65 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(62): Show | 66 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.1798+1992G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665258 | ||||||
chr11:64665279
|
CA | C | 10 | a0001c0001t0001g0157a0001c0003t0002g0140a0001c0003t0002g0233others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1798+1970delT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665279 | ||||||
chr11:64665289
|
AAAAG | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1798+1957_1798+196 others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665289 | ||||||
chr11:64665431
|
T | C | 1 | a0001c0017t0007g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1798+1819A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665431 | ||||||
chr11:64665468
|
G | C | 1 | a0002c0004t0001g0279 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1798+1782C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665468 | ||||||
chr11:64665561
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0052 | 2 | NA18960.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1798+1689C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665561 | ||||||
chr11:64665606
|
G | A | 79 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0002t0001g0058others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1798+1644C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665606 | ||||||
chr11:64665923
|
A | T | 1 | a0001c0007t0001g0042 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1798+1327T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665923 | ||||||
chr11:64665962
|
C | T | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1798+1288G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665962 | ||||||
chr11:64665972
|
T | C | 145 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(142): Show | 147 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.1798+1278A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64665972 | ||||||
chr11:64666204
|
A | AT | 21 | a0001c0001t0004g0160a0001c0001t0004g0165a0001c0001t0004g0250others(18): Show | 21 | HG00738.hp1 HG01106.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1798+1045dupA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64666204 | ||||||
chr11:64666204
|
AT | A | 115 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(112): Show | 117 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.1798+1045delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64666204 | ||||||
chr11:64666584
|
G | A | 1 | a0001c0017t0007g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1798+666C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64666584 | ||||||
chr11:64666603
|
G | A | 1 | a0001c0007t0001g0044 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1798+647C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64666603 | ||||||
chr11:64666679
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(60): Show | 63 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1798+571A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64666679 | ||||||
chr11:64667057
|
T | C | 1 | a0001c0023t0001g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1798+193A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 9/22 | chr11 | 64667057 | ||||||
chr11:64667876
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1360-188G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 8/22 | chr11 | 64667876 | ||||||
chr11:64667884
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1360-196C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 8/22 | chr11 | 64667884 | ||||||
chr11:64667895
|
T | TGTCTTCT others(5): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1360-208_1360-207i others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 8/22 | chr11 | 64667895 | ||||||
chr11:64667911
|
A | G | 2 | a0001c0003t0005g0105a0001c0003t0005g0203 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1360-223T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 8/22 | chr11 | 64667911 | ||||||
chr11:64668425
|
C | T | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1359+18G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 8/22 | chr11 | 64668425 | ||||||
chr11:64668434
|
C | T | 27 | a0001c0003t0003g0103a0001c0003t0003g0142a0001c0003t0003g0145others(24): Show | 28 | HG00609.hp2 HG00673.hp2 HG01978.hp1 others(25): Show |
intron_variant | MODIFIER | c.1359+9G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 8/22 | chr11 | 64668434 | ||||||
chr11:64668641
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1198-37G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64668641 | ||||||
chr11:64668671
|
C | T | 2 | a0002c0004t0001g0222a0002c0004t0001g0223 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1198-67G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64668671 | ||||||
chr11:64668960
|
C | A | 1 | a0001c0002t0001g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1198-356G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64668960 | ||||||
chr11:64669013
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1198-409A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669013 | ||||||
chr11:64669121
|
A | G | 19 | a0001c0001t0001g0248a0001c0001t0004g0012a0001c0001t0004g0160others(16): Show | 19 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1198-517T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669121 | ||||||
chr11:64669420
|
G | C | 1 | a0001c0002t0001g0102 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1198-816C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669420 | ||||||
chr11:64669492
|
C | A | 1 | a0002c0004t0011g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1198-888G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669492 | ||||||
chr11:64669590
|
C | G | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1198-986G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669590 | ||||||
chr11:64669678
|
C | G | 1 | a0001c0001t0001g0045 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1198-1074G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669678 | ||||||
chr11:64669718
|
C | T | 1 | a0001c0001t0004g0261 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1198-1114G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669718 | ||||||
chr11:64669762
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1198-1158G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669762 | ||||||
chr11:64669903
|
C | T | 21 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0001t0004g0012others(18): Show | 21 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1198-1299G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64669903 | ||||||
chr11:64670018
|
T | C | 80 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0002t0001g0058others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1198-1414A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64670018 | ||||||
chr11:64670020
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1198-1416C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64670020 | ||||||
chr11:64670195
|
G | A | 1 | a0001c0003t0006g0302 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1198-1591C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64670195 | ||||||
chr11:64670242
|
A | C | 50 | a0002c0004t0001g0001a0002c0004t0001g0019a0002c0004t0001g0020others(47): Show | 51 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1198-1638T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64670242 | ||||||
chr11:64670572
|
C | T | 1 | a0002c0004t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1198-1968G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64670572 | ||||||
chr11:64670695
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1198-2091T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64670695 | ||||||
chr11:64670815
|
C | T | 3 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0203 | 3 | HG03927.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1198-2211G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64670815 | ||||||
chr11:64671145
|
C | T | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1198-2541G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671145 | ||||||
chr11:64671183
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1198-2579C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671183 | ||||||
chr11:64671239
|
C | A | 7 | a0001c0003t0002g0141a0001c0003t0002g0147a0001c0003t0002g0292others(4): Show | 7 | HG00639.hp2 HG00738.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1198-2635G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671239 | ||||||
chr11:64671272
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1198-2668G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671272 | ||||||
chr11:64671507
|
G | A | 1 | a0002c0004t0001g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1198-2903C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671507 | ||||||
chr11:64671531
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1198-2927C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671531 | ||||||
chr11:64671670
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1198-3066C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671670 | ||||||
chr11:64671755
|
G | T | 77 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1198-3151C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64671755 | ||||||
chr11:64672178
|
G | C | 1 | a0001c0001t0004g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1198-3574C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64672178 | ||||||
chr11:64672290
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1198-3686C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64672290 | ||||||
chr11:64672327
|
T | C | 34 | a0001c0003t0001g0144a0001c0003t0003g0103a0001c0003t0003g0142others(31): Show | 35 | HG00609.hp2 HG00673.hp2 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.1198-3723A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64672327 | ||||||
chr11:64672344
|
T | C | 145 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(142): Show | 147 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.1198-3740A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64672344 | ||||||
chr11:64672727
|
AG | A | 50 | a0002c0004t0001g0001a0002c0004t0001g0019a0002c0004t0001g0110others(47): Show | 51 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1198-4124delC | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64672727 | ||||||
chr11:64672779
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1198-4175C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64672779 | ||||||
chr11:64672906
|
G | A | 1 | a0001c0003t0003g0237 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1197+4087C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64672906 | ||||||
chr11:64673020
|
G | A | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1197+3973C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64673020 | ||||||
chr11:64673045
|
T | C | 4 | a0002c0005t0002g0219a0002c0005t0002g0220a0002c0005t0002g0277others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+3948A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64673045 | ||||||
chr11:64673090
|
C | T | 2 | a0001c0003t0002g0141a0001c0003t0002g0292 | 2 | HG00738.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1197+3903G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64673090 | ||||||
chr11:64673445
|
G | A | 1 | a0002c0004t0001g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1197+3548C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64673445 | ||||||
chr11:64673448
|
T | C | 79 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0002t0001g0058others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1197+3545A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64673448 | ||||||
chr11:64673688
|
T | TTG | 80 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0002t0001g0058others(77): Show | 80 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.1197+3303_1197+330 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64673688 | ||||||
chr11:64674006
|
C | A | 2 | a0001c0001t0004g0252a0001c0001t0004g0257 | 2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1197+2987G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674006 | ||||||
chr11:64674021
|
C | A | 1 | a0002c0013t0001g0191 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1197+2972G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674021 | ||||||
chr11:64674038
|
C | CA | 33 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0045others(30): Show | 33 | HG00597.hp2 HG01175.hp2 HG01978.hp1 others(30): Show |
intron_variant | MODIFIER | c.1197+2954dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674038 | ||||||
chr11:64674384
|
T | G | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1197+2609A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674384 | ||||||
chr11:64674397
|
G | C | 47 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(44): Show | 48 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1197+2596C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674397 | ||||||
chr11:64674491
|
T | C | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1197+2502A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674491 | ||||||
chr11:64674900
|
C | T | 294 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(291): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.1197+2093G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674900 | ||||||
chr11:64674926
|
T | C | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1197+2067A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64674926 | ||||||
chr11:64675026
|
TC | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+1966delG | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675026 | ||||||
chr11:64675069
|
C | T | 2 | a0001c0002t0001g0286a0001c0003t0002g0234 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1197+1924G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675069 | ||||||
chr11:64675110
|
A | G | 3 | a0002c0005t0002g0170a0002c0005t0002g0280a0002c0005t0002g0300 | 3 | HG02922.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1197+1883T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675110 | ||||||
chr11:64675113
|
G | A | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1197+1880C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675113 | ||||||
chr11:64675327
|
T | C | 1 | a0002c0004t0001g0214 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1197+1666A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675327 | ||||||
chr11:64675657
|
G | A | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1197+1336C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675657 | ||||||
chr11:64675875
|
C | T | 4 | a0001c0003t0001g0144a0001c0003t0003g0143a0001c0003t0003g0242others(1): Show | 4 | NA18747.hp2 NA18947.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+1118G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675875 | ||||||
chr11:64675993
|
T | C | 145 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(142): Show | 147 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(144): Show |
intron_variant | MODIFIER | c.1197+1000A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64675993 | ||||||
chr11:64676067
|
C | T | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1197+926G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64676067 | ||||||
chr11:64676126
|
G | A | 2 | a0002c0004t0001g0222a0002c0004t0001g0223 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1197+867C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64676126 | ||||||
chr11:64676368
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1197+625A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64676368 | ||||||
chr11:64676374
|
G | A | 1 | a0002c0004t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1197+619C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64676374 | ||||||
chr11:64676643
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1197+350G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 7/22 | chr11 | 64676643 | ||||||
chr11:64677179
|
T | C | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1153-142A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64677179 | ||||||
chr11:64677494
|
G | A | 4 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(1): Show | 4 | HG00597.hp1 HG00621.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-457C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64677494 | ||||||
chr11:64677517
|
C | T | 1 | a0002c0004t0001g0167 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1153-480G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64677517 | ||||||
chr11:64677566
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1153-529C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64677566 | ||||||
chr11:64677765
|
T | C | 10 | a0001c0003t0003g0103a0001c0003t0003g0145a0001c0003t0003g0148others(7): Show | 10 | HG00609.hp2 HG02083.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.1153-728A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64677765 | ||||||
chr11:64677934
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1153-897C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64677934 | ||||||
chr11:64678019
|
G | A | 4 | a0002c0005t0002g0170a0002c0005t0002g0274a0002c0005t0002g0280others(1): Show | 4 | HG02922.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-982C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678019 | ||||||
chr11:64678210
|
C | A | 1 | a0001c0003t0001g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1153-1173G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678210 | ||||||
chr11:64678307
|
T | C | 4 | a0001c0003t0002g0147a0001c0003t0002g0294a0001c0003t0002g0295others(1): Show | 4 | HG01168.hp2 HG01257.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-1270A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678307 | ||||||
chr11:64678345
|
C | T | 1 | a0002c0015t0002g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1153-1308G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678345 | ||||||
chr11:64678656
|
G | T | 1 | a0001c0002t0001g0075 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1153-1619C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678656 | ||||||
chr11:64678773
|
T | C | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1153-1736A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678773 | ||||||
chr11:64678790
|
G | A | 1 | a0001c0001t0004g0256 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1153-1753C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678790 | ||||||
chr11:64678844
|
G | A | 1 | a0001c0003t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1153-1807C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64678844 | ||||||
chr11:64679513
|
C | A | 19 | a0001c0001t0001g0270a0001c0001t0004g0012a0001c0001t0004g0160others(16): Show | 19 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1153-2476G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64679513 | ||||||
chr11:64679554
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(60): Show | 63 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1153-2517C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64679554 | ||||||
chr11:64679595
|
C | A | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1153-2558G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64679595 | ||||||
chr11:64679718
|
A | G | 3 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260 | 3 | HG02976.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1153-2681T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64679718 | ||||||
chr11:64679850
|
A | G | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1153-2813T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64679850 | ||||||
chr11:64679881
|
C | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(301): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1153-2844G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64679881 | ||||||
chr11:64679948
|
G | A | 19 | a0001c0001t0001g0270a0001c0001t0004g0012a0001c0001t0004g0160others(16): Show | 19 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1153-2911C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64679948 | ||||||
chr11:64680033
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1153-2996C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64680033 | ||||||
chr11:64680335
|
A | G | 4 | a0002c0005t0002g0219a0002c0005t0002g0220a0002c0005t0002g0277others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-3298T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64680335 | ||||||
chr11:64680722
|
T | C | 9 | a0001c0002t0001g0060a0001c0002t0001g0062a0001c0002t0001g0063others(6): Show | 9 | HG01070.hp1 HG01074.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1153-3685A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64680722 | ||||||
chr11:64680777
|
C | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1153-3740G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64680777 | ||||||
chr11:64680802
|
T | C | 1 | a0001c0003t0003g0235 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1153-3765A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64680802 | ||||||
chr11:64680951
|
G | T | 1 | a0001c0003t0002g0290 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1153-3914C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64680951 | ||||||
chr11:64681018
|
AC | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG01109.hp1 HG01109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1153-3982delG | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681018 | ||||||
chr11:64681116
|
TA | T | 24 | a0001c0001t0001g0054a0001c0001t0001g0190a0001c0001t0001g0270others(21): Show | 24 | HG01168.hp2 HG02015.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1153-4080delT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681116 | ||||||
chr11:64681229
|
G | A | 1 | a0001c0003t0002g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153-4192C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681229 | ||||||
chr11:64681503
|
G | T | 4 | a0002c0005t0002g0219a0002c0005t0002g0220a0002c0005t0002g0277others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+4143C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681503 | ||||||
chr11:64681564
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1152+4082A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681564 | ||||||
chr11:64681751
|
G | A | 51 | a0002c0004t0001g0001a0002c0004t0001g0019a0002c0004t0001g0020others(48): Show | 52 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1152+3895C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681751 | ||||||
chr11:64681813
|
T | TGGCAC | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1152+3832_1152+383 others(9): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681813 | ||||||
chr11:64681835
|
C | T | 76 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1152+3811G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681835 | ||||||
chr11:64681881
|
G | C | 1 | a0001c0001t0001g0271 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1152+3765C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681881 | ||||||
chr11:64681893
|
A | G | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3753T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681893 | ||||||
chr11:64681953
|
G | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(127): Show | 132 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.1152+3693C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681953 | ||||||
chr11:64681980
|
C | A | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3666G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681980 | ||||||
chr11:64681982
|
A | G | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3664T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64681982 | ||||||
chr11:64682070
|
C | G | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3576G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682070 | ||||||
chr11:64682071
|
T | G | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3575A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682071 | ||||||
chr11:64682102
|
T | A | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3544A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682102 | ||||||
chr11:64682108
|
C | T | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3538G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682108 | ||||||
chr11:64682120
|
A | T | 8 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0166others(5): Show | 8 | HG00609.hp1 HG02056.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1152+3526T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682120 | ||||||
chr11:64682127
|
T | C | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3519A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682127 | ||||||
chr11:64682136
|
T | C | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3510A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682136 | ||||||
chr11:64682142
|
C | T | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3504G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682142 | ||||||
chr11:64682143
|
T | C | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3503A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682143 | ||||||
chr11:64682158
|
C | T | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3488G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682158 | ||||||
chr11:64682166
|
C | T | 1 | a0005c0016t0003g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1152+3480G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682166 | ||||||
chr11:64682217
|
G | A | 1 | a0002c0006t0001g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1152+3429C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682217 | ||||||
chr11:64682218
|
C | A | 1 | a0002c0006t0001g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1152+3428G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682218 | ||||||
chr11:64682459
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1152+3187C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682459 | ||||||
chr11:64682466
|
ACATCTTT others(24): Show |
A | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1152+3149_1152+317 others(35): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682466 | ||||||
chr11:64682492
|
G | A | 1 | a0008c0026t0003g0244 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1152+3154C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682492 | ||||||
chr11:64682826
|
T | C | 298 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(295): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1152+2820A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682826 | ||||||
chr11:64682838
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1152+2808G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682838 | ||||||
chr11:64682876
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0175a0001c0001t0001g0248 | 3 | HG00438.hp1 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1152+2770C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64682876 | ||||||
chr11:64683007
|
C | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(67): Show | 71 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1152+2639G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683007 | ||||||
chr11:64683094
|
T | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(60): Show | 63 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1152+2552A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683094 | ||||||
chr11:64683174
|
A | G | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 151 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.1152+2472T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683174 | ||||||
chr11:64683187
|
T | C | 2 | a0002c0004t0001g0222a0002c0004t0001g0223 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1152+2459A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683187 | ||||||
chr11:64683307
|
T | C | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1152+2339A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683307 | ||||||
chr11:64683323
|
C | T | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 151 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.1152+2323G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683323 | ||||||
chr11:64683489
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(67): Show | 71 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1152+2157C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683489 | ||||||
chr11:64683512
|
C | T | 1 | a0001c0002t0005g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1152+2134G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683512 | ||||||
chr11:64683514
|
G | C | 2 | a0001c0001t0008g0026a0001c0001t0008g0173 | 2 | HG00735.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1152+2132C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683514 | ||||||
chr11:64683569
|
G | A | 3 | a0001c0002t0001g0067a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG00735.hp2 HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1152+2077C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683569 | ||||||
chr11:64683576
|
C | T | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1152+2070G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683576 | ||||||
chr11:64683614
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1152+2032G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683614 | ||||||
chr11:64683615
|
A | G | 298 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(295): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1152+2031T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683615 | ||||||
chr11:64683619
|
C | CA | 8 | a0001c0001t0001g0031a0001c0001t0001g0186a0001c0002t0001g0137others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1152+2026dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683619 | ||||||
chr11:64683619
|
CA | C | 35 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(32): Show | 35 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1152+2026delT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683619 | ||||||
chr11:64683809
|
C | G | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1152+1837G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64683809 | ||||||
chr11:64684199
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1152+1447G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64684199 | ||||||
chr11:64684222
|
T | C | 1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1152+1424A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64684222 | ||||||
chr11:64684746
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1152+900G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64684746 | ||||||
chr11:64684844
|
G | A | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1152+802C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64684844 | ||||||
chr11:64684850
|
C | G | 8 | a0001c0001t0004g0165a0001c0001t0004g0252a0001c0001t0004g0257others(5): Show | 8 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1152+796G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64684850 | ||||||
chr11:64685247
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1152+399G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64685247 | ||||||
chr11:64685359
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1152+287T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64685359 | ||||||
chr11:64685371
|
C | A | 1 | a0001c0003t0002g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1152+275G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64685371 | ||||||
chr11:64685534
|
C | T | 1 | a0001c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1152+112G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 6/22 | chr11 | 64685534 | ||||||
chr11:64686146
|
G | T | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.851-199C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686146 | ||||||
chr11:64686282
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.851-335C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686282 | ||||||
chr11:64686289
|
C | T | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.851-342G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686289 | ||||||
chr11:64686357
|
G | A | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.851-410C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686357 | ||||||
chr11:64686385
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.851-438G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686385 | ||||||
chr11:64686587
|
C | T | 2 | a0002c0005t0002g0219a0002c0005t0002g0220 | 2 | HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.851-640G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686587 | ||||||
chr11:64686624
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.851-677A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686624 | ||||||
chr11:64686679
|
C | T | 1 | a0001c0003t0002g0232 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.851-732G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686679 | ||||||
chr11:64686883
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.851-936T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686883 | ||||||
chr11:64686904
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.851-957C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64686904 | ||||||
chr11:64687261
|
G | C | 1 | a0002c0005t0002g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.851-1314C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64687261 | ||||||
chr11:64687372
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.851-1425G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64687372 | ||||||
chr11:64687385
|
A | G | 1 | a0001c0002t0001g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.851-1438T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64687385 | ||||||
chr11:64687733
|
G | T | 1 | a0001c0002t0001g0287 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.851-1786C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64687733 | ||||||
chr11:64688079
|
A | C | 12 | a0001c0002t0001g0065a0001c0002t0001g0072a0001c0002t0001g0078others(9): Show | 12 | HG00558.hp2 HG02027.hp2 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.851-2132T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688079 | ||||||
chr11:64688118
|
C | CAA | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 150 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.851-2173_851-2172d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688118 | ||||||
chr11:64688210
|
A | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(3): Show | 6 | HG01109.hp1 HG01109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+2195T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688210 | ||||||
chr11:64688341
|
C | A | 3 | a0001c0003t0002g0230a0001c0003t0002g0231a0001c0003t0002g0232 | 3 | NA18945.hp2 NA19056.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.850+2064G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688341 | ||||||
chr11:64688454
|
C | T | 6 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0156others(3): Show | 6 | NA18944.hp1 NA18954.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.850+1951G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688454 | ||||||
chr11:64688509
|
G | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG00621.hp1 HG02165.hp2 NA18963.hp1 others(8): Show |
intron_variant | MODIFIER | c.850+1896C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688509 | ||||||
chr11:64688529
|
G | C | 1 | a0001c0003t0003g0242 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.850+1876C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688529 | ||||||
chr11:64688627
|
C | T | 74 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.850+1778G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688627 | ||||||
chr11:64688676
|
G | A | 2 | a0001c0002t0001g0068a0001c0002t0001g0070 | 2 | HG01257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.850+1729C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688676 | ||||||
chr11:64688757
|
C | G | 3 | a0001c0003t0005g0105a0001c0003t0005g0106a0001c0003t0005g0203 | 3 | HG03927.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.850+1648G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688757 | ||||||
chr11:64688768
|
G | C | 74 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.850+1637C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688768 | ||||||
chr11:64688885
|
C | A | 10 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0166others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+1520G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64688885 | ||||||
chr11:64689021
|
CTTCGCTG others(7): Show |
C | 1 | a0001c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.850+1370_850+1383d others(16): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64689021 | ||||||
chr11:64689243
|
AT | A | 50 | a0001c0003t0003g0143a0002c0004t0001g0001a0002c0004t0001g0019others(47): Show | 51 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.850+1161delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64689243 | ||||||
chr11:64689269
|
C | T | 1 | a0002c0004t0001g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.850+1136G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64689269 | ||||||
chr11:64689514
|
C | T | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.850+891G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64689514 | ||||||
chr11:64689710
|
A | G | 1 | a0001c0003t0002g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.850+695T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64689710 | ||||||
chr11:64689799
|
C | T | 1 | a0002c0004t0001g0121 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.850+606G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64689799 | ||||||
chr11:64689949
|
A | G | 1 | a0002c0004t0001g0169 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.850+456T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64689949 | ||||||
chr11:64690262
|
C | T | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.850+143G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64690262 | ||||||
chr11:64690337
|
C | G | 2 | a0002c0004t0001g0121a0002c0004t0001g0211 | 2 | NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.850+68G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 5/22 | chr11 | 64690337 | ||||||
chr11:64690579
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.779-103C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64690579 | ||||||
chr11:64690664
|
G | C | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.779-188C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64690664 | ||||||
chr11:64690887
|
A | C | 1 | a0002c0004t0001g0214 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.779-411T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64690887 | ||||||
chr11:64690957
|
C | T | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.779-481G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64690957 | ||||||
chr11:64691247
|
G | A | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.779-771C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64691247 | ||||||
chr11:64691805
|
C | T | 1 | a0002c0005t0002g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.778+1042G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64691805 | ||||||
chr11:64691922
|
G | A | 1 | a0001c0003t0001g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.778+925C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64691922 | ||||||
chr11:64691934
|
C | T | 41 | a0002c0004t0001g0001a0002c0004t0001g0110a0002c0004t0001g0111others(38): Show | 42 | HG00280.hp1 HG00438.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.778+913G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64691934 | ||||||
chr11:64692281
|
C | G | 1 | a0001c0002t0001g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.778+566G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64692281 | ||||||
chr11:64692447
|
A | C | 4 | a0002c0005t0002g0219a0002c0005t0002g0220a0002c0005t0002g0277others(1): Show | 4 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+400T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64692447 | ||||||
chr11:64692675
|
C | G | 1 | a0002c0006t0001g0162 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.778+172G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 4/22 | chr11 | 64692675 | ||||||
chr11:64692894
|
G | A | 1 | a0001c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.749-18C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64692894 | ||||||
chr11:64693049
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.749-173C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64693049 | ||||||
chr11:64693107
|
G | A | 1 | a0002c0004t0001g0221 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.749-231C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64693107 | ||||||
chr11:64693200
|
A | G | 297 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(294): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.749-324T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64693200 | ||||||
chr11:64693247
|
G | GA | 8 | a0001c0003t0002g0140a0001c0003t0002g0233a0001c0003t0002g0234others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.749-372dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64693247 | ||||||
chr11:64693495
|
C | A | 2 | a0002c0004t0001g0125a0002c0004t0001g0216 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.749-619G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64693495 | ||||||
chr11:64694125
|
C | T | 1 | a0002c0006t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.749-1249G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694125 | ||||||
chr11:64694253
|
T | G | 1 | a0007c0025t0001g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.749-1377A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694253 | ||||||
chr11:64694293
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.749-1417C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694293 | ||||||
chr11:64694482
|
T | G | 1 | a0001c0003t0003g0237 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.749-1606A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694482 | ||||||
chr11:64694501
|
C | G | 39 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0065others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.749-1625G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694501 | ||||||
chr11:64694772
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.749-1896G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694772 | ||||||
chr11:64694779
|
C | T | 1 | a0001c0003t0002g0226 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.749-1903G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694779 | ||||||
chr11:64694797
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.749-1921C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694797 | ||||||
chr11:64694989
|
G | A | 11 | a0001c0001t0004g0165a0001c0001t0004g0252a0001c0001t0004g0254others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.749-2113C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64694989 | ||||||
chr11:64695010
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.749-2134G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695010 | ||||||
chr11:64695011
|
G | A | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.749-2135C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695011 | ||||||
chr11:64695475
|
GAGGGCTG others(1): Show |
G | 8 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(5): Show | 8 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.748+2292_748+2299d others(10): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695475 | ||||||
chr11:64695676
|
G | GTCTCAGA others(39): Show |
1 | a0001c0001t0004g0251 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.748+2053_748+2098d others(48): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695676 | ||||||
chr11:64695730
|
G | GCA | 4 | a0001c0002t0001g0193a0001c0002t0001g0198a0001c0002t0005g0055others(1): Show | 4 | HG01261.hp1 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+2043_748+2044d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695730 | ||||||
chr11:64695754
|
A | G | 2 | a0001c0002t0001g0074a0001c0002t0001g0138 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.748+2021T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695754 | ||||||
chr11:64695765
|
T | C | 17 | a0001c0001t0004g0012a0001c0001t0004g0165a0001c0001t0004g0250others(14): Show | 17 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.748+2010A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695765 | ||||||
chr11:64695924
|
T | G | 1 | a0001c0003t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.748+1851A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695924 | ||||||
chr11:64695927
|
T | G | 5 | a0001c0003t0001g0144a0001c0003t0003g0143a0001c0003t0003g0150others(2): Show | 5 | NA18747.hp2 NA18947.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+1848A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64695927 | ||||||
chr11:64696013
|
C | A | 1 | a0001c0002t0001g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.748+1762G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696013 | ||||||
chr11:64696036
|
T | C | 1 | a0002c0004t0001g0155 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.748+1739A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696036 | ||||||
chr11:64696062
|
CT | C | 65 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(62): Show | 66 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.748+1712delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696062 | ||||||
chr11:64696385
|
C | T | 1 | a0001c0007t0007g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.748+1390G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696385 | ||||||
chr11:64696528
|
T | TAC | 122 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0031others(119): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.748+1245_748+1246d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
T | TACAC | 36 | a0001c0002t0001g0072a0001c0002t0001g0076a0001c0002t0001g0078others(33): Show | 36 | HG00558.hp2 HG00735.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.748+1243_748+1246d others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
T | TACACAC | 4 | a0001c0002t0001g0065a0001c0002t0001g0087a0001c0002t0001g0093others(1): Show | 4 | NA18950.hp1 NA18979.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+1241_748+1246d others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
T | TACACACA others(1): Show |
25 | a0001c0007t0007g0013a0002c0004t0001g0020a0002c0004t0001g0111others(22): Show | 25 | HG00438.hp2 HG00609.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.748+1239_748+1246d others(10): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
T | TACACACA others(3): Show |
18 | a0002c0004t0001g0001a0002c0004t0001g0110a0002c0004t0001g0113others(15): Show | 19 | HG00280.hp1 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.748+1237_748+1246d others(12): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
T | TACACACA others(5): Show |
8 | a0002c0004t0001g0119a0002c0004t0001g0156a0002c0004t0001g0221others(5): Show | 8 | HG03654.hp1 HG03669.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.748+1235_748+1246d others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
T | TACACACA others(7): Show |
6 | a0002c0004t0001g0117a0002c0004t0001g0121a0002c0004t0001g0128others(3): Show | 6 | HG01123.hp1 NA18954.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.748+1233_748+1246d others(16): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
T | TACACACA others(9): Show |
1 | a0002c0004t0001g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.748+1231_748+1246d others(18): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
TACAC | T | 17 | a0001c0001t0004g0012a0001c0001t0004g0165a0001c0001t0004g0250others(14): Show | 17 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.748+1243_748+1246d others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696528
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.748+1235_748+1246d others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696528 | ||||||
chr11:64696589
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG01496.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.748+1186C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696589 | ||||||
chr11:64696613
|
T | A | 75 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.748+1162A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64696613 | ||||||
chr11:64697005
|
G | A | 1 | a0001c0001t0004g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.748+770C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64697005 | ||||||
chr11:64697028
|
G | A | 1 | a0001c0007t0007g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.748+747C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64697028 | ||||||
chr11:64697658
|
C | T | 2 | a0001c0001t0001g0267a0001c0019t0001g0263 | 2 | NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.748+117G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64697658 | ||||||
chr11:64697714
|
C | T | 2 | a0001c0003t0002g0140a0001c0003t0002g0289 | 2 | HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.748+61G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 3/22 | chr11 | 64697714 | ||||||
chr11:64697803
|
C | T | 1 | a0001c0002t0013g0061 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.731-11G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64697803 | ||||||
chr11:64697810
|
C | T | 2 | a0001c0002t0001g0068a0001c0002t0001g0070 | 2 | HG01257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.731-18G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64697810 | ||||||
chr11:64697880
|
AAGGGGAG others(5): Show |
A | 1 | a0001c0003t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.731-100_731-89delC others(11): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64697880 | ||||||
chr11:64697931
|
T | C | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 150 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.731-139A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64697931 | ||||||
chr11:64698042
|
C | T | 64 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(61): Show | 64 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.731-250G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64698042 | ||||||
chr11:64698136
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-344G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64698136 | ||||||
chr11:64698253
|
T | C | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.731-461A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64698253 | ||||||
chr11:64698301
|
C | T | 1 | a0001c0003t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.731-509G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64698301 | ||||||
chr11:64698307
|
G | A | 1 | a0001c0003t0002g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.731-515C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64698307 | ||||||
chr11:64698389
|
A | C | 1 | a0002c0005t0002g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.731-597T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64698389 | ||||||
chr11:64698887
|
G | A | 1 | a0001c0018t0001g0047 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.731-1095C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64698887 | ||||||
chr11:64699007
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.731-1215G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699007 | ||||||
chr11:64699070
|
T | G | 25 | a0002c0004t0001g0001a0002c0004t0001g0110a0002c0004t0001g0113others(22): Show | 26 | HG00280.hp1 HG00438.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.731-1278A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699070 | ||||||
chr11:64699425
|
C | CTT | 13 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0179others(10): Show | 13 | HG00609.hp2 HG01109.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.731-1635_731-1634d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699425 | ||||||
chr11:64699425
|
C | CTTT | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.731-1636_731-1634d others(5): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699425 | ||||||
chr11:64699425
|
C | CTTTT | 71 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0053others(68): Show | 72 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.731-1637_731-1634d others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699425 | ||||||
chr11:64699425
|
C | CTTTTT | 10 | a0001c0001t0001g0032a0001c0001t0004g0251a0001c0001t0004g0252others(7): Show | 10 | HG01175.hp1 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.731-1638_731-1634d others(7): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699425 | ||||||
chr11:64699425
|
CT | C | 6 | a0001c0001t0001g0264a0001c0001t0001g0266a0001c0001t0001g0267others(3): Show | 6 | HG02630.hp2 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1634delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699425 | ||||||
chr11:64699573
|
C | T | 3 | a0001c0007t0007g0013a0001c0017t0007g0189a0002c0011t0007g0014 | 3 | HG01109.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.731-1781G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699573 | ||||||
chr11:64699930
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.731-2138T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64699930 | ||||||
chr11:64700187
|
G | A | 1 | a0001c0003t0003g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.731-2395C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700187 | ||||||
chr11:64700218
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.731-2426G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700218 | ||||||
chr11:64700325
|
G | A | 4 | a0002c0004t0001g0166a0002c0004t0001g0167a0002c0004t0001g0169others(1): Show | 4 | HG00609.hp1 HG02083.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-2533C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700325 | ||||||
chr11:64700432
|
T | C | 5 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0253others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-2640A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700432 | ||||||
chr11:64700570
|
G | A | 1 | a0002c0006t0001g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.731-2778C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700570 | ||||||
chr11:64700646
|
G | C | 1 | a0001c0002t0001g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.731-2854C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700646 | ||||||
chr11:64700700
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.731-2908G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700700 | ||||||
chr11:64700789
|
C | T | 3 | a0002c0004t0001g0110a0002c0004t0001g0113a0002c0004t0001g0114 | 3 | HG00280.hp1 HG01175.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.731-2997G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700789 | ||||||
chr11:64700961
|
C | T | 1 | a0001c0002t0001g0088 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.731-3169G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64700961 | ||||||
chr11:64701767
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.731-3975C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701767 | ||||||
chr11:64701776
|
G | C | 4 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(1): Show | 4 | HG02818.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-3984C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701776 | ||||||
chr11:64701779
|
G | A | 7 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0008others(4): Show | 7 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.731-3987C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701779 | ||||||
chr11:64701838
|
G | A | 1 | a0001c0002t0001g0091 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.731-4046C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701838 | ||||||
chr11:64701886
|
C | G | 1 | a0002c0004t0001g0279 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.731-4094G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701886 | ||||||
chr11:64701887
|
TGTCCGGG others(43): Show |
T | 1 | a0001c0002t0001g0067 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.731-4145_731-4096d others(52): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701887 | ||||||
chr11:64701902
|
TG | T | 147 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(144): Show | 149 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.731-4111delC | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701902 | ||||||
chr11:64701912
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.731-4120G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701912 | ||||||
chr11:64701921
|
G | A | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.731-4129C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701921 | ||||||
chr11:64701942
|
AGGAGGGA others(42): Show |
A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.731-4199_731-4151d others(51): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701942 | ||||||
chr11:64701956
|
G | C | 1 | a0009c0012t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.731-4164C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701956 | ||||||
chr11:64701981
|
T | C | 1 | a0001c0002t0001g0085 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.731-4189A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64701981 | ||||||
chr11:64702052
|
G | A | 124 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(121): Show | 126 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.731-4260C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702052 | ||||||
chr11:64702065
|
TGCCGCCC others(168): Show |
T | 1 | a0002c0004t0001g0208 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.731-4448_731-4274d others(2): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702065 | ||||||
chr11:64702102
|
G | A | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.731-4310C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702102 | ||||||
chr11:64702166
|
C | T | 18 | a0001c0001t0004g0012a0001c0001t0004g0160a0001c0001t0004g0165others(15): Show | 18 | HG02055.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.731-4374G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702166 | ||||||
chr11:64702194
|
C | T | 4 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(1): Show | 4 | HG02818.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-4402G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702194 | ||||||
chr11:64702215
|
C | T | 2 | a0001c0002t0001g0076a0001c0002t0001g0077 | 2 | HG00735.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.731-4423G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702215 | ||||||
chr11:64702239
|
C | T | 2 | a0002c0004t0001g0110a0002c0004t0001g0114 | 2 | HG01175.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.731-4447G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702239 | ||||||
chr11:64702433
|
A | G | 1 | a0002c0004t0001g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.731-4641T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702433 | ||||||
chr11:64702519
|
T | G | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.731-4727A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702519 | ||||||
chr11:64702627
|
C | A | 1 | a0001c0024t0001g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.731-4835G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702627 | ||||||
chr11:64702774
|
G | A | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.731-4982C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702774 | ||||||
chr11:64702790
|
T | C | 1 | a0002c0013t0001g0191 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.731-4998A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702790 | ||||||
chr11:64702814
|
A | G | 1 | a0001c0003t0003g0236 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.731-5022T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702814 | ||||||
chr11:64702824
|
A | T | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.731-5032T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702824 | ||||||
chr11:64702971
|
T | TA | 12 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0004g0252others(9): Show | 12 | HG00621.hp1 HG02055.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.731-5180dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702971 | ||||||
chr11:64702971
|
TA | T | 17 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0158others(14): Show | 17 | HG01070.hp1 HG01168.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.731-5180delT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64702971 | ||||||
chr11:64703897
|
G | A | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 150 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.731-6105C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64703897 | ||||||
chr11:64703914
|
A | G | 1 | a0001c0003t0006g0303 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.731-6122T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64703914 | ||||||
chr11:64704073
|
C | G | 2 | a0002c0005t0002g0170a0002c0005t0002g0300 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.731-6281G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704073 | ||||||
chr11:64704107
|
CAG | C | 41 | a0002c0004t0001g0001a0002c0004t0001g0110a0002c0004t0001g0111others(38): Show | 42 | HG00280.hp1 HG00438.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.731-6317_731-6316d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704107 | ||||||
chr11:64704185
|
T | C | 2 | a0001c0002t0001g0072a0001c0002t0001g0082 | 2 | NA18981.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.731-6393A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704185 | ||||||
chr11:64704437
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.731-6645C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704437 | ||||||
chr11:64704510
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.731-6718G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704510 | ||||||
chr11:64704514
|
T | C | 130 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(127): Show | 132 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.731-6722A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704514 | ||||||
chr11:64704598
|
T | TCA | 41 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0024others(38): Show | 41 | HG00438.hp1 HG00558.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.731-6808_731-6807d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704598 | ||||||
chr11:64704598
|
T | TCACA | 10 | a0001c0001t0001g0016a0001c0001t0001g0164a0001c0001t0001g0179others(7): Show | 10 | HG00438.hp2 HG02132.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.731-6810_731-6807d others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704598 | ||||||
chr11:64704598
|
T | TCACACA | 4 | a0001c0003t0001g0057a0001c0017t0007g0189a0002c0004t0001g0116others(1): Show | 4 | HG02083.hp1 HG02129.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-6812_731-6807d others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704598 | ||||||
chr11:64704613
|
CACACACA others(7): Show |
C | 1 | a0002c0006t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.731-6835_731-6822d others(16): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704613 | ||||||
chr11:64704617
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0172 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.731-6835_731-6826d others(12): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704617 | ||||||
chr11:64704623
|
C | CACACAG | 9 | a0001c0001t0001g0248a0001c0003t0001g0249a0002c0004t0001g0111others(6): Show | 9 | HG01175.hp1 HG02109.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-6832_731-6831i others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACACAGA others(1): Show |
3 | a0002c0004t0001g0110a0002c0004t0001g0113a0002c0004t0001g0214 | 3 | HG00280.hp1 HG02135.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.731-6832_731-6831i others(10): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACACAGA others(3): Show |
1 | a0001c0003t0001g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.731-6832_731-6831i others(12): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACACAGA others(5): Show |
3 | a0001c0001t0001g0011a0002c0013t0001g0191a0003c0027t0001g0056 | 3 | HG03041.hp1 NA18944.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.731-6832_731-6831i others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACAG | 14 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0051others(11): Show | 14 | HG00621.hp1 HG00735.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.731-6832_731-6831i others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACAGAG | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0050others(3): Show | 6 | HG02055.hp2 HG02976.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-6832_731-6831i others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACAGAGA others(3): Show |
2 | a0001c0002t0001g0154a0001c0002t0001g0206 | 2 | NA18950.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.731-6832_731-6831i others(12): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACAGAGA others(5): Show |
4 | a0001c0001t0001g0053a0001c0001t0004g0258a0001c0001t0004g0259others(1): Show | 4 | HG00140.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-6832_731-6831i others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACAGAGA others(7): Show |
5 | a0001c0002t0001g0087a0001c0002t0001g0098a0001c0002t0001g0130others(2): Show | 5 | HG00408.hp2 HG02027.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-6832_731-6831i others(16): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CACAGAGA others(9): Show |
3 | a0001c0002t0001g0102a0001c0002t0001g0139a0001c0002t0001g0200 | 3 | NA18951.hp2 NA18994.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.731-6832_731-6831i others(18): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAG | 11 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0271others(8): Show | 11 | HG01346.hp2 HG01943.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.731-6833_731-6832d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAG | 14 | a0001c0002t0001g0060a0001c0002t0001g0067a0001c0002t0001g0068others(11): Show | 14 | HG00597.hp1 HG00621.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.731-6835_731-6832d others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAG | 6 | a0001c0002t0001g0069a0001c0002t0001g0193a0001c0002t0001g0196others(3): Show | 6 | HG00280.hp2 HG01261.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-6837_731-6832d others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAGA others(1): Show |
8 | a0001c0002t0001g0058a0001c0002t0001g0075a0001c0002t0001g0082others(5): Show | 8 | HG01256.hp2 HG01358.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-6839_731-6832d others(10): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAGA others(3): Show |
4 | a0001c0002t0001g0088a0001c0002t0001g0286a0002c0008t0001g0188others(1): Show | 4 | HG02109.hp2 HG02698.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-6841_731-6832d others(12): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAGA others(5): Show |
5 | a0001c0002t0001g0066a0001c0002t0001g0072a0001c0002t0001g0081others(2): Show | 5 | HG00558.hp2 HG02602.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-6843_731-6832d others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAGA others(7): Show |
6 | a0001c0002t0001g0065a0001c0002t0001g0074a0001c0002t0001g0078others(3): Show | 6 | HG04199.hp2 NA18971.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-6845_731-6832d others(16): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAGA others(9): Show |
2 | a0001c0002t0001g0205a0002c0008t0001g0281 | 2 | HG01243.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.731-6847_731-6832d others(18): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAGA others(11): Show |
2 | a0001c0002t0001g0199a0001c0002t0001g0243 | 2 | HG03669.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.731-6849_731-6832d others(20): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | CAGAGAGA others(13): Show |
1 | a0001c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.731-6851_731-6832d others(22): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
C | G | 2 | a0001c0002t0001g0076a0002c0005t0002g0276 | 2 | HG00735.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.731-6831G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
CAG | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0159others(22): Show | 26 | HG00597.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.731-6833_731-6832d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
CAGAG | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(3): Show | 7 | HG02145.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.731-6835_731-6832d others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
CAGAGAG | C | 8 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0247others(5): Show | 8 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-6837_731-6832d others(8): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
CAGAGAGA others(1): Show |
C | 3 | a0001c0001t0001g0269a0001c0003t0001g0144a0002c0004t0001g0118 | 3 | HG02572.hp1 NA18947.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.731-6839_731-6832d others(10): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
CAGAGAGA others(3): Show |
C | 8 | a0001c0003t0002g0134a0001c0003t0002g0234a0001c0003t0002g0292others(5): Show | 8 | HG01256.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.731-6841_731-6832d others(12): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
CAGAGAGA others(5): Show |
C | 47 | a0001c0001t0004g0262a0001c0003t0002g0133a0001c0003t0002g0135others(44): Show | 48 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.731-6843_731-6832d others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704623
|
CAGAGAGA others(7): Show |
C | 5 | a0001c0003t0003g0145a0001c0003t0003g0242a0002c0005t0002g0170others(2): Show | 5 | HG02922.hp2 HG03471.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-6845_731-6832d others(16): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704623 | ||||||
chr11:64704625
|
G | C | 48 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 48 | HG00140.hp1 HG00609.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.731-6833C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704625 | ||||||
chr11:64704627
|
G | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(42): Show | 46 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.731-6835C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704627 | ||||||
chr11:64704629
|
G | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0004g0160others(15): Show | 20 | HG00609.hp1 HG01106.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.731-6837C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704629 | ||||||
chr11:64704631
|
G | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0184a0001c0001t0001g0185others(3): Show | 7 | HG00408.hp1 HG00673.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.731-6839C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704631 | ||||||
chr11:64704633
|
G | C | 4 | a0001c0001t0001g0247a0001c0001t0001g0269a0001c0003t0001g0144others(1): Show | 4 | HG02486.hp2 HG02572.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-6841C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704633 | ||||||
chr11:64704635
|
G | C | 11 | a0001c0001t0001g0269a0001c0003t0001g0144a0001c0003t0002g0134others(8): Show | 11 | HG01256.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.731-6843C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704635 | ||||||
chr11:64704637
|
G | C | 57 | a0001c0001t0001g0269a0001c0001t0004g0262a0001c0003t0001g0144others(54): Show | 58 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.731-6845C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704637 | ||||||
chr11:64704639
|
G | C | 59 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(56): Show | 60 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.731-6847C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704639 | ||||||
chr11:64704641
|
G | C | 55 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0135others(52): Show | 56 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.731-6849C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704641 | ||||||
chr11:64704643
|
G | C | 1 | a0001c0003t0003g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.731-6851C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704643 | ||||||
chr11:64704663
|
G | GAGAGAGA others(11): Show |
1 | a0001c0002t0001g0288 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.731-6872_731-6871i others(20): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704663 | ||||||
chr11:64704703
|
G | A | 1 | a0002c0015t0002g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.731-6911C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704703 | ||||||
chr11:64704786
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.731-6994G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704786 | ||||||
chr11:64704847
|
T | C | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 150 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(147): Show |
intron_variant | MODIFIER | c.731-7055A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704847 | ||||||
chr11:64704984
|
G | C | 1 | a0001c0001t0001g0267 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.731-7192C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64704984 | ||||||
chr11:64705146
|
T | A | 1 | a0002c0004t0001g0213 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.731-7354A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64705146 | ||||||
chr11:64705505
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 61 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.730+7465G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64705505 | ||||||
chr11:64705728
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.730+7242T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64705728 | ||||||
chr11:64705925
|
C | A | 1 | a0001c0001t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.730+7045G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64705925 | ||||||
chr11:64705944
|
A | G | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.730+7026T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64705944 | ||||||
chr11:64705968
|
A | G | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.730+7002T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64705968 | ||||||
chr11:64706025
|
C | T | 1 | a0001c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.730+6945G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706025 | ||||||
chr11:64706064
|
T | TTA | 68 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(65): Show | 69 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.730+6904_730+6905d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706064 | ||||||
chr11:64706087
|
A | T | 1 | a0002c0004t0001g0208 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.730+6883T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706087 | ||||||
chr11:64706108
|
GTA | G | 192 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(189): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.730+6860_730+6861d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706108 | ||||||
chr11:64706110
|
A | ATATATAT others(292): Show |
1 | a0001c0003t0003g0240 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.730+6859_730+6860i others(301): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706110 | ||||||
chr11:64706110
|
A | ATATATAT others(276): Show |
1 | a0001c0003t0003g0242 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.730+6859_730+6860i others(285): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706110 | ||||||
chr11:64706110
|
A | G | 1 | a0001c0003t0002g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.730+6860T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706110 | ||||||
chr11:64706129
|
A | T | 34 | a0001c0001t0001g0175a0001c0001t0004g0252a0001c0001t0004g0257others(31): Show | 34 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.730+6841T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706129 | ||||||
chr11:64706148
|
A | AGTATATA others(461): Show |
1 | a0001c0003t0003g0145 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.730+6821_730+6822i others(470): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706148 | ||||||
chr11:64706148
|
A | ATATATAT others(174): Show |
1 | a0001c0001t0001g0175 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.730+6821_730+6822i others(183): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706148 | ||||||
chr11:64706148
|
A | C | 2 | a0001c0002t0001g0073a0001c0002t0001g0080 | 2 | HG00639.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.730+6822T>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706148 | ||||||
chr11:64706150
|
G | T | 2 | a0001c0001t0001g0175a0001c0003t0003g0145 | 2 | HG00438.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.730+6820C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706150 | ||||||
chr11:64706152
|
A | ATATAAAG others(459): Show |
1 | a0001c0003t0003g0148 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.730+6817_730+6818i others(468): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706152 | ||||||
chr11:64706152
|
A | ATATAAAG others(488): Show |
1 | a0001c0003t0003g0239 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.730+6817_730+6818i others(497): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706152 | ||||||
chr11:64706159
|
T | TA | 289 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(286): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.730+6810dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706159 | ||||||
chr11:64706161
|
T | A | 2 | a0001c0001t0001g0175a0001c0003t0003g0145 | 2 | HG00438.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.730+6809A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706161 | ||||||
chr11:64706162
|
A | AATATATA others(191): Show |
1 | a0001c0003t0001g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(200): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | AATATATA others(271): Show |
5 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(280): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | AATATATA others(271): Show |
2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(280): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATAATA others(104): Show |
2 | a0001c0003t0003g0240a0001c0003t0003g0242 | 2 | NA18952.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(113): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATAATA others(266): Show |
2 | a0001c0002t0001g0078a0001c0002t0001g0079 | 2 | NA18971.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(275): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(302): Show |
3 | a0002c0004t0001g0128a0002c0004t0001g0129a0010c0014t0001g0127 | 3 | NA18954.hp2 NA18971.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(311): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(344): Show |
2 | a0002c0005t0002g0219a0002c0005t0002g0220 | 2 | HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(353): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(226): Show |
1 | a0001c0001t0012g0048 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(235): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(246): Show |
1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(255): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(186): Show |
32 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 32 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(195): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(146): Show |
6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG00140.hp1 HG01433.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(155): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(177): Show |
1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(186): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(177): Show |
13 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG00735.hp1 HG01070.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(186): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(228): Show |
1 | a0001c0002t0001g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(237): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(197): Show |
2 | a0002c0008t0001g0188a0002c0008t0001g0281 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(206): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(224): Show |
1 | a0001c0002t0001g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(233): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(378): Show |
1 | a0002c0005t0002g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(387): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(460): Show |
2 | a0001c0003t0003g0103a0001c0003t0003g0238 | 2 | NA19054.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(469): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(500): Show |
1 | a0001c0003t0003g0229 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(509): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(418): Show |
4 | a0001c0003t0002g0230a0001c0003t0002g0231a0001c0003t0002g0232others(1): Show | 4 | HG02280.hp1 NA18945.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(427): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(380): Show |
2 | a0001c0003t0003g0146a0001c0003t0003g0149 | 2 | NA18954.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(389): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(300): Show |
3 | a0001c0003t0002g0134a0001c0003t0002g0135a0001c0003t0002g0226 | 3 | HG02818.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(309): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(302): Show |
1 | a0002c0004t0011g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(311): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(342): Show |
2 | a0002c0004t0001g0117a0002c0004t0001g0131 | 2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(351): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(409): Show |
1 | a0001c0003t0003g0150 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(418): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(380): Show |
12 | a0001c0003t0001g0144a0001c0003t0002g0141a0001c0003t0002g0292others(9): Show | 13 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(389): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(351): Show |
5 | a0001c0003t0002g0147a0001c0003t0002g0294a0001c0003t0002g0295others(2): Show | 5 | HG01168.hp2 HG01257.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(360): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(460): Show |
11 | a0001c0003t0003g0151a0001c0003t0003g0227a0001c0003t0003g0236others(8): Show | 11 | HG00609.hp2 HG02027.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(469): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(500): Show |
1 | a0001c0003t0006g0302 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(509): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(371): Show |
1 | a0001c0003t0003g0228 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(380): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(222): Show |
1 | a0001c0001t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(231): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(342): Show |
1 | a0002c0004t0001g0167 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(351): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(333): Show |
10 | a0002c0004t0001g0001a0002c0004t0001g0110a0002c0004t0001g0113others(7): Show | 11 | HG00280.hp1 HG00438.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(342): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(304): Show |
13 | a0002c0004t0001g0111a0002c0004t0001g0119a0002c0004t0001g0120others(10): Show | 13 | HG02135.hp2 HG03669.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(313): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(342): Show |
5 | a0002c0004t0001g0124a0002c0004t0001g0125a0002c0004t0001g0216others(2): Show | 5 | HG01123.hp1 HG01346.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(351): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(273): Show |
1 | a0002c0004t0001g0208 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(282): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(342): Show |
1 | a0002c0015t0002g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(351): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(344): Show |
5 | a0002c0004t0001g0166a0002c0004t0001g0168a0002c0004t0001g0169others(2): Show | 5 | HG00609.hp1 HG02132.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(353): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(384): Show |
4 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0222others(1): Show | 4 | HG02071.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(393): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(255): Show |
1 | a0002c0004t0001g0211 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(264): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(329): Show |
1 | a0002c0005t0002g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(338): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(359): Show |
1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(368): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(617): Show |
2 | a0001c0001t0004g0251a0001c0001t0004g0256 | 2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(626): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(340): Show |
1 | a0001c0003t0002g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(349): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(420): Show |
8 | a0001c0003t0002g0140a0001c0003t0002g0233a0001c0003t0002g0234others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(429): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(500): Show |
1 | a0008c0026t0003g0244 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(509): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(344): Show |
3 | a0002c0004t0001g0118a0002c0004t0001g0126a0002c0004t0001g0213 | 3 | HG03831.hp2 NA18951.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.730+6807_730+6808i others(353): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(344): Show |
1 | a0009c0012t0001g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(353): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(435): Show |
1 | a0001c0007t0007g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(444): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(697): Show |
1 | a0001c0001t0004g0250 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(706): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(617): Show |
1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(626): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(606): Show |
1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(615): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(698): Show |
1 | a0001c0001t0004g0262 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(707): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(228): Show |
1 | a0001c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(237): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(657): Show |
1 | a0001c0001t0004g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(666): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(386): Show |
1 | a0001c0001t0001g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(395): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(415): Show |
1 | a0001c0001t0001g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(424): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(386): Show |
1 | a0001c0001t0001g0015 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(395): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(384): Show |
1 | a0002c0005t0009g0004 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(393): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(437): Show |
1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(446): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(357): Show |
1 | a0001c0017t0007g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(366): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(308): Show |
4 | a0001c0002t0001g0081a0001c0002t0001g0082a0001c0002t0001g0102others(1): Show | 4 | HG00558.hp2 HG02027.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(317): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(737): Show |
1 | a0001c0001t0004g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(746): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(268): Show |
10 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0065others(7): Show | 10 | HG00280.hp2 HG00639.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(277): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(346): Show |
1 | a0001c0001t0001g0164 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(355): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(386): Show |
1 | a0001c0001t0001g0248 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(395): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(228): Show |
43 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0066others(40): Show | 43 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(237): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(695): Show |
1 | a0001c0001t0004g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(704): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(697): Show |
4 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(706): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(697): Show |
1 | a0001c0001t0004g0165 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(706): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(697): Show |
1 | a0001c0001t0004g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(706): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(657): Show |
1 | a0001c0001t0004g0254 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(666): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(188): Show |
22 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(19): Show | 23 | HG00408.hp2 HG01070.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(197): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(148): Show |
1 | a0001c0003t0005g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(157): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(617): Show |
1 | a0001c0001t0004g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(626): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATAA others(277): Show |
1 | a0001c0002t0001g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(286): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATTA others(186): Show |
1 | a0001c0001t0014g0039 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(195): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATTA others(344): Show |
1 | a0002c0004t0001g0279 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(353): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATTA others(268): Show |
1 | a0001c0024t0001g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(277): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATTA others(355): Show |
1 | a0002c0006t0001g0008 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.730+6807_730+6808i others(364): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATTA others(391): Show |
1 | a0002c0006t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.730+6807_730+6808i others(400): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | ATATATTA others(315): Show |
6 | a0002c0006t0001g0006a0002c0006t0001g0007a0002c0006t0001g0010others(3): Show | 6 | HG01106.hp1 HG01934.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+6807_730+6808i others(324): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706162
|
A | G | 2 | a0001c0001t0001g0175a0001c0003t0003g0145 | 2 | HG00438.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.730+6808T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706162 | ||||||
chr11:64706171
|
A | T | 2 | a0002c0004t0001g0221a0002c0008t0001g0188 | 2 | HG02109.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.730+6799T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706171 | ||||||
chr11:64706173
|
T | G | 1 | a0001c0002t0001g0094 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.730+6797A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706173 | ||||||
chr11:64706173
|
T | TATATATT others(616): Show |
1 | a0001c0001t0004g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730+6796_730+6797i others(625): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706173 | ||||||
chr11:64706347
|
G | A | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG00621.hp1 HG02165.hp2 NA18963.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+6623C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706347 | ||||||
chr11:64706418
|
C | A | 2 | a0002c0004t0001g0222a0002c0004t0001g0223 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.730+6552G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706418 | ||||||
chr11:64706419
|
G | A | 1 | a0002c0004t0001g0279 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.730+6551C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706419 | ||||||
chr11:64706952
|
A | AT | 12 | a0001c0001t0001g0247a0001c0001t0004g0160a0001c0001t0004g0250others(9): Show | 12 | HG02451.hp1 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.730+6017dupA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706952 | ||||||
chr11:64706952
|
AT | A | 90 | a0001c0001t0001g0024a0001c0001t0001g0269a0001c0002t0001g0058others(87): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.730+6017delA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64706952 | ||||||
chr11:64707087
|
G | T | 116 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(113): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.730+5883C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707087 | ||||||
chr11:64707280
|
A | G | 147 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(144): Show | 149 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.730+5690T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707280 | ||||||
chr11:64707312
|
G | A | 8 | a0002c0004t0001g0019a0002c0004t0001g0020a0002c0004t0001g0166others(5): Show | 8 | HG00609.hp1 HG02056.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.730+5658C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707312 | ||||||
chr11:64707384
|
C | CA | 6 | a0002c0004t0001g0128a0002c0004t0001g0129a0002c0004t0001g0156others(3): Show | 6 | NA18944.hp1 NA18954.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+5585dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707384 | ||||||
chr11:64707384
|
CA | C | 8 | a0001c0001t0008g0026a0001c0002t0001g0070a0001c0002t0001g0071others(5): Show | 8 | HG00609.hp2 HG01070.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+5585delT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707384 | ||||||
chr11:64707674
|
T | C | 1 | a0001c0002t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.730+5296A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707674 | ||||||
chr11:64707941
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247others(3): Show | 7 | HG02486.hp2 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.730+5029T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707941 | ||||||
chr11:64707991
|
G | T | 1 | a0001c0002t0001g0098 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.730+4979C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64707991 | ||||||
chr11:64708040
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0186 | 2 | HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.730+4930C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708040 | ||||||
chr11:64708094
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.730+4876C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708094 | ||||||
chr11:64708098
|
C | CA | 14 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0003t0001g0107others(11): Show | 14 | HG01106.hp1 HG01934.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.730+4871dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708098 | ||||||
chr11:64708140
|
T | G | 1 | a0001c0001t0004g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730+4830A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708140 | ||||||
chr11:64708377
|
C | T | 1 | a0002c0004t0001g0110 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.730+4593G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708377 | ||||||
chr11:64708418
|
T | C | 1 | a0001c0001t0004g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730+4552A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708418 | ||||||
chr11:64708419
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.730+4551G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708419 | ||||||
chr11:64708453
|
T | C | 1 | a0001c0003t0006g0305 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.730+4517A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708453 | ||||||
chr11:64708618
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.730+4352C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708618 | ||||||
chr11:64708638
|
C | A | 2 | a0001c0002t0001g0096a0001c0002t0001g0097 | 2 | NA18984.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.730+4332G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708638 | ||||||
chr11:64708706
|
T | C | 1 | a0001c0003t0002g0299 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.730+4264A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708706 | ||||||
chr11:64708734
|
C | T | 1 | a0001c0002t0001g0069 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.730+4236G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708734 | ||||||
chr11:64708793
|
A | G | 21 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 21 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.730+4177T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708793 | ||||||
chr11:64708966
|
C | T | 1 | a0001c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.730+4004G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708966 | ||||||
chr11:64708973
|
C | A | 81 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0002t0001g0058others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.730+3997G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64708973 | ||||||
chr11:64709190
|
C | CA | 20 | a0001c0001t0001g0005a0001c0001t0001g0049a0001c0001t0001g0053others(17): Show | 20 | HG00408.hp2 HG01175.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.730+3779dupT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709190 | ||||||
chr11:64709190
|
CA | C | 8 | a0001c0001t0001g0003a0001c0017t0007g0189a0002c0006t0001g0006others(5): Show | 9 | HG01106.hp1 HG01934.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.730+3779delT | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709190 | ||||||
chr11:64709190
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0002t0001g0197a0001c0003t0003g0149 | 2 | HG01074.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.730+3769_730+3779d others(13): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709190 | ||||||
chr11:64709190
|
CAAAAAAA others(5): Show |
C | 115 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(112): Show | 117 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.730+3768_730+3779d others(14): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709190 | ||||||
chr11:64709245
|
T | C | 1 | a0001c0002t0001g0102 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.730+3725A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709245 | ||||||
chr11:64709337
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(3): Show | 6 | HG00140.hp1 HG01433.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+3633G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709337 | ||||||
chr11:64709363
|
A | G | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.730+3607T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709363 | ||||||
chr11:64709522
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.730+3448C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709522 | ||||||
chr11:64709578
|
T | G | 56 | a0001c0003t0001g0144a0001c0003t0002g0133a0001c0003t0002g0134others(53): Show | 57 | HG00609.hp2 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.730+3392A>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709578 | ||||||
chr11:64709908
|
C | CT | 9 | a0001c0001t0001g0003a0001c0001t0001g0157a0001c0001t0004g0251others(6): Show | 10 | HG00609.hp2 HG02056.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.730+3061dupA | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709908 | ||||||
chr11:64709915
|
T | A | 1 | a0001c0002t0001g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730+3055A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64709915 | ||||||
chr11:64710033
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(276): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.730+2937T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710033 | ||||||
chr11:64710211
|
G | A | 3 | a0001c0001t0001g0003a0002c0004t0001g0222a0002c0004t0001g0223 | 4 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+2759C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710211 | ||||||
chr11:64710527
|
C | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.730+2443G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710527 | ||||||
chr11:64710591
|
G | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.730+2379C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710591 | ||||||
chr11:64710674
|
T | A | 1 | a0001c0023t0001g0192 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.730+2296A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710674 | ||||||
chr11:64710714
|
C | T | 1 | a0001c0002t0001g0068 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.730+2256G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710714 | ||||||
chr11:64710748
|
A | T | 4 | a0001c0003t0002g0133a0001c0003t0002g0134a0001c0003t0002g0135others(1): Show | 4 | HG02818.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+2222T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710748 | ||||||
chr11:64710848
|
C | T | 131 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(128): Show | 132 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.730+2122G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710848 | ||||||
chr11:64710903
|
G | A | 4 | a0001c0003t0006g0301a0001c0003t0006g0303a0001c0003t0006g0304others(1): Show | 4 | HG02040.hp2 HG02071.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+2067C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64710903 | ||||||
chr11:64711438
|
G | A | 1 | a0001c0001t0004g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.730+1532C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711438 | ||||||
chr11:64711458
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.730+1512C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711458 | ||||||
chr11:64711516
|
C | T | 10 | a0002c0005t0002g0170a0002c0005t0002g0274a0002c0005t0002g0276others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.730+1454G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711516 | ||||||
chr11:64711526
|
T | C | 1 | a0001c0002t0001g0205 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.730+1444A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711526 | ||||||
chr11:64711640
|
G | T | 63 | a0002c0004t0001g0001a0002c0004t0001g0019a0002c0004t0001g0020others(60): Show | 64 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.730+1330C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711640 | ||||||
chr11:64711776
|
C | G | 1 | a0001c0002t0001g0067 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.730+1194G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711776 | ||||||
chr11:64711778
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0248 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.730+1192G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711778 | ||||||
chr11:64711857
|
G | A | 1 | a0001c0003t0003g0150 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.730+1113C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711857 | ||||||
chr11:64711872
|
T | C | 1 | a0001c0001t0004g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.730+1098A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711872 | ||||||
chr11:64711966
|
ACT | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.730+1002_730+1003d others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64711966 | ||||||
chr11:64712285
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(276): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.730+685A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64712285 | ||||||
chr11:64712331
|
G | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0247 | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+639C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64712331 | ||||||
chr11:64712693
|
C | A | 1 | a0001c0003t0003g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.730+277G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64712693 | ||||||
chr11:64712836
|
C | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.730+134G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64712836 | ||||||
chr11:64712838
|
C | G | 10 | a0002c0005t0002g0170a0002c0005t0002g0274a0002c0005t0002g0276others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.730+132G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64712838 | ||||||
chr11:64712887
|
C | T | 1 | a0002c0004t0015g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.730+83G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64712887 | ||||||
chr11:64712927
|
A | AC | 7 | a0001c0001t0004g0250a0001c0002t0001g0065a0001c0002t0001g0066others(4): Show | 7 | HG01106.hp1 HG01106.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.730+42dupG | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 2/22 | chr11 | 64712927 | ||||||
chr11:64713976
|
G | C | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-244-33C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64713976 | ||||||
chr11:64714107
|
G | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-244-164C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714107 | ||||||
chr11:64714116
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-244-173C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714116 | ||||||
chr11:64714216
|
C | CCA | 207 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(204): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-244-274_-244-273i others(4): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714216 | ||||||
chr11:64714388
|
T | C | 1 | a0001c0002t0001g0205 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-244-445A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714388 | ||||||
chr11:64714408
|
G | A | 135 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(132): Show | 136 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-244-465C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714408 | ||||||
chr11:64714597
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-244-654G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714597 | ||||||
chr11:64714733
|
T | C | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-244-790A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714733 | ||||||
chr11:64714829
|
A | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG01109.hp1 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-244-886T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64714829 | ||||||
chr11:64715069
|
G | T | 10 | a0002c0005t0002g0170a0002c0005t0002g0274a0002c0005t0002g0276others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-244-1126C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715069 | ||||||
chr11:64715074
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(61): Show | 65 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-244-1131C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715074 | ||||||
chr11:64715106
|
G | T | 1 | a0002c0015t0002g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-244-1163C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715106 | ||||||
chr11:64715270
|
A | G | 1 | a0001c0003t0003g0246 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-244-1327T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715270 | ||||||
chr11:64715273
|
C | A | 1 | a0001c0003t0003g0246 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-244-1330G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715273 | ||||||
chr11:64715323
|
G | A | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-244-1380C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715323 | ||||||
chr11:64715475
|
G | C | 201 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(198): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.-244-1532C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715475 | ||||||
chr11:64715504
|
C | T | 2 | a0001c0007t0007g0013a0001c0017t0007g0189 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-244-1561G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715504 | ||||||
chr11:64715538
|
G | A | 1 | a0001c0002t0001g0205 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-244-1595C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64715538 | ||||||
chr11:64716157
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(276): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-244-2214A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716157 | ||||||
chr11:64716177
|
C | T | 7 | a0001c0002t0001g0060a0001c0002t0001g0062a0001c0002t0001g0063others(4): Show | 7 | HG01070.hp1 HG01123.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-2234G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716177 | ||||||
chr11:64716229
|
A | T | 1 | a0002c0005t0002g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-244-2286T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716229 | ||||||
chr11:64716266
|
G | A | 2 | a0001c0007t0007g0013a0001c0017t0007g0189 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-244-2323C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716266 | ||||||
chr11:64716638
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.-244-2695C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716638 | ||||||
chr11:64716865
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-244-2922C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716865 | ||||||
chr11:64716944
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0186 | 3 | HG02602.hp2 HG02738.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-244-3001C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716944 | ||||||
chr11:64716951
|
C | A | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-244-3008G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64716951 | ||||||
chr11:64717305
|
T | C | 1 | a0001c0002t0001g0206 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-244-3362A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64717305 | ||||||
chr11:64717519
|
T | C | 1 | a0002c0004t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-244-3576A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64717519 | ||||||
chr11:64717642
|
C | T | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-244-3699G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64717642 | ||||||
chr11:64717684
|
C | A | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-244-3741G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64717684 | ||||||
chr11:64717721
|
C | T | 67 | a0001c0002t0001g0130a0001c0002t0001g0225a0002c0004t0001g0001others(64): Show | 68 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-244-3778G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64717721 | ||||||
chr11:64717734
|
A | T | 1 | a0001c0007t0001g0018 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-244-3791T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64717734 | ||||||
chr11:64717893
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-244-3950G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64717893 | ||||||
chr11:64718545
|
C | A | 1 | a0001c0001t0004g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-245+4426G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718545 | ||||||
chr11:64718599
|
C | T | 2 | a0001c0002t0001g0058a0001c0002t0001g0059 | 2 | HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-245+4372G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718599 | ||||||
chr11:64718667
|
C | T | 2 | a0002c0005t0002g0277a0002c0015t0002g0275 | 2 | HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-245+4304G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718667 | ||||||
chr11:64718706
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-245+4265G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718706 | ||||||
chr11:64718802
|
C | A | 1 | a0001c0003t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-245+4169G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718802 | ||||||
chr11:64718835
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-245+4136T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718835 | ||||||
chr11:64718841
|
G | C | 2 | a0001c0007t0007g0013a0001c0017t0007g0189 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-245+4130C>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718841 | ||||||
chr11:64718880
|
G | A | 2 | a0001c0007t0007g0013a0001c0017t0007g0189 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-245+4091C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718880 | ||||||
chr11:64718881
|
C | A | 2 | a0001c0007t0007g0013a0001c0017t0007g0189 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-245+4090G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64718881 | ||||||
chr11:64719100
|
C | T | 1 | a0002c0005t0002g0276 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-245+3871G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719100 | ||||||
chr11:64719265
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-245+3706C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719265 | ||||||
chr11:64719547
|
G | T | 74 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(71): Show | 74 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-245+3424C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719547 | ||||||
chr11:64719606
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-245+3365G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719606 | ||||||
chr11:64719636
|
A | T | 1 | a0002c0004t0001g0284 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-245+3335T>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719636 | ||||||
chr11:64719907
|
AATAGCTA others(15): Show |
A | 1 | a0001c0001t0001g0187 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-245+3042_-245+306 others(26): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719907 | ||||||
chr11:64719922
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0015others(195): Show | 201 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-245+3049G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719922 | ||||||
chr11:64719975
|
T | C | 5 | a0002c0005t0002g0170a0002c0005t0002g0274a0002c0005t0002g0280others(2): Show | 5 | HG01243.hp1 HG02922.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-245+2996A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64719975 | ||||||
chr11:64720051
|
C | T | 1 | a0002c0015t0002g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-245+2920G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720051 | ||||||
chr11:64720137
|
G | A | 1 | a0001c0003t0003g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-245+2834C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720137 | ||||||
chr11:64720367
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-245+2604C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720367 | ||||||
chr11:64720375
|
C | T | 1 | a0001c0002t0001g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-245+2596G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720375 | ||||||
chr11:64720402
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-245+2569C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720402 | ||||||
chr11:64720467
|
C | T | 1 | a0002c0011t0007g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-245+2504G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720467 | ||||||
chr11:64720549
|
G | A | 1 | a0001c0003t0003g0246 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-245+2422C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720549 | ||||||
chr11:64720582
|
G | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(76): Show | 79 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-245+2389C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720582 | ||||||
chr11:64720671
|
CAT | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 61 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-245+2298_-245+229 others(6): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720671 | ||||||
chr11:64720754
|
A | G | 1 | a0001c0001t0004g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-245+2217T>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720754 | ||||||
chr11:64720802
|
G | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0247a0001c0023t0001g0192 | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-245+2169C>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720802 | ||||||
chr11:64720817
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-245+2154C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720817 | ||||||
chr11:64720819
|
G | A | 81 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0016others(78): Show | 81 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-245+2152C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64720819 | ||||||
chr11:64721098
|
G | A | 1 | a0002c0008t0001g0188 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-245+1873C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64721098 | ||||||
chr11:64721134
|
C | T | 3 | a0001c0002t0005g0055a0002c0013t0001g0191a0003c0027t0001g0056 | 3 | HG01346.hp2 NA18944.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-245+1837G>A | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64721134 | ||||||
chr11:64721230
|
G | A | 1 | a0001c0017t0007g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-245+1741C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64721230 | ||||||
chr11:64721433
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG01175.hp2 HG01496.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-245+1538G>C | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64721433 | ||||||
chr11:64721883
|
T | C | 1 | a0001c0002t0001g0154 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-245+1088A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64721883 | ||||||
chr11:64721902
|
T | C | 1 | a0002c0004t0001g0155 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-245+1069A>G | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64721902 | ||||||
chr11:64721986
|
G | A | 1 | a0002c0004t0001g0156 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-245+985C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64721986 | ||||||
chr11:64722286
|
T | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0190 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-245+685A>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64722286 | ||||||
chr11:64722651
|
G | A | 181 | a0001c0001t0001g0108a0001c0001t0001g0152a0001c0002t0001g0058others(178): Show | 183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-245+320C>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64722651 | ||||||
chr11:64722950
|
GC | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0157a0001c0001t0001g0158others(93): Show | 97 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-245+20delG | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64722950 | ||||||
chr11:64722950
|
GCC | G | 156 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0015others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-245+19_-245+20del others(2): Show |
NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64722950 | ||||||
chr11:64722963
|
C | A | 1 | a0002c0005t0002g0300 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.-245+8G>T | NRXN2 | ENSG00000110076.21 | transcript | ENST00000265459.11 | protein_coding | 1/22 | chr11 | 64722963 |