Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84628 |
|---|---|
| ensemblid | ENSG00000196358.12 |
| hgncid | 14288 |
| symbol | NTNG2 |
| name | netrin G2 |
| refseq_nuc | NM_032536.4 |
| refseq_prot | NP_115925.2 |
| ensembl_nuc | ENST00000393229.4 |
| ensembl_prot | ENSP00000376921.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 132162058 |
| end | 132244526 |
| strand | + |
| ver | v1.2 |
| region | chr9:132162058-132244526 |
| region5000 | chr9:132157058-132249526 |
| regionname0 | NTNG2_chr9_132162058_132244526 |
| regionname5000 | NTNG2_chr9_132157058_132249526 |
| 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 | 0/1 | 530 | 352 | 91 | 66 | 142 | 13 | 39 | 98 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0002 | 0/0 | 530 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0003 | 1/0 | 530 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0004 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0005 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| 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 | 0/1 | 1593 | 118 | 37 | 19 | 45 | 6 | 10 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0002 | 0/0 | 1593 | 94 | 34 | 22 | 24 | 3 | 11 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0003 | 0/0 | 1593 | 60 | 8 | 17 | 25 | 3 | 7 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0004 | 0/0 | 1593 | 49 | 9 | 3 | 31 | 1 | 5 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0005 | 0/0 | 1593 | 16 | 3 | 3 | 8 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0006 | 0/0 | 1593 | 12 | 0 | 2 | 8 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0007 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0008 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0009 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0010 | 1/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0011 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0012 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0013 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0014 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| c0015 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| 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 | 1/0 | 3081 | 125 | 18 | 35 | 52 | 5 | 14 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0002 | 0/0 | 3079 | 86 | 20 | 15 | 40 | 1 | 10 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0003 | 0/1 | 3081 | 34 | 5 | 3 | 16 | 3 | 6 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0004 | 0/0 | 3080 | 16 | 14 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0005 | 0/0 | 3081 | 11 | 9 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0006 | 0/0 | 3081 | 8 | 2 | 0 | 5 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0007 | 0/0 | 3079 | 6 | 0 | 0 | 5 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0008 | 0/0 | 3082 | 6 | 0 | 2 | 3 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0009 | 0/0 | 3081 | 5 | 0 | 1 | 1 | 2 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0010 | 0/0 | 3079 | 4 | 0 | 0 | 4 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0011 | 0/0 | 3080 | 4 | 1 | 0 | 3 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0012 | 0/0 | 3081 | 4 | 4 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0013 | 0/0 | 3082 | 3 | 3 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0014 | 0/0 | 3090 | 3 | 0 | 0 | 0 | 2 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0015 | 0/0 | 3081 | 2 | 0 | 0 | 2 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0016 | 0/0 | 3082 | 2 | 2 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0017 | 0/0 | 3082 | 2 | 0 | 0 | 2 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0018 | 0/0 | 3079 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0019 | 0/0 | 3079 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0020 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0021 | 0/0 | 3080 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0022 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0023 | 0/0 | 3080 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0024 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0025 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0026 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0027 | 0/0 | 3081 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0028 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0029 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0030 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0031 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0032 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0033 | 0/0 | 3079 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0034 | 0/0 | 3079 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0035 | 0/0 | 3081 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0036 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0037 | 0/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0038 | 0/0 | 3081 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0039 | 0/0 | 3081 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0040 | 0/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0041 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0042 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0043 | 0/0 | 3081 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0044 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0045 | 0/0 | 3080 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0046 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0047 | 0/0 | 3082 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0048 | 0/0 | 3079 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0049 | 0/0 | 3079 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0050 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0051 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0052 | 0/0 | 3081 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| t0053 | 0/0 | 3090 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| 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 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| 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 | 0/1 | 1593 | 118 | 37 | 19 | 45 | 6 | 10 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002 | 0/0 | 1593 | 94 | 34 | 22 | 24 | 3 | 11 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003 | 0/0 | 1593 | 60 | 8 | 17 | 25 | 3 | 7 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004 | 0/0 | 1593 | 49 | 9 | 3 | 31 | 1 | 5 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0005 | 0/0 | 1593 | 16 | 3 | 3 | 8 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0006 | 0/0 | 1593 | 12 | 0 | 2 | 8 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0012 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0014 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0015 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0002c0007 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0002c0008 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0003c0010 | 1/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0003c0013 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0004c0009 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0005c0011 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4673 | 28 | 4 | 6 | 14 | 2 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0002 | 0/0 | 4671 | 28 | 6 | 6 | 13 | 0 | 3 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0003 | 0/1 | 4673 | 19 | 1 | 0 | 10 | 3 | 4 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0004 | 0/0 | 4672 | 3 | 3 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0005 | 0/0 | 4673 | 10 | 8 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0006 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0007 | 0/0 | 4671 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0008 | 0/0 | 4674 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0009 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0011 | 0/0 | 4672 | 4 | 1 | 0 | 3 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0012 | 0/0 | 4673 | 3 | 3 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0013 | 0/0 | 4674 | 3 | 3 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0016 | 0/0 | 4674 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0018 | 0/0 | 4671 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0019 | 0/0 | 4671 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0020 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0027 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0030 | 0/0 | 4671 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0033 | 0/0 | 4671 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0034 | 0/0 | 4671 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0036 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0042 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0043 | 0/0 | 4673 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0046 | 0/0 | 4674 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0048 | 0/0 | 4671 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0050 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0001t0051 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0001 | 0/0 | 4673 | 47 | 12 | 15 | 14 | 1 | 5 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0002 | 0/0 | 4671 | 21 | 8 | 3 | 6 | 0 | 4 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0003 | 0/0 | 4673 | 2 | 1 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0004 | 0/0 | 4672 | 11 | 9 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0005 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0006 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0008 | 0/0 | 4674 | 2 | 0 | 1 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0009 | 0/0 | 4673 | 3 | 0 | 1 | 0 | 1 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0014 | 0/0 | 4682 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0021 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0039 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0044 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0045 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0002t0049 | 0/0 | 4671 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0001 | 0/0 | 4673 | 26 | 1 | 10 | 10 | 2 | 3 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0002 | 0/0 | 4671 | 12 | 2 | 4 | 6 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0003 | 0/0 | 4673 | 4 | 2 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0004 | 0/0 | 4672 | 2 | 2 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0006 | 0/0 | 4673 | 4 | 1 | 0 | 2 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0007 | 0/0 | 4671 | 2 | 0 | 0 | 1 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0010 | 0/0 | 4671 | 4 | 0 | 0 | 4 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0014 | 0/0 | 4682 | 2 | 0 | 0 | 0 | 1 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0023 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0026 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0037 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0003t0038 | 0/0 | 4673 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0001 | 0/0 | 4673 | 10 | 0 | 1 | 8 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0002 | 0/0 | 4671 | 11 | 2 | 1 | 6 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0003 | 0/0 | 4673 | 8 | 1 | 1 | 5 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0006 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0007 | 0/0 | 4671 | 3 | 0 | 0 | 3 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0008 | 0/0 | 4674 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0012 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0015 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0016 | 0/0 | 4674 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0017 | 0/0 | 4674 | 2 | 0 | 0 | 2 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0022 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0024 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0025 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0028 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0029 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0032 | 0/0 | 4671 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0035 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0041 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0047 | 0/0 | 4674 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0004t0053 | 0/0 | 4682 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0005t0001 | 0/0 | 4673 | 4 | 0 | 2 | 1 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0005t0002 | 0/0 | 4671 | 7 | 2 | 1 | 4 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0005t0006 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0005t0008 | 0/0 | 4674 | 2 | 0 | 0 | 2 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0005t0009 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0005t0040 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0006t0001 | 0/0 | 4673 | 5 | 0 | 1 | 4 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0006t0002 | 0/0 | 4671 | 5 | 0 | 0 | 4 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0006t0003 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0006t0031 | 0/0 | 4671 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0012t0015 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0014t0001 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0001c0015t0052 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0002c0007t0002 | 0/0 | 4671 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0002c0008t0001 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0003c0010t0001 | 1/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0003c0013t0001 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0004c0009t0001 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| a0005c0011t0002 | 0/0 | 4671 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | copy fasta | chr9 | 132157058 | 132249526 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0012g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0013g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0013g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0018g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0018g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0019g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0020g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0027g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0030g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0033g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0034g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0036g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0042g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0043g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0046g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0048g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0050g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0051g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0008g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0009g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0009g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0009g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0014g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0021g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0039g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0044g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0045g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0049g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0007g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0010g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0010g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0010g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0010g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0014g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0014g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0023g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0026g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0037g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0038g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0008g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0015g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0016g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0017g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0017g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0022g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0024g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0025g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0028g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0029g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0032g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0035g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0041g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0047g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0053g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0008g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0009g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0040g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0031g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0012t0015g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0014t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0015t0052g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0002c0007t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0002c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0003c0010t0001g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0003c0013t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0004c0009t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0005c0011t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0113 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0160 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0062 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00140 | hp2 | a0001 | c0004 | t0053 | g0298 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00280 | hp1 | a0001 | c0003 | t0014 | g0293 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00280 | hp2 | a0001 | c0002 | t0009 | g0112 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00323 | hp1 | a0002 | c0007 | t0002 | g0131 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00423 | hp1 | a0001 | c0003 | t0006 | g0219 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0324 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0135 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0332 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00621 | hp1 | a0001 | c0004 | t0007 | g0211 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0156 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0288 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0071 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0149 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0087 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00741 | hp1 | a0001 | c0001 | t0048 | g0065 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0270 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0336 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01071 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01074 | hp2 | a0001 | c0001 | t0018 | g0091 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0337 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01099 | hp2 | a0001 | c0001 | t0018 | g0088 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0234 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0339 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0133 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0256 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0345 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0326 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0327 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01175 | hp1 | a0001 | c0006 | t0001 | g0271 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01192 | hp1 | a0001 | c0005 | t0002 | g0303 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01243 | hp2 | a0001 | c0002 | t0009 | g0304 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0309 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01257 | hp1 | a0001 | c0005 | t0001 | g0277 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0310 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01261 | hp1 | a0001 | c0004 | t0002 | g0042 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0299 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01516 | hp1 | a0001 | c0002 | t0014 | g0294 | EUR | IBS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0198 | EUR | IBS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01884 | hp2 | a0001 | c0001 | t0046 | g0077 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0350 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0081 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01943 | hp1 | a0001 | c0003 | t0002 | g0311 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01952 | hp1 | a0001 | c0004 | t0003 | g0202 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0166 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01981 | hp1 | a0001 | c0002 | t0008 | g0319 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01981 | hp2 | a0001 | c0001 | t0043 | g0060 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02004 | hp1 | a0001 | c0003 | t0038 | g0128 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02015 | hp1 | a0001 | c0003 | t0010 | g0316 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02027 | hp1 | a0001 | c0005 | t0008 | g0349 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02027 | hp2 | a0001 | c0006 | t0001 | g0005 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0054 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02056 | hp2 | a0001 | c0004 | t0015 | g0241 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0046 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0325 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02080 | hp1 | a0001 | c0001 | t0011 | g0061 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0028 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02132 | hp1 | a0001 | c0001 | t0011 | g0007 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02132 | hp2 | a0001 | c0005 | t0001 | g0329 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02145 | hp1 | a0001 | c0004 | t0025 | g0225 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0138 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02155 | hp1 | a0001 | c0004 | t0028 | g0116 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02155 | hp2 | a0001 | c0006 | t0002 | g0004 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02165 | hp2 | a0001 | c0006 | t0001 | g0295 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02257 | hp1 | a0003 | c0013 | t0001 | g0130 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0272 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0296 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02451 | hp1 | a0001 | c0004 | t0003 | g0273 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0300 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02572 | hp1 | a0001 | c0004 | t0012 | g0279 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0233 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0224 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0280 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02622 | hp2 | a0001 | c0002 | t0021 | g0230 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0351 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02683 | hp1 | a0001 | c0002 | t0009 | g0035 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0334 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0267 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0301 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02735 | hp2 | a0001 | c0005 | t0040 | g0239 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02738 | hp1 | a0001 | c0003 | t0006 | g0205 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02738 | hp2 | a0001 | c0003 | t0014 | g0297 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0353 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0250 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02818 | hp2 | a0001 | c0003 | t0004 | g0226 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0352 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02886 | hp2 | a0001 | c0001 | t0042 | g0158 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02895 | hp1 | a0001 | c0001 | t0051 | g0236 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0252 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02922 | hp2 | a0001 | c0002 | t0049 | g0238 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0119 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0264 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03041 | hp1 | a0001 | c0001 | t0050 | g0237 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03041 | hp2 | a0001 | c0004 | t0024 | g0228 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0340 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03130 | hp1 | a0001 | c0004 | t0016 | g0229 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0248 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03139 | hp1 | a0001 | c0002 | t0044 | g0274 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03139 | hp2 | a0001 | c0001 | t0020 | g0302 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03195 | hp1 | a0001 | c0004 | t0002 | g0247 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0261 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0254 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03225 | hp1 | a0001 | c0005 | t0002 | g0341 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0101 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03239 | hp1 | a0001 | c0001 | t0019 | g0027 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0276 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0240 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0232 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0275 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03492 | hp2 | a0001 | c0004 | t0002 | g0085 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0257 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0125 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03579 | hp1 | a0001 | c0004 | t0041 | g0249 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03654 | hp1 | a0001 | c0014 | t0001 | g0287 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03669 | hp2 | a0001 | c0002 | t0045 | g0183 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0171 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03688 | hp2 | a0001 | c0004 | t0003 | g0118 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03704 | hp1 | a0001 | c0003 | t0007 | g0209 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0331 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03831 | hp1 | a0001 | c0006 | t0003 | g0347 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0145 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03834 | hp2 | a0002 | c0008 | t0001 | g0132 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0181 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04115 | hp2 | a0001 | c0003 | t0037 | g0137 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04184 | hp1 | a0001 | c0006 | t0002 | g0084 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04199 | hp1 | a0001 | c0005 | t0001 | g0269 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04204 | hp2 | a0001 | c0004 | t0008 | g0032 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04228 | hp1 | a0001 | c0004 | t0002 | g0139 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | YRI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | YRI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | CHB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | CHB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | CHB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18939 | hp1 | a0001 | c0004 | t0002 | g0323 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18939 | hp2 | a0001 | c0002 | t0039 | g0045 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18941 | hp1 | a0001 | c0004 | t0003 | g0136 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18944 | hp1 | a0001 | c0006 | t0002 | g0072 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18944 | hp2 | a0001 | c0004 | t0022 | g0039 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18946 | hp1 | a0005 | c0011 | t0002 | g0117 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18948 | hp1 | a0001 | c0003 | t0010 | g0315 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18948 | hp2 | a0001 | c0004 | t0047 | g0322 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18949 | hp1 | a0001 | c0004 | t0017 | g0220 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18949 | hp2 | a0001 | c0004 | t0003 | g0142 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18950 | hp1 | a0001 | c0002 | t0008 | g0164 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0342 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18952 | hp2 | a0001 | c0004 | t0003 | g0070 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18960 | hp1 | a0001 | c0006 | t0001 | g0284 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18960 | hp2 | a0001 | c0003 | t0002 | g0147 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18961 | hp2 | a0001 | c0006 | t0002 | g0292 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18963 | hp1 | a0001 | c0003 | t0010 | g0314 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18966 | hp2 | a0001 | c0001 | t0027 | g0053 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0221 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18967 | hp2 | a0001 | c0006 | t0002 | g0354 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0178 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18969 | hp2 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18970 | hp1 | a0001 | c0004 | t0007 | g0214 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18974 | hp1 | a0001 | c0003 | t0023 | g0216 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18974 | hp2 | a0001 | c0004 | t0002 | g0003 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18977 | hp1 | a0001 | c0004 | t0002 | g0338 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18977 | hp2 | a0001 | c0004 | t0001 | g0317 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18979 | hp2 | a0001 | c0004 | t0035 | g0193 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18984 | hp1 | a0001 | c0004 | t0006 | g0207 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18986 | hp1 | a0004 | c0009 | t0001 | g0355 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0330 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18993 | hp1 | a0001 | c0003 | t0007 | g0213 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18993 | hp2 | a0001 | c0002 | t0006 | g0206 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18995 | hp2 | a0001 | c0003 | t0006 | g0217 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18999 | hp2 | a0001 | c0005 | t0009 | g0356 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19000 | hp2 | a0001 | c0004 | t0017 | g0215 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19002 | hp1 | a0001 | c0001 | t0030 | g0022 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19002 | hp2 | a0001 | c0004 | t0002 | g0083 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19004 | hp1 | a0001 | c0004 | t0002 | g0100 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0126 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19005 | hp2 | a0001 | c0004 | t0007 | g0208 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0305 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19011 | hp1 | a0001 | c0004 | t0032 | g0162 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0082 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19012 | hp1 | a0001 | c0003 | t0010 | g0313 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0328 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0318 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19043 | hp2 | a0001 | c0003 | t0006 | g0222 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0306 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19057 | hp2 | a0001 | c0001 | t0011 | g0197 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19063 | hp1 | a0001 | c0005 | t0002 | g0290 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19063 | hp2 | a0001 | c0005 | t0008 | g0199 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19067 | hp1 | a0001 | c0001 | t0034 | g0041 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19067 | hp2 | a0001 | c0012 | t0015 | g0210 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19068 | hp2 | a0001 | c0005 | t0002 | g0015 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19070 | hp2 | a0001 | c0006 | t0001 | g0006 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19074 | hp2 | a0001 | c0005 | t0002 | g0124 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0286 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19080 | hp2 | a0001 | c0004 | t0003 | g0195 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19084 | hp2 | a0001 | c0003 | t0026 | g0308 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19087 | hp1 | a0001 | c0004 | t0001 | g0026 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19087 | hp2 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19088 | hp2 | a0001 | c0005 | t0002 | g0291 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19090 | hp2 | a0001 | c0004 | t0002 | g0335 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0009 | AFR | YRI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | YRI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0231 | AFR | ASW | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20129 | hp2 | a0001 | c0001 | t0033 | g0074 | AFR | ASW | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0073 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0177 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0283 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | GIH | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20905 | hp2 | a0001 | c0015 | t0052 | g0203 | SAS | GIH | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01123 | hp2 | a0001 | c0006 | t0031 | g0268 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0259 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02109 | hp2 | a0001 | c0005 | t0002 | g0235 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0263 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02486 | hp2 | a0001 | c0005 | t0006 | g0218 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03471 | hp1 | a0001 | c0001 | t0036 | g0285 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG06807 | hp1 | a0001 | c0004 | t0029 | g0227 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0201 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0194 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0044 | REF | REF | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| homoSapiens_grch38 | hp1 | a0003 | c0010 | t0001 | g0063 | REF | REF | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132166965
|
G | A | 1 | a0002 | 2 | HG00323.hp1 HG03834.hp2 |
missense_variant | MODERATE | c.134G>A | p.Arg45His | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/8 | 799/4673 | 134/1593 | 45/530 | chr9 | 132166965 | ||
| chr9:132198516
|
G | A | 1 | a0004 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.764G>A | p.Arg255Gln | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/8 | 1429/4673 | 764/1593 | 255/530 | chr9 | 132198516 | ||
| chr9:132230577
|
A | G | 4 | a0001a0002a0004others(1): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
missense_variant | MODERATE | c.1036A>G | p.Thr346Ala | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/8 | 1701/4673 | 1036/1593 | 346/530 | chr9 | 132230577 | ||
| chr9:132241926
|
C | A | 1 | a0005 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1408C>A | p.Leu470Met | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 2073/4673 | 1408/1593 | 470/530 | chr9 | 132241926 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132198469
|
C | T | 1 | a0001c0015 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.717C>T | p.Ser239Ser | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/8 | 1382/4673 | 717/1593 | 239/530 | chr9 | 132198469 | ||
| chr9:132198490
|
C | T | 8 | a0001c0003a0001c0004a0001c0012others(5): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
synonymous_variant | LOW | c.738C>T | p.Phe246Phe | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/8 | 1403/4673 | 738/1593 | 246/530 | chr9 | 132198490 | ||
| chr9:132198556
|
G | A | 1 | a0001c0012 | 1 | NA19067.hp2 | synonymous_variant | LOW | c.804G>A | p.Arg268Arg | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/8 | 1469/4673 | 804/1593 | 268/530 | chr9 | 132198556 | ||
| chr9:132198580
|
C | T | 3 | a0001c0005a0001c0006a0004c0009 | 29 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(26): Show |
synonymous_variant | LOW | c.828C>T | p.Tyr276Tyr | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/8 | 1493/4673 | 828/1593 | 276/530 | chr9 | 132198580 | ||
| chr9:132226867
|
C | T | 8 | a0001c0002a0001c0003a0001c0005others(5): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
synonymous_variant | LOW | c.876C>T | p.His292His | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/8 | 1541/4673 | 876/1593 | 292/530 | chr9 | 132226867 | ||
| chr9:132226888
|
C | T | 1 | a0001c0014 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.897C>T | p.Arg299Arg | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/8 | 1562/4673 | 897/1593 | 299/530 | chr9 | 132226888 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132162064
|
A | ACGGCGGC others(2): Show |
3 | a0001c0002t0014a0001c0003t0014a0001c0004t0053 | 4 | HG00140.hp2 HG00280.hp1 HG01516.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-648_-640dupGGCGGC others(3): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/8 | 4748 | INFO_REALIGN_3_PRIME | chr9 | 132162064 | ||||
| chr9:132162184
|
G | A | 1 | a0001c0001t0019 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-539G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/8 | 4648 | chr9 | 132162184 | |||||
| chr9:132162218
|
C | T | 1 | a0001c0015t0052 | 1 | NA20905.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-505C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/8 | chr9 | 132162218 | ||||||
| chr9:132166409
|
C | G | 3 | a0001c0001t0050a0001c0001t0051a0001c0002t0049 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
5_prime_UTR_variant | MODIFIER | c.-423C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/8 | 423 | chr9 | 132166409 | |||||
| chr9:132166759
|
C | T | 1 | a0001c0001t0048 | 1 | HG00741.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-73C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/8 | chr9 | 132166759 | ||||||
| chr9:132166779
|
G | A | 19 | a0001c0001t0006a0001c0001t0007a0001c0001t0016others(16): Show | 26 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-53G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/8 | 53 | chr9 | 132166779 | |||||
| chr9:132166809
|
G | A | 2 | a0001c0003t0010a0001c0003t0026 | 5 | HG02015.hp1 NA18948.hp1 NA18963.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-23G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/8 | 23 | chr9 | 132166809 | |||||
| chr9:132242188
|
C | G | 1 | a0001c0004t0047 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 77 | chr9 | 132242188 | |||||
| chr9:132242201
|
G | A | 2 | a0001c0001t0027a0001c0004t0028 | 2 | HG02155.hp1 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*90G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 90 | chr9 | 132242201 | |||||
| chr9:132242247
|
G | C | 1 | a0001c0004t0047 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 136 | chr9 | 132242247 | |||||
| chr9:132242308
|
G | A | 2 | a0001c0001t0020a0001c0004t0029 | 2 | HG03139.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*197G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 197 | chr9 | 132242308 | |||||
| chr9:132242354
|
G | A | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(37): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*243G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 243 | chr9 | 132242354 | |||||
| chr9:132242355
|
C | T | 3 | a0001c0001t0009a0001c0002t0009a0001c0005t0009 | 5 | HG00280.hp2 HG01243.hp2 HG02683.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*244C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 244 | chr9 | 132242355 | |||||
| chr9:132242389
|
C | CT | 13 | a0001c0001t0008a0001c0001t0013a0001c0001t0016others(10): Show | 18 | HG00738.hp2 HG01884.hp2 HG01981.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*295dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 296 | INFO_REALIGN_3_PRIME | chr9 | 132242389 | ||||
| chr9:132242389
|
CT | C | 26 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(23): Show | 124 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*295delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 295 | INFO_REALIGN_3_PRIME | chr9 | 132242389 | ||||
| chr9:132242749
|
G | A | 1 | a0001c0001t0030 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 638 | chr9 | 132242749 | |||||
| chr9:132243060
|
CA | C | 23 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(20): Show | 111 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*950delA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 950 | chr9 | 132243060 | |||||
| chr9:132243158
|
A | C | 1 | a0001c0001t0034 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1047A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1047 | chr9 | 132243158 | |||||
| chr9:132243197
|
T | G | 49 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(46): Show | 190 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1086T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1086 | chr9 | 132243197 | |||||
| chr9:132243355
|
C | T | 1 | a0001c0001t0033 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1244C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1244 | chr9 | 132243355 | |||||
| chr9:132243520
|
C | T | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(37): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1409C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1409 | chr9 | 132243520 | |||||
| chr9:132243590
|
G | C | 49 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(46): Show | 190 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*1479G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1479 | chr9 | 132243590 | |||||
| chr9:132243591
|
T | C | 4 | a0001c0001t0013a0001c0001t0016a0001c0001t0042others(1): Show | 6 | HG02486.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1480T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1480 | chr9 | 132243591 | |||||
| chr9:132243629
|
G | A | 1 | a0001c0004t0035 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1518G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1518 | chr9 | 132243629 | |||||
| chr9:132243657
|
A | G | 1 | a0001c0001t0018 | 2 | HG01074.hp2 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1546A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1546 | chr9 | 132243657 | |||||
| chr9:132243831
|
A | G | 1 | a0001c0004t0032 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1720A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1720 | chr9 | 132243831 | |||||
| chr9:132243884
|
C | A | 1 | a0001c0001t0027 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1773C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1773 | chr9 | 132243884 | |||||
| chr9:132243938
|
C | T | 1 | a0001c0006t0031 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1827C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1827 | chr9 | 132243938 | |||||
| chr9:132244010
|
A | C | 6 | a0001c0001t0012a0001c0001t0020a0001c0001t0051others(3): Show | 8 | HG02145.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1899A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1899 | chr9 | 132244010 | |||||
| chr9:132244085
|
C | G | 52 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(49): Show | 193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1974C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 1974 | chr9 | 132244085 | |||||
| chr9:132244197
|
G | A | 23 | a0001c0001t0002a0001c0001t0007a0001c0001t0011others(20): Show | 111 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2086G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 2086 | chr9 | 132244197 | |||||
| chr9:132244266
|
T | C | 12 | a0001c0001t0012a0001c0001t0013a0001c0001t0016others(9): Show | 16 | HG01884.hp2 HG02145.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2155T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 2155 | chr9 | 132244266 | |||||
| chr9:132244339
|
T | C | 1 | a0001c0001t0043 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2228T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 2228 | chr9 | 132244339 | |||||
| chr9:132244368
|
T | C | 6 | a0001c0001t0013a0001c0001t0016a0001c0001t0042others(3): Show | 8 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2257T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 2257 | chr9 | 132244368 | |||||
| chr9:132244460
|
A | G | 7 | a0001c0001t0013a0001c0001t0016a0001c0001t0042others(4): Show | 9 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2349A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 2349 | chr9 | 132244460 | |||||
| chr9:132244470
|
G | A | 3 | a0001c0001t0005a0001c0001t0050a0001c0002t0005 | 12 | HG01081.hp1 HG01106.hp1 HG02809.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2359G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 8/8 | 2359 | chr9 | 132244470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132162423
|
A | G | 157 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0204others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.-484+184A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162423 | ||||||
| chr9:132162521
|
G | A | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-484+282G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162521 | ||||||
| chr9:132162535
|
A | AGT | 14 | a0001c0001t0004g0260a0001c0001t0006g0221a0001c0001t0011g0197others(11): Show | 14 | HG01516.hp2 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-484+316_-484+317d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162535 | |||||
| chr9:132162535
|
A | T | 13 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0001t0002g0348others(10): Show | 13 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-484+296A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162535 | ||||||
| chr9:132162537
|
T | A | 1 | a0001c0004t0003g0202 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-484+298T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162537 | ||||||
| chr9:132162555
|
T | A | 1 | a0001c0004t0002g0003 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-484+316T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162555 | ||||||
| chr9:132162555
|
T | TGTGA | 12 | a0001c0001t0002g0223a0001c0001t0005g0234a0001c0001t0011g0231others(9): Show | 12 | HG01106.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-484+317_-484+318i others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162555 | |||||
| chr9:132162555
|
T | TGTGAGA | 3 | a0001c0001t0001g0346a0001c0002t0049g0238a0001c0005t0040g0239 | 3 | HG02735.hp2 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-484+317_-484+318i others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162555 | |||||
| chr9:132162555
|
T | TGTGTGA | 10 | a0001c0001t0005g0265a0001c0001t0005g0266a0001c0001t0013g0264others(7): Show | 10 | HG01123.hp2 HG02647.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.-484+317_-484+318i others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162555 | |||||
| chr9:132162555
|
T | TGTGTGAG others(1): Show |
34 | a0001c0001t0002g0281a0001c0001t0003g0283a0001c0001t0036g0285others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-484+317_-484+318i others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162555 | |||||
| chr9:132162555
|
T | TGTGTGTG others(1): Show |
3 | a0001c0001t0004g0301a0001c0001t0020g0302a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-484+317_-484+318i others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162555 | |||||
| chr9:132162557
|
A | T | 89 | a0001c0001t0001g0196a0001c0001t0001g0343a0001c0001t0002g0204others(86): Show | 90 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.-484+318A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162557 | ||||||
| chr9:132162559
|
A | T | 65 | a0001c0001t0001g0343a0001c0001t0002g0348a0001c0001t0003g0251others(62): Show | 66 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.-484+320A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162559 | ||||||
| chr9:132162561
|
A | T | 42 | a0001c0001t0001g0343a0001c0001t0003g0320a0001c0001t0003g0321others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.-484+322A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162561 | ||||||
| chr9:132162563
|
A | T | 2 | a0001c0001t0001g0343a0001c0003t0002g0342 | 2 | NA18951.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-484+324A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162563 | ||||||
| chr9:132162564
|
GAC | G | 56 | a0001c0001t0001g0343a0001c0001t0003g0251a0001c0001t0003g0320others(53): Show | 57 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-484+327_-484+328d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162564 | |||||
| chr9:132162566
|
C | G | 51 | a0001c0001t0001g0196a0001c0001t0001g0346a0001c0001t0002g0204others(48): Show | 51 | HG00423.hp1 HG01074.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.-484+327C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162566 | ||||||
| chr9:132162568
|
G | C | 15 | a0001c0001t0001g0196a0001c0001t0001g0346a0001c0001t0005g0234others(12): Show | 15 | HG01106.hp1 HG01123.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-484+329G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162568 | ||||||
| chr9:132162569
|
A | AGAGTGT | 3 | a0001c0001t0011g0007a0001c0006t0001g0005a0001c0006t0001g0006 | 3 | HG02027.hp2 HG02132.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-484+331_-484+332i others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGAGTGTG others(3): Show |
1 | a0001c0003t0002g0008 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-484+331_-484+332i others(12): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGT | 37 | a0001c0001t0001g0095a0001c0001t0001g0109a0001c0001t0001g0111others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-484+377_-484+378d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGT | 43 | a0001c0001t0001g0129a0001c0001t0001g0140a0001c0001t0001g0143others(40): Show | 43 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-484+375_-484+378d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGTGT | 37 | a0001c0001t0001g0155a0001c0001t0001g0169a0001c0001t0002g0161others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.-484+373_-484+378d others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGTGTG others(1): Show |
10 | a0001c0001t0003g0174a0001c0001t0003g0176a0001c0001t0003g0177others(7): Show | 10 | HG00140.hp2 HG00621.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-484+371_-484+378d others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGTGTG others(3): Show |
5 | a0001c0001t0002g0179a0001c0001t0002g0182a0001c0002t0001g0180others(2): Show | 5 | HG02129.hp1 HG03516.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-484+369_-484+378d others(12): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGTGTG others(5): Show |
6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0184others(3): Show | 6 | HG01975.hp2 HG02300.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-484+367_-484+378d others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGTGTG others(7): Show |
5 | a0001c0001t0001g0191a0001c0002t0001g0190a0001c0002t0001g0192others(2): Show | 5 | HG02148.hp2 HG02572.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-484+365_-484+378d others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGTGTG others(9): Show |
1 | a0001c0002t0005g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-484+363_-484+378d others(18): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | AGTGTGTG others(11): Show |
1 | a0001c0004t0003g0195 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-484+361_-484+378d others(20): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
A | T | 1 | a0001c0002t0002g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-484+330A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162569 | ||||||
| chr9:132162569
|
AGT | A | 25 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0047others(22): Show | 26 | HG00408.hp1 HG00597.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-484+377_-484+378d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
AGTGT | A | 23 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0002g0348others(20): Show | 23 | HG01081.hp1 HG01256.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.-484+375_-484+378d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
AGTGTGT | A | 14 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0021others(11): Show | 14 | HG00609.hp2 HG01074.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-484+373_-484+378d others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-484+367_-484+378d others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0002g0012 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-484+365_-484+378d others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-484+363_-484+378d others(18): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162569
|
AGTGTGTG others(11): Show |
A | 2 | a0001c0001t0001g0010a0001c0001t0013g0009 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-484+361_-484+378d others(20): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132162569 | |||||
| chr9:132162570
|
G | C | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0003t0006g0219 | 3 | HG00423.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-484+331G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162570 | ||||||
| chr9:132162571
|
T | A | 90 | a0001c0001t0001g0196a0001c0001t0001g0343a0001c0001t0001g0346others(87): Show | 91 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.-484+332T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162571 | ||||||
| chr9:132162572
|
G | C | 22 | a0001c0001t0002g0344a0001c0001t0004g0260a0001c0001t0007g0212others(19): Show | 22 | HG00621.hp1 HG01167.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.-484+333G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162572 | ||||||
| chr9:132162573
|
T | A | 76 | a0001c0001t0001g0196a0001c0001t0001g0343a0001c0001t0002g0344others(73): Show | 77 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.-484+334T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162573 | ||||||
| chr9:132162574
|
G | C | 6 | a0001c0001t0012g0257a0001c0002t0001g0258a0001c0002t0004g0256others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-484+335G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162574 | ||||||
| chr9:132162575
|
T | A | 83 | a0001c0001t0001g0343a0001c0001t0002g0344a0001c0001t0002g0348others(80): Show | 84 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.-484+336T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162575 | ||||||
| chr9:132162576
|
G | C | 7 | a0001c0001t0003g0251a0001c0001t0004g0340a0001c0002t0001g0253others(4): Show | 7 | HG02818.hp1 HG02897.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-484+337G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162576 | ||||||
| chr9:132162577
|
T | A | 65 | a0001c0001t0001g0343a0001c0001t0002g0348a0001c0001t0003g0251others(62): Show | 66 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.-484+338T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162577 | ||||||
| chr9:132162578
|
G | C | 45 | a0001c0001t0002g0348a0001c0001t0003g0320a0001c0001t0003g0321others(42): Show | 46 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.-484+339G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162578 | ||||||
| chr9:132162579
|
T | A | 59 | a0001c0001t0001g0343a0001c0001t0002g0348a0001c0001t0003g0251others(56): Show | 60 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.-484+340T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162579 | ||||||
| chr9:132162580
|
G | C | 5 | a0001c0001t0001g0343a0001c0002t0002g0243a0001c0002t0002g0244others(2): Show | 5 | HG01074.hp1 HG01175.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-484+341G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162580 | ||||||
| chr9:132162581
|
T | A | 52 | a0001c0001t0001g0343a0001c0001t0002g0348a0001c0001t0003g0320others(49): Show | 53 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.-484+342T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162581 | ||||||
| chr9:132162582
|
G | C | 3 | a0001c0001t0002g0204a0001c0002t0009g0304a0001c0005t0002g0303 | 3 | HG01192.hp1 HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-484+343G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162582 | ||||||
| chr9:132162583
|
T | A | 8 | a0001c0001t0001g0343a0001c0001t0002g0204a0001c0002t0002g0243others(5): Show | 8 | HG01074.hp1 HG01175.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-484+344T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162583 | ||||||
| chr9:132162585
|
T | A | 3 | a0001c0001t0002g0204a0001c0002t0009g0304a0001c0005t0002g0303 | 3 | HG01192.hp1 HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-484+346T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162585 | ||||||
| chr9:132162586
|
G | C | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-484+347G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162586 | ||||||
| chr9:132162587
|
T | A | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-484+348T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162587 | ||||||
| chr9:132162589
|
T | A | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-484+350T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162589 | ||||||
| chr9:132162602
|
GTGTGTGT others(8): Show |
G | 1 | a0001c0002t0001g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-484+364_-484+378d others(17): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162602 | ||||||
| chr9:132162689
|
C | T | 1 | a0001c0005t0001g0269 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-484+450C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162689 | ||||||
| chr9:132162774
|
G | T | 1 | a0001c0002t0044g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-484+535G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162774 | ||||||
| chr9:132162783
|
A | G | 1 | a0001c0004t0025g0225 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-484+544A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162783 | ||||||
| chr9:132162804
|
G | A | 59 | a0001c0001t0001g0343a0001c0001t0003g0251a0001c0001t0003g0320others(56): Show | 60 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.-484+565G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162804 | ||||||
| chr9:132162864
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-484+625G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162864 | ||||||
| chr9:132162906
|
G | T | 7 | a0001c0001t0002g0348a0001c0001t0011g0007a0001c0005t0008g0349others(4): Show | 7 | HG02027.hp1 HG02132.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.-484+667G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132162906 | ||||||
| chr9:132163073
|
G | A | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-484+834G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163073 | ||||||
| chr9:132163199
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-484+960G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163199 | ||||||
| chr9:132163384
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0003g0037a0001c0001t0003g0038others(2): Show | 5 | HG02683.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.-484+1145G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163384 | ||||||
| chr9:132163409
|
C | CG | 9 | a0001c0001t0001g0034a0001c0002t0001g0094a0001c0002t0001g0172others(6): Show | 9 | HG00597.hp1 HG01192.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-484+1176dupG | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132163409 | |||||
| chr9:132163576
|
C | A | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-484+1337C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163576 | ||||||
| chr9:132163621
|
G | A | 2 | a0001c0001t0003g0056a0001c0002t0002g0096 | 2 | HG02040.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-484+1382G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163621 | ||||||
| chr9:132163667
|
C | G | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0004g0301others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(32): Show |
intron_variant | MODIFIER | c.-484+1428C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163667 | ||||||
| chr9:132163717
|
G | A | 4 | a0001c0001t0002g0184a0001c0002t0001g0173a0001c0002t0001g0190others(1): Show | 4 | HG01952.hp2 HG01975.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.-484+1478G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163717 | ||||||
| chr9:132163768
|
G | A | 1 | a0001c0002t0001g0307 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-484+1529G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163768 | ||||||
| chr9:132163775
|
G | A | 1 | a0001c0003t0006g0219 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-484+1536G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163775 | ||||||
| chr9:132163816
|
G | A | 1 | a0001c0002t0001g0013 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-484+1577G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163816 | ||||||
| chr9:132163983
|
G | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-484+1744G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132163983 | ||||||
| chr9:132164051
|
G | A | 1 | a0001c0002t0002g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-484+1812G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164051 | ||||||
| chr9:132164083
|
T | C | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-484+1844T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164083 | ||||||
| chr9:132164128
|
G | GT | 6 | a0001c0001t0005g0265a0001c0001t0005g0266a0001c0001t0013g0263others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-484+1890dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132164128 | |||||
| chr9:132164169
|
T | C | 44 | a0001c0001t0002g0281a0001c0001t0003g0283a0001c0001t0005g0234others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-484+1930T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164169 | ||||||
| chr9:132164221
|
T | A | 59 | a0001c0001t0001g0343a0001c0001t0003g0251a0001c0001t0003g0320others(56): Show | 60 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.-484+1982T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164221 | ||||||
| chr9:132164288
|
G | T | 1 | a0001c0001t0020g0302 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-484+2049G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164288 | ||||||
| chr9:132164649
|
G | T | 150 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0204others(147): Show | 151 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-483-1700G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164649 | ||||||
| chr9:132164706
|
T | C | 33 | a0001c0001t0002g0281a0001c0001t0003g0283a0001c0002t0001g0280others(30): Show | 33 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-483-1643T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164706 | ||||||
| chr9:132164861
|
G | T | 1 | a0001c0003t0001g0296 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-483-1488G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132164861 | ||||||
| chr9:132165084
|
A | C | 2 | a0001c0002t0001g0151a0001c0002t0001g0152 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-483-1265A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165084 | ||||||
| chr9:132165213
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-483-1136C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165213 | ||||||
| chr9:132165338
|
A | G | 1 | a0001c0004t0002g0338 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-483-1011A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165338 | ||||||
| chr9:132165356
|
ACAG | A | 9 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0002t0002g0272others(6): Show | 9 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.-483-990_-483-988d others(5): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 132165356 | |||||
| chr9:132165396
|
C | G | 1 | a0001c0004t0025g0225 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-483-953C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165396 | ||||||
| chr9:132165678
|
C | G | 1 | a0001c0002t0001g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-483-671C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165678 | ||||||
| chr9:132165762
|
G | A | 1 | a0001c0003t0026g0308 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-483-587G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165762 | ||||||
| chr9:132165845
|
G | T | 1 | a0001c0004t0035g0193 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-483-504G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165845 | ||||||
| chr9:132165881
|
C | T | 1 | a0001c0001t0030g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-483-468C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165881 | ||||||
| chr9:132165945
|
C | T | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-483-404C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165945 | ||||||
| chr9:132165959
|
C | T | 1 | a0001c0001t0012g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-483-390C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132165959 | ||||||
| chr9:132166085
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-483-264T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 1/7 | chr9 | 132166085 | ||||||
| chr9:132167129
|
G | A | 1 | a0001c0003t0004g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.213+85G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167129 | ||||||
| chr9:132167193
|
G | A | 33 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(30): Show | 33 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.213+149G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167193 | ||||||
| chr9:132167268
|
C | T | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+224C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167268 | ||||||
| chr9:132167340
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0003g0251a0001c0001t0004g0301others(2): Show | 5 | HG01071.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+296G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167340 | ||||||
| chr9:132167498
|
A | G | 176 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0092others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.213+454A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167498 | ||||||
| chr9:132167574
|
G | A | 1 | a0001c0002t0003g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.213+530G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167574 | ||||||
| chr9:132167798
|
C | A | 8 | a0001c0001t0002g0097a0001c0002t0001g0120a0001c0002t0001g0121others(5): Show | 8 | HG00738.hp1 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.213+754C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167798 | ||||||
| chr9:132167816
|
G | A | 2 | a0001c0002t0002g0243a0001c0002t0002g0244 | 2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.213+772G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167816 | ||||||
| chr9:132167828
|
C | G | 2 | a0001c0006t0001g0284a0001c0006t0001g0295 | 2 | HG02165.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.213+784C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167828 | ||||||
| chr9:132167897
|
G | A | 1 | a0001c0004t0001g0023 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.213+853G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167897 | ||||||
| chr9:132167924
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.213+880G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167924 | ||||||
| chr9:132167950
|
G | A | 33 | a0001c0001t0001g0346a0001c0001t0002g0092a0001c0001t0002g0093others(30): Show | 33 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.213+906G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167950 | ||||||
| chr9:132167977
|
C | T | 1 | a0001c0001t0020g0302 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.213+933C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132167977 | ||||||
| chr9:132168125
|
G | C | 1 | a0001c0001t0012g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.213+1081G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168125 | ||||||
| chr9:132168132
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.213+1088G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168132 | ||||||
| chr9:132168146
|
G | A | 1 | a0001c0002t0006g0206 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.213+1102G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168146 | ||||||
| chr9:132168255
|
G | T | 2 | a0001c0003t0002g0248a0001c0004t0041g0249 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.213+1211G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168255 | ||||||
| chr9:132168500
|
T | C | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+1456T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168500 | ||||||
| chr9:132168559
|
G | A | 1 | a0001c0002t0006g0206 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.213+1515G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168559 | ||||||
| chr9:132168589
|
A | G | 179 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(176): Show | 180 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.213+1545A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168589 | ||||||
| chr9:132168648
|
A | G | 183 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(180): Show | 184 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.213+1604A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168648 | ||||||
| chr9:132168695
|
G | A | 2 | a0001c0001t0003g0251a0001c0003t0004g0250 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.213+1651G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168695 | ||||||
| chr9:132168756
|
G | A | 5 | a0001c0001t0002g0059a0001c0001t0043g0060a0001c0002t0001g0001others(2): Show | 6 | HG01168.hp2 HG01169.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.213+1712G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132168756 | ||||||
| chr9:132169164
|
G | T | 2 | a0001c0001t0008g0087a0001c0001t0018g0088 | 2 | HG00738.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.213+2120G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169164 | ||||||
| chr9:132169186
|
C | T | 1 | a0001c0001t0002g0189 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.213+2142C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169186 | ||||||
| chr9:132169192
|
C | T | 13 | a0001c0001t0001g0114a0001c0001t0001g0169a0001c0001t0002g0148others(10): Show | 13 | HG00099.hp1 HG01346.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.213+2148C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169192 | ||||||
| chr9:132169450
|
T | C | 3 | a0001c0002t0001g0170a0001c0002t0001g0200a0001c0005t0002g0235 | 3 | HG01884.hp1 HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.213+2406T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169450 | ||||||
| chr9:132169507
|
T | C | 33 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(30): Show | 33 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.213+2463T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169507 | ||||||
| chr9:132169706
|
G | A | 19 | a0001c0001t0006g0221a0001c0001t0007g0212a0001c0002t0001g0152others(16): Show | 19 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.213+2662G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169706 | ||||||
| chr9:132169741
|
C | T | 1 | a0001c0001t0006g0221 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+2697C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169741 | ||||||
| chr9:132169745
|
G | T | 1 | a0001c0001t0005g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+2701G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169745 | ||||||
| chr9:132169943
|
C | T | 1 | a0001c0004t0025g0225 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+2899C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132169943 | ||||||
| chr9:132170050
|
C | T | 2 | a0001c0002t0001g0336a0001c0002t0001g0337 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.213+3006C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170050 | ||||||
| chr9:132170067
|
T | C | 178 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(175): Show | 179 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.213+3023T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170067 | ||||||
| chr9:132170102
|
C | T | 1 | a0001c0001t0005g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.213+3058C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170102 | ||||||
| chr9:132170128
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0003g0251 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+3084G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170128 | ||||||
| chr9:132170132
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.213+3088G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170132 | ||||||
| chr9:132170367
|
G | A | 177 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(174): Show | 178 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.213+3323G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170367 | ||||||
| chr9:132170466
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.213+3422G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170466 | ||||||
| chr9:132170585
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.213+3541G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170585 | ||||||
| chr9:132170598
|
C | G | 176 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(173): Show | 177 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.213+3554C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170598 | ||||||
| chr9:132170682
|
G | A | 44 | a0001c0001t0002g0182a0001c0001t0002g0281a0001c0001t0003g0251others(41): Show | 44 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.213+3638G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170682 | ||||||
| chr9:132170702
|
C | T | 2 | a0001c0001t0016g0224a0001c0003t0006g0222 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.213+3658C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170702 | ||||||
| chr9:132170725
|
G | A | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+3681G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170725 | ||||||
| chr9:132170893
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.213+3849G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170893 | ||||||
| chr9:132170899
|
G | T | 2 | a0001c0001t0001g0111a0001c0002t0009g0112 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.213+3855G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170899 | ||||||
| chr9:132170940
|
G | T | 34 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(31): Show |
intron_variant | MODIFIER | c.213+3896G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132170940 | ||||||
| chr9:132171064
|
G | A | 1 | a0001c0002t0001g0312 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.213+4020G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171064 | ||||||
| chr9:132171334
|
G | C | 116 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(113): Show | 117 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.213+4290G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171334 | ||||||
| chr9:132171498
|
C | T | 44 | a0001c0001t0002g0182a0001c0001t0002g0281a0001c0001t0003g0251others(41): Show | 44 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.213+4454C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171498 | ||||||
| chr9:132171543
|
G | T | 45 | a0001c0001t0002g0182a0001c0001t0002g0281a0001c0001t0003g0251others(42): Show | 45 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.213+4499G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171543 | ||||||
| chr9:132171640
|
G | T | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.213+4596G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171640 | ||||||
| chr9:132171662
|
T | C | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+4618T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171662 | ||||||
| chr9:132171773
|
C | T | 1 | a0001c0001t0016g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.213+4729C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171773 | ||||||
| chr9:132171776
|
C | T | 3 | a0001c0001t0003g0283a0001c0006t0001g0271a0001c0006t0031g0268 | 3 | HG01123.hp2 HG01175.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.213+4732C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171776 | ||||||
| chr9:132171853
|
C | G | 3 | a0001c0001t0004g0301a0001c0002t0002g0300a0001c0003t0004g0250 | 3 | HG02451.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.213+4809C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171853 | ||||||
| chr9:132171858
|
G | A | 1 | a0001c0001t0011g0061 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.213+4814G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171858 | ||||||
| chr9:132171886
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.213+4842C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171886 | ||||||
| chr9:132171887
|
G | A | 1 | a0001c0003t0003g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.213+4843G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171887 | ||||||
| chr9:132171918
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.213+4874C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132171918 | ||||||
| chr9:132172087
|
C | T | 2 | a0001c0001t0002g0182a0001c0001t0003g0251 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+5043C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172087 | ||||||
| chr9:132172205
|
C | G | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+5161C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172205 | ||||||
| chr9:132172236
|
C | A | 1 | a0001c0001t0030g0022 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.213+5192C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172236 | ||||||
| chr9:132172390
|
T | A | 2 | a0001c0002t0001g0170a0001c0005t0002g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.213+5346T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172390 | ||||||
| chr9:132172492
|
T | G | 3 | a0001c0001t0004g0301a0001c0002t0002g0300a0001c0003t0004g0250 | 3 | HG02451.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.213+5448T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172492 | ||||||
| chr9:132172722
|
A | AT | 161 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0034others(158): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.213+5702dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132172722 | |||||
| chr9:132172722
|
A | ATT | 103 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0049others(100): Show | 103 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.213+5701_213+5702d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132172722 | |||||
| chr9:132172722
|
A | ATTT | 26 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0109others(23): Show | 26 | HG02080.hp2 HG02145.hp1 HG02572.hp2 others(23): Show |
intron_variant | MODIFIER | c.213+5700_213+5702d others(5): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132172722 | |||||
| chr9:132172753
|
A | G | 2 | a0001c0002t0001g0170a0001c0005t0002g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.213+5709A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172753 | ||||||
| chr9:132172760
|
C | T | 1 | a0001c0001t0033g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.213+5716C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172760 | ||||||
| chr9:132172804
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.213+5760G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172804 | ||||||
| chr9:132172830
|
C | T | 2 | a0001c0002t0001g0134a0001c0002t0002g0107 | 2 | NA18941.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.213+5786C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172830 | ||||||
| chr9:132172831
|
G | A | 39 | a0001c0001t0002g0182a0001c0001t0002g0204a0001c0001t0002g0223others(36): Show | 39 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.213+5787G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132172831 | ||||||
| chr9:132173131
|
G | A | 17 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0001t0002g0348others(14): Show | 17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.213+6087G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173131 | ||||||
| chr9:132173145
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0003g0251 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+6101G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173145 | ||||||
| chr9:132173172
|
G | A | 34 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(31): Show |
intron_variant | MODIFIER | c.213+6128G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173172 | ||||||
| chr9:132173363
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.213+6319C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173363 | ||||||
| chr9:132173447
|
T | C | 329 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(326): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.213+6403T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173447 | ||||||
| chr9:132173502
|
C | T | 161 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(158): Show | 162 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.213+6458C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173502 | ||||||
| chr9:132173591
|
T | C | 13 | a0001c0002t0002g0276a0001c0002t0014g0294a0001c0003t0001g0149others(10): Show | 13 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+6547T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173591 | ||||||
| chr9:132173641
|
T | C | 161 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(158): Show | 162 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.213+6597T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173641 | ||||||
| chr9:132173681
|
T | C | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.213+6637T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173681 | ||||||
| chr9:132173717
|
G | A | 1 | a0001c0001t0003g0089 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.213+6673G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173717 | ||||||
| chr9:132173741
|
G | C | 2 | a0001c0002t0001g0170a0001c0005t0002g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.213+6697G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173741 | ||||||
| chr9:132173752
|
T | TGGAC | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+6714_213+6717d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132173752 | |||||
| chr9:132173757
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0003g0251 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+6713G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173757 | ||||||
| chr9:132173761
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0003g0251 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+6717G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173761 | ||||||
| chr9:132173781
|
C | G | 2 | a0001c0001t0004g0301a0001c0002t0002g0300 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.213+6737C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173781 | ||||||
| chr9:132173869
|
A | G | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+6825A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173869 | ||||||
| chr9:132173910
|
C | T | 3 | a0001c0001t0036g0285a0001c0002t0002g0272a0001c0004t0003g0273 | 3 | HG02257.hp2 HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.213+6866C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173910 | ||||||
| chr9:132173939
|
G | GCACCATG others(97): Show |
1 | a0001c0001t0002g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.213+6931_213+6932i others(106): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132173939 | |||||
| chr9:132173939
|
G | GCACCATG others(97): Show |
116 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.213+6931_213+6932i others(106): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132173939 | |||||
| chr9:132173971
|
C | T | 1 | a0001c0001t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.213+6927C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173971 | ||||||
| chr9:132173976
|
A | G | 158 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(155): Show | 159 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.213+6932A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173976 | ||||||
| chr9:132174017
|
C | T | 2 | a0001c0002t0001g0170a0001c0005t0002g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.213+6973C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174017 | ||||||
| chr9:132174036
|
G | A | 34 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(31): Show |
intron_variant | MODIFIER | c.213+6992G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174036 | ||||||
| chr9:132174043
|
A | ACACCATG others(47): Show |
3 | a0001c0001t0004g0301a0001c0002t0002g0300a0001c0003t0004g0250 | 3 | HG02451.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.213+7035_213+7088d others(56): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174043 | |||||
| chr9:132174067
|
C | T | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7023C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174067 | ||||||
| chr9:132174068
|
A | G | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7024A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174068 | ||||||
| chr9:132174071
|
CGGACAGA others(39): Show |
C | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+7073_213+7118d others(48): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174071 | |||||
| chr9:132174072
|
G | A | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7028G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174072 | ||||||
| chr9:132174076
|
A | G | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7032A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174076 | ||||||
| chr9:132174077
|
G | A | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7033G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174077 | ||||||
| chr9:132174086
|
A | G | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7042A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174086 | ||||||
| chr9:132174087
|
T | C | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7043T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174087 | ||||||
| chr9:132174095
|
C | T | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7051C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174095 | ||||||
| chr9:132174098
|
C | A | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.213+7054C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174098 | ||||||
| chr9:132174108
|
C | T | 19 | a0001c0001t0001g0346a0001c0001t0002g0182a0001c0001t0002g0344others(16): Show | 19 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.213+7064C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174108 | ||||||
| chr9:132174117
|
T | TGGACAGA others(1): Show |
38 | a0001c0001t0002g0182a0001c0001t0002g0204a0001c0001t0002g0223others(35): Show | 38 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.213+7081_213+7088d others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174117 | |||||
| chr9:132174143
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0003g0251 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+7099G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174143 | ||||||
| chr9:132174163
|
C | T | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7119C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174163 | ||||||
| chr9:132174168
|
G | A | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7124G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174168 | ||||||
| chr9:132174175
|
C | CAGACGGA others(5): Show |
2 | a0001c0002t0001g0170a0001c0005t0002g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.213+7133_213+7134i others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174175 | |||||
| chr9:132174175
|
C | CAGATGGA others(5): Show |
34 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(31): Show | 34 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(31): Show |
intron_variant | MODIFIER | c.213+7133_213+7134i others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174175 | |||||
| chr9:132174183
|
T | C | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7139T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174183 | ||||||
| chr9:132174186
|
A | C | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7142A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174186 | ||||||
| chr9:132174197
|
A | G | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7153A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174197 | ||||||
| chr9:132174201
|
T | G | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7157T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174201 | ||||||
| chr9:132174205
|
C | T | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7161C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174205 | ||||||
| chr9:132174213
|
T | C | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7169T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174213 | ||||||
| chr9:132174213
|
TGGAC | T | 6 | a0001c0001t0004g0301a0001c0001t0050g0237a0001c0001t0051g0236others(3): Show | 6 | HG02451.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+7178_213+7181d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174213 | |||||
| chr9:132174218
|
G | A | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7174G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174218 | ||||||
| chr9:132174229
|
C | T | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7185C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174229 | ||||||
| chr9:132174250
|
T | C | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7206T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174250 | ||||||
| chr9:132174256
|
AGATGGAT others(5): Show |
A | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7215_213+7226d others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174256 | |||||
| chr9:132174260
|
G | A | 2 | a0001c0002t0001g0120a0001c0002t0001g0121 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.213+7216G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174260 | ||||||
| chr9:132174263
|
T | C | 1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7219T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174263 | ||||||
| chr9:132174267
|
T | C | 1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7223T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174267 | ||||||
| chr9:132174272
|
A | G | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7228A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174272 | ||||||
| chr9:132174280
|
A | G | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7236A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174280 | ||||||
| chr9:132174283
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7239C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174283 | ||||||
| chr9:132174291
|
C | T | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7247C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174291 | ||||||
| chr9:132174294
|
C | A | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7250C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174294 | ||||||
| chr9:132174294
|
CACCATGC others(43): Show |
C | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+7261_213+7310d others(52): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174294 | |||||
| chr9:132174305
|
G | A | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7261G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174305 | ||||||
| chr9:132174309
|
G | T | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7265G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174309 | ||||||
| chr9:132174313
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7269C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174313 | ||||||
| chr9:132174317
|
C | CAGACGGA others(93): Show |
1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7273_213+7274i others(102): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174317 | ||||||
| chr9:132174317
|
C | CAGAT | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7273_213+7274i others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174317 | ||||||
| chr9:132174318
|
G | A | 1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7274G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174318 | ||||||
| chr9:132174326
|
G | A | 2 | a0001c0003t0002g0339a0001c0005t0006g0218 | 2 | HG01106.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.213+7282G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174326 | ||||||
| chr9:132174326
|
G | GGACA | 117 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.213+7292_213+7295d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174326 | |||||
| chr9:132174326
|
GGACA | G | 6 | a0001c0001t0002g0059a0001c0001t0030g0022a0001c0001t0043g0060others(3): Show | 7 | HG01168.hp2 HG01169.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.213+7292_213+7295d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174326 | |||||
| chr9:132174330
|
A | G | 1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7286A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174330 | ||||||
| chr9:132174336
|
A | G | 36 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(33): Show | 36 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7292A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174336 | ||||||
| chr9:132174341
|
T | C | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7297T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174341 | ||||||
| chr9:132174344
|
A | C | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7300A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174344 | ||||||
| chr9:132174354
|
C | T | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7310C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174354 | ||||||
| chr9:132174355
|
A | G | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7311A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174355 | ||||||
| chr9:132174359
|
T | G | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7315T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174359 | ||||||
| chr9:132174363
|
C | T | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7319C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174363 | ||||||
| chr9:132174364
|
G | T | 36 | a0001c0001t0001g0033a0001c0001t0001g0109a0001c0001t0001g0143others(33): Show | 36 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.213+7320G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174364 | ||||||
| chr9:132174367
|
C | T | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7323C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174367 | ||||||
| chr9:132174368
|
A | G | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7324A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174368 | ||||||
| chr9:132174376
|
G | A | 35 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+7332G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174376 | ||||||
| chr9:132174376
|
G | GGACGGAC others(47): Show |
1 | a0001c0002t0001g0152 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.213+7363_213+7364i others(56): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174376 | |||||
| chr9:132174417
|
A | G | 1 | a0001c0003t0003g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.213+7373A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174417 | ||||||
| chr9:132174578
|
G | C | 3 | a0001c0001t0002g0182a0001c0001t0003g0251a0001c0003t0004g0250 | 3 | HG02818.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+7534G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174578 | ||||||
| chr9:132174588
|
G | A | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+7544G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174588 | ||||||
| chr9:132174684
|
G | C | 1 | a0001c0003t0004g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.213+7640G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174684 | ||||||
| chr9:132174779
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.213+7735G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174779 | ||||||
| chr9:132174793
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0003g0251 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.213+7749G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174793 | ||||||
| chr9:132174885
|
G | A | 8 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0002t0002g0242others(5): Show | 8 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+7841G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132174885 | ||||||
| chr9:132174904
|
AGAGCAAG others(5): Show |
A | 116 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0281others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.213+7862_213+7873d others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174904 | |||||
| chr9:132174921
|
C | CA | 192 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(189): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.213+7888dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174921 | |||||
| chr9:132174921
|
C | CAAA | 37 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0004g0301others(34): Show | 37 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(34): Show |
intron_variant | MODIFIER | c.213+7886_213+7888d others(5): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132174921 | |||||
| chr9:132175146
|
T | C | 353 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(350): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.213+8102T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175146 | ||||||
| chr9:132175228
|
G | A | 2 | a0001c0001t0004g0301a0001c0002t0002g0300 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.213+8184G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175228 | ||||||
| chr9:132175306
|
G | T | 1 | a0001c0003t0001g0334 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.213+8262G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175306 | ||||||
| chr9:132175336
|
A | G | 166 | a0001c0001t0001g0031a0001c0001t0001g0343a0001c0001t0001g0346others(163): Show | 167 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.213+8292A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175336 | ||||||
| chr9:132175518
|
A | C | 1 | a0001c0002t0001g0333 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.213+8474A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175518 | ||||||
| chr9:132175519
|
G | C | 1 | a0001c0002t0001g0333 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.213+8475G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175519 | ||||||
| chr9:132175553
|
C | T | 5 | a0001c0001t0002g0223a0001c0001t0011g0231a0001c0003t0003g0233others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+8509C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175553 | ||||||
| chr9:132175554
|
A | G | 159 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(156): Show | 160 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.213+8510A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175554 | ||||||
| chr9:132175590
|
C | T | 1 | a0001c0002t0001g0052 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.213+8546C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132175590 | ||||||
| chr9:132175869
|
C | CA | 32 | a0001c0001t0002g0204a0001c0001t0002g0223a0001c0001t0006g0221others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.213+8826dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132175869 | |||||
| chr9:132176048
|
A | C | 2 | a0001c0002t0001g0282a0001c0004t0012g0279 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.213+9004A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176048 | ||||||
| chr9:132176117
|
G | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.213+9073G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176117 | ||||||
| chr9:132176184
|
C | CA | 83 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(80): Show | 84 | HG00558.hp2 HG00639.hp1 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.213+9151dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132176184 | |||||
| chr9:132176198
|
C | G | 17 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0001t0002g0348others(14): Show | 17 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.213+9154C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176198 | ||||||
| chr9:132176302
|
G | A | 1 | a0001c0002t0002g0350 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.213+9258G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176302 | ||||||
| chr9:132176304
|
T | G | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+9260T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176304 | ||||||
| chr9:132176376
|
C | T | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+9332C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176376 | ||||||
| chr9:132176426
|
G | A | 2 | a0001c0003t0002g0126a0001c0004t0001g0305 | 2 | NA19004.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.213+9382G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176426 | ||||||
| chr9:132176507
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.213+9463G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176507 | ||||||
| chr9:132176555
|
C | A | 87 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(84): Show | 88 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.213+9511C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176555 | ||||||
| chr9:132176821
|
A | G | 83 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(80): Show | 84 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.213+9777A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176821 | ||||||
| chr9:132176844
|
T | C | 1 | a0004c0009t0001g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.213+9800T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176844 | ||||||
| chr9:132176886
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.213+9842T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176886 | ||||||
| chr9:132176907
|
A | C | 1 | a0001c0006t0002g0354 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.213+9863A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176907 | ||||||
| chr9:132176996
|
G | T | 196 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(193): Show | 197 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.213+9952G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132176996 | ||||||
| chr9:132177052
|
T | C | 237 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(234): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.213+10008T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177052 | ||||||
| chr9:132177063
|
C | G | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+10019C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177063 | ||||||
| chr9:132177123
|
A | G | 3 | a0001c0001t0050g0237a0001c0001t0051g0236a0001c0002t0049g0238 | 3 | HG02895.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.213+10079A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177123 | ||||||
| chr9:132177223
|
A | G | 83 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(80): Show | 84 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.213+10179A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177223 | ||||||
| chr9:132177239
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.213+10195G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177239 | ||||||
| chr9:132177247
|
G | A | 4 | a0001c0001t0002g0115a0001c0001t0027g0053a0001c0002t0001g0171others(1): Show | 4 | HG00673.hp1 HG03688.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+10203G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177247 | ||||||
| chr9:132177308
|
C | G | 1 | a0001c0002t0002g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.213+10264C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177308 | ||||||
| chr9:132177472
|
G | A | 6 | a0001c0003t0010g0313a0001c0003t0010g0314a0001c0003t0010g0315others(3): Show | 6 | HG02015.hp1 NA18948.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+10428G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177472 | ||||||
| chr9:132177652
|
T | G | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.213+10608T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177652 | ||||||
| chr9:132177936
|
C | T | 62 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(59): Show | 62 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.213+10892C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132177936 | ||||||
| chr9:132178038
|
C | T | 1 | a0001c0001t0016g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.213+10994C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178038 | ||||||
| chr9:132178060
|
A | G | 4 | a0001c0001t0004g0301a0001c0002t0002g0300a0001c0002t0004g0259others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+11016A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178060 | ||||||
| chr9:132178152
|
G | A | 1 | a0001c0001t0034g0041 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.213+11108G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178152 | ||||||
| chr9:132178187
|
C | T | 1 | a0001c0005t0002g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.213+11143C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178187 | ||||||
| chr9:132178262
|
C | A | 2 | a0001c0001t0002g0018a0001c0002t0002g0030 | 2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.213+11218C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178262 | ||||||
| chr9:132178369
|
C | T | 84 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(81): Show | 85 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.213+11325C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178369 | ||||||
| chr9:132178513
|
T | C | 64 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(61): Show | 64 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.213+11469T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178513 | ||||||
| chr9:132178544
|
G | A | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+11500G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178544 | ||||||
| chr9:132178547
|
C | A | 83 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(80): Show | 84 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.213+11503C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178547 | ||||||
| chr9:132178711
|
C | T | 1 | a0001c0005t0002g0341 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.213+11667C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178711 | ||||||
| chr9:132178715
|
C | T | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+11671C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178715 | ||||||
| chr9:132178786
|
C | CA | 32 | a0001c0001t0001g0019a0001c0001t0001g0187a0001c0001t0002g0223others(29): Show | 32 | HG00735.hp2 HG00741.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.213+11762dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178786 | |||||
| chr9:132178786
|
CA | C | 35 | a0001c0001t0001g0047a0001c0001t0002g0204a0001c0001t0003g0056others(32): Show | 35 | HG00423.hp1 HG00621.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.213+11762delA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178786 | |||||
| chr9:132178786
|
CAAAAA | C | 21 | a0001c0001t0001g0346a0001c0001t0002g0020a0001c0001t0002g0344others(18): Show | 21 | HG01167.hp1 HG01361.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.213+11758_213+1176 others(9): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178786 | |||||
| chr9:132178786
|
CAAAAAA | C | 67 | a0001c0001t0001g0343a0001c0001t0003g0320a0001c0001t0003g0321others(64): Show | 68 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.213+11757_213+1176 others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178786 | |||||
| chr9:132178879
|
C | T | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+11835C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178879 | ||||||
| chr9:132178928
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0011g0231a0001c0003t0001g0288 | 3 | HG00639.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.213+11884C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132178928 | ||||||
| chr9:132178961
|
C | CA | 89 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0196others(86): Show | 90 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.213+11938dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178961 | |||||
| chr9:132178961
|
C | CAA | 16 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0001t0002g0348others(13): Show | 16 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.213+11937_213+1193 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178961 | |||||
| chr9:132178961
|
CA | C | 100 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(97): Show | 100 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.213+11938delA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178961 | |||||
| chr9:132178961
|
CAA | C | 26 | a0001c0001t0002g0204a0001c0001t0007g0212a0001c0001t0016g0224others(23): Show | 26 | HG00423.hp1 HG02145.hp1 HG02572.hp2 others(23): Show |
intron_variant | MODIFIER | c.213+11937_213+1193 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178961 | |||||
| chr9:132178999
|
TCCC | T | 93 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(90): Show | 94 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.213+11960_213+1196 others(7): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132178999 | |||||
| chr9:132179274
|
C | A | 1 | a0001c0005t0002g0235 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.213+12230C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179274 | ||||||
| chr9:132179404
|
G | A | 1 | a0001c0003t0001g0332 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.213+12360G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179404 | ||||||
| chr9:132179418
|
T | C | 192 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(189): Show | 193 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.213+12374T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179418 | ||||||
| chr9:132179429
|
C | T | 5 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0005g0103others(2): Show | 5 | HG01884.hp2 HG03486.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+12385C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179429 | ||||||
| chr9:132179594
|
G | A | 1 | a0001c0001t0005g0234 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.213+12550G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179594 | ||||||
| chr9:132179709
|
C | T | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+12665C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179709 | ||||||
| chr9:132179812
|
G | T | 4 | a0001c0001t0004g0301a0001c0002t0002g0300a0001c0002t0004g0259others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+12768G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179812 | ||||||
| chr9:132179846
|
G | T | 27 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0140others(24): Show | 27 | HG01256.hp2 HG01884.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.213+12802G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179846 | ||||||
| chr9:132179900
|
G | A | 1 | a0001c0002t0002g0242 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.213+12856G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179900 | ||||||
| chr9:132179935
|
G | A | 2 | a0001c0001t0001g0346a0001c0001t0002g0344 | 2 | HG01361.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.213+12891G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132179935 | ||||||
| chr9:132180101
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.213+13057C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180101 | ||||||
| chr9:132180131
|
T | C | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+13087T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180131 | ||||||
| chr9:132180138
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.213+13094C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180138 | ||||||
| chr9:132180304
|
A | G | 191 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(188): Show | 192 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.213+13260A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180304 | ||||||
| chr9:132180308
|
A | C | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.213+13264A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180308 | ||||||
| chr9:132180427
|
A | C | 88 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(85): Show | 89 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.213+13383A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180427 | ||||||
| chr9:132180449
|
T | C | 65 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(62): Show | 65 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.213+13405T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180449 | ||||||
| chr9:132180497
|
T | C | 122 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.213+13453T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180497 | ||||||
| chr9:132180577
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.213+13533G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180577 | ||||||
| chr9:132180692
|
G | A | 1 | a0001c0003t0003g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.213+13648G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180692 | ||||||
| chr9:132180763
|
A | C | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.213+13719A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180763 | ||||||
| chr9:132180807
|
A | G | 4 | a0001c0001t0004g0301a0001c0002t0002g0300a0001c0002t0004g0259others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+13763A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180807 | ||||||
| chr9:132180922
|
A | G | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+13878A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132180922 | ||||||
| chr9:132181001
|
G | A | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+13957G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181001 | ||||||
| chr9:132181006
|
T | G | 1 | a0001c0003t0001g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.213+13962T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181006 | ||||||
| chr9:132181110
|
G | A | 4 | a0001c0001t0004g0301a0001c0002t0002g0300a0001c0002t0004g0259others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+14066G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181110 | ||||||
| chr9:132181110
|
G | T | 2 | a0001c0002t0001g0170a0001c0005t0002g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.213+14066G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181110 | ||||||
| chr9:132181118
|
C | T | 1 | a0001c0004t0003g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.213+14074C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181118 | ||||||
| chr9:132181168
|
C | A | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.213+14124C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181168 | ||||||
| chr9:132181168
|
C | G | 1 | a0001c0003t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.213+14124C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181168 | ||||||
| chr9:132181198
|
T | C | 196 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(193): Show | 197 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.213+14154T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181198 | ||||||
| chr9:132181322
|
C | CT | 25 | a0001c0001t0001g0114a0001c0001t0003g0051a0001c0001t0006g0221others(22): Show | 25 | HG00423.hp1 HG00621.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.213+14294dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132181322 | |||||
| chr9:132181494
|
T | C | 4 | a0001c0001t0003g0251a0001c0001t0050g0237a0001c0001t0051g0236others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+14450T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181494 | ||||||
| chr9:132181583
|
G | A | 62 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(59): Show | 62 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.213+14539G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181583 | ||||||
| chr9:132181604
|
C | T | 97 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(94): Show | 98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.213+14560C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181604 | ||||||
| chr9:132181823
|
C | G | 1 | a0001c0001t0003g0174 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.213+14779C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181823 | ||||||
| chr9:132181864
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.213+14820G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132181864 | ||||||
| chr9:132182066
|
C | T | 4 | a0001c0001t0005g0246a0001c0003t0002g0248a0001c0004t0002g0247others(1): Show | 4 | HG03130.hp2 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+15022C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182066 | ||||||
| chr9:132182092
|
C | A | 1 | a0001c0004t0003g0118 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.213+15048C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182092 | ||||||
| chr9:132182260
|
A | G | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.213+15216A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182260 | ||||||
| chr9:132182361
|
C | T | 3 | a0001c0004t0016g0229a0001c0004t0024g0228a0001c0004t0025g0225 | 3 | HG02145.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.213+15317C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182361 | ||||||
| chr9:132182558
|
C | T | 5 | a0001c0001t0002g0204a0001c0001t0012g0257a0001c0003t0003g0233others(2): Show | 5 | HG02572.hp2 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-15408C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182558 | ||||||
| chr9:132182708
|
G | A | 9 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0002t0001g0258others(6): Show | 9 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-15258G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182708 | ||||||
| chr9:132182880
|
C | T | 1 | a0001c0003t0026g0308 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.214-15086C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182880 | ||||||
| chr9:132182900
|
C | A | 1 | a0001c0003t0023g0216 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.214-15066C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182900 | ||||||
| chr9:132182999
|
G | A | 8 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0005g0103others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-14967G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132182999 | ||||||
| chr9:132183107
|
C | CT | 9 | a0001c0001t0002g0348a0001c0001t0036g0285a0001c0002t0002g0272others(6): Show | 9 | HG02027.hp1 HG02165.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.214-14858dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132183107 | |||||
| chr9:132183112
|
A | G | 130 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(127): Show | 131 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.214-14854A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183112 | ||||||
| chr9:132183146
|
A | G | 86 | a0001c0001t0001g0343a0001c0001t0001g0346a0001c0001t0002g0020others(83): Show | 87 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.214-14820A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183146 | ||||||
| chr9:132183211
|
A | C | 1 | a0001c0002t0006g0206 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.214-14755A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183211 | ||||||
| chr9:132183278
|
G | C | 64 | a0001c0001t0001g0343a0001c0001t0003g0163a0001c0001t0003g0320others(61): Show | 65 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.214-14688G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183278 | ||||||
| chr9:132183292
|
G | A | 74 | a0001c0001t0001g0343a0001c0001t0002g0020a0001c0001t0002g0281others(71): Show | 75 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.214-14674G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183292 | ||||||
| chr9:132183351
|
G | A | 66 | a0001c0001t0001g0343a0001c0001t0002g0020a0001c0001t0003g0163others(63): Show | 67 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.214-14615G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183351 | ||||||
| chr9:132183546
|
G | A | 26 | a0001c0001t0007g0212a0001c0001t0020g0302a0001c0002t0001g0200others(23): Show | 26 | HG00423.hp1 HG00621.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.214-14420G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183546 | ||||||
| chr9:132183757
|
G | A | 2 | a0001c0001t0004g0340a0001c0003t0004g0250 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.214-14209G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183757 | ||||||
| chr9:132183760
|
C | A | 1 | a0001c0003t0001g0062 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.214-14206C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132183760 | ||||||
| chr9:132184100
|
G | C | 321 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(318): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.214-13866G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184100 | ||||||
| chr9:132184126
|
G | C | 1 | a0001c0003t0006g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214-13840G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184126 | ||||||
| chr9:132184269
|
G | A | 6 | a0001c0001t0005g0265a0001c0001t0005g0266a0001c0001t0013g0263others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-13697G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184269 | ||||||
| chr9:132184339
|
G | A | 1 | a0001c0002t0004g0252 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.214-13627G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184339 | ||||||
| chr9:132184426
|
G | A | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.214-13540G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184426 | ||||||
| chr9:132184472
|
G | T | 1 | a0001c0002t0001g0058 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.214-13494G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184472 | ||||||
| chr9:132184675
|
G | A | 26 | a0001c0001t0007g0212a0001c0001t0020g0302a0001c0002t0001g0200others(23): Show | 26 | HG00423.hp1 HG00621.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.214-13291G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184675 | ||||||
| chr9:132184690
|
G | A | 1 | a0001c0001t0012g0257 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.214-13276G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184690 | ||||||
| chr9:132184695
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.214-13271G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184695 | ||||||
| chr9:132184886
|
C | T | 1 | a0001c0005t0040g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214-13080C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184886 | ||||||
| chr9:132184947
|
A | G | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.214-13019A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184947 | ||||||
| chr9:132184971
|
A | C | 1 | a0001c0001t0002g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.214-12995A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132184971 | ||||||
| chr9:132185041
|
G | C | 1 | a0001c0001t0003g0160 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.214-12925G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185041 | ||||||
| chr9:132185113
|
A | G | 64 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0140others(61): Show | 64 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.214-12853A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185113 | ||||||
| chr9:132185169
|
A | T | 1 | a0001c0003t0004g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.214-12797A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185169 | ||||||
| chr9:132185239
|
C | G | 2 | a0001c0002t0001g0170a0001c0005t0002g0235 | 2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.214-12727C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185239 | ||||||
| chr9:132185360
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-12606G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185360 | ||||||
| chr9:132185389
|
G | C | 42 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0140others(39): Show | 42 | HG01081.hp1 HG01109.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.214-12577G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185389 | ||||||
| chr9:132185408
|
C | G | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.214-12558C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185408 | ||||||
| chr9:132185450
|
C | T | 1 | a0001c0001t0003g0177 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.214-12516C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185450 | ||||||
| chr9:132185477
|
G | C | 1 | a0001c0005t0002g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.214-12489G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185477 | ||||||
| chr9:132185763
|
A | G | 2 | a0001c0002t0009g0304a0001c0005t0002g0303 | 2 | HG01192.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.214-12203A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185763 | ||||||
| chr9:132185820
|
C | CAGGGAGG others(18): Show |
1 | a0001c0004t0001g0317 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.214-12142_214-1211 others(29): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185820 | |||||
| chr9:132185821
|
A | AGGGAGGA others(11): Show |
32 | a0001c0001t0001g0068a0001c0001t0002g0092a0001c0001t0002g0093others(29): Show | 32 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.214-12091_214-1207 others(22): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185821 | |||||
| chr9:132185821
|
A | AGGGAGGA others(47): Show |
1 | a0001c0001t0001g0014 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214-12127_214-1207 others(58): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185821 | |||||
| chr9:132185821
|
AGGGAGGA others(11): Show |
A | 62 | a0001c0001t0002g0020a0001c0001t0002g0182a0001c0001t0002g0204others(59): Show | 62 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.214-12091_214-1207 others(22): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185821 | |||||
| chr9:132185821
|
AGGGAGGA others(29): Show |
A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.214-12109_214-1207 others(40): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185821 | |||||
| chr9:132185840
|
GGGAGGAG others(32): Show |
G | 2 | a0001c0004t0016g0229a0001c0004t0024g0228 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.214-12111_214-1207 others(43): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185840 | |||||
| chr9:132185846
|
AGGAGGAG others(5): Show |
A | 2 | a0001c0002t0001g0312a0001c0004t0001g0305 | 2 | HG02074.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.214-12109_214-1209 others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185846 | |||||
| chr9:132185875
|
T | G | 2 | a0001c0005t0002g0303a0001c0005t0040g0239 | 2 | HG01192.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.214-12091T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185875 | ||||||
| chr9:132185876
|
G | GGGAGGAG others(14): Show |
1 | a0001c0004t0001g0054 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.214-12079_214-1205 others(25): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132185876 | |||||
| chr9:132185877
|
G | A | 1 | a0001c0005t0040g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214-12089G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185877 | ||||||
| chr9:132185878
|
G | A | 1 | a0001c0005t0040g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214-12088G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185878 | ||||||
| chr9:132185893
|
G | T | 1 | a0001c0001t0002g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.214-12073G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185893 | ||||||
| chr9:132185894
|
G | A | 1 | a0001c0002t0001g0282 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.214-12072G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185894 | ||||||
| chr9:132185895
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.214-12071A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185895 | ||||||
| chr9:132185896
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.214-12070A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185896 | ||||||
| chr9:132185901
|
G | A | 1 | a0001c0003t0010g0313 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.214-12065G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132185901 | ||||||
| chr9:132186008
|
T | A | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-11958T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186008 | ||||||
| chr9:132186009
|
C | A | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-11957C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186009 | ||||||
| chr9:132186130
|
G | A | 3 | a0001c0001t0004g0340a0001c0001t0012g0257a0001c0002t0001g0200 | 3 | HG03098.hp2 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.214-11836G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186130 | ||||||
| chr9:132186223
|
G | A | 12 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0005g0265others(9): Show | 12 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.214-11743G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186223 | ||||||
| chr9:132186404
|
C | A | 1 | a0001c0002t0009g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.214-11562C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186404 | ||||||
| chr9:132186405
|
AT | A | 3 | a0001c0003t0002g0248a0001c0004t0029g0227a0001c0004t0041g0249 | 3 | HG03130.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.214-11556delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132186405 | |||||
| chr9:132186465
|
G | A | 8 | a0001c0001t0002g0075a0001c0001t0002g0092a0001c0001t0002g0093others(5): Show | 8 | HG00408.hp2 HG00673.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.214-11501G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186465 | ||||||
| chr9:132186595
|
T | A | 203 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(200): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.214-11371T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186595 | ||||||
| chr9:132186763
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.214-11203C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186763 | ||||||
| chr9:132186827
|
G | A | 25 | a0001c0001t0007g0212a0001c0002t0021g0230a0001c0003t0002g0028others(22): Show | 25 | HG00621.hp1 HG02015.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.214-11139G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186827 | ||||||
| chr9:132186887
|
A | G | 206 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.214-11079A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132186887 | ||||||
| chr9:132187072
|
C | T | 3 | a0001c0001t0004g0301a0001c0002t0001g0200a0001c0002t0004g0252 | 3 | HG02717.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.214-10894C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187072 | ||||||
| chr9:132187157
|
C | T | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-10809C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187157 | ||||||
| chr9:132187173
|
A | G | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-10793A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187173 | ||||||
| chr9:132187182
|
C | T | 2 | a0001c0003t0001g0043a0001c0005t0002g0124 | 2 | NA18951.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.214-10784C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187182 | ||||||
| chr9:132187183
|
G | A | 24 | a0001c0001t0001g0187a0001c0001t0002g0018a0001c0001t0004g0260others(21): Show | 24 | HG01109.hp2 HG01891.hp2 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.214-10783G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187183 | ||||||
| chr9:132187359
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0002g0182a0001c0001t0005g0234 | 3 | HG01106.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.214-10607G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187359 | ||||||
| chr9:132187384
|
G | A | 36 | a0001c0001t0011g0061a0001c0001t0012g0257a0001c0002t0001g0258others(33): Show | 36 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.214-10582G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187384 | ||||||
| chr9:132187388
|
G | A | 26 | a0001c0001t0001g0187a0001c0001t0002g0018a0001c0001t0002g0020others(23): Show | 26 | HG01109.hp2 HG01891.hp2 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.214-10578G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187388 | ||||||
| chr9:132187429
|
C | T | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.214-10537C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187429 | ||||||
| chr9:132187471
|
T | C | 1 | a0001c0002t0002g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.214-10495T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187471 | ||||||
| chr9:132187541
|
A | AAC | 37 | a0001c0001t0002g0204a0001c0001t0011g0061a0001c0001t0012g0257others(34): Show | 37 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.214-10415_214-1041 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132187541 | |||||
| chr9:132187569
|
AAG | A | 9 | a0001c0001t0001g0034a0001c0001t0001g0140a0001c0001t0002g0182others(6): Show | 9 | HG00597.hp1 HG01106.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-10370_214-1036 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132187569 | |||||
| chr9:132187569
|
AAGAG | A | 136 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0001t0003g0037others(133): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.214-10372_214-1036 others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132187569 | |||||
| chr9:132187569
|
AAGAGAG | A | 61 | a0001c0001t0001g0187a0001c0001t0002g0018a0001c0001t0002g0020others(58): Show | 61 | HG00741.hp2 HG01109.hp2 HG01123.hp2 others(58): Show |
intron_variant | MODIFIER | c.214-10374_214-1036 others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132187569 | |||||
| chr9:132187573
|
G | A | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.214-10393G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187573 | ||||||
| chr9:132187609
|
A | G | 136 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0177others(133): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.214-10357A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187609 | ||||||
| chr9:132187872
|
G | C | 137 | a0001c0001t0001g0140a0001c0001t0002g0182a0001c0001t0003g0037others(134): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.214-10094G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187872 | ||||||
| chr9:132187882
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.214-10084G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187882 | ||||||
| chr9:132187899
|
C | T | 16 | a0001c0001t0004g0301a0001c0001t0005g0265a0001c0001t0005g0266others(13): Show | 16 | HG01167.hp1 HG01891.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.214-10067C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132187899 | ||||||
| chr9:132188313
|
C | T | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-9653C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188313 | ||||||
| chr9:132188325
|
G | A | 2 | a0001c0006t0001g0284a0001c0006t0001g0295 | 2 | HG02165.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.214-9641G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188325 | ||||||
| chr9:132188335
|
C | A | 1 | a0001c0003t0001g0275 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.214-9631C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188335 | ||||||
| chr9:132188362
|
G | A | 1 | a0001c0003t0003g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.214-9604G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188362 | ||||||
| chr9:132188374
|
C | T | 7 | a0001c0003t0006g0205a0001c0005t0008g0349a0001c0005t0009g0356others(4): Show | 7 | HG02027.hp1 HG02738.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-9592C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188374 | ||||||
| chr9:132188382
|
G | A | 1 | a0001c0002t0002g0105 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.214-9584G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188382 | ||||||
| chr9:132188477
|
C | T | 1 | a0001c0001t0001g0346 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.214-9489C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188477 | ||||||
| chr9:132188547
|
C | G | 1 | a0001c0002t0001g0180 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.214-9419C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188547 | ||||||
| chr9:132188588
|
A | G | 165 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.214-9378A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188588 | ||||||
| chr9:132188645
|
G | A | 3 | a0001c0003t0001g0024a0001c0003t0001g0330a0001c0004t0035g0193 | 3 | NA18979.hp2 NA18986.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.214-9321G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188645 | ||||||
| chr9:132188657
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-9309G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188657 | ||||||
| chr9:132188705
|
T | A | 168 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(165): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.214-9261T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188705 | ||||||
| chr9:132188804
|
G | A | 8 | a0001c0001t0002g0012a0001c0001t0002g0080a0001c0001t0002g0148others(5): Show | 8 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.214-9162G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188804 | ||||||
| chr9:132188847
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(3): Show | 6 | HG01106.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-9119C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188847 | ||||||
| chr9:132188874
|
G | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(2): Show | 5 | HG01106.hp1 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.214-9092G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188874 | ||||||
| chr9:132188884
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-9082G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188884 | ||||||
| chr9:132188887
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(3): Show | 6 | HG01106.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-9079C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188887 | ||||||
| chr9:132188895
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-9071G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188895 | ||||||
| chr9:132188916
|
A | T | 39 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(36): Show | 39 | HG00741.hp2 HG01106.hp1 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.214-9050A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188916 | ||||||
| chr9:132188952
|
T | C | 6 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(3): Show | 6 | HG01106.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-9014T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188952 | ||||||
| chr9:132188953
|
T | C | 6 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(3): Show | 6 | HG01106.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-9013T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132188953 | ||||||
| chr9:132189054
|
G | C | 33 | a0001c0001t0011g0061a0001c0001t0012g0257a0001c0002t0001g0258others(30): Show | 33 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.214-8912G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189054 | ||||||
| chr9:132189062
|
GCCTT | G | 23 | a0001c0001t0012g0257a0001c0002t0021g0230a0001c0005t0001g0269others(20): Show | 23 | HG01257.hp1 HG02027.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.214-8903_214-8900d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189062 | ||||||
| chr9:132189063
|
C | G | 155 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(152): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.214-8903C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189063 | ||||||
| chr9:132189065
|
TTTC | T | 9 | a0001c0001t0011g0061a0001c0002t0001g0258a0001c0005t0001g0270others(6): Show | 9 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-8898_214-8896d others(5): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189065 | |||||
| chr9:132189067
|
T | G | 23 | a0001c0001t0012g0257a0001c0002t0021g0230a0001c0005t0001g0269others(20): Show | 23 | HG01257.hp1 HG02027.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.214-8899T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189067 | ||||||
| chr9:132189068
|
C | CT | 46 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0095others(43): Show | 46 | HG00438.hp1 HG01109.hp2 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.214-8871dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTT | 6 | a0001c0001t0002g0348a0001c0001t0004g0260a0001c0001t0006g0221others(3): Show | 6 | HG02165.hp1 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-8872_214-8871d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTT | 8 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-8873_214-8871d others(5): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0005g0246others(4): Show | 7 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-8878_214-8871d others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0005g0265a0001c0002t0004g0345a0001c0002t0044g0274others(1): Show | 4 | HG01167.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-8881_214-8871d others(13): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(5): Show |
14 | a0001c0001t0002g0223a0001c0001t0005g0266a0001c0001t0011g0231others(11): Show | 14 | HG02109.hp1 HG02145.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.214-8882_214-8871d others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(6): Show |
21 | a0001c0001t0002g0344a0001c0002t0002g0255a0001c0002t0002g0272others(18): Show | 21 | HG01361.hp2 HG01891.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.214-8883_214-8871d others(15): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(7): Show |
28 | a0001c0001t0001g0346a0001c0002t0002g0325a0001c0003t0001g0062others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.214-8884_214-8871d others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(8): Show |
36 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0036g0285others(33): Show | 37 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.214-8885_214-8871d others(17): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(9): Show |
10 | a0001c0003t0001g0064a0001c0003t0001g0149a0001c0003t0001g0306others(7): Show | 10 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.214-8886_214-8871d others(18): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(10): Show |
2 | a0001c0003t0001g0104a0001c0003t0001g0332 | 2 | HG00609.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.214-8887_214-8871d others(19): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(11): Show |
1 | a0001c0003t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.214-8888_214-8871d others(20): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0046g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214-8890_214-8871d others(22): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0004t0002g0338 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.214-8881_214-8871d others(13): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0003t0001g0024a0001c0004t0001g0026a0001c0004t0035g0193 | 3 | NA18979.hp2 NA19085.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.214-8882_214-8871d others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0001g0330 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.214-8883_214-8871d others(15): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189068
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0002t0001g0200a0001c0002t0004g0252 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.214-8884_214-8871d others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189068 | |||||
| chr9:132189147
|
G | A | 1 | a0001c0002t0002g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.214-8819G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189147 | ||||||
| chr9:132189220
|
G | A | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.214-8746G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189220 | ||||||
| chr9:132189237
|
C | T | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-8729C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189237 | ||||||
| chr9:132189238
|
G | A | 3 | a0001c0001t0009g0073a0001c0002t0001g0200a0001c0002t0004g0252 | 3 | HG02922.hp1 NA19240.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.214-8728G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189238 | ||||||
| chr9:132189273
|
C | T | 1 | a0001c0005t0006g0218 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.214-8693C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189273 | ||||||
| chr9:132189315
|
G | C | 24 | a0001c0001t0011g0061a0001c0005t0001g0269a0001c0005t0001g0270others(21): Show | 24 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.214-8651G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189315 | ||||||
| chr9:132189378
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.214-8588G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189378 | ||||||
| chr9:132189401
|
C | T | 171 | a0001c0001t0001g0346a0001c0001t0002g0020a0001c0001t0002g0223others(168): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.214-8565C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189401 | ||||||
| chr9:132189402
|
G | A | 3 | a0001c0001t0033g0074a0001c0002t0001g0336a0001c0002t0001g0337 | 3 | HG01070.hp2 HG01081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.214-8564G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189402 | ||||||
| chr9:132189410
|
T | TA | 6 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0002g0182others(3): Show | 6 | HG01106.hp1 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-8548dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189410 | |||||
| chr9:132189418
|
AG | A | 138 | a0001c0001t0001g0346a0001c0001t0002g0020a0001c0001t0002g0223others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.214-8546delG | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132189418 | |||||
| chr9:132189419
|
G | A | 33 | a0001c0001t0011g0061a0001c0001t0012g0257a0001c0002t0001g0258others(30): Show | 33 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.214-8547G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189419 | ||||||
| chr9:132189464
|
G | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0169a0001c0001t0003g0160others(1): Show | 4 | HG00099.hp2 HG03669.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-8502G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189464 | ||||||
| chr9:132189597
|
A | G | 3 | a0001c0005t0001g0270a0001c0005t0001g0277a0001c0005t0002g0303 | 3 | HG00741.hp2 HG01192.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.214-8369A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189597 | ||||||
| chr9:132189608
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-8358G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189608 | ||||||
| chr9:132189639
|
T | C | 33 | a0001c0001t0011g0061a0001c0001t0012g0257a0001c0002t0001g0258others(30): Show | 33 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.214-8327T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189639 | ||||||
| chr9:132189650
|
T | A | 146 | a0001c0001t0001g0346a0001c0001t0002g0020a0001c0001t0002g0223others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.214-8316T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189650 | ||||||
| chr9:132189749
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0005g0234a0001c0002t0004g0261 | 3 | HG01106.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.214-8217C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189749 | ||||||
| chr9:132189891
|
G | A | 1 | a0001c0001t0027g0053 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.214-8075G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189891 | ||||||
| chr9:132189931
|
G | C | 1 | a0001c0002t0045g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.214-8035G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189931 | ||||||
| chr9:132189948
|
C | A | 33 | a0001c0001t0011g0061a0001c0001t0012g0257a0001c0002t0001g0258others(30): Show | 33 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.214-8018C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132189948 | ||||||
| chr9:132190015
|
T | C | 180 | a0001c0001t0001g0346a0001c0001t0002g0020a0001c0001t0002g0223others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.214-7951T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190015 | ||||||
| chr9:132190030
|
G | C | 173 | a0001c0001t0001g0346a0001c0001t0002g0020a0001c0001t0002g0223others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.214-7936G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190030 | ||||||
| chr9:132190049
|
C | T | 3 | a0001c0001t0002g0189a0001c0001t0030g0022a0001c0002t0001g0150 | 3 | HG02056.hp1 NA18970.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.214-7917C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190049 | ||||||
| chr9:132190125
|
T | C | 220 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(217): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.214-7841T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190125 | ||||||
| chr9:132190203
|
A | G | 173 | a0001c0001t0001g0346a0001c0001t0002g0020a0001c0001t0002g0223others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.214-7763A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190203 | ||||||
| chr9:132190232
|
C | CA | 31 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0114others(28): Show | 31 | HG00597.hp2 HG01081.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.214-7705dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132190232 | |||||
| chr9:132190232
|
C | CAA | 14 | a0001c0001t0001g0010a0001c0001t0002g0204a0001c0001t0002g0281others(11): Show | 14 | HG01884.hp1 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.214-7706_214-7705d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132190232 | |||||
| chr9:132190232
|
CA | C | 8 | a0001c0001t0001g0068a0001c0001t0001g0188a0001c0001t0002g0148others(5): Show | 8 | HG01081.hp2 HG02004.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-7705delA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132190232 | |||||
| chr9:132190232
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0002t0004g0259a0001c0002t0044g0274a0001c0003t0002g0008others(3): Show | 6 | HG00423.hp2 HG02109.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-7713_214-7705d others(11): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132190232 | |||||
| chr9:132190232
|
CAAAAAAA others(3): Show |
C | 106 | a0001c0001t0001g0346a0001c0001t0002g0223a0001c0001t0002g0344others(103): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.214-7714_214-7705d others(12): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132190232 | |||||
| chr9:132190232
|
CAAAAAAA others(4): Show |
C | 59 | a0001c0001t0002g0020a0001c0001t0005g0266a0001c0001t0011g0061others(56): Show | 59 | HG00621.hp1 HG00741.hp2 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.214-7715_214-7705d others(13): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132190232 | |||||
| chr9:132190232
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0002t0021g0230a0001c0004t0017g0220 | 2 | HG02622.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.214-7716_214-7705d others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132190232 | |||||
| chr9:132190320
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-7646G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190320 | ||||||
| chr9:132190441
|
C | G | 31 | a0001c0001t0011g0061a0001c0002t0001g0258a0001c0005t0001g0269others(28): Show | 31 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.214-7525C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190441 | ||||||
| chr9:132190472
|
C | T | 1 | a0001c0001t0002g0348 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.214-7494C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190472 | ||||||
| chr9:132190532
|
T | C | 12 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0001t0005g0265others(9): Show | 12 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.214-7434T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190532 | ||||||
| chr9:132190550
|
G | A | 26 | a0001c0001t0002g0018a0001c0001t0004g0260a0001c0001t0005g0165others(23): Show | 26 | HG01109.hp2 HG01891.hp2 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.214-7416G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190550 | ||||||
| chr9:132190726
|
T | C | 3 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-7240T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190726 | ||||||
| chr9:132190938
|
T | C | 3 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-7028T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132190938 | ||||||
| chr9:132191000
|
T | C | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-6966T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191000 | ||||||
| chr9:132191064
|
C | G | 1 | a0001c0003t0004g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.214-6902C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191064 | ||||||
| chr9:132191331
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-6635C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191331 | ||||||
| chr9:132191361
|
A | G | 143 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.214-6605A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191361 | ||||||
| chr9:132191372
|
T | C | 146 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0223others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.214-6594T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191372 | ||||||
| chr9:132191426
|
T | G | 1 | a0001c0002t0021g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214-6540T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191426 | ||||||
| chr9:132191551
|
T | C | 1 | a0001c0002t0002g0105 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.214-6415T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191551 | ||||||
| chr9:132191558
|
T | TG | 221 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(218): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.214-6408_214-6407i others(3): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191558 | ||||||
| chr9:132191662
|
C | A | 3 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0002t0002g0300 | 3 | HG02451.hp2 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-6304C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191662 | ||||||
| chr9:132191717
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.214-6249G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191717 | ||||||
| chr9:132191778
|
T | C | 1 | a0001c0015t0052g0203 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.214-6188T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191778 | ||||||
| chr9:132191835
|
T | C | 33 | a0001c0001t0011g0061a0001c0001t0012g0257a0001c0002t0001g0258others(30): Show | 33 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.214-6131T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191835 | ||||||
| chr9:132191967
|
G | A | 1 | a0001c0003t0001g0334 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.214-5999G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132191967 | ||||||
| chr9:132192143
|
G | T | 1 | a0001c0001t0002g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.214-5823G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132192143 | ||||||
| chr9:132192158
|
C | G | 3 | a0001c0001t0012g0257a0001c0002t0021g0230a0001c0004t0002g0085 | 3 | HG02622.hp2 HG03492.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.214-5808C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132192158 | ||||||
| chr9:132192361
|
T | C | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-5605T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132192361 | ||||||
| chr9:132192451
|
C | T | 1 | a0001c0002t0002g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.214-5515C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132192451 | ||||||
| chr9:132192705
|
C | G | 1 | a0001c0004t0007g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.214-5261C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132192705 | ||||||
| chr9:132192813
|
C | T | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.214-5153C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132192813 | ||||||
| chr9:132192936
|
G | A | 31 | a0001c0001t0011g0061a0001c0002t0001g0258a0001c0005t0001g0269others(28): Show | 31 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.214-5030G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132192936 | ||||||
| chr9:132193036
|
G | A | 1 | a0001c0005t0006g0218 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.214-4930G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193036 | ||||||
| chr9:132193075
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0002g0182a0001c0001t0005g0234 | 3 | HG01106.hp1 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.214-4891A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193075 | ||||||
| chr9:132193240
|
C | A | 5 | a0001c0001t0001g0010a0001c0001t0002g0204a0001c0001t0005g0029others(2): Show | 5 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-4726C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193240 | ||||||
| chr9:132193314
|
G | T | 4 | a0001c0001t0002g0018a0001c0002t0001g0280a0001c0002t0002g0030others(1): Show | 4 | HG01891.hp2 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-4652G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193314 | ||||||
| chr9:132193553
|
A | G | 6 | a0001c0001t0001g0140a0001c0001t0002g0020a0001c0001t0002g0182others(3): Show | 6 | HG01106.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-4413A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193553 | ||||||
| chr9:132193651
|
T | C | 1 | a0001c0004t0002g0335 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.214-4315T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193651 | ||||||
| chr9:132193670
|
T | C | 1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.214-4296T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193670 | ||||||
| chr9:132193742
|
A | G | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.214-4224A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193742 | ||||||
| chr9:132193773
|
C | T | 8 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0005g0103others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-4193C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193773 | ||||||
| chr9:132193843
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-4123G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193843 | ||||||
| chr9:132193866
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.214-4100G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193866 | ||||||
| chr9:132193951
|
G | A | 2 | a0001c0005t0001g0269a0001c0006t0002g0084 | 2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.214-4015G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132193951 | ||||||
| chr9:132194109
|
T | C | 148 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0223others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.214-3857T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194109 | ||||||
| chr9:132194283
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.214-3683C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194283 | ||||||
| chr9:132194349
|
G | A | 9 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0004g0340others(6): Show | 9 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-3617G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194349 | ||||||
| chr9:132194687
|
T | C | 2 | a0001c0002t0001g0123a0001c0002t0014g0294 | 2 | HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.214-3279T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194687 | ||||||
| chr9:132194717
|
A | G | 221 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(218): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.214-3249A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194717 | ||||||
| chr9:132194799
|
G | A | 8 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0005g0103others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-3167G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194799 | ||||||
| chr9:132194886
|
G | A | 9 | a0001c0001t0002g0204a0001c0001t0002g0281a0001c0001t0003g0251others(6): Show | 9 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-3080G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194886 | ||||||
| chr9:132194892
|
C | T | 1 | a0001c0001t0004g0340 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.214-3074C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194892 | ||||||
| chr9:132194897
|
C | G | 6 | a0001c0001t0002g0204a0001c0001t0004g0340a0001c0001t0005g0103others(3): Show | 6 | HG02895.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-3069C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194897 | ||||||
| chr9:132194918
|
G | T | 2 | a0001c0001t0002g0020a0001c0001t0012g0125 | 2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.214-3048G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132194918 | ||||||
| chr9:132195091
|
TTTTCTTT others(7): Show |
T | 1 | a0001c0004t0007g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.214-2861_214-2848d others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132195091 | |||||
| chr9:132195371
|
C | T | 117 | a0001c0001t0002g0182a0001c0001t0003g0037a0001c0001t0003g0038others(114): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.214-2595C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195371 | ||||||
| chr9:132195372
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0005g0029a0001c0001t0013g0009others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-2594G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195372 | ||||||
| chr9:132195444
|
G | A | 1 | a0001c0005t0002g0015 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.214-2522G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195444 | ||||||
| chr9:132195458
|
A | G | 32 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0002g0204others(29): Show | 32 | HG01109.hp2 HG01891.hp2 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.214-2508A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195458 | ||||||
| chr9:132195474
|
A | AT | 33 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0066others(30): Show | 33 | HG00741.hp1 HG00741.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.214-2466dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132195474 | |||||
| chr9:132195474
|
AT | A | 62 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0155others(59): Show | 62 | HG00558.hp1 HG01109.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.214-2466delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132195474 | |||||
| chr9:132195474
|
ATT | A | 12 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0016g0224others(9): Show | 12 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-2467_214-2466d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132195474 | |||||
| chr9:132195474
|
ATTT | A | 102 | a0001c0001t0002g0182a0001c0001t0003g0037a0001c0001t0003g0038others(99): Show | 103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.214-2468_214-2466d others(5): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132195474 | |||||
| chr9:132195474
|
ATTTT | A | 8 | a0001c0001t0004g0340a0001c0003t0001g0156a0001c0003t0001g0198others(5): Show | 8 | HG00423.hp1 HG00609.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-2469_214-2466d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 132195474 | |||||
| chr9:132195546
|
G | C | 1 | a0001c0001t0002g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.214-2420G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195546 | ||||||
| chr9:132195552
|
C | T | 8 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0005g0103others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-2414C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195552 | ||||||
| chr9:132195558
|
A | T | 1 | a0001c0001t0002g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.214-2408A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195558 | ||||||
| chr9:132195570
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.214-2396A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195570 | ||||||
| chr9:132195571
|
C | A | 1 | a0001c0001t0002g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.214-2395C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195571 | ||||||
| chr9:132195574
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.214-2392G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195574 | ||||||
| chr9:132195742
|
C | T | 1 | a0001c0003t0001g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.214-2224C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195742 | ||||||
| chr9:132195891
|
C | T | 1 | a0001c0002t0002g0325 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.214-2075C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132195891 | ||||||
| chr9:132196126
|
G | A | 1 | a0001c0003t0004g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.214-1840G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196126 | ||||||
| chr9:132196335
|
C | T | 1 | a0001c0002t0039g0045 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.214-1631C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196335 | ||||||
| chr9:132196445
|
G | A | 211 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.214-1521G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196445 | ||||||
| chr9:132196503
|
G | A | 1 | a0001c0004t0002g0085 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.214-1463G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196503 | ||||||
| chr9:132196550
|
C | T | 148 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0004g0340others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.214-1416C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196550 | ||||||
| chr9:132196612
|
G | A | 3 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0014g0294 | 3 | HG00738.hp1 HG01346.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.214-1354G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196612 | ||||||
| chr9:132196622
|
G | A | 211 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.214-1344G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196622 | ||||||
| chr9:132196818
|
T | C | 1 | a0001c0002t0001g0013 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.214-1148T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196818 | ||||||
| chr9:132196877
|
G | A | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214-1089G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132196877 | ||||||
| chr9:132197112
|
G | A | 211 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.214-854G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197112 | ||||||
| chr9:132197337
|
C | T | 2 | a0001c0002t0001g0094a0001c0002t0008g0164 | 2 | NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.214-629C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197337 | ||||||
| chr9:132197471
|
G | A | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.214-495G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197471 | ||||||
| chr9:132197492
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0005g0029a0001c0001t0013g0009others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-474G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197492 | ||||||
| chr9:132197511
|
A | G | 6 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0016g0224others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-455A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197511 | ||||||
| chr9:132197600
|
C | G | 211 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.214-366C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197600 | ||||||
| chr9:132197637
|
T | C | 1 | a0001c0001t0019g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.214-329T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197637 | ||||||
| chr9:132197671
|
G | A | 2 | a0001c0005t0001g0269a0001c0006t0002g0084 | 2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.214-295G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197671 | ||||||
| chr9:132197708
|
C | T | 31 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(28): Show | 31 | HG01106.hp1 HG01167.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.214-258C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197708 | ||||||
| chr9:132197922
|
G | A | 146 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0002t0002g0325others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.214-44G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197922 | ||||||
| chr9:132197928
|
C | G | 148 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0004g0340others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.214-38C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197928 | ||||||
| chr9:132197941
|
T | C | 2 | a0001c0004t0032g0162a0001c0004t0047g0322 | 2 | NA18948.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.214-25T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197941 | ||||||
| chr9:132197958
|
C | G | 1 | a0001c0001t0002g0182 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.214-8C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132197958 | ||||||
| chr9:132198672
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0011g0231 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.857+63G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198672 | ||||||
| chr9:132198676
|
T | C | 32 | a0001c0001t0004g0340a0001c0003t0007g0209a0001c0003t0037g0137others(29): Show | 32 | HG00741.hp2 HG01123.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.857+67T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198676 | ||||||
| chr9:132198716
|
G | A | 169 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(166): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.857+107G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198716 | ||||||
| chr9:132198769
|
C | T | 2 | a0001c0002t0021g0230a0001c0005t0008g0349 | 2 | HG02027.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.857+160C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198769 | ||||||
| chr9:132198801
|
G | C | 38 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(35): Show | 38 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.857+192G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198801 | ||||||
| chr9:132198811
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.857+202G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198811 | ||||||
| chr9:132198815
|
C | T | 8 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0005g0103others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.857+206C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198815 | ||||||
| chr9:132198822
|
C | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(35): Show | 38 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.857+213C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132198822 | ||||||
| chr9:132199062
|
G | A | 35 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(32): Show | 35 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.857+453G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132199062 | ||||||
| chr9:132199193
|
A | G | 1 | a0001c0003t0001g0288 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.857+584A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132199193 | ||||||
| chr9:132199356
|
G | T | 5 | a0001c0001t0002g0184a0001c0002t0001g0017a0001c0002t0001g0173others(2): Show | 5 | HG01952.hp2 HG01975.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.857+747G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132199356 | ||||||
| chr9:132199707
|
ACT | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(26): Show | 29 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.857+1101_857+1102d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132199707 | |||||
| chr9:132199726
|
G | C | 355 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(352): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.857+1117G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132199726 | ||||||
| chr9:132199770
|
C | T | 8 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0005g0103others(5): Show | 8 | HG02280.hp1 HG02647.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.857+1161C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132199770 | ||||||
| chr9:132199914
|
C | G | 2 | a0001c0001t0003g0089a0001c0001t0011g0197 | 2 | NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.857+1305C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132199914 | ||||||
| chr9:132199983
|
A | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(37): Show | 40 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.857+1374A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132199983 | ||||||
| chr9:132200262
|
G | A | 1 | a0001c0003t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.857+1653G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132200262 | ||||||
| chr9:132200354
|
T | C | 114 | a0001c0001t0002g0189a0001c0002t0044g0274a0001c0003t0001g0024others(111): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.857+1745T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132200354 | ||||||
| chr9:132200519
|
T | C | 1 | a0001c0002t0002g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.857+1910T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132200519 | ||||||
| chr9:132200650
|
G | C | 115 | a0001c0001t0002g0189a0001c0002t0044g0274a0001c0003t0001g0024others(112): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.857+2041G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132200650 | ||||||
| chr9:132201139
|
T | C | 1 | a0001c0001t0027g0053 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.857+2530T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201139 | ||||||
| chr9:132201176
|
C | T | 3 | a0001c0001t0001g0196a0001c0001t0003g0089a0001c0001t0011g0197 | 3 | NA18984.hp2 NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.857+2567C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201176 | ||||||
| chr9:132201300
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.857+2691C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201300 | ||||||
| chr9:132201410
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0005g0029a0001c0001t0013g0009others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+2801C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201410 | ||||||
| chr9:132201707
|
C | T | 4 | a0001c0003t0002g0339a0001c0004t0001g0166a0001c0004t0001g0331others(1): Show | 4 | HG01106.hp2 HG01975.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+3098C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201707 | ||||||
| chr9:132201865
|
A | G | 8 | a0001c0001t0002g0020a0001c0001t0002g0182a0001c0001t0002g0223others(5): Show | 8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.857+3256A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201865 | ||||||
| chr9:132201866
|
C | A | 112 | a0001c0001t0002g0097a0001c0001t0002g0281a0001c0001t0002g0348others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.857+3257C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201866 | ||||||
| chr9:132201877
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0012g0125a0001c0001t0036g0285others(1): Show | 4 | HG02922.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+3268G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201877 | ||||||
| chr9:132201909
|
G | A | 183 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(180): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.857+3300G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201909 | ||||||
| chr9:132201957
|
G | C | 32 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(29): Show | 32 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.857+3348G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201957 | ||||||
| chr9:132201974
|
C | A | 66 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(63): Show | 66 | HG00621.hp1 HG01081.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.857+3365C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201974 | ||||||
| chr9:132201996
|
C | T | 1 | a0001c0002t0002g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.857+3387C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132201996 | ||||||
| chr9:132202059
|
C | T | 4 | a0001c0001t0001g0031a0001c0001t0005g0076a0001c0001t0005g0078others(1): Show | 4 | HG01256.hp2 HG01884.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+3450C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132202059 | ||||||
| chr9:132202114
|
G | A | 4 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0005t0002g0341others(1): Show | 4 | HG02486.hp2 HG03225.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+3505G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132202114 | ||||||
| chr9:132202449
|
G | T | 1 | a0001c0002t0001g0262 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.857+3840G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132202449 | ||||||
| chr9:132202482
|
G | T | 1 | a0001c0001t0012g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.857+3873G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132202482 | ||||||
| chr9:132202689
|
C | T | 6 | a0001c0001t0002g0012a0001c0001t0002g0080a0001c0001t0002g0148others(3): Show | 6 | HG00741.hp1 HG02004.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.857+4080C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132202689 | ||||||
| chr9:132202901
|
T | C | 1 | a0001c0001t0005g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.857+4292T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132202901 | ||||||
| chr9:132202913
|
A | G | 3 | a0001c0003t0001g0299a0001c0003t0038g0128a0001c0015t0052g0203 | 3 | HG01261.hp2 HG02004.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.857+4304A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132202913 | ||||||
| chr9:132203187
|
C | T | 1 | a0001c0003t0003g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.857+4578C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132203187 | ||||||
| chr9:132203391
|
A | T | 38 | a0001c0001t0005g0186a0001c0001t0005g0234a0001c0001t0012g0101others(35): Show | 38 | HG00621.hp1 HG01106.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.857+4782A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132203391 | ||||||
| chr9:132203428
|
C | T | 2 | a0001c0004t0002g0247a0001c0004t0003g0273 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.857+4819C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132203428 | ||||||
| chr9:132203464
|
C | T | 1 | a0001c0004t0017g0220 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.857+4855C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132203464 | ||||||
| chr9:132203766
|
G | A | 1 | a0001c0003t0001g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.857+5157G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132203766 | ||||||
| chr9:132203980
|
G | A | 1 | a0001c0001t0012g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.857+5371G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132203980 | ||||||
| chr9:132203993
|
C | A | 1 | a0001c0002t0002g0352 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.857+5384C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132203993 | ||||||
| chr9:132204116
|
C | T | 65 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(62): Show | 65 | HG00621.hp1 HG01081.hp1 HG01106.hp1 others(62): Show |
intron_variant | MODIFIER | c.857+5507C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204116 | ||||||
| chr9:132204359
|
G | A | 1 | a0001c0003t0002g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.857+5750G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204359 | ||||||
| chr9:132204376
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0005g0029a0001c0001t0013g0009others(1): Show | 4 | HG01081.hp1 HG01884.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+5767C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204376 | ||||||
| chr9:132204398
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.857+5789G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204398 | ||||||
| chr9:132204405
|
G | A | 4 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0004g0301others(1): Show | 4 | HG02717.hp1 HG02809.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+5796G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204405 | ||||||
| chr9:132204538
|
T | G | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.857+5929T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204538 | ||||||
| chr9:132204711
|
A | G | 21 | a0001c0001t0002g0018a0001c0001t0005g0165a0001c0001t0013g0263others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.857+6102A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204711 | ||||||
| chr9:132204844
|
C | T | 37 | a0001c0001t0005g0186a0001c0001t0005g0234a0001c0001t0012g0101others(34): Show | 37 | HG00621.hp1 HG01106.hp1 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.857+6235C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132204844 | ||||||
| chr9:132205048
|
G | A | 3 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0046g0077 | 3 | HG01884.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.857+6439G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205048 | ||||||
| chr9:132205101
|
C | T | 3 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0046g0077 | 3 | HG01884.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.857+6492C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205101 | ||||||
| chr9:132205117
|
C | A | 20 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0301others(17): Show | 20 | HG01109.hp2 HG01891.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.857+6508C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205117 | ||||||
| chr9:132205218
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.857+6609C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205218 | ||||||
| chr9:132205255
|
A | T | 2 | a0001c0003t0001g0024a0001c0004t0035g0193 | 2 | NA18979.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.857+6646A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205255 | ||||||
| chr9:132205302
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.857+6693C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205302 | ||||||
| chr9:132205362
|
G | A | 1 | a0001c0001t0013g0263 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.857+6753G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205362 | ||||||
| chr9:132205393
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.857+6784C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205393 | ||||||
| chr9:132205394
|
G | A | 1 | a0001c0002t0003g0135 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.857+6785G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205394 | ||||||
| chr9:132205448
|
G | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0066a0001c0002t0009g0112 | 3 | HG00280.hp2 HG01123.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.857+6839G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205448 | ||||||
| chr9:132205502
|
C | G | 68 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0301others(65): Show | 68 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.857+6893C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205502 | ||||||
| chr9:132205602
|
T | C | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+6993T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205602 | ||||||
| chr9:132205609
|
G | A | 3 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0046g0077 | 3 | HG01884.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.857+7000G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205609 | ||||||
| chr9:132205647
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0034others(6): Show | 9 | HG00597.hp1 HG00609.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+7038G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205647 | ||||||
| chr9:132205655
|
C | T | 3 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0046g0077 | 3 | HG01884.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.857+7046C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205655 | ||||||
| chr9:132205697
|
A | G | 1 | a0001c0004t0002g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.857+7088A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205697 | ||||||
| chr9:132205758
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.857+7149G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205758 | ||||||
| chr9:132205897
|
G | C | 4 | a0001c0001t0001g0343a0001c0001t0011g0007a0001c0002t0001g0333others(1): Show | 4 | HG02071.hp2 HG02083.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+7288G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205897 | ||||||
| chr9:132205984
|
G | C | 68 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0301others(65): Show | 68 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.857+7375G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132205984 | ||||||
| chr9:132206112
|
A | G | 78 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0301others(75): Show | 78 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(75): Show |
intron_variant | MODIFIER | c.857+7503A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206112 | ||||||
| chr9:132206123
|
A | T | 225 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(222): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.857+7514A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206123 | ||||||
| chr9:132206127
|
A | G | 78 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0301others(75): Show | 78 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(75): Show |
intron_variant | MODIFIER | c.857+7518A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206127 | ||||||
| chr9:132206194
|
C | T | 2 | a0001c0001t0012g0257a0001c0002t0021g0230 | 2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.857+7585C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206194 | ||||||
| chr9:132206195
|
G | A | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+7586G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206195 | ||||||
| chr9:132206351
|
G | A | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+7742G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206351 | ||||||
| chr9:132206443
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.857+7834C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206443 | ||||||
| chr9:132206508
|
G | A | 69 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0301others(66): Show | 69 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.857+7899G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206508 | ||||||
| chr9:132206559
|
C | T | 1 | a0001c0002t0039g0045 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.857+7950C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206559 | ||||||
| chr9:132206590
|
C | T | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+7981C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206590 | ||||||
| chr9:132206591
|
C | T | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+7982C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206591 | ||||||
| chr9:132206592
|
A | G | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+7983A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206592 | ||||||
| chr9:132206594
|
A | G | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+7985A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206594 | ||||||
| chr9:132206615
|
C | T | 2 | a0001c0004t0016g0229a0001c0004t0024g0228 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.857+8006C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206615 | ||||||
| chr9:132206674
|
T | A | 1 | a0001c0003t0001g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.857+8065T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206674 | ||||||
| chr9:132206777
|
G | T | 38 | a0001c0001t0005g0186a0001c0001t0005g0234a0001c0001t0012g0101others(35): Show | 38 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.857+8168G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206777 | ||||||
| chr9:132206810
|
G | A | 1 | a0001c0001t0004g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.857+8201G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206810 | ||||||
| chr9:132206832
|
C | T | 1 | a0001c0004t0047g0322 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.857+8223C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206832 | ||||||
| chr9:132206855
|
C | G | 1 | a0001c0002t0003g0135 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.857+8246C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206855 | ||||||
| chr9:132206855
|
C | T | 1 | a0001c0003t0001g0306 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.857+8246C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206855 | ||||||
| chr9:132206919
|
A | G | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+8310A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206919 | ||||||
| chr9:132206941
|
C | G | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+8332C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206941 | ||||||
| chr9:132206953
|
G | A | 13 | a0001c0001t0002g0018a0001c0001t0005g0165a0001c0001t0042g0158others(10): Show | 13 | HG01891.hp2 HG01943.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.857+8344G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132206953 | ||||||
| chr9:132207007
|
C | T | 9 | a0001c0004t0002g0003a0001c0004t0002g0247a0001c0004t0003g0273others(6): Show | 9 | HG02027.hp1 HG02451.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.857+8398C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207007 | ||||||
| chr9:132207100
|
G | A | 56 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0340others(53): Show | 56 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.857+8491G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207100 | ||||||
| chr9:132207156
|
G | A | 3 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0046g0077 | 3 | HG01884.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.857+8547G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207156 | ||||||
| chr9:132207196
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.857+8587C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207196 | ||||||
| chr9:132207263
|
T | A | 212 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(209): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.857+8654T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207263 | ||||||
| chr9:132207360
|
G | T | 1 | a0001c0001t0004g0301 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.857+8751G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207360 | ||||||
| chr9:132207371
|
G | C | 7 | a0001c0004t0002g0003a0001c0004t0017g0220a0001c0005t0008g0349others(4): Show | 7 | HG02027.hp1 NA18944.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.857+8762G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207371 | ||||||
| chr9:132207445
|
C | T | 1 | a0001c0001t0020g0302 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.857+8836C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207445 | ||||||
| chr9:132207461
|
G | A | 16 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0344others(13): Show | 16 | HG01167.hp1 HG01361.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.857+8852G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207461 | ||||||
| chr9:132207592
|
G | A | 144 | a0001c0001t0001g0010a0001c0001t0001g0187a0001c0001t0001g0346others(141): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.857+8983G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207592 | ||||||
| chr9:132207659
|
C | T | 1 | a0001c0006t0002g0084 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.857+9050C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207659 | ||||||
| chr9:132207744
|
G | A | 2 | a0001c0003t0004g0250a0001c0003t0006g0222 | 2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.857+9135G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207744 | ||||||
| chr9:132207744
|
G | T | 18 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0340others(15): Show | 18 | HG01891.hp2 HG01943.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.857+9135G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207744 | ||||||
| chr9:132207970
|
G | A | 1 | a0001c0004t0001g0331 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.857+9361G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207970 | ||||||
| chr9:132207995
|
C | G | 67 | a0001c0001t0001g0140a0001c0001t0002g0018a0001c0001t0004g0301others(64): Show | 67 | HG00621.hp1 HG01106.hp1 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.857+9386C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132207995 | ||||||
| chr9:132208214
|
G | T | 1 | a0001c0002t0004g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.857+9605G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208214 | ||||||
| chr9:132208283
|
G | A | 152 | a0001c0001t0001g0010a0001c0001t0001g0187a0001c0001t0001g0346others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.857+9674G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208283 | ||||||
| chr9:132208484
|
T | C | 187 | a0001c0001t0001g0010a0001c0001t0001g0109a0001c0001t0001g0188others(184): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.857+9875T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208484 | ||||||
| chr9:132208558
|
T | G | 1 | a0001c0001t0004g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.857+9949T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208558 | ||||||
| chr9:132208596
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.857+9987A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208596 | ||||||
| chr9:132208634
|
A | G | 1 | a0001c0004t0053g0298 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.857+10025A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208634 | ||||||
| chr9:132208638
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.857+10029A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208638 | ||||||
| chr9:132208728
|
T | A | 210 | a0001c0001t0001g0010a0001c0001t0001g0187a0001c0001t0001g0346others(207): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.857+10119T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208728 | ||||||
| chr9:132208827
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.857+10218A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208827 | ||||||
| chr9:132208866
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.857+10257G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208866 | ||||||
| chr9:132208870
|
T | TCCCTGTG others(25): Show |
1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.857+10264_857+1026 others(36): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132208870 | |||||
| chr9:132208967
|
G | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0223a0001c0001t0011g0231 | 3 | HG02717.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.857+10358G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132208967 | ||||||
| chr9:132209037
|
A | G | 4 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0005g0246others(1): Show | 4 | HG01884.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.857+10428A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209037 | ||||||
| chr9:132209090
|
G | A | 160 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.857+10481G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209090 | ||||||
| chr9:132209147
|
G | A | 2 | a0001c0003t0003g0233a0001c0003t0004g0226 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.857+10538G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209147 | ||||||
| chr9:132209178
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.857+10569C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209178 | ||||||
| chr9:132209368
|
G | A | 1 | a0001c0002t0001g0190 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.857+10759G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209368 | ||||||
| chr9:132209537
|
G | A | 2 | a0001c0001t0003g0320a0001c0001t0003g0321 | 2 | NA18950.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.857+10928G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209537 | ||||||
| chr9:132209769
|
C | T | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.857+11160C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209769 | ||||||
| chr9:132209860
|
G | C | 191 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(188): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.857+11251G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209860 | ||||||
| chr9:132209894
|
A | G | 8 | a0001c0001t0001g0140a0001c0001t0002g0020a0001c0001t0012g0125others(5): Show | 8 | HG02257.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.857+11285A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132209894 | ||||||
| chr9:132210267
|
C | G | 1 | a0001c0001t0005g0186 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.857+11658C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210267 | ||||||
| chr9:132210308
|
G | A | 226 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(223): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.857+11699G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210308 | ||||||
| chr9:132210449
|
C | T | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.857+11840C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210449 | ||||||
| chr9:132210477
|
G | A | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.857+11868G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210477 | ||||||
| chr9:132210553
|
C | T | 2 | a0001c0001t0011g0061a0001c0002t0001g0013 | 2 | HG02080.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.857+11944C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210553 | ||||||
| chr9:132210610
|
T | C | 226 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(223): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.857+12001T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210610 | ||||||
| chr9:132210626
|
C | T | 1 | a0001c0004t0022g0039 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.857+12017C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210626 | ||||||
| chr9:132210637
|
G | A | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.857+12028G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210637 | ||||||
| chr9:132210675
|
G | A | 34 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0004g0260others(31): Show | 34 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.857+12066G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210675 | ||||||
| chr9:132210709
|
G | T | 1 | a0001c0004t0002g0232 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.857+12100G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210709 | ||||||
| chr9:132210894
|
G | A | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.857+12285G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210894 | ||||||
| chr9:132210900
|
T | TCA | 34 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0004g0260others(31): Show | 34 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.857+12301_857+1230 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132210900 | |||||
| chr9:132210950
|
A | G | 1 | a0001c0004t0001g0023 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.857+12341A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132210950 | ||||||
| chr9:132211023
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.857+12414C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211023 | ||||||
| chr9:132211223
|
C | A | 2 | a0001c0001t0012g0257a0001c0002t0021g0230 | 2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.857+12614C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211223 | ||||||
| chr9:132211333
|
G | A | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.857+12724G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211333 | ||||||
| chr9:132211349
|
G | A | 3 | a0001c0001t0001g0343a0001c0001t0011g0007a0001c0002t0002g0159 | 3 | HG02071.hp2 HG02132.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.857+12740G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211349 | ||||||
| chr9:132211561
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.857+12952C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211561 | ||||||
| chr9:132211653
|
C | G | 7 | a0001c0001t0001g0049a0001c0001t0001g0066a0001c0001t0001g0111others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.857+13044C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211653 | ||||||
| chr9:132211751
|
T | C | 228 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(225): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.857+13142T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211751 | ||||||
| chr9:132211826
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.857+13217A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211826 | ||||||
| chr9:132211981
|
C | G | 2 | a0001c0004t0001g0166a0001c0004t0001g0331 | 2 | HG01975.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.857+13372C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211981 | ||||||
| chr9:132212205
|
C | A | 1 | a0001c0003t0006g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.857+13596C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212205 | ||||||
| chr9:132212224
|
A | C | 229 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.857+13615A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212224 | ||||||
| chr9:132212307
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.857+13698C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212307 | ||||||
| chr9:132212331
|
C | T | 3 | a0001c0001t0018g0091a0001c0002t0001g0167a0001c0003t0001g0153 | 3 | HG01074.hp2 HG01192.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.857+13722C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212331 | ||||||
| chr9:132212335
|
C | T | 2 | a0001c0001t0001g0140a0001c0002t0002g0272 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.857+13726C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212335 | ||||||
| chr9:132212505
|
G | A | 227 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.857+13896G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212505 | ||||||
| chr9:132212615
|
G | A | 1 | a0001c0006t0031g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.857+14006G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212615 | ||||||
| chr9:132212750
|
G | C | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858-14099G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212750 | ||||||
| chr9:132212833
|
C | T | 1 | a0001c0002t0045g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.858-14016C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212833 | ||||||
| chr9:132212931
|
AC | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(27): Show | 30 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.858-13912delC | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132212931 | |||||
| chr9:132212936
|
C | G | 1 | a0001c0004t0047g0322 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.858-13913C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132212936 | ||||||
| chr9:132213041
|
G | A | 1 | a0001c0001t0006g0221 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.858-13808G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213041 | ||||||
| chr9:132213099
|
C | T | 1 | a0001c0004t0002g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.858-13750C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213099 | ||||||
| chr9:132213108
|
A | G | 228 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.858-13741A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213108 | ||||||
| chr9:132213139
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858-13710C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213139 | ||||||
| chr9:132213140
|
G | A | 4 | a0001c0001t0005g0186a0001c0001t0005g0234a0001c0001t0012g0101others(1): Show | 4 | HG01106.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-13709G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213140 | ||||||
| chr9:132213261
|
A | G | 229 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.858-13588A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213261 | ||||||
| chr9:132213262
|
A | C | 229 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.858-13587A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213262 | ||||||
| chr9:132213331
|
C | CA | 28 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0040others(25): Show | 28 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.858-13488dupA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132213331 | |||||
| chr9:132213331
|
CA | C | 9 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0002g0050others(6): Show | 9 | HG01074.hp1 HG01975.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.858-13488delA | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132213331 | |||||
| chr9:132213331
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0003g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.858-13499_858-1348 others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132213331 | |||||
| chr9:132213331
|
CAAAAAAA others(6): Show |
C | 30 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0004g0260others(27): Show | 30 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.858-13500_858-1348 others(17): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132213331 | |||||
| chr9:132213331
|
CAAAAAAA others(7): Show |
C | 193 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.858-13501_858-1348 others(18): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132213331 | |||||
| chr9:132213331
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0002t0001g0055a0001c0002t0001g0113a0001c0006t0001g0284 | 3 | HG00099.hp1 HG02630.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.858-13502_858-1348 others(19): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132213331 | |||||
| chr9:132213345
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858-13504A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213345 | ||||||
| chr9:132213350
|
A | G | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858-13499A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213350 | ||||||
| chr9:132213443
|
G | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858-13406G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213443 | ||||||
| chr9:132213509
|
C | G | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.858-13340C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213509 | ||||||
| chr9:132213515
|
A | G | 226 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.858-13334A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213515 | ||||||
| chr9:132213591
|
C | G | 1 | a0001c0002t0001g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.858-13258C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213591 | ||||||
| chr9:132213694
|
GT | G | 194 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.858-13149delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132213694 | |||||
| chr9:132213785
|
A | C | 226 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.858-13064A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213785 | ||||||
| chr9:132213867
|
C | T | 79 | a0001c0001t0002g0348a0001c0001t0003g0098a0001c0001t0003g0160others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.858-12982C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132213867 | ||||||
| chr9:132214581
|
G | A | 3 | a0001c0003t0001g0064a0002c0007t0002g0131a0002c0008t0001g0132 | 3 | HG00323.hp1 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.858-12268G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132214581 | ||||||
| chr9:132214730
|
G | T | 1 | a0001c0004t0002g0003 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.858-12119G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132214730 | ||||||
| chr9:132214800
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.858-12049G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132214800 | ||||||
| chr9:132214874
|
AT | A | 228 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.858-11961delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132214874 | |||||
| chr9:132214875
|
T | A | 2 | a0001c0004t0001g0331a0001c0006t0001g0005 | 2 | HG02027.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.858-11974T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132214875 | ||||||
| chr9:132214876
|
T | A | 227 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.858-11973T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132214876 | ||||||
| chr9:132215059
|
T | A | 190 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.858-11790T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215059 | ||||||
| chr9:132215077
|
TG | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0196others(19): Show | 22 | HG00423.hp1 HG00609.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.858-11761delG | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132215077 | |||||
| chr9:132215077
|
TGG | T | 182 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.858-11762_858-1176 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132215077 | |||||
| chr9:132215079
|
G | C | 1 | a0001c0001t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.858-11770G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215079 | ||||||
| chr9:132215082
|
G | T | 2 | a0001c0001t0001g0191a0001c0002t0002g0107 | 2 | NA18952.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.858-11767G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215082 | ||||||
| chr9:132215087
|
G | T | 2 | a0001c0001t0001g0140a0001c0002t0002g0272 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.858-11762G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215087 | ||||||
| chr9:132215173
|
C | A | 229 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.858-11676C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215173 | ||||||
| chr9:132215486
|
AG | A | 190 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.858-11361delG | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132215486 | |||||
| chr9:132215490
|
T | G | 190 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.858-11359T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215490 | ||||||
| chr9:132215550
|
G | A | 1 | a0001c0001t0018g0088 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.858-11299G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215550 | ||||||
| chr9:132215551
|
G | A | 1 | a0001c0004t0002g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.858-11298G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215551 | ||||||
| chr9:132215849
|
C | G | 2 | a0001c0002t0002g0145a0001c0002t0002g0146 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.858-11000C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215849 | ||||||
| chr9:132215853
|
G | A | 1 | a0001c0001t0009g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.858-10996G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215853 | ||||||
| chr9:132215955
|
G | A | 189 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.858-10894G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132215955 | ||||||
| chr9:132216033
|
G | A | 1 | a0001c0004t0007g0208 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.858-10816G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216033 | ||||||
| chr9:132216191
|
T | A | 32 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0004g0260others(29): Show | 32 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.858-10658T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216191 | ||||||
| chr9:132216219
|
T | C | 32 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0004g0260others(29): Show | 32 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.858-10630T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216219 | ||||||
| chr9:132216244
|
G | T | 1 | a0001c0002t0002g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.858-10605G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216244 | ||||||
| chr9:132216245
|
C | T | 1 | a0001c0002t0002g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.858-10604C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216245 | ||||||
| chr9:132216276
|
G | T | 1 | a0001c0002t0001g0150 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.858-10573G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216276 | ||||||
| chr9:132216381
|
C | CCT | 4 | a0001c0002t0004g0138a0001c0003t0003g0201a0001c0006t0002g0072others(1): Show | 4 | HG02145.hp2 NA18944.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-10435_858-1043 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216381 | |||||
| chr9:132216381
|
CCTCT | C | 4 | a0001c0001t0006g0221a0001c0002t0001g0336a0001c0002t0001g0337others(1): Show | 4 | HG01070.hp2 HG01081.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-10437_858-1043 others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216381 | |||||
| chr9:132216381
|
CCTCTCT | C | 5 | a0001c0001t0003g0051a0001c0001t0027g0053a0001c0002t0002g0245others(2): Show | 5 | HG02015.hp2 NA18747.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.858-10439_858-1043 others(10): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216381 | |||||
| chr9:132216410
|
CTCTCTGT others(11): Show |
C | 2 | a0001c0001t0001g0140a0001c0002t0002g0272 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.858-10437_858-1042 others(22): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216410 | |||||
| chr9:132216410
|
CTCTCTGT others(13): Show |
C | 1 | a0001c0003t0001g0306 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.858-10437_858-1041 others(24): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216410 | |||||
| chr9:132216412
|
CTCTGTGT others(3): Show |
C | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858-10435_858-1042 others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216412 | |||||
| chr9:132216412
|
CTCTGTGT others(13): Show |
C | 1 | a0001c0004t0003g0118 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.858-10435_858-1041 others(24): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216412 | |||||
| chr9:132216412
|
CTCTGTGT others(15): Show |
C | 5 | a0001c0001t0002g0020a0001c0001t0003g0037a0001c0001t0003g0038others(2): Show | 5 | HG02965.hp2 HG03471.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-10435_858-1041 others(26): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216412 | |||||
| chr9:132216412
|
CTCTGTGT others(17): Show |
C | 2 | a0001c0003t0002g0028a0001c0003t0037g0137 | 2 | HG02129.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.858-10435_858-1041 others(28): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216412 | |||||
| chr9:132216414
|
C | CTCTCTCT others(5): Show |
1 | a0001c0002t0001g0253 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.858-10434_858-1043 others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
C | CTCTCTCT others(9): Show |
2 | a0001c0002t0004g0254a0001c0002t0005g0194 | 2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.858-10434_858-1043 others(20): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
C | CTCTCTCT others(11): Show |
1 | a0001c0002t0001g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.858-10434_858-1043 others(22): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
C | CTCTCTCT others(13): Show |
1 | a0001c0002t0001g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.858-10434_858-1043 others(24): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
C | CTCTCTCT others(1): Show |
3 | a0001c0001t0002g0018a0001c0001t0005g0165a0001c0004t0002g0247 | 3 | HG02970.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.858-10434_858-1043 others(12): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
C | CTCTCTCT others(3): Show |
1 | a0001c0002t0002g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.858-10434_858-1043 others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
C | CTCTCTGT others(5): Show |
1 | a0001c0004t0002g0003 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.858-10434_858-1043 others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
C | G | 13 | a0001c0001t0001g0109a0001c0001t0001g0191a0001c0001t0002g0144others(10): Show | 13 | HG00438.hp2 HG00558.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.858-10435C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216414 | ||||||
| chr9:132216414
|
CTGTGTGT others(3): Show |
C | 5 | a0001c0001t0001g0187a0001c0002t0001g0113a0001c0003t0001g0328others(2): Show | 5 | HG00099.hp1 HG03453.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-10431_858-1042 others(14): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
CTGTGTGT others(5): Show |
C | 32 | a0001c0001t0001g0346a0001c0001t0002g0344a0001c0001t0002g0348others(29): Show | 32 | HG00323.hp1 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.858-10433_858-1042 others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
CTGTGTGT others(7): Show |
C | 71 | a0001c0001t0002g0097a0001c0001t0003g0086a0001c0001t0003g0160others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.858-10421_858-1040 others(18): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
CTGTGTGT others(9): Show |
C | 48 | a0001c0001t0002g0182a0001c0001t0002g0223a0001c0001t0002g0281others(45): Show | 48 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.858-10421_858-1040 others(20): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
CTGTGTGT others(11): Show |
C | 13 | a0001c0001t0002g0204a0001c0001t0004g0301a0001c0001t0013g0263others(10): Show | 13 | HG02015.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.858-10421_858-1040 others(22): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216414
|
CTGTGTGT others(13): Show |
C | 14 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0046g0077others(11): Show | 14 | HG00621.hp1 HG01884.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.858-10421_858-1040 others(24): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216414 | |||||
| chr9:132216416
|
G | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0047others(36): Show | 39 | HG01081.hp1 HG01099.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.858-10433G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216416 | ||||||
| chr9:132216418
|
G | C | 13 | a0001c0001t0001g0010a0001c0001t0004g0260a0001c0001t0005g0029others(10): Show | 13 | HG01081.hp1 HG01099.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.858-10431G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216418 | ||||||
| chr9:132216420
|
G | C | 5 | a0001c0001t0001g0010a0001c0001t0013g0009a0001c0001t0042g0158others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.858-10429G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216420 | ||||||
| chr9:132216422
|
G | C | 5 | a0001c0001t0001g0010a0001c0001t0013g0009a0001c0002t0001g0170others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-10427G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216422 | ||||||
| chr9:132216424
|
G | C | 2 | a0001c0003t0001g0330a0001c0003t0004g0250 | 2 | HG02818.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.858-10425G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216424 | ||||||
| chr9:132216426
|
G | C | 7 | a0001c0001t0001g0187a0001c0002t0001g0113a0001c0003t0001g0328others(4): Show | 7 | HG00099.hp1 HG02818.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.858-10423G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216426 | ||||||
| chr9:132216426
|
GTA | G | 27 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0001g0047others(24): Show | 27 | HG01123.hp2 HG01243.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.858-10421_858-1042 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216426 | |||||
| chr9:132216428
|
A | C | 39 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0344others(36): Show | 39 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.858-10421A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216428 | ||||||
| chr9:132216428
|
A | G | 26 | a0001c0001t0002g0018a0001c0001t0005g0165a0001c0001t0018g0088others(23): Show | 26 | HG01099.hp2 HG01891.hp2 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.858-10421A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216428 | ||||||
| chr9:132216428
|
ATG | A | 5 | a0001c0001t0002g0050a0001c0001t0002g0106a0001c0002t0001g0154others(2): Show | 5 | HG00558.hp1 HG00597.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.858-10381_858-1038 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216428 | |||||
| chr9:132216428
|
ATGTG | A | 93 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0031others(90): Show | 95 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.858-10383_858-1038 others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132216428 | |||||
| chr9:132216430
|
G | C | 108 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0097others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.858-10419G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216430 | ||||||
| chr9:132216432
|
G | A | 24 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0001g0114others(21): Show | 24 | HG01099.hp2 HG01123.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.858-10417G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216432 | ||||||
| chr9:132216432
|
G | C | 136 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0097others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.858-10417G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216432 | ||||||
| chr9:132216434
|
G | C | 72 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0182others(69): Show | 72 | HG00673.hp2 HG00741.hp2 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.858-10415G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216434 | ||||||
| chr9:132216436
|
G | C | 23 | a0001c0001t0002g0182a0001c0001t0002g0223a0001c0001t0005g0076others(20): Show | 23 | HG00621.hp1 HG01884.hp2 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.858-10413G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216436 | ||||||
| chr9:132216438
|
G | C | 4 | a0001c0001t0005g0076a0001c0001t0005g0078a0001c0001t0046g0077others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-10411G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216438 | ||||||
| chr9:132216455
|
TGTGTGTG others(6): Show |
T | 1 | a0001c0002t0006g0206 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.858-10393_858-1038 others(17): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216455 | ||||||
| chr9:132216469
|
T | C | 1 | a0001c0002t0006g0206 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.858-10380T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216469 | ||||||
| chr9:132216492
|
G | A | 194 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.858-10357G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216492 | ||||||
| chr9:132216512
|
A | G | 229 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0187others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.858-10337A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216512 | ||||||
| chr9:132216572
|
G | A | 196 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.858-10277G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216572 | ||||||
| chr9:132216660
|
C | T | 1 | a0001c0002t0002g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.858-10189C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216660 | ||||||
| chr9:132216731
|
C | T | 33 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0004g0260others(30): Show | 33 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.858-10118C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216731 | ||||||
| chr9:132216861
|
G | T | 5 | a0001c0001t0002g0020a0001c0001t0003g0037a0001c0001t0003g0038others(2): Show | 5 | HG02965.hp2 HG03471.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.858-9988G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132216861 | ||||||
| chr9:132217321
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.858-9528G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217321 | ||||||
| chr9:132217372
|
T | C | 1 | a0001c0001t0002g0075 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.858-9477T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217372 | ||||||
| chr9:132217522
|
G | A | 1 | a0001c0004t0003g0273 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.858-9327G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217522 | ||||||
| chr9:132217562
|
G | T | 1 | a0001c0004t0001g0046 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.858-9287G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217562 | ||||||
| chr9:132217605
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.858-9244G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217605 | ||||||
| chr9:132217654
|
T | C | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-9195T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217654 | ||||||
| chr9:132217844
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0002g0018others(33): Show | 36 | HG01081.hp1 HG01261.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.858-9005A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217844 | ||||||
| chr9:132217987
|
G | A | 2 | a0001c0001t0027g0053a0001c0004t0003g0195 | 2 | NA18966.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.858-8862G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132217987 | ||||||
| chr9:132218016
|
G | A | 1 | a0001c0002t0002g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.858-8833G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218016 | ||||||
| chr9:132218161
|
G | T | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-8688G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218161 | ||||||
| chr9:132218176
|
C | T | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-8673C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218176 | ||||||
| chr9:132218349
|
G | A | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-8500G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218349 | ||||||
| chr9:132218448
|
A | C | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-8401A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218448 | ||||||
| chr9:132218488
|
G | GT | 193 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0020others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.858-8353dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132218488 | |||||
| chr9:132218488
|
G | T | 1 | a0001c0004t0047g0322 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.858-8361G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218488 | ||||||
| chr9:132218523
|
T | A | 1 | a0001c0003t0001g0306 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.858-8326T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218523 | ||||||
| chr9:132218560
|
G | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0223a0001c0001t0011g0231 | 3 | HG02717.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.858-8289G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218560 | ||||||
| chr9:132218648
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.858-8201C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218648 | ||||||
| chr9:132218685
|
C | T | 1 | a0001c0002t0021g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.858-8164C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218685 | ||||||
| chr9:132218880
|
T | C | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-7969T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218880 | ||||||
| chr9:132218986
|
G | T | 3 | a0001c0001t0005g0265a0001c0001t0005g0266a0001c0002t0003g0119 | 3 | HG02895.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.858-7863G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132218986 | ||||||
| chr9:132219049
|
A | G | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.858-7800A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219049 | ||||||
| chr9:132219446
|
G | A | 2 | a0001c0003t0004g0250a0001c0003t0006g0222 | 2 | HG02818.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.858-7403G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219446 | ||||||
| chr9:132219516
|
T | C | 1 | a0001c0003t0001g0175 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.858-7333T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219516 | ||||||
| chr9:132219587
|
AAG | A | 191 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0001g0346others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.858-7260_858-7259d others(4): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132219587 | |||||
| chr9:132219588
|
AG | A | 31 | a0001c0001t0001g0010a0001c0001t0002g0018a0001c0001t0002g0204others(28): Show | 31 | HG01081.hp1 HG01261.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.858-7260delG | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219588 | ||||||
| chr9:132219589
|
G | A | 1 | a0001c0002t0021g0230 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.858-7260G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219589 | ||||||
| chr9:132219818
|
A | T | 1 | a0001c0003t0010g0316 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.858-7031A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219818 | ||||||
| chr9:132219889
|
C | G | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-6960C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219889 | ||||||
| chr9:132219894
|
T | C | 3 | a0001c0001t0001g0140a0001c0002t0002g0272a0001c0002t0044g0274 | 3 | HG02257.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.858-6955T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132219894 | ||||||
| chr9:132220136
|
T | C | 1 | a0001c0004t0047g0322 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.858-6713T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132220136 | ||||||
| chr9:132220169
|
C | T | 2 | a0001c0006t0002g0072a0001c0006t0002g0354 | 2 | NA18944.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.858-6680C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132220169 | ||||||
| chr9:132220461
|
C | CT | 19 | a0001c0001t0002g0067a0001c0001t0003g0098a0001c0001t0006g0221others(16): Show | 19 | HG00438.hp1 HG01109.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.858-6371dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132220461 | |||||
| chr9:132220461
|
CT | C | 30 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0169others(27): Show | 31 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.858-6371delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132220461 | |||||
| chr9:132220728
|
G | A | 3 | a0001c0005t0008g0199a0001c0006t0002g0072a0001c0006t0002g0354 | 3 | NA18944.hp1 NA18967.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.858-6121G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132220728 | ||||||
| chr9:132221102
|
T | C | 2 | a0001c0004t0016g0229a0001c0004t0024g0228 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.858-5747T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221102 | ||||||
| chr9:132221159
|
C | A | 1 | a0001c0001t0004g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.858-5690C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221159 | ||||||
| chr9:132221380
|
G | A | 7 | a0001c0001t0001g0049a0001c0001t0001g0066a0001c0001t0001g0111others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.858-5469G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221380 | ||||||
| chr9:132221412
|
C | T | 2 | a0001c0001t0002g0161a0001c0002t0001g0052 | 2 | HG04228.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.858-5437C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221412 | ||||||
| chr9:132221474
|
C | T | 4 | a0001c0001t0013g0263a0001c0001t0013g0264a0001c0001t0016g0224others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.858-5375C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221474 | ||||||
| chr9:132221537
|
G | T | 1 | a0001c0002t0002g0300 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.858-5312G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221537 | ||||||
| chr9:132221564
|
G | A | 1 | a0001c0005t0002g0341 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.858-5285G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221564 | ||||||
| chr9:132221576
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.858-5273C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221576 | ||||||
| chr9:132221620
|
G | A | 1 | a0001c0004t0047g0322 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.858-5229G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221620 | ||||||
| chr9:132221655
|
G | A | 1 | a0001c0004t0007g0208 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.858-5194G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221655 | ||||||
| chr9:132221683
|
G | A | 2 | a0001c0001t0011g0061a0001c0002t0001g0013 | 2 | HG02080.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.858-5166G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221683 | ||||||
| chr9:132221695
|
G | A | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.858-5154G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221695 | ||||||
| chr9:132221870
|
C | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0223a0001c0001t0011g0231 | 3 | HG02717.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.858-4979C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221870 | ||||||
| chr9:132221973
|
G | A | 2 | a0001c0005t0008g0349a0001c0005t0009g0356 | 2 | HG02027.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.858-4876G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132221973 | ||||||
| chr9:132222458
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0005g0029a0001c0002t0001g0170 | 3 | HG01081.hp1 HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.858-4391A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132222458 | ||||||
| chr9:132222610
|
G | A | 46 | a0001c0001t0001g0095a0001c0001t0001g0169a0001c0001t0002g0020others(43): Show | 46 | HG00621.hp1 HG00741.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.858-4239G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132222610 | ||||||
| chr9:132222617
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.858-4232G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132222617 | ||||||
| chr9:132222695
|
G | A | 1 | a0001c0004t0002g0003 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.858-4154G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132222695 | ||||||
| chr9:132222703
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.858-4146C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132222703 | ||||||
| chr9:132222891
|
A | C | 1 | a0001c0002t0001g0333 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.858-3958A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132222891 | ||||||
| chr9:132222985
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0036g0285 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.858-3864G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132222985 | ||||||
| chr9:132223007
|
G | A | 1 | a0001c0002t0004g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.858-3842G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223007 | ||||||
| chr9:132223075
|
C | T | 1 | a0001c0005t0006g0218 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.858-3774C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223075 | ||||||
| chr9:132223185
|
C | T | 1 | a0001c0004t0003g0118 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.858-3664C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223185 | ||||||
| chr9:132223270
|
C | T | 4 | a0001c0001t0005g0186a0001c0001t0020g0302a0001c0002t0021g0230others(1): Show | 4 | HG02622.hp2 HG02809.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-3579C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223270 | ||||||
| chr9:132223278
|
C | T | 1 | a0001c0002t0009g0304 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.858-3571C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223278 | ||||||
| chr9:132223280
|
G | A | 186 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0155others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.858-3569G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223280 | ||||||
| chr9:132223314
|
C | T | 1 | a0001c0005t0006g0218 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.858-3535C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223314 | ||||||
| chr9:132223328
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.858-3521C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223328 | ||||||
| chr9:132223355
|
G | C | 9 | a0001c0002t0001g0200a0001c0002t0001g0253a0001c0002t0001g0280others(6): Show | 9 | HG01943.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.858-3494G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223355 | ||||||
| chr9:132223430
|
C | T | 1 | a0001c0004t0001g0026 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.858-3419C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223430 | ||||||
| chr9:132223705
|
C | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0344others(4): Show | 7 | HG01361.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.858-3144C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223705 | ||||||
| chr9:132223706
|
G | A | 1 | a0001c0003t0006g0219 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.858-3143G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223706 | ||||||
| chr9:132223783
|
G | A | 3 | a0001c0003t0001g0064a0002c0007t0002g0131a0002c0008t0001g0132 | 3 | HG00323.hp1 HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.858-3066G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223783 | ||||||
| chr9:132223886
|
G | T | 15 | a0001c0001t0005g0103a0001c0001t0005g0234a0001c0001t0046g0077others(12): Show | 15 | HG01106.hp1 HG01167.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.858-2963G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132223886 | ||||||
| chr9:132224015
|
C | T | 184 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(181): Show | 186 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.858-2834C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224015 | ||||||
| chr9:132224016
|
G | A | 2 | a0001c0002t0044g0274a0001c0003t0006g0222 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.858-2833G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224016 | ||||||
| chr9:132224020
|
A | T | 5 | a0001c0001t0005g0186a0001c0001t0020g0302a0001c0002t0021g0230others(2): Show | 5 | HG02622.hp2 HG02809.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.858-2829A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224020 | ||||||
| chr9:132224030
|
C | G | 206 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(203): Show | 208 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.858-2819C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224030 | ||||||
| chr9:132224099
|
C | T | 178 | a0001c0001t0001g0031a0001c0001t0001g0095a0001c0001t0001g0140others(175): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.858-2750C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224099 | ||||||
| chr9:132224359
|
C | T | 1 | a0001c0005t0002g0015 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.858-2490C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224359 | ||||||
| chr9:132224430
|
G | T | 1 | a0001c0002t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.858-2419G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224430 | ||||||
| chr9:132224519
|
G | A | 1 | a0001c0004t0032g0162 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.858-2330G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224519 | ||||||
| chr9:132224523
|
C | A | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858-2326C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224523 | ||||||
| chr9:132224644
|
G | A | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.858-2205G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224644 | ||||||
| chr9:132224924
|
CT | C | 12 | a0001c0001t0005g0029a0001c0001t0005g0076a0001c0001t0005g0078others(9): Show | 12 | HG01081.hp1 HG01106.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.858-1915delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132224924 | |||||
| chr9:132224982
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.858-1867G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224982 | ||||||
| chr9:132225155
|
T | G | 240 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0049others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.858-1694T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225155 | ||||||
| chr9:132225224
|
TTTGTC | T | 193 | a0001c0001t0001g0034a0001c0001t0002g0018a0001c0001t0002g0020others(190): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.858-1620_858-1616d others(7): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132225224 | |||||
| chr9:132225229
|
C | T | 66 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0057others(63): Show | 66 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.858-1620C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225229 | ||||||
| chr9:132225244
|
T | TTTTGTTT others(7): Show |
1 | a0001c0002t0044g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.858-1602_858-1601i others(16): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | 132225244 | |||||
| chr9:132225258
|
G | T | 1 | a0001c0002t0044g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.858-1591G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225258 | ||||||
| chr9:132225304
|
T | A | 1 | a0001c0004t0029g0227 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.858-1545T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225304 | ||||||
| chr9:132225519
|
G | A | 42 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0066others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.858-1330G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225519 | ||||||
| chr9:132225532
|
A | C | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.858-1317A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225532 | ||||||
| chr9:132225562
|
G | A | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.858-1287G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225562 | ||||||
| chr9:132225591
|
A | G | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.858-1258A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225591 | ||||||
| chr9:132225656
|
G | A | 4 | a0001c0001t0002g0204a0001c0003t0014g0293a0001c0003t0014g0297others(1): Show | 4 | HG00280.hp1 HG02738.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.858-1193G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225656 | ||||||
| chr9:132225837
|
C | T | 16 | a0001c0001t0004g0301a0001c0001t0005g0029a0001c0001t0005g0076others(13): Show | 16 | HG01081.hp1 HG01106.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.858-1012C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225837 | ||||||
| chr9:132225877
|
C | T | 16 | a0001c0001t0004g0301a0001c0001t0005g0029a0001c0001t0005g0076others(13): Show | 16 | HG01081.hp1 HG01106.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.858-972C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225877 | ||||||
| chr9:132225896
|
G | A | 1 | a0001c0003t0006g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.858-953G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225896 | ||||||
| chr9:132226181
|
G | A | 11 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0013g0263others(8): Show | 11 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.858-668G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132226181 | ||||||
| chr9:132226193
|
A | G | 2 | a0001c0001t0002g0204a0001c0004t0024g0228 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.858-656A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132226193 | ||||||
| chr9:132226353
|
C | T | 8 | a0001c0001t0002g0281a0001c0001t0003g0251a0001c0001t0004g0260others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.858-496C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132226353 | ||||||
| chr9:132226477
|
C | G | 1 | a0001c0002t0002g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.858-372C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132226477 | ||||||
| chr9:132226573
|
C | G | 1 | a0001c0001t0003g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.858-276C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132226573 | ||||||
| chr9:132226817
|
C | T | 1 | a0001c0001t0012g0125 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.858-32C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132226817 | ||||||
| chr9:132226846
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0020 | 2 | HG02965.hp2 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.858-3C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132226846 | ||||||
| chr9:132227045
|
C | T | 1 | a0001c0004t0002g0323 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1030+24C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227045 | ||||||
| chr9:132227076
|
G | A | 1 | a0001c0003t0006g0205 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1030+55G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227076 | ||||||
| chr9:132227083
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1030+62C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227083 | ||||||
| chr9:132227155
|
G | A | 4 | a0001c0002t0001g0123a0001c0003t0001g0156a0001c0003t0001g0198others(1): Show | 4 | HG00639.hp1 HG01106.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030+134G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227155 | ||||||
| chr9:132227287
|
C | T | 177 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0008g0087others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1030+266C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227287 | ||||||
| chr9:132227421
|
C | A | 52 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0068others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1030+400C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227421 | ||||||
| chr9:132227453
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0020 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1030+432G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227453 | ||||||
| chr9:132227474
|
A | T | 2 | a0001c0002t0002g0272a0001c0005t0002g0341 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1030+453A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227474 | ||||||
| chr9:132227542
|
C | T | 24 | a0001c0002t0001g0200a0001c0002t0001g0253a0001c0002t0001g0262others(21): Show | 24 | HG01167.hp1 HG01891.hp2 HG01943.hp2 others(21): Show |
intron_variant | MODIFIER | c.1030+521C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227542 | ||||||
| chr9:132227661
|
G | T | 1 | a0001c0002t0004g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1030+640G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227661 | ||||||
| chr9:132227756
|
A | T | 1 | a0001c0002t0001g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1030+735A>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227756 | ||||||
| chr9:132227782
|
C | T | 1 | a0001c0004t0003g0118 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1030+761C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227782 | ||||||
| chr9:132227955
|
A | G | 1 | a0001c0003t0001g0286 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1030+934A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132227955 | ||||||
| chr9:132228327
|
C | T | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1030+1306C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228327 | ||||||
| chr9:132228328
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0169a0001c0004t0001g0166others(1): Show | 4 | HG00140.hp2 HG01975.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030+1307G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228328 | ||||||
| chr9:132228453
|
C | T | 1 | a0001c0005t0040g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1030+1432C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228453 | ||||||
| chr9:132228454
|
G | C | 87 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0095others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1030+1433G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228454 | ||||||
| chr9:132228558
|
C | CT | 291 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(288): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1030+1549dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 132228558 | |||||
| chr9:132228558
|
CT | C | 16 | a0001c0001t0004g0301a0001c0001t0005g0029a0001c0001t0005g0076others(13): Show | 16 | HG01081.hp1 HG01106.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1030+1549delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 132228558 | |||||
| chr9:132228706
|
C | T | 2 | a0001c0002t0001g0102a0001c0005t0002g0235 | 2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1030+1685C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228706 | ||||||
| chr9:132228730
|
G | A | 3 | a0001c0001t0002g0182a0001c0001t0002g0223a0001c0001t0011g0231 | 3 | HG02717.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1030+1709G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228730 | ||||||
| chr9:132228849
|
C | G | 1 | a0001c0004t0001g0331 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1031-1723C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228849 | ||||||
| chr9:132228994
|
G | A | 1 | a0001c0001t0002g0344 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1031-1578G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132228994 | ||||||
| chr9:132229005
|
G | C | 1 | a0001c0004t0024g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1031-1567G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229005 | ||||||
| chr9:132229119
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1031-1453G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229119 | ||||||
| chr9:132229129
|
C | T | 138 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0095others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1031-1443C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229129 | ||||||
| chr9:132229313
|
C | T | 2 | a0001c0002t0001g0180a0001c0003t0006g0222 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1031-1259C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229313 | ||||||
| chr9:132229322
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1031-1250C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229322 | ||||||
| chr9:132229323
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1031-1249G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229323 | ||||||
| chr9:132229399
|
C | T | 89 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(86): Show | 89 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1031-1173C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229399 | ||||||
| chr9:132229489
|
G | C | 1 | a0001c0003t0002g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1031-1083G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229489 | ||||||
| chr9:132229540
|
G | A | 1 | a0001c0003t0002g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1031-1032G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229540 | ||||||
| chr9:132229637
|
C | T | 1 | a0001c0003t0002g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1031-935C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229637 | ||||||
| chr9:132229672
|
G | A | 268 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(265): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1031-900G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229672 | ||||||
| chr9:132229783
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0002g0059a0001c0001t0043g0060 | 3 | HG01934.hp1 HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1031-789C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229783 | ||||||
| chr9:132229794
|
C | T | 22 | a0001c0001t0001g0187a0001c0001t0001g0346a0001c0001t0002g0182others(19): Show | 22 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1031-778C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229794 | ||||||
| chr9:132229858
|
T | G | 2 | a0001c0002t0002g0243a0001c0002t0002g0244 | 2 | HG01074.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1031-714T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132229858 | ||||||
| chr9:132230054
|
C | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0004t0041g0249 | 3 | HG02965.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1031-518C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230054 | ||||||
| chr9:132230068
|
C | T | 270 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(267): Show | 272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1031-504C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230068 | ||||||
| chr9:132230085
|
G | A | 10 | a0001c0002t0001g0333a0001c0002t0002g0159a0001c0002t0009g0035others(7): Show | 11 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1031-487G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230085 | ||||||
| chr9:132230114
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1031-458G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230114 | ||||||
| chr9:132230168
|
TAGAC | T | 6 | a0001c0002t0001g0013a0001c0002t0001g0017a0001c0002t0001g0134others(3): Show | 6 | NA18941.hp2 NA18950.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1031-401_1031-398d others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 132230168 | |||||
| chr9:132230210
|
G | T | 267 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(264): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1031-362G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230210 | ||||||
| chr9:132230228
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1031-344T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230228 | ||||||
| chr9:132230311
|
G | A | 18 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0004g0301others(15): Show | 18 | HG01081.hp1 HG01106.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.1031-261G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230311 | ||||||
| chr9:132230398
|
C | T | 1 | a0001c0003t0002g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1031-174C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230398 | ||||||
| chr9:132230410
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0002g0281a0001c0001t0003g0251others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1031-162C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230410 | ||||||
| chr9:132230424
|
G | C | 285 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(282): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1031-148G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230424 | ||||||
| chr9:132230468
|
G | A | 1 | a0001c0001t0006g0221 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1031-104G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230468 | ||||||
| chr9:132230557
|
G | A | 87 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(84): Show | 87 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1031-15G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 4/7 | chr9 | 132230557 | ||||||
| chr9:132230639
|
G | A | 1 | a0001c0002t0001g0253 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1054+44G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132230639 | ||||||
| chr9:132230667
|
T | A | 292 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(289): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1054+72T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132230667 | ||||||
| chr9:132230762
|
C | A | 1 | a0001c0003t0002g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1054+167C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132230762 | ||||||
| chr9:132231018
|
C | A | 2 | a0001c0001t0002g0075a0001c0004t0001g0305 | 2 | NA18979.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1054+423C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132231018 | ||||||
| chr9:132231200
|
G | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0020 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1054+605G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132231200 | ||||||
| chr9:132231336
|
C | A | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1054+741C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132231336 | ||||||
| chr9:132231554
|
G | A | 1 | a0001c0001t0018g0091 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1054+959G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132231554 | ||||||
| chr9:132232031
|
G | A | 173 | a0001c0001t0001g0033a0001c0001t0001g0095a0001c0001t0001g0140others(170): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1054+1436G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232031 | ||||||
| chr9:132232034
|
G | A | 24 | a0001c0001t0001g0019a0001c0001t0001g0187a0001c0001t0001g0346others(21): Show | 24 | HG01361.hp2 HG02145.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1054+1439G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232034 | ||||||
| chr9:132232093
|
C | T | 2 | a0001c0001t0001g0346a0001c0004t0002g0232 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1054+1498C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232093 | ||||||
| chr9:132232271
|
C | T | 1 | a0001c0002t0009g0304 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1054+1676C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232271 | ||||||
| chr9:132232420
|
G | A | 1 | a0001c0001t0002g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1054+1825G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232420 | ||||||
| chr9:132232484
|
G | A | 1 | a0001c0004t0007g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1054+1889G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232484 | ||||||
| chr9:132232582
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1054+1987G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232582 | ||||||
| chr9:132232610
|
T | C | 1 | a0001c0003t0002g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1054+2015T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232610 | ||||||
| chr9:132232658
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1054+2063T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232658 | ||||||
| chr9:132232715
|
C | A | 1 | a0001c0004t0002g0338 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1054+2120C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232715 | ||||||
| chr9:132232812
|
TG | T | 148 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(145): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1054+2223delG | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 132232812 | |||||
| chr9:132232852
|
G | T | 3 | a0001c0001t0001g0188a0001c0001t0011g0197a0001c0002t0001g0192 | 3 | NA18946.hp2 NA19057.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1054+2257G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232852 | ||||||
| chr9:132232862
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1054+2267C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232862 | ||||||
| chr9:132232973
|
C | T | 6 | a0001c0001t0001g0095a0001c0001t0001g0169a0001c0002t0001g0120others(3): Show | 6 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054+2378C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132232973 | ||||||
| chr9:132233075
|
C | A | 16 | a0001c0001t0004g0301a0001c0001t0005g0029a0001c0001t0005g0076others(13): Show | 16 | HG01081.hp1 HG01106.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1054+2480C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233075 | ||||||
| chr9:132233123
|
G | A | 14 | a0001c0002t0001g0058a0001c0002t0001g0090a0001c0002t0001g0122others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1054+2528G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233123 | ||||||
| chr9:132233139
|
G | T | 16 | a0001c0001t0004g0301a0001c0001t0005g0029a0001c0001t0005g0076others(13): Show | 16 | HG01081.hp1 HG01106.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1054+2544G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233139 | ||||||
| chr9:132233164
|
C | A | 128 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(125): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1054+2569C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233164 | ||||||
| chr9:132233251
|
A | G | 3 | a0001c0004t0001g0026a0001c0004t0002g0100a0001c0004t0002g0338 | 3 | NA18977.hp1 NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1054+2656A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233251 | ||||||
| chr9:132233325
|
G | T | 1 | a0001c0002t0001g0113 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1054+2730G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233325 | ||||||
| chr9:132233332
|
T | TAC | 108 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(105): Show | 108 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1054+2753_1054+275 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 132233332 | |||||
| chr9:132233332
|
T | TACAC | 5 | a0001c0001t0001g0155a0001c0002t0001g0282a0001c0004t0001g0324others(2): Show | 5 | HG00558.hp2 HG02647.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054+2751_1054+275 others(8): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 132233332 | |||||
| chr9:132233350
|
G | C | 7 | a0001c0002t0001g0253a0001c0002t0001g0280a0001c0002t0002g0242others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+2755G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233350 | ||||||
| chr9:132233409
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1054+2814G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233409 | ||||||
| chr9:132233475
|
G | T | 278 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(275): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1054+2880G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233475 | ||||||
| chr9:132233667
|
C | T | 1 | a0001c0001t0005g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1054+3072C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233667 | ||||||
| chr9:132233844
|
C | T | 1 | a0001c0002t0001g0069 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1054+3249C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233844 | ||||||
| chr9:132233965
|
G | A | 3 | a0001c0001t0013g0263a0001c0002t0004g0261a0001c0003t0004g0250 | 3 | HG02486.hp1 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1054+3370G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132233965 | ||||||
| chr9:132234026
|
C | CT | 24 | a0001c0001t0001g0111a0001c0001t0002g0223a0001c0001t0004g0260others(21): Show | 24 | HG00323.hp2 HG01081.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1054+3449dupT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 132234026 | |||||
| chr9:132234026
|
CT | C | 99 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(96): Show | 99 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1054+3449delT | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 132234026 | |||||
| chr9:132234026
|
CTT | C | 160 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1054+3448_1054+344 others(6): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 132234026 | |||||
| chr9:132234113
|
C | T | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1054+3518C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234113 | ||||||
| chr9:132234121
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0040a0001c0001t0001g0114others(1): Show | 4 | HG00408.hp1 HG01243.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054+3526C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234121 | ||||||
| chr9:132234146
|
A | C | 1 | a0001c0005t0040g0239 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1054+3551A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234146 | ||||||
| chr9:132234387
|
G | A | 1 | a0001c0001t0003g0283 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1054+3792G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234387 | ||||||
| chr9:132234446
|
A | G | 25 | a0001c0002t0001g0157a0001c0002t0001g0180a0001c0002t0001g0253others(22): Show | 26 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1054+3851A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234446 | ||||||
| chr9:132234482
|
T | C | 176 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(173): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1054+3887T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234482 | ||||||
| chr9:132234523
|
C | A | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1054+3928C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234523 | ||||||
| chr9:132234551
|
G | A | 1 | a0001c0003t0002g0028 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1054+3956G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234551 | ||||||
| chr9:132234588
|
C | T | 3 | a0001c0003t0001g0064a0001c0003t0001g0288a0001c0005t0001g0270 | 3 | HG00639.hp2 HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1054+3993C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234588 | ||||||
| chr9:132234647
|
G | A | 104 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0021others(101): Show | 104 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1054+4052G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234647 | ||||||
| chr9:132234689
|
G | C | 1 | a0001c0001t0013g0009 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1054+4094G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234689 | ||||||
| chr9:132234939
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1055-4165A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132234939 | ||||||
| chr9:132235048
|
T | G | 1 | a0001c0001t0003g0321 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1055-4056T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235048 | ||||||
| chr9:132235056
|
G | A | 1 | a0001c0001t0046g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1055-4048G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235056 | ||||||
| chr9:132235069
|
C | T | 210 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0031others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1055-4035C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235069 | ||||||
| chr9:132235224
|
A | G | 147 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0031others(144): Show | 147 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1055-3880A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235224 | ||||||
| chr9:132235239
|
G | C | 10 | a0001c0001t0002g0012a0001c0001t0002g0080a0001c0001t0002g0148others(7): Show | 10 | HG00741.hp1 HG01106.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1055-3865G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235239 | ||||||
| chr9:132235301
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1055-3803C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235301 | ||||||
| chr9:132235324
|
CTCTGTCC others(1): Show |
C | 3 | a0001c0004t0001g0026a0001c0004t0002g0100a0001c0004t0002g0338 | 3 | NA18977.hp1 NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1055-3777_1055-377 others(12): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 132235324 | |||||
| chr9:132235343
|
C | T | 1 | a0001c0001t0006g0221 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1055-3761C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235343 | ||||||
| chr9:132235358
|
G | A | 8 | a0001c0001t0004g0260a0001c0001t0012g0101a0001c0001t0012g0125others(5): Show | 8 | HG01884.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1055-3746G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235358 | ||||||
| chr9:132235497
|
A | G | 59 | a0001c0001t0001g0346a0001c0001t0003g0037a0001c0001t0003g0038others(56): Show | 60 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1055-3607A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235497 | ||||||
| chr9:132235711
|
G | A | 3 | a0001c0001t0003g0251a0001c0002t0001g0253a0001c0002t0001g0280 | 3 | HG02622.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1055-3393G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235711 | ||||||
| chr9:132235714
|
C | A | 3 | a0001c0001t0003g0251a0001c0002t0001g0253a0001c0002t0001g0280 | 3 | HG02622.hp1 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1055-3390C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235714 | ||||||
| chr9:132235747
|
C | G | 1 | a0001c0003t0001g0275 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1055-3357C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235747 | ||||||
| chr9:132236013
|
C | T | 1 | a0001c0001t0046g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1055-3091C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236013 | ||||||
| chr9:132236171
|
G | A | 27 | a0001c0001t0005g0029a0001c0001t0005g0076a0001c0001t0005g0078others(24): Show | 27 | HG01081.hp1 HG01106.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1055-2933G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236171 | ||||||
| chr9:132236183
|
T | C | 237 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0031others(234): Show | 239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1055-2921T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236183 | ||||||
| chr9:132236195
|
G | C | 6 | a0001c0001t0013g0009a0001c0001t0013g0263a0001c0001t0013g0264others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1055-2909G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236195 | ||||||
| chr9:132236216
|
G | A | 1 | a0001c0003t0004g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1055-2888G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236216 | ||||||
| chr9:132236237
|
G | T | 1 | a0001c0003t0001g0275 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1055-2867G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236237 | ||||||
| chr9:132236289
|
A | C | 1 | a0001c0003t0007g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1055-2815A>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236289 | ||||||
| chr9:132236465
|
G | A | 1 | a0001c0002t0002g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1055-2639G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236465 | ||||||
| chr9:132236612
|
G | C | 1 | a0001c0002t0009g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1055-2492G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236612 | ||||||
| chr9:132236898
|
C | T | 53 | a0001c0001t0001g0140a0001c0001t0001g0187a0001c0001t0003g0037others(50): Show | 54 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.1055-2206C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132236898 | ||||||
| chr9:132237090
|
G | A | 1 | a0001c0004t0008g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1055-2014G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237090 | ||||||
| chr9:132237287
|
T | A | 6 | a0001c0001t0013g0009a0001c0001t0013g0263a0001c0001t0013g0264others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1055-1817T>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237287 | ||||||
| chr9:132237341
|
G | C | 13 | a0001c0001t0005g0029a0001c0001t0005g0076a0001c0001t0005g0078others(10): Show | 13 | HG01081.hp1 HG01106.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1055-1763G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237341 | ||||||
| chr9:132237438
|
G | A | 9 | a0001c0001t0012g0101a0001c0001t0012g0125a0001c0001t0012g0257others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1055-1666G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237438 | ||||||
| chr9:132237597
|
G | A | 1 | a0001c0001t0005g0234 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1055-1507G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237597 | ||||||
| chr9:132237612
|
G | A | 13 | a0001c0001t0005g0029a0001c0001t0005g0076a0001c0001t0005g0078others(10): Show | 13 | HG01081.hp1 HG01106.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1055-1492G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237612 | ||||||
| chr9:132237643
|
G | T | 1 | a0001c0001t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1055-1461G>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237643 | ||||||
| chr9:132237819
|
G | A | 1 | a0001c0002t0002g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1055-1285G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237819 | ||||||
| chr9:132237861
|
C | T | 13 | a0001c0001t0005g0029a0001c0001t0005g0076a0001c0001t0005g0078others(10): Show | 13 | HG01081.hp1 HG01106.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1055-1243C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132237861 | ||||||
| chr9:132238100
|
T | G | 1 | a0001c0004t0017g0215 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1055-1004T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238100 | ||||||
| chr9:132238110
|
G | A | 1 | a0001c0002t0004g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1055-994G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238110 | ||||||
| chr9:132238313
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1055-791G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238313 | ||||||
| chr9:132238329
|
G | C | 13 | a0001c0001t0005g0029a0001c0001t0005g0076a0001c0001t0005g0078others(10): Show | 13 | HG01081.hp1 HG01106.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1055-775G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238329 | ||||||
| chr9:132238679
|
C | T | 106 | a0001c0001t0001g0155a0001c0001t0002g0012a0001c0001t0002g0018others(103): Show | 106 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1055-425C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238679 | ||||||
| chr9:132238697
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1055-407C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238697 | ||||||
| chr9:132238938
|
C | A | 3 | a0001c0004t0001g0026a0001c0004t0002g0100a0001c0004t0002g0338 | 3 | NA18977.hp1 NA19004.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1055-166C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238938 | ||||||
| chr9:132238978
|
G | A | 103 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0020others(100): Show | 103 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1055-126G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132238978 | ||||||
| chr9:132239009
|
C | T | 12 | a0001c0001t0004g0301a0001c0001t0004g0340a0001c0002t0004g0081others(9): Show | 12 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1055-95C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132239009 | ||||||
| chr9:132239284
|
G | A | 1 | a0001c0003t0006g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1222+13G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132239284 | ||||||
| chr9:132239391
|
T | G | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1222+120T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132239391 | ||||||
| chr9:132239599
|
C | T | 1 | a0001c0004t0041g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1222+328C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132239599 | ||||||
| chr9:132239640
|
T | TG | 47 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0044others(44): Show | 48 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1222+376dupG | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 132239640 | |||||
| chr9:132239642
|
G | A | 1 | a0001c0001t0043g0060 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1222+371G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132239642 | ||||||
| chr9:132239648
|
T | C | 1 | a0001c0002t0008g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1222+377T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132239648 | ||||||
| chr9:132239676
|
G | A | 1 | a0001c0003t0006g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1222+405G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132239676 | ||||||
| chr9:132239701
|
C | T | 103 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0020others(100): Show | 103 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1222+430C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132239701 | ||||||
| chr9:132240210
|
C | T | 1 | a0001c0002t0001g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1223-700C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240210 | ||||||
| chr9:132240211
|
G | A | 2 | a0001c0002t0001g0094a0001c0002t0008g0164 | 2 | NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1223-699G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240211 | ||||||
| chr9:132240223
|
A | G | 1 | a0001c0001t0003g0251 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1223-687A>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240223 | ||||||
| chr9:132240259
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1223-651C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240259 | ||||||
| chr9:132240270
|
G | A | 104 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0020others(101): Show | 104 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1223-640G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240270 | ||||||
| chr9:132240292
|
G | A | 1 | a0001c0004t0003g0070 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1223-618G>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240292 | ||||||
| chr9:132240372
|
C | T | 1 | a0001c0002t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1223-538C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240372 | ||||||
| chr9:132240609
|
C | A | 2 | a0001c0003t0001g0149a0001c0004t0001g0166 | 2 | HG00735.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1223-301C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 6/7 | chr9 | 132240609 | ||||||
| chr9:132241097
|
G | C | 6 | a0001c0001t0013g0009a0001c0001t0013g0263a0001c0001t0013g0264others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1357+53G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241097 | ||||||
| chr9:132241101
|
C | G | 1 | a0001c0004t0003g0070 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1357+57C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241101 | ||||||
| chr9:132241210
|
C | A | 1 | a0001c0001t0002g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1357+166C>A | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241210 | ||||||
| chr9:132241600
|
C | T | 41 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0044others(38): Show | 42 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1358-276C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241600 | ||||||
| chr9:132241724
|
G | C | 193 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0020others(190): Show | 194 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.1358-152G>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241724 | ||||||
| chr9:132241759
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1358-117C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241759 | ||||||
| chr9:132241791
|
T | G | 255 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0021others(252): Show | 256 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1358-85T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241791 | ||||||
| chr9:132241796
|
C | T | 1 | a0001c0001t0033g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1358-80C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241796 |