Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MLHLL others(525): Show |
chr9 | 132157058 | 132249526 |
| a0002 | 1/0 | 530 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | MLHLL others(525): Show |
chr9 | 132157058 | 132249526 |
| a0003 | 0/0 | 530 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | MLHLL others(525): Show |
chr9 | 132157058 | 132249526 |
| a0004 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | MLHLL others(525): Show |
chr9 | 132157058 | 132249526 |
| a0005 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | MLHLL others(525): Show |
chr9 | 132157058 | 132249526 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1590 | 118 | 37 | 19 | 45 | 6 | 10 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0002 | 0/0 | 1590 | 94 | 34 | 22 | 24 | 3 | 11 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0003 | 0/0 | 1590 | 60 | 8 | 17 | 25 | 3 | 7 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0004 | 0/0 | 1590 | 49 | 9 | 3 | 31 | 1 | 5 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0005 | 0/0 | 1590 | 16 | 3 | 3 | 8 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0006 | 0/0 | 1590 | 12 | 0 | 2 | 8 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0012 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0014 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0001c0015 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0002c0010 | 1/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0002c0013 | 0/0 | 1590 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0003c0007 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0003c0008 | 0/0 | 1590 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0004c0011 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 | ||
| a0005c0009 | 0/0 | 1590 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | ATGCT others(1585): Show |
chr9 | 132157058 | 132249526 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4673 | 29 | 4 | 7 | 14 | 2 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0002 | 0/0 | 4672 | 32 | 7 | 6 | 16 | 0 | 3 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0003 | 0/1 | 4673 | 22 | 4 | 0 | 10 | 3 | 4 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0004 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0005 | 0/0 | 4673 | 10 | 8 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0006 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0007 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0010 | 0/0 | 4673 | 3 | 3 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0011 | 0/0 | 4673 | 4 | 4 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0013 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0014 | 0/0 | 4672 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0015 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0016 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0020 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0023 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0025 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0029 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0030 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0035 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0036 | 0/0 | 4673 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0040 | 0/0 | 4672 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0041 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0001t0043 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0001 | 0/0 | 4673 | 49 | 12 | 16 | 15 | 1 | 5 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0002 | 0/0 | 4672 | 21 | 8 | 3 | 6 | 0 | 4 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0003 | 0/0 | 4673 | 13 | 10 | 2 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0004 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0005 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0007 | 0/0 | 4673 | 3 | 0 | 1 | 0 | 1 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0008 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0012 | 0/0 | 4682 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4677): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0032 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0037 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0038 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0002t0042 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0001 | 0/0 | 4673 | 26 | 1 | 10 | 10 | 2 | 3 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0002 | 0/0 | 4672 | 12 | 2 | 4 | 6 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0003 | 0/0 | 4673 | 6 | 4 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0004 | 0/0 | 4673 | 5 | 1 | 0 | 3 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0006 | 0/0 | 4672 | 2 | 0 | 0 | 1 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0009 | 0/0 | 4672 | 4 | 0 | 0 | 4 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0012 | 0/0 | 4682 | 2 | 0 | 0 | 0 | 1 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4677): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0019 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0026 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0003t0031 | 0/0 | 4673 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0001 | 0/0 | 4673 | 11 | 0 | 1 | 8 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0002 | 0/0 | 4672 | 11 | 2 | 1 | 6 | 0 | 2 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0003 | 0/0 | 4673 | 8 | 1 | 1 | 5 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0004 | 0/0 | 4673 | 3 | 0 | 0 | 3 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0006 | 0/0 | 4672 | 3 | 0 | 0 | 3 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0008 | 0/0 | 4673 | 2 | 0 | 0 | 2 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0010 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0013 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0017 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0018 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0021 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0022 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0024 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0028 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0034 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0039 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0004t0045 | 0/0 | 4682 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4677): Show |
chr9 | 132157058 | 132249526 |
| a0001c0005t0001 | 0/0 | 4673 | 6 | 0 | 2 | 3 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0005t0002 | 0/0 | 4672 | 7 | 2 | 1 | 4 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0005t0004 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0005t0007 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0005t0033 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0006t0001 | 0/0 | 4673 | 5 | 0 | 1 | 4 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0006t0002 | 0/0 | 4672 | 5 | 0 | 0 | 4 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0006t0003 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0006t0027 | 0/0 | 4672 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0001c0012t0008 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0014t0001 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0001c0015t0044 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0002c0010t0001 | 1/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0002c0013t0001 | 0/0 | 4673 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0003c0007t0002 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0003c0008t0001 | 0/0 | 4673 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| a0004c0011t0002 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4667): Show |
chr9 | 132157058 | 132249526 |
| a0005c0009t0001 | 0/0 | 4673 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | GATCT others(4668): Show |
chr9 | 132157058 | 132249526 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0215 | 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 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0010g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0010g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0014g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0016g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0020g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0023g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0025g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0029g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0030g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0035g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0036g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0040g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0041g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0001t0043g0212 | 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 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0014 | 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 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0002g0326 | 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 |
| a0001c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0007g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0012g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0032g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0037g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0038g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0002t0042g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0148 | 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 |
| a0001c0003t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0006g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0009g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0009g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0009g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0009g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0012g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0012g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0019g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0026g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0003t0031g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0238 | 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 |
| a0001c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0017g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0021g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0022g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0024g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0028g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0034g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0039g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0004t0045g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0005t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0007g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0005t0033g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0006t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0006t0027g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0012t0008g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0014t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0001c0015t0044g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0002c0010t0001g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0002c0013t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0003c0007t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0003c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0004c0011t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| a0005c0009t0001g0354 | 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 | g0114 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0161 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0063 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00140 | hp2 | a0001 | c0004 | t0045 | g0299 | EUR | GBR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00280 | hp1 | a0001 | c0003 | t0012 | g0294 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00280 | hp2 | a0001 | c0002 | t0007 | g0113 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00323 | hp1 | a0003 | c0007 | t0002 | g0133 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00423 | hp1 | a0001 | c0003 | t0004 | g0207 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0009 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0325 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0333 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00621 | hp1 | a0001 | c0004 | t0006 | g0221 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0157 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0289 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0072 | EAS | CHS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00741 | hp1 | a0001 | c0001 | t0040 | g0066 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG00741 | hp2 | a0001 | c0005 | t0001 | g0271 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0337 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01071 | hp2 | a0001 | c0003 | t0003 | g0003 | 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 | t0014 | g0092 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0338 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0279 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01099 | hp2 | a0001 | c0001 | t0014 | g0089 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0215 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0340 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0250 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0344 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0327 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0111 | 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 | g0328 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01175 | hp1 | a0001 | c0006 | t0001 | g0272 | 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 | g0301 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0154 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01243 | hp2 | a0001 | c0002 | t0007 | g0302 | AMR | PUR | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01257 | hp1 | a0001 | c0005 | t0001 | g0278 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0002 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01261 | hp1 | a0001 | c0004 | t0002 | g0043 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0300 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01516 | hp1 | a0001 | c0002 | t0012 | g0295 | EUR | IBS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0200 | EUR | IBS | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01884 | hp2 | a0001 | c0001 | t0035 | g0078 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0352 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0082 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01943 | hp1 | a0001 | c0003 | t0002 | g0312 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01952 | hp1 | a0001 | c0004 | t0003 | g0203 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01975 | hp1 | a0001 | c0004 | t0001 | g0167 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0320 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01981 | hp2 | a0001 | c0001 | t0036 | g0061 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02004 | hp1 | a0001 | c0003 | t0031 | g0129 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02015 | hp1 | a0001 | c0003 | t0009 | g0317 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02027 | hp1 | a0001 | c0005 | t0001 | g0348 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02027 | hp2 | a0001 | c0006 | t0001 | g0006 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0055 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02056 | hp2 | a0001 | c0004 | t0008 | g0242 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0326 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0029 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02132 | hp2 | a0001 | c0005 | t0001 | g0330 | EAS | KHV | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02145 | hp1 | a0001 | c0004 | t0018 | g0231 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0139 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02155 | hp1 | a0001 | c0004 | t0021 | g0117 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02155 | hp2 | a0001 | c0006 | t0002 | g0005 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02165 | hp2 | a0001 | c0006 | t0001 | g0296 | EAS | CDX | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02257 | hp1 | a0002 | c0013 | t0001 | g0131 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0273 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0297 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02451 | hp1 | a0001 | c0004 | t0003 | g0274 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0307 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02572 | hp1 | a0001 | c0004 | t0010 | g0280 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0239 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02615 | hp1 | a0001 | c0001 | t0013 | g0230 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0281 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02622 | hp2 | a0001 | c0002 | t0008 | g0236 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0349 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0283 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02683 | hp1 | a0001 | c0002 | t0007 | g0036 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02683 | hp2 | a0001 | c0003 | t0001 | g0335 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0261 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02735 | hp2 | a0001 | c0005 | t0033 | g0241 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02738 | hp1 | a0001 | c0003 | t0004 | g0206 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02738 | hp2 | a0001 | c0003 | t0012 | g0298 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0351 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0265 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0232 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0350 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0159 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02895 | hp1 | a0001 | c0001 | t0043 | g0212 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0267 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02922 | hp2 | a0001 | c0002 | t0042 | g0240 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0120 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0270 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0258 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03041 | hp1 | a0001 | c0001 | t0041 | g0213 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03041 | hp2 | a0001 | c0004 | t0017 | g0234 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0305 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03130 | hp1 | a0001 | c0004 | t0013 | g0235 | 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 | t0037 | g0275 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0309 | 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 | g0141 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0255 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0269 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03225 | hp1 | a0001 | c0005 | t0002 | g0306 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0102 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03239 | hp1 | a0001 | c0001 | t0015 | g0028 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0277 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0214 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0238 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0276 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03492 | hp2 | a0001 | c0004 | t0002 | g0086 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0251 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ESN | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0126 | AFR | GWD | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03579 | hp1 | a0001 | c0004 | t0034 | g0249 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03654 | hp1 | a0001 | c0014 | t0001 | g0288 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03669 | hp2 | a0001 | c0002 | t0038 | g0184 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03688 | hp2 | a0001 | c0004 | t0003 | g0119 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03704 | hp1 | a0001 | c0003 | t0006 | g0219 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0332 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03831 | hp1 | a0001 | c0006 | t0003 | g0346 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03834 | hp2 | a0003 | c0008 | t0001 | g0132 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0182 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04115 | hp2 | a0001 | c0003 | t0026 | g0138 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04184 | hp1 | a0001 | c0006 | t0002 | g0085 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | BEB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04199 | hp1 | a0001 | c0005 | t0001 | g0263 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0147 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0033 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04228 | hp1 | a0001 | c0004 | t0002 | g0140 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0264 | 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 | g0094 | EAS | CHB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | CHB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0080 | 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 | g0324 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18939 | hp2 | a0001 | c0002 | t0032 | g0046 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18941 | hp1 | a0001 | c0004 | t0003 | g0137 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18944 | hp1 | a0001 | c0006 | t0002 | g0073 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18944 | hp2 | a0001 | c0004 | t0008 | g0040 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18946 | hp1 | a0004 | c0011 | t0002 | g0118 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18948 | hp1 | a0001 | c0003 | t0009 | g0316 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18948 | hp2 | a0001 | c0004 | t0039 | g0323 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18949 | hp1 | a0001 | c0004 | t0004 | g0209 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18949 | hp2 | a0001 | c0004 | t0003 | g0143 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18951 | hp1 | a0001 | c0003 | t0002 | g0341 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18952 | hp2 | a0001 | c0004 | t0003 | g0071 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18960 | hp1 | a0001 | c0006 | t0001 | g0285 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18960 | hp2 | a0001 | c0003 | t0002 | g0148 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18961 | hp2 | a0001 | c0006 | t0002 | g0293 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18963 | hp1 | a0001 | c0003 | t0009 | g0315 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18966 | hp2 | a0001 | c0001 | t0020 | g0054 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18967 | hp2 | a0001 | c0006 | t0002 | g0353 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0179 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18969 | hp2 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18970 | hp1 | a0001 | c0004 | t0006 | g0224 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18974 | hp1 | a0001 | c0003 | t0004 | g0226 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18974 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18977 | hp1 | a0001 | c0004 | t0002 | g0339 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18977 | hp2 | a0001 | c0004 | t0001 | g0318 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18979 | hp2 | a0001 | c0004 | t0024 | g0194 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18984 | hp1 | a0001 | c0004 | t0004 | g0217 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18986 | hp1 | a0005 | c0009 | t0001 | g0354 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0331 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18993 | hp1 | a0001 | c0003 | t0006 | g0223 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18993 | hp2 | a0001 | c0002 | t0004 | g0216 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18995 | hp2 | a0001 | c0003 | t0004 | g0227 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA18999 | hp2 | a0001 | c0005 | t0007 | g0355 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19000 | hp2 | a0001 | c0004 | t0004 | g0225 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0023 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19002 | hp2 | a0001 | c0004 | t0002 | g0084 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19004 | hp1 | a0001 | c0004 | t0002 | g0101 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19005 | hp2 | a0001 | c0004 | t0006 | g0218 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0303 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19011 | hp1 | a0001 | c0004 | t0028 | g0163 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0083 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19012 | hp1 | a0001 | c0003 | t0009 | g0314 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0329 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0319 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0211 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19054 | hp2 | a0001 | c0003 | t0001 | g0304 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19063 | hp1 | a0001 | c0005 | t0002 | g0291 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19063 | hp2 | a0001 | c0005 | t0001 | g0201 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19067 | hp1 | a0001 | c0001 | t0030 | g0042 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19067 | hp2 | a0001 | c0012 | t0008 | g0220 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19068 | hp2 | a0001 | c0005 | t0002 | g0016 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19070 | hp2 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19074 | hp2 | a0001 | c0005 | t0002 | g0125 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19080 | hp2 | a0001 | c0004 | t0003 | g0196 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19084 | hp2 | a0001 | c0003 | t0019 | g0311 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19087 | hp1 | a0001 | c0004 | t0001 | g0027 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19088 | hp2 | a0001 | c0005 | t0002 | g0292 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19090 | hp2 | a0001 | c0004 | t0002 | g0336 | EAS | JPT | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | YRI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | YRI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ASW | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20129 | hp2 | a0001 | c0001 | t0029 | g0075 | AFR | ASW | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0074 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0178 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0284 | EUR | TSI | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | GIH | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20905 | hp2 | a0001 | c0015 | t0044 | g0204 | SAS | GIH | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG01123 | hp2 | a0001 | c0006 | t0027 | g0262 | AMR | CLM | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0253 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02109 | hp2 | a0001 | c0005 | t0002 | g0208 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0257 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02486 | hp2 | a0001 | c0005 | t0004 | g0228 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0286 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG06807 | hp1 | a0001 | c0004 | t0022 | g0233 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | USA | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0202 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0195 | AFR | LWK | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0045 | REF | REF | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| homoSapiens | grch38p0 | a0002 | c0010 | t0001 | g0064 | REF | REF | NTNG2_chr9_132157058_132249526 | NTNG2 | chr9 | 132157058 | 132249526 |
| view | 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 | a0003 | 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 | a0005 | 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 | a0001 a0003 a0004 others(1): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): 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 | a0004 | 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 |
| view | 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 | a0001c0003 a0001c0004 a0001c0012 others(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 | a0001c0005 a0001c0006 a0005c0009 |
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 | a0001c0002 a0001c0003 a0001c0005 others(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 |
| view | 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 | a0001c0002t0012 a0001c0003t0012 a0001c0004t0045 |
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 | a0001c0001t0015 | 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 | a0001c0015t0044 | 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 | a0001c0001t0041 a0001c0001t0043 a0001c0002t0042 |
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 | a0001c0001t0040 | 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 | 16 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0013 others(13): 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 | a0001c0003t0009 a0001c0003t0019 |
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 | a0001c0004t0039 | 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 | a0001c0001t0020 a0001c0004t0021 |
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 | a0001c0004t0039 | 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 | a0001c0001t0016 a0001c0004t0022 |
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 | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(32): Show |
178 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(175): 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 | a0001c0001t0007 a0001c0002t0007 a0001c0005t0007 |
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 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0013 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(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 | a0001c0001t0023 | 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 | 22 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0014 others(19): 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 | a0001c0001t0030 | 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 | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(41): Show |
189 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(186): 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 | a0001c0001t0029 | 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 | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(32): Show |
178 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(175): 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 | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(41): Show |
189 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(186): 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 | 3 | a0001c0001t0011 a0001c0001t0013 a0001c0004t0013 |
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 | a0001c0004t0024 | 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 | a0001c0001t0014 | 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 | a0001c0004t0028 | 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 | a0001c0001t0020 | 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 | a0001c0006t0027 | 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 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0043 others(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 | 47 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(44): Show |
192 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(189): 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 | 22 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0014 others(19): 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 | 11 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0013 others(8): 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 | a0001c0001t0036 | 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 | 5 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0035 others(2): 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 | 6 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0035 others(3): 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 | a0001c0001t0005 a0001c0001t0041 a0001c0002t0005 |
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 |
| view | 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 | 156 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0205 others(153): 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 | a0001c0003t0003g0202 | 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 | a0001c0001t0002g0199 a0001c0001t0003g0254 a0001c0001t0004g0210 others(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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0001t0002g0347 others(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 | a0001c0004t0003g0203 | 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 | a0001c0004t0002g0004 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 a0001c0001t0005g0215 others(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 | a0001c0001t0001g0345 a0001c0002t0042g0240 a0001c0005t0033g0241 |
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 | a0001c0001t0005g0259 a0001c0001t0005g0260 a0001c0001t0011g0258 others(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 | a0001c0001t0002g0282 a0001c0001t0003g0284 a0001c0001t0025g0286 others(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 | a0001c0001t0003g0308 a0001c0001t0016g0309 a0001c0002t0002g0307 |
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 | 88 | a0001c0001t0001g0197 a0001c0001t0001g0342 a0001c0001t0002g0205 others(85): 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 | 64 | a0001c0001t0001g0342 a0001c0001t0002g0347 a0001c0001t0003g0266 others(61): 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 | 41 | a0001c0001t0001g0342 a0001c0001t0003g0305 a0001c0001t0003g0321 others(38): 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 | a0001c0001t0001g0342 a0001c0003t0002g0341 |
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 | 55 | a0001c0001t0001g0342 a0001c0001t0003g0266 a0001c0001t0003g0321 others(52): 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 | a0001c0001t0001g0197 a0001c0001t0001g0345 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0345 a0001c0001t0004g0210 others(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 | a0001c0001t0002g0008 a0001c0006t0001g0006 a0001c0006t0001g0007 |
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 | a0001c0003t0002g0009 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0110 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0141 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0170 a0001c0001t0002g0162 others(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 | a0001c0001t0002g0237 a0001c0001t0003g0175 a0001c0001t0003g0177 others(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 | a0001c0001t0002g0180 a0001c0001t0002g0183 a0001c0002t0001g0181 others(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 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0002g0185 others(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 | a0001c0001t0001g0192 a0001c0002t0001g0191 a0001c0002t0001g0193 others(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 | a0001c0002t0005g0195 | 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 | a0001c0004t0003g0196 | 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 | a0001c0002t0002g0264 | 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 | 24 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0048 others(21): Show |
25 | HG00408.hp1 HG00597.hp1 HG01123.hp1 others(22): 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 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0002g0347 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0022 others(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 | a0001c0001t0002g0205 | 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 | a0001c0001t0002g0013 | 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 | a0001c0002t0001g0198 | 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 | a0001c0001t0001g0011 a0001c0001t0011g0010 |
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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0003t0004g0207 |
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 | 89 | a0001c0001t0001g0197 a0001c0001t0001g0342 a0001c0001t0001g0345 others(86): 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 | a0001c0001t0002g0343 a0001c0001t0003g0254 a0001c0001t0006g0222 others(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 | 75 | a0001c0001t0001g0197 a0001c0001t0001g0342 a0001c0001t0002g0343 others(72): 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 | a0001c0001t0010g0251 a0001c0002t0001g0252 a0001c0002t0003g0250 others(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 | 82 | a0001c0001t0001g0342 a0001c0001t0002g0343 a0001c0001t0002g0347 others(79): 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 | a0001c0001t0003g0266 a0001c0001t0003g0305 a0001c0002t0001g0268 others(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 | 64 | a0001c0001t0001g0342 a0001c0001t0002g0347 a0001c0001t0003g0266 others(61): 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 | 44 | a0001c0001t0002g0347 a0001c0001t0003g0321 a0001c0001t0003g0322 others(41): 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 | 58 | a0001c0001t0001g0342 a0001c0001t0002g0347 a0001c0001t0003g0266 others(55): 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 | a0001c0001t0001g0342 a0001c0002t0002g0243 a0001c0002t0002g0244 others(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 | 51 | a0001c0001t0001g0342 a0001c0001t0002g0347 a0001c0001t0003g0321 others(48): 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 | a0001c0001t0002g0205 a0001c0002t0007g0302 a0001c0005t0002g0301 |
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 | a0001c0001t0001g0342 a0001c0001t0002g0205 a0001c0002t0002g0243 others(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 | a0001c0001t0002g0205 a0001c0002t0007g0302 a0001c0005t0002g0301 |
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 | a0001c0002t0001g0198 | 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 | a0001c0002t0001g0198 | 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 | a0001c0002t0001g0198 | 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 | a0001c0002t0001g0012 | 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 | a0001c0005t0001g0263 | 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 | a0001c0002t0037g0275 | 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 | a0001c0004t0018g0231 | 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 | 58 | a0001c0001t0001g0342 a0001c0001t0003g0254 a0001c0001t0003g0266 others(55): 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0002g0008 a0001c0001t0002g0347 a0001c0005t0001g0348 others(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 | a0001c0002t0001g0198 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0096 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0035 a0001c0002t0001g0095 a0001c0002t0001g0173 others(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 | a0001c0001t0002g0205 | 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 | a0001c0001t0003g0057 a0001c0002t0002g0097 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0185 a0001c0002t0001g0174 a0001c0002t0001g0191 others(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 | a0001c0002t0001g0310 | 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 | a0001c0003t0004g0207 | 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 | a0001c0002t0001g0014 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0002g0264 | 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 | a0001c0002t0001g0198 | 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 | a0001c0001t0005g0259 a0001c0001t0005g0260 a0001c0001t0011g0257 others(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 | a0001c0001t0002g0282 a0001c0001t0003g0284 a0001c0001t0005g0215 others(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 | 58 | a0001c0001t0001g0342 a0001c0001t0003g0254 a0001c0001t0003g0266 others(55): 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 | a0001c0001t0016g0309 | 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 | 149 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0205 others(146): 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 | a0001c0001t0002g0282 a0001c0001t0003g0284 a0001c0002t0001g0281 others(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 | a0001c0003t0001g0297 | 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 | a0001c0002t0001g0152 a0001c0002t0001g0153 |
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 | a0001c0002t0001g0056 | 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 | a0001c0004t0002g0339 | 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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0002t0002g0273 others(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 | a0001c0004t0018g0231 | 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 | a0001c0002t0001g0151 | 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 | a0001c0003t0019g0311 | 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 | a0001c0004t0024g0194 | 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 | a0001c0001t0023g0023 | 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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0001t0010g0251 | 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 | a0001c0001t0001g0035 | 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 | a0001c0003t0003g0265 | 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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0003g0305 | 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 | a0001c0001t0001g0058 a0001c0001t0003g0266 a0001c0001t0003g0308 others(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 | 175 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0008 others(172): 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 | a0001c0002t0003g0120 | 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 | 7 | a0001c0001t0002g0098 a0001c0002t0001g0121 a0001c0002t0001g0122 others(4): 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 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
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 | a0001c0006t0001g0285 a0001c0006t0001g0296 |
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 | a0001c0004t0001g0024 | 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0001g0345 a0001c0001t0002g0093 a0001c0001t0002g0094 others(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 | a0001c0001t0016g0309 | 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 | a0001c0001t0010g0126 | 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 | a0001c0001t0001g0022 | 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 | a0001c0002t0004g0216 | 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 | a0001c0003t0002g0248 a0001c0004t0034g0249 |
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 | a0001c0001t0003g0305 | 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 | a0001c0002t0004g0216 | 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 | 178 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0008 others(175): 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 | 182 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0008 others(179): 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 | a0001c0001t0003g0266 a0001c0003t0003g0265 |
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 | a0001c0001t0002g0060 a0001c0001t0036g0061 a0001c0002t0001g0001 others(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 | a0001c0001t0001g0088 a0001c0001t0014g0089 |
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 | a0001c0001t0002g0190 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0170 a0001c0001t0002g0149 others(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 | a0001c0002t0001g0171 a0001c0002t0001g0198 a0001c0005t0002g0208 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0004g0210 a0001c0001t0006g0222 a0001c0002t0001g0153 others(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 | a0001c0001t0004g0210 | 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 | a0001c0001t0005g0166 | 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 | a0001c0004t0018g0231 | 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 | a0001c0002t0001g0337 a0001c0002t0001g0338 |
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 | 177 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(174): 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 | a0001c0001t0005g0166 | 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 | a0001c0001t0002g0183 a0001c0001t0003g0266 |
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 | a0001c0001t0001g0015 | 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 | 176 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(173): 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 | a0001c0001t0002g0149 | 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 | a0001c0001t0002g0021 | 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 | 175 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(172): 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 | a0001c0001t0002g0183 a0001c0001t0002g0282 a0001c0001t0003g0266 others(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 | a0001c0001t0013g0230 a0001c0003t0004g0211 |
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 | a0001c0001t0003g0305 | 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0001g0112 a0001c0002t0007g0113 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0313 | 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 | 115 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(112): 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 | a0001c0001t0002g0183 a0001c0001t0002g0282 a0001c0001t0003g0266 others(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 | a0001c0001t0002g0183 a0001c0001t0002g0282 a0001c0001t0003g0266 others(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 | a0001c0002t0001g0198 | 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 | a0001c0001t0003g0305 | 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 | a0001c0001t0013g0230 | 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 | a0001c0001t0003g0284 a0001c0006t0001g0272 a0001c0006t0027g0262 |
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 | a0001c0001t0003g0308 a0001c0002t0002g0307 a0001c0003t0003g0265 |
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 | a0001c0001t0002g0062 | 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 | a0001c0002t0001g0111 | 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 | a0001c0003t0003g0003 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0002g0183 a0001c0001t0003g0266 |
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 | a0001c0001t0003g0305 | 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 | a0001c0001t0023g0023 | 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 | a0001c0002t0001g0171 a0001c0005t0002g0208 |
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 | a0001c0001t0003g0308 a0001c0002t0002g0307 a0001c0003t0003g0265 |
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 | 160 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0035 others(157): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): 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 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0110 others(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 | a0001c0002t0001g0171 a0001c0005t0002g0208 |
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 | a0001c0001t0029g0075 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0135 a0001c0002t0002g0108 |
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 | a0001c0001t0002g0183 a0001c0001t0002g0205 a0001c0001t0002g0229 others(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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0001t0002g0347 others(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 | a0001c0001t0002g0183 a0001c0001t0003g0266 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0001g0112 | 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 | 327 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(324): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.213+6403T>C | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | chr9 | 132173447 | |||||||
| chr9:132173502 | C | T | 160 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(157): 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 | a0001c0002t0002g0277 a0001c0002t0012g0295 a0001c0003t0001g0150 others(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 | 160 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(157): 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0003g0090 | 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 | a0001c0002t0001g0171 a0001c0005t0002g0208 |
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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0001t0002g0183 a0001c0001t0003g0266 |
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 | a0001c0001t0002g0183 a0001c0001t0003g0266 |
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 | a0001c0001t0003g0308 a0001c0002t0002g0307 |
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 | a0001c0001t0003g0305 | 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 | a0001c0001t0025g0286 a0001c0002t0002g0273 a0001c0004t0003g0274 |
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 | a0001c0001t0002g0282 | 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 |
115 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(112): 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 | a0001c0001t0003g0049 | 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 | 157 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(154): 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 | a0001c0002t0001g0171 a0001c0005t0002g0208 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0003g0308 a0001c0002t0002g0307 a0001c0003t0003g0265 |
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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0277 | 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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0277 | 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 | a0001c0002t0002g0277 | 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 | a0001c0001t0001g0345 a0001c0001t0002g0183 a0001c0001t0002g0343 others(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 | a0001c0001t0002g0183 a0001c0001t0002g0205 a0001c0001t0002g0229 others(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 | a0001c0001t0002g0183 a0001c0001t0003g0266 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0171 a0001c0005t0002g0208 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0003g0308 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
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 | a0001c0002t0001g0153 | 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 | a0001c0002t0001g0153 | 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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0153 | 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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0153 | 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 | a0001c0002t0001g0153 | 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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0153 | 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 | a0001c0003t0002g0340 a0001c0005t0004g0228 |
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 | 116 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(113): 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 | a0001c0001t0002g0060 a0001c0001t0023g0023 a0001c0001t0036g0061 others(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 | a0001c0002t0001g0153 | 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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0110 a0001c0001t0001g0144 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0153 | 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 | a0001c0003t0003g0003 | 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 | a0001c0001t0002g0183 a0001c0001t0003g0266 a0001c0003t0003g0265 |
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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0003t0003g0265 | 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 | a0001c0001t0002g0051 | 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 | a0001c0001t0002g0183 a0001c0001t0003g0266 |
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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0002t0002g0264 others(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 | 115 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0282 others(112): 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 | 191 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(188): 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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | 351 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(348): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(351): 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 | a0001c0001t0003g0308 a0001c0002t0002g0307 |
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 | a0001c0003t0001g0335 | 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 | 165 | a0001c0001t0001g0032 a0001c0001t0001g0342 a0001c0001t0001g0345 others(162): 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 | a0001c0002t0001g0334 | 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 | a0001c0002t0001g0334 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 a0001c0003t0003g0232 others(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 | 158 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(155): 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 | a0001c0002t0001g0053 | 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 | a0001c0001t0002g0205 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0002t0001g0283 a0001c0004t0010g0280 |
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 | a0001c0002t0001g0252 | 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 | 82 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(79): 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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0001t0002g0347 others(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 | a0001c0002t0002g0352 | 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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0003t0002g0127 a0001c0004t0001g0303 |
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 | a0001c0001t0002g0183 | 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 | 86 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(83): 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 | 82 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(79): 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 | a0005c0009t0001g0354 | 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 | a0001c0001t0001g0041 | 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 | a0001c0006t0002g0353 | 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 | 195 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(192): 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 | 236 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(233): 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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | a0001c0001t0041g0213 a0001c0001t0043g0212 a0001c0002t0042g0240 |
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 | 82 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(79): 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0002g0116 a0001c0001t0020g0054 a0001c0002t0001g0172 others(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 | a0001c0002t0002g0273 | 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 | a0001c0003t0009g0314 a0001c0003t0009g0315 a0001c0003t0009g0316 others(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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(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 | a0001c0001t0013g0230 | 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 | a0001c0001t0003g0308 a0001c0002t0002g0307 a0001c0002t0003g0253 others(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 | a0001c0001t0030g0042 | 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 | a0001c0005t0002g0125 | 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 | a0001c0001t0002g0019 a0001c0002t0002g0031 |
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 | 83 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(80): 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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | 82 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(79): 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 | a0001c0005t0002g0306 | 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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0002g0062 others(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 | a0001c0001t0001g0048 a0001c0001t0002g0205 a0001c0001t0003g0057 others(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 | a0001c0001t0001g0345 a0001c0001t0002g0021 a0001c0001t0002g0343 others(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 | 66 | a0001c0001t0001g0342 a0001c0001t0003g0254 a0001c0001t0003g0321 others(63): 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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0001t0002g0229 a0001c0001t0002g0237 a0001c0003t0001g0289 |
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 | 88 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0197 others(85): 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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0001t0002g0347 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(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 | a0001c0001t0002g0205 a0001c0001t0006g0222 a0001c0001t0013g0230 others(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 | 92 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(89): 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 | a0001c0005t0002g0208 | 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 | a0001c0003t0001g0333 | 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 | 191 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(188): 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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0005g0104 others(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 | a0001c0001t0005g0215 | 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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0001t0003g0308 a0001c0002t0002g0307 a0001c0002t0003g0253 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0141 others(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 | a0001c0002t0002g0264 | 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 | a0001c0001t0001g0345 a0001c0001t0002g0343 |
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 | a0001c0001t0002g0183 | 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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | 190 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(187): 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | 87 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(84): 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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(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 | 121 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(118): 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0003t0003g0003 | 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 | a0001c0001t0003g0305 | 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 | a0001c0001t0003g0308 a0001c0002t0002g0307 a0001c0002t0003g0253 others(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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0003t0001g0065 | 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 | a0001c0001t0003g0308 a0001c0002t0002g0307 a0001c0002t0003g0253 others(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 | a0001c0002t0001g0171 a0001c0005t0002g0208 |
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 | a0001c0004t0003g0274 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0003t0001g0154 | 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 | 195 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(192): 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 | a0001c0001t0001g0115 a0001c0001t0003g0052 a0001c0001t0004g0210 others(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 | a0001c0001t0003g0266 a0001c0001t0041g0213 a0001c0001t0043g0212 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(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 | 96 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(93): 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 | a0001c0001t0003g0175 | 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0005g0246 a0001c0003t0002g0248 a0001c0004t0002g0247 others(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 | a0001c0004t0003g0119 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0004t0013g0235 a0001c0004t0017g0234 a0001c0004t0018g0231 |
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 | a0001c0001t0002g0205 a0001c0001t0010g0251 a0001c0003t0003g0232 others(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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0002t0001g0252 others(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 | a0001c0003t0019g0311 | 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 | a0001c0003t0004g0226 | 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 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0005g0104 others(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 | a0001c0001t0002g0347 a0001c0001t0025g0286 a0001c0002t0002g0273 others(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 | 129 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(126): 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 | 85 | a0001c0001t0001g0342 a0001c0001t0001g0345 a0001c0001t0002g0021 others(82): 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 | a0001c0002t0004g0216 | 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 | 63 | a0001c0001t0001g0342 a0001c0001t0003g0164 a0001c0001t0003g0308 others(60): 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 | 73 | a0001c0001t0001g0342 a0001c0001t0002g0021 a0001c0001t0002g0282 others(70): 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 | 65 | a0001c0001t0001g0342 a0001c0001t0002g0021 a0001c0001t0003g0164 others(62): 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 | a0001c0001t0006g0222 a0001c0001t0016g0309 a0001c0002t0001g0198 others(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 | a0001c0001t0003g0305 a0001c0003t0003g0265 |
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 | a0001c0003t0001g0063 | 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 | 319 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(316): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): 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 | a0001c0003t0004g0211 | 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 | a0001c0001t0005g0259 a0001c0001t0005g0260 a0001c0001t0011g0257 others(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 | a0001c0002t0003g0267 | 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 | a0001c0002t0001g0198 | 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 | a0001c0002t0001g0059 | 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 | a0001c0001t0006g0222 a0001c0001t0016g0309 a0001c0002t0001g0198 others(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 | a0001c0001t0010g0251 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0005t0033g0241 | 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 | a0001c0001t0003g0305 | 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 | a0001c0001t0002g0183 | 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 | a0001c0001t0003g0161 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0141 others(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 | a0001c0003t0003g0265 | 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 | a0001c0002t0001g0171 a0001c0005t0002g0208 |
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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0141 others(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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0001t0003g0178 | 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 | a0001c0005t0002g0125 | 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 | a0001c0002t0007g0302 a0001c0005t0002g0301 |
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 | a0001c0004t0001g0318 | 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 | a0001c0001t0001g0069 a0001c0001t0002g0093 a0001c0001t0002g0094 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0002g0021 a0001c0001t0002g0183 a0001c0001t0002g0205 others(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 | a0001c0002t0001g0252 | 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 | a0001c0004t0013g0235 a0001c0004t0017g0234 |
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 | a0001c0002t0001g0313 a0001c0004t0001g0303 |
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 | a0001c0005t0002g0301 a0001c0005t0033g0241 |
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 | a0001c0004t0001g0055 | 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 | a0001c0005t0033g0241 | 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 | a0001c0005t0033g0241 | 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 | a0001c0001t0002g0145 | 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 | a0001c0002t0001g0283 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0002g0145 | 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 | a0001c0003t0009g0314 | 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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | a0001c0001t0003g0305 a0001c0001t0010g0251 a0001c0002t0001g0198 |
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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0005g0259 others(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 | a0001c0002t0007g0036 | 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 | a0001c0003t0002g0248 a0001c0004t0022g0233 a0001c0004t0034g0249 |
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 | a0001c0001t0002g0076 a0001c0001t0002g0093 a0001c0001t0002g0094 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(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 | a0001c0002t0001g0056 | 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 | a0001c0001t0006g0222 a0001c0002t0008g0236 a0001c0003t0002g0029 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(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 | a0001c0001t0003g0308 a0001c0002t0001g0198 a0001c0002t0003g0267 |
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 | a0001c0002t0002g0307 | 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 | a0001c0002t0002g0307 | 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 | a0001c0003t0001g0044 a0001c0005t0002g0125 |
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 | a0001c0001t0001g0188 a0001c0001t0002g0019 a0001c0001t0003g0254 others(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 | a0001c0001t0001g0141 a0001c0001t0002g0183 a0001c0001t0005g0215 |
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 | a0001c0001t0002g0062 a0001c0001t0010g0251 a0001c0002t0001g0252 others(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 | a0001c0001t0001g0188 a0001c0001t0002g0019 a0001c0001t0002g0021 others(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 | a0001c0001t0003g0305 | 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 | a0001c0002t0002g0146 | 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 | a0001c0001t0002g0062 a0001c0001t0002g0205 a0001c0001t0010g0251 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0141 a0001c0001t0002g0183 others(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 | 135 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0001t0003g0038 others(132): 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 | a0001c0001t0001g0188 a0001c0001t0002g0019 a0001c0001t0002g0021 others(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 | a0001c0001t0003g0305 | 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 | 135 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0178 others(132): 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 | 136 | a0001c0001t0001g0141 a0001c0001t0002g0183 a0001c0001t0003g0038 others(133): 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 | a0001c0002t0001g0056 | 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 | a0001c0001t0003g0308 a0001c0001t0005g0259 a0001c0001t0005g0260 others(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 | a0001c0002t0002g0307 | 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 | a0001c0006t0001g0285 a0001c0006t0001g0296 |
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 | a0001c0003t0001g0276 | 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 | a0001c0003t0003g0239 | 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 | a0001c0003t0004g0206 a0001c0005t0001g0348 a0001c0005t0007g0355 others(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 | a0001c0002t0002g0106 | 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 | a0001c0001t0001g0345 | 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 | a0001c0002t0001g0181 | 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 | 164 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0001g0345 others(161): 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 | a0001c0003t0001g0025 a0001c0003t0001g0331 a0001c0004t0024g0194 |
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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | 167 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0001g0345 others(164): 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 | a0001c0001t0001g0088 a0001c0001t0002g0013 a0001c0001t0002g0081 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0183 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0183 others(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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0183 others(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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0002t0002g0307 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0062 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0183 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0183 others(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 | a0001c0001t0002g0062 a0001c0001t0010g0251 a0001c0002t0001g0252 others(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 | a0001c0001t0010g0251 a0001c0002t0008g0236 a0001c0005t0001g0263 others(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 | 154 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0001g0345 others(151): 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 | a0001c0001t0002g0062 a0001c0002t0001g0252 a0001c0005t0001g0271 others(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 | a0001c0001t0010g0251 a0001c0002t0008g0236 a0001c0005t0001g0263 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0096 others(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 | a0001c0001t0002g0347 a0001c0001t0003g0254 a0001c0001t0004g0210 others(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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0183 others(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 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0005g0246 others(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 | a0001c0001t0005g0259 a0001c0002t0003g0344 a0001c0002t0037g0275 others(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 | a0001c0001t0002g0229 a0001c0001t0002g0237 a0001c0001t0005g0260 others(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 | a0001c0001t0002g0343 a0001c0002t0002g0270 a0001c0002t0002g0273 others(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 | a0001c0001t0001g0345 a0001c0002t0002g0326 a0001c0003t0001g0063 others(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 |
35 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0025g0286 others(32): 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 | a0001c0003t0001g0065 a0001c0003t0001g0150 a0001c0003t0001g0304 others(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 | a0001c0003t0001g0105 a0001c0003t0001g0333 |
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 | a0001c0003t0001g0154 | 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 | a0001c0001t0035g0078 | 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 | a0001c0004t0002g0339 | 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 | a0001c0003t0001g0025 a0001c0004t0001g0027 a0001c0004t0024g0194 |
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 | a0001c0003t0001g0331 | 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 | a0001c0002t0001g0198 a0001c0002t0003g0267 |
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 | a0001c0002t0002g0273 | 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 | a0001c0002t0001g0198 | 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 | a0001c0002t0002g0307 | 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 | a0001c0001t0007g0074 a0001c0002t0001g0198 a0001c0002t0003g0267 |
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 | a0001c0005t0004g0228 | 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 | a0001c0001t0002g0062 a0001c0005t0001g0201 a0001c0005t0001g0263 others(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 | a0001c0002t0001g0252 | 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 | 170 | a0001c0001t0001g0345 a0001c0001t0002g0021 a0001c0001t0002g0062 others(167): 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 | a0001c0001t0029g0075 a0001c0002t0001g0337 a0001c0002t0001g0338 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0002g0183 others(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 | 137 | a0001c0001t0001g0345 a0001c0001t0002g0021 a0001c0001t0002g0229 others(134): 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 | a0001c0001t0002g0062 a0001c0001t0010g0251 a0001c0002t0001g0252 others(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 | a0001c0001t0001g0096 a0001c0001t0001g0170 a0001c0001t0003g0161 others(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 | a0001c0005t0001g0271 a0001c0005t0001g0278 a0001c0005t0002g0301 |
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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0002t0002g0307 |
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 | a0001c0001t0002g0062 a0001c0001t0010g0251 a0001c0002t0001g0252 others(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 | 145 | a0001c0001t0001g0345 a0001c0001t0002g0021 a0001c0001t0002g0229 others(142): 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 | a0001c0001t0001g0188 a0001c0001t0005g0215 a0001c0002t0003g0255 |
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 | a0001c0001t0020g0054 | 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 | a0001c0002t0038g0184 | 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 | a0001c0001t0002g0062 a0001c0001t0010g0251 a0001c0002t0001g0252 others(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 | 179 | a0001c0001t0001g0345 a0001c0001t0002g0021 a0001c0001t0002g0062 others(176): 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 | 172 | a0001c0001t0001g0345 a0001c0001t0002g0021 a0001c0001t0002g0062 others(169): 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 | a0001c0001t0002g0190 a0001c0001t0023g0023 a0001c0002t0001g0151 |
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 | 219 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(216): 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 | 172 | a0001c0001t0001g0345 a0001c0001t0002g0021 a0001c0001t0002g0062 others(169): 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 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0011 a0001c0001t0002g0205 a0001c0001t0002g0282 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0189 a0001c0001t0002g0149 others(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 | a0001c0002t0003g0253 a0001c0002t0037g0275 a0001c0003t0002g0009 others(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 | 105 | a0001c0001t0001g0345 a0001c0001t0002g0229 a0001c0001t0002g0237 others(102): 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 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0005g0260 others(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 | a0001c0002t0008g0236 a0001c0004t0004g0209 |
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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0002t0002g0307 |
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 | a0001c0001t0002g0062 a0001c0002t0001g0252 a0001c0005t0001g0201 others(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 | a0001c0001t0002g0347 | 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 | a0001c0001t0001g0345 a0001c0001t0002g0343 a0001c0001t0005g0259 others(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 | a0001c0001t0002g0019 a0001c0001t0003g0254 a0001c0001t0005g0166 others(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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0002t0002g0307 |
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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0002t0002g0307 |
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 | a0001c0001t0002g0205 | 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 | a0001c0003t0003g0232 | 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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0002t0002g0307 |
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 | 142 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0021 others(139): 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 | 145 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0229 others(142): 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 | a0001c0002t0008g0236 | 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 | a0001c0002t0002g0106 | 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 | 220 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(217): 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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0002t0002g0307 |
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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0015t0044g0204 | 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 | a0001c0001t0002g0062 a0001c0001t0010g0251 a0001c0002t0001g0252 others(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 | a0001c0003t0001g0335 | 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0010g0251 a0001c0002t0008g0236 a0001c0004t0002g0086 |
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 | a0001c0002t0002g0307 | 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 | a0001c0002t0002g0273 | 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 | a0001c0004t0006g0221 | 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 | a0001c0002t0002g0307 | 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 | a0001c0001t0002g0062 a0001c0002t0001g0252 a0001c0005t0001g0201 others(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 | a0001c0005t0004g0228 | 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 | a0001c0001t0001g0141 a0001c0001t0002g0183 a0001c0001t0005g0215 |
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 | a0001c0001t0001g0011 a0001c0001t0002g0205 a0001c0001t0005g0030 others(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 | a0001c0001t0002g0019 a0001c0002t0001g0281 a0001c0002t0002g0031 others(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 | a0001c0001t0001g0141 a0001c0001t0002g0021 a0001c0001t0002g0183 others(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 | a0001c0004t0002g0336 | 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 | a0001c0002t0001g0198 | 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0005g0104 others(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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | a0001c0001t0002g0145 | 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 | a0001c0005t0001g0263 a0001c0006t0002g0085 |
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 | 147 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0229 others(144): 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0003g0305 others(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 | a0001c0002t0001g0124 a0001c0002t0012g0295 |
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 | 220 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(217): 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 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0005g0104 others(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 | a0001c0001t0002g0205 a0001c0001t0002g0282 a0001c0001t0003g0266 others(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 | a0001c0001t0003g0305 | 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 | a0001c0001t0002g0205 a0001c0001t0003g0305 a0001c0001t0005g0104 others(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 | a0001c0001t0002g0021 a0001c0001t0010g0126 |
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 | a0001c0004t0006g0224 | 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 | 116 | a0001c0001t0002g0183 a0001c0001t0003g0038 a0001c0001t0003g0039 others(113): 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 | a0001c0001t0001g0011 a0001c0001t0005g0030 a0001c0001t0011g0010 others(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 | a0001c0005t0002g0016 | 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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0002g0205 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0156 others(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 | a0001c0001t0011g0257 a0001c0001t0011g0258 a0001c0001t0013g0230 others(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 | a0001c0001t0002g0183 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0003g0305 a0001c0003t0001g0157 a0001c0003t0001g0200 others(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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0005g0104 others(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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0180 | 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 | a0001c0003t0001g0261 | 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 | a0001c0002t0002g0326 | 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 | a0001c0003t0003g0265 | 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 | a0001c0002t0032g0046 | 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 | 210 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(207): 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 | a0001c0004t0002g0086 | 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 | 147 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0305 others(144): 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 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0012g0295 |
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 | 210 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(207): 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 | a0001c0002t0001g0014 | 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 | a0001c0003t0003g0202 | 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 | 210 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(207): 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 | a0001c0002t0001g0095 a0001c0002t0001g0165 |
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 | a0001c0003t0003g0202 | 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 | a0001c0001t0001g0011 a0001c0001t0005g0030 a0001c0001t0011g0010 others(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 | a0001c0001t0011g0257 a0001c0001t0011g0258 a0001c0001t0013g0230 others(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 | 210 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0001g0188 others(207): 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 | a0001c0001t0015g0028 | 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 | a0001c0005t0001g0263 a0001c0006t0002g0085 |
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 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0021 others(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 | 145 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0002t0002g0326 others(142): 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 | 147 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0305 others(144): 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 | a0001c0004t0028g0163 a0001c0004t0039g0323 |
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 | a0001c0001t0002g0183 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0001t0003g0305 a0001c0003t0006g0219 a0001c0003t0026g0138 others(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 | 168 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0021 others(165): 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 | a0001c0002t0008g0236 a0001c0005t0001g0348 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0001t0002g0205 | 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 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0005g0104 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0003t0001g0289 | 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 | a0001c0001t0002g0185 a0001c0002t0001g0018 a0001c0002t0001g0174 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | ||||||
| chr9:132199770 | C | T | 8 | a0001c0001t0002g0282 a0001c0001t0003g0266 a0001c0001t0005g0104 others(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 | a0001c0001t0002g0199 a0001c0001t0003g0090 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0003t0001g0154 | 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 | 113 | a0001c0001t0002g0190 a0001c0002t0037g0275 a0001c0003t0001g0025 others(110): 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 | a0001c0002t0002g0273 | 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 | 114 | a0001c0001t0002g0190 a0001c0002t0037g0275 a0001c0003t0001g0025 others(111): 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 | a0001c0001t0020g0054 | 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 | a0001c0001t0001g0197 a0001c0001t0002g0199 a0001c0001t0003g0090 |
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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0011 a0001c0001t0005g0030 a0001c0001t0011g0010 others(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 | a0001c0003t0002g0340 a0001c0004t0001g0167 a0001c0004t0001g0332 others(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 | a0001c0001t0002g0021 a0001c0001t0002g0183 a0001c0001t0002g0229 others(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 | 111 | a0001c0001t0001g0088 a0001c0001t0002g0098 a0001c0001t0002g0282 others(108): 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 | a0001c0001t0002g0021 a0001c0001t0010g0126 a0001c0001t0025g0286 others(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 | 182 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(179): 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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0002t0002g0031 | 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 | a0001c0001t0001g0032 a0001c0001t0005g0077 a0001c0001t0005g0079 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0005t0002g0306 others(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 | a0001c0002t0001g0256 | 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 | a0001c0001t0010g0126 | 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 | a0001c0001t0002g0013 a0001c0001t0002g0081 a0001c0001t0002g0149 others(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 | a0001c0001t0005g0166 | 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 | a0001c0003t0001g0300 a0001c0003t0031g0129 a0001c0015t0044g0204 |
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 | a0001c0003t0003g0003 | 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 | a0001c0001t0005g0187 a0001c0001t0005g0215 a0001c0001t0010g0102 others(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 | a0001c0004t0002g0247 a0001c0004t0003g0274 |
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 | a0001c0004t0004g0209 | 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 | a0001c0003t0001g0065 | 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 | a0001c0001t0010g0102 | 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 | a0001c0002t0002g0350 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0003t0002g0319 | 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 | a0001c0001t0001g0011 a0001c0001t0005g0030 a0001c0001t0011g0010 others(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 | a0001c0001t0001g0112 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0308 others(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 | a0001c0002t0001g0056 | 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 | a0001c0001t0002g0019 a0001c0001t0005g0166 a0001c0001t0011g0159 others(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 | a0001c0001t0005g0187 a0001c0001t0005g0215 a0001c0001t0010g0102 others(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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0035g0078 |
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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0035g0078 |
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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0001t0003g0308 | 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 | a0001c0003t0001g0025 a0001c0004t0024g0194 |
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 | a0001c0001t0002g0162 | 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 | a0001c0001t0011g0257 | 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 | a0001c0001t0001g0022 | 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 | a0001c0002t0003g0136 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0002t0007g0113 |
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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0035g0078 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0035 others(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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0035g0078 |
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 | a0001c0004t0002g0140 | 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 | a0001c0002t0001g0056 | 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 | a0001c0001t0001g0342 a0001c0001t0002g0008 a0001c0002t0001g0334 others(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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | 224 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(221): 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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0001t0010g0251 a0001c0002t0008g0236 |
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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0001t0003g0308 | 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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0002t0032g0046 | 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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0004t0013g0235 a0001c0004t0017g0234 |
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 | a0001c0003t0001g0080 | 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 | a0001c0001t0005g0187 a0001c0001t0005g0215 a0001c0001t0010g0102 others(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 | a0001c0001t0003g0308 | 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 | a0001c0004t0039g0323 | 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 | a0001c0002t0003g0136 | 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 | a0001c0003t0001g0304 | 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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0001t0002g0019 a0001c0001t0005g0166 a0001c0001t0011g0159 others(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 | a0001c0004t0002g0004 a0001c0004t0002g0247 a0001c0004t0003g0274 others(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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0035g0078 |
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 | a0001c0001t0003g0308 | 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 | 211 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(208): 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 | a0001c0001t0003g0308 | 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 | a0001c0004t0002g0004 a0001c0004t0004g0209 a0001c0005t0001g0348 others(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 | a0001c0001t0016g0309 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0343 others(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 | 143 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0188 others(140): 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 | a0001c0006t0002g0085 | 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 | a0001c0003t0003g0265 a0001c0003t0004g0211 |
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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0004t0001g0332 | 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 | a0001c0001t0001g0141 a0001c0001t0002g0019 a0001c0001t0003g0305 others(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 | a0001c0002t0003g0255 | 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 | 151 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0188 others(148): 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 | 186 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0110 others(183): 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 | a0001c0001t0003g0254 | 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 | a0001c0002t0001g0252 | 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 | a0001c0004t0045g0299 | 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 | a0001c0002t0001g0252 | 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 | 209 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0188 others(206): 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0002g0183 a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0005g0246 others(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 | 159 | a0001c0001t0001g0088 a0001c0001t0001g0141 a0001c0001t0001g0188 others(156): 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 | a0001c0003t0003g0232 a0001c0003t0003g0239 |
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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0191 | 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 | a0001c0001t0003g0321 a0001c0001t0003g0322 |
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 | a0001c0003t0003g0202 | 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 | 190 | a0001c0001t0001g0088 a0001c0001t0001g0141 a0001c0001t0001g0188 others(187): 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 | a0001c0001t0001g0141 a0001c0001t0002g0021 a0001c0001t0010g0126 others(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 | a0001c0001t0005g0187 | 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 | 225 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(222): 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 | a0001c0003t0003g0202 | 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 | a0001c0003t0003g0202 | 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 | a0001c0001t0002g0062 a0001c0002t0001g0014 |
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 | 225 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(222): 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 | a0001c0004t0008g0040 | 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 | a0001c0003t0003g0202 | 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 | a0001c0001t0001g0011 a0001c0001t0002g0019 a0001c0001t0003g0254 others(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 | a0001c0004t0002g0238 | 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 | a0001c0002t0002g0307 | 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 | a0001c0001t0001g0011 a0001c0001t0002g0019 a0001c0001t0003g0254 others(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 | a0001c0004t0001g0024 | 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 | a0001c0002t0001g0056 | 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 | a0001c0001t0010g0251 a0001c0002t0008g0236 |
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 | a0001c0003t0003g0202 | 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 | a0001c0001t0001g0342 a0001c0001t0002g0008 a0001c0002t0002g0160 |
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 | a0001c0001t0002g0068 | 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 | 6 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0112 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.857+13044C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132211653 | |||||||
| chr9:132211751 | T | C | 227 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(224): 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 | a0001c0001t0001g0156 | 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 | a0001c0004t0001g0167 a0001c0004t0001g0332 |
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 | a0001c0003t0004g0206 | 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 | 228 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(225): 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0014g0092 a0001c0002t0001g0168 a0001c0003t0001g0154 |
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 | a0001c0001t0001g0141 a0001c0002t0002g0273 |
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 | 226 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(223): 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 | a0001c0006t0027g0262 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0038g0184 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0004t0039g0323 | 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 | a0001c0001t0004g0210 | 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 | a0001c0004t0002g0140 | 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 | 227 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(224): 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0005g0187 a0001c0001t0005g0215 a0001c0001t0010g0102 others(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 | 228 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(225): 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 | 228 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(225): 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 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0002g0051 others(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 | a0001c0003t0003g0202 | 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 | a0001c0001t0001g0011 a0001c0001t0002g0019 a0001c0001t0003g0254 others(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 | 192 | a0001c0001t0001g0088 a0001c0001t0001g0141 a0001c0001t0001g0188 others(189): 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 | a0001c0002t0001g0056 a0001c0002t0001g0114 a0001c0006t0001g0285 |
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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0252 | 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 | a0001c0002t0001g0056 | 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 | 225 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(222): 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 | a0001c0002t0001g0155 | 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 | 193 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(190): 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 | 225 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(222): 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 | 78 | a0001c0001t0001g0088 a0001c0001t0002g0347 a0001c0001t0003g0099 others(75): 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 | a0001c0003t0001g0065 a0003c0007t0002g0133 a0003c0008t0001g0132 |
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 | a0001c0004t0002g0004 | 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 | a0001c0002t0001g0056 | 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 | 227 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(224): 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 | a0001c0004t0001g0332 a0001c0006t0001g0006 |
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 | 226 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(223): 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 | 189 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(186): 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 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(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 | 181 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0021 others(178): 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 | a0001c0001t0003g0049 | 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 | a0001c0001t0001g0192 a0001c0002t0002g0108 |
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 | a0001c0001t0001g0141 a0001c0002t0002g0273 |
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 | 228 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(225): 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 | 189 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(186): 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 | 189 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(186): 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 | a0001c0001t0014g0089 | 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 | a0001c0004t0002g0140 | 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 | a0001c0002t0002g0146 a0001c0002t0002g0147 |
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 | a0001c0001t0007g0074 | 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 | 188 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(185): 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 | a0001c0004t0006g0218 | 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 | a0001c0001t0001g0011 a0001c0001t0002g0019 a0001c0001t0003g0254 others(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 | a0001c0001t0001g0011 a0001c0001t0002g0019 a0001c0001t0003g0254 others(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 | a0001c0002t0002g0273 | 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 | a0001c0002t0002g0273 | 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 | a0001c0002t0001g0151 | 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 | a0001c0002t0003g0139 a0001c0003t0003g0202 a0001c0006t0002g0073 others(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 | a0001c0001t0004g0210 a0001c0002t0001g0337 a0001c0002t0001g0338 others(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 | a0001c0001t0003g0052 a0001c0001t0020g0054 a0001c0002t0002g0245 others(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 | a0001c0001t0001g0141 a0001c0002t0002g0273 |
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 | a0001c0003t0001g0304 | 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 | a0001c0002t0001g0252 | 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 | a0001c0004t0003g0119 | 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 | a0001c0001t0002g0021 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0003t0002g0029 a0001c0003t0026g0138 |
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 | a0001c0002t0001g0268 | 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 | a0001c0002t0003g0269 a0001c0002t0005g0195 |
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 | a0001c0002t0001g0198 | 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 | a0001c0002t0001g0290 | 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 | a0001c0001t0002g0019 a0001c0001t0005g0166 a0001c0004t0002g0247 |
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 | a0001c0002t0002g0031 | 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 | a0001c0004t0002g0004 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0192 a0001c0001t0002g0145 others(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 | a0001c0001t0001g0188 a0001c0002t0001g0114 a0001c0003t0001g0329 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0345 a0001c0001t0002g0343 others(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 | 70 | a0001c0001t0002g0098 a0001c0001t0002g0237 a0001c0001t0003g0087 others(67): 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 | a0001c0001t0002g0183 a0001c0001t0002g0229 a0001c0001t0002g0282 others(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 | a0001c0001t0002g0205 a0001c0001t0003g0308 a0001c0001t0011g0257 others(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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0035g0078 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0011 a0001c0001t0003g0254 a0001c0001t0005g0030 others(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 | a0001c0001t0001g0011 a0001c0001t0011g0010 a0001c0001t0011g0159 others(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 | a0001c0001t0001g0011 a0001c0001t0011g0010 a0001c0002t0001g0171 others(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 | a0001c0003t0001g0331 a0001c0003t0003g0265 |
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 | a0001c0001t0001g0188 a0001c0002t0001g0114 a0001c0003t0001g0329 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(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 | a0001c0001t0002g0019 a0001c0001t0005g0166 a0001c0001t0011g0159 others(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 | a0001c0001t0002g0051 a0001c0001t0002g0107 a0001c0002t0001g0155 others(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 | 92 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(89): Show |
94 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(91): 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 | 107 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(104): 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 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0115 others(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 | 135 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0098 others(132): 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 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0183 others(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 | a0001c0001t0002g0183 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0005g0077 a0001c0001t0005g0079 a0001c0001t0035g0078 others(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 | a0001c0002t0004g0216 | 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 | a0001c0002t0004g0216 | 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 | 193 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(190): 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 | 228 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0141 others(225): 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 | 195 | a0001c0001t0001g0088 a0001c0001t0001g0141 a0001c0001t0001g0188 others(192): 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 | a0001c0002t0002g0186 | 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 | a0001c0001t0001g0011 a0001c0001t0002g0019 a0001c0001t0003g0254 others(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 | a0001c0001t0002g0021 a0001c0001t0003g0038 a0001c0001t0003g0039 others(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 | a0001c0001t0002g0205 | 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 | a0001c0001t0002g0076 | 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 | a0001c0004t0003g0274 | 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 | a0001c0004t0001g0047 | 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0141 a0001c0001t0002g0019 others(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 | a0001c0001t0020g0054 a0001c0004t0003g0196 |
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 | a0001c0002t0002g0273 | 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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | 192 | a0001c0001t0001g0088 a0001c0001t0001g0188 a0001c0001t0001g0345 others(189): 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 | a0001c0004t0039g0323 | 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 | a0001c0003t0001g0304 | 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 | a0001c0001t0002g0183 a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0001t0001g0141 | 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 | a0001c0002t0008g0236 | 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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | a0001c0001t0005g0259 a0001c0001t0005g0260 a0001c0002t0003g0120 |
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 | a0001c0001t0002g0205 | 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 | a0001c0003t0003g0265 a0001c0003t0004g0211 |
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 | a0001c0003t0001g0176 | 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 | a0001c0001t0001g0088 a0001c0001t0001g0141 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0011 a0001c0001t0002g0019 a0001c0001t0002g0205 others(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 | a0001c0002t0008g0236 | 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 | a0001c0003t0009g0317 | 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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | a0001c0001t0001g0141 a0001c0002t0002g0273 a0001c0002t0037g0275 |
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 | a0001c0004t0039g0323 | 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 | a0001c0006t0002g0073 a0001c0006t0002g0353 |
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 | a0001c0001t0002g0068 a0001c0001t0003g0099 a0001c0001t0004g0210 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0096 a0001c0001t0001g0170 others(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 | a0001c0005t0001g0201 a0001c0006t0002g0073 a0001c0006t0002g0353 |
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 | a0001c0004t0013g0235 a0001c0004t0017g0234 |
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 | a0001c0001t0003g0254 | 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 | 6 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0112 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG01123.hp1 others(3): 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 | a0001c0001t0002g0162 a0001c0002t0001g0053 |
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 | a0001c0001t0011g0257 a0001c0001t0011g0258 a0001c0001t0013g0230 others(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 | a0001c0002t0002g0307 | 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 | a0001c0005t0002g0306 | 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 | a0001c0002t0001g0056 | 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 | a0001c0004t0039g0323 | 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 | a0001c0004t0006g0218 | 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 | a0001c0001t0002g0062 a0001c0002t0001g0014 |
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 | a0001c0002t0001g0056 | 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 | a0001c0001t0002g0183 a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0005t0001g0348 a0001c0005t0007g0355 |
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 | a0001c0001t0001g0011 a0001c0001t0005g0030 a0001c0002t0001g0171 |
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 | a0001c0001t0001g0096 a0001c0001t0001g0170 a0001c0001t0002g0021 others(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 | a0001c0001t0002g0142 | 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 | a0001c0004t0002g0004 | 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 | a0001c0002t0001g0056 | 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 | a0001c0002t0001g0334 | 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 | a0001c0001t0001g0141 a0001c0001t0025g0286 |
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 | a0001c0002t0003g0082 | 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 | a0001c0005t0004g0228 | 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 | a0001c0004t0003g0119 | 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 | a0001c0001t0005g0187 a0001c0001t0016g0309 a0001c0002t0008g0236 others(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 | a0001c0002t0007g0302 | 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 | 185 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0141 others(182): 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 | a0001c0005t0004g0228 | 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 | a0001c0001t0001g0041 | 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 | a0001c0002t0001g0198 a0001c0002t0001g0268 a0001c0002t0001g0281 others(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 | a0001c0004t0001g0027 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0343 others(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 | a0001c0003t0004g0207 | 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 | a0001c0003t0001g0065 a0003c0007t0002g0133 a0003c0008t0001g0132 |
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 | a0001c0001t0005g0104 a0001c0001t0005g0215 a0001c0001t0035g0078 others(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 | 183 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(180): Show |
185 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(182): 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 | a0001c0002t0037g0275 a0001c0003t0004g0211 |
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 | a0001c0001t0005g0187 a0001c0001t0016g0309 a0001c0002t0008g0236 others(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 | 205 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(202): Show |
207 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.858-2819C>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132224030 | |||||||
| chr9:132224099 | C | T | 177 | a0001c0001t0001g0032 a0001c0001t0001g0096 a0001c0001t0001g0141 others(174): 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 | a0001c0005t0002g0016 | 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 | a0001c0002t0001g0171 | 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 | a0001c0004t0028g0163 | 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 | a0001c0002t0001g0252 | 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 | a0001c0001t0011g0010 | 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 | a0001c0001t0005g0030 a0001c0001t0005g0077 a0001c0001t0005g0079 others(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 | a0001c0002t0001g0123 | 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 | 238 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0050 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.858-1694T>G | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | chr9 | 132225155 | |||||||
| chr9:132225224 | TTTGTC | T | 192 | a0001c0001t0001g0035 a0001c0001t0001g0088 a0001c0001t0002g0019 others(189): 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 | 65 | a0001c0001t0001g0032 a0001c0001t0001g0050 a0001c0001t0001g0058 others(62): Show |
65 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(62): 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 | a0001c0002t0037g0275 | 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 | a0001c0002t0037g0275 | 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 | a0001c0004t0022g0233 | 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 | 41 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0067 others(38): Show |
41 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(38): 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 | a0001c0001t0011g0010 | 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 | a0001c0001t0011g0010 | 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 | a0001c0001t0011g0010 | 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 | a0001c0001t0002g0205 a0001c0003t0012g0294 a0001c0003t0012g0298 others(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 | a0001c0001t0003g0308 a0001c0001t0005g0030 a0001c0001t0005g0077 others(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 | a0001c0001t0003g0308 a0001c0001t0005g0030 a0001c0001t0005g0077 others(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 | a0001c0003t0004g0211 | 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 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0011g0159 others(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 | a0001c0001t0002g0205 a0001c0004t0017g0234 |
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 | a0001c0001t0002g0282 a0001c0001t0003g0254 a0001c0001t0003g0266 others(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 | a0001c0002t0002g0186 | 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 | a0001c0001t0003g0052 | 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 | a0001c0001t0010g0126 | 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 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
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 | a0001c0004t0002g0324 | 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 | a0001c0003t0004g0206 | 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 | a0001c0001t0002g0205 | 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 | a0001c0002t0001g0124 a0001c0003t0001g0157 a0001c0003t0001g0200 others(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 | 176 | a0001c0001t0001g0088 a0001c0001t0002g0019 a0001c0001t0002g0021 others(173): 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 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0069 others(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 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
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 | a0001c0002t0002g0273 a0001c0005t0002g0306 |
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 | a0001c0002t0001g0198 a0001c0002t0001g0256 a0001c0002t0001g0268 others(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 | a0001c0002t0003g0214 | 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 | a0001c0002t0001g0290 | 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 | a0001c0004t0003g0119 | 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 | a0001c0003t0001g0287 | 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 | a0001c0001t0011g0010 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0170 a0001c0004t0001g0167 others(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 | a0001c0005t0033g0241 | 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 | 86 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0088 others(83): 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 | 290 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(287): 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 | a0001c0001t0003g0308 a0001c0001t0005g0030 a0001c0001t0005g0077 others(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 | a0001c0002t0001g0103 a0001c0005t0002g0208 |
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 | a0001c0001t0002g0183 a0001c0001t0002g0229 a0001c0001t0002g0237 |
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 | a0001c0004t0001g0332 | 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 | a0001c0001t0002g0343 | 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 | a0001c0004t0017g0234 | 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 | a0001c0001t0001g0115 | 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 | 137 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0088 others(134): 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 | a0001c0002t0001g0181 a0001c0003t0004g0211 |
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 | a0001c0001t0001g0011 | 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 | a0001c0002t0001g0103 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(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 | a0001c0003t0002g0319 | 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 | a0001c0003t0002g0319 | 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 | a0001c0003t0002g0319 | 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 | 267 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(264): 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 | a0001c0001t0001g0144 a0001c0001t0002g0060 a0001c0001t0036g0061 |
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 | a0001c0001t0001g0188 a0001c0001t0001g0345 a0001c0001t0002g0183 others(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 | a0001c0002t0002g0243 a0001c0002t0002g0244 |
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 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0004t0034g0249 |
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 | 269 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(266): 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 | a0001c0002t0001g0334 a0001c0002t0002g0160 a0001c0002t0007g0036 others(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 | a0001c0001t0002g0162 | 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 | a0001c0002t0001g0014 a0001c0002t0001g0018 a0001c0002t0001g0135 others(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 | 266 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(263): 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 | a0001c0001t0002g0060 | 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 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0003g0308 others(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 | a0001c0003t0002g0319 | 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 | a0001c0001t0001g0188 a0001c0001t0002g0282 a0001c0001t0003g0254 others(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 | 284 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(281): 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 | a0001c0001t0004g0210 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(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 | a0001c0002t0001g0268 | 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 | 291 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(288): 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 | a0001c0003t0002g0319 | 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 | a0001c0001t0002g0076 a0001c0004t0001g0303 |
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 | a0001c0001t0002g0019 a0001c0001t0002g0021 |
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 | a0001c0001t0011g0010 | 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 | a0001c0001t0014g0092 | 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 | 172 | a0001c0001t0001g0034 a0001c0001t0001g0088 a0001c0001t0001g0096 others(169): 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 | a0001c0001t0001g0020 a0001c0001t0001g0188 a0001c0001t0001g0345 others(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 | a0001c0001t0001g0345 a0001c0004t0002g0238 |
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 | a0001c0002t0007g0302 | 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 | a0001c0001t0002g0205 | 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 | a0001c0004t0006g0224 | 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 | a0001c0001t0002g0142 | 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 | a0001c0003t0002g0319 | 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 | a0001c0001t0001g0141 | 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 | a0001c0004t0002g0339 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0189 a0001c0001t0002g0199 a0001c0002t0001g0193 |
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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0096 a0001c0001t0001g0170 a0001c0002t0001g0121 others(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 | a0001c0001t0003g0308 a0001c0001t0005g0030 a0001c0001t0005g0077 others(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 | a0001c0002t0001g0059 a0001c0002t0001g0091 a0001c0002t0001g0123 others(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 | a0001c0001t0003g0308 a0001c0001t0005g0030 a0001c0001t0005g0077 others(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 | 127 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(124): 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 | a0001c0004t0001g0027 a0001c0004t0002g0101 a0001c0004t0002g0339 |
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 | a0001c0002t0001g0114 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0156 a0001c0002t0001g0283 a0001c0004t0001g0325 others(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 | a0001c0002t0001g0268 a0001c0002t0001g0281 a0001c0002t0002g0264 others(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 | a0001c0001t0001g0069 | 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 | 277 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(274): 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 | a0001c0001t0005g0166 | 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 | a0001c0002t0001g0070 | 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 | a0001c0001t0011g0257 a0001c0002t0003g0255 a0001c0003t0003g0265 |
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 | a0001c0001t0001g0112 a0001c0001t0002g0229 a0001c0001t0002g0237 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0020 others(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 | 159 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(156): 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 | a0001c0001t0011g0010 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0115 others(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 | a0001c0005t0033g0241 | 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 | a0001c0001t0003g0284 | 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 | a0001c0002t0001g0158 a0001c0002t0001g0181 a0001c0002t0001g0268 others(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 | 174 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(171): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): 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 | a0001c0001t0011g0010 | 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 | a0001c0003t0002g0029 | 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 | a0001c0003t0001g0065 a0001c0003t0001g0289 a0001c0005t0001g0271 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0022 others(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 | a0001c0001t0011g0010 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0003g0322 | 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 | a0001c0001t0035g0078 | 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 | 208 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(205): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1055-4035C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 5/7 | chr9 | 132235069 | |||||||
| chr9:132235224 | A | G | 145 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(142): Show |
146 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(143): 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 | a0001c0001t0002g0013 a0001c0001t0002g0081 a0001c0001t0002g0149 others(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 | a0001c0001t0001g0170 | 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 | a0001c0004t0001g0027 a0001c0004t0002g0101 a0001c0004t0002g0339 |
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 | a0001c0001t0004g0210 | 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 | a0001c0001t0003g0254 a0001c0001t0010g0102 a0001c0001t0010g0126 others(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 | 58 | a0001c0001t0001g0345 a0001c0001t0003g0038 a0001c0001t0003g0039 others(55): Show |
59 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(56): 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 | a0001c0001t0003g0266 a0001c0002t0001g0268 a0001c0002t0001g0281 |
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 | a0001c0001t0003g0266 a0001c0002t0001g0268 a0001c0002t0001g0281 |
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 | a0001c0003t0001g0276 | 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 | a0001c0001t0035g0078 | 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 | a0001c0001t0005g0030 a0001c0001t0005g0077 a0001c0001t0005g0079 others(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 | 235 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(232): Show |
238 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(235): 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 | a0001c0001t0011g0010 a0001c0001t0011g0159 a0001c0001t0011g0257 others(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 | a0001c0003t0003g0232 | 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 | a0001c0003t0001g0276 | 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 | a0001c0003t0006g0219 | 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 | a0001c0002t0002g0160 | 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 | a0001c0002t0007g0036 | 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 | 52 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0003g0038 others(49): Show |
53 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(50): 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 | a0001c0004t0001g0033 | 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 | a0001c0001t0011g0010 a0001c0001t0011g0159 a0001c0001t0011g0257 others(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 | a0001c0001t0005g0030 a0001c0001t0005g0077 a0001c0001t0005g0079 others(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 | a0001c0001t0010g0102 a0001c0001t0010g0126 a0001c0001t0010g0251 others(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 | a0001c0001t0005g0215 | 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 | a0001c0001t0005g0030 a0001c0001t0005g0077 a0001c0001t0005g0079 others(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 | a0001c0001t0003g0266 | 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 | a0001c0002t0002g0277 | 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 | a0001c0001t0005g0030 a0001c0001t0005g0077 a0001c0001t0005g0079 others(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 | a0001c0004t0004g0225 | 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 | a0001c0002t0003g0214 | 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 | a0001c0002t0001g0123 | 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 | a0001c0001t0005g0030 a0001c0001t0005g0077 a0001c0001t0005g0079 others(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 | 105 | a0001c0001t0001g0156 a0001c0001t0002g0008 a0001c0001t0002g0013 others(102): 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 | a0001c0002t0001g0252 | 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 | a0001c0004t0001g0027 a0001c0004t0002g0101 a0001c0004t0002g0339 |
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 | 102 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0019 others(99): 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 | a0001c0001t0003g0305 a0001c0001t0003g0308 a0001c0002t0003g0082 others(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 | a0001c0003t0004g0211 | 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 | a0001c0002t0001g0252 | 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 | a0001c0004t0034g0249 | 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 | 46 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0049 others(43): Show |
47 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(44): 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 | a0001c0001t0036g0061 | 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 | a0001c0002t0001g0165 | 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 | a0001c0003t0004g0211 | 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 | 102 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0019 others(99): 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 | a0001c0002t0001g0290 | 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 | a0001c0002t0001g0095 a0001c0002t0001g0165 |
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 | a0001c0001t0003g0266 | 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 | a0001c0002t0001g0252 | 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 | 103 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0019 others(100): 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 | a0001c0004t0003g0071 | 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 | a0001c0002t0001g0252 | 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 | a0001c0003t0001g0150 a0001c0004t0001g0167 |
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 | a0001c0001t0011g0010 a0001c0001t0011g0159 a0001c0001t0011g0257 others(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 | a0001c0004t0003g0071 | 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 | a0001c0001t0002g0183 | 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 | 40 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0049 others(37): Show |
41 | HG00099.hp2 HG00597.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1358-276C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241600 | |||||||
| chr9:132241724 | G | C | 191 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0019 others(188): Show |
193 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(190): 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 | a0001c0001t0001g0170 | 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 | 253 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0022 others(250): Show |
255 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(252): 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 | a0001c0001t0029g0075 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1358-80C>T | NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 7/7 | chr9 | 132241796 |