Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 126147 |
| ensemblid | ENSG00000142233.14 |
| hgncid | 25208 |
| symbol | NTN5 |
| name | netrin 5 |
| refseq_nuc | NM_145807.4 |
| refseq_prot | NP_665806.1 |
| ensembl_nuc | ENST00000270235.11 |
| ensembl_prot | ENSP00000270235.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 48661407 |
| end | 48673017 |
| strand | - |
| ver | v1.2 |
| region | chr19:48661407-48673017 |
| region5000 | chr19:48656407-48678017 |
| regionname0 | NTN5_chr19_48661407_48673017 |
| regionname5000 | NTN5_chr19_48656407_48678017 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 489 | 398 | 89 | 71 | 185 | 12 | 40 | 151 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| a0002 | 0/0 | 489 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| a0003 | 0/0 | 489 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| a0004 | 0/0 | 489 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| a0005 | 0/1 | 489 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| a0006 | 0/0 | 489 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| a0007 | 0/0 | 489 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| a0008 | 0/0 | 489 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | MPVTF others(484): Show |
chr19 | 48656407 | 48678017 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1467 | 209 | 37 | 32 | 105 | 6 | 29 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0002 | 1/0 | 1467 | 163 | 47 | 35 | 69 | 2 | 9 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0003 | 0/0 | 1467 | 11 | 2 | 3 | 0 | 4 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0004 | 0/0 | 1467 | 8 | 0 | 0 | 8 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0007 | 0/0 | 1467 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0010 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0011 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0012 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0001c0015 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0002c0005 | 0/0 | 1467 | 4 | 3 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0003c0006 | 0/0 | 1467 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0004c0008 | 0/0 | 1467 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0005c0009 | 0/1 | 1467 | 2 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0006c0016 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0007c0013 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 | ||
| a0008c0014 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ATGCC others(1462): Show |
chr19 | 48656407 | 48678017 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1846 | 208 | 36 | 32 | 105 | 6 | 29 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0001t0002 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0002t0001 | 0/0 | 1846 | 8 | 7 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0002t0002 | 1/0 | 1846 | 154 | 39 | 35 | 68 | 2 | 9 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0002t0003 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0003t0001 | 0/0 | 1846 | 11 | 2 | 3 | 0 | 4 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0004t0001 | 0/0 | 1846 | 8 | 0 | 0 | 8 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0007t0001 | 0/0 | 1846 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0010t0002 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0011t0002 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0012t0001 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0001c0015t0001 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0002c0005t0002 | 0/0 | 1846 | 4 | 3 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0003c0006t0002 | 0/0 | 1846 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0004c0008t0001 | 0/0 | 1846 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0005c0009t0001 | 0/1 | 1846 | 2 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0006c0016t0002 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0007c0013t0002 | 0/0 | 1846 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| a0008c0014t0001 | 0/0 | 1846 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | ACTCC others(1841): Show |
chr19 | 48656407 | 48678017 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 39 | 7 | 17 | 0 | 4 | 11 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0003 | 0/0 | 25 | 2 | 0 | 20 | 0 | 3 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0004 | 0/0 | 25 | 0 | 1 | 20 | 0 | 4 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0005 | 0/0 | 21 | 0 | 0 | 21 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0008 | 0/0 | 15 | 0 | 2 | 9 | 1 | 3 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0009 | 0/0 | 14 | 11 | 1 | 0 | 0 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0011 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0001 | 0/0 | 45 | 1 | 14 | 28 | 1 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0006 | 0/0 | 20 | 0 | 6 | 8 | 0 | 6 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0007 | 0/0 | 16 | 0 | 7 | 8 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0010 | 0/0 | 12 | 11 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0016 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0018 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0003t0001g0012 | 0/0 | 8 | 1 | 1 | 0 | 4 | 2 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0004t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0004t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0007t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0010t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0011t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0012t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0001c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0002c0005t0002g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0002c0005t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0003c0006t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0003c0006t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0004c0008t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0005c0009t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0005c0009t0001g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0006c0016t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0007c0013t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| a0008c0014t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00597 | hp2 | a0003 | c0006 | t0002 | g0091 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00621 | hp1 | a0006 | c0016 | t0002 | g0105 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01106 | hp1 | a0004 | c0008 | t0001 | g0033 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01346 | hp2 | a0002 | c0005 | t0002 | g0103 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01358 | hp2 | a0004 | c0008 | t0001 | g0033 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01433 | hp2 | a0001 | c0007 | t0001 | g0021 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0012 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0012 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0016 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0012 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0012 | EUR | IBS | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | CDX | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0110 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0098 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02818 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02886 | hp1 | a0002 | c0005 | t0002 | g0029 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02922 | hp2 | a0001 | c0012 | t0001 | g0082 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03139 | hp2 | a0007 | c0013 | t0002 | g0097 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0113 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03453 | hp2 | a0002 | c0005 | t0002 | g0029 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0012 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0012 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0089 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18612 | hp2 | a0001 | c0011 | t0002 | g0100 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18949 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18950 | hp1 | a0003 | c0006 | t0002 | g0036 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18961 | hp2 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18971 | hp2 | a0001 | c0015 | t0001 | g0046 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18972 | hp1 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19007 | hp2 | a0003 | c0006 | t0002 | g0036 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19009 | hp1 | a0001 | c0010 | t0002 | g0099 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19030 | hp1 | a0002 | c0005 | t0002 | g0029 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19060 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19065 | hp2 | a0008 | c0014 | t0001 | g0057 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0024 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19085 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0096 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ASW | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | GIH | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | GIH | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | MSL | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG06807 | hp1 | a0005 | c0009 | t0001 | g0060 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | USA | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| homoSapiens | chm13v2 | a0005 | c0009 | t0001 | g0079 | REF | REF | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0018 | REF | REF | NTN5_chr19_48656407_48678017 | NTN5 | chr19 | 48656407 | 48678017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48661687 | G | A | 1 | a0002 | 4 | HG01346.hp2 HG02886.hp1 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.1460C>T | p.Pro487Leu | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1566/1846 | 1460/1470 | 487/489 | chr19 | 48661687 | |||
| chr19:48661696 | C | T | 1 | a0008 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.1451G>A | p.Ser484Asn | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1557/1846 | 1451/1470 | 484/489 | chr19 | 48661696 | |||
| chr19:48661900 | A | C | 1 | a0003 | 3 | HG00597.hp2 NA18950.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.1247T>G | p.Leu416Arg | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1353/1846 | 1247/1470 | 416/489 | chr19 | 48661900 | |||
| chr19:48661960 | T | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1187A>G | p.Lys396Arg | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1293/1846 | 1187/1470 | 396/489 | chr19 | 48661960 | |||
| chr19:48661961 | T | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1186A>G | p.Lys396Glu | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1292/1846 | 1186/1470 | 396/489 | chr19 | 48661961 | |||
| chr19:48661962 | G | C | 1 | a0006 | 1 | HG00621.hp1 | stop_gained | HIGH | c.1185C>G | p.Tyr395* | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1291/1846 | 1185/1470 | 395/489 | chr19 | 48661962 | |||
| chr19:48661963 | T | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1184A>G | p.Tyr395Cys | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1290/1846 | 1184/1470 | 395/489 | chr19 | 48661963 | |||
| chr19:48661964 | A | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1183T>G | p.Tyr395Asp | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1289/1846 | 1183/1470 | 395/489 | chr19 | 48661964 | |||
| chr19:48661966 | A | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1181T>G | p.Val394Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1287/1846 | 1181/1470 | 394/489 | chr19 | 48661966 | |||
| chr19:48661969 | G | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1178C>G | p.Ala393Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1284/1846 | 1178/1470 | 393/489 | chr19 | 48661969 | |||
| chr19:48661972 | A | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1175T>G | p.Leu392Arg | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1281/1846 | 1175/1470 | 392/489 | chr19 | 48661972 | |||
| chr19:48661973 | G | C | 1 | a0006 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1174C>G | p.Leu392Val | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1280/1846 | 1174/1470 | 392/489 | chr19 | 48661973 | |||
| chr19:48662015 | C | T | 1 | a0007 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1132G>A | p.Glu378Lys | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1238/1846 | 1132/1470 | 378/489 | chr19 | 48662015 | |||
| chr19:48663484 | T | C | 1 | a0005 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1084A>G | p.Arg362Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/7 | 1190/1846 | 1084/1470 | 362/489 | chr19 | 48663484 | |||
| chr19:48664274 | A | G | 1 | a0004 | 2 | HG01106.hp1 HG01358.hp2 |
missense_variant | MODERATE | c.839T>C | p.Ile280Thr | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/7 | 945/1846 | 839/1470 | 280/489 | chr19 | 48664274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48661695 | A | G | 6 | a0001c0001 a0001c0007 a0001c0015 others(3): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
synonymous_variant | LOW | c.1452T>C | p.Ser484Ser | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1558/1846 | 1452/1470 | 484/489 | chr19 | 48661695 | |||
| chr19:48661698 | G | T | 1 | a0001c0007 | 3 | HG01433.hp2 HG02145.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.1449C>A | p.Pro483Pro | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1555/1846 | 1449/1470 | 483/489 | chr19 | 48661698 | |||
| chr19:48661890 | G | C | 1 | a0001c0015 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1257C>G | p.Gly419Gly | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1363/1846 | 1257/1470 | 419/489 | chr19 | 48661890 | |||
| chr19:48661965 | A | C | 1 | a0006c0016 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.1182T>G | p.Val394Val | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1288/1846 | 1182/1470 | 394/489 | chr19 | 48661965 | |||
| chr19:48661968 | G | C | 1 | a0006c0016 | 1 | HG00621.hp1 | synonymous_variant | LOW | c.1179C>G | p.Ala393Ala | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1285/1846 | 1179/1470 | 393/489 | chr19 | 48661968 | |||
| chr19:48662001 | C | G | 1 | a0001c0012 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1146G>C | p.Pro382Pro | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 1252/1846 | 1146/1470 | 382/489 | chr19 | 48662001 | |||
| chr19:48664748 | G | A | 1 | a0001c0003 | 11 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
synonymous_variant | LOW | c.651C>T | p.His217His | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/7 | 757/1846 | 651/1470 | 217/489 | chr19 | 48664748 | |||
| chr19:48670414 | C | T | 2 | a0001c0004 a0001c0012 |
9 | HG02922.hp2 NA18949.hp1 NA18952.hp2 others(6): Show |
synonymous_variant | LOW | c.573G>A | p.Pro191Pro | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/7 | 679/1846 | 573/1470 | 191/489 | chr19 | 48670414 | |||
| chr19:48670540 | C | T | 1 | a0001c0011 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.447G>A | p.Ala149Ala | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/7 | 553/1846 | 447/1470 | 149/489 | chr19 | 48670540 | |||
| chr19:48670585 | C | T | 1 | a0001c0010 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.402G>A | p.Ala134Ala | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/7 | 508/1846 | 402/1470 | 134/489 | chr19 | 48670585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48661483 | T | C | 10 | a0001c0001t0001 a0001c0002t0001 a0001c0003t0001 others(7): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*194A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 7/7 | 194 | chr19 | 48661483 | ||||||
| chr19:48673003 | C | A | 1 | a0001c0002t0003 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/7 | 2017 | chr19 | 48673003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48662066 | C | G | 1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1106-25G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662066 | |||||||
| chr19:48662307 | T | TGCA | 2 | a0001c0002t0002g0010 a0001c0002t0003g0113 |
13 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1106-267_1106-266i others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662307 | |||||||
| chr19:48662308 | A | T | 2 | a0001c0002t0002g0010 a0001c0002t0003g0113 |
13 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1106-267T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662308 | |||||||
| chr19:48662356 | G | A | 1 | a0001c0002t0002g0106 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1106-315C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662356 | |||||||
| chr19:48662510 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1106-469T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662510 | |||||||
| chr19:48662819 | G | GGAGATCC others(90): Show |
1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1105+547_1105+643d others(99): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48662819 | |||||||
| chr19:48663019 | T | C | 1 | a0001c0002t0002g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1105+444A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663019 | |||||||
| chr19:48663033 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0092 |
3 | HG01070.hp1 HG01071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1105+430A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663033 | |||||||
| chr19:48663054 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1105+409C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663054 | |||||||
| chr19:48663063 | G | A | 1 | a0001c0002t0002g0107 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1105+400C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663063 | |||||||
| chr19:48663286 | C | T | 1 | a0001c0002t0002g0019 | 4 | HG02622.hp2 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+177G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 6/6 | chr19 | 48663286 | |||||||
| chr19:48663618 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(51): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1025-75C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 5/6 | chr19 | 48663618 | |||||||
| chr19:48663840 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.971-26G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48663840 | |||||||
| chr19:48663876 | C | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0002g0010 others(1): Show |
15 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-62G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48663876 | |||||||
| chr19:48664006 | G | A | 1 | a0001c0003t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.970+137C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48664006 | |||||||
| chr19:48664085 | C | G | 1 | a0001c0002t0002g0025 | 3 | NA18960.hp1 NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.970+58G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48664085 | |||||||
| chr19:48664104 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0052 others(5): Show |
22 | HG01074.hp2 HG01243.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.970+39C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 4/6 | chr19 | 48664104 | |||||||
| chr19:48664416 | GGAGTCCA others(29): Show |
G | 3 | a0001c0001t0001g0056 a0001c0002t0002g0086 a0001c0002t0002g0090 |
3 | NA18747.hp1 NA18954.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.820+127_821-125del others(36): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664416 | |||||||
| chr19:48664426 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.821-134G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664426 | |||||||
| chr19:48664521 | C | A | 1 | a0001c0003t0001g0040 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.820+58G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664521 | |||||||
| chr19:48664522 | C | T | 1 | a0001c0003t0001g0040 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.820+57G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664522 | |||||||
| chr19:48664529 | G | A | 1 | a0001c0003t0001g0040 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.820+50C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 3/6 | chr19 | 48664529 | |||||||
| chr19:48664851 | C | T | 1 | a0001c0004t0001g0024 | 3 | NA18961.hp2 NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.632-84G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664851 | |||||||
| chr19:48664925 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(20): Show |
96 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.632-158A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664925 | |||||||
| chr19:48664936 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0054 a0001c0001t0001g0064 others(1): Show |
5 | HG01074.hp2 HG02735.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-169C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664936 | |||||||
| chr19:48664973 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.632-206G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48664973 | |||||||
| chr19:48665079 | A | AT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0070 others(3): Show |
8 | HG01934.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.632-313dupA | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665079 | |||||||
| chr19:48665079 | AT | A | 8 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
13 | HG02258.hp1 HG02615.hp1 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.632-313delA | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665079 | |||||||
| chr19:48665135 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0063 |
11 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(8): Show |
intron_variant | MODIFIER | c.632-368C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665135 | |||||||
| chr19:48665139 | G | T | 1 | a0001c0002t0002g0043 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.632-372C>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665139 | |||||||
| chr19:48665171 | C | T | 6 | a0001c0002t0002g0015 a0001c0002t0002g0027 a0001c0002t0002g0095 others(3): Show |
12 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.632-404G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665171 | |||||||
| chr19:48665202 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.632-435T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665202 | |||||||
| chr19:48665300 | A | G | 45 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0102 others(42): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.632-533T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665300 | |||||||
| chr19:48665435 | C | CA | 8 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0002t0002g0007 others(5): Show |
25 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.632-669dupT | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665435 | |||||||
| chr19:48665480 | G | A | 45 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0102 others(42): Show |
146 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.632-713C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665480 | |||||||
| chr19:48665540 | TC | T | 3 | a0001c0002t0001g0041 a0001c0002t0001g0111 a0001c0002t0001g0112 |
4 | HG02280.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.632-774delG | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665540 | |||||||
| chr19:48665543 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
407 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.632-776T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665543 | |||||||
| chr19:48665685 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0050 others(1): Show |
44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.632-918C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665685 | |||||||
| chr19:48665833 | C | A | 2 | a0001c0002t0002g0019 a0001c0002t0002g0038 |
6 | HG02486.hp1 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.632-1066G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665833 | |||||||
| chr19:48665959 | TG | T | 37 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0102 others(34): Show |
128 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.632-1193delC | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48665959 | |||||||
| chr19:48666259 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.632-1492C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666259 | |||||||
| chr19:48666455 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.632-1688C>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666455 | |||||||
| chr19:48666677 | CTT | C | 17 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0032 others(14): Show |
30 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.632-1912_632-1911d others(4): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666677 | |||||||
| chr19:48666677 | CTTT | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.632-1913_632-1911d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666677 | |||||||
| chr19:48666677 | CTTTT | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0067 others(4): Show |
15 | HG01106.hp2 HG01167.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.632-1914_632-1911d others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666677 | |||||||
| chr19:48666807 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0045 |
3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.632-2040G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666807 | |||||||
| chr19:48666811 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(33): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.632-2044C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666811 | |||||||
| chr19:48666836 | A | G | 1 | a0001c0002t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.632-2069T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666836 | |||||||
| chr19:48666874 | G | A | 2 | a0001c0002t0001g0031 a0001c0002t0001g0045 |
3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.632-2107C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666874 | |||||||
| chr19:48666960 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.632-2193G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48666960 | |||||||
| chr19:48667056 | C | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0045 |
3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.632-2289G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667056 | |||||||
| chr19:48667211 | C | A | 22 | a0001c0001t0001g0102 a0001c0001t0002g0104 a0001c0002t0002g0001 others(19): Show |
89 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.632-2444G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667211 | |||||||
| chr19:48667236 | AGAG | A | 4 | a0001c0002t0001g0084 a0001c0004t0001g0014 a0001c0004t0001g0024 others(1): Show |
10 | HG02027.hp1 HG02922.hp2 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.632-2472_632-2470d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667236 | |||||||
| chr19:48667306 | C | T | 1 | a0001c0002t0002g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.632-2539G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667306 | |||||||
| chr19:48667778 | C | G | 7 | a0001c0001t0001g0042 a0001c0002t0001g0041 a0001c0002t0001g0111 others(4): Show |
17 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.631+2578G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667778 | |||||||
| chr19:48667938 | G | A | 1 | a0001c0002t0002g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.631+2418C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48667938 | |||||||
| chr19:48668049 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(3): Show |
46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.631+2307G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668049 | |||||||
| chr19:48668122 | G | T | 1 | a0001c0002t0002g0101 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.631+2234C>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668122 | |||||||
| chr19:48668336 | T | C | 37 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0102 others(34): Show |
128 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.631+2020A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668336 | |||||||
| chr19:48668404 | GC | G | 2 | a0001c0002t0002g0019 a0001c0002t0002g0038 |
6 | HG02486.hp1 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1951delG | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668404 | |||||||
| chr19:48668749 | G | A | 1 | a0001c0002t0002g0043 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.631+1607C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668749 | |||||||
| chr19:48668849 | C | T | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1507G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668849 | |||||||
| chr19:48668857 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.631+1499T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668857 | |||||||
| chr19:48668899 | C | G | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1457G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668899 | |||||||
| chr19:48668909 | G | A | 4 | a0001c0001t0001g0042 a0001c0002t0001g0041 a0001c0002t0001g0111 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1447C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668909 | |||||||
| chr19:48668921 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0045 |
3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1435G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668921 | |||||||
| chr19:48668938 | T | A | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1418A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668938 | |||||||
| chr19:48668945 | C | A | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1411G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668945 | |||||||
| chr19:48668949 | A | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0045 |
3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1407T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668949 | |||||||
| chr19:48668956 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1400A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668956 | |||||||
| chr19:48668963 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1393A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668963 | |||||||
| chr19:48668963 | TATCACCA others(5): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.631+1381_631+1392d others(14): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668963 | |||||||
| chr19:48668965 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1391A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668965 | |||||||
| chr19:48668966 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1390G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668966 | |||||||
| chr19:48668968 | C | T | 2 | a0001c0001t0001g0068 a0003c0006t0002g0091 |
2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1388G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668968 | |||||||
| chr19:48668969 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1387G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668969 | |||||||
| chr19:48668972 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1384G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668972 | |||||||
| chr19:48668975 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1381G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668975 | |||||||
| chr19:48668978 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1378G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668978 | |||||||
| chr19:48668979 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1377T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668979 | |||||||
| chr19:48668980 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1376G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668980 | |||||||
| chr19:48668981 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1375G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668981 | |||||||
| chr19:48668983 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1373G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668983 | |||||||
| chr19:48668987 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1369G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668987 | |||||||
| chr19:48668989 | C | T | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1367G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668989 | |||||||
| chr19:48668992 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1364A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48668992 | |||||||
| chr19:48669001 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1355A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669001 | |||||||
| chr19:48669002 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1354G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669002 | |||||||
| chr19:48669004 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1352G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669004 | |||||||
| chr19:48669008 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1348A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669008 | |||||||
| chr19:48669009 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1347T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669009 | |||||||
| chr19:48669011 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1345G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669011 | |||||||
| chr19:48669018 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1338T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669018 | |||||||
| chr19:48669025 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1331G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669025 | |||||||
| chr19:48669029 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1327A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669029 | |||||||
| chr19:48669035 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1321A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669035 | |||||||
| chr19:48669040 | T | A | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1316A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669040 | |||||||
| chr19:48669040 | TCACCACC others(608): Show |
T | 3 | a0001c0002t0002g0015 a0001c0002t0002g0095 a0001c0002t0002g0096 |
7 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+701_631+1315de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669040 | |||||||
| chr19:48669045 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1311T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669045 | |||||||
| chr19:48669046 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1310G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669046 | |||||||
| chr19:48669049 | C | T | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1307G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669049 | |||||||
| chr19:48669055 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1301G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669055 | |||||||
| chr19:48669058 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1298A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669058 | |||||||
| chr19:48669058 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1298A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669058 | |||||||
| chr19:48669061 | C | T | 2 | a0001c0002t0002g0098 a0007c0013t0002g0097 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+1295G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669061 | |||||||
| chr19:48669065 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1291G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669065 | |||||||
| chr19:48669067 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1289G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669067 | |||||||
| chr19:48669067 | CCACCACT others(23): Show |
C | 1 | a0001c0002t0002g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.631+1259_631+1288d others(32): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669067 | |||||||
| chr19:48669070 | C | T | 3 | a0001c0002t0002g0098 a0003c0006t0002g0091 a0007c0013t0002g0097 |
3 | HG00597.hp2 HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+1286G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669070 | |||||||
| chr19:48669073 | CTATCACC others(274): Show |
C | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+1002_631+1282d others(2): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669073 | |||||||
| chr19:48669074 | T | C | 1 | a0001c0002t0002g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+1282A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669074 | |||||||
| chr19:48669076 | T | C | 2 | a0001c0002t0002g0098 a0003c0006t0002g0091 |
2 | HG00597.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.631+1280A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669076 | |||||||
| chr19:48669076 | TCACCATC others(41): Show |
T | 1 | a0001c0002t0002g0007 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.631+1232_631+1279d others(50): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669076 | |||||||
| chr19:48669085 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1271A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669085 | |||||||
| chr19:48669085 | TCACCACC others(469): Show |
T | 1 | a0001c0002t0002g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+795_631+1270de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669085 | |||||||
| chr19:48669088 | C | T | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1268G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669088 | |||||||
| chr19:48669104 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1252A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669104 | |||||||
| chr19:48669105 | A | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1251T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669105 | |||||||
| chr19:48669106 | T | A | 2 | a0001c0001t0001g0068 a0003c0006t0002g0091 |
2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1250A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669106 | |||||||
| chr19:48669108 | A | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1248T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669108 | |||||||
| chr19:48669109 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1247G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669109 | |||||||
| chr19:48669112 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1244A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669112 | |||||||
| chr19:48669115 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1241A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669115 | |||||||
| chr19:48669121 | C | T | 2 | a0001c0001t0001g0068 a0003c0006t0002g0091 |
2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1235G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669121 | |||||||
| chr19:48669127 | C | T | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1229G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669127 | |||||||
| chr19:48669133 | T | C | 2 | a0001c0001t0001g0068 a0003c0006t0002g0091 |
2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1223A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669133 | |||||||
| chr19:48669136 | T | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1220A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669136 | |||||||
| chr19:48669144 | TCATCACC others(489): Show |
T | 1 | a0001c0004t0001g0014 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.631+716_631+1211de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669144 | |||||||
| chr19:48669147 | T | C | 2 | a0001c0001t0001g0068 a0003c0006t0002g0091 |
2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+1209A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669147 | |||||||
| chr19:48669150 | CCACCATC others(272): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.631+927_631+1205de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669150 | |||||||
| chr19:48669152 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1204T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669152 | |||||||
| chr19:48669153 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1203G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669153 | |||||||
| chr19:48669153 | CCATCACC others(269): Show |
C | 1 | a0001c0002t0002g0016 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.631+927_631+1202de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669153 | |||||||
| chr19:48669156 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.631+1200A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669156 | |||||||
| chr19:48669158 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1198T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669158 | |||||||
| chr19:48669165 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1191G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669165 | |||||||
| chr19:48669171 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1185A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669171 | |||||||
| chr19:48669176 | ACCATGAC others(54): Show |
A | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+1119_631+1179d others(63): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669176 | |||||||
| chr19:48669181 | G | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1175C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669181 | |||||||
| chr19:48669195 | CCACCATC others(7): Show |
C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1147_631+1160d others(16): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669195 | |||||||
| chr19:48669198 | CCATCACC others(26): Show |
C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(36): Show |
114 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.631+1125_631+1157d others(35): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669198 | |||||||
| chr19:48669198 | CCATCACC others(62): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631+1089_631+1157d others(71): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669198 | |||||||
| chr19:48669201 | T | TCAC | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(34): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.631+1152_631+1154d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669201 | |||||||
| chr19:48669201 | TCACCATC others(35): Show |
T | 4 | a0001c0001t0001g0042 a0001c0002t0001g0041 a0001c0002t0001g0111 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1113_631+1154d others(44): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669201 | |||||||
| chr19:48669201 | TCACCATC others(122): Show |
T | 3 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0003g0113 |
14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+1026_631+1154d others(2): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669201 | |||||||
| chr19:48669204 | C | CCACCATC others(347): Show |
1 | a0001c0001t0001g0058 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.631+1151_631+1152i others(356): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669204 | |||||||
| chr19:48669207 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0069 others(3): Show |
32 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.631+1149A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669207 | |||||||
| chr19:48669210 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1146G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669210 | |||||||
| chr19:48669213 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(35): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.631+1143G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669213 | |||||||
| chr19:48669216 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0069 others(3): Show |
32 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.631+1140G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669216 | |||||||
| chr19:48669222 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1134G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669222 | |||||||
| chr19:48669223 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1133G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669223 | |||||||
| chr19:48669225 | CGACCAT | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0069 |
4 | HG00438.hp2 HG02040.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+1125_631+1130d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669225 | |||||||
| chr19:48669225 | CGACCATC others(323): Show |
C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(8): Show |
54 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.631+801_631+1130de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669225 | |||||||
| chr19:48669226 | G | C | 2 | a0001c0001t0001g0053 a0001c0002t0001g0031 |
3 | HG01891.hp1 HG02080.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1130C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669226 | |||||||
| chr19:48669231 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.631+1125A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669231 | |||||||
| chr19:48669234 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1122A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669234 | |||||||
| chr19:48669240 | C | CCACCACC others(41): Show |
2 | a0001c0001t0001g0002 a0001c0002t0002g0001 |
6 | HG00280.hp1 HG01081.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+1115_631+1116i others(50): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669240 | |||||||
| chr19:48669240 | C | T | 1 | a0001c0002t0002g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1116G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669240 | |||||||
| chr19:48669243 | C | CCACCACC others(32): Show |
1 | a0001c0002t0002g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1112_631+1113i others(41): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | |||||||
| chr19:48669243 | C | CCACCATC others(50): Show |
1 | a0001c0002t0002g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.631+1112_631+1113i others(59): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | |||||||
| chr19:48669243 | C | CCACCATC others(47): Show |
13 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(10): Show |
60 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+1112_631+1113i others(56): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | |||||||
| chr19:48669243 | C | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(38): Show |
118 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.631+1113G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669243 | |||||||
| chr19:48669244 | C | T | 1 | a0001c0002t0002g0007 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.631+1112G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669244 | |||||||
| chr19:48669246 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1110G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669246 | |||||||
| chr19:48669246 | CCATCACC others(71): Show |
C | 1 | a0001c0001t0001g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.631+1032_631+1109d others(80): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669246 | |||||||
| chr19:48669248 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1108T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669248 | |||||||
| chr19:48669249 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1107A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669249 | |||||||
| chr19:48669249 | T | C | 1 | a0001c0002t0002g0007 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.631+1107A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669249 | |||||||
| chr19:48669252 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1104G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669252 | |||||||
| chr19:48669252 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1104G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669252 | |||||||
| chr19:48669255 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1101G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669255 | |||||||
| chr19:48669258 | C | CCAT | 16 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(13): Show |
52 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(49): Show |
intron_variant | MODIFIER | c.631+1097_631+1098i others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | |||||||
| chr19:48669258 | C | CCATCACC others(23): Show |
1 | a0001c0001t0001g0008 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.631+1097_631+1098i others(32): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | |||||||
| chr19:48669258 | C | CCATCACC others(250): Show |
1 | a0001c0001t0001g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.631+1097_631+1098i others(259): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | |||||||
| chr19:48669258 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1098G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | |||||||
| chr19:48669258 | CCACGACC others(2): Show |
C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0002t0002g0001 others(1): Show |
12 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.631+1089_631+1097d others(11): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669258 | |||||||
| chr19:48669259 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1097G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669259 | |||||||
| chr19:48669261 | C | T | 3 | a0001c0001t0001g0058 a0001c0002t0001g0031 a0003c0006t0002g0091 |
4 | HG00597.hp2 HG00735.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+1095G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669261 | |||||||
| chr19:48669262 | G | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(21): Show |
62 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.631+1094C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669262 | |||||||
| chr19:48669264 | C | T | 1 | a0001c0002t0002g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1092G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669264 | |||||||
| chr19:48669267 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1089A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669267 | |||||||
| chr19:48669267 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(31): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.631+1089A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669267 | |||||||
| chr19:48669270 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(18): Show |
57 | HG00408.hp1 HG00544.hp1 HG01258.hp1 others(54): Show |
intron_variant | MODIFIER | c.631+1086A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669270 | |||||||
| chr19:48669273 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(14): Show |
53 | HG00408.hp1 HG01258.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.631+1083G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669273 | |||||||
| chr19:48669275 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1081T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669275 | |||||||
| chr19:48669276 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0052 |
2 | HG00099.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.631+1080G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669276 | |||||||
| chr19:48669282 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+1074G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669282 | |||||||
| chr19:48669285 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1071A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669285 | |||||||
| chr19:48669285 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0058 others(4): Show |
8 | HG00544.hp1 HG00735.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+1071A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669285 | |||||||
| chr19:48669285 | TCACCACC others(104): Show |
T | 2 | a0001c0003t0001g0012 a0001c0003t0001g0040 |
6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+960_631+1070de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669285 | |||||||
| chr19:48669287 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1069T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669287 | |||||||
| chr19:48669288 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(14): Show |
72 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.631+1068G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669288 | |||||||
| chr19:48669291 | C | CCACCATC others(131): Show |
1 | a0001c0002t0002g0007 | 2 | HG03490.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.631+927_631+1064du others(139): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669291 | |||||||
| chr19:48669294 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1062G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669294 | |||||||
| chr19:48669294 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(14): Show |
54 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(51): Show |
intron_variant | MODIFIER | c.631+1062G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669294 | |||||||
| chr19:48669297 | T | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(15): Show |
55 | HG00408.hp1 HG01258.hp1 HG01361.hp2 others(52): Show |
intron_variant | MODIFIER | c.631+1059A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669297 | |||||||
| chr19:48669297 | TCACCACC others(212): Show |
T | 1 | a0001c0003t0001g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.631+840_631+1058de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669297 | |||||||
| chr19:48669303 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1053G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669303 | |||||||
| chr19:48669303 | CCACCACC others(2): Show |
C | 1 | a0001c0003t0001g0012 | 4 | HG01515.hp1 HG01517.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+1044_631+1052d others(11): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669303 | |||||||
| chr19:48669304 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1052G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669304 | |||||||
| chr19:48669306 | C | CCATCAT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(11): Show |
67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.631+1049_631+1050i others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669306 | |||||||
| chr19:48669306 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(2): Show |
12 | HG00544.hp1 HG01123.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.631+1050G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669306 | |||||||
| chr19:48669307 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1049G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669307 | |||||||
| chr19:48669308 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1048T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669308 | |||||||
| chr19:48669309 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0069 others(2): Show |
7 | HG00438.hp2 HG02040.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+1047G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669309 | |||||||
| chr19:48669312 | T | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(16): Show |
55 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(52): Show |
intron_variant | MODIFIER | c.631+1044A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669312 | |||||||
| chr19:48669312 | TCACCAC | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0069 |
5 | HG00438.hp2 HG02040.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1038_631+1043d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669312 | |||||||
| chr19:48669315 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0002t0001g0031 others(1): Show |
5 | HG00544.hp1 HG01261.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1041G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669315 | |||||||
| chr19:48669318 | C | T | 1 | a0001c0003t0001g0012 | 4 | HG01515.hp1 HG01517.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+1038G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669318 | |||||||
| chr19:48669318 | CCACCAT | C | 3 | a0001c0001t0001g0004 a0001c0002t0002g0001 a0001c0002t0002g0028 |
10 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.631+1032_631+1037d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669318 | |||||||
| chr19:48669319 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1037G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669319 | |||||||
| chr19:48669320 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1036T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669320 | |||||||
| chr19:48669324 | T | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(11): Show |
65 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.631+1032A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | |||||||
| chr19:48669324 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0020 others(2): Show |
5 | HG02622.hp1 HG02647.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1032A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | |||||||
| chr19:48669324 | TCACCAC | T | 2 | a0001c0001t0001g0009 a0001c0002t0001g0031 |
3 | HG01891.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1026_631+1031d others(8): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | |||||||
| chr19:48669324 | TCACCACC others(227): Show |
T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0092 others(2): Show |
5 | HG02148.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.631+798_631+1031de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669324 | |||||||
| chr19:48669327 | C | A | 1 | a0001c0001t0001g0009 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.631+1029G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669327 | |||||||
| chr19:48669327 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+1029G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669327 | |||||||
| chr19:48669328 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1028G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669328 | |||||||
| chr19:48669329 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1027T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669329 | |||||||
| chr19:48669331 | C | G | 2 | a0001c0002t0002g0001 a0001c0002t0002g0028 |
9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+1025G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669331 | |||||||
| chr19:48669333 | C | T | 39 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(36): Show |
118 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.631+1023G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669333 | |||||||
| chr19:48669334 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+1022G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669334 | |||||||
| chr19:48669336 | C | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0069 |
5 | HG00438.hp2 HG02040.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.631+1020G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | |||||||
| chr19:48669336 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0020 others(13): Show |
67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.631+1020G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | |||||||
| chr19:48669336 | CCAT | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(11): Show |
44 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.631+1017_631+1019d others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | |||||||
| chr19:48669336 | CCATCACC others(224): Show |
C | 2 | a0001c0001t0001g0061 a0002c0005t0002g0029 |
2 | HG03453.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.631+789_631+1019de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669336 | |||||||
| chr19:48669339 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(17): Show |
73 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.631+1017A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669339 | |||||||
| chr19:48669342 | C | CCAT | 3 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0054 |
3 | HG02622.hp1 HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.631+1013_631+1014i others(5): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669342 | |||||||
| chr19:48669342 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(29): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.631+1014G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669342 | |||||||
| chr19:48669342 | CCACCACC others(227): Show |
C | 23 | a0001c0001t0001g0042 a0001c0001t0002g0104 a0001c0002t0001g0041 others(20): Show |
68 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.631+780_631+1013de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669342 | |||||||
| chr19:48669345 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.631+1011G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669345 | |||||||
| chr19:48669348 | C | CCACGACC others(5): Show |
1 | a0001c0002t0002g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+1007_631+1008i others(14): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669348 | |||||||
| chr19:48669348 | C | CCATCACC others(295): Show |
1 | a0001c0001t0001g0011 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+1007_631+1008i others(304): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669348 | |||||||
| chr19:48669348 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+1008G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669348 | |||||||
| chr19:48669351 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(14): Show |
46 | HG00408.hp1 HG00735.hp1 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.631+1005G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669351 | |||||||
| chr19:48669351 | CCATCACC others(152): Show |
C | 1 | a0001c0003t0001g0012 | 4 | HG01515.hp1 HG01517.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+846_631+1004de others(1): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669351 | |||||||
| chr19:48669354 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(30): Show |
105 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.631+1002A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669354 | |||||||
| chr19:48669355 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+1001G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669355 | |||||||
| chr19:48669357 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0069 others(4): Show |
16 | HG00438.hp2 HG01123.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+999G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669357 | |||||||
| chr19:48669358 | C | G | 5 | a0001c0001t0001g0093 a0001c0002t0002g0001 a0001c0002t0002g0010 others(2): Show |
16 | HG01243.hp1 HG01884.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+998G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669358 | |||||||
| chr19:48669360 | C | CCATCACC others(107): Show |
1 | a0001c0002t0002g0001 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.631+995_631+996ins others(114): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669360 | |||||||
| chr19:48669360 | C | CCATCATC others(62): Show |
13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(10): Show |
41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+995_631+996ins others(69): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669360 | |||||||
| chr19:48669360 | CCACCATC others(209): Show |
C | 1 | a0001c0001t0001g0004 | 2 | NA18966.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.631+780_631+995del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669360 | |||||||
| chr19:48669363 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0059 others(6): Show |
21 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.631+993G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669363 | |||||||
| chr19:48669366 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+990A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669366 | |||||||
| chr19:48669366 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.631+990A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669366 | |||||||
| chr19:48669369 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+987G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669369 | |||||||
| chr19:48669369 | C | CCAT | 4 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG00735.hp1 HG02293.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+986_631+987ins others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669369 | |||||||
| chr19:48669369 | C | T | 2 | a0001c0002t0002g0001 a0001c0002t0002g0043 |
2 | HG01261.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.631+987G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669369 | |||||||
| chr19:48669372 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(14): Show |
70 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.631+984G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669372 | |||||||
| chr19:48669373 | C | G | 1 | a0001c0001t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631+983G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669373 | |||||||
| chr19:48669373 | CACCACCA others(125): Show |
C | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+851_631+982del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669373 | |||||||
| chr19:48669375 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(13): Show |
44 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.631+981G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669375 | |||||||
| chr19:48669378 | C | T | 3 | a0001c0001t0001g0005 a0001c0002t0002g0001 a0001c0002t0002g0028 |
10 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.631+978G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669378 | |||||||
| chr19:48669381 | T | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG00735.hp1 HG02293.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+975A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669381 | |||||||
| chr19:48669381 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(12): Show |
43 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(40): Show |
intron_variant | MODIFIER | c.631+975A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669381 | |||||||
| chr19:48669381 | TCACCACC others(14): Show |
T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+954_631+974del others(21): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669381 | |||||||
| chr19:48669384 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(14): Show |
49 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.631+972G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669384 | |||||||
| chr19:48669384 | CCACCACC others(185): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.631+780_631+971del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669384 | |||||||
| chr19:48669385 | C | G | 1 | a0001c0001t0001g0009 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.631+971G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669385 | |||||||
| chr19:48669387 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0077 others(3): Show |
19 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.631+969G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669387 | |||||||
| chr19:48669390 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(1): Show |
10 | HG00099.hp1 HG04115.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.631+966G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669390 | |||||||
| chr19:48669390 | CCAT | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0020 others(15): Show |
71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.631+963_631+965del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669390 | |||||||
| chr19:48669392 | A | C | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+964T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669392 | |||||||
| chr19:48669393 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0054 others(3): Show |
19 | HG00099.hp1 HG01123.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.631+963A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669393 | |||||||
| chr19:48669393 | TCACCACC others(32): Show |
T | 1 | a0001c0002t0002g0001 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.631+924_631+962del others(39): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669393 | |||||||
| chr19:48669396 | C | CCAT | 16 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(13): Show |
45 | HG00408.hp1 HG00735.hp1 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.631+959_631+960ins others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669396 | |||||||
| chr19:48669397 | C | T | 1 | a0001c0001t0001g0011 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+959G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669397 | |||||||
| chr19:48669399 | C | A | 2 | a0001c0002t0002g0001 a0001c0002t0002g0028 |
9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+957G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669399 | |||||||
| chr19:48669399 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0058 others(5): Show |
8 | HG00735.hp1 HG02293.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+957G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669399 | |||||||
| chr19:48669402 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(14): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.631+954G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669402 | |||||||
| chr19:48669405 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(15): Show |
51 | HG00099.hp1 HG00621.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.631+951G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669405 | |||||||
| chr19:48669407 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+949T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669407 | |||||||
| chr19:48669408 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+948A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669408 | |||||||
| chr19:48669408 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0077 others(3): Show |
13 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.631+948A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669408 | |||||||
| chr19:48669411 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+945G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669411 | |||||||
| chr19:48669411 | C | T | 3 | a0001c0002t0002g0001 a0001c0002t0002g0028 a0001c0002t0002g0043 |
11 | HG01123.hp2 HG01257.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.631+945G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669411 | |||||||
| chr19:48669412 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+944G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669412 | |||||||
| chr19:48669414 | C | CCACCATC others(133): Show |
1 | a0001c0002t0002g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.631+941_631+942ins others(140): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | |||||||
| chr19:48669414 | C | CCACCATC others(2): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG00735.hp1 HG02293.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+941_631+942ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | |||||||
| chr19:48669414 | C | CCATCACC others(74): Show |
1 | a0001c0001t0001g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.631+941_631+942ins others(81): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | |||||||
| chr19:48669414 | C | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(13): Show |
49 | HG00544.hp1 HG00621.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.631+942G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669414 | |||||||
| chr19:48669416 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+940T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669416 | |||||||
| chr19:48669417 | C | T | 2 | a0001c0002t0002g0001 a0001c0002t0002g0028 |
9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+939G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669417 | |||||||
| chr19:48669419 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+937T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669419 | |||||||
| chr19:48669420 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+936A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669420 | |||||||
| chr19:48669420 | T | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(14): Show |
46 | HG00597.hp2 HG00621.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.631+936A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669420 | |||||||
| chr19:48669420 | TCAC | T | 2 | a0001c0003t0001g0012 a0001c0003t0001g0040 |
6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+933_631+935del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669420 | |||||||
| chr19:48669423 | C | T | 4 | a0001c0001t0001g0054 a0001c0002t0001g0031 a0001c0002t0002g0001 others(1): Show |
5 | HG01261.hp1 HG01891.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.631+933G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669423 | |||||||
| chr19:48669426 | C | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(11): Show |
44 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.631+930G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669426 | |||||||
| chr19:48669426 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(13): Show |
73 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.631+930G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669426 | |||||||
| chr19:48669429 | T | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(15): Show |
51 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.631+927A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669429 | |||||||
| chr19:48669432 | C | CCACCACC others(2): Show |
1 | a0001c0001t0001g0011 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+923_631+924ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669432 | |||||||
| chr19:48669432 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631+924G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669432 | |||||||
| chr19:48669435 | C | A | 2 | a0001c0002t0002g0001 a0001c0002t0002g0109 |
2 | HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.631+921G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | |||||||
| chr19:48669435 | C | CTACCATC others(34): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(3): Show |
40 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.631+920_631+921ins others(41): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | |||||||
| chr19:48669435 | C | CTACCATC others(55): Show |
1 | a0001c0001t0001g0002 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+920_631+921ins others(62): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | |||||||
| chr19:48669435 | C | CTACCATC others(79): Show |
1 | a0001c0002t0002g0028 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.631+920_631+921ins others(86): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | |||||||
| chr19:48669435 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(16): Show |
58 | HG00408.hp1 HG01243.hp1 HG01258.hp1 others(55): Show |
intron_variant | MODIFIER | c.631+921G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669435 | |||||||
| chr19:48669436 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0002t0002g0001 others(7): Show |
21 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.631+920G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669436 | |||||||
| chr19:48669437 | AC | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(10): Show |
41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+918delG | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669437 | |||||||
| chr19:48669438 | C | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(13): Show |
46 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.631+918G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669438 | |||||||
| chr19:48669438 | CCACCACC others(131): Show |
C | 1 | a0001c0001t0001g0005 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.631+780_631+917del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669438 | |||||||
| chr19:48669439 | C | G | 1 | a0001c0002t0002g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.631+917G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669439 | |||||||
| chr19:48669441 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0002t0002g0001 others(8): Show |
30 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.631+915G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669441 | |||||||
| chr19:48669441 | CCACCATC others(65): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.631+843_631+914del others(72): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669441 | |||||||
| chr19:48669441 | CCACCATC others(128): Show |
C | 1 | a0001c0001t0001g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.631+780_631+914del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669441 | |||||||
| chr19:48669444 | C | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(16): Show |
54 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.631+912G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669444 | |||||||
| chr19:48669446 | ATCACCAC others(283): Show |
A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+620_631+909del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669446 | |||||||
| chr19:48669447 | T | A | 1 | a0001c0001t0001g0002 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+909A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669447 | |||||||
| chr19:48669447 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(10): Show |
41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+909A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669447 | |||||||
| chr19:48669447 | TCACCACC others(65): Show |
T | 1 | a0001c0001t0001g0009 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.631+837_631+908del others(72): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669447 | |||||||
| chr19:48669448 | C | CACACCAC others(61): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0020 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.631+907_631+908ins others(68): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669448 | |||||||
| chr19:48669448 | C | G | 3 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0003g0113 |
14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+908G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669448 | |||||||
| chr19:48669450 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(17): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.631+906G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669450 | |||||||
| chr19:48669450 | CCACCATG | C | 8 | a0001c0002t0002g0001 a0001c0002t0002g0030 a0001c0002t0002g0101 others(5): Show |
19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+899_631+905del others(7): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669450 | |||||||
| chr19:48669451 | CACCATG | C | 2 | a0001c0003t0001g0012 a0001c0003t0001g0040 |
6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+899_631+904del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669451 | |||||||
| chr19:48669453 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(9): Show |
20 | HG00099.hp1 HG00735.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.631+903G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669453 | |||||||
| chr19:48669453 | CCATGACC others(5): Show |
C | 2 | a0001c0002t0002g0001 a0001c0002t0002g0028 |
9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+891_631+902del others(12): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669453 | |||||||
| chr19:48669456 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(6): Show |
15 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.631+900A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669456 | |||||||
| chr19:48669456 | T | TCACCAC | 3 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0003g0113 |
14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+899_631+900ins others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669456 | |||||||
| chr19:48669457 | G | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(42): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.631+899C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669457 | |||||||
| chr19:48669459 | C | T | 1 | a0001c0001t0001g0002 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+897G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669459 | |||||||
| chr19:48669463 | C | T | 1 | a0001c0002t0002g0028 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.631+893G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669463 | |||||||
| chr19:48669465 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.631+891A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669465 | |||||||
| chr19:48669465 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
107 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.631+891A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669465 | |||||||
| chr19:48669468 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(3): Show |
40 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.631+888A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669468 | |||||||
| chr19:48669468 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(11): Show |
27 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.631+888A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669468 | |||||||
| chr19:48669468 | TCAC | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(10): Show |
41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+885_631+887del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669468 | |||||||
| chr19:48669471 | C | T | 14 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(11): Show |
44 | HG01074.hp1 HG01074.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.631+885G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669471 | |||||||
| chr19:48669472 | C | A | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+884G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669472 | |||||||
| chr19:48669473 | A | G | 1 | a0003c0006t0002g0091 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.631+883T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669473 | |||||||
| chr19:48669474 | C | T | 9 | a0001c0002t0002g0001 a0001c0002t0002g0028 a0001c0002t0002g0030 others(6): Show |
20 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.631+882G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669474 | |||||||
| chr19:48669477 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(18): Show |
79 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.631+879A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669477 | |||||||
| chr19:48669480 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0020 others(6): Show |
53 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.631+876G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669480 | |||||||
| chr19:48669483 | C | T | 12 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0078 others(9): Show |
24 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.631+873G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669483 | |||||||
| chr19:48669486 | T | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(19): Show |
69 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.631+870A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669486 | |||||||
| chr19:48669486 | T | TCAC | 2 | a0001c0001t0001g0011 a0001c0001t0001g0054 |
8 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+867_631+869dup others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669486 | |||||||
| chr19:48669489 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0048 others(6): Show |
54 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.631+867G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669489 | |||||||
| chr19:48669492 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
85 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.631+864A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669492 | |||||||
| chr19:48669495 | C | CACCACCA others(28): Show |
1 | a0001c0001t0001g0003 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.631+860_631+861ins others(35): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669495 | |||||||
| chr19:48669495 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+861G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669495 | |||||||
| chr19:48669498 | C | CCACCACC others(92): Show |
1 | a0001c0001t0001g0008 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.631+857_631+858ins others(99): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669498 | |||||||
| chr19:48669498 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(19): Show |
99 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.631+858G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669498 | |||||||
| chr19:48669501 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+855G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669501 | |||||||
| chr19:48669502 | CACG | C | 1 | a0001c0001t0001g0002 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+851_631+853del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669502 | |||||||
| chr19:48669504 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(12): Show |
52 | HG01074.hp1 HG01074.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.631+852G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669504 | |||||||
| chr19:48669504 | CGACCAT | C | 3 | a0001c0003t0001g0012 a0001c0003t0001g0040 a0007c0013t0002g0097 |
7 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+846_631+851del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669504 | |||||||
| chr19:48669505 | G | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(46): Show |
182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.631+851C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669505 | |||||||
| chr19:48669507 | C | T | 8 | a0001c0001t0001g0054 a0001c0002t0002g0001 a0001c0002t0002g0030 others(5): Show |
19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+849G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669507 | |||||||
| chr19:48669508 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(10): Show |
41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+848G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669508 | |||||||
| chr19:48669510 | T | A | 3 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0003g0113 |
14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+846A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | |||||||
| chr19:48669510 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(24): Show |
68 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.631+846A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | |||||||
| chr19:48669510 | T | TCATCACC others(142): Show |
1 | a0001c0002t0002g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.631+845_631+846ins others(149): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | |||||||
| chr19:48669510 | TCATCACC others(26): Show |
T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0022 others(9): Show |
42 | HG01074.hp1 HG01074.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.631+813_631+845del others(33): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669510 | |||||||
| chr19:48669513 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0052 others(8): Show |
32 | HG00280.hp2 HG00621.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.631+843A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669513 | |||||||
| chr19:48669513 | TCAC | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(10): Show |
41 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.631+840_631+842del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669513 | |||||||
| chr19:48669513 | TCACCACC others(201): Show |
T | 2 | a0001c0002t0002g0001 a0001c0002t0002g0028 |
9 | HG01123.hp2 HG01257.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.631+635_631+842del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669513 | |||||||
| chr19:48669516 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0077 others(4): Show |
13 | HG01978.hp2 HG01981.hp1 HG03669.hp1 others(10): Show |
intron_variant | MODIFIER | c.631+840G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669516 | |||||||
| chr19:48669519 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0020 others(6): Show |
43 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.631+837G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669519 | |||||||
| chr19:48669522 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0093 a0001c0002t0002g0010 others(2): Show |
16 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+834G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669522 | |||||||
| chr19:48669523 | C | T | 8 | a0001c0001t0001g0003 a0001c0002t0002g0001 a0001c0002t0002g0030 others(5): Show |
19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+833G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669523 | |||||||
| chr19:48669525 | C | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0003t0001g0012 others(1): Show |
8 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+831G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669525 | |||||||
| chr19:48669528 | T | C | 8 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0058 others(5): Show |
12 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.631+828A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669528 | |||||||
| chr19:48669528 | T | TCATCACC others(215): Show |
1 | a0001c0001t0001g0008 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.631+827_631+828ins others(222): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669528 | |||||||
| chr19:48669531 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0020 others(6): Show |
21 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.631+825G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669531 | |||||||
| chr19:48669534 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(16): Show |
50 | HG00280.hp2 HG00408.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.631+822G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669534 | |||||||
| chr19:48669537 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(12): Show |
43 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(40): Show |
intron_variant | MODIFIER | c.631+819G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669537 | |||||||
| chr19:48669540 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(21): Show |
90 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.631+816A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669540 | |||||||
| chr19:48669543 | C | CCACCACC others(134): Show |
1 | a0001c0001t0001g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.631+812_631+813ins others(141): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | |||||||
| chr19:48669543 | C | CCACCACC others(289): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0020 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.631+812_631+813ins others(296): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | |||||||
| chr19:48669543 | C | CCATCACC others(2): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0020 others(4): Show |
41 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.631+812_631+813ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | |||||||
| chr19:48669543 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.631+813G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669543 | |||||||
| chr19:48669544 | C | CACCATCA others(106): Show |
1 | a0001c0001t0001g0011 | 7 | NA18939.hp1 NA18944.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+811_631+812ins others(113): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669544 | |||||||
| chr19:48669544 | C | CATCATCA others(5): Show |
8 | a0001c0001t0001g0003 a0001c0002t0002g0001 a0001c0002t0002g0030 others(5): Show |
19 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.631+811_631+812ins others(12): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669544 | |||||||
| chr19:48669544 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(12): Show |
43 | HG00408.hp1 HG01258.hp1 HG01433.hp2 others(40): Show |
intron_variant | MODIFIER | c.631+812G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669544 | |||||||
| chr19:48669546 | C | CCACCATC others(83): Show |
1 | a0001c0002t0002g0018 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.631+809_631+810ins others(90): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669546 | |||||||
| chr19:48669546 | C | CCACCATC others(44): Show |
1 | a0001c0001t0001g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+809_631+810ins others(51): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669546 | |||||||
| chr19:48669546 | C | T | 1 | a0001c0001t0001g0002 | 4 | HG00280.hp2 HG00741.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.631+810G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669546 | |||||||
| chr19:48669549 | C | CCATCATC others(71): Show |
1 | a0001c0002t0002g0001 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.631+806_631+807ins others(78): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | |||||||
| chr19:48669549 | C | CCATCATC others(32): Show |
1 | a0001c0001t0001g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631+806_631+807ins others(39): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | |||||||
| chr19:48669549 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(21): Show |
73 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.631+807G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | |||||||
| chr19:48669549 | CCACCAT | C | 2 | a0001c0003t0001g0012 a0001c0003t0001g0040 |
6 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.631+801_631+806del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669549 | |||||||
| chr19:48669552 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0093 a0001c0002t0002g0010 others(2): Show |
16 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.631+804G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669552 | |||||||
| chr19:48669555 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0002t0002g0001 others(1): Show |
8 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.631+801A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669555 | |||||||
| chr19:48669555 | TCACCAC | T | 3 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0003g0113 |
14 | HG01243.hp1 HG01884.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.631+795_631+800del others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669555 | |||||||
| chr19:48669558 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(14): Show |
67 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.631+798G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669558 | |||||||
| chr19:48669558 | CCACCACC others(11): Show |
C | 1 | a0001c0015t0001g0046 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.631+780_631+797del others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669558 | |||||||
| chr19:48669565 | C | T | 1 | a0001c0002t0002g0028 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.631+791G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669565 | |||||||
| chr19:48669567 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0031 others(3): Show |
7 | HG01891.hp1 HG01978.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.631+789A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669567 | |||||||
| chr19:48669568 | C | G | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+788G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669568 | |||||||
| chr19:48669570 | C | T | 6 | a0001c0001t0001g0065 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG01978.hp2 HG01981.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.631+786G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669570 | |||||||
| chr19:48669573 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(33): Show |
135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.631+783G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669573 | |||||||
| chr19:48669573 | CCATCACC others(105): Show |
C | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+671_631+782del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669573 | |||||||
| chr19:48669575 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+781T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669575 | |||||||
| chr19:48669576 | T | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(43): Show |
145 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.631+780A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | |||||||
| chr19:48669576 | T | TCACCACC others(2): Show |
9 | a0001c0002t0002g0006 a0001c0002t0002g0007 a0001c0002t0002g0044 others(6): Show |
41 | HG00597.hp2 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.631+771_631+779dup others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | |||||||
| chr19:48669576 | T | TCACCACC others(269): Show |
1 | a0001c0002t0002g0007 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.631+779_631+780ins others(276): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | |||||||
| chr19:48669576 | T | TCACCACC others(86): Show |
1 | a0001c0002t0002g0018 | 2 | HG00544.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.631+779_631+780ins others(93): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | |||||||
| chr19:48669576 | T | TCACCACC others(353): Show |
1 | a0001c0002t0002g0025 | 3 | NA18960.hp1 NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.631+779_631+780ins others(360): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | |||||||
| chr19:48669576 | T | TCACCACC others(386): Show |
1 | a0001c0002t0002g0089 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.631+779_631+780ins others(393): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | |||||||
| chr19:48669576 | T | TCACCATC others(2): Show |
26 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(23): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.631+779_631+780ins others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669576 | |||||||
| chr19:48669582 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+774G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669582 | |||||||
| chr19:48669583 | C | T | 2 | a0001c0001t0001g0069 a0001c0002t0002g0028 |
2 | HG02040.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.631+773G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669583 | |||||||
| chr19:48669585 | C | T | 3 | a0001c0001t0001g0094 a0001c0002t0002g0001 a0001c0002t0002g0109 |
3 | HG00733.hp2 HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.631+771G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669585 | |||||||
| chr19:48669586 | G | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0061 others(14): Show |
29 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.631+770C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669586 | |||||||
| chr19:48669588 | C | T | 2 | a0001c0001t0001g0069 a0001c0002t0002g0028 |
2 | HG02040.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.631+768G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669588 | |||||||
| chr19:48669591 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+765G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669591 | |||||||
| chr19:48669594 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+762A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669594 | |||||||
| chr19:48669597 | CCACCACC others(176): Show |
C | 2 | a0001c0002t0002g0001 a0001c0002t0002g0109 |
2 | HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.631+576_631+758del | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669597 | |||||||
| chr19:48669600 | C | T | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+756G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669600 | |||||||
| chr19:48669603 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+753G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669603 | |||||||
| chr19:48669609 | T | C | 5 | a0001c0001t0001g0093 a0001c0002t0001g0031 a0001c0002t0002g0010 others(2): Show |
17 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.631+747A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669609 | |||||||
| chr19:48669615 | C | T | 2 | a0001c0001t0001g0065 a0001c0002t0001g0031 |
3 | HG01891.hp1 HG02293.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+741G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669615 | |||||||
| chr19:48669618 | C | T | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+738G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669618 | |||||||
| chr19:48669628 | C | T | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+728G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669628 | |||||||
| chr19:48669630 | CCAGT | C | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+722_631+725del others(4): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669630 | |||||||
| chr19:48669632 | AG | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.631+723delC | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669632 | |||||||
| chr19:48669633 | G | A | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+723C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669633 | |||||||
| chr19:48669634 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0031 |
4 | HG01891.hp1 HG06807.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+722A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669634 | |||||||
| chr19:48669644 | CACCACCA others(3): Show |
C | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+702_631+711del others(10): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669644 | |||||||
| chr19:48669646 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.631+710G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669646 | |||||||
| chr19:48669655 | A | C | 2 | a0001c0001t0001g0065 a0001c0004t0001g0014 |
2 | HG02293.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.631+701T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669655 | |||||||
| chr19:48669655 | A | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0031 |
4 | HG01891.hp1 HG06807.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+701T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669655 | |||||||
| chr19:48669661 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+695G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669661 | |||||||
| chr19:48669667 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(10): Show |
58 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.631+689A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669667 | |||||||
| chr19:48669673 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0001g0031 |
4 | HG01891.hp1 HG06807.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+683A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669673 | |||||||
| chr19:48669676 | T | C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
20 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.631+680A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669676 | |||||||
| chr19:48669679 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.631+677G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669679 | |||||||
| chr19:48669680 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+676G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669680 | |||||||
| chr19:48669682 | C | T | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+674G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669682 | |||||||
| chr19:48669688 | CCACCACC others(2): Show |
C | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+659_631+667del others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669688 | |||||||
| chr19:48669691 | C | T | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+665G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669691 | |||||||
| chr19:48669694 | CCAT | C | 19 | a0001c0001t0001g0102 a0001c0001t0002g0104 a0001c0002t0001g0084 others(16): Show |
70 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.631+659_631+661del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669694 | |||||||
| chr19:48669697 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+659A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669697 | |||||||
| chr19:48669706 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0093 others(3): Show |
17 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.631+650A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669706 | |||||||
| chr19:48669710 | C | T | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+646G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669710 | |||||||
| chr19:48669712 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+644G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669712 | |||||||
| chr19:48669715 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02040.hp1 NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+641A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669715 | |||||||
| chr19:48669721 | C | CCACCACC others(11): Show |
3 | a0001c0003t0001g0012 a0001c0003t0001g0040 a0001c0003t0001g0110 |
11 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.631+617_631+634dup others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669721 | |||||||
| chr19:48669721 | C | T | 5 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(2): Show |
16 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.631+635G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669721 | |||||||
| chr19:48669724 | C | CCACCACC others(2): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0070 others(3): Show |
27 | NA18939.hp2 NA18944.hp2 NA18945.hp1 others(24): Show |
intron_variant | MODIFIER | c.631+623_631+631dup others(9): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669724 | |||||||
| chr19:48669724 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02040.hp1 NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+632G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669724 | |||||||
| chr19:48669730 | CCAT | C | 4 | a0001c0001t0001g0093 a0001c0002t0002g0010 a0001c0002t0002g0098 others(1): Show |
15 | HG01243.hp1 HG01884.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.631+623_631+625del others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669730 | |||||||
| chr19:48669733 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | HG02040.hp1 NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+623A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669733 | |||||||
| chr19:48669734 | C | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0093 a0001c0002t0002g0010 others(2): Show |
16 | HG01243.hp1 HG01884.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.631+622G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669734 | |||||||
| chr19:48669742 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+614G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669742 | |||||||
| chr19:48669749 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+607G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669749 | |||||||
| chr19:48669750 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+606T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669750 | |||||||
| chr19:48669751 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+605A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669751 | |||||||
| chr19:48669754 | CCATCGTC others(19): Show |
C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+576_631+601del others(26): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669754 | |||||||
| chr19:48669759 | G | A | 38 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0093 others(35): Show |
115 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.631+597C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669759 | |||||||
| chr19:48669760 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+596A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669760 | |||||||
| chr19:48669767 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+589A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669767 | |||||||
| chr19:48669768 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+588T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669768 | |||||||
| chr19:48669771 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+585T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669771 | |||||||
| chr19:48669772 | TCACCATC others(40): Show |
T | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+537_631+583del others(47): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669772 | |||||||
| chr19:48669776 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.631+580G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669776 | |||||||
| chr19:48669789 | C | T | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+567G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669789 | |||||||
| chr19:48669792 | T | C | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+564A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669792 | |||||||
| chr19:48669795 | C | T | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+561G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669795 | |||||||
| chr19:48669807 | T | C | 2 | a0001c0002t0002g0098 a0007c0013t0002g0097 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+549A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669807 | |||||||
| chr19:48669810 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0078 |
3 | NA18942.hp2 NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.631+546A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669810 | |||||||
| chr19:48669812 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+544T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669812 | |||||||
| chr19:48669816 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+540A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669816 | |||||||
| chr19:48669819 | C | CCACCACC others(47): Show |
1 | a0001c0001t0001g0003 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.631+483_631+536dup others(54): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669819 | |||||||
| chr19:48669819 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+537G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669819 | |||||||
| chr19:48669825 | C | T | 5 | a0001c0001t0001g0042 a0001c0002t0001g0041 a0001c0002t0001g0111 others(2): Show |
8 | HG01070.hp1 HG01071.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.631+531G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669825 | |||||||
| chr19:48669826 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.631+530G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669826 | |||||||
| chr19:48669831 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+525A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669831 | |||||||
| chr19:48669835 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+521G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669835 | |||||||
| chr19:48669836 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+520T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669836 | |||||||
| chr19:48669837 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.631+519A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669837 | |||||||
| chr19:48669840 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.631+516G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669840 | |||||||
| chr19:48669845 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+511T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669845 | |||||||
| chr19:48669846 | C | T | 1 | a0007c0013t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.631+510G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669846 | |||||||
| chr19:48669847 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+509A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669847 | |||||||
| chr19:48669847 | T | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0002t0002g0098 others(1): Show |
4 | HG02615.hp1 HG03139.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+509A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669847 | |||||||
| chr19:48669848 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+508T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669848 | |||||||
| chr19:48669849 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+507G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669849 | |||||||
| chr19:48669849 | C | T | 2 | a0001c0002t0002g0098 a0007c0013t0002g0097 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+507G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669849 | |||||||
| chr19:48669852 | T | C | 2 | a0001c0002t0002g0098 a0007c0013t0002g0097 |
2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.631+504A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669852 | |||||||
| chr19:48669855 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+501G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669855 | |||||||
| chr19:48669858 | CCACCATC others(20): Show |
C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.631+471_631+497del others(27): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669858 | |||||||
| chr19:48669868 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+488G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669868 | |||||||
| chr19:48669869 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+487T>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669869 | |||||||
| chr19:48669870 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+486A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669870 | |||||||
| chr19:48669873 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+483A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669873 | |||||||
| chr19:48669879 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+477G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669879 | |||||||
| chr19:48669880 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+476A>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669880 | |||||||
| chr19:48669881 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+475T>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669881 | |||||||
| chr19:48669891 | T | C | 1 | a0001c0001t0001g0017 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+465A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669891 | |||||||
| chr19:48669891 | T | TCACCAC | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | HG01168.hp2 HG01993.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.631+459_631+464dup others(6): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669891 | |||||||
| chr19:48669897 | C | T | 1 | a0001c0001t0001g0017 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+459G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669897 | |||||||
| chr19:48669900 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0002g0010 others(1): Show |
15 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.631+456G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669900 | |||||||
| chr19:48669903 | T | TCATCACC others(5): Show |
1 | a0001c0001t0001g0017 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+452_631+453ins others(12): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669903 | |||||||
| chr19:48669906 | C | T | 1 | a0001c0001t0001g0017 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+450G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669906 | |||||||
| chr19:48669909 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+447G>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669909 | |||||||
| chr19:48669913 | C | CACCATCA others(14): Show |
1 | a0001c0015t0001g0046 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.631+422_631+442dup others(21): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669913 | |||||||
| chr19:48669918 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+438A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669918 | |||||||
| chr19:48669947 | ACCACCAC others(30): Show |
A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0035 others(10): Show |
58 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.631+372_631+408del others(37): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669947 | |||||||
| chr19:48669952 | CACCATCA others(33): Show |
C | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.631+364_631+403del others(40): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669952 | |||||||
| chr19:48669954 | CCATCACC others(11): Show |
C | 1 | a0001c0001t0001g0003 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.631+384_631+401del others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669954 | |||||||
| chr19:48669960 | C | CCAT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(82): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.631+393_631+395dup others(3): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669960 | |||||||
| chr19:48669963 | T | C | 1 | a0001c0001t0001g0017 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+393A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669963 | |||||||
| chr19:48669966 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.631+390G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669966 | |||||||
| chr19:48669972 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(82): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.631+384A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669972 | |||||||
| chr19:48669972 | T | TCACCATC others(11): Show |
1 | a0001c0001t0001g0017 | 4 | HG00408.hp2 HG02129.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.631+383_631+384ins others(18): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669972 | |||||||
| chr19:48669983 | AT | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(82): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.631+372delA | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669983 | |||||||
| chr19:48669990 | C | CTACCATC others(8): Show |
1 | a0001c0001t0001g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.631+365_631+366ins others(15): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669990 | |||||||
| chr19:48669996 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.631+360A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48669996 | |||||||
| chr19:48670002 | TCACCACC others(8): Show |
T | 1 | a0001c0002t0002g0037 | 2 | HG00558.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.631+339_631+353del others(15): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48670002 | |||||||
| chr19:48670026 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.631+330A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 2/6 | chr19 | 48670026 | |||||||
| chr19:48671017 | G | A | 1 | a0001c0002t0002g0026 | 3 | HG02896.hp2 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-20-11C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671017 | |||||||
| chr19:48671035 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-20-29C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671035 | |||||||
| chr19:48671275 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20-269C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671275 | |||||||
| chr19:48671478 | A | G | 42 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0093 others(39): Show |
141 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-20-472T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671478 | |||||||
| chr19:48671642 | G | A | 1 | a0001c0002t0002g0109 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-20-636C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48671642 | |||||||
| chr19:48672012 | C | T | 5 | a0001c0002t0002g0015 a0001c0002t0002g0095 a0001c0002t0002g0096 others(2): Show |
9 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+920G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672012 | |||||||
| chr19:48672094 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(48): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-21+838G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672094 | |||||||
| chr19:48672151 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0045 |
3 | HG01891.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-21+781G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672151 | |||||||
| chr19:48672353 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-21+579C>T | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672353 | |||||||
| chr19:48672429 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0002g0010 others(1): Show |
15 | HG00733.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21+503G>A | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672429 | |||||||
| chr19:48672496 | A | G | 2 | a0001c0002t0002g0013 a0001c0002t0002g0026 |
9 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+436T>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672496 | |||||||
| chr19:48672642 | CTT | C | 33 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0102 others(30): Show |
118 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-21+288_-21+289del others(2): Show |
NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672642 | |||||||
| chr19:48672707 | G | C | 7 | a0001c0001t0001g0042 a0001c0002t0001g0041 a0001c0002t0001g0111 others(4): Show |
17 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21+225C>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672707 | |||||||
| chr19:48672778 | C | G | 1 | a0001c0002t0002g0044 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-21+154G>C | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672778 | |||||||
| chr19:48672909 | T | C | 1 | a0001c0002t0002g0043 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-21+23A>G | NTN5 | ENSG00000142233.14 | transcript | ENST00000270235.11 | protein_coding | 1/6 | chr19 | 48672909 |