Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2596 |
| ensemblid | ENSG00000172020.13 |
| hgncid | 4140 |
| symbol | GAP43 |
| name | growth associated protein 43 |
| refseq_nuc | NM_002045.4 |
| refseq_prot | NP_002036.1 |
| ensembl_nuc | ENST00000305124.11 |
| ensembl_prot | ENSP00000305010.7 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 115623510 |
| end | 115721483 |
| strand | + |
| ver | v1.2 |
| region | chr3:115623510-115721483 |
| region5000 | chr3:115618510-115726483 |
| regionname0 | GAP43_chr3_115623510_115721483 |
| regionname5000 | GAP43_chr3_115618510_115726483 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 714 | 338 | 84 | 70 | 128 | 10 | 44 | GAP43_chr3_115618510_115726483 | GAP43 | ATGCT others(709): Show |
chr3 | 115618510 | 115726483 | ||
| a0001c0002 | 0/0 | 714 | 14 | 8 | 2 | 4 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ATGCT others(709): Show |
chr3 | 115618510 | 115726483 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1498 | 128 | 52 | 22 | 28 | 5 | 19 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0002 | 0/0 | 1500 | 99 | 5 | 17 | 66 | 2 | 9 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1495): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0003 | 0/0 | 1498 | 43 | 8 | 12 | 6 | 3 | 14 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0004 | 0/0 | 1498 | 31 | 0 | 11 | 20 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0005 | 0/0 | 1499 | 17 | 15 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1494): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0006 | 0/0 | 1501 | 3 | 0 | 0 | 3 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1496): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0007 | 0/0 | 1499 | 3 | 0 | 0 | 2 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1494): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0008 | 0/0 | 1499 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1494): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0009 | 0/0 | 1497 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1492): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0010 | 0/0 | 1498 | 2 | 2 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0011 | 0/0 | 1498 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0012 | 0/0 | 1498 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0013 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1494): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0014 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1495): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0015 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1495): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0016 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1495): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0018 | 0/0 | 1497 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1492): Show |
chr3 | 115618510 | 115726483 |
| a0001c0001t0019 | 0/0 | 1499 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1494): Show |
chr3 | 115618510 | 115726483 |
| a0001c0002t0001 | 0/0 | 1498 | 10 | 5 | 1 | 4 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| a0001c0002t0002 | 0/0 | 1500 | 3 | 2 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1495): Show |
chr3 | 115618510 | 115726483 |
| a0001c0002t0017 | 0/0 | 1498 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | ACAGT others(1493): Show |
chr3 | 115618510 | 115726483 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0044 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0008g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0009g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0010g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0011g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0012g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0014g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0015g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0016g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0018g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0019g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0017g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0197 | EUR | GBR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0243 | EUR | FIN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | FIN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00438 | hp1 | a0001 | c0001 | t0014 | g0253 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0062 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00735 | hp2 | a0001 | c0001 | t0012 | g0301 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0244 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0245 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0344 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0081 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0188 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0079 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0340 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | IBS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0307 | EUR | IBS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0183 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0257 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0308 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0336 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0312 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0242 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0337 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0239 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0238 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0274 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0100 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0193 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0339 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0295 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0283 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0273 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04228 | hp2 | a0001 | c0001 | t0019 | g0017 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CHB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0033 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18962 | hp2 | a0001 | c0001 | t0016 | g0270 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19081 | hp1 | a0001 | c0001 | t0018 | g0331 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | ASW | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | GIH | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02486 | hp2 | a0001 | c0002 | t0017 | g0310 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0219 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA21309 | hp1 | a0001 | c0001 | t0015 | g0155 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0044 | REF | REF | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0087 | REF | REF | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:115676474 | G | A | 1 | a0001c0002 | 14 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(11): Show |
synonymous_variant | LOW | c.492G>A | p.Glu164Glu | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/3 | 672/1498 | 492/717 | 164/238 | chr3 | 115676474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:115623548 | G | C | 1 | a0001c0001t0011 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/3 | 142 | chr3 | 115623548 | ||||||
| chr3:115623556 | G | C | 1 | a0001c0001t0012 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-134G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/3 | 134 | chr3 | 115623556 | ||||||
| chr3:115623673 | C | T | 1 | a0001c0001t0019 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-17C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/3 | 17 | chr3 | 115623673 | ||||||
| chr3:115720905 | A | G | 1 | a0001c0001t0010 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*23A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 23 | chr3 | 115720905 | ||||||
| chr3:115721047 | T | TA | 5 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(2): Show |
24 | HG01069.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*182dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 183 | INFO_REALIGN_3_PRIME | chr3 | 115721047 | |||||
| chr3:115721047 | TA | T | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0018 |
6 | HG01169.hp1 HG01169.hp2 HG03017.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*182delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 182 | INFO_REALIGN_3_PRIME | chr3 | 115721047 | |||||
| chr3:115721071 | A | G | 1 | a0001c0002t0017 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 189 | chr3 | 115721071 | ||||||
| chr3:115721119 | G | A | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*237G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 237 | chr3 | 115721119 | ||||||
| chr3:115721160 | T | G | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(3): Show |
80 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*278T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 278 | chr3 | 115721160 | ||||||
| chr3:115721185 | G | C | 1 | a0001c0001t0016 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 303 | chr3 | 115721185 | ||||||
| chr3:115721227 | C | CCT | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(4): Show |
111 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*362_*363dupCT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 364 | INFO_REALIGN_3_PRIME | chr3 | 115721227 | |||||
| chr3:115721295 | C | T | 1 | a0001c0001t0005 | 17 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*413C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 413 | chr3 | 115721295 | ||||||
| chr3:115721324 | C | T | 1 | a0001c0001t0004 | 31 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*442C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 442 | chr3 | 115721324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:115623781 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0005g0007 others(2): Show |
5 | HG01433.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+62G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115623781 | |||||||
| chr3:115623929 | G | A | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.30+210G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115623929 | |||||||
| chr3:115623963 | AT | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(14): Show |
17 | HG01255.hp2 HG01261.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.30+255delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115623963 | ||||||
| chr3:115624098 | CA | C | 279 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(276): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.30+385delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624098 | ||||||
| chr3:115624201 | A | C | 1 | a0001c0001t0002g0347 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.30+482A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624201 | |||||||
| chr3:115624300 | AT | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
14 | HG01255.hp2 HG01975.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.30+595delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624300 | ||||||
| chr3:115624300 | ATT | A | 146 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(143): Show |
148 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.30+594_30+595delTT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624300 | ||||||
| chr3:115624300 | ATTT | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(120): Show |
125 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.30+593_30+595delTT others(1): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624300 | ||||||
| chr3:115624366 | A | G | 272 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(269): Show |
276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.30+647A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624366 | |||||||
| chr3:115624443 | G | C | 3 | a0001c0001t0001g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 |
3 | HG00558.hp2 NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.30+724G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624443 | |||||||
| chr3:115624548 | A | G | 36 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0207 others(33): Show |
36 | HG00609.hp1 HG00609.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.30+829A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624548 | |||||||
| chr3:115624853 | G | T | 1 | a0001c0001t0002g0205 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.30+1134G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624853 | |||||||
| chr3:115625051 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0213 others(8): Show |
11 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+1332G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625051 | |||||||
| chr3:115625132 | G | C | 1 | a0001c0001t0002g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.30+1413G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625132 | |||||||
| chr3:115625206 | C | CATAA | 94 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0026 others(91): Show |
96 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.30+1508_30+1511dup others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | ||||||
| chr3:115625206 | C | CATAAATA others(1): Show |
44 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(41): Show |
44 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.30+1504_30+1511dup others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | ||||||
| chr3:115625206 | C | CATAAATA others(5): Show |
16 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0040 others(13): Show |
16 | HG01261.hp1 HG01517.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+1500_30+1511dup others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | ||||||
| chr3:115625206 | C | CATAAATA others(13): Show |
4 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(1): Show |
4 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+1492_30+1511dup others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | ||||||
| chr3:115625250 | T | C | 8 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+1531T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625250 | |||||||
| chr3:115625272 | T | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0026 others(104): Show |
109 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.30+1553T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625272 | |||||||
| chr3:115625361 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+1642C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625361 | |||||||
| chr3:115625494 | A | G | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+1775A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625494 | |||||||
| chr3:115625596 | C | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(1): Show |
4 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+1877C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625596 | |||||||
| chr3:115625663 | A | G | 1 | a0001c0001t0004g0305 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.30+1944A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625663 | |||||||
| chr3:115625761 | G | T | 1 | a0001c0001t0001g0346 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.30+2042G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625761 | |||||||
| chr3:115625840 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+2121T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625840 | |||||||
| chr3:115626093 | C | T | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+2374C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626093 | |||||||
| chr3:115626140 | C | T | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0002g0217 others(1): Show |
4 | HG01975.hp1 HG02004.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+2421C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626140 | |||||||
| chr3:115626202 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.30+2483T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626202 | |||||||
| chr3:115626219 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0228 others(8): Show |
11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+2500C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626219 | |||||||
| chr3:115626478 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+2759G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626478 | |||||||
| chr3:115626481 | T | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0228 others(8): Show |
11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+2762T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626481 | |||||||
| chr3:115626553 | T | C | 1 | a0001c0002t0002g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+2834T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626553 | |||||||
| chr3:115626610 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.30+2891G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626610 | |||||||
| chr3:115626710 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+2991G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626710 | |||||||
| chr3:115626721 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.30+3002G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626721 | |||||||
| chr3:115626817 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+3098C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626817 | |||||||
| chr3:115627045 | T | C | 3 | a0001c0001t0001g0309 a0001c0001t0005g0339 a0001c0001t0005g0340 |
3 | HG01361.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.30+3326T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627045 | |||||||
| chr3:115627105 | T | G | 1 | a0001c0001t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.30+3386T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627105 | |||||||
| chr3:115627122 | CTTTTTTC others(5): Show |
C | 4 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(1): Show |
4 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+3410_30+3421del others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627122 | ||||||
| chr3:115627133 | CT | C | 190 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0035 others(187): Show |
192 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.30+3430delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627133 | ||||||
| chr3:115627133 | CTT | C | 131 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(128): Show |
134 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.30+3429_30+3430del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627133 | ||||||
| chr3:115627133 | CTTT | C | 13 | a0001c0001t0001g0068 a0001c0001t0001g0090 a0001c0001t0001g0091 others(10): Show |
13 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+3428_30+3430del others(3): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627133 | ||||||
| chr3:115627286 | CAG | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0304 a0001c0001t0002g0303 others(3): Show |
6 | HG02280.hp1 HG02451.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+3570_30+3571del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627286 | ||||||
| chr3:115627349 | T | C | 2 | a0001c0001t0001g0209 a0001c0002t0001g0039 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.30+3630T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627349 | |||||||
| chr3:115627571 | T | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(77): Show |
81 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.30+3852T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627571 | |||||||
| chr3:115627646 | A | G | 6 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(3): Show |
6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+3927A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627646 | |||||||
| chr3:115627901 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.30+4182T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627901 | |||||||
| chr3:115627987 | C | A | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+4268C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627987 | |||||||
| chr3:115627989 | A | C | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+4270A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627989 | |||||||
| chr3:115628002 | A | G | 2 | a0001c0001t0001g0302 a0001c0001t0001g0304 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+4283A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628002 | |||||||
| chr3:115628018 | T | G | 4 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4299T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628018 | |||||||
| chr3:115628028 | A | C | 6 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(3): Show |
6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4309A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628028 | |||||||
| chr3:115628029 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+4310T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628029 | |||||||
| chr3:115628237 | C | T | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+4518C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628237 | |||||||
| chr3:115628302 | T | C | 90 | a0001c0001t0001g0028 a0001c0001t0001g0040 a0001c0001t0001g0041 others(87): Show |
92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.30+4583T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628302 | |||||||
| chr3:115628337 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.30+4618C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628337 | |||||||
| chr3:115628367 | T | C | 6 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(3): Show |
6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4648T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628367 | |||||||
| chr3:115628382 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+4663C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628382 | |||||||
| chr3:115628709 | G | T | 79 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0069 others(76): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.30+4990G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628709 | |||||||
| chr3:115628745 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+5026A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628745 | |||||||
| chr3:115628778 | A | G | 1 | a0001c0001t0002g0330 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.30+5059A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628778 | |||||||
| chr3:115628793 | C | G | 6 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(3): Show |
6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5074C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628793 | |||||||
| chr3:115628829 | A | G | 74 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(71): Show |
75 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.30+5110A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628829 | |||||||
| chr3:115628972 | G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+5253G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628972 | |||||||
| chr3:115629104 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+5385C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629104 | |||||||
| chr3:115629162 | T | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0228 others(8): Show |
11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+5443T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629162 | |||||||
| chr3:115629323 | T | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0228 others(14): Show |
17 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.30+5604T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629323 | |||||||
| chr3:115629408 | C | CT | 135 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(132): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.30+5703dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115629408 | ||||||
| chr3:115629408 | C | CTT | 10 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+5702_30+5703dup others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115629408 | ||||||
| chr3:115629540 | G | C | 1 | a0001c0001t0003g0312 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.30+5821G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629540 | |||||||
| chr3:115629691 | G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+5972G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629691 | |||||||
| chr3:115629862 | A | T | 2 | a0001c0001t0001g0203 a0001c0001t0002g0202 |
2 | NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.30+6143A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629862 | |||||||
| chr3:115629959 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0228 others(8): Show |
11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+6240G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629959 | |||||||
| chr3:115630067 | C | G | 11 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0213 others(8): Show |
11 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+6348C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630067 | |||||||
| chr3:115630309 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0002g0211 |
2 | HG00558.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.30+6590G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630309 | |||||||
| chr3:115630309 | G | C | 50 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0045 others(47): Show |
51 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+6590G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630309 | |||||||
| chr3:115630417 | A | G | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0002g0236 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+6698A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630417 | |||||||
| chr3:115630479 | T | G | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0002g0236 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+6760T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630479 | |||||||
| chr3:115630543 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0213 a0001c0001t0002g0022 |
3 | NA18939.hp1 NA18943.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.30+6824C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630543 | |||||||
| chr3:115630621 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0002g0303 a0001c0001t0005g0007 others(2): Show |
5 | HG02280.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+6902G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630621 | |||||||
| chr3:115630949 | A | G | 316 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(313): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.30+7230A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630949 | |||||||
| chr3:115630995 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0234 |
3 | HG02109.hp2 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+7276A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630995 | |||||||
| chr3:115631084 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0223 a0001c0001t0001g0224 others(4): Show |
7 | HG01433.hp1 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.30+7365T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631084 | |||||||
| chr3:115631156 | A | C | 1 | a0001c0001t0003g0295 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.30+7437A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631156 | |||||||
| chr3:115631279 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.30+7560C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631279 | |||||||
| chr3:115631335 | G | T | 1 | a0001c0001t0004g0329 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30+7616G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631335 | |||||||
| chr3:115631359 | G | A | 68 | a0001c0001t0001g0098 a0001c0001t0001g0108 a0001c0001t0001g0114 others(65): Show |
70 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.30+7640G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631359 | |||||||
| chr3:115631400 | T | G | 42 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(39): Show |
42 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.30+7681T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631400 | |||||||
| chr3:115631435 | G | C | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+7716G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631435 | |||||||
| chr3:115631516 | A | G | 2 | a0001c0001t0004g0160 a0001c0001t0004g0161 |
2 | NA18968.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.30+7797A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631516 | |||||||
| chr3:115631826 | G | A | 4 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0003g0206 others(1): Show |
4 | NA18975.hp2 NA18986.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+8107G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631826 | |||||||
| chr3:115632661 | G | A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0213 others(9): Show |
12 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+8942G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632661 | |||||||
| chr3:115632954 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.30+9235G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632954 | |||||||
| chr3:115632969 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.30+9250G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632969 | |||||||
| chr3:115632977 | A | G | 5 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(2): Show |
5 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9258A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632977 | |||||||
| chr3:115633002 | T | G | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9283T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633002 | |||||||
| chr3:115633023 | AG | A | 80 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0068 others(77): Show |
82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.30+9305delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633023 | |||||||
| chr3:115633024 | G | A | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+9305G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633024 | |||||||
| chr3:115633037 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0002g0303 a0001c0001t0005g0007 others(2): Show |
5 | HG02280.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9318G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633037 | |||||||
| chr3:115633037 | G | C | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+9318G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633037 | |||||||
| chr3:115633128 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0002g0303 a0001c0001t0005g0007 others(2): Show |
5 | HG02280.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9409C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633128 | |||||||
| chr3:115633132 | A | G | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+9413A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633132 | |||||||
| chr3:115633242 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9523G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633242 | |||||||
| chr3:115633338 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9619A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633338 | |||||||
| chr3:115633480 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+9761G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633480 | |||||||
| chr3:115633511 | G | A | 4 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0003g0206 others(1): Show |
4 | NA18975.hp2 NA18986.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9792G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633511 | |||||||
| chr3:115633591 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+9872C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633591 | |||||||
| chr3:115633625 | C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+9906C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633625 | |||||||
| chr3:115634071 | C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+10352C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634071 | |||||||
| chr3:115634185 | T | C | 87 | a0001c0001t0001g0028 a0001c0001t0001g0040 a0001c0001t0001g0041 others(84): Show |
89 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.30+10466T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634185 | |||||||
| chr3:115634500 | A | C | 7 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0005g0336 others(4): Show |
7 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+10781A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634500 | |||||||
| chr3:115634567 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
2 | HG01261.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+10848C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634567 | |||||||
| chr3:115634663 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.30+10944T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634663 | |||||||
| chr3:115634668 | G | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+10949G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634668 | |||||||
| chr3:115634693 | C | T | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+10974C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634693 | |||||||
| chr3:115634723 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+11004T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634723 | |||||||
| chr3:115634770 | AAAATAAA others(1): Show |
A | 4 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+11070_30+11077d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115634770 | ||||||
| chr3:115634826 | C | T | 12 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0213 others(9): Show |
12 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+11107C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634826 | |||||||
| chr3:115634916 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.30+11197T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634916 | |||||||
| chr3:115634972 | A | G | 125 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0035 others(122): Show |
127 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.30+11253A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634972 | |||||||
| chr3:115635062 | T | C | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+11343T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635062 | |||||||
| chr3:115635358 | A | T | 41 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0186 others(38): Show |
41 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+11639A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635358 | |||||||
| chr3:115635392 | A | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0234 a0001c0001t0005g0100 others(3): Show |
6 | HG01433.hp1 HG02109.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+11673A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635392 | |||||||
| chr3:115635408 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.30+11689C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635408 | |||||||
| chr3:115635440 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.30+11721A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635440 | |||||||
| chr3:115635701 | C | G | 3 | a0001c0001t0003g0156 a0001c0001t0003g0157 a0001c0001t0003g0158 |
3 | HG00642.hp2 HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.30+11982C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635701 | |||||||
| chr3:115635703 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.30+11984G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635703 | |||||||
| chr3:115635761 | A | C | 2 | a0001c0001t0002g0292 a0001c0001t0002g0293 |
2 | HG03704.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.30+12042A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635761 | |||||||
| chr3:115635864 | T | C | 5 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+12145T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635864 | |||||||
| chr3:115635933 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12214G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635933 | |||||||
| chr3:115635948 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.30+12229C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635948 | |||||||
| chr3:115635968 | C | G | 1 | a0001c0001t0003g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.30+12249C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635968 | |||||||
| chr3:115635988 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+12269C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635988 | |||||||
| chr3:115636099 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0015g0155 |
2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.30+12380C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636099 | |||||||
| chr3:115636282 | T | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12563T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636282 | |||||||
| chr3:115636358 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12639T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636358 | |||||||
| chr3:115636369 | T | G | 1 | a0001c0001t0005g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+12650T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636369 | |||||||
| chr3:115636414 | A | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12695A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636414 | |||||||
| chr3:115636571 | T | G | 196 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(193): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.30+12852T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636571 | |||||||
| chr3:115636682 | G | A | 2 | a0001c0001t0004g0250 a0001c0001t0004g0251 |
2 | HG00673.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.30+12963G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636682 | |||||||
| chr3:115636739 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+13020G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636739 | |||||||
| chr3:115637031 | T | C | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.30+13312T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637031 | |||||||
| chr3:115637114 | A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+13395A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637114 | |||||||
| chr3:115637117 | A | G | 44 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0051 others(41): Show |
45 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.30+13398A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637117 | |||||||
| chr3:115637126 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0002g0152 |
2 | NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.30+13407C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637126 | |||||||
| chr3:115637160 | A | T | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG01074.hp2 HG01099.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13441A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637160 | |||||||
| chr3:115637162 | A | C | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+13443A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637162 | |||||||
| chr3:115637329 | C | G | 49 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.30+13610C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637329 | |||||||
| chr3:115637755 | C | T | 2 | a0001c0001t0003g0287 a0001c0001t0004g0286 |
2 | NA18970.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.30+14036C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637755 | |||||||
| chr3:115637813 | T | C | 22 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0116 others(19): Show |
22 | HG00408.hp2 HG00621.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.30+14094T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637813 | |||||||
| chr3:115638167 | G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+14448G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638167 | |||||||
| chr3:115638511 | CT | C | 124 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0021 others(121): Show |
126 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+14806delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115638511 | ||||||
| chr3:115638559 | T | A | 2 | a0001c0001t0005g0172 a0001c0001t0005g0233 |
2 | HG02895.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.30+14840T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638559 | |||||||
| chr3:115638773 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+15054C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638773 | |||||||
| chr3:115638851 | A | G | 2 | a0001c0001t0001g0298 a0001c0001t0005g0299 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.30+15132A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638851 | |||||||
| chr3:115638958 | G | A | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+15239G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638958 | |||||||
| chr3:115638995 | T | A | 2 | a0001c0001t0001g0019 a0001c0001t0003g0020 |
2 | HG01261.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+15276T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638995 | |||||||
| chr3:115639004 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.30+15285A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639004 | |||||||
| chr3:115639308 | G | A | 180 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(177): Show |
183 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.30+15589G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639308 | |||||||
| chr3:115639326 | G | A | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+15607G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639326 | |||||||
| chr3:115639376 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.30+15657C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639376 | |||||||
| chr3:115639471 | C | T | 1 | a0001c0001t0002g0285 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.30+15752C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639471 | |||||||
| chr3:115639511 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.30+15792G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639511 | |||||||
| chr3:115639600 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+15881T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639600 | |||||||
| chr3:115639820 | A | T | 1 | a0001c0001t0001g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.30+16101A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639820 | |||||||
| chr3:115639977 | A | C | 141 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0032 others(138): Show |
143 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.30+16258A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639977 | |||||||
| chr3:115640034 | T | G | 1 | a0001c0002t0002g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+16315T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640034 | |||||||
| chr3:115640263 | T | G | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.30+16544T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640263 | |||||||
| chr3:115640418 | C | T | 43 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.30+16699C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640418 | |||||||
| chr3:115640534 | G | T | 9 | a0001c0001t0001g0309 a0001c0001t0001g0342 a0001c0001t0001g0343 others(6): Show |
9 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+16815G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640534 | |||||||
| chr3:115640586 | C | T | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.30+16867C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640586 | |||||||
| chr3:115640708 | G | C | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG00733.hp1 HG00735.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.30+16989G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640708 | |||||||
| chr3:115640759 | G | T | 4 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0003g0206 others(1): Show |
4 | NA18975.hp2 NA18986.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+17040G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640759 | |||||||
| chr3:115640880 | G | A | 1 | a0001c0001t0005g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.30+17161G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640880 | |||||||
| chr3:115640925 | C | CT | 92 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0063 others(89): Show |
94 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.30+17213dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115640925 | ||||||
| chr3:115640925 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.30+17206C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640925 | |||||||
| chr3:115640965 | C | CCCTT | 95 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0063 others(92): Show |
97 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.30+17260_30+17263d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115640965 | ||||||
| chr3:115641035 | T | C | 91 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0063 others(88): Show |
93 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.30+17316T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641035 | |||||||
| chr3:115641036 | T | C | 1 | a0001c0001t0015g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17317T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641036 | |||||||
| chr3:115641036 | TC | T | 91 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0063 others(88): Show |
93 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.30+17318delC | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641036 | |||||||
| chr3:115641037 | C | T | 1 | a0001c0001t0015g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17318C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641037 | |||||||
| chr3:115641130 | G | A | 85 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0064 others(82): Show |
87 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.30+17411G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641130 | |||||||
| chr3:115641241 | A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+17522A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641241 | |||||||
| chr3:115641332 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0302 a0001c0001t0001g0304 others(3): Show |
6 | HG02451.hp2 HG03195.hp1 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+17613G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641332 | |||||||
| chr3:115641345 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0092 a0001c0001t0001g0093 others(37): Show |
40 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.30+17626C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641345 | |||||||
| chr3:115641365 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.30+17646C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641365 | |||||||
| chr3:115641382 | TTG | T | 3 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0346 |
3 | HG01891.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.30+17677_30+17678d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641382 | ||||||
| chr3:115641401 | C | A | 2 | a0001c0001t0002g0255 a0001c0002t0001g0004 |
3 | NA18939.hp2 NA18999.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.30+17682C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641401 | |||||||
| chr3:115641450 | T | G | 1 | a0001c0001t0002g0200 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.30+17731T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641450 | |||||||
| chr3:115641452 | T | G | 105 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0042 others(102): Show |
106 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.30+17733T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641452 | |||||||
| chr3:115641454 | T | G | 238 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(235): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.30+17735T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641454 | |||||||
| chr3:115641456 | G | T | 2 | a0001c0001t0002g0313 a0001c0001t0002g0314 |
2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.30+17737G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641456 | |||||||
| chr3:115641510 | T | TCA | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0210 others(5): Show |
8 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+17823_30+17824d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641510 | T | TCACACAC others(1): Show |
18 | a0001c0001t0001g0083 a0001c0001t0001g0095 a0001c0001t0001g0096 others(15): Show |
18 | HG01106.hp1 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.30+17817_30+17824d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641510 | T | TCACACAC others(3): Show |
52 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0076 others(49): Show |
55 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.30+17815_30+17824d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641510 | T | TCACACAC others(5): Show |
45 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(42): Show |
45 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.30+17813_30+17824d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641510 | T | TCACACAC others(7): Show |
13 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0123 others(10): Show |
13 | HG00642.hp1 HG00642.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+17811_30+17824d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641510 | T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+17809_30+17824d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641510 | T | TCACACAC others(11): Show |
1 | a0001c0001t0001g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.30+17807_30+17824d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641510 | T | TCACACAC others(15): Show |
1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.30+17803_30+17824d others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | ||||||
| chr3:115641539 | C | CACACACA others(3): Show |
2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641539 | ||||||
| chr3:115641543 | C | CACACACA others(9): Show |
3 | a0001c0001t0003g0020 a0001c0001t0008g0244 a0001c0001t0008g0245 |
3 | HG01069.hp2 HG01081.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CACACACA others(7): Show |
2 | a0001c0001t0002g0246 a0001c0001t0002g0333 |
2 | HG01192.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CACACACA others(5): Show |
24 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0054 others(21): Show |
24 | HG00738.hp1 HG00741.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CACACACA others(3): Show |
3 | a0001c0001t0001g0207 a0001c0001t0002g0208 a0001c0001t0005g0233 |
3 | HG03017.hp2 HG03516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CACACACA others(1): Show |
5 | a0001c0001t0001g0061 a0001c0001t0001g0328 a0001c0001t0002g0316 others(2): Show |
5 | HG00609.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CACACAGA others(3): Show |
16 | a0001c0001t0001g0175 a0001c0001t0001g0335 a0001c0001t0001g0338 others(13): Show |
16 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CACACAT | 35 | a0001c0001t0001g0006 a0001c0001t0001g0092 a0001c0001t0001g0093 others(32): Show |
35 | HG00609.hp1 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CACAGACA others(1): Show |
28 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(25): Show |
28 | HG00140.hp1 HG00140.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CAGACAT | 5 | a0001c0001t0001g0174 a0001c0001t0001g0198 a0001c0001t0001g0241 others(2): Show |
5 | HG00280.hp1 HG01934.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641543 | C | CAT | 11 | a0001c0001t0001g0309 a0001c0001t0001g0342 a0001c0001t0001g0343 others(8): Show |
11 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | |||||||
| chr3:115641555 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+17836G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641555 | |||||||
| chr3:115641582 | A | C | 51 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+17863A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641582 | |||||||
| chr3:115641753 | G | A | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+18034G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641753 | |||||||
| chr3:115641861 | C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+18142C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641861 | |||||||
| chr3:115641981 | A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+18262A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641981 | |||||||
| chr3:115642160 | A | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0002g0217 |
3 | HG01975.hp1 HG02004.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.30+18441A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642160 | |||||||
| chr3:115642289 | C | G | 6 | a0001c0001t0001g0332 a0001c0001t0002g0148 a0001c0001t0002g0149 others(3): Show |
6 | NA18970.hp2 NA19000.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+18570C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642289 | |||||||
| chr3:115642304 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.30+18585A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642304 | |||||||
| chr3:115642406 | A | AT | 54 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(51): Show |
54 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.30+18702dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115642406 | ||||||
| chr3:115642406 | AT | A | 7 | a0001c0001t0001g0263 a0001c0001t0001g0304 a0001c0001t0002g0179 others(4): Show |
7 | HG01069.hp1 HG01069.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+18702delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115642406 | ||||||
| chr3:115642482 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.30+18763G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642482 | |||||||
| chr3:115642703 | A | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0185 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.30+18984A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642703 | |||||||
| chr3:115642773 | A | C | 50 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.30+19054A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642773 | |||||||
| chr3:115642890 | A | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(54): Show |
57 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+19171A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642890 | |||||||
| chr3:115642989 | G | A | 343 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(340): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.30+19270G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642989 | |||||||
| chr3:115643031 | T | C | 1 | a0001c0001t0003g0031 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.30+19312T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643031 | |||||||
| chr3:115643170 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0304 a0001c0001t0005g0007 others(2): Show |
5 | HG02451.hp2 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+19451T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643170 | |||||||
| chr3:115643179 | C | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+19460C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643179 | |||||||
| chr3:115643514 | A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+19795A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643514 | |||||||
| chr3:115643534 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0054 |
2 | HG00741.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.30+19815C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643534 | |||||||
| chr3:115643586 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+19867T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643586 | |||||||
| chr3:115643689 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00609.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.30+19970C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643689 | |||||||
| chr3:115643690 | A | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.30+19971A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643690 | |||||||
| chr3:115643706 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+19987C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643706 | |||||||
| chr3:115643752 | C | G | 50 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.30+20033C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643752 | |||||||
| chr3:115643770 | A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+20051A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643770 | |||||||
| chr3:115643774 | A | C | 50 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.30+20055A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643774 | |||||||
| chr3:115643800 | C | T | 123 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(120): Show |
126 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+20081C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643800 | |||||||
| chr3:115644190 | T | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0092 others(44): Show |
47 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.30+20471T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644190 | |||||||
| chr3:115644561 | A | G | 44 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.30+20842A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644561 | |||||||
| chr3:115644668 | C | A | 1 | a0001c0001t0002g0264 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.30+20949C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644668 | |||||||
| chr3:115644722 | C | T | 36 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0051 others(33): Show |
37 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.30+21003C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644722 | |||||||
| chr3:115644824 | A | C | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.30+21105A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644824 | |||||||
| chr3:115645189 | G | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0092 others(31): Show |
34 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.30+21470G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645189 | |||||||
| chr3:115645209 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+21490T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645209 | |||||||
| chr3:115645297 | T | C | 46 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0092 others(43): Show |
46 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(43): Show |
intron_variant | MODIFIER | c.30+21578T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645297 | |||||||
| chr3:115645366 | T | C | 1 | a0001c0001t0002g0317 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.30+21647T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645366 | |||||||
| chr3:115645611 | GA | G | 171 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(168): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.30+21900delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115645611 | ||||||
| chr3:115645980 | G | A | 36 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0051 others(33): Show |
37 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.30+22261G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645980 | |||||||
| chr3:115646165 | A | G | 49 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.30+22446A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646165 | |||||||
| chr3:115646189 | T | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(54): Show |
57 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+22470T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646189 | |||||||
| chr3:115646437 | T | C | 1 | a0001c0001t0005g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.30+22718T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646437 | |||||||
| chr3:115646608 | A | C | 13 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(10): Show |
13 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+22889A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646608 | |||||||
| chr3:115646646 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0237 others(1): Show |
4 | HG00735.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+22927C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646646 | |||||||
| chr3:115646780 | G | T | 1 | a0001c0001t0003g0312 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.30+23061G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646780 | |||||||
| chr3:115646798 | G | A | 81 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0064 others(78): Show |
83 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.30+23079G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646798 | |||||||
| chr3:115646812 | A | C | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.30+23093A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646812 | |||||||
| chr3:115647136 | T | C | 340 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(337): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.30+23417T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647136 | |||||||
| chr3:115647174 | G | A | 41 | a0001c0001t0001g0006 a0001c0001t0001g0092 a0001c0001t0001g0093 others(38): Show |
41 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+23455G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647174 | |||||||
| chr3:115647180 | CCTTG | C | 230 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(227): Show |
233 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.30+23466_30+23469d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647180 | ||||||
| chr3:115647221 | C | T | 7 | a0001c0001t0001g0174 a0001c0001t0001g0194 a0001c0001t0001g0198 others(4): Show |
7 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+23502C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647221 | |||||||
| chr3:115647503 | C | T | 37 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0051 others(34): Show |
38 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.30+23784C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647503 | |||||||
| chr3:115647517 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+23798C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647517 | |||||||
| chr3:115647739 | A | C | 43 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.30+24020A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647739 | |||||||
| chr3:115647754 | A | AAAAC | 7 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG01934.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+24039_30+24042d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647754 | ||||||
| chr3:115647754 | A | C | 1 | a0001c0001t0001g0045 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.30+24035A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647754 | |||||||
| chr3:115647758 | C | A | 1 | a0001c0001t0019g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.30+24039C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647758 | |||||||
| chr3:115647758 | C | CA | 58 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0032 others(55): Show |
58 | HG00280.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+24051dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647758 | ||||||
| chr3:115647758 | C | CAA | 87 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0064 others(84): Show |
89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.30+24050_30+24051d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647758 | ||||||
| chr3:115647758 | C | CAAA | 30 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0042 others(27): Show |
31 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+24049_30+24051d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647758 | ||||||
| chr3:115647759 | A | AAAC | 49 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.30+24042_30+24043i others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647759 | ||||||
| chr3:115647925 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.30+24206T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647925 | |||||||
| chr3:115648102 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+24383T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648102 | |||||||
| chr3:115648119 | C | T | 175 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(172): Show |
178 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.30+24400C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648119 | |||||||
| chr3:115648139 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0304 a0001c0001t0005g0007 others(2): Show |
5 | HG02451.hp2 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+24420T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648139 | |||||||
| chr3:115648168 | G | C | 3 | a0001c0001t0002g0256 a0001c0001t0003g0267 a0001c0001t0004g0257 |
3 | HG01952.hp2 HG02300.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.30+24449G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648168 | |||||||
| chr3:115648274 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+24555G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648274 | |||||||
| chr3:115648287 | A | G | 58 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(55): Show |
58 | HG00609.hp1 HG00609.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+24568A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648287 | |||||||
| chr3:115648367 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+24648A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648367 | |||||||
| chr3:115648370 | T | C | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+24651T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648370 | |||||||
| chr3:115648382 | C | T | 1 | a0001c0001t0005g0339 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+24663C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648382 | |||||||
| chr3:115648731 | A | G | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+25012A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648731 | |||||||
| chr3:115648755 | G | A | 174 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(171): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.30+25036G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648755 | |||||||
| chr3:115648936 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.30+25217A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648936 | |||||||
| chr3:115648954 | T | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(54): Show |
57 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+25235T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648954 | |||||||
| chr3:115649143 | T | C | 185 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(182): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.30+25424T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649143 | |||||||
| chr3:115649221 | T | G | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+25502T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649221 | |||||||
| chr3:115649297 | C | G | 9 | a0001c0001t0001g0309 a0001c0001t0001g0342 a0001c0001t0001g0343 others(6): Show |
9 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+25578C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649297 | |||||||
| chr3:115649359 | C | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+25640C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649359 | |||||||
| chr3:115649822 | A | AAAAAG | 156 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0032 others(153): Show |
158 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.30+26106_30+26107i others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115649822 | ||||||
| chr3:115649822 | A | AAAAG | 96 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0045 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.30+26119_30+26122d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115649822 | ||||||
| chr3:115650221 | T | G | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-25792T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650221 | |||||||
| chr3:115650256 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-25757A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650256 | |||||||
| chr3:115650289 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.31-25724C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650289 | |||||||
| chr3:115650324 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.31-25689G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650324 | |||||||
| chr3:115650351 | A | C | 1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31-25662A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650351 | |||||||
| chr3:115650386 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.31-25627G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650386 | |||||||
| chr3:115650731 | TTTTTAAA others(14): Show |
T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-25256_31-25236d others(23): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115650731 | ||||||
| chr3:115650782 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-25231C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650782 | |||||||
| chr3:115650834 | G | A | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | NA18982.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.31-25179G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650834 | |||||||
| chr3:115650859 | T | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0342 a0001c0001t0001g0343 others(5): Show |
8 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-25154T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650859 | |||||||
| chr3:115650893 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-25120C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650893 | |||||||
| chr3:115650907 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0005g0100 a0001c0001t0005g0101 others(1): Show |
4 | HG01433.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-25106T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650907 | |||||||
| chr3:115650945 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0311 a0001c0001t0003g0024 others(3): Show |
6 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-25068C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650945 | |||||||
| chr3:115651413 | A | T | 4 | a0001c0001t0002g0145 a0001c0001t0002g0199 a0001c0001t0004g0003 others(1): Show |
5 | HG01358.hp2 HG01496.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-24600A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115651413 | |||||||
| chr3:115651768 | G | T | 1 | a0001c0001t0003g0082 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.31-24245G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115651768 | |||||||
| chr3:115651771 | G | T | 1 | a0001c0001t0002g0303 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.31-24242G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115651771 | |||||||
| chr3:115652050 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.31-23963A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652050 | |||||||
| chr3:115652233 | G | T | 140 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(137): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.31-23780G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652233 | |||||||
| chr3:115652356 | C | CT | 29 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0153 others(26): Show |
29 | HG01106.hp1 HG01257.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-23628dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | C | CTT | 68 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0040 others(65): Show |
69 | HG00280.hp1 HG00544.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.31-23629_31-23628d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | C | CTTT | 54 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0054 others(51): Show |
54 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-23630_31-23628d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | C | CTTTT | 18 | a0001c0001t0001g0192 a0001c0001t0001g0203 a0001c0001t0002g0144 others(15): Show |
18 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-23631_31-23628d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CT | C | 60 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0045 others(57): Show |
61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.31-23628delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CTT | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0168 a0001c0001t0001g0169 others(6): Show |
10 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23629_31-23628d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CTTT | C | 12 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0170 others(9): Show |
12 | HG01106.hp2 HG01496.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-23630_31-23628d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0309 others(3): Show |
6 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-23635_31-23628d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.31-23638_31-23628d others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0338 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.31-23641_31-23628d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0137 a0001c0001t0001g0296 a0001c0001t0001g0335 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-23642_31-23628d others(17): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652356 | CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0162 |
2 | HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.31-23646_31-23628d others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | ||||||
| chr3:115652386 | G | T | 9 | a0001c0001t0001g0023 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
9 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-23627G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652386 | |||||||
| chr3:115652388 | G | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0103 others(7): Show |
10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23625G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652388 | |||||||
| chr3:115652389 | A | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0103 others(7): Show |
10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23624A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652389 | |||||||
| chr3:115652391 | A | T | 10 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0103 others(7): Show |
10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23622A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652391 | |||||||
| chr3:115652413 | T | C | 110 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(107): Show |
111 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.31-23600T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652413 | |||||||
| chr3:115652565 | T | C | 109 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(106): Show |
110 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.31-23448T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652565 | |||||||
| chr3:115652584 | T | C | 261 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(258): Show |
263 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.31-23429T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652584 | |||||||
| chr3:115652585 | G | A | 47 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0092 others(44): Show |
47 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-23428G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652585 | |||||||
| chr3:115652636 | C | G | 112 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(109): Show |
113 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.31-23377C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652636 | |||||||
| chr3:115652686 | G | T | 262 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(259): Show |
264 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.31-23327G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652686 | |||||||
| chr3:115652722 | C | T | 32 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(29): Show |
33 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.31-23291C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652722 | |||||||
| chr3:115652773 | T | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-23240T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652773 | |||||||
| chr3:115652836 | C | T | 12 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0091 others(9): Show |
12 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-23177C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652836 | |||||||
| chr3:115653167 | C | T | 1 | a0001c0001t0016g0270 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.31-22846C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653167 | |||||||
| chr3:115653313 | A | G | 257 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(254): Show |
259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.31-22700A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653313 | |||||||
| chr3:115653319 | G | A | 10 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0103 others(7): Show |
10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-22694G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653319 | |||||||
| chr3:115653328 | C | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0023 others(133): Show |
137 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.31-22685C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653328 | |||||||
| chr3:115653329 | C | T | 84 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0054 others(81): Show |
85 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.31-22684C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653329 | |||||||
| chr3:115653427 | G | A | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-22586G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653427 | |||||||
| chr3:115653576 | C | T | 1 | a0001c0001t0005g0009 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.31-22437C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653576 | |||||||
| chr3:115653607 | T | A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0309 others(3): Show |
6 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-22406T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653607 | |||||||
| chr3:115653674 | C | T | 24 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0069 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-22339C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653674 | |||||||
| chr3:115653805 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.31-22208T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653805 | |||||||
| chr3:115653943 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0198 |
2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.31-22070C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653943 | |||||||
| chr3:115654476 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.31-21537T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654476 | |||||||
| chr3:115654480 | A | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0235 a0001c0001t0001g0260 others(4): Show |
7 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-21533A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654480 | |||||||
| chr3:115654588 | C | T | 50 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0077 others(47): Show |
50 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-21425C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654588 | |||||||
| chr3:115654743 | A | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA18747.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.31-21270A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654743 | |||||||
| chr3:115654882 | C | G | 265 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(262): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.31-21131C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654882 | |||||||
| chr3:115654948 | A | G | 88 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0054 others(85): Show |
89 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.31-21065A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654948 | |||||||
| chr3:115655238 | T | G | 2 | a0001c0001t0003g0024 a0001c0001t0003g0025 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.31-20775T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655238 | |||||||
| chr3:115655260 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-20753G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655260 | |||||||
| chr3:115655525 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.31-20488C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655525 | |||||||
| chr3:115655704 | A | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0091 others(13): Show |
16 | HG01106.hp2 HG01884.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-20309A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655704 | |||||||
| chr3:115655741 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.31-20272A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655741 | |||||||
| chr3:115655819 | A | C | 2 | a0001c0001t0002g0272 a0001c0001t0003g0005 |
3 | NA18995.hp1 NA19002.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.31-20194A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655819 | |||||||
| chr3:115655850 | G | C | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-20163G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655850 | |||||||
| chr3:115655950 | C | G | 1 | a0001c0001t0001g0263 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.31-20063C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655950 | |||||||
| chr3:115656028 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.31-19985C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656028 | |||||||
| chr3:115656231 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.31-19782T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656231 | |||||||
| chr3:115656252 | C | A | 2 | a0001c0001t0002g0313 a0001c0001t0002g0314 |
2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.31-19761C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656252 | |||||||
| chr3:115656393 | A | G | 23 | a0001c0001t0001g0026 a0001c0001t0001g0076 a0001c0001t0001g0089 others(20): Show |
23 | HG01106.hp2 HG01109.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-19620A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656393 | |||||||
| chr3:115656788 | C | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-19225C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656788 | |||||||
| chr3:115656848 | A | T | 1 | a0001c0001t0004g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.31-19165A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656848 | |||||||
| chr3:115656852 | G | A | 2 | a0001c0001t0005g0007 a0001c0002t0001g0010 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-19161G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656852 | |||||||
| chr3:115656909 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.31-19104C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656909 | |||||||
| chr3:115656922 | T | C | 1 | a0001c0001t0005g0340 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.31-19091T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656922 | |||||||
| chr3:115657035 | G | C | 31 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(28): Show |
32 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-18978G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657035 | |||||||
| chr3:115657125 | T | C | 84 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0054 others(81): Show |
85 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.31-18888T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657125 | |||||||
| chr3:115657199 | G | T | 16 | a0001c0001t0001g0059 a0001c0001t0001g0108 a0001c0001t0001g0241 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-18814G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657199 | |||||||
| chr3:115657263 | G | A | 108 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(105): Show |
109 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-18750G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657263 | |||||||
| chr3:115657347 | T | C | 27 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0040 others(24): Show |
27 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-18666T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657347 | |||||||
| chr3:115657363 | G | C | 8 | a0001c0001t0001g0061 a0001c0001t0001g0289 a0001c0001t0001g0290 others(5): Show |
8 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-18650G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657363 | |||||||
| chr3:115657445 | A | G | 7 | a0001c0001t0001g0296 a0001c0001t0001g0335 a0001c0001t0001g0338 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-18568A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657445 | |||||||
| chr3:115657465 | C | A | 1 | a0001c0001t0002g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31-18548C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657465 | |||||||
| chr3:115657476 | A | AT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01081.hp2 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-18531dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115657476 | ||||||
| chr3:115657502 | C | T | 82 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0054 others(79): Show |
83 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.31-18511C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657502 | |||||||
| chr3:115657590 | G | A | 51 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0064 others(48): Show |
51 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.31-18423G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657590 | |||||||
| chr3:115657703 | G | A | 23 | a0001c0001t0001g0026 a0001c0001t0001g0076 a0001c0001t0001g0089 others(20): Show |
23 | HG01106.hp2 HG01109.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-18310G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657703 | |||||||
| chr3:115657834 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0260 a0001c0001t0001g0328 |
3 | HG02717.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.31-18179A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657834 | |||||||
| chr3:115657838 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-18175G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657838 | |||||||
| chr3:115657844 | C | T | 2 | a0001c0001t0005g0007 a0001c0002t0001g0010 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-18169C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657844 | |||||||
| chr3:115658022 | G | C | 243 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(240): Show |
245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.31-17991G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658022 | |||||||
| chr3:115658187 | A | G | 243 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(240): Show |
245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.31-17826A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658187 | |||||||
| chr3:115658280 | G | A | 107 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0035 others(104): Show |
108 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.31-17733G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658280 | |||||||
| chr3:115658305 | C | T | 1 | a0001c0001t0001g0346 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-17708C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658305 | |||||||
| chr3:115658407 | C | A | 237 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(234): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.31-17606C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658407 | |||||||
| chr3:115658535 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0003g0070 |
2 | HG01993.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.31-17478C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658535 | |||||||
| chr3:115658697 | G | A | 8 | a0001c0001t0001g0296 a0001c0001t0001g0335 a0001c0001t0001g0338 others(5): Show |
8 | HG00544.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-17316G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658697 | |||||||
| chr3:115658968 | G | C | 9 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0266 others(6): Show |
9 | HG01109.hp1 HG01361.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-17045G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658968 | |||||||
| chr3:115659005 | G | A | 86 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0054 others(83): Show |
87 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.31-17008G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659005 | |||||||
| chr3:115659010 | T | C | 79 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(76): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.31-17003T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659010 | |||||||
| chr3:115659103 | C | G | 2 | a0001c0001t0001g0054 a0001c0001t0003g0070 |
2 | HG01993.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.31-16910C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659103 | |||||||
| chr3:115659270 | T | C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(33): Show |
37 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.31-16743T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659270 | |||||||
| chr3:115659345 | C | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-16668C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659345 | |||||||
| chr3:115659618 | TAGAG | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(31): Show |
35 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.31-16387_31-16384d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115659618 | ||||||
| chr3:115659623 | A | G | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-16390A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659623 | |||||||
| chr3:115659770 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0068 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.31-16243G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659770 | |||||||
| chr3:115659846 | A | C | 1 | a0001c0001t0005g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-16167A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659846 | |||||||
| chr3:115659900 | C | G | 1 | a0001c0002t0001g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.31-16113C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659900 | |||||||
| chr3:115659914 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0003g0070 |
2 | HG01993.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.31-16099A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659914 | |||||||
| chr3:115660109 | G | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-15904G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660109 | |||||||
| chr3:115660536 | A | G | 14 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
14 | HG01106.hp2 HG01884.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-15477A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660536 | |||||||
| chr3:115660555 | T | A | 17 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0069 others(14): Show |
17 | HG01081.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-15458T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660555 | |||||||
| chr3:115660893 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-15120A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660893 | |||||||
| chr3:115661088 | C | A | 1 | a0001c0001t0002g0227 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.31-14925C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661088 | |||||||
| chr3:115661124 | T | TA | 8 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0170 others(5): Show |
8 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-14879dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661124 | ||||||
| chr3:115661134 | ACT | A | 21 | a0001c0001t0001g0209 a0001c0001t0001g0302 a0001c0001t0001g0320 others(18): Show |
22 | HG00609.hp2 HG01106.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-14878_31-14877d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661134 | |||||||
| chr3:115661248 | A | G | 25 | a0001c0001t0001g0023 a0001c0001t0001g0209 a0001c0001t0001g0302 others(22): Show |
26 | HG00609.hp2 HG01106.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.31-14765A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661248 | |||||||
| chr3:115661258 | C | T | 284 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(281): Show |
287 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.31-14755C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661258 | |||||||
| chr3:115661422 | G | A | 1 | a0001c0001t0003g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.31-14591G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661422 | |||||||
| chr3:115661512 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-14501G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661512 | |||||||
| chr3:115661527 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0002g0164 |
2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.31-14486C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661527 | |||||||
| chr3:115661539 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.31-14474A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661539 | |||||||
| chr3:115661673 | A | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(14): Show |
17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-14340A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661673 | |||||||
| chr3:115661710 | G | A | 49 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0077 others(46): Show |
49 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.31-14303G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661710 | |||||||
| chr3:115661778 | G | A | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-14235G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661778 | |||||||
| chr3:115661802 | C | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0309 others(3): Show |
6 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-14211C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661802 | |||||||
| chr3:115661812 | G | A | 1 | a0001c0001t0002g0324 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.31-14201G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661812 | |||||||
| chr3:115661831 | C | CTTTTTTT others(3): Show |
33 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(30): Show |
34 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.31-14177_31-14168d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(4): Show |
49 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0064 others(46): Show |
49 | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.31-14178_31-14168d others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(5): Show |
44 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0069 others(41): Show |
45 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.31-14179_31-14168d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(6): Show |
74 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(71): Show |
75 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.31-14180_31-14168d others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(7): Show |
33 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0085 others(30): Show |
33 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-14181_31-14168d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(8): Show |
15 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0076 others(12): Show |
15 | HG00735.hp2 HG01109.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-14168_31-14167i others(17): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.31-14168_31-14167i others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(15): Show |
3 | a0001c0001t0001g0235 a0001c0001t0001g0342 a0001c0001t0002g0236 |
3 | HG01891.hp2 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-14168_31-14167i others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(16): Show |
8 | a0001c0001t0001g0006 a0001c0001t0001g0174 a0001c0001t0001g0198 others(5): Show |
8 | HG01433.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-14168_31-14167i others(25): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(17): Show |
7 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG02109.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-14168_31-14167i others(26): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115661831 | C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0094 a0001c0001t0005g0015 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.31-14168_31-14167i others(27): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | ||||||
| chr3:115662016 | G | A | 4 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-13997G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662016 | |||||||
| chr3:115662043 | G | T | 264 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(261): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.31-13970G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662043 | |||||||
| chr3:115662057 | G | C | 264 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(261): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.31-13956G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662057 | |||||||
| chr3:115662085 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.31-13928G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662085 | |||||||
| chr3:115662123 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.31-13890T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662123 | |||||||
| chr3:115662185 | G | A | 269 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(266): Show |
272 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.31-13828G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662185 | |||||||
| chr3:115662462 | G | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(31): Show |
35 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.31-13551G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662462 | |||||||
| chr3:115662579 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-13434C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662579 | |||||||
| chr3:115662692 | T | A | 1 | a0001c0001t0003g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.31-13321T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662692 | |||||||
| chr3:115662955 | G | A | 13 | a0001c0001t0001g0302 a0001c0001t0002g0199 a0001c0001t0004g0003 others(10): Show |
15 | HG01106.hp1 HG01496.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-13058G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662955 | |||||||
| chr3:115663116 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.31-12897C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663116 | |||||||
| chr3:115663188 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.31-12825C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663188 | |||||||
| chr3:115663252 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0002g0138 |
2 | NA18951.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.31-12761G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663252 | |||||||
| chr3:115663274 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0054 others(77): Show |
80 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.31-12739G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663274 | |||||||
| chr3:115663449 | G | T | 12 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0090 others(9): Show |
12 | HG02683.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-12564G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663449 | |||||||
| chr3:115663627 | G | A | 1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31-12386G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663627 | |||||||
| chr3:115663734 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-12279A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663734 | |||||||
| chr3:115663790 | C | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0304 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-12223C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663790 | |||||||
| chr3:115663808 | C | T | 21 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0302 others(18): Show |
23 | HG01106.hp1 HG01496.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.31-12205C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663808 | |||||||
| chr3:115663938 | C | T | 1 | a0001c0001t0004g0250 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.31-12075C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663938 | |||||||
| chr3:115663963 | C | A | 1 | a0001c0001t0003g0005 | 2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.31-12050C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663963 | |||||||
| chr3:115663975 | C | G | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-12038C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663975 | |||||||
| chr3:115663997 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-12016G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663997 | |||||||
| chr3:115664061 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.31-11952G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664061 | |||||||
| chr3:115664067 | AT | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-11944delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664067 | ||||||
| chr3:115664204 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.31-11809T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664204 | |||||||
| chr3:115664221 | AG | A | 71 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0076 others(68): Show |
72 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.31-11789delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664221 | ||||||
| chr3:115664230 | T | TATGTCAT others(328): Show |
11 | a0001c0001t0002g0126 a0001c0001t0002g0195 a0001c0001t0002g0202 others(8): Show |
11 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(337): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(328): Show |
1 | a0001c0001t0001g0269 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.31-11769_31-11768i others(337): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(329): Show |
1 | a0001c0001t0001g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.31-11769_31-11768i others(338): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(329): Show |
29 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0077 others(26): Show |
29 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(338): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(330): Show |
1 | a0001c0001t0004g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.31-11769_31-11768i others(339): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(330): Show |
16 | a0001c0001t0001g0322 a0001c0001t0002g0200 a0001c0001t0002g0261 others(13): Show |
16 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(339): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(330): Show |
1 | a0001c0001t0002g0204 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31-11769_31-11768i others(339): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(331): Show |
4 | a0001c0001t0002g0112 a0001c0001t0003g0013 a0001c0001t0003g0240 others(1): Show |
4 | HG01884.hp2 HG02738.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(340): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664230 | T | TATGTCAT others(332): Show |
2 | a0001c0001t0004g0160 a0001c0001t0004g0161 |
2 | NA18968.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.31-11769_31-11768i others(341): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | ||||||
| chr3:115664378 | A | G | 2 | a0001c0001t0001g0343 a0001c0001t0005g0007 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-11635A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664378 | |||||||
| chr3:115664532 | G | A | 2 | a0001c0001t0001g0343 a0001c0001t0005g0007 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-11481G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664532 | |||||||
| chr3:115665188 | T | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0054 others(74): Show |
77 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.31-10825T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665188 | |||||||
| chr3:115665251 | C | A | 1 | a0001c0001t0003g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.31-10762C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665251 | |||||||
| chr3:115665254 | C | G | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-10759C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665254 | |||||||
| chr3:115665507 | G | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(17): Show |
20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-10506G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665507 | |||||||
| chr3:115665512 | G | A | 1 | a0001c0001t0002g0276 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.31-10501G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665512 | |||||||
| chr3:115665568 | C | T | 31 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(28): Show |
31 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.31-10445C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665568 | |||||||
| chr3:115665686 | G | A | 5 | a0001c0001t0001g0174 a0001c0001t0001g0198 a0001c0001t0001g0334 others(2): Show |
5 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-10327G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665686 | |||||||
| chr3:115665733 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.31-10280A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665733 | |||||||
| chr3:115665852 | T | C | 1 | a0001c0001t0003g0308 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.31-10161T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665852 | |||||||
| chr3:115665989 | A | AGT | 9 | a0001c0001t0001g0116 a0001c0001t0001g0311 a0001c0001t0002g0171 others(6): Show |
9 | HG02257.hp2 HG04199.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-9982_31-9981dup others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | A | AGTGT | 5 | a0001c0001t0001g0019 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG01261.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9984_31-9981dup others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | A | AGTTT | 5 | a0001c0001t0001g0221 a0001c0001t0003g0273 a0001c0002t0001g0010 others(2): Show |
5 | HG02486.hp2 HG02630.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | A | AGTTTGT | 11 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0002g0199 others(8): Show |
13 | HG01106.hp1 HG01496.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | A | AGTTTGTG others(1): Show |
6 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(3): Show |
6 | HG02280.hp2 HG02622.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | A | AGTTTGTG others(9): Show |
2 | a0001c0001t0001g0234 a0001c0001t0001g0304 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-10022_31-10021i others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | AGT | A | 25 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0041 others(22): Show |
25 | HG00738.hp1 HG01071.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.31-9982_31-9981del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | AGTGT | A | 166 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0028 others(163): Show |
168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.31-9984_31-9981del others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | AGTGTGT | A | 56 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(53): Show |
57 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.31-9986_31-9981del others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | AGTGTGTG others(1): Show |
A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0002g0204 others(3): Show |
6 | HG00673.hp1 HG02257.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-9988_31-9981del others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0002g0165 a0001c0001t0009g0188 |
2 | HG01169.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.31-9990_31-9981del others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665989 | AGTGTGTG others(9): Show |
A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(8): Show |
11 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-9996_31-9981del others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | ||||||
| chr3:115665990 | G | GTT | 5 | a0001c0001t0001g0173 a0001c0001t0001g0249 a0001c0001t0002g0119 others(2): Show |
5 | HG02895.hp2 HG02896.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665990 | ||||||
| chr3:115665992 | G | T | 9 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
9 | HG01884.hp1 HG02683.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-10021G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665992 | |||||||
| chr3:115665994 | G | T | 14 | a0001c0001t0001g0053 a0001c0001t0001g0114 a0001c0001t0001g0168 others(11): Show |
14 | HG01175.hp1 HG02074.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-10019G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665994 | |||||||
| chr3:115665996 | G | T | 146 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0028 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.31-10017G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665996 | |||||||
| chr3:115665998 | G | T | 56 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(53): Show |
57 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.31-10015G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665998 | |||||||
| chr3:115666000 | G | T | 4 | a0001c0001t0002g0204 a0001c0001t0002g0272 a0001c0001t0003g0206 others(1): Show |
4 | HG00673.hp1 NA18986.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-10013G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666000 | |||||||
| chr3:115666002 | G | T | 1 | a0001c0001t0002g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.31-10011G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666002 | |||||||
| chr3:115666003 | T | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.31-10010T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666003 | |||||||
| chr3:115666008 | G | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0095 others(8): Show |
11 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-10005G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666008 | |||||||
| chr3:115666168 | CAGTT | C | 8 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0309 others(5): Show |
8 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-9844_31-9841del others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666168 | |||||||
| chr3:115666404 | C | T | 2 | a0001c0001t0001g0343 a0001c0001t0005g0007 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-9609C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666404 | |||||||
| chr3:115666465 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.31-9548C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666465 | |||||||
| chr3:115666472 | C | G | 9 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-9541C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666472 | |||||||
| chr3:115666486 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.31-9527G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666486 | |||||||
| chr3:115666622 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-9391A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666622 | |||||||
| chr3:115666731 | A | G | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.31-9282A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666731 | |||||||
| chr3:115666743 | G | A | 1 | a0001c0001t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.31-9270G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666743 | |||||||
| chr3:115666835 | A | G | 221 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(218): Show |
224 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.31-9178A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666835 | |||||||
| chr3:115666852 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-9161C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666852 | |||||||
| chr3:115666867 | T | C | 2 | a0001c0001t0002g0313 a0001c0001t0002g0314 |
2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.31-9146T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666867 | |||||||
| chr3:115666991 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-9022G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666991 | |||||||
| chr3:115667031 | C | T | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-8982C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667031 | |||||||
| chr3:115667117 | C | G | 73 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0076 others(70): Show |
74 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.31-8896C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667117 | |||||||
| chr3:115667128 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.31-8885A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667128 | |||||||
| chr3:115667139 | G | C | 1 | a0001c0001t0009g0188 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.31-8874G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667139 | |||||||
| chr3:115667186 | T | C | 2 | a0001c0001t0001g0343 a0001c0001t0005g0007 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-8827T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667186 | |||||||
| chr3:115667199 | G | T | 1 | a0001c0001t0003g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31-8814G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667199 | |||||||
| chr3:115667317 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0304 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-8696G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667317 | |||||||
| chr3:115667724 | G | T | 85 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0053 others(82): Show |
85 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.31-8289G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667724 | |||||||
| chr3:115667763 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-8250A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667763 | |||||||
| chr3:115667777 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-8236G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667777 | |||||||
| chr3:115667816 | A | T | 2 | a0001c0001t0001g0343 a0001c0001t0005g0007 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-8197A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667816 | |||||||
| chr3:115668013 | G | A | 55 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(52): Show |
56 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.31-8000G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668013 | |||||||
| chr3:115668163 | T | C | 180 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0032 others(177): Show |
184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.31-7850T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668163 | |||||||
| chr3:115668240 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.31-7773G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668240 | |||||||
| chr3:115668278 | T | G | 2 | a0001c0001t0001g0234 a0001c0001t0001g0304 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-7735T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668278 | |||||||
| chr3:115668725 | C | T | 210 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(207): Show |
213 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.31-7288C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668725 | |||||||
| chr3:115669044 | TA | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(18): Show |
21 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-6956delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669044 | ||||||
| chr3:115669069 | T | TAC | 93 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(90): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.31-6922_31-6921dup others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669069 | ||||||
| chr3:115669069 | T | TACAC | 21 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(18): Show |
21 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-6924_31-6921dup others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669069 | ||||||
| chr3:115669104 | T | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0090 others(7): Show |
10 | HG02683.hp2 HG02886.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-6909T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669104 | |||||||
| chr3:115669151 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-6862T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669151 | |||||||
| chr3:115669480 | G | A | 1 | a0001c0001t0002g0107 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-6533G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669480 | |||||||
| chr3:115669497 | A | C | 1 | a0001c0002t0002g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.31-6516A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669497 | |||||||
| chr3:115669551 | T | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-6462T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669551 | |||||||
| chr3:115669711 | G | A | 12 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0090 others(9): Show |
12 | HG02683.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-6302G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669711 | |||||||
| chr3:115669869 | G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-6144G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669869 | |||||||
| chr3:115669873 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-6140C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669873 | |||||||
| chr3:115669912 | A | G | 2 | a0001c0001t0003g0287 a0001c0001t0004g0286 |
2 | NA18970.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.31-6101A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669912 | |||||||
| chr3:115669922 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0266 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-6091T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669922 | |||||||
| chr3:115669932 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.31-6081C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669932 | |||||||
| chr3:115669965 | A | AT | 3 | a0001c0001t0001g0322 a0001c0001t0003g0013 a0001c0001t0003g0240 |
3 | HG01496.hp2 HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.31-6043dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669965 | ||||||
| chr3:115669969 | TTA | T | 7 | a0001c0001t0001g0137 a0001c0001t0002g0112 a0001c0001t0002g0138 others(4): Show |
7 | HG01169.hp1 NA18951.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-6042_31-6041del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669969 | ||||||
| chr3:115669970 | TA | T | 53 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(50): Show |
53 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.31-6042delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669970 | |||||||
| chr3:115669971 | A | T | 5 | a0001c0001t0001g0322 a0001c0001t0003g0013 a0001c0001t0003g0189 others(2): Show |
5 | HG01496.hp2 HG01884.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-6042A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669971 | |||||||
| chr3:115669971 | AT | A | 12 | a0001c0001t0001g0026 a0001c0001t0001g0167 a0001c0001t0001g0173 others(9): Show |
12 | HG01081.hp2 HG01943.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-6030delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669971 | ||||||
| chr3:115669973 | TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0005g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-6017_31-6006del others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669973 | ||||||
| chr3:115669977 | T | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0304 a0001c0001t0005g0015 others(1): Show |
4 | HG01361.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-6036T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669977 | |||||||
| chr3:115669982 | TTA | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(17): Show |
20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-6030_31-6029del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669982 | |||||||
| chr3:115669983 | T | A | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-6030T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669983 | |||||||
| chr3:115669985 | A | AT | 9 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0002g0171 others(6): Show |
9 | HG02451.hp1 HG02630.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-6018dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669985 | ||||||
| chr3:115669985 | A | T | 1 | a0001c0001t0002g0120 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.31-6028A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669985 | |||||||
| chr3:115669986 | T | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(17): Show |
20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-6027T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669986 | |||||||
| chr3:115669995 | T | A | 8 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0091 others(5): Show |
8 | HG02683.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-6018T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669995 | |||||||
| chr3:115669997 | A | AT | 175 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0035 others(172): Show |
178 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.31-6005dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669997 | ||||||
| chr3:115669997 | A | T | 8 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0091 others(5): Show |
8 | HG02683.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-6016A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669997 | |||||||
| chr3:115670013 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-6000T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670013 | |||||||
| chr3:115670072 | TG | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(17): Show |
20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-5940delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670072 | |||||||
| chr3:115670085 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.31-5928C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670085 | |||||||
| chr3:115670101 | G | A | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.31-5912G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670101 | |||||||
| chr3:115670144 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-5869C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670144 | |||||||
| chr3:115670274 | A | G | 2 | a0001c0001t0003g0287 a0001c0001t0004g0286 |
2 | NA18970.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.31-5739A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670274 | |||||||
| chr3:115670294 | A | G | 2 | a0001c0001t0002g0265 a0001c0001t0007g0274 |
2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.31-5719A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670294 | |||||||
| chr3:115670362 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0046 others(19): Show |
22 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.31-5651T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670362 | |||||||
| chr3:115670437 | A | T | 1 | a0001c0001t0003g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.31-5576A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670437 | |||||||
| chr3:115670510 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.31-5503C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670510 | |||||||
| chr3:115670539 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.31-5474G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670539 | |||||||
| chr3:115670707 | G | A | 213 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(210): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.31-5306G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670707 | |||||||
| chr3:115670720 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.31-5293T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670720 | |||||||
| chr3:115670842 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0304 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-5171G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670842 | |||||||
| chr3:115670949 | G | A | 128 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0026 others(125): Show |
131 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.31-5064G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670949 | |||||||
| chr3:115670972 | T | C | 19 | a0001c0001t0001g0263 a0001c0001t0001g0332 a0001c0001t0002g0109 others(16): Show |
20 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-5041T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670972 | |||||||
| chr3:115671002 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5011T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671002 | |||||||
| chr3:115671284 | C | T | 274 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(271): Show |
278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.31-4729C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671284 | |||||||
| chr3:115671450 | G | A | 1 | a0001c0001t0005g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-4563G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671450 | |||||||
| chr3:115671989 | G | A | 2 | a0001c0001t0001g0343 a0001c0001t0005g0007 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-4024G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671989 | |||||||
| chr3:115672020 | G | C | 1 | a0001c0001t0002g0124 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.31-3993G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672020 | |||||||
| chr3:115672048 | C | G | 272 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(269): Show |
276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.31-3965C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672048 | |||||||
| chr3:115672389 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-3624T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672389 | |||||||
| chr3:115672732 | C | CCCTCT | 25 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0053 others(22): Show |
25 | HG00558.hp1 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.31-3247_31-3243dup others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | C | CCCTCTCC others(3): Show |
96 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0028 others(93): Show |
98 | HG00280.hp1 HG00408.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.31-3252_31-3243dup others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | C | CCCTCTCC others(8): Show |
101 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0047 others(98): Show |
102 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.31-3257_31-3243dup others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | C | CCCTCTCC others(13): Show |
46 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0071 others(43): Show |
47 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-3262_31-3243dup others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | C | CCCTCTCC others(18): Show |
9 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0194 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-3267_31-3243dup others(25): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | C | CCCTCTCC others(23): Show |
3 | a0001c0001t0001g0006 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG01433.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.31-3272_31-3243dup others(30): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | C | CCCTCTCC others(28): Show |
1 | a0001c0001t0001g0315 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.31-3277_31-3243dup others(35): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | C | CCTCTCCT others(12): Show |
1 | a0001c0001t0002g0122 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.31-3280_31-3279ins others(19): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672732 | CCCTCTCC others(3): Show |
C | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.31-3252_31-3243del others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | ||||||
| chr3:115672761 | CTCCTCTC others(3): Show |
C | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.31-3247_31-3238del others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672761 | ||||||
| chr3:115672771 | T | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-3242T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672771 | |||||||
| chr3:115672784 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.31-3229A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672784 | |||||||
| chr3:115672794 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-3219G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672794 | |||||||
| chr3:115672845 | T | C | 9 | a0001c0001t0001g0069 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
9 | HG02683.hp2 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-3168T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672845 | |||||||
| chr3:115672899 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-3114C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672899 | |||||||
| chr3:115672942 | C | T | 1 | a0001c0001t0004g0281 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.31-3071C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672942 | |||||||
| chr3:115673167 | G | A | 11 | a0001c0001t0001g0054 a0001c0001t0002g0248 a0001c0001t0003g0070 others(8): Show |
11 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-2846G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673167 | |||||||
| chr3:115673184 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-2829C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673184 | |||||||
| chr3:115673253 | G | A | 62 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0108 others(59): Show |
63 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.31-2760G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673253 | |||||||
| chr3:115673317 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.31-2696C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673317 | |||||||
| chr3:115673475 | A | G | 1 | a0001c0001t0005g0007 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.31-2538A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673475 | |||||||
| chr3:115673616 | T | A | 66 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(63): Show |
66 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.31-2397T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673616 | |||||||
| chr3:115673617 | C | T | 66 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 others(63): Show |
66 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.31-2396C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673617 | |||||||
| chr3:115673712 | T | A | 148 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0054 others(145): Show |
149 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.31-2301T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673712 | |||||||
| chr3:115673720 | C | T | 3 | a0001c0001t0002g0163 a0001c0001t0004g0251 a0001c0001t0004g0281 |
3 | HG00673.hp2 NA18985.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.31-2293C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673720 | |||||||
| chr3:115673833 | C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-2180C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673833 | |||||||
| chr3:115673916 | G | A | 262 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(259): Show |
266 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.31-2097G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673916 | |||||||
| chr3:115674009 | C | T | 6 | a0001c0001t0002g0142 a0001c0001t0002g0148 a0001c0001t0002g0149 others(3): Show |
6 | HG00558.hp2 NA18970.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2004C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674009 | |||||||
| chr3:115674031 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-1982C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674031 | |||||||
| chr3:115674170 | G | C | 154 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0054 others(151): Show |
155 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.31-1843G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674170 | |||||||
| chr3:115674286 | A | G | 7 | a0001c0001t0002g0145 a0001c0001t0002g0179 a0001c0001t0002g0185 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-1727A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674286 | |||||||
| chr3:115674390 | C | T | 104 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0032 others(101): Show |
107 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.31-1623C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674390 | |||||||
| chr3:115674391 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0054 others(74): Show |
77 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.31-1622C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674391 | |||||||
| chr3:115674445 | T | C | 3 | a0001c0002t0001g0099 a0001c0002t0001g0102 a0001c0002t0001g0284 |
3 | HG03579.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.31-1568T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674445 | |||||||
| chr3:115674489 | G | A | 73 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(70): Show |
76 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.31-1524G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674489 | |||||||
| chr3:115674496 | T | G | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.31-1517T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674496 | |||||||
| chr3:115674585 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-1428A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674585 | |||||||
| chr3:115674624 | A | T | 283 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(280): Show |
287 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.31-1389A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674624 | |||||||
| chr3:115674685 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.31-1328G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674685 | |||||||
| chr3:115674779 | T | C | 83 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0037 others(80): Show |
86 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.31-1234T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674779 | |||||||
| chr3:115674939 | C | T | 1 | a0001c0001t0002g0136 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.31-1074C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674939 | |||||||
| chr3:115675027 | A | G | 285 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(282): Show |
289 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.31-986A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675027 | |||||||
| chr3:115675162 | C | T | 5 | a0001c0001t0002g0199 a0001c0001t0004g0003 a0001c0001t0004g0181 others(2): Show |
7 | HG01496.hp1 HG01943.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-851C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675162 | |||||||
| chr3:115675291 | C | T | 32 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0055 others(29): Show |
32 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-722C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675291 | |||||||
| chr3:115675355 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-658C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675355 | |||||||
| chr3:115675412 | G | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0304 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-601G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675412 | |||||||
| chr3:115675446 | C | T | 199 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0026 others(196): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.31-567C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675446 | |||||||
| chr3:115675463 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-550T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675463 | |||||||
| chr3:115675536 | C | T | 123 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0026 others(120): Show |
126 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.31-477C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675536 | |||||||
| chr3:115675589 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-424C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675589 | |||||||
| chr3:115675716 | G | C | 115 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0028 others(112): Show |
118 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.31-297G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675716 | |||||||
| chr3:115675758 | C | CA | 43 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0056 others(40): Show |
44 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.31-225dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | ||||||
| chr3:115675758 | C | CAA | 11 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
11 | HG00609.hp2 HG00741.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-226_31-225dupAA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | ||||||
| chr3:115675758 | CA | C | 47 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0032 others(44): Show |
47 | HG00673.hp2 HG01106.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-225delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | ||||||
| chr3:115675758 | CAA | C | 128 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0045 others(125): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.31-226_31-225delAA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | ||||||
| chr3:115675758 | CAAA | C | 78 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0054 others(75): Show |
78 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.31-227_31-225delAA others(1): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | ||||||
| chr3:115675758 | CAAAA | C | 10 | a0001c0001t0001g0053 a0001c0001t0001g0104 a0001c0001t0001g0223 others(7): Show |
10 | HG00621.hp1 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-228_31-225delAA others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | ||||||
| chr3:115675758 | CAAAAAAA | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-231_31-225delAA others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | ||||||
| chr3:115675858 | T | C | 295 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(292): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.31-155T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675858 | |||||||
| chr3:115676700 | G | C | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+90G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676700 | |||||||
| chr3:115676799 | CCA | C | 17 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0302 others(14): Show |
18 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+190_628+191del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676799 | |||||||
| chr3:115676871 | C | T | 24 | a0001c0001t0001g0046 a0001c0001t0001g0073 a0001c0001t0001g0074 others(21): Show |
24 | HG01106.hp2 HG01891.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.628+261C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676871 | |||||||
| chr3:115676973 | T | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0072 others(18): Show |
21 | HG01081.hp2 HG01433.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.628+363T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676973 | |||||||
| chr3:115677154 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.628+544C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677154 | |||||||
| chr3:115677335 | C | T | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+725C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677335 | |||||||
| chr3:115677404 | T | G | 318 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(315): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.628+794T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677404 | |||||||
| chr3:115677422 | A | C | 100 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0032 others(97): Show |
102 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.628+812A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677422 | |||||||
| chr3:115677508 | C | T | 1 | a0001c0001t0004g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.628+898C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677508 | |||||||
| chr3:115677625 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+1015A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677625 | |||||||
| chr3:115677681 | T | C | 27 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0073 others(24): Show |
27 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.628+1071T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677681 | |||||||
| chr3:115677734 | C | T | 73 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0059 others(70): Show |
74 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.628+1124C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677734 | |||||||
| chr3:115677747 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.628+1137C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677747 | |||||||
| chr3:115677781 | A | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0002t0001g0102 |
3 | HG03516.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.628+1171A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677781 | |||||||
| chr3:115678353 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0170 others(5): Show |
8 | HG02683.hp2 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+1743G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678353 | |||||||
| chr3:115678452 | A | G | 59 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0045 others(56): Show |
60 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.628+1842A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678452 | |||||||
| chr3:115678575 | GATA | G | 19 | a0001c0001t0001g0046 a0001c0001t0001g0073 a0001c0001t0001g0074 others(16): Show |
19 | HG01106.hp2 HG01934.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+1971_628+1973d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115678575 | ||||||
| chr3:115678767 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.628+2157A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678767 | |||||||
| chr3:115678938 | G | A | 197 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0028 others(194): Show |
201 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.628+2328G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678938 | |||||||
| chr3:115679099 | G | C | 2 | a0001c0001t0002g0211 a0001c0001t0006g0150 |
2 | HG00558.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.628+2489G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679099 | |||||||
| chr3:115679184 | G | A | 1 | a0001c0001t0003g0307 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.628+2574G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679184 | |||||||
| chr3:115679272 | T | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+2662T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679272 | |||||||
| chr3:115679277 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0073 a0001c0001t0001g0074 |
3 | HG03491.hp2 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.628+2667A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679277 | |||||||
| chr3:115679866 | A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+3256A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679866 | |||||||
| chr3:115679910 | A | G | 1 | a0001c0002t0001g0284 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.628+3300A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679910 | |||||||
| chr3:115679993 | T | A | 204 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(201): Show |
208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.628+3383T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679993 | |||||||
| chr3:115680179 | T | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(202): Show |
209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.628+3569T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680179 | |||||||
| chr3:115680188 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0003g0024 others(2): Show |
5 | HG02615.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+3578G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680188 | |||||||
| chr3:115680381 | G | A | 16 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0315 others(13): Show |
17 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+3771G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680381 | |||||||
| chr3:115680557 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+3947A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680557 | |||||||
| chr3:115680656 | G | A | 67 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0071 others(64): Show |
68 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.628+4046G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680656 | |||||||
| chr3:115680666 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.628+4056G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680666 | |||||||
| chr3:115680980 | G | T | 1 | a0001c0001t0007g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.628+4370G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680980 | |||||||
| chr3:115681211 | C | T | 56 | a0001c0001t0001g0054 a0001c0001t0001g0125 a0001c0001t0001g0168 others(53): Show |
58 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.628+4601C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681211 | |||||||
| chr3:115681356 | C | T | 12 | a0001c0001t0001g0046 a0001c0001t0001g0073 a0001c0001t0001g0074 others(9): Show |
12 | HG01106.hp2 HG01934.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.628+4746C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681356 | |||||||
| chr3:115681435 | G | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0035 others(70): Show |
74 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.628+4825G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681435 | |||||||
| chr3:115681745 | T | C | 1 | a0001c0001t0002g0276 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.628+5135T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681745 | |||||||
| chr3:115681997 | C | A | 1 | a0001c0001t0004g0279 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.628+5387C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681997 | |||||||
| chr3:115682201 | A | G | 7 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0103 others(4): Show |
7 | HG01361.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.628+5591A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682201 | |||||||
| chr3:115682451 | C | A | 26 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.628+5841C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682451 | |||||||
| chr3:115682599 | T | C | 308 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(305): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.628+5989T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682599 | |||||||
| chr3:115682729 | A | G | 307 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0023 others(304): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.628+6119A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682729 | |||||||
| chr3:115682780 | G | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0346 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.628+6170G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682780 | |||||||
| chr3:115682834 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.628+6224T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682834 | |||||||
| chr3:115682896 | G | A | 2 | a0001c0001t0003g0156 a0001c0001t0003g0157 |
2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.628+6286G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682896 | |||||||
| chr3:115682952 | A | G | 1 | a0001c0001t0005g0015 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.628+6342A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682952 | |||||||
| chr3:115683032 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0035 others(73): Show |
77 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.628+6422G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683032 | |||||||
| chr3:115683113 | CTACA | C | 21 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0085 others(18): Show |
22 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.628+6509_628+6512d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683113 | ||||||
| chr3:115683118 | TACATGTG others(7): Show |
T | 2 | a0001c0001t0001g0207 a0001c0002t0001g0099 |
2 | HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+6509_628+6522d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683118 | |||||||
| chr3:115683121 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.628+6511A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683121 | |||||||
| chr3:115683122 | TGTGCGCG others(7): Show |
T | 1 | a0001c0001t0005g0340 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.628+6514_628+6527d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683122 | ||||||
| chr3:115683122 | TGTGCGCG others(9): Show |
T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0309 others(1): Show |
4 | HG02257.hp1 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+6514_628+6529d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683122 | ||||||
| chr3:115683124 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0249 |
3 | HG02896.hp2 HG02897.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.628+6514T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683124 | |||||||
| chr3:115683124 | T | TGCGCGCG others(3): Show |
1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628+6521_628+6522i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | ||||||
| chr3:115683124 | T | TGCGCGCG others(5): Show |
1 | a0001c0001t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.628+6521_628+6522i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | ||||||
| chr3:115683124 | TGC | T | 85 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0047 others(82): Show |
87 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.628+6522_628+6523d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | ||||||
| chr3:115683124 | TGCGCGCG others(5): Show |
T | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+6524_628+6535d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | ||||||
| chr3:115683126 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.628+6516C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683126 | |||||||
| chr3:115683126 | CGCGCGCG others(1): Show |
C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0065 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.628+6524_628+6531d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683126 | ||||||
| chr3:115683128 | C | CGCGT | 3 | a0001c0001t0001g0088 a0001c0001t0005g0015 a0001c0001t0005g0344 |
3 | HG01081.hp2 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.628+6521_628+6522i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683128 | ||||||
| chr3:115683128 | CGCGCGT | C | 21 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0067 others(18): Show |
21 | HG00140.hp2 HG00738.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.628+6524_628+6529d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683128 | ||||||
| chr3:115683129 | G | GTGTGCGC others(7): Show |
1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+6519_628+6520i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683129 | |||||||
| chr3:115683130 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+6520C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683130 | |||||||
| chr3:115683130 | C | CGT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0174 a0001c0001t0001g0198 others(6): Show |
9 | HG01433.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.628+6521_628+6522i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683130 | ||||||
| chr3:115683130 | CGCGT | C | 47 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0054 others(44): Show |
47 | HG00544.hp2 HG00621.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.628+6524_628+6527d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683130 | ||||||
| chr3:115683132 | C | A | 1 | a0001c0001t0001g0338 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.628+6522C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683132 | |||||||
| chr3:115683132 | C | T | 56 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0046 others(53): Show |
56 | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.628+6522C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683132 | |||||||
| chr3:115683132 | CGT | C | 25 | a0001c0001t0001g0083 a0001c0001t0001g0168 a0001c0001t0001g0169 others(22): Show |
27 | HG00408.hp1 HG01261.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.628+6524_628+6525d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683132 | ||||||
| chr3:115683133 | GTGCGCGC others(11): Show |
G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.628+6524_628+6541d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683133 | |||||||
| chr3:115683134 | T | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0023 others(104): Show |
108 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.628+6524T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683134 | |||||||
| chr3:115683134 | T | TGC | 3 | a0001c0001t0001g0092 a0001c0001t0001g0311 a0001c0001t0002g0327 |
3 | HG00609.hp1 NA18966.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.628+6537_628+6538d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683134 | ||||||
| chr3:115683136 | C | T | 13 | a0001c0001t0002g0012 a0001c0001t0002g0048 a0001c0001t0002g0119 others(10): Show |
13 | HG00673.hp2 HG01255.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.628+6526C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683136 | |||||||
| chr3:115683137 | GCGCGCGC others(21): Show |
G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0346 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.628+6529_628+6556d others(30): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683137 | ||||||
| chr3:115683138 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.628+6528C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683138 | |||||||
| chr3:115683139 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.628+6529G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683139 | |||||||
| chr3:115683141 | G | A | 8 | a0001c0001t0001g0221 a0001c0001t0001g0249 a0001c0001t0001g0315 others(5): Show |
9 | HG02293.hp2 HG02486.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.628+6531G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683141 | |||||||
| chr3:115683141 | G | GCACACAC others(3): Show |
1 | a0001c0001t0003g0191 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.628+6532_628+6533i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683141 | ||||||
| chr3:115683141 | GCGCGCGC others(3): Show |
G | 2 | a0001c0001t0001g0154 a0001c0001t0002g0218 |
2 | HG01192.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.628+6533_628+6542d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683141 | ||||||
| chr3:115683141 | GCGCGCGC others(5): Show |
G | 2 | a0001c0001t0001g0064 a0001c0001t0004g0329 |
2 | HG00609.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.628+6533_628+6544d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683141 | ||||||
| chr3:115683143 | G | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0066 a0001c0001t0001g0170 others(23): Show |
28 | HG00673.hp1 HG00738.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.628+6533G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683143 | |||||||
| chr3:115683143 | G | GCA | 3 | a0001c0001t0002g0333 a0001c0001t0003g0156 a0001c0001t0003g0158 |
3 | HG00642.hp2 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.628+6534_628+6535i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683143 | ||||||
| chr3:115683143 | G | GCACA | 5 | a0001c0001t0002g0030 a0001c0001t0002g0226 a0001c0001t0002g0319 others(2): Show |
5 | HG00741.hp1 HG02523.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+6534_628+6535i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683143 | ||||||
| chr3:115683143 | G | GCACACAC others(3): Show |
1 | a0001c0001t0003g0283 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.628+6534_628+6535i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683143 | ||||||
| chr3:115683143 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.628+6533G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683143 | |||||||
| chr3:115683144 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.628+6534C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683144 | |||||||
| chr3:115683145 | G | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0058 a0001c0001t0001g0066 others(74): Show |
79 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.628+6535G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683145 | |||||||
| chr3:115683145 | G | GCA | 3 | a0001c0001t0008g0244 a0001c0001t0008g0245 a0001c0001t0009g0081 |
3 | HG01069.hp2 HG01081.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.628+6536_628+6537i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683145 | ||||||
| chr3:115683145 | G | GCACA | 3 | a0001c0001t0001g0041 a0001c0001t0002g0180 a0001c0001t0002g0202 |
3 | HG03516.hp2 NA18985.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.628+6536_628+6537i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683145 | ||||||
| chr3:115683145 | GCGCA | G | 11 | a0001c0001t0002g0106 a0001c0001t0002g0124 a0001c0001t0002g0293 others(8): Show |
11 | HG01517.hp2 HG01952.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.628+6537_628+6540d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683145 | ||||||
| chr3:115683146 | C | T | 6 | a0001c0001t0001g0059 a0001c0001t0001g0289 a0001c0001t0002g0121 others(3): Show |
6 | HG00642.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.628+6536C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683146 | |||||||
| chr3:115683147 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0028 others(159): Show |
166 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.628+6537G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683147 | |||||||
| chr3:115683147 | G | GCA | 4 | a0001c0001t0001g0053 a0001c0001t0001g0063 a0001c0001t0004g0062 others(1): Show |
4 | HG00438.hp2 HG03225.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+6577_628+6578d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCACA | 3 | a0001c0001t0001g0077 a0001c0001t0004g0252 a0001c0001t0010g0239 |
3 | HG02683.hp1 HG02895.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.628+6575_628+6578d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCACACA | 4 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0001c0001t0002g0129 others(1): Show |
4 | HG01934.hp1 HG02897.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+6573_628+6578d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCGCGCGC others(3): Show |
1 | a0001c0001t0005g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCGCGCGC others(5): Show |
1 | a0001c0001t0005g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCGCGCGC others(7): Show |
4 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0002g0164 others(1): Show |
4 | HG02280.hp1 HG03471.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+6538_628+6539i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCGCGCGC others(7): Show |
1 | a0001c0001t0002g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCGCGCGC others(5): Show |
1 | a0001c0001t0003g0295 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.628+6538_628+6539i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | G | GCGCGCGC others(7): Show |
1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | GCA | G | 18 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0123 others(15): Show |
18 | HG00558.hp1 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.628+6577_628+6578d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | GCACA | G | 29 | a0001c0001t0001g0059 a0001c0001t0001g0071 a0001c0001t0001g0146 others(26): Show |
30 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.628+6575_628+6578d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | GCACACA | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0228 others(5): Show |
8 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+6573_628+6578d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683147 | GCACACAC others(3): Show |
G | 1 | a0001c0001t0002g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.628+6569_628+6578d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | ||||||
| chr3:115683148 | C | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0122 |
2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.628+6538C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683148 | |||||||
| chr3:115683149 | A | G | 31 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0054 others(28): Show |
31 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.628+6539A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683149 | |||||||
| chr3:115683151 | A | G | 6 | a0001c0001t0001g0088 a0001c0001t0001g0123 a0001c0001t0002g0171 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+6541A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683151 | |||||||
| chr3:115683153 | A | G | 1 | a0001c0001t0002g0231 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.628+6543A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683153 | |||||||
| chr3:115683155 | A | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
6 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+6545A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683155 | |||||||
| chr3:115683157 | A | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0228 a0001c0001t0001g0229 others(3): Show |
6 | HG00733.hp1 HG00735.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.628+6547A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683157 | |||||||
| chr3:115683159 | A | G | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
5 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+6549A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683159 | |||||||
| chr3:115683161 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.628+6551A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683161 | |||||||
| chr3:115683360 | G | C | 1 | a0001c0001t0004g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.628+6750G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683360 | |||||||
| chr3:115683375 | A | G | 2 | a0001c0001t0001g0289 a0001c0001t0002g0288 |
2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.628+6765A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683375 | |||||||
| chr3:115683399 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA18747.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.628+6789G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683399 | |||||||
| chr3:115683604 | A | AG | 285 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(282): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.628+6994_628+6995i others(3): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683604 | |||||||
| chr3:115683609 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.628+6999A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683609 | |||||||
| chr3:115683688 | G | T | 2 | a0001c0001t0002g0142 a0001c0001t0002g0148 |
2 | NA18970.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.628+7078G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683688 | |||||||
| chr3:115683766 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0209 a0001c0001t0001g0302 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+7156C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683766 | |||||||
| chr3:115683838 | A | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0035 others(77): Show |
81 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.628+7228A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683838 | |||||||
| chr3:115683895 | T | C | 286 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(283): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.628+7285T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683895 | |||||||
| chr3:115683928 | G | A | 2 | a0001c0002t0002g0193 a0001c0002t0002g0225 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.628+7318G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683928 | |||||||
| chr3:115684208 | C | T | 204 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(201): Show |
208 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.628+7598C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684208 | |||||||
| chr3:115684368 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.628+7758A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684368 | |||||||
| chr3:115684495 | C | T | 1 | a0001c0001t0002g0294 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.628+7885C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684495 | |||||||
| chr3:115684563 | G | A | 2 | a0001c0001t0008g0244 a0001c0001t0008g0245 |
2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.628+7953G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684563 | |||||||
| chr3:115684564 | G | GT | 8 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+7955dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115684564 | ||||||
| chr3:115684744 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0088 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+8134G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684744 | |||||||
| chr3:115684886 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0085 a0001c0001t0001g0170 others(6): Show |
9 | HG02683.hp2 HG02970.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.628+8276C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684886 | |||||||
| chr3:115684968 | C | A | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+8358C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684968 | |||||||
| chr3:115684971 | C | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0035 others(78): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.628+8361C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684971 | |||||||
| chr3:115685022 | T | C | 1 | a0001c0001t0009g0188 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.628+8412T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685022 | |||||||
| chr3:115685081 | T | G | 281 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(278): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.628+8471T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685081 | |||||||
| chr3:115685746 | T | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(202): Show |
209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.628+9136T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685746 | |||||||
| chr3:115685799 | G | A | 8 | a0001c0001t0001g0069 a0001c0001t0001g0297 a0001c0001t0001g0341 others(5): Show |
8 | HG01081.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+9189G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685799 | |||||||
| chr3:115685830 | C | T | 1 | a0001c0001t0004g0279 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.628+9220C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685830 | |||||||
| chr3:115685866 | C | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
33 | HG01106.hp1 HG01361.hp1 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.628+9256C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685866 | |||||||
| chr3:115686144 | C | T | 307 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(304): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.628+9534C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686144 | |||||||
| chr3:115686321 | C | G | 307 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(304): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.628+9711C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686321 | |||||||
| chr3:115686344 | C | T | 104 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0059 others(101): Show |
106 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.628+9734C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686344 | |||||||
| chr3:115686550 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0001g0209 a0001c0001t0001g0302 others(1): Show |
4 | HG01891.hp1 HG02055.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+9940A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686550 | |||||||
| chr3:115686658 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0035 others(79): Show |
83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.628+10048T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686658 | |||||||
| chr3:115686940 | G | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0025 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.628+10330G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686940 | |||||||
| chr3:115687108 | C | G | 3 | a0001c0001t0002g0180 a0001c0001t0002g0195 a0001c0001t0002g0202 |
3 | NA18974.hp2 NA18985.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.628+10498C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687108 | |||||||
| chr3:115687114 | TC | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0035 others(85): Show |
89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.628+10505delC | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687114 | |||||||
| chr3:115687115 | C | CT | 236 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(233): Show |
240 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.628+10518dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115687115 | ||||||
| chr3:115687115 | C | CTT | 14 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0085 others(11): Show |
14 | HG01069.hp2 HG01081.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.628+10517_628+1051 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115687115 | ||||||
| chr3:115687209 | A | T | 1 | a0001c0001t0002g0317 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.628+10599A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687209 | |||||||
| chr3:115687239 | T | C | 314 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(311): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.628+10629T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687239 | |||||||
| chr3:115687380 | C | T | 1 | a0001c0001t0005g0009 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.628+10770C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687380 | |||||||
| chr3:115687421 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628+10811A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687421 | |||||||
| chr3:115687438 | A | G | 2 | a0001c0001t0002g0110 a0001c0001t0002g0294 |
2 | NA18969.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.628+10828A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687438 | |||||||
| chr3:115687631 | T | C | 198 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0026 others(195): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.628+11021T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687631 | |||||||
| chr3:115687634 | C | T | 74 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0055 others(71): Show |
75 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.628+11024C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687634 | |||||||
| chr3:115687706 | C | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0289 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.628+11096C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687706 | |||||||
| chr3:115687729 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.628+11119A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687729 | |||||||
| chr3:115687750 | C | G | 338 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(335): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.628+11140C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687750 | |||||||
| chr3:115687960 | A | C | 95 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0032 others(92): Show |
97 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.628+11350A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687960 | |||||||
| chr3:115687995 | G | A | 1 | a0001c0001t0004g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.628+11385G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687995 | |||||||
| chr3:115688006 | A | ATTAT | 138 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(135): Show |
139 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.628+11417_628+1142 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115688006 | ||||||
| chr3:115688006 | A | T | 2 | a0001c0001t0001g0338 a0001c0001t0005g0337 |
2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.628+11396A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688006 | |||||||
| chr3:115688051 | C | G | 1 | a0001c0001t0002g0220 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.628+11441C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688051 | |||||||
| chr3:115688137 | C | T | 19 | a0001c0001t0001g0046 a0001c0001t0001g0073 a0001c0001t0001g0074 others(16): Show |
19 | HG01106.hp2 HG01934.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+11527C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688137 | |||||||
| chr3:115688152 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0035 others(77): Show |
81 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.628+11542G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688152 | |||||||
| chr3:115688187 | T | A | 3 | a0001c0001t0003g0075 a0001c0001t0003g0082 a0001c0001t0011g0079 |
3 | HG01261.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.628+11577T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688187 | |||||||
| chr3:115688215 | G | A | 16 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0315 others(13): Show |
17 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+11605G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688215 | |||||||
| chr3:115688307 | G | C | 338 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(335): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.628+11697G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688307 | |||||||
| chr3:115688406 | T | C | 62 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0040 others(59): Show |
62 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.628+11796T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688406 | |||||||
| chr3:115688462 | CTCTA | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0028 others(78): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.628+11858_628+1186 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115688462 | ||||||
| chr3:115688463 | T | C | 62 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0040 others(59): Show |
62 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.628+11853T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688463 | |||||||
| chr3:115688655 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+12045A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688655 | |||||||
| chr3:115688715 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.628+12105C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688715 | |||||||
| chr3:115688877 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.628+12267T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688877 | |||||||
| chr3:115688937 | G | A | 19 | a0001c0001t0001g0046 a0001c0001t0001g0073 a0001c0001t0001g0074 others(16): Show |
19 | HG01074.hp2 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+12327G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688937 | |||||||
| chr3:115689149 | T | C | 1 | a0001c0001t0004g0252 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.628+12539T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689149 | |||||||
| chr3:115689258 | G | T | 3 | a0001c0001t0002g0112 a0001c0001t0002g0126 a0001c0001t0002g0127 |
3 | NA18955.hp2 NA19003.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.628+12648G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689258 | |||||||
| chr3:115689355 | A | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0041 others(8): Show |
11 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.628+12745A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689355 | |||||||
| chr3:115689445 | GA | G | 4 | a0001c0002t0001g0039 a0001c0002t0002g0043 a0001c0002t0002g0193 others(1): Show |
4 | HG01106.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+12838delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115689445 | ||||||
| chr3:115689465 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+12855A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689465 | |||||||
| chr3:115689506 | T | C | 42 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0040 others(39): Show |
42 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.628+12896T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689506 | |||||||
| chr3:115689814 | A | T | 1 | a0001c0001t0004g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.628+13204A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689814 | |||||||
| chr3:115690061 | T | C | 1 | a0001c0001t0004g0286 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.628+13451T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690061 | |||||||
| chr3:115690197 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.628+13587C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690197 | |||||||
| chr3:115690223 | C | G | 1 | a0001c0001t0001g0328 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.628+13613C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690223 | |||||||
| chr3:115690237 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0002g0248 |
2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.628+13627C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690237 | |||||||
| chr3:115690549 | G | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+13939G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690549 | |||||||
| chr3:115690602 | T | C | 4 | a0001c0001t0010g0238 a0001c0001t0010g0239 a0001c0002t0002g0193 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+13992T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690602 | |||||||
| chr3:115690620 | T | C | 1 | a0001c0001t0002g0272 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.628+14010T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690620 | |||||||
| chr3:115690711 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.628+14101A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690711 | |||||||
| chr3:115690746 | T | C | 1 | a0001c0001t0014g0253 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.628+14136T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690746 | |||||||
| chr3:115690757 | C | CT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0170 others(22): Show |
26 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.628+14163dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115690757 | ||||||
| chr3:115690778 | C | T | 17 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0093 others(14): Show |
18 | HG02071.hp2 HG02293.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+14168C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690778 | |||||||
| chr3:115690792 | G | A | 1 | a0001c0001t0019g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.628+14182G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690792 | |||||||
| chr3:115690807 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.628+14197G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690807 | |||||||
| chr3:115690842 | G | A | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+14232G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690842 | |||||||
| chr3:115691307 | T | A | 1 | a0001c0001t0003g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.628+14697T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115691307 | |||||||
| chr3:115691469 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+14859C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115691469 | |||||||
| chr3:115691470 | G | A | 1 | a0001c0001t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.628+14860G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115691470 | |||||||
| chr3:115692016 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0018g0331 |
2 | NA18982.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.628+15406G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692016 | |||||||
| chr3:115692083 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0198 a0001c0001t0001g0334 |
3 | HG02258.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.628+15473C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692083 | |||||||
| chr3:115692144 | A | G | 36 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(33): Show |
36 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.628+15534A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692144 | |||||||
| chr3:115692386 | G | T | 81 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0041 others(78): Show |
82 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.628+15776G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692386 | |||||||
| chr3:115692568 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+15958C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692568 | |||||||
| chr3:115692631 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.628+16021G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692631 | |||||||
| chr3:115692691 | G | C | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.628+16081G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692691 | |||||||
| chr3:115692702 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+16092T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692702 | |||||||
| chr3:115692728 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.628+16118G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692728 | |||||||
| chr3:115692818 | T | A | 1 | a0001c0001t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.628+16208T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692818 | |||||||
| chr3:115692818 | T | C | 2 | a0001c0001t0001g0028 a0001c0002t0001g0039 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.628+16208T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692818 | |||||||
| chr3:115692837 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.628+16227T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692837 | |||||||
| chr3:115692908 | C | T | 1 | a0001c0001t0004g0034 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.628+16298C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692908 | |||||||
| chr3:115692986 | T | C | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+16376T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692986 | |||||||
| chr3:115693000 | C | T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(34): Show |
37 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.628+16390C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693000 | |||||||
| chr3:115693267 | A | G | 1 | a0001c0002t0001g0135 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.628+16657A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693267 | |||||||
| chr3:115693339 | C | G | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+16729C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693339 | |||||||
| chr3:115693485 | TAA | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+16877_628+1687 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115693485 | ||||||
| chr3:115693487 | AATTATT | A | 55 | a0001c0001t0001g0019 a0001c0001t0001g0167 a0001c0001t0001g0345 others(52): Show |
55 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.628+16893_628+1689 others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115693487 | ||||||
| chr3:115693716 | G | A | 54 | a0001c0001t0001g0019 a0001c0001t0001g0167 a0001c0001t0002g0014 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.628+17106G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693716 | |||||||
| chr3:115694215 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+17605T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694215 | |||||||
| chr3:115694232 | C | T | 24 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0271 others(21): Show |
24 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.628+17622C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694232 | |||||||
| chr3:115694578 | A | T | 39 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(36): Show |
39 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.628+17968A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694578 | |||||||
| chr3:115694812 | C | G | 1 | a0001c0001t0002g0127 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.628+18202C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694812 | |||||||
| chr3:115694869 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+18259A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694869 | |||||||
| chr3:115694960 | C | T | 21 | a0001c0001t0001g0167 a0001c0001t0002g0271 a0001c0001t0002g0293 others(18): Show |
21 | HG00544.hp1 HG00673.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+18350C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694960 | |||||||
| chr3:115694963 | C | A | 338 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(335): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.628+18353C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694963 | |||||||
| chr3:115695005 | G | A | 1 | a0001c0001t0005g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.628+18395G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695005 | |||||||
| chr3:115695026 | A | T | 215 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(212): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.628+18416A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695026 | |||||||
| chr3:115695134 | A | G | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.628+18524A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695134 | |||||||
| chr3:115695341 | C | G | 215 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(212): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.628+18731C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695341 | |||||||
| chr3:115695730 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.628+19120C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695730 | |||||||
| chr3:115695899 | G | T | 338 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(335): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.628+19289G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695899 | |||||||
| chr3:115696104 | T | C | 37 | a0001c0001t0001g0023 a0001c0001t0001g0167 a0001c0001t0001g0221 others(34): Show |
38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+19494T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696104 | |||||||
| chr3:115696174 | A | G | 2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628+19564A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696174 | |||||||
| chr3:115696211 | A | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0167 a0001c0001t0001g0221 others(34): Show |
38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+19601A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696211 | |||||||
| chr3:115696294 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+19684C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696294 | |||||||
| chr3:115696575 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.628+19965A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696575 | |||||||
| chr3:115696576 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.628+19966C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696576 | |||||||
| chr3:115696576 | C | CCA | 8 | a0001c0001t0001g0169 a0001c0001t0002g0014 a0001c0001t0002g0036 others(5): Show |
8 | HG03486.hp2 NA18944.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+19967_628+1996 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696576 | ||||||
| chr3:115696577 | C | CA | 60 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0084 others(57): Show |
60 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.628+19967_628+1996 others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696577 | |||||||
| chr3:115696577 | CG | C | 15 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0073 others(12): Show |
16 | HG00738.hp1 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.628+19968delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696577 | |||||||
| chr3:115696578 | G | A | 126 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0032 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.628+19968G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696578 | |||||||
| chr3:115696578 | G | C | 72 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0084 others(69): Show |
72 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.628+19968G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696578 | |||||||
| chr3:115696578 | G | GC | 16 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0077 others(13): Show |
16 | HG02148.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.628+19980dupC | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | ||||||
| chr3:115696578 | G | GCC | 24 | a0001c0001t0001g0021 a0001c0001t0001g0091 a0001c0001t0001g0095 others(21): Show |
24 | HG01361.hp1 HG01884.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.628+19979_628+1998 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | ||||||
| chr3:115696578 | G | GCCC | 25 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0041 others(22): Show |
25 | HG00673.hp2 HG01081.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+19978_628+1998 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | ||||||
| chr3:115696578 | G | GCCCC | 15 | a0001c0001t0001g0263 a0001c0001t0001g0345 a0001c0001t0004g0132 others(12): Show |
15 | HG00544.hp1 HG01109.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.628+19977_628+1998 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | ||||||
| chr3:115696579 | C | A | 16 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0073 others(13): Show |
17 | HG00738.hp1 HG01071.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+19969C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696579 | |||||||
| chr3:115696584 | C | A | 20 | a0001c0001t0001g0040 a0001c0001t0001g0066 a0001c0001t0001g0067 others(17): Show |
21 | HG02055.hp1 HG02071.hp2 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+19974C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696584 | |||||||
| chr3:115696808 | T | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0167 a0001c0001t0001g0221 others(34): Show |
38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+20198T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696808 | |||||||
| chr3:115696852 | G | GACAGAGT others(277): Show |
1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.628+20255_628+2025 others(288): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696852 | ||||||
| chr3:115696862 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0304 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.628+20252C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696862 | |||||||
| chr3:115696902 | A | G | 338 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(335): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.628+20292A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696902 | |||||||
| chr3:115696987 | A | G | 44 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0028 others(41): Show |
44 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.628+20377A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696987 | |||||||
| chr3:115696991 | G | A | 12 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.628+20381G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696991 | |||||||
| chr3:115696994 | TA | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+20387delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696994 | ||||||
| chr3:115697057 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+20447T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697057 | |||||||
| chr3:115697187 | T | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+20577T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697187 | |||||||
| chr3:115697207 | A | AATAAT | 342 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(339): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.628+20601_628+2060 others(9): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697207 | ||||||
| chr3:115697284 | A | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0167 a0001c0001t0001g0221 others(34): Show |
38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+20674A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697284 | |||||||
| chr3:115697379 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628+20769C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697379 | |||||||
| chr3:115697466 | C | A | 25 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0271 others(22): Show |
25 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+20856C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697466 | |||||||
| chr3:115697489 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+20879C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697489 | |||||||
| chr3:115697668 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0341 a0001c0001t0003g0321 |
3 | HG02886.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.628+21058A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697668 | |||||||
| chr3:115697701 | G | C | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+21091G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697701 | |||||||
| chr3:115697815 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21205T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697815 | |||||||
| chr3:115697831 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+21221A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697831 | |||||||
| chr3:115697896 | A | T | 1 | a0001c0001t0003g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.628+21286A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697896 | |||||||
| chr3:115697908 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.628+21298T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697908 | |||||||
| chr3:115697950 | G | A | 2 | a0001c0002t0001g0099 a0001c0002t0001g0102 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21340G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697950 | |||||||
| chr3:115697982 | T | TGC | 191 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(188): Show |
194 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.628+21374_628+2137 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697982 | ||||||
| chr3:115697984 | C | CGCGT | 14 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0085 others(11): Show |
14 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.628+21375_628+2137 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697984 | ||||||
| chr3:115697984 | CGT | C | 125 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(122): Show |
127 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.628+21399_628+2140 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697984 | ||||||
| chr3:115697986 | T | C | 8 | a0001c0001t0002g0014 a0001c0001t0002g0036 a0001c0001t0002g0136 others(5): Show |
8 | HG01943.hp2 HG02523.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+21376T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697986 | |||||||
| chr3:115698000 | T | C | 125 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(122): Show |
127 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.628+21390T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698000 | |||||||
| chr3:115698021 | T | C | 20 | a0001c0001t0001g0041 a0001c0001t0002g0164 a0001c0001t0002g0303 others(17): Show |
21 | HG00438.hp2 HG00609.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+21411T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698021 | |||||||
| chr3:115698024 | C | T | 25 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0271 others(22): Show |
25 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+21414C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698024 | |||||||
| chr3:115698027 | GTATATAA others(16): Show |
G | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628+21441_628+2146 others(27): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698027 | ||||||
| chr3:115698035 | A | AATATATA others(66): Show |
1 | a0001c0001t0003g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.628+21477_628+2147 others(77): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698035 | ||||||
| chr3:115698043 | TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0266 a0001c0001t0001g0302 others(1): Show |
4 | HG02280.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21447_628+2146 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698043 | ||||||
| chr3:115698044 | TATATATT others(7): Show |
T | 2 | a0001c0001t0001g0222 a0001c0001t0005g0009 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.628+21441_628+2145 others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698044 | ||||||
| chr3:115698050 | T | TAA | 23 | a0001c0001t0001g0167 a0001c0001t0002g0271 a0001c0001t0002g0293 others(20): Show |
23 | HG00544.hp1 HG00673.hp2 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.628+21440_628+2144 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | |||||||
| chr3:115698050 | T | TAATATAT others(4): Show |
1 | a0001c0001t0004g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21440_628+2144 others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | |||||||
| chr3:115698050 | T | TAATATAT others(258): Show |
1 | a0001c0001t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.628+21440_628+2144 others(269): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | |||||||
| chr3:115698050 | T | TAATATAT others(4): Show |
30 | a0001c0001t0001g0041 a0001c0001t0001g0094 a0001c0001t0001g0095 others(27): Show |
31 | HG00438.hp2 HG00609.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.628+21440_628+2144 others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | |||||||
| chr3:115698050 | T | TAATATAT others(8): Show |
20 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(17): Show |
21 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+21440_628+2144 others(19): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | |||||||
| chr3:115698050 | T | TAATATAT others(29): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0311 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.628+21440_628+2144 others(40): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | |||||||
| chr3:115698050 | TTATATAA | T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(34): Show |
37 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.628+21441_628+2144 others(11): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | |||||||
| chr3:115698051 | T | A | 2 | a0001c0001t0002g0237 a0001c0001t0003g0011 |
2 | HG02145.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.628+21441T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698051 | |||||||
| chr3:115698057 | A | T | 9 | a0001c0001t0002g0237 a0001c0001t0004g0003 a0001c0001t0004g0029 others(6): Show |
10 | HG00438.hp2 HG00609.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.628+21447A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698057 | |||||||
| chr3:115698058 | A | T | 1 | a0001c0001t0004g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21448A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698058 | |||||||
| chr3:115698058 | AATATATA others(68): Show |
A | 1 | a0001c0001t0002g0237 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.628+21456_628+2153 others(79): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698058 | ||||||
| chr3:115698066 | T | A | 26 | a0001c0001t0001g0167 a0001c0001t0001g0222 a0001c0001t0002g0271 others(23): Show |
26 | HG00544.hp1 HG00673.hp2 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.628+21456T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698066 | |||||||
| chr3:115698067 | T | A | 42 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(39): Show |
42 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(39): Show |
intron_variant | MODIFIER | c.628+21457T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698067 | |||||||
| chr3:115698070 | ATAT | A | 37 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(34): Show |
37 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.628+21461_628+2146 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698070 | |||||||
| chr3:115698074 | A | ATTATATA others(197): Show |
1 | a0001c0001t0004g0252 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(208): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698074 | A | ATTATATA others(231): Show |
13 | a0001c0001t0001g0167 a0001c0001t0002g0293 a0001c0001t0004g0132 others(10): Show |
13 | HG00544.hp1 HG01928.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.628+21464_628+2146 others(242): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698074 | A | ATTATATA others(299): Show |
1 | a0001c0001t0004g0201 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(310): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698074 | A | ATTATATA others(265): Show |
2 | a0001c0001t0004g0057 a0001c0001t0004g0305 |
2 | HG02083.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.628+21464_628+2146 others(276): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698074 | A | ATTATATA others(265): Show |
1 | a0001c0001t0003g0027 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.628+21464_628+2146 others(276): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698074 | A | ATTATATA others(299): Show |
1 | a0001c0001t0015g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(310): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698074 | A | ATTATATA others(299): Show |
1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(310): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698074 | A | ATTATATA others(197): Show |
3 | a0001c0001t0002g0271 a0001c0001t0004g0251 a0001c0001t0004g0281 |
3 | HG00673.hp2 NA18990.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.628+21464_628+2146 others(208): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | |||||||
| chr3:115698076 | T | A | 1 | a0001c0001t0001g0247 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.628+21466T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698076 | |||||||
| chr3:115698082 | A | AAATATAT | 16 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(13): Show |
17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21477_628+2147 others(11): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698082 | ||||||
| chr3:115698082 | A | T | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21472A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698082 | |||||||
| chr3:115698083 | A | AATATATA others(9): Show |
1 | a0001c0001t0005g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.628+21477_628+2147 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698083 | ||||||
| chr3:115698083 | A | T | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21473A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698083 | |||||||
| chr3:115698088 | G | A | 337 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(334): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.628+21478G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698088 | |||||||
| chr3:115698091 | T | A | 15 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0002g0086 others(12): Show |
16 | HG00438.hp2 HG00609.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.628+21481T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698091 | |||||||
| chr3:115698099 | A | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0002g0086 others(1): Show |
4 | HG02647.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21489A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698099 | |||||||
| chr3:115698107 | A | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(13): Show |
17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21497A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698107 | |||||||
| chr3:115698108 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0266 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+21498A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698108 | |||||||
| chr3:115698108 | A | T | 28 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0167 others(25): Show |
28 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.628+21498A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698108 | |||||||
| chr3:115698109 | ATATATAA others(7): Show |
A | 3 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 |
3 | HG02280.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.628+21506_628+2151 others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698109 | ||||||
| chr3:115698114 | T | TAA | 24 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0271 others(21): Show |
24 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.628+21505_628+2150 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698114 | ||||||
| chr3:115698114 | T | TCTTATAT others(215): Show |
1 | a0001c0001t0004g0181 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.628+21504_628+2150 others(226): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | |||||||
| chr3:115698114 | T | TCTTATAT others(224): Show |
6 | a0001c0001t0004g0029 a0001c0001t0004g0062 a0001c0001t0004g0160 others(3): Show |
6 | HG00438.hp2 HG00609.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21504_628+2150 others(235): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | |||||||
| chr3:115698114 | T | TCTTATAT others(249): Show |
1 | a0001c0001t0004g0003 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.628+21504_628+2150 others(260): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | |||||||
| chr3:115698114 | T | TCTTATAT others(283): Show |
1 | a0001c0001t0004g0003 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.628+21504_628+2150 others(294): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | |||||||
| chr3:115698115 | A | C | 1 | a0001c0001t0004g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21505A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698115 | |||||||
| chr3:115698115 | A | T | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21505A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698115 | |||||||
| chr3:115698116 | A | T | 2 | a0001c0001t0001g0222 a0001c0001t0004g0139 |
2 | HG02129.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.628+21506A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698116 | |||||||
| chr3:115698117 | T | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21507T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698117 | |||||||
| chr3:115698121 | T | A | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21511T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698121 | |||||||
| chr3:115698122 | A | T | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21512A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698122 | |||||||
| chr3:115698123 | T | A | 3 | a0001c0001t0002g0086 a0001c0001t0003g0011 a0001c0001t0005g0233 |
3 | HG02647.hp2 HG03516.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.628+21513T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698123 | |||||||
| chr3:115698124 | T | A | 6 | a0001c0001t0001g0222 a0001c0001t0002g0086 a0001c0001t0004g0139 others(3): Show |
6 | HG02129.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21514T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698124 | |||||||
| chr3:115698126 | T | A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(13): Show |
17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21516T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698126 | |||||||
| chr3:115698130 | T | A | 16 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(13): Show |
17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21520T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698130 | |||||||
| chr3:115698130 | TAA | T | 50 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0297 others(47): Show |
53 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.628+21521_628+2152 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698130 | |||||||
| chr3:115698131 | A | T | 178 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(175): Show |
179 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.628+21521A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698131 | |||||||
| chr3:115698131 | AAT | A | 3 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 |
3 | HG02280.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.628+21529_628+2153 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698131 | ||||||
| chr3:115698131 | AATATATA others(10): Show |
A | 1 | a0001c0001t0001g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.628+21522_628+2153 others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698131 | |||||||
| chr3:115698132 | ATATATAT others(9): Show |
A | 32 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(29): Show |
32 | HG01361.hp1 HG01884.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.628+21538_628+2155 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698132 | ||||||
| chr3:115698133 | T | A | 3 | a0001c0001t0003g0011 a0001c0002t0001g0099 a0001c0002t0001g0102 |
3 | NA19084.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21523T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698133 | |||||||
| chr3:115698134 | A | ATATATTA others(32): Show |
2 | a0001c0002t0001g0099 a0001c0002t0001g0102 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21529_628+2153 others(43): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698134 | ||||||
| chr3:115698139 | T | A | 33 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0212 others(30): Show |
34 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.628+21529T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698139 | |||||||
| chr3:115698139 | T | TAAAATAT others(272): Show |
1 | a0001c0001t0004g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21531_628+2153 others(283): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698139 | ||||||
| chr3:115698139 | T | TTA | 16 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(13): Show |
17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21529_628+2153 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698139 | |||||||
| chr3:115698140 | A | AATATATA others(18): Show |
2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628+21537_628+2153 others(29): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698140 | ||||||
| chr3:115698140 | A | T | 52 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0297 others(49): Show |
55 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.628+21530A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698140 | |||||||
| chr3:115698140 | AATATATA others(2): Show |
A | 158 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0032 others(155): Show |
158 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.628+21538_628+2154 others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698140 | ||||||
| chr3:115698141 | A | T | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21531A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698141 | |||||||
| chr3:115698142 | T | A | 2 | a0001c0002t0001g0099 a0001c0002t0001g0102 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21532T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698142 | |||||||
| chr3:115698147 | A | AAAATATA others(34): Show |
10 | a0001c0001t0002g0164 a0001c0001t0002g0303 a0001c0001t0005g0007 others(7): Show |
10 | HG01081.hp2 HG01106.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.628+21537_628+2153 others(45): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698147 | |||||||
| chr3:115698147 | A | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+21537A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698147 | |||||||
| chr3:115698147 | A | T | 2 | a0001c0001t0001g0041 a0001c0001t0005g0337 |
2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.628+21537A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698147 | |||||||
| chr3:115698148 | T | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(10): Show |
13 | HG00733.hp1 HG00735.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.628+21538T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698148 | |||||||
| chr3:115698149 | T | A | 61 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0077 others(58): Show |
64 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.628+21539T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698149 | |||||||
| chr3:115698149 | T | TATATATA others(41): Show |
1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.628+21561_628+2156 others(52): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698149 | ||||||
| chr3:115698155 | T | A | 1 | a0001c0001t0003g0011 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21545T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698155 | |||||||
| chr3:115698156 | A | T | 21 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(18): Show |
22 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.628+21546A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698156 | |||||||
| chr3:115698158 | T | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21548T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698158 | |||||||
| chr3:115698162 | T | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(18): Show |
22 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.628+21552T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698162 | |||||||
| chr3:115698163 | A | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21553A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698163 | |||||||
| chr3:115698165 | A | T | 24 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+21555A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698165 | |||||||
| chr3:115698169 | TA | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0304 |
3 | HG02109.hp2 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.628+21560delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698169 | |||||||
| chr3:115698171 | T | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21561T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698171 | |||||||
| chr3:115698172 | T | A | 2 | a0001c0002t0001g0099 a0001c0002t0001g0102 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21562T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698172 | |||||||
| chr3:115698172 | TAAA | T | 33 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0271 others(30): Show |
34 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.628+21563_628+2156 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698172 | |||||||
| chr3:115698174 | A | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21564A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698174 | |||||||
| chr3:115698177 | A | ATATATT | 5 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21567_628+2156 others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698177 | |||||||
| chr3:115698177 | AAT | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+21576_628+2157 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698177 | ||||||
| chr3:115698179 | T | C | 27 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0094 others(24): Show |
27 | HG01081.hp2 HG01106.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.628+21569T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698179 | |||||||
| chr3:115698179 | T | TATATA | 16 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(13): Show |
17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21570_628+2157 others(9): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698179 | ||||||
| chr3:115698182 | A | AT | 5 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21573dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698182 | ||||||
| chr3:115698188 | T | A | 56 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(53): Show |
58 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.628+21578T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698188 | |||||||
| chr3:115698189 | A | T | 2 | a0001c0002t0001g0099 a0001c0002t0001g0102 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21579A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698189 | |||||||
| chr3:115698198 | T | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(4): Show |
7 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.628+21588T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698198 | |||||||
| chr3:115698199 | T | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21589T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698199 | |||||||
| chr3:115698205 | T | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21595T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698205 | |||||||
| chr3:115698205 | T | TAATA | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21595_628+2159 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698205 | |||||||
| chr3:115698205 | TTATATAA others(2): Show |
T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+21603_628+2161 others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698205 | ||||||
| chr3:115698210 | T | TAATATAT others(18): Show |
1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.628+21602_628+2160 others(29): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698210 | ||||||
| chr3:115698210 | T | TAATATAT others(4): Show |
5 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0228 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21602_628+2160 others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698210 | ||||||
| chr3:115698210 | TAA | T | 15 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0164 others(12): Show |
15 | HG01081.hp2 HG01106.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.628+21603_628+2160 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698210 | ||||||
| chr3:115698212 | A | AAATATAT | 44 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(41): Show |
44 | HG01361.hp1 HG01884.hp1 HG01943.hp2 others(41): Show |
intron_variant | MODIFIER | c.628+21618_628+2162 others(11): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(41): Show |
1 | a0001c0001t0001g0046 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.628+21624_628+2162 others(52): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(34): Show |
110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0032 others(107): Show |
110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(45): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(68): Show |
73 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0045 others(70): Show |
75 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(79): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(102): Show |
6 | a0001c0001t0001g0050 a0001c0001t0002g0133 a0001c0001t0003g0082 others(3): Show |
6 | HG00140.hp1 HG00140.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(113): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(170): Show |
8 | a0001c0001t0001g0054 a0001c0001t0003g0002 a0001c0001t0003g0070 others(5): Show |
9 | HG00642.hp2 HG00738.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(181): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(204): Show |
1 | a0001c0001t0003g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.628+21624_628+2162 others(215): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(105): Show |
3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0342 |
3 | HG01891.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.628+21624_628+2162 others(116): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | AAATATAT others(32): Show |
1 | a0001c0001t0002g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.628+21623_628+2162 others(43): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | ||||||
| chr3:115698212 | A | T | 2 | a0001c0002t0001g0099 a0001c0002t0001g0102 |
2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21602A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698212 | |||||||
| chr3:115698213 | A | AAT | 18 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(15): Show |
19 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+21609_628+2161 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698213 | ||||||
| chr3:115698213 | A | AATATATA others(27): Show |
1 | a0001c0001t0001g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.628+21624_628+2162 others(38): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698213 | ||||||
| chr3:115698213 | A | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0077 a0001c0001t0001g0170 others(3): Show |
6 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21603A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698213 | |||||||
| chr3:115698214 | A | ATATATAA others(66): Show |
5 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0180 others(2): Show |
5 | NA18974.hp2 NA18983.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(77): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698214 | ||||||
| chr3:115698229 | T | TATATAAT others(32): Show |
1 | a0001c0001t0002g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.628+21624_628+2162 others(43): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698229 | ||||||
| chr3:115698231 | T | C | 5 | a0001c0001t0001g0186 a0001c0001t0001g0223 a0001c0001t0001g0335 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21621T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698231 | |||||||
| chr3:115698237 | A | T | 1 | a0001c0001t0002g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.628+21627A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698237 | |||||||
| chr3:115698240 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.628+21630T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698240 | |||||||
| chr3:115698247 | A | ATTATATA others(28): Show |
30 | a0001c0001t0001g0167 a0001c0001t0002g0271 a0001c0001t0002g0293 others(27): Show |
31 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.628+21637_628+2163 others(39): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698247 | |||||||
| chr3:115698247 | A | ATTATATA others(30): Show |
2 | a0001c0001t0001g0345 a0001c0001t0013g0219 |
2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.628+21637_628+2163 others(41): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698247 | |||||||
| chr3:115698247 | A | T | 19 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(16): Show |
20 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.628+21637A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698247 | |||||||
| chr3:115698249 | T | A | 32 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0271 others(29): Show |
33 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.628+21639T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698249 | |||||||
| chr3:115698255 | AT | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21646delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698255 | |||||||
| chr3:115698262 | T | A | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21652T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698262 | |||||||
| chr3:115698263 | A | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(14): Show |
18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21653A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698263 | |||||||
| chr3:115698265 | A | AATATATA others(72): Show |
1 | a0001c0001t0001g0315 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.628+21663_628+2166 others(83): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698265 | ||||||
| chr3:115698265 | A | T | 18 | a0001c0001t0001g0019 a0001c0001t0001g0066 a0001c0001t0001g0067 others(15): Show |
19 | HG01261.hp1 HG01943.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+21655A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698265 | |||||||
| chr3:115698282 | A | AATATAAT others(24): Show |
1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(35): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698282 | ||||||
| chr3:115698282 | A | T | 1 | a0001c0001t0002g0199 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.628+21672A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698282 | |||||||
| chr3:115698287 | A | AAT | 119 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(116): Show |
121 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.628+21686_628+2168 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATAT | 3 | a0001c0001t0001g0041 a0001c0001t0005g0007 a0001c0001t0005g0009 |
3 | HG03195.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.628+21684_628+2168 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(26): Show |
1 | a0001c0001t0001g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(26): Show |
10 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0047 others(7): Show |
10 | HG00140.hp2 HG00741.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.628+21687_628+2168 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(28): Show |
184 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0045 others(181): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.628+21687_628+2168 others(39): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(30): Show |
1 | a0001c0001t0002g0294 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(41): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(59): Show |
1 | a0001c0001t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(70): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(61): Show |
7 | a0001c0001t0001g0032 a0001c0001t0002g0129 a0001c0001t0002g0130 others(4): Show |
7 | HG01433.hp2 NA18944.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.628+21687_628+2168 others(72): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(24): Show |
1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(35): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(26): Show |
1 | a0001c0001t0002g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(54): Show |
1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(65): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(30): Show |
1 | a0001c0001t0002g0200 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(41): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | AATATATA others(26): Show |
3 | a0001c0001t0001g0085 a0001c0001t0001g0269 a0001c0001t0002g0171 |
3 | NA18522.hp1 NA18943.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.628+21687_628+2171 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | ||||||
| chr3:115698287 | A | ATATATAT others(60): Show |
1 | a0001c0001t0002g0199 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.628+21677_628+2167 others(71): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698287 | |||||||
| chr3:115698287 | A | ATATATAT others(23): Show |
1 | a0001c0001t0003g0312 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.628+21677_628+2167 others(34): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698287 | |||||||
| chr3:115698298 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+21688T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698298 | |||||||
| chr3:115698299 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+21689A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698299 | |||||||
| chr3:115698312 | A | G | 1 | a0001c0001t0002g0226 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.628+21702A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698312 | |||||||
| chr3:115698316 | A | AAT | 33 | a0001c0001t0001g0167 a0001c0001t0001g0345 a0001c0001t0002g0271 others(30): Show |
34 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.628+21718_628+2171 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698316 | ||||||
| chr3:115698316 | A | T | 2 | a0001c0001t0002g0109 a0001c0001t0002g0147 |
2 | NA19012.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.628+21706A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698316 | |||||||
| chr3:115698326 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21716T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698326 | |||||||
| chr3:115698343 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.628+21733C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698343 | |||||||
| chr3:115698473 | G | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0221 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.628+21863G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698473 | |||||||
| chr3:115698925 | C | T | 12 | a0001c0001t0001g0041 a0001c0001t0002g0164 a0001c0001t0002g0303 others(9): Show |
12 | HG01081.hp2 HG01106.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.629-21869C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698925 | |||||||
| chr3:115698926 | G | A | 82 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0167 others(79): Show |
86 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.629-21868G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698926 | |||||||
| chr3:115698968 | T | A | 1 | a0001c0001t0005g0009 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.629-21826T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698968 | |||||||
| chr3:115698982 | CTG | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0093 |
3 | NA18747.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.629-21808_629-2180 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698982 | ||||||
| chr3:115699018 | C | T | 83 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0054 others(80): Show |
87 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.629-21776C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699018 | |||||||
| chr3:115699070 | A | G | 82 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0167 others(79): Show |
86 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.629-21724A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699070 | |||||||
| chr3:115699119 | G | A | 3 | a0001c0001t0001g0209 a0001c0001t0010g0238 a0001c0001t0010g0239 |
3 | HG02895.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.629-21675G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699119 | |||||||
| chr3:115699199 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-21595C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699199 | |||||||
| chr3:115699201 | C | G | 1 | a0001c0001t0001g0345 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.629-21593C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699201 | |||||||
| chr3:115699201 | C | T | 8 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-21593C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699201 | |||||||
| chr3:115699333 | C | T | 1 | a0001c0001t0002g0276 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.629-21461C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699333 | |||||||
| chr3:115699531 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-21263C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699531 | |||||||
| chr3:115699646 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.629-21148G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699646 | |||||||
| chr3:115699687 | T | C | 1 | a0001c0001t0004g0143 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.629-21107T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699687 | |||||||
| chr3:115699871 | G | T | 1 | a0001c0001t0002g0205 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.629-20923G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699871 | |||||||
| chr3:115700234 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.629-20560G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700234 | |||||||
| chr3:115700494 | A | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0266 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-20300A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700494 | |||||||
| chr3:115700520 | G | T | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.629-20274G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700520 | |||||||
| chr3:115700533 | A | C | 1 | a0001c0001t0002g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.629-20261A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700533 | |||||||
| chr3:115700556 | A | G | 8 | a0001c0001t0005g0007 a0001c0001t0005g0015 a0001c0001t0005g0016 others(5): Show |
8 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.629-20238A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700556 | |||||||
| chr3:115700889 | T | C | 1 | a0001c0001t0004g0190 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.629-19905T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700889 | |||||||
| chr3:115700895 | A | C | 11 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(8): Show |
11 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.629-19899A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700895 | |||||||
| chr3:115700948 | G | A | 175 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0032 others(172): Show |
175 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.629-19846G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700948 | |||||||
| chr3:115701065 | T | A | 1 | a0001c0001t0004g0201 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.629-19729T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701065 | |||||||
| chr3:115701257 | C | T | 165 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(162): Show |
165 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.629-19537C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701257 | |||||||
| chr3:115701345 | T | G | 11 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(8): Show |
11 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.629-19449T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701345 | |||||||
| chr3:115701671 | T | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0093 |
3 | NA18747.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.629-19123T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701671 | |||||||
| chr3:115701747 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-19047A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701747 | |||||||
| chr3:115701790 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-19004C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701790 | |||||||
| chr3:115702463 | C | T | 1 | a0001c0001t0005g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.629-18331C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702463 | |||||||
| chr3:115702738 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.629-18056C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702738 | |||||||
| chr3:115702769 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-18025C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702769 | |||||||
| chr3:115702843 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17951G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702843 | |||||||
| chr3:115702844 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17950G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702844 | |||||||
| chr3:115702845 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17949G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702845 | |||||||
| chr3:115702848 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17946A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702848 | |||||||
| chr3:115702850 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17944G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702850 | |||||||
| chr3:115702852 | T | A | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17942T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702852 | |||||||
| chr3:115702854 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17940T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702854 | |||||||
| chr3:115702857 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17937A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702857 | |||||||
| chr3:115702946 | G | A | 29 | a0001c0001t0001g0167 a0001c0001t0002g0271 a0001c0001t0002g0293 others(26): Show |
30 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.629-17848G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702946 | |||||||
| chr3:115702966 | T | A | 1 | a0001c0001t0001g0241 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17828T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702966 | |||||||
| chr3:115703023 | T | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0311 a0001c0001t0001g0338 |
3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-17771T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703023 | |||||||
| chr3:115703085 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-17709A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703085 | |||||||
| chr3:115703092 | A | G | 2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-17702A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703092 | |||||||
| chr3:115703218 | A | G | 11 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(8): Show |
11 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.629-17576A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703218 | |||||||
| chr3:115703457 | A | G | 1 | a0001c0001t0002g0326 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.629-17337A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703457 | |||||||
| chr3:115703494 | C | A | 173 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(170): Show |
178 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.629-17300C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703494 | |||||||
| chr3:115703700 | A | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0342 |
3 | HG01891.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.629-17094A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703700 | |||||||
| chr3:115703701 | T | C | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.629-17093T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703701 | |||||||
| chr3:115703760 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-17034C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703760 | |||||||
| chr3:115703777 | A | T | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.629-17017A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703777 | |||||||
| chr3:115703805 | G | A | 2 | a0001c0001t0003g0307 a0001c0001t0003g0308 |
2 | HG01517.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.629-16989G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703805 | |||||||
| chr3:115703912 | G | A | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(159): Show |
167 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.629-16882G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703912 | |||||||
| chr3:115703986 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.629-16808T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703986 | |||||||
| chr3:115704007 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.629-16787T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704007 | |||||||
| chr3:115704079 | C | A | 2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-16715C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704079 | |||||||
| chr3:115704257 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0247 |
2 | HG01071.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.629-16537T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704257 | |||||||
| chr3:115704279 | C | T | 1 | a0001c0001t0002g0030 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.629-16515C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704279 | |||||||
| chr3:115704292 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-16502C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704292 | |||||||
| chr3:115704382 | C | T | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-16412C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704382 | |||||||
| chr3:115704481 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.629-16313C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704481 | |||||||
| chr3:115704498 | A | G | 1 | a0001c0001t0003g0031 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.629-16296A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704498 | |||||||
| chr3:115704551 | C | T | 1 | a0001c0001t0019g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.629-16243C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704551 | |||||||
| chr3:115704662 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-16132G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704662 | |||||||
| chr3:115704753 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629-16041G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704753 | |||||||
| chr3:115704871 | A | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0346 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.629-15923A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704871 | |||||||
| chr3:115704957 | T | C | 8 | a0001c0001t0001g0059 a0001c0001t0001g0192 a0001c0001t0001g0232 others(5): Show |
8 | HG01071.hp2 HG01074.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-15837T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704957 | |||||||
| chr3:115704964 | G | T | 79 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0167 others(76): Show |
83 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.629-15830G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704964 | |||||||
| chr3:115704966 | C | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0311 a0001c0001t0001g0338 |
3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-15828C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704966 | |||||||
| chr3:115705129 | C | T | 9 | a0001c0001t0005g0007 a0001c0001t0005g0015 a0001c0001t0005g0016 others(6): Show |
9 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.629-15665C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705129 | |||||||
| chr3:115705200 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0173 a0001c0001t0001g0174 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-15594G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705200 | |||||||
| chr3:115705212 | G | A | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-15582G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705212 | |||||||
| chr3:115705226 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.629-15568G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705226 | |||||||
| chr3:115705302 | G | T | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-15492G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705302 | |||||||
| chr3:115705376 | CT | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-15417delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705376 | |||||||
| chr3:115705473 | T | G | 2 | a0001c0001t0003g0283 a0001c0001t0003g0312 |
2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.629-15321T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705473 | |||||||
| chr3:115705659 | C | T | 3 | a0001c0001t0002g0272 a0001c0001t0002g0313 a0001c0001t0002g0314 |
3 | NA18975.hp2 NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.629-15135C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705659 | |||||||
| chr3:115706127 | A | G | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-14667A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706127 | |||||||
| chr3:115706180 | CA | C | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-14607delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115706180 | ||||||
| chr3:115706298 | C | G | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0028 others(57): Show |
61 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.629-14496C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706298 | |||||||
| chr3:115706341 | G | C | 142 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0028 others(139): Show |
147 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.629-14453G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706341 | |||||||
| chr3:115706383 | A | G | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-14411A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706383 | |||||||
| chr3:115706397 | TG | T | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-14391delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115706397 | ||||||
| chr3:115706496 | A | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-14298A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706496 | |||||||
| chr3:115706664 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0002g0133 a0001c0001t0003g0196 others(2): Show |
5 | HG00140.hp1 HG00140.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-14130C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706664 | |||||||
| chr3:115706758 | C | G | 1 | a0001c0001t0002g0112 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.629-14036C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706758 | |||||||
| chr3:115706863 | A | T | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0028 others(57): Show |
61 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.629-13931A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706863 | |||||||
| chr3:115707178 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.629-13616T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707178 | |||||||
| chr3:115707332 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.629-13462G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707332 | |||||||
| chr3:115707427 | T | C | 339 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(336): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.629-13367T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707427 | |||||||
| chr3:115707463 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.629-13331T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707463 | |||||||
| chr3:115707532 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.629-13262C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707532 | |||||||
| chr3:115707762 | C | G | 80 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0167 others(77): Show |
84 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.629-13032C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707762 | |||||||
| chr3:115707781 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-13013G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707781 | |||||||
| chr3:115707886 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 |
3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.629-12908A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707886 | |||||||
| chr3:115707972 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.629-12822A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707972 | |||||||
| chr3:115707985 | C | T | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-12809C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707985 | |||||||
| chr3:115707990 | T | TAC | 5 | a0001c0001t0001g0041 a0001c0001t0001g0222 a0001c0001t0001g0302 others(2): Show |
5 | HG01069.hp2 HG01081.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-12780_629-1277 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115707990 | ||||||
| chr3:115707990 | T | TACAC | 12 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(9): Show |
12 | HG01081.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.629-12782_629-1277 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115707990 | ||||||
| chr3:115707990 | TAC | T | 126 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0035 others(123): Show |
130 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.629-12780_629-1277 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115707990 | ||||||
| chr3:115708000 | CACACACA others(9): Show |
C | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-12792_629-1277 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708000 | ||||||
| chr3:115708014 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0003g0001 a0001c0001t0003g0075 others(3): Show |
7 | HG01257.hp1 HG01258.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.629-12780C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708014 | |||||||
| chr3:115708016 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-12778T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708016 | |||||||
| chr3:115708024 | T | C | 4 | a0001c0001t0003g0001 a0001c0001t0003g0075 a0001c0001t0003g0117 others(1): Show |
5 | HG01257.hp1 HG01258.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-12770T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708024 | |||||||
| chr3:115708050 | A | T | 1 | a0001c0001t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.629-12744A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708050 | |||||||
| chr3:115708157 | A | G | 142 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0028 others(139): Show |
147 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.629-12637A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708157 | |||||||
| chr3:115708234 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-12560G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708234 | |||||||
| chr3:115708265 | G | T | 1 | a0001c0001t0002g0276 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.629-12529G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708265 | |||||||
| chr3:115708460 | A | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0311 a0001c0001t0001g0338 |
3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-12334A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708460 | |||||||
| chr3:115708528 | G | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0311 a0001c0001t0001g0338 |
3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-12266G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708528 | |||||||
| chr3:115708726 | A | G | 1 | a0001c0002t0002g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.629-12068A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708726 | |||||||
| chr3:115708903 | G | A | 1 | a0001c0001t0004g0279 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.629-11891G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708903 | |||||||
| chr3:115708940 | G | GT | 38 | a0001c0001t0001g0069 a0001c0001t0001g0076 a0001c0001t0001g0089 others(35): Show |
39 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.629-11830dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | ||||||
| chr3:115708940 | GT | G | 12 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0103 others(9): Show |
13 | HG00733.hp1 HG01069.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.629-11830delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | ||||||
| chr3:115708940 | GTTT | G | 25 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0072 others(22): Show |
25 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.629-11832_629-1183 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | ||||||
| chr3:115708940 | GTTTT | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(143): Show |
146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.629-11833_629-1183 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | ||||||
| chr3:115709251 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0311 a0001c0001t0001g0338 |
3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-11543G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709251 | |||||||
| chr3:115709391 | A | G | 339 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(336): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.629-11403A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709391 | |||||||
| chr3:115709582 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.629-11212G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709582 | |||||||
| chr3:115709661 | A | G | 1 | a0001c0001t0004g0184 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.629-11133A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709661 | |||||||
| chr3:115709762 | T | C | 177 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(174): Show |
177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-11032T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709762 | |||||||
| chr3:115709844 | C | CAT | 70 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0167 others(67): Show |
73 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.629-10930_629-1092 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | ||||||
| chr3:115709844 | C | CATAT | 20 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0066 others(17): Show |
20 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.629-10932_629-1092 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | ||||||
| chr3:115709844 | C | CATATAT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0341 a0001c0001t0003g0011 others(3): Show |
7 | HG02293.hp2 HG03453.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.629-10934_629-1092 others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | ||||||
| chr3:115709844 | C | CATATATA others(3): Show |
9 | a0001c0001t0001g0203 a0001c0001t0005g0007 a0001c0001t0005g0015 others(6): Show |
9 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.629-10938_629-1092 others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | ||||||
| chr3:115709844 | CAT | C | 175 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(172): Show |
175 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.629-10930_629-1092 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | ||||||
| chr3:115709848 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.629-10946T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709848 | |||||||
| chr3:115709856 | T | C | 4 | a0001c0001t0002g0111 a0001c0001t0002g0152 a0001c0001t0002g0227 others(1): Show |
4 | HG00621.hp2 NA18979.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-10938T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709856 | |||||||
| chr3:115709864 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.629-10930T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709864 | |||||||
| chr3:115709864 | T | TATATATA others(5): Show |
1 | a0001c0001t0005g0337 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.629-10929_629-1092 others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709864 | ||||||
| chr3:115709938 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.629-10856A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709938 | |||||||
| chr3:115710256 | CT | C | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-10527delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115710256 | ||||||
| chr3:115710405 | C | T | 6 | a0001c0001t0004g0177 a0001c0001t0004g0178 a0001c0001t0004g0182 others(3): Show |
6 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-10389C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710405 | |||||||
| chr3:115710633 | T | A | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-10161T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710633 | |||||||
| chr3:115710700 | A | T | 336 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(333): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.629-10094A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710700 | |||||||
| chr3:115710795 | T | G | 1 | a0001c0001t0004g0201 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.629-9999T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710795 | |||||||
| chr3:115710858 | T | C | 1 | a0001c0001t0002g0276 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.629-9936T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710858 | |||||||
| chr3:115710890 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-9904C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710890 | |||||||
| chr3:115711253 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0061 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.629-9541C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711253 | |||||||
| chr3:115711494 | TAC | T | 168 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(165): Show |
168 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.629-9283_629-9282d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115711494 | ||||||
| chr3:115711498 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0005g0007 a0001c0001t0005g0015 others(7): Show |
10 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.629-9296C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711498 | |||||||
| chr3:115711506 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.629-9288C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711506 | |||||||
| chr3:115711511 | A | C | 137 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0028 others(134): Show |
141 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.629-9283A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711511 | |||||||
| chr3:115711511 | ACC | A | 8 | a0001c0001t0001g0064 a0001c0001t0002g0060 a0001c0001t0002g0121 others(5): Show |
8 | HG00642.hp1 HG00733.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.629-9278_629-9277d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115711511 | ||||||
| chr3:115711513 | C | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-9281C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711513 | |||||||
| chr3:115711516 | C | A | 2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-9278C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711516 | |||||||
| chr3:115711561 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.629-9233T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711561 | |||||||
| chr3:115711595 | G | A | 2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-9199G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711595 | |||||||
| chr3:115711658 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0221 a0001c0001t0001g0266 |
3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-9136G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711658 | |||||||
| chr3:115711736 | C | T | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.629-9058C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711736 | |||||||
| chr3:115711763 | T | A | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-9031T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711763 | |||||||
| chr3:115711807 | CTGTT | C | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-8982_629-8979d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115711807 | ||||||
| chr3:115711948 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.629-8846A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711948 | |||||||
| chr3:115711958 | A | G | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-8836A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711958 | |||||||
| chr3:115712033 | C | T | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-8761C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712033 | |||||||
| chr3:115712183 | C | A | 176 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-8611C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712183 | |||||||
| chr3:115712193 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.629-8601A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712193 | |||||||
| chr3:115712321 | A | C | 54 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0042 others(51): Show |
54 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.629-8473A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712321 | |||||||
| chr3:115712360 | G | A | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-8434G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712360 | |||||||
| chr3:115712437 | TA | T | 163 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(160): Show |
168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-8353delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115712437 | ||||||
| chr3:115712621 | C | T | 1 | a0001c0001t0005g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.629-8173C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712621 | |||||||
| chr3:115712636 | C | G | 164 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(161): Show |
169 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.629-8158C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712636 | |||||||
| chr3:115712637 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.629-8157G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712637 | |||||||
| chr3:115712661 | T | C | 176 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0032 others(173): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-8133T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712661 | |||||||
| chr3:115712960 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.629-7834A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712960 | |||||||
| chr3:115712982 | GA | G | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-7809delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115712982 | ||||||
| chr3:115713026 | A | T | 1 | a0001c0001t0002g0347 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.629-7768A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713026 | |||||||
| chr3:115713040 | C | T | 177 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(174): Show |
177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-7754C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713040 | |||||||
| chr3:115713041 | G | A | 139 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0028 others(136): Show |
144 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.629-7753G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713041 | |||||||
| chr3:115713174 | A | T | 177 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0026 others(174): Show |
177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-7620A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713174 | |||||||
| chr3:115713389 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0153 a0001c0001t0001g0175 others(1): Show |
4 | HG02074.hp1 NA18968.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-7405G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713389 | |||||||
| chr3:115713637 | A | G | 1 | a0001c0002t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.629-7157A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713637 | |||||||
| chr3:115713709 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0001g0302 a0001c0001t0002g0236 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-7085T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713709 | |||||||
| chr3:115713724 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.629-7070A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713724 | |||||||
| chr3:115713800 | T | A | 1 | a0001c0001t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.629-6994T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713800 | |||||||
| chr3:115713977 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-6817T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713977 | |||||||
| chr3:115714097 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.629-6697G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714097 | |||||||
| chr3:115714197 | A | T | 1 | a0001c0001t0001g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.629-6597A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714197 | |||||||
| chr3:115714248 | A | G | 19 | a0001c0001t0001g0041 a0001c0001t0005g0007 a0001c0001t0005g0009 others(16): Show |
19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-6546A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714248 | |||||||
| chr3:115714403 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629-6391A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714403 | |||||||
| chr3:115714407 | GCAGGTTA | G | 5 | a0001c0001t0001g0224 a0001c0001t0001g0234 a0001c0001t0001g0235 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-6383_629-6377d others(9): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714407 | ||||||
| chr3:115714708 | GT | G | 339 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(336): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.629-6074delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714708 | ||||||
| chr3:115714827 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-5967T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714827 | |||||||
| chr3:115714869 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0213 |
2 | NA18939.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.629-5925G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714869 | |||||||
| chr3:115714873 | G | GCA | 114 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0028 others(111): Show |
118 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.629-5898_629-5897d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714873 | ||||||
| chr3:115714873 | G | GCACACAC others(1): Show |
18 | a0001c0001t0005g0007 a0001c0001t0005g0009 a0001c0001t0005g0015 others(15): Show |
18 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-5904_629-5897d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714873 | ||||||
| chr3:115714873 | GCA | G | 6 | a0001c0001t0001g0209 a0001c0001t0001g0224 a0001c0001t0001g0234 others(3): Show |
6 | HG02109.hp2 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-5898_629-5897d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714873 | ||||||
| chr3:115714890 | C | T | 171 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0042 others(168): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.629-5904C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714890 | |||||||
| chr3:115714964 | C | A | 81 | a0001c0001t0001g0167 a0001c0001t0002g0129 a0001c0001t0002g0130 others(78): Show |
85 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.629-5830C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714964 | |||||||
| chr3:115715019 | A | G | 19 | a0001c0001t0001g0041 a0001c0001t0005g0007 a0001c0001t0005g0009 others(16): Show |
19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-5775A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715019 | |||||||
| chr3:115715079 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.629-5715C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715079 | |||||||
| chr3:115715129 | G | A | 1 | a0001c0001t0003g0031 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.629-5665G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715129 | |||||||
| chr3:115715273 | A | T | 1 | a0001c0001t0002g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.629-5521A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715273 | |||||||
| chr3:115715323 | C | T | 25 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0028 others(22): Show |
25 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.629-5471C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715323 | |||||||
| chr3:115715466 | C | T | 293 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0032 others(290): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.629-5328C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715466 | |||||||
| chr3:115715477 | A | G | 4 | a0001c0001t0002g0086 a0001c0001t0002g0164 a0001c0001t0002g0303 others(1): Show |
4 | HG01106.hp1 HG02280.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-5317A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715477 | |||||||
| chr3:115715604 | G | T | 1 | a0001c0001t0001g0332 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.629-5190G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715604 | |||||||
| chr3:115715912 | A | G | 1 | a0001c0001t0009g0188 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.629-4882A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715912 | |||||||
| chr3:115715914 | G | A | 1 | a0001c0001t0005g0009 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.629-4880G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715914 | |||||||
| chr3:115715933 | C | G | 19 | a0001c0001t0001g0041 a0001c0001t0005g0007 a0001c0001t0005g0009 others(16): Show |
19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-4861C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715933 | |||||||
| chr3:115716158 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.629-4636A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716158 | |||||||
| chr3:115716195 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.629-4599G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716195 | |||||||
| chr3:115716510 | T | C | 4 | a0001c0001t0002g0012 a0001c0001t0002g0106 a0001c0001t0002g0124 others(1): Show |
4 | HG01255.hp2 HG02735.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4284T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716510 | |||||||
| chr3:115716710 | TCAGA | T | 12 | a0001c0001t0001g0054 a0001c0001t0001g0083 a0001c0001t0001g0173 others(9): Show |
12 | HG00621.hp1 HG01099.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.629-4081_629-4078d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716710 | ||||||
| chr3:115716711 | C | CAA | 3 | a0001c0001t0002g0205 a0001c0001t0002g0243 a0001c0001t0002g0265 |
3 | HG00280.hp1 HG00280.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.629-4082_629-4081i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAG | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0056 others(13): Show |
16 | HG00621.hp2 HG01074.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.629-4081_629-4080d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAA | C | 26 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0058 others(23): Show |
26 | HG00438.hp1 HG01175.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.629-4081_629-4076d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(1): Show |
C | 49 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0059 others(46): Show |
49 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.629-4081_629-4074d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(3): Show |
C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0049 a0001c0001t0001g0050 others(11): Show |
14 | HG00140.hp1 HG01256.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-4081_629-4072d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(5): Show |
C | 18 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0092 others(15): Show |
18 | HG00609.hp1 HG01106.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-4081_629-4070d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(7): Show |
C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0097 others(3): Show |
6 | HG00733.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4081_629-4068d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(9): Show |
C | 4 | a0001c0001t0001g0094 a0001c0001t0001g0187 a0001c0001t0001g0247 others(1): Show |
4 | HG01071.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4081_629-4066d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(11): Show |
C | 1 | a0001c0001t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629-4081_629-4064d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(13): Show |
C | 4 | a0001c0001t0002g0212 a0001c0001t0002g0226 a0001c0001t0002g0280 others(1): Show |
4 | HG03927.hp2 NA18965.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4081_629-4062d others(22): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(15): Show |
C | 4 | a0001c0001t0001g0174 a0001c0001t0001g0198 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG06807.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4081_629-4060d others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(17): Show |
C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0346 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.629-4081_629-4058d others(26): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716711 | CAGACAAA others(23): Show |
C | 1 | a0001c0001t0016g0270 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.629-4081_629-4052d others(32): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | ||||||
| chr3:115716713 | G | A | 8 | a0001c0001t0001g0055 a0001c0001t0001g0146 a0001c0001t0002g0131 others(5): Show |
8 | HG00738.hp1 HG01943.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-4081G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716713 | |||||||
| chr3:115716713 | G | T | 5 | a0001c0001t0001g0241 a0001c0001t0002g0205 a0001c0001t0002g0243 others(2): Show |
5 | HG00280.hp1 HG00280.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-4081G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716713 | |||||||
| chr3:115716715 | C | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0056 others(13): Show |
16 | HG00621.hp2 HG01074.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.629-4079C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716715 | |||||||
| chr3:115716715 | C | T | 14 | a0001c0001t0001g0055 a0001c0001t0001g0146 a0001c0001t0001g0241 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-4079C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716715 | |||||||
| chr3:115716716 | AAATATAT others(6): Show |
A | 1 | a0001c0001t0003g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.629-4076_629-4064d others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716716 | ||||||
| chr3:115716717 | A | AAT | 4 | a0001c0001t0001g0093 a0001c0001t0001g0266 a0001c0001t0003g0156 others(1): Show |
4 | HG00642.hp2 HG02970.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4027_629-4026d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | A | AATATATA others(5): Show |
1 | a0001c0001t0003g0287 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.629-4037_629-4026d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | A | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0055 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.629-4077A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716717 | |||||||
| chr3:115716717 | AAT | A | 18 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0091 others(15): Show |
18 | HG01433.hp2 HG02071.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-4027_629-4026d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATAT | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0108 others(14): Show |
18 | HG00738.hp2 HG01169.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.629-4029_629-4026d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATAT | A | 18 | a0001c0001t0001g0028 a0001c0001t0001g0071 a0001c0001t0001g0194 others(15): Show |
18 | HG00544.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.629-4031_629-4026d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(1): Show |
A | 33 | a0001c0001t0001g0021 a0001c0001t0001g0167 a0001c0001t0001g0228 others(30): Show |
33 | HG00609.hp2 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.629-4033_629-4026d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(3): Show |
A | 3 | a0001c0001t0001g0170 a0001c0001t0003g0082 a0001c0001t0004g0161 |
3 | HG02683.hp2 HG03942.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.629-4035_629-4026d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(5): Show |
A | 13 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0003g0295 others(10): Show |
13 | HG00438.hp2 HG01361.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.629-4037_629-4026d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(7): Show |
A | 6 | a0001c0001t0001g0345 a0001c0001t0005g0016 a0001c0001t0005g0277 others(3): Show |
6 | HG01081.hp2 HG01109.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4039_629-4026d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(9): Show |
A | 4 | a0001c0001t0004g0057 a0001c0001t0005g0105 a0001c0001t0005g0233 others(1): Show |
4 | HG02083.hp2 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4041_629-4026d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(11): Show |
A | 2 | a0001c0001t0001g0221 a0001c0001t0005g0172 |
2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.629-4043_629-4026d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(13): Show |
A | 2 | a0001c0001t0002g0130 a0001c0001t0013g0219 |
2 | NA19066.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.629-4045_629-4026d others(22): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(15): Show |
A | 1 | a0001c0001t0004g0305 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.629-4047_629-4026d others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(19): Show |
A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0298 others(1): Show |
4 | HG02055.hp1 HG03139.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4051_629-4026d others(28): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716717 | AATATATA others(25): Show |
A | 1 | a0001c0001t0001g0186 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.629-4057_629-4026d others(34): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | ||||||
| chr3:115716719 | T | A | 26 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0058 others(23): Show |
26 | HG00438.hp1 HG01175.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.629-4075T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716719 | |||||||
| chr3:115716721 | T | A | 49 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0059 others(46): Show |
49 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.629-4073T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716721 | |||||||
| chr3:115716723 | T | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0049 a0001c0001t0001g0050 others(11): Show |
14 | HG00140.hp1 HG01256.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-4071T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716723 | |||||||
| chr3:115716725 | T | A | 18 | a0001c0001t0001g0061 a0001c0001t0001g0072 a0001c0001t0001g0092 others(15): Show |
18 | HG00609.hp1 HG01106.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-4069T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716725 | |||||||
| chr3:115716727 | T | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0097 others(3): Show |
6 | HG00733.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4067T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716727 | |||||||
| chr3:115716729 | T | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0187 a0001c0001t0001g0247 others(1): Show |
4 | HG01071.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4065T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716729 | |||||||
| chr3:115716729 | T | TATATATA others(12): Show |
1 | a0001c0001t0003g0031 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.629-4064_629-4046d others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716729 | ||||||
| chr3:115716731 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629-4063T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716731 | |||||||
| chr3:115716733 | T | A | 4 | a0001c0001t0002g0212 a0001c0001t0002g0226 a0001c0001t0002g0280 others(1): Show |
4 | HG03927.hp2 NA18965.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4061T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716733 | |||||||
| chr3:115716735 | T | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0198 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG06807.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4059T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716735 | |||||||
| chr3:115716736 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-4058A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716736 | |||||||
| chr3:115716737 | T | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0346 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.629-4057T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716737 | |||||||
| chr3:115716737 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-4057T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716737 | |||||||
| chr3:115716739 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-4055T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716739 | |||||||
| chr3:115716743 | T | A | 1 | a0001c0001t0016g0270 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.629-4051T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716743 | |||||||
| chr3:115716749 | TATATATA others(19): Show |
T | 1 | a0001c0001t0001g0335 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.629-4043_629-4018d others(28): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716749 | ||||||
| chr3:115716754 | A | G | 1 | a0001c0002t0017g0310 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.629-4040A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716754 | |||||||
| chr3:115716757 | TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0116 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.629-4035_629-4020d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716757 | ||||||
| chr3:115716759 | T | C | 24 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0035 others(21): Show |
24 | HG00733.hp1 HG00735.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.629-4035T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716759 | |||||||
| chr3:115716759 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-4033_629-4020d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716759 | ||||||
| chr3:115716761 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0023 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.629-4031_629-4018d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716761 | ||||||
| chr3:115716763 | TATATACA others(5): Show |
T | 2 | a0001c0001t0001g0315 a0001c0002t0001g0004 |
2 | HG03654.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.629-4029_629-4018d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716763 | ||||||
| chr3:115716765 | T | C | 18 | a0001c0001t0001g0041 a0001c0001t0001g0216 a0001c0001t0005g0007 others(15): Show |
18 | HG01081.hp2 HG01361.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.629-4029T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716765 | |||||||
| chr3:115716765 | TATACAGA others(3): Show |
T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0077 |
2 | HG01261.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.629-4027_629-4018d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716765 | ||||||
| chr3:115716767 | T | C | 14 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.629-4027T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716767 | |||||||
| chr3:115716767 | T | G | 16 | a0001c0001t0001g0041 a0001c0001t0001g0338 a0001c0001t0005g0007 others(13): Show |
16 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.629-4027T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716767 | |||||||
| chr3:115716767 | TACAG | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0203 a0001c0002t0001g0151 |
3 | HG02293.hp2 NA18747.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.629-4025_629-4022d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716767 | ||||||
| chr3:115716769 | C | CAGAG | 4 | a0001c0001t0005g0105 a0001c0001t0005g0172 a0001c0001t0005g0233 others(1): Show |
4 | HG02559.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4006_629-4003d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716769 | ||||||
| chr3:115716769 | C | G | 19 | a0001c0001t0001g0041 a0001c0001t0001g0260 a0001c0001t0001g0338 others(16): Show |
19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-4025C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716769 | |||||||
| chr3:115716769 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.629-4025C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716769 | |||||||
| chr3:115716769 | CAGAGAGA others(1): Show |
C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0223 a0001c0001t0001g0343 others(1): Show |
4 | HG02922.hp1 HG02970.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4010_629-4003d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716769 | ||||||
| chr3:115716771 | G | T | 3 | a0001c0001t0001g0093 a0001c0001t0019g0017 a0001c0002t0001g0134 |
3 | HG04228.hp2 NA18945.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.629-4023G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716771 | |||||||
| chr3:115716773 | G | T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0093 a0001c0001t0001g0203 others(3): Show |
6 | HG02293.hp2 HG04228.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-4021G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716773 | |||||||
| chr3:115716775 | G | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0222 a0001c0001t0019g0017 |
3 | HG02717.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.629-4019G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716775 | |||||||
| chr3:115716775 | G | T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0093 a0001c0001t0001g0203 others(3): Show |
6 | HG02293.hp2 NA18747.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4019G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716775 | |||||||
| chr3:115716777 | G | C | 13 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0066 others(10): Show |
14 | HG01261.hp1 HG02293.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.629-4017G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716777 | |||||||
| chr3:115716841 | A | C | 1 | a0001c0001t0003g0018 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.629-3953A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716841 | |||||||
| chr3:115716847 | T | C | 338 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(335): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.629-3947T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716847 | |||||||
| chr3:115716964 | C | A | 7 | a0001c0001t0001g0069 a0001c0001t0001g0224 a0001c0001t0001g0234 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.629-3830C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716964 | |||||||
| chr3:115716985 | G | A | 3 | a0001c0001t0001g0209 a0001c0001t0010g0238 a0001c0001t0010g0239 |
3 | HG02895.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.629-3809G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716985 | |||||||
| chr3:115717001 | C | T | 1 | a0001c0001t0003g0013 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.629-3793C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717001 | |||||||
| chr3:115717043 | G | T | 17 | a0001c0001t0005g0007 a0001c0001t0005g0009 a0001c0001t0005g0015 others(14): Show |
17 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.629-3751G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717043 | |||||||
| chr3:115717159 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0221 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-3635G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717159 | |||||||
| chr3:115717214 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0338 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-3580G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717214 | |||||||
| chr3:115717315 | C | CT | 194 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0042 others(191): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.629-3466dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717315 | ||||||
| chr3:115717315 | C | CTT | 91 | a0001c0001t0001g0041 a0001c0001t0001g0167 a0001c0001t0001g0260 others(88): Show |
95 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.629-3467_629-3466d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717315 | ||||||
| chr3:115717358 | G | A | 5 | a0001c0001t0001g0209 a0001c0001t0002g0236 a0001c0001t0002g0237 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-3436G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717358 | |||||||
| chr3:115717497 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0259 |
2 | NA18943.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.629-3297C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717497 | |||||||
| chr3:115717498 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.629-3296G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717498 | |||||||
| chr3:115717669 | C | CT | 12 | a0001c0001t0003g0002 a0001c0001t0003g0070 a0001c0001t0003g0078 others(9): Show |
13 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.629-3109dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717669 | ||||||
| chr3:115717669 | CT | C | 24 | a0001c0001t0001g0041 a0001c0001t0001g0198 a0001c0001t0001g0260 others(21): Show |
24 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.629-3109delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717669 | ||||||
| chr3:115717797 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0221 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-2997G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717797 | |||||||
| chr3:115718277 | G | T | 1 | a0001c0001t0012g0301 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.629-2517G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718277 | |||||||
| chr3:115718328 | T | C | 180 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0042 others(177): Show |
180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.629-2466T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718328 | |||||||
| chr3:115718358 | T | A | 1 | a0001c0001t0004g0250 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.629-2436T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718358 | |||||||
| chr3:115718427 | C | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0338 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-2367C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718427 | |||||||
| chr3:115718460 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0221 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-2334G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718460 | |||||||
| chr3:115718552 | A | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0185 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.629-2242A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718552 | |||||||
| chr3:115718595 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0338 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-2199A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718595 | |||||||
| chr3:115718728 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.629-2066G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718728 | |||||||
| chr3:115718757 | T | C | 5 | a0001c0001t0001g0209 a0001c0001t0002g0236 a0001c0001t0002g0237 others(2): Show |
5 | HG02145.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-2037T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718757 | |||||||
| chr3:115718852 | A | G | 2 | a0001c0001t0002g0236 a0001c0001t0002g0237 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.629-1942A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718852 | |||||||
| chr3:115718912 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-1882T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718912 | |||||||
| chr3:115719078 | C | G | 2 | a0001c0001t0010g0238 a0001c0001t0010g0239 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-1716C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719078 | |||||||
| chr3:115719268 | GA | G | 179 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0042 others(176): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.629-1515delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115719268 | ||||||
| chr3:115719295 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.629-1499G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719295 | |||||||
| chr3:115719416 | C | G | 1 | a0001c0002t0001g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.629-1378C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719416 | |||||||
| chr3:115719441 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.629-1353G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719441 | |||||||
| chr3:115719448 | C | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0021 others(43): Show |
47 | HG01109.hp1 HG01261.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.629-1346C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719448 | |||||||
| chr3:115719456 | C | G | 3 | a0001c0001t0002g0272 a0001c0001t0002g0313 a0001c0001t0002g0314 |
3 | NA18975.hp2 NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.629-1338C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719456 | |||||||
| chr3:115719811 | G | A | 75 | a0001c0001t0002g0293 a0001c0001t0003g0001 a0001c0001t0003g0002 others(72): Show |
79 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.629-983G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719811 | |||||||
| chr3:115719907 | A | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
2 | NA18950.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.629-887A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719907 | |||||||
| chr3:115720003 | G | A | 338 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0019 others(335): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.629-791G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115720003 | |||||||
| chr3:115720405 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0338 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-389C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115720405 | |||||||
| chr3:115720529 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0338 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-265T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115720529 |