Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2650 |
| ensemblid | ENSG00000187210.14 |
| hgncid | 4203 |
| symbol | GCNT1 |
| name | glucosaminyl (N-acetyl) transferase 1 |
| refseq_nuc | NM_001490.5 |
| refseq_prot | NP_001481.2 |
| ensembl_nuc | ENST00000376730.5 |
| ensembl_prot | ENSP00000365920.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 76459182 |
| end | 76507416 |
| strand | + |
| ver | v1.2 |
| region | chr9:76459182-76507416 |
| region5000 | chr9:76454182-76512416 |
| regionname0 | GCNT1_chr9_76459182_76507416 |
| regionname5000 | GCNT1_chr9_76454182_76512416 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 428 | 252 | 63 | 50 | 99 | 12 | 26 | 67 | GCNT1_chr9_76454182_76512416 | GCNT1 | MLRTL others(423): Show |
chr9 | 76454182 | 76512416 |
| a0002 | 0/0 | 428 | 111 | 21 | 21 | 46 | 5 | 18 | 34 | GCNT1_chr9_76454182_76512416 | GCNT1 | MLRTL others(423): Show |
chr9 | 76454182 | 76512416 |
| a0003 | 0/0 | 428 | 3 | 2 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | MLRTL others(423): Show |
chr9 | 76454182 | 76512416 |
| a0004 | 0/0 | 428 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | MLRTL others(423): Show |
chr9 | 76454182 | 76512416 |
| a0005 | 0/0 | 428 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | MLRTL others(423): Show |
chr9 | 76454182 | 76512416 |
| a0006 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | MLRTL others(423): Show |
chr9 | 76454182 | 76512416 |
| a0007 | 0/0 | 428 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | MLRTL others(423): Show |
chr9 | 76454182 | 76512416 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1284 | 251 | 63 | 50 | 99 | 12 | 25 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0001c0007 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0002c0002 | 0/0 | 1284 | 108 | 20 | 21 | 46 | 5 | 16 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0002c0004 | 0/0 | 1284 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0002c0006 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0003c0003 | 0/0 | 1284 | 3 | 2 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0004c0009 | 0/0 | 1284 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0005c0010 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0006c0005 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 | ||
| a0007c0008 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ATGCT others(1279): Show |
chr9 | 76454182 | 76512416 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 5566 | 77 | 1 | 11 | 54 | 4 | 6 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0003 | 1/0 | 5566 | 39 | 5 | 12 | 10 | 5 | 6 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0004 | 0/0 | 5566 | 25 | 7 | 9 | 2 | 0 | 7 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0005 | 0/0 | 5569 | 19 | 3 | 6 | 6 | 3 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0006 | 0/0 | 5570 | 17 | 2 | 2 | 11 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5565): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0007 | 0/0 | 5568 | 12 | 10 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0008 | 0/0 | 5566 | 10 | 9 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0010 | 0/0 | 5566 | 6 | 0 | 0 | 6 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0011 | 0/0 | 5565 | 6 | 4 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5560): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0012 | 0/0 | 5569 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0013 | 0/0 | 5570 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5565): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0014 | 0/0 | 5568 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0018 | 0/0 | 5568 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0019 | 0/0 | 5566 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0020 | 0/0 | 5568 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0021 | 0/0 | 5568 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0022 | 0/0 | 5566 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0023 | 0/0 | 5566 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0024 | 0/0 | 5569 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0025 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0026 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0027 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0029 | 0/0 | 5566 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0030 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0031 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0032 | 0/0 | 5544 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5539): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0033 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0034 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0035 | 0/0 | 5569 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0036 | 0/0 | 5569 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0037 | 0/0 | 5570 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5565): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0038 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0040 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0045 | 0/0 | 5565 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5560): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0046 | 0/0 | 5566 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0001t0047 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0001c0007t0003 | 0/0 | 5566 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0001 | 0/0 | 5568 | 92 | 14 | 17 | 40 | 5 | 16 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0009 | 0/0 | 5568 | 6 | 5 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0015 | 0/0 | 5565 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5560): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0016 | 0/0 | 5568 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0041 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0042 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0043 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0002t0044 | 0/0 | 5568 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0004t0001 | 0/0 | 5568 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0002c0004t0028 | 0/0 | 5569 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5564): Show |
chr9 | 76454182 | 76512416 |
| a0002c0006t0009 | 0/0 | 5568 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5563): Show |
chr9 | 76454182 | 76512416 |
| a0003c0003t0017 | 0/0 | 5565 | 3 | 2 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5560): Show |
chr9 | 76454182 | 76512416 |
| a0004c0009t0003 | 0/0 | 5566 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0005c0010t0039 | 0/0 | 5565 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5560): Show |
chr9 | 76454182 | 76512416 |
| a0006c0005t0002 | 0/0 | 5566 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| a0007c0008t0004 | 0/0 | 5566 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | ACGCT others(5561): Show |
chr9 | 76454182 | 76512416 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0005 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0006g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0012g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0012g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0013g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0013g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0018g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0018g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0019g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0019g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0020g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0020g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0021g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0021g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0022g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0022g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0023g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0023g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0024g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0025g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0026g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0027g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0029g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0030g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0031g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0032g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0033g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0035g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0036g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0037g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0038g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0040g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0045g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0046g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0001t0047g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0001c0007t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0015g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0015g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0016g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0016g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0041g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0042g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0043g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0002t0044g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0004t0028g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0002c0006t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0003c0003t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0003c0003t0017g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0003c0003t0017g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0004c0009t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0005c0010t0039g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0006c0005t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| a0007c0008t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0058 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | GBR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0259 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0324 | EUR | FIN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00408 | hp2 | a0001 | c0001 | t0030 | g0116 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0166 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | CHS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0158 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0304 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0113 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0130 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01074 | hp2 | a0002 | c0002 | t0016 | g0004 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01099 | hp2 | a0004 | c0009 | t0003 | g0054 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01106 | hp2 | a0002 | c0002 | t0009 | g0267 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0303 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0025 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01168 | hp2 | a0002 | c0002 | t0016 | g0004 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01169 | hp1 | a0002 | c0002 | t0016 | g0027 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0025 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0168 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0292 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0017 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0298 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01257 | hp1 | a0001 | c0001 | t0013 | g0325 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01361 | hp2 | a0001 | c0001 | t0024 | g0162 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0170 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01496 | hp1 | a0001 | c0001 | t0037 | g0323 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01496 | hp2 | a0001 | c0001 | t0029 | g0094 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0252 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0072 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0021 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0095 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0021 | EUR | IBS | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01884 | hp1 | a0001 | c0001 | t0021 | g0318 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0320 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01891 | hp2 | a0001 | c0001 | t0035 | g0194 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01928 | hp1 | a0001 | c0001 | t0046 | g0096 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0245 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02040 | hp2 | a0001 | c0001 | t0011 | g0216 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02055 | hp1 | a0003 | c0003 | t0017 | g0186 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0226 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0309 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02135 | hp1 | a0001 | c0001 | t0010 | g0211 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02145 | hp2 | a0002 | c0002 | t0041 | g0274 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | CDX | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0257 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0032 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0167 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | KHV | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02572 | hp2 | a0001 | c0001 | t0040 | g0047 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0190 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0197 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02698 | hp1 | a0001 | c0001 | t0031 | g0154 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02698 | hp2 | a0001 | c0001 | t0025 | g0059 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02717 | hp1 | a0001 | c0001 | t0045 | g0037 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02717 | hp2 | a0005 | c0010 | t0039 | g0048 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0306 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0276 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0312 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0308 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0241 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02818 | hp1 | a0002 | c0002 | t0009 | g0040 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0213 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02886 | hp1 | a0001 | c0001 | t0018 | g0087 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0227 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0050 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02897 | hp2 | a0002 | c0002 | t0009 | g0046 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0028 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02965 | hp2 | a0001 | c0001 | t0034 | g0031 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0256 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02976 | hp1 | a0002 | c0006 | t0009 | g0041 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0086 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03130 | hp1 | a0001 | c0001 | t0023 | g0177 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03453 | hp2 | a0001 | c0001 | t0022 | g0083 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0280 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0044 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0174 | AFR | ESN | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | GWD | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0322 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0199 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0275 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0321 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03704 | hp2 | a0001 | c0007 | t0003 | g0010 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03710 | hp1 | a0002 | c0004 | t0001 | g0281 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0183 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03927 | hp1 | a0001 | c0001 | t0027 | g0103 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0290 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0269 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0289 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04184 | hp2 | a0002 | c0004 | t0028 | g0151 | SAS | BEB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0278 | SAS | STU | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18522 | hp1 | a0001 | c0001 | t0026 | g0326 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18522 | hp2 | a0001 | c0001 | t0023 | g0176 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18906 | hp1 | a0002 | c0002 | t0009 | g0039 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18948 | hp1 | a0002 | c0002 | t0044 | g0286 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18949 | hp1 | a0001 | c0001 | t0032 | g0135 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18950 | hp2 | a0001 | c0001 | t0047 | g0287 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18960 | hp1 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18960 | hp2 | a0006 | c0005 | t0002 | g0144 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0314 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18964 | hp2 | a0001 | c0001 | t0038 | g0143 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0316 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18966 | hp1 | a0002 | c0002 | t0015 | g0019 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18969 | hp1 | a0001 | c0001 | t0006 | g0024 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18983 | hp2 | a0001 | c0001 | t0033 | g0084 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18986 | hp1 | a0001 | c0001 | t0019 | g0147 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18991 | hp1 | a0002 | c0002 | t0043 | g0279 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18999 | hp1 | a0002 | c0002 | t0015 | g0019 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0311 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0205 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19004 | hp1 | a0002 | c0002 | t0042 | g0223 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19005 | hp2 | a0001 | c0001 | t0010 | g0212 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19011 | hp1 | a0001 | c0001 | t0019 | g0185 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19012 | hp2 | a0001 | c0001 | t0036 | g0107 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0172 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0299 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19060 | hp2 | a0002 | c0002 | t0015 | g0020 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0215 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19079 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19084 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19089 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19091 | hp2 | a0001 | c0001 | t0010 | g0208 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA19240 | hp2 | a0002 | c0002 | t0009 | g0268 | AFR | YRI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | ASW | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ASW | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0157 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20752 | hp2 | a0003 | c0003 | t0017 | g0222 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0243 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | TSI | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | GIH | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0288 | SAS | GIH | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0240 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0307 | AMR | CLM | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02109 | hp2 | a0001 | c0001 | t0022 | g0082 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02486 | hp1 | a0001 | c0001 | t0021 | g0319 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02486 | hp2 | a0002 | c0002 | t0009 | g0045 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0228 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | ACB | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0171 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG03471 | hp2 | a0003 | c0003 | t0017 | g0236 | AFR | MSL | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0300 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA20300 | hp2 | a0001 | c0001 | t0018 | g0088 | AFR | USA | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA21309 | hp1 | a0007 | c0008 | t0004 | g0201 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| NA21309 | hp2 | a0001 | c0001 | t0012 | g0164 | AFR | LWK | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0102 | REF | REF | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0180 | REF | REF | GCNT1_chr9_76454182_76512416 | GCNT1 | chr9 | 76454182 | 76512416 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76460061 | G | T | 1 | a0001 | 2 | HG01884.hp1 HG02486.hp1 |
splice_region_variant | LOW | c.-406G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/4 | chr9 | 76460061 | |||||||
| chr9:76460062 | C | T | 1 | a0001 | 2 | HG01884.hp1 HG02486.hp1 |
splice_region_variant | LOW | c.-405C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/4 | chr9 | 76460062 | |||||||
| chr9:76502475 | T | A | 1 | a0006 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.94T>A | p.Leu32Ile | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 625/5566 | 94/1287 | 32/428 | chr9 | 76502475 | |||
| chr9:76502737 | C | A | 1 | a0003 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.356C>A | p.Ala119Glu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 887/5566 | 356/1287 | 119/428 | chr9 | 76502737 | |||
| chr9:76502835 | A | G | 2 | a0002 a0005 |
112 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
missense_variant | MODERATE | c.454A>G | p.Ile152Val | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 985/5566 | 454/1287 | 152/428 | chr9 | 76502835 | |||
| chr9:76502854 | C | G | 1 | a0004 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.473C>G | p.Ser158Cys | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1004/5566 | 473/1287 | 158/428 | chr9 | 76502854 | |||
| chr9:76503484 | C | T | 1 | a0007 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1103C>T | p.Pro368Leu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1634/5566 | 1103/1287 | 368/428 | chr9 | 76503484 | |||
| chr9:76503612 | A | T | 1 | a0005 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1231A>T | p.Ile411Phe | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1762/5566 | 1231/1287 | 411/428 | chr9 | 76503612 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76502573 | G | A | 1 | a0002c0006 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.192G>A | p.Gln64Gln | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 723/5566 | 192/1287 | 64/428 | chr9 | 76502573 | |||
| chr9:76503084 | T | C | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.703T>C | p.Leu235Leu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1234/5566 | 703/1287 | 235/428 | chr9 | 76503084 | |||
| chr9:76503413 | G | A | 3 | a0002c0002 a0002c0006 a0005c0010 |
110 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
synonymous_variant | LOW | c.1032G>A | p.Leu344Leu | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1563/5566 | 1032/1287 | 344/428 | chr9 | 76503413 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76459239 | G | C | 1 | a0001c0001t0024 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-474G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/4 | 43143 | chr9 | 76459239 | ||||||
| chr9:76459244 | C | T | 2 | a0001c0001t0022 a0001c0001t0023 |
4 | HG02109.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-469C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/4 | 43138 | chr9 | 76459244 | ||||||
| chr9:76460114 | C | T | 1 | a0001c0001t0047 | 1 | NA18950.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-353C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/4 | chr9 | 76460114 | |||||||
| chr9:76500928 | A | C | 39 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(36): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
5_prime_UTR_variant | MODIFIER | c.-277A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/4 | 1454 | chr9 | 76500928 | ||||||
| chr9:76500965 | A | G | 1 | a0001c0001t0046 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-240A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/4 | 1417 | chr9 | 76500965 | ||||||
| chr9:76502376 | T | C | 1 | a0001c0001t0046 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 6 | chr9 | 76502376 | ||||||
| chr9:76503675 | C | T | 1 | a0001c0001t0018 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 7 | chr9 | 76503675 | ||||||
| chr9:76503681 | A | G | 1 | a0003c0003t0017 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 13 | chr9 | 76503681 | ||||||
| chr9:76503712 | C | T | 5 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0020 others(2): Show |
15 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*44C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 44 | chr9 | 76503712 | ||||||
| chr9:76503715 | AC | A | 20 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0014 others(17): Show |
144 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*50delC | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 50 | INFO_REALIGN_3_PRIME | chr9 | 76503715 | |||||
| chr9:76503745 | A | G | 37 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(34): Show |
260 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*77A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 77 | chr9 | 76503745 | ||||||
| chr9:76503769 | C | T | 1 | a0001c0001t0021 | 2 | HG01884.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*101C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 101 | chr9 | 76503769 | ||||||
| chr9:76503962 | G | A | 1 | a0001c0001t0029 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 294 | chr9 | 76503962 | ||||||
| chr9:76503987 | A | C | 8 | a0002c0002t0001 a0002c0002t0015 a0002c0002t0016 others(5): Show |
103 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*319A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 319 | chr9 | 76503987 | ||||||
| chr9:76504300 | C | T | 1 | a0001c0001t0023 | 2 | HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*632C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 632 | chr9 | 76504300 | ||||||
| chr9:76504363 | C | T | 1 | a0001c0001t0038 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 695 | chr9 | 76504363 | ||||||
| chr9:76504454 | C | T | 1 | a0001c0001t0018 | 3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*786C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 786 | chr9 | 76504454 | ||||||
| chr9:76504548 | A | T | 1 | a0001c0001t0037 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 880 | chr9 | 76504548 | ||||||
| chr9:76504566 | G | A | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0019 others(3): Show |
41 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*898G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 898 | chr9 | 76504566 | ||||||
| chr9:76504836 | C | T | 19 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(16): Show |
81 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1168C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1168 | chr9 | 76504836 | ||||||
| chr9:76504913 | A | AT | 3 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0037 |
21 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1256dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1257 | INFO_REALIGN_3_PRIME | chr9 | 76504913 | |||||
| chr9:76505052 | G | T | 1 | a0002c0002t0016 | 3 | HG01074.hp2 HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1384G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1384 | chr9 | 76505052 | ||||||
| chr9:76505382 | C | T | 4 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0021 others(1): Show |
9 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1714C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1714 | chr9 | 76505382 | ||||||
| chr9:76505438 | T | C | 1 | a0001c0001t0012 | 3 | HG01891.hp1 NA19030.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1770 | chr9 | 76505438 | ||||||
| chr9:76505543 | A | G | 1 | a0001c0001t0033 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1875A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1875 | chr9 | 76505543 | ||||||
| chr9:76505559 | A | T | 21 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0012 others(18): Show |
156 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*1891A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1891 | chr9 | 76505559 | ||||||
| chr9:76505560 | G | C | 1 | a0002c0002t0041 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1892G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1892 | chr9 | 76505560 | ||||||
| chr9:76505636 | C | CAGT | 26 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(23): Show |
179 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1971_*1973dupTAG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 1974 | INFO_REALIGN_3_PRIME | chr9 | 76505636 | |||||
| chr9:76505821 | C | T | 1 | a0001c0001t0010 | 6 | HG02135.hp1 NA18960.hp1 NA19005.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2153C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2153 | chr9 | 76505821 | ||||||
| chr9:76505824 | G | A | 2 | a0001c0001t0013 a0001c0001t0037 |
4 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2156G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2156 | chr9 | 76505824 | ||||||
| chr9:76505839 | T | G | 1 | a0003c0003t0017 | 3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2171T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2171 | chr9 | 76505839 | ||||||
| chr9:76505889 | C | T | 1 | a0001c0001t0035 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2221C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2221 | chr9 | 76505889 | ||||||
| chr9:76506169 | G | T | 45 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(42): Show |
313 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(310): Show |
3_prime_UTR_variant | MODIFIER | c.*2501G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2501 | chr9 | 76506169 | ||||||
| chr9:76506183 | A | G | 1 | a0001c0001t0025 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2515A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2515 | chr9 | 76506183 | ||||||
| chr9:76506266 | AATCACAT others(15): Show |
A | 1 | a0001c0001t0032 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2599_*2620delATCA others(18): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2599 | chr9 | 76506266 | ||||||
| chr9:76506282 | T | A | 1 | a0001c0001t0011 | 4 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2614T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2614 | chr9 | 76506282 | ||||||
| chr9:76506359 | C | T | 1 | a0001c0001t0014 | 3 | HG02280.hp1 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2691C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2691 | chr9 | 76506359 | ||||||
| chr9:76506360 | G | A | 1 | a0001c0001t0045 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2692G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2692 | chr9 | 76506360 | ||||||
| chr9:76506370 | C | G | 8 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0014 others(5): Show |
31 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2702C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2702 | chr9 | 76506370 | ||||||
| chr9:76506464 | A | G | 11 | a0002c0002t0001 a0002c0002t0009 a0002c0002t0015 others(8): Show |
111 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2796A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2796 | chr9 | 76506464 | ||||||
| chr9:76506468 | G | A | 13 | a0001c0001t0006 a0001c0001t0034 a0001c0001t0035 others(10): Show |
129 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2800G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2800 | chr9 | 76506468 | ||||||
| chr9:76506605 | G | A | 1 | a0002c0002t0042 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2937G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 2937 | chr9 | 76506605 | ||||||
| chr9:76506795 | A | G | 2 | a0002c0002t0042 a0002c0002t0044 |
2 | NA18948.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3127A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3127 | chr9 | 76506795 | ||||||
| chr9:76506840 | G | A | 1 | a0001c0001t0019 | 2 | NA18986.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3172G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3172 | chr9 | 76506840 | ||||||
| chr9:76506846 | G | A | 1 | a0002c0002t0043 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3178G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3178 | chr9 | 76506846 | ||||||
| chr9:76506866 | C | T | 1 | a0001c0001t0031 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3198C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3198 | chr9 | 76506866 | ||||||
| chr9:76506867 | G | A | 3 | a0001c0001t0006 a0001c0001t0034 a0001c0001t0035 |
19 | HG01123.hp2 HG01257.hp2 HG01891.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3199G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3199 | chr9 | 76506867 | ||||||
| chr9:76506990 | C | T | 29 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(26): Show |
176 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*3322C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3322 | chr9 | 76506990 | ||||||
| chr9:76507104 | A | G | 1 | a0001c0001t0030 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3436A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3436 | chr9 | 76507104 | ||||||
| chr9:76507263 | T | C | 1 | a0001c0001t0007 | 12 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3595T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3595 | chr9 | 76507263 | ||||||
| chr9:76507329 | G | A | 1 | a0001c0001t0007 | 12 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3661G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 4/4 | 3661 | chr9 | 76507329 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:76459429 | C | T | 11 | a0001c0001t0003g0324 a0001c0001t0003g0327 a0001c0001t0003g0328 others(8): Show |
14 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-408+124C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459429 | |||||||
| chr9:76459432 | G | A | 11 | a0001c0001t0020g0028 a0001c0001t0020g0032 a0001c0001t0034g0031 others(8): Show |
12 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-408+127G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459432 | |||||||
| chr9:76459509 | T | A | 1 | a0001c0001t0003g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-408+204T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459509 | |||||||
| chr9:76459609 | G | T | 1 | a0002c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-408+304G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459609 | |||||||
| chr9:76459610 | C | A | 1 | a0002c0002t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-408+305C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459610 | |||||||
| chr9:76459618 | G | T | 2 | a0001c0001t0021g0318 a0001c0001t0021g0319 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-408+313G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459618 | |||||||
| chr9:76459709 | C | T | 1 | a0001c0001t0005g0317 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-407-351C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459709 | |||||||
| chr9:76459983 | C | A | 2 | a0001c0001t0021g0318 a0001c0001t0021g0319 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-407-77C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 1/3 | chr9 | 76459983 | |||||||
| chr9:76460332 | A | C | 20 | a0001c0001t0002g0313 a0001c0001t0003g0305 a0001c0001t0004g0298 others(17): Show |
21 | HG00735.hp2 HG01123.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-290+155A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460332 | |||||||
| chr9:76460516 | G | T | 3 | a0001c0001t0006g0314 a0001c0001t0006g0315 a0001c0001t0006g0316 |
3 | NA18962.hp1 NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-290+339G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460516 | |||||||
| chr9:76460525 | A | G | 3 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 |
3 | HG02056.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-290+348A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460525 | |||||||
| chr9:76460657 | T | C | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+480T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460657 | |||||||
| chr9:76460672 | G | T | 1 | a0001c0001t0002g0294 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-290+495G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460672 | |||||||
| chr9:76460736 | A | G | 132 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(129): Show |
148 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-290+559A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460736 | |||||||
| chr9:76460738 | A | T | 1 | a0002c0002t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-290+561A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460738 | |||||||
| chr9:76460739 | CTA | C | 20 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(17): Show |
21 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-290+564_-290+565d others(4): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76460739 | ||||||
| chr9:76460862 | T | C | 38 | a0001c0001t0003g0042 a0001c0001t0004g0018 a0001c0001t0004g0187 others(35): Show |
39 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.-290+685T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76460862 | |||||||
| chr9:76461011 | C | T | 1 | a0001c0001t0019g0185 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-290+834C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461011 | |||||||
| chr9:76461194 | CT | C | 222 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(219): Show |
252 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.-290+1038delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76461194 | ||||||
| chr9:76461194 | CTT | C | 54 | a0001c0001t0002g0071 a0001c0001t0002g0209 a0001c0001t0002g0210 others(51): Show |
55 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.-290+1037_-290+103 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76461194 | ||||||
| chr9:76461194 | CTTT | C | 25 | a0001c0001t0002g0060 a0001c0001t0003g0003 a0001c0001t0003g0010 others(22): Show |
30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.-290+1036_-290+103 others(7): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76461194 | ||||||
| chr9:76461277 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-290+1100G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461277 | |||||||
| chr9:76461376 | A | G | 2 | a0001c0001t0023g0176 a0001c0001t0023g0177 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-290+1199A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461376 | |||||||
| chr9:76461444 | G | A | 1 | a0002c0002t0001g0220 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-290+1267G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461444 | |||||||
| chr9:76461456 | C | T | 1 | a0002c0002t0001g0285 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-290+1279C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461456 | |||||||
| chr9:76461473 | A | G | 1 | a0001c0001t0003g0328 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-290+1296A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461473 | |||||||
| chr9:76461509 | G | A | 12 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(9): Show |
12 | HG02486.hp2 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-290+1332G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461509 | |||||||
| chr9:76461592 | A | C | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+1415A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461592 | |||||||
| chr9:76461651 | G | T | 35 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 others(32): Show |
37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-290+1474G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461651 | |||||||
| chr9:76461652 | C | T | 35 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 others(32): Show |
37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-290+1475C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461652 | |||||||
| chr9:76461865 | G | T | 1 | a0001c0001t0002g0149 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-290+1688G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461865 | |||||||
| chr9:76461883 | C | T | 20 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(17): Show |
21 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-290+1706C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461883 | |||||||
| chr9:76461884 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-290+1707G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76461884 | |||||||
| chr9:76462133 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-290+1956G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462133 | |||||||
| chr9:76462143 | AT | A | 232 | a0001c0001t0002g0060 a0001c0001t0002g0209 a0001c0001t0002g0210 others(229): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-290+1980delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76462143 | ||||||
| chr9:76462363 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-290+2186C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462363 | |||||||
| chr9:76462580 | G | A | 1 | a0002c0002t0001g0221 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-290+2403G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462580 | |||||||
| chr9:76462602 | T | C | 1 | a0001c0001t0003g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-290+2425T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462602 | |||||||
| chr9:76462997 | T | G | 1 | a0003c0003t0017g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-290+2820T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76462997 | |||||||
| chr9:76463028 | C | T | 2 | a0001c0001t0019g0147 a0001c0001t0019g0185 |
2 | NA18986.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-290+2851C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463028 | |||||||
| chr9:76463040 | G | A | 1 | a0001c0001t0033g0084 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-290+2863G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463040 | |||||||
| chr9:76463122 | C | A | 243 | a0001c0001t0002g0060 a0001c0001t0002g0209 a0001c0001t0002g0210 others(240): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-290+2945C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463122 | |||||||
| chr9:76463204 | C | T | 12 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(9): Show |
12 | HG02486.hp2 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-290+3027C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463204 | |||||||
| chr9:76463205 | T | A | 1 | a0001c0001t0006g0321 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-290+3028T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463205 | |||||||
| chr9:76463265 | G | C | 1 | a0001c0001t0045g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-290+3088G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463265 | |||||||
| chr9:76463275 | T | TA | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3105dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76463275 | ||||||
| chr9:76463371 | G | A | 35 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 others(32): Show |
37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.-290+3194G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463371 | |||||||
| chr9:76463372 | G | A | 2 | a0001c0001t0007g0038 a0002c0002t0009g0039 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-290+3195G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463372 | |||||||
| chr9:76463419 | C | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3242C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463419 | |||||||
| chr9:76463425 | T | C | 2 | a0001c0001t0007g0009 a0001c0001t0007g0322 |
4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+3248T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463425 | |||||||
| chr9:76463496 | A | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3319A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463496 | |||||||
| chr9:76463507 | T | A | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+3330T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463507 | |||||||
| chr9:76463673 | A | T | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3496A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463673 | |||||||
| chr9:76463680 | C | T | 1 | a0001c0001t0003g0069 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-290+3503C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463680 | |||||||
| chr9:76463687 | G | T | 9 | a0002c0002t0001g0008 a0002c0002t0001g0023 a0002c0002t0001g0277 others(6): Show |
12 | HG03490.hp2 HG03491.hp1 HG03492.hp2 others(9): Show |
intron_variant | MODIFIER | c.-290+3510G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463687 | |||||||
| chr9:76463733 | T | TTTATGAG others(1): Show |
215 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(212): Show |
237 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.-290+3565_-290+357 others(12): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76463733 | ||||||
| chr9:76463787 | T | C | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+3610T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76463787 | |||||||
| chr9:76464038 | G | GT | 12 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0182 others(9): Show |
12 | HG02040.hp2 HG02071.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-290+3876dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76464038 | ||||||
| chr9:76464038 | G | T | 10 | a0001c0001t0002g0015 a0001c0001t0002g0079 a0001c0001t0002g0142 others(7): Show |
11 | HG02074.hp2 HG02145.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.-290+3861G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464038 | |||||||
| chr9:76464038 | GT | G | 81 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 others(78): Show |
87 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.-290+3876delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76464038 | ||||||
| chr9:76464048 | T | G | 2 | a0002c0002t0042g0223 a0002c0002t0044g0286 |
2 | NA18948.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-290+3871T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464048 | |||||||
| chr9:76464068 | A | T | 1 | a0001c0001t0026g0326 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-290+3891A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464068 | |||||||
| chr9:76464077 | G | A | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+3900G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464077 | |||||||
| chr9:76464155 | A | G | 5 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0139 others(2): Show |
5 | NA18946.hp2 NA18969.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+3978A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464155 | |||||||
| chr9:76464155 | A | T | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+3978A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464155 | |||||||
| chr9:76464251 | C | G | 24 | a0001c0001t0003g0042 a0001c0001t0003g0324 a0001c0001t0003g0327 others(21): Show |
27 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-290+4074C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464251 | |||||||
| chr9:76464417 | A | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+4240A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464417 | |||||||
| chr9:76464455 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-290+4278G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464455 | |||||||
| chr9:76464515 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+4338C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464515 | |||||||
| chr9:76464615 | A | G | 2 | a0002c0002t0001g0073 a0002c0002t0001g0074 |
2 | NA18961.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-290+4438A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464615 | |||||||
| chr9:76464676 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-290+4499G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464676 | |||||||
| chr9:76464685 | A | G | 1 | a0001c0001t0002g0270 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-290+4508A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464685 | |||||||
| chr9:76464779 | A | T | 2 | a0001c0001t0007g0038 a0002c0002t0009g0039 |
2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-290+4602A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464779 | |||||||
| chr9:76464975 | A | T | 1 | a0002c0002t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-290+4798A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76464975 | |||||||
| chr9:76465027 | G | A | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+4850G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465027 | |||||||
| chr9:76465130 | C | A | 214 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(211): Show |
236 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.-290+4953C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465130 | |||||||
| chr9:76465155 | G | GT | 26 | a0001c0001t0003g0042 a0001c0001t0003g0324 a0001c0001t0003g0327 others(23): Show |
29 | HG00323.hp2 HG01099.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.-290+4991dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76465155 | ||||||
| chr9:76465155 | G | GTT | 22 | a0001c0001t0004g0018 a0001c0001t0004g0188 a0001c0001t0004g0189 others(19): Show |
23 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-290+4990_-290+499 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76465155 | ||||||
| chr9:76465156 | T | G | 1 | a0002c0002t0001g0206 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-290+4979T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465156 | |||||||
| chr9:76465169 | A | T | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+4992A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465169 | |||||||
| chr9:76465413 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+5236C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465413 | |||||||
| chr9:76465414 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-290+5237G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465414 | |||||||
| chr9:76465520 | G | A | 27 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(24): Show |
28 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-290+5343G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465520 | |||||||
| chr9:76465547 | T | C | 1 | a0001c0001t0003g0224 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-290+5370T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465547 | |||||||
| chr9:76465700 | C | A | 23 | a0001c0001t0002g0060 a0001c0001t0003g0003 a0001c0001t0003g0010 others(20): Show |
28 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-290+5523C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465700 | |||||||
| chr9:76465979 | T | C | 2 | a0002c0002t0009g0040 a0002c0006t0009g0041 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-290+5802T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76465979 | |||||||
| chr9:76466169 | G | A | 1 | a0002c0002t0001g0225 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-290+5992G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466169 | |||||||
| chr9:76466303 | TTTTG | T | 7 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+6134_-290+613 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76466303 | ||||||
| chr9:76466513 | G | A | 3 | a0001c0001t0011g0226 a0001c0001t0011g0227 a0001c0001t0011g0228 |
3 | HG02055.hp2 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-290+6336G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466513 | |||||||
| chr9:76466538 | G | A | 201 | a0001c0001t0002g0090 a0001c0001t0002g0182 a0001c0001t0002g0209 others(198): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.-290+6361G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466538 | |||||||
| chr9:76466666 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-290+6489G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466666 | |||||||
| chr9:76466729 | G | GGA | 7 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+6556_-290+655 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76466729 | ||||||
| chr9:76466928 | A | G | 7 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+6751A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466928 | |||||||
| chr9:76466994 | C | A | 13 | a0002c0002t0001g0020 a0002c0002t0001g0221 a0002c0002t0001g0229 others(10): Show |
14 | HG00438.hp1 HG00544.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-290+6817C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76466994 | |||||||
| chr9:76467042 | A | C | 6 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+6865A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467042 | |||||||
| chr9:76467044 | C | CT | 21 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0004g0018 others(18): Show |
22 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-290+6879dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467044 | ||||||
| chr9:76467105 | C | T | 6 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+6928C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467105 | |||||||
| chr9:76467109 | C | T | 1 | a0001c0001t0023g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-290+6932C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467109 | |||||||
| chr9:76467232 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-290+7055T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467232 | |||||||
| chr9:76467264 | A | G | 231 | a0001c0001t0002g0060 a0001c0001t0002g0090 a0001c0001t0002g0146 others(228): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-290+7087A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467264 | |||||||
| chr9:76467277 | A | C | 231 | a0001c0001t0002g0060 a0001c0001t0002g0090 a0001c0001t0002g0146 others(228): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-290+7100A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467277 | |||||||
| chr9:76467332 | T | A | 1 | a0001c0001t0004g0187 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-290+7155T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467332 | |||||||
| chr9:76467450 | G | A | 3 | a0001c0001t0018g0086 a0001c0001t0018g0087 a0001c0001t0018g0088 |
3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+7273G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467450 | |||||||
| chr9:76467489 | C | G | 123 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(120): Show |
139 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.-290+7312C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467489 | |||||||
| chr9:76467494 | A | T | 1 | a0001c0001t0003g0012 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-290+7317A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467494 | |||||||
| chr9:76467553 | G | T | 3 | a0001c0001t0004g0187 a0001c0001t0004g0203 a0001c0001t0004g0204 |
3 | HG01069.hp2 HG01099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-290+7376G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467553 | |||||||
| chr9:76467763 | G | A | 7 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(4): Show |
9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+7586G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467763 | |||||||
| chr9:76467796 | G | A | 3 | a0001c0001t0018g0086 a0001c0001t0018g0087 a0001c0001t0018g0088 |
3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+7619G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467796 | |||||||
| chr9:76467850 | T | C | 6 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 others(3): Show |
6 | HG02056.hp1 HG02155.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+7673T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467850 | |||||||
| chr9:76467897 | G | GT | 79 | a0001c0001t0002g0005 a0001c0001t0002g0014 a0001c0001t0002g0060 others(76): Show |
88 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.-290+7749dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | ||||||
| chr9:76467897 | G | GTT | 21 | a0001c0001t0002g0182 a0001c0001t0003g0067 a0001c0001t0004g0198 others(18): Show |
22 | HG01109.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-290+7748_-290+774 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | ||||||
| chr9:76467897 | GT | G | 78 | a0001c0001t0002g0091 a0001c0001t0002g0209 a0001c0001t0002g0210 others(75): Show |
91 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.-290+7749delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | ||||||
| chr9:76467897 | GTT | G | 8 | a0001c0001t0003g0042 a0001c0001t0004g0298 a0001c0001t0007g0038 others(5): Show |
8 | HG01256.hp1 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-290+7748_-290+774 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | ||||||
| chr9:76467897 | GTTTT | G | 8 | a0001c0001t0003g0324 a0001c0001t0003g0328 a0001c0001t0006g0321 others(5): Show |
9 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-290+7746_-290+774 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | ||||||
| chr9:76467897 | GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0003c0003t0017g0222 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-290+7740_-290+774 others(14): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76467897 | ||||||
| chr9:76467902 | T | G | 1 | a0001c0001t0018g0088 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-290+7725T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467902 | |||||||
| chr9:76467903 | T | G | 2 | a0001c0001t0018g0086 a0001c0001t0018g0087 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-290+7726T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467903 | |||||||
| chr9:76467916 | T | G | 1 | a0001c0001t0007g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-290+7739T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76467916 | |||||||
| chr9:76468026 | C | A | 1 | a0001c0001t0002g0092 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-290+7849C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468026 | |||||||
| chr9:76468115 | C | T | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0133 |
3 | HG00099.hp1 HG01081.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-290+7938C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468115 | |||||||
| chr9:76468156 | C | T | 21 | a0001c0001t0003g0042 a0001c0001t0003g0324 a0001c0001t0003g0327 others(18): Show |
22 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-290+7979C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468156 | |||||||
| chr9:76468187 | G | A | 28 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0003g0324 others(25): Show |
31 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.-290+8010G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468187 | |||||||
| chr9:76468454 | C | T | 2 | a0001c0001t0008g0044 a0001c0001t0045g0037 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-290+8277C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468454 | |||||||
| chr9:76468550 | C | T | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+8373C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468550 | |||||||
| chr9:76468556 | C | T | 36 | a0001c0001t0002g0090 a0001c0001t0002g0182 a0001c0001t0002g0295 others(33): Show |
39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+8379C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468556 | |||||||
| chr9:76468609 | A | G | 51 | a0001c0001t0002g0263 a0001c0001t0002g0270 a0001c0001t0003g0006 others(48): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-290+8432A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468609 | |||||||
| chr9:76468743 | G | C | 1 | a0001c0001t0006g0178 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-290+8566G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468743 | |||||||
| chr9:76468848 | G | A | 1 | a0001c0001t0012g0320 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+8671G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468848 | |||||||
| chr9:76468855 | G | C | 1 | a0001c0001t0004g0191 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-290+8678G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468855 | |||||||
| chr9:76468857 | A | T | 29 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0003g0324 others(26): Show |
32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+8680A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468857 | |||||||
| chr9:76468898 | A | G | 1 | a0001c0001t0025g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-290+8721A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468898 | |||||||
| chr9:76468904 | G | T | 1 | a0002c0002t0001g0138 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-290+8727G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468904 | |||||||
| chr9:76468960 | C | G | 2 | a0001c0001t0007g0009 a0001c0001t0007g0322 |
4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+8783C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468960 | |||||||
| chr9:76468979 | A | G | 2 | a0002c0002t0001g0073 a0002c0002t0001g0074 |
2 | NA18961.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-290+8802A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468979 | |||||||
| chr9:76468981 | T | A | 29 | a0001c0001t0002g0090 a0001c0001t0002g0182 a0001c0001t0002g0295 others(26): Show |
31 | HG00733.hp2 HG01070.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-290+8804T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76468981 | |||||||
| chr9:76469044 | C | A | 29 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0003g0324 others(26): Show |
32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+8867C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469044 | |||||||
| chr9:76469051 | A | G | 29 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0003g0324 others(26): Show |
32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+8874A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469051 | |||||||
| chr9:76469054 | G | A | 2 | a0001c0001t0007g0009 a0001c0001t0007g0322 |
4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+8877G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469054 | |||||||
| chr9:76469106 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-290+8929G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469106 | |||||||
| chr9:76469113 | CTAAG | C | 22 | a0001c0001t0002g0060 a0001c0001t0003g0003 a0001c0001t0003g0010 others(19): Show |
27 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.-290+8938_-290+894 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76469113 | ||||||
| chr9:76469261 | C | T | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+9084C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469261 | |||||||
| chr9:76469299 | G | A | 27 | a0001c0001t0002g0060 a0001c0001t0003g0003 a0001c0001t0003g0010 others(24): Show |
32 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.-290+9122G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469299 | |||||||
| chr9:76469322 | T | C | 29 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0003g0324 others(26): Show |
32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+9145T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469322 | |||||||
| chr9:76469405 | A | G | 22 | a0001c0001t0003g0042 a0001c0001t0003g0324 a0001c0001t0003g0327 others(19): Show |
23 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-290+9228A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469405 | |||||||
| chr9:76469460 | T | G | 1 | a0001c0001t0002g0313 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-290+9283T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469460 | |||||||
| chr9:76469508 | C | T | 7 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-290+9331C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469508 | |||||||
| chr9:76469564 | C | T | 4 | a0001c0001t0022g0082 a0001c0001t0022g0083 a0001c0001t0023g0176 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+9387C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469564 | |||||||
| chr9:76469720 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-290+9543G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469720 | |||||||
| chr9:76469737 | G | C | 29 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0003g0324 others(26): Show |
32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+9560G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469737 | |||||||
| chr9:76469743 | G | T | 10 | a0001c0001t0020g0028 a0001c0001t0020g0032 a0002c0002t0001g0004 others(7): Show |
11 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-290+9566G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469743 | |||||||
| chr9:76469818 | C | T | 7 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(4): Show |
9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+9641C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469818 | |||||||
| chr9:76469827 | T | G | 6 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+9650T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76469827 | |||||||
| chr9:76470109 | T | C | 1 | a0001c0001t0012g0320 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+9932T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470109 | |||||||
| chr9:76470208 | C | T | 2 | a0002c0002t0001g0258 a0002c0002t0001g0259 |
2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-290+10031C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470208 | |||||||
| chr9:76470477 | C | G | 1 | a0001c0001t0002g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-290+10300C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470477 | |||||||
| chr9:76470478 | G | A | 2 | a0002c0002t0009g0267 a0002c0002t0009g0268 |
2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-290+10301G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470478 | |||||||
| chr9:76470603 | C | CA | 13 | a0001c0001t0002g0093 a0001c0001t0002g0126 a0001c0001t0002g0127 others(10): Show |
14 | HG00438.hp2 HG00741.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+10447dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76470603 | ||||||
| chr9:76470603 | CA | C | 184 | a0001c0001t0002g0090 a0001c0001t0002g0209 a0001c0001t0002g0210 others(181): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-290+10447delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76470603 | ||||||
| chr9:76470603 | CAA | C | 20 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(17): Show |
21 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-290+10446_-290+10 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76470603 | ||||||
| chr9:76470814 | G | A | 29 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0003g0324 others(26): Show |
32 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.-290+10637G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470814 | |||||||
| chr9:76470840 | G | A | 1 | a0001c0001t0004g0018 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-290+10663G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470840 | |||||||
| chr9:76470923 | C | T | 36 | a0001c0001t0002g0090 a0001c0001t0002g0182 a0001c0001t0002g0295 others(33): Show |
39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+10746C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76470923 | |||||||
| chr9:76471238 | G | A | 5 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+11061G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471238 | |||||||
| chr9:76471245 | A | G | 1 | a0001c0001t0002g0145 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-290+11068A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471245 | |||||||
| chr9:76471552 | T | C | 2 | a0001c0001t0007g0009 a0001c0001t0007g0322 |
4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+11375T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471552 | |||||||
| chr9:76471579 | C | T | 20 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0004g0237 others(17): Show |
22 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-290+11402C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471579 | |||||||
| chr9:76471657 | A | G | 2 | a0001c0001t0008g0044 a0001c0001t0045g0037 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-290+11480A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471657 | |||||||
| chr9:76471667 | TAA | T | 20 | a0001c0001t0003g0042 a0001c0001t0003g0077 a0001c0001t0004g0237 others(17): Show |
22 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-290+11491_-290+11 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471667 | |||||||
| chr9:76471818 | A | G | 3 | a0002c0002t0001g0043 a0002c0002t0009g0045 a0002c0002t0009g0046 |
3 | HG02486.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-290+11641A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76471818 | |||||||
| chr9:76472068 | G | T | 1 | a0001c0001t0002g0182 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-290+11891G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472068 | |||||||
| chr9:76472120 | T | TA | 12 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(9): Show |
12 | HG02486.hp2 HG02572.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-290+11951dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472120 | ||||||
| chr9:76472191 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-290+12014C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472191 | |||||||
| chr9:76472281 | T | G | 7 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(4): Show |
9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+12104T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472281 | |||||||
| chr9:76472577 | A | G | 2 | a0002c0002t0009g0267 a0002c0002t0009g0268 |
2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-290+12400A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472577 | |||||||
| chr9:76472650 | T | C | 13 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(10): Show |
13 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-290+12473T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472650 | |||||||
| chr9:76472720 | C | CTTTCT | 5 | a0001c0001t0002g0128 a0001c0001t0002g0136 a0001c0001t0002g0139 others(2): Show |
5 | HG01928.hp1 HG03669.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(11): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472720 | ||||||
| chr9:76472720 | CTTTCT | C | 48 | a0001c0001t0002g0060 a0001c0001t0002g0120 a0001c0001t0002g0121 others(45): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(11): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472720 | ||||||
| chr9:76472744 | CTTTTCTT others(1): Show |
C | 131 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(128): Show |
148 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(14): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472744 | ||||||
| chr9:76472745 | TTTTC | T | 32 | a0001c0001t0002g0296 a0001c0001t0003g0042 a0001c0001t0003g0324 others(29): Show |
32 | HG00323.hp2 HG01257.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472745 | ||||||
| chr9:76472746 | TTTC | T | 29 | a0001c0001t0002g0090 a0001c0001t0002g0182 a0001c0001t0002g0295 others(26): Show |
31 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-290+12572_-290+12 others(9): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472746 | ||||||
| chr9:76472749 | C | CT | 7 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0071 others(4): Show |
8 | HG01261.hp1 HG01358.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-290+12589dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76472749 | ||||||
| chr9:76472749 | C | T | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+12572C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472749 | |||||||
| chr9:76472754 | T | C | 3 | a0001c0001t0018g0086 a0001c0001t0018g0087 a0001c0001t0018g0088 |
3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+12577T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472754 | |||||||
| chr9:76472761 | TTTTTTGA others(4): Show |
T | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+12585_-290+12 others(17): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472761 | |||||||
| chr9:76472772 | G | T | 3 | a0001c0001t0018g0086 a0001c0001t0018g0087 a0001c0001t0018g0088 |
3 | HG02886.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-290+12595G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472772 | |||||||
| chr9:76472937 | C | T | 2 | a0001c0001t0006g0308 a0002c0002t0001g0244 |
2 | HG00642.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-290+12760C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472937 | |||||||
| chr9:76472958 | G | A | 23 | a0001c0001t0002g0060 a0001c0001t0003g0003 a0001c0001t0003g0010 others(20): Show |
28 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-290+12781G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76472958 | |||||||
| chr9:76473048 | G | C | 136 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(133): Show |
154 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-290+12871G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473048 | |||||||
| chr9:76473373 | G | T | 4 | a0001c0001t0004g0262 a0002c0002t0001g0007 a0002c0002t0001g0021 others(1): Show |
7 | HG00738.hp2 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-290+13196G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473373 | |||||||
| chr9:76473401 | TAAACTGG others(15): Show |
T | 1 | a0001c0001t0002g0119 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-290+13225_-290+13 others(28): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473401 | |||||||
| chr9:76473571 | A | T | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+13394A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473571 | |||||||
| chr9:76473607 | A | C | 158 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(155): Show |
176 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.-290+13430A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473607 | |||||||
| chr9:76473641 | T | A | 1 | a0001c0001t0003g0011 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-290+13464T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473641 | |||||||
| chr9:76473697 | G | T | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0003c0003t0017g0222 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-290+13520G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473697 | |||||||
| chr9:76473743 | C | A | 9 | a0001c0001t0003g0324 a0001c0001t0003g0327 a0001c0001t0003g0328 others(6): Show |
10 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-290+13566C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473743 | |||||||
| chr9:76473771 | T | C | 1 | a0002c0002t0001g0240 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-290+13594T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473771 | |||||||
| chr9:76473816 | T | A | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+13639T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473816 | |||||||
| chr9:76473832 | G | A | 5 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+13655G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76473832 | |||||||
| chr9:76474056 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+13879C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474056 | |||||||
| chr9:76474061 | C | T | 1 | a0001c0001t0013g0325 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-290+13884C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474061 | |||||||
| chr9:76474076 | G | T | 1 | a0001c0001t0026g0326 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-290+13899G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474076 | |||||||
| chr9:76474147 | T | C | 8 | a0001c0001t0007g0038 a0002c0002t0001g0043 a0002c0002t0009g0039 others(5): Show |
8 | HG02486.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-290+13970T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474147 | |||||||
| chr9:76474193 | C | T | 1 | a0002c0002t0001g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-290+14016C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474193 | |||||||
| chr9:76474194 | G | A | 143 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(140): Show |
159 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.-290+14017G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474194 | |||||||
| chr9:76474207 | A | T | 150 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(147): Show |
168 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.-290+14030A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474207 | |||||||
| chr9:76474297 | G | A | 1 | a0001c0001t0008g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-290+14120G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474297 | |||||||
| chr9:76474466 | A | G | 2 | a0001c0001t0022g0082 a0001c0001t0022g0083 |
2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-290+14289A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474466 | |||||||
| chr9:76474537 | C | G | 4 | a0001c0001t0008g0044 a0001c0001t0022g0082 a0001c0001t0022g0083 others(1): Show |
4 | HG02109.hp2 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+14360C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474537 | |||||||
| chr9:76474540 | A | G | 1 | a0001c0001t0008g0050 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-290+14363A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474540 | |||||||
| chr9:76474586 | C | G | 14 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(11): Show |
14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+14409C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474586 | |||||||
| chr9:76474648 | C | T | 14 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(11): Show |
14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+14471C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474648 | |||||||
| chr9:76474772 | C | A | 1 | a0001c0001t0002g0126 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-290+14595C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474772 | |||||||
| chr9:76474849 | C | G | 136 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(133): Show |
154 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-290+14672C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76474849 | |||||||
| chr9:76475060 | C | T | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0003c0003t0017g0222 others(1): Show |
4 | HG01884.hp2 HG03471.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-290+14883C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475060 | |||||||
| chr9:76475115 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-290+14938C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475115 | |||||||
| chr9:76475146 | A | G | 3 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02622.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-290+14969A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475146 | |||||||
| chr9:76475172 | G | A | 1 | a0001c0001t0010g0211 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-290+14995G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475172 | |||||||
| chr9:76475280 | C | T | 1 | a0002c0002t0001g0118 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-290+15103C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475280 | |||||||
| chr9:76475365 | A | G | 1 | a0001c0001t0003g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-290+15188A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475365 | |||||||
| chr9:76475383 | A | G | 1 | a0001c0001t0012g0320 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+15206A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475383 | |||||||
| chr9:76475402 | G | A | 320 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(317): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-290+15225G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475402 | |||||||
| chr9:76475448 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-290+15271A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475448 | |||||||
| chr9:76475497 | G | T | 6 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+15320G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475497 | |||||||
| chr9:76475537 | T | A | 1 | a0001c0001t0002g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-290+15360T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475537 | |||||||
| chr9:76475544 | T | A | 1 | a0001c0001t0012g0320 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+15367T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475544 | |||||||
| chr9:76475575 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-290+15398C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475575 | |||||||
| chr9:76475577 | G | T | 2 | a0001c0001t0007g0009 a0001c0001t0007g0322 |
4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-290+15400G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475577 | |||||||
| chr9:76475618 | TAAG | T | 7 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(4): Show |
9 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-290+15442_-290+15 others(9): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475618 | |||||||
| chr9:76475662 | G | A | 1 | a0002c0002t0001g0073 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-290+15485G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475662 | |||||||
| chr9:76475857 | G | A | 5 | a0001c0001t0002g0014 a0001c0001t0002g0093 a0001c0001t0002g0098 others(2): Show |
6 | HG00423.hp1 HG00438.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+15680G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475857 | |||||||
| chr9:76475858 | G | A | 1 | a0001c0001t0005g0089 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-290+15681G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76475858 | |||||||
| chr9:76475877 | GTAAC | G | 157 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(154): Show |
175 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.-290+15705_-290+15 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76475877 | ||||||
| chr9:76476030 | A | T | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+15853A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476030 | |||||||
| chr9:76476046 | G | A | 6 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-290+15869G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476046 | |||||||
| chr9:76476259 | A | G | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+16082A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476259 | |||||||
| chr9:76476443 | A | T | 2 | a0002c0002t0001g0282 a0002c0004t0001g0281 |
2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-290+16266A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476443 | |||||||
| chr9:76476456 | C | T | 34 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(31): Show |
35 | HG00558.hp2 HG00735.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-290+16279C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476456 | |||||||
| chr9:76476550 | TA | T | 134 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(131): Show |
152 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-290+16384delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76476550 | ||||||
| chr9:76476663 | T | C | 14 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(11): Show |
14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+16486T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476663 | |||||||
| chr9:76476710 | T | TG | 15 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0003g0053 others(12): Show |
15 | HG00423.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+16537dupG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76476710 | ||||||
| chr9:76476822 | G | T | 36 | a0001c0001t0002g0090 a0001c0001t0002g0182 a0001c0001t0002g0295 others(33): Show |
39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+16645G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76476822 | |||||||
| chr9:76477185 | G | T | 5 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0003c0003t0017g0186 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-290+17008G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477185 | |||||||
| chr9:76477207 | G | A | 1 | a0001c0001t0003g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-290+17030G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477207 | |||||||
| chr9:76477259 | G | A | 1 | a0001c0001t0008g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-290+17082G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477259 | |||||||
| chr9:76477295 | A | AG | 8 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(5): Show |
10 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-290+17120dupG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477295 | ||||||
| chr9:76477299 | G | C | 1 | a0001c0001t0012g0320 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-290+17122G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477299 | |||||||
| chr9:76477310 | G | A | 128 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(125): Show |
144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+17133G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477310 | |||||||
| chr9:76477509 | G | A | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+17332G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477509 | |||||||
| chr9:76477519 | C | CT | 126 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(123): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-290+17343dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477519 | ||||||
| chr9:76477526 | C | CA | 8 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(5): Show |
10 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-290+17360dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477526 | ||||||
| chr9:76477526 | CA | C | 128 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(125): Show |
144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+17360delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76477526 | ||||||
| chr9:76477603 | C | A | 2 | a0001c0001t0022g0082 a0001c0001t0022g0083 |
2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-290+17426C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477603 | |||||||
| chr9:76477611 | G | A | 14 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(11): Show |
14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+17434G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477611 | |||||||
| chr9:76477739 | T | G | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+17562T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477739 | |||||||
| chr9:76477767 | C | A | 1 | a0001c0001t0011g0205 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-290+17590C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477767 | |||||||
| chr9:76477790 | C | T | 24 | a0001c0001t0004g0018 a0001c0001t0004g0187 a0001c0001t0004g0188 others(21): Show |
25 | HG00639.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-290+17613C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477790 | |||||||
| chr9:76477797 | C | A | 1 | a0001c0001t0003g0006 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-290+17620C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477797 | |||||||
| chr9:76477846 | C | G | 126 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(123): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-290+17669C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477846 | |||||||
| chr9:76477874 | C | T | 2 | a0001c0001t0023g0176 a0001c0001t0023g0177 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-290+17697C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477874 | |||||||
| chr9:76477879 | T | C | 2 | a0001c0001t0021g0318 a0001c0001t0021g0319 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-290+17702T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477879 | |||||||
| chr9:76477962 | G | A | 321 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(318): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-290+17785G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477962 | |||||||
| chr9:76477969 | G | A | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+17792G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76477969 | |||||||
| chr9:76478073 | A | G | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-290+17896A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478073 | |||||||
| chr9:76478179 | T | C | 304 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(301): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-290+18002T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478179 | |||||||
| chr9:76478189 | T | G | 126 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(123): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-290+18012T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478189 | |||||||
| chr9:76478190 | A | G | 23 | a0001c0001t0008g0241 a0001c0001t0008g0242 a0002c0002t0001g0008 others(20): Show |
26 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-290+18013A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478190 | |||||||
| chr9:76478190 | A | T | 126 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(123): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-290+18013A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478190 | |||||||
| chr9:76478213 | C | G | 1 | a0001c0001t0002g0015 | 2 | NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-290+18036C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478213 | |||||||
| chr9:76478251 | C | T | 21 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(18): Show |
21 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.-290+18074C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478251 | |||||||
| chr9:76478351 | T | C | 3 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 |
3 | HG02622.hp1 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-290+18174T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478351 | |||||||
| chr9:76478385 | G | A | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+18208G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478385 | |||||||
| chr9:76478388 | T | G | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18211T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478388 | |||||||
| chr9:76478429 | A | G | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+18252A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478429 | |||||||
| chr9:76478479 | T | C | 319 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(316): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.-290+18302T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478479 | |||||||
| chr9:76478506 | G | A | 1 | a0002c0002t0001g0023 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-290+18329G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478506 | |||||||
| chr9:76478586 | C | T | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18409C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478586 | |||||||
| chr9:76478587 | T | G | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18410T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478587 | |||||||
| chr9:76478588 | G | T | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-290+18411G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478588 | |||||||
| chr9:76478694 | G | A | 1 | a0001c0001t0007g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-290+18517G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478694 | |||||||
| chr9:76478711 | C | G | 36 | a0001c0001t0002g0090 a0001c0001t0002g0182 a0001c0001t0002g0295 others(33): Show |
39 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-290+18534C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478711 | |||||||
| chr9:76478748 | A | G | 162 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(159): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-290+18571A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478748 | |||||||
| chr9:76478833 | T | C | 1 | a0001c0001t0006g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-290+18656T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478833 | |||||||
| chr9:76478870 | TATTGTAT others(4): Show |
T | 1 | a0001c0001t0003g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-290+18695_-290+18 others(17): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76478870 | ||||||
| chr9:76478877 | T | G | 1 | a0001c0001t0002g0139 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-290+18700T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478877 | |||||||
| chr9:76478905 | T | C | 313 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(310): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-290+18728T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478905 | |||||||
| chr9:76478931 | A | G | 1 | a0001c0001t0003g0022 | 2 | HG00544.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-290+18754A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478931 | |||||||
| chr9:76478984 | T | A | 162 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(159): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.-290+18807T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76478984 | |||||||
| chr9:76479306 | G | A | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-290+19129G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479306 | |||||||
| chr9:76479309 | A | G | 14 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(11): Show |
14 | HG02109.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-290+19132A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479309 | |||||||
| chr9:76479315 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-290+19138C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479315 | |||||||
| chr9:76479319 | G | A | 126 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(123): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-290+19142G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479319 | |||||||
| chr9:76479392 | G | A | 1 | a0001c0001t0027g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-290+19215G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479392 | |||||||
| chr9:76479528 | A | T | 1 | a0002c0002t0001g0230 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-290+19351A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479528 | |||||||
| chr9:76479688 | G | A | 1 | a0001c0001t0026g0326 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-290+19511G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479688 | |||||||
| chr9:76479730 | G | C | 2 | a0001c0001t0010g0211 a0001c0001t0010g0212 |
2 | HG02135.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-290+19553G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76479730 | |||||||
| chr9:76480020 | T | A | 1 | a0001c0001t0013g0025 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-290+19843T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480020 | |||||||
| chr9:76480067 | A | G | 2 | a0001c0001t0002g0296 a0001c0001t0002g0297 |
2 | NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-290+19890A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480067 | |||||||
| chr9:76480266 | C | T | 144 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(141): Show |
160 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.-290+20089C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480266 | |||||||
| chr9:76480335 | C | T | 128 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(125): Show |
144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-290+20158C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480335 | |||||||
| chr9:76480354 | A | G | 129 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(126): Show |
145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-290+20177A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480354 | |||||||
| chr9:76480630 | G | A | 6 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(3): Show |
6 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-20286G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480630 | |||||||
| chr9:76480691 | T | C | 1 | a0001c0001t0008g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-289-20225T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480691 | |||||||
| chr9:76480730 | C | T | 8 | a0002c0002t0001g0004 a0002c0002t0001g0026 a0002c0002t0001g0029 others(5): Show |
9 | HG01074.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-289-20186C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480730 | |||||||
| chr9:76480788 | C | T | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-20128C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480788 | |||||||
| chr9:76480797 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-289-20119A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480797 | |||||||
| chr9:76480923 | T | C | 2 | a0001c0001t0007g0009 a0001c0001t0007g0322 |
4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-19993T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76480923 | |||||||
| chr9:76481133 | G | A | 1 | a0003c0003t0017g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-289-19783G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481133 | |||||||
| chr9:76481164 | C | T | 2 | a0002c0002t0001g0258 a0002c0002t0001g0259 |
2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-289-19752C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481164 | |||||||
| chr9:76481200 | C | T | 1 | a0002c0002t0001g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-289-19716C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481200 | |||||||
| chr9:76481304 | G | T | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-19612G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481304 | |||||||
| chr9:76481411 | AT | A | 96 | a0001c0001t0002g0090 a0001c0001t0002g0104 a0001c0001t0002g0182 others(93): Show |
101 | HG00558.hp2 HG00642.hp1 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.-289-19492delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76481411 | ||||||
| chr9:76481460 | A | G | 2 | a0002c0002t0009g0040 a0002c0006t0009g0041 |
2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-289-19456A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481460 | |||||||
| chr9:76481694 | G | A | 3 | a0001c0001t0007g0076 a0001c0001t0007g0173 a0001c0001t0014g0174 |
3 | HG03195.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-289-19222G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481694 | |||||||
| chr9:76481743 | C | T | 126 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(123): Show |
142 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-289-19173C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481743 | |||||||
| chr9:76481794 | G | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0120 |
2 | HG00323.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.-289-19122G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481794 | |||||||
| chr9:76481829 | G | A | 2 | a0001c0001t0020g0028 a0001c0001t0020g0032 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-289-19087G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76481829 | |||||||
| chr9:76482050 | C | T | 1 | a0002c0002t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-289-18866C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482050 | |||||||
| chr9:76482107 | G | C | 2 | a0001c0001t0020g0028 a0001c0001t0020g0032 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-289-18809G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482107 | |||||||
| chr9:76482129 | C | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0129 a0001c0001t0004g0179 |
3 | HG02083.hp1 HG02165.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-289-18787C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482129 | |||||||
| chr9:76482183 | G | A | 2 | a0001c0001t0021g0318 a0001c0001t0021g0319 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-289-18733G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482183 | |||||||
| chr9:76482198 | A | C | 1 | a0002c0002t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-289-18718A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482198 | |||||||
| chr9:76482201 | G | A | 34 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(31): Show |
35 | HG00558.hp2 HG00735.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-289-18715G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482201 | |||||||
| chr9:76482228 | T | C | 129 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(126): Show |
145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-289-18688T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482228 | |||||||
| chr9:76482245 | C | G | 2 | a0002c0002t0042g0223 a0002c0002t0044g0286 |
2 | NA18948.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-289-18671C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482245 | |||||||
| chr9:76482347 | G | T | 2 | a0002c0002t0001g0288 a0002c0002t0001g0293 |
2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-289-18569G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482347 | |||||||
| chr9:76482393 | G | A | 6 | a0001c0001t0003g0077 a0001c0001t0004g0237 a0001c0001t0004g0238 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-18523G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482393 | |||||||
| chr9:76482397 | G | A | 1 | a0002c0002t0001g0248 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-289-18519G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482397 | |||||||
| chr9:76482410 | A | G | 1 | a0001c0001t0003g0324 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-289-18506A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482410 | |||||||
| chr9:76482437 | C | T | 130 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(127): Show |
146 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-289-18479C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482437 | |||||||
| chr9:76482465 | C | CA | 128 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(125): Show |
144 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-289-18442dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482465 | ||||||
| chr9:76482479 | C | T | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-18437C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482479 | |||||||
| chr9:76482530 | A | G | 129 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(126): Show |
145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-289-18386A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482530 | |||||||
| chr9:76482731 | A | G | 1 | a0001c0001t0003g0327 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-289-18185A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482731 | |||||||
| chr9:76482811 | A | AT | 133 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(130): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-289-18086dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482811 | ||||||
| chr9:76482811 | A | ATT | 126 | a0001c0001t0002g0097 a0001c0001t0002g0115 a0001c0001t0002g0131 others(123): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.-289-18087_-289-18 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482811 | ||||||
| chr9:76482811 | A | ATTT | 22 | a0001c0001t0003g0305 a0001c0001t0004g0202 a0001c0001t0004g0312 others(19): Show |
22 | HG00544.hp1 HG01123.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-289-18088_-289-18 others(9): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76482811 | ||||||
| chr9:76482831 | G | T | 1 | a0001c0001t0002g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-289-18085G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482831 | |||||||
| chr9:76482832 | G | A | 1 | a0002c0002t0001g0225 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-289-18084G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482832 | |||||||
| chr9:76482840 | G | T | 1 | a0001c0001t0002g0112 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-289-18076G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482840 | |||||||
| chr9:76482872 | A | G | 313 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(310): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-289-18044A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482872 | |||||||
| chr9:76482950 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-289-17966C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482950 | |||||||
| chr9:76482981 | T | C | 129 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(126): Show |
145 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-289-17935T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76482981 | |||||||
| chr9:76483044 | C | T | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-17872C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483044 | |||||||
| chr9:76483194 | A | C | 1 | a0001c0001t0002g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-289-17722A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483194 | |||||||
| chr9:76483243 | T | A | 127 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(124): Show |
143 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-289-17673T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483243 | |||||||
| chr9:76483270 | G | A | 1 | a0001c0001t0010g0208 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-289-17646G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483270 | |||||||
| chr9:76483403 | G | GT | 7 | a0001c0001t0003g0011 a0001c0001t0003g0053 a0001c0001t0003g0058 others(4): Show |
8 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-289-17503dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76483403 | ||||||
| chr9:76483403 | G | T | 3 | a0002c0002t0001g0043 a0002c0002t0009g0045 a0002c0002t0009g0046 |
3 | HG02486.hp2 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-289-17513G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483403 | |||||||
| chr9:76483403 | GT | G | 131 | a0001c0001t0002g0104 a0001c0001t0002g0209 a0001c0001t0002g0210 others(128): Show |
147 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-289-17503delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76483403 | ||||||
| chr9:76483554 | A | G | 1 | a0001c0001t0014g0036 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-289-17362A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483554 | |||||||
| chr9:76483575 | C | A | 1 | a0001c0001t0006g0309 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-17341C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483575 | |||||||
| chr9:76483609 | G | A | 2 | a0001c0001t0002g0142 a0006c0005t0002g0144 |
2 | NA18947.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-289-17307G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483609 | |||||||
| chr9:76483737 | A | C | 2 | a0001c0001t0002g0139 a0002c0002t0001g0138 |
2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.-289-17179A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483737 | |||||||
| chr9:76483926 | C | T | 16 | a0001c0001t0031g0154 a0002c0002t0001g0002 a0002c0002t0001g0075 others(13): Show |
20 | HG00621.hp2 HG00673.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-289-16990C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483926 | |||||||
| chr9:76483958 | G | A | 20 | a0001c0001t0003g0305 a0001c0001t0004g0132 a0001c0001t0004g0298 others(17): Show |
21 | HG00735.hp2 HG01123.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-289-16958G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76483958 | |||||||
| chr9:76484001 | ACT | A | 15 | a0001c0001t0003g0042 a0001c0001t0007g0038 a0001c0001t0008g0044 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-16914_-289-16 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484001 | |||||||
| chr9:76484158 | C | A | 141 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0218 others(138): Show |
157 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.-289-16758C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484158 | |||||||
| chr9:76484281 | G | T | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-289-16635G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484281 | |||||||
| chr9:76484285 | A | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(72): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-289-16631A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484285 | |||||||
| chr9:76484369 | T | TA | 13 | a0001c0001t0003g0042 a0001c0001t0007g0009 a0001c0001t0007g0038 others(10): Show |
15 | HG01243.hp2 HG01891.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-289-16533dupA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484369 | ||||||
| chr9:76484369 | TA | T | 7 | a0001c0001t0002g0114 a0001c0001t0023g0176 a0001c0001t0023g0177 others(4): Show |
7 | HG01975.hp2 HG02897.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-289-16533delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484369 | ||||||
| chr9:76484651 | G | C | 1 | a0001c0001t0027g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-289-16265G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484651 | |||||||
| chr9:76484710 | T | A | 1 | a0001c0001t0002g0133 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-289-16206T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484710 | |||||||
| chr9:76484724 | C | A | 5 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0003c0003t0017g0186 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-289-16192C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484724 | |||||||
| chr9:76484751 | G | A | 246 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(243): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.-289-16165G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484751 | |||||||
| chr9:76484766 | A | C | 2 | a0001c0001t0002g0210 a0001c0001t0002g0218 |
2 | NA18939.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-289-16150A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484766 | |||||||
| chr9:76484786 | C | CT | 16 | a0001c0001t0002g0104 a0001c0001t0002g0182 a0001c0001t0004g0262 others(13): Show |
16 | HG01175.hp2 HG01981.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.-289-16112dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484786 | ||||||
| chr9:76484786 | C | CTT | 88 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(85): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-289-16113_-289-16 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76484786 | ||||||
| chr9:76484815 | A | G | 285 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(282): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-289-16101A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484815 | |||||||
| chr9:76484886 | T | A | 1 | a0001c0001t0010g0212 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-289-16030T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484886 | |||||||
| chr9:76484934 | T | G | 322 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(319): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.-289-15982T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484934 | |||||||
| chr9:76484994 | G | A | 14 | a0001c0001t0003g0305 a0001c0001t0006g0013 a0001c0001t0006g0178 others(11): Show |
18 | HG03490.hp2 HG03491.hp1 HG03492.hp2 others(15): Show |
intron_variant | MODIFIER | c.-289-15922G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76484994 | |||||||
| chr9:76485003 | T | G | 1 | a0001c0001t0002g0115 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-289-15913T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485003 | |||||||
| chr9:76485074 | G | A | 115 | a0001c0001t0002g0060 a0001c0001t0002g0263 a0001c0001t0003g0003 others(112): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-289-15842G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485074 | |||||||
| chr9:76485076 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-289-15840C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485076 | |||||||
| chr9:76485106 | A | G | 149 | a0001c0001t0002g0014 a0001c0001t0002g0060 a0001c0001t0002g0085 others(146): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-289-15810A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485106 | |||||||
| chr9:76485253 | A | G | 2 | a0001c0001t0005g0159 a0001c0001t0005g0160 |
2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-289-15663A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485253 | |||||||
| chr9:76485318 | G | A | 1 | a0001c0001t0034g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-15598G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485318 | |||||||
| chr9:76485480 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-289-15436C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485480 | |||||||
| chr9:76485511 | A | T | 6 | a0001c0001t0005g0150 a0001c0001t0005g0159 a0001c0001t0005g0160 others(3): Show |
6 | HG02040.hp1 HG02135.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-15405A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485511 | |||||||
| chr9:76485580 | A | G | 4 | a0002c0002t0001g0023 a0002c0002t0001g0278 a0002c0002t0001g0280 others(1): Show |
5 | HG03490.hp2 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-289-15336A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485580 | |||||||
| chr9:76485736 | CT | C | 106 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(103): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-289-15168delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76485736 | ||||||
| chr9:76485831 | C | T | 2 | a0001c0001t0023g0176 a0001c0001t0023g0177 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-15085C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485831 | |||||||
| chr9:76485855 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-289-15061C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485855 | |||||||
| chr9:76485879 | T | C | 297 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(294): Show |
328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.-289-15037T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485879 | |||||||
| chr9:76485881 | C | T | 9 | a0001c0001t0003g0003 a0001c0001t0003g0010 a0001c0001t0003g0012 others(6): Show |
13 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-15035C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485881 | |||||||
| chr9:76485893 | T | G | 1 | a0001c0001t0003g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-289-15023T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76485893 | |||||||
| chr9:76486065 | G | A | 297 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(294): Show |
328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.-289-14851G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486065 | |||||||
| chr9:76486090 | A | G | 297 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(294): Show |
328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.-289-14826A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486090 | |||||||
| chr9:76486174 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(73): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.-289-14742G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486174 | |||||||
| chr9:76486217 | G | A | 10 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(7): Show |
13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-14699G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486217 | |||||||
| chr9:76486311 | T | G | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-14605T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486311 | |||||||
| chr9:76486344 | C | T | 1 | a0002c0002t0001g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-289-14572C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486344 | |||||||
| chr9:76486384 | G | A | 3 | a0001c0001t0002g0142 a0001c0001t0036g0107 a0006c0005t0002g0144 |
3 | NA18947.hp1 NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-289-14532G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486384 | |||||||
| chr9:76486471 | A | G | 3 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 |
3 | HG02056.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-289-14445A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486471 | |||||||
| chr9:76486490 | C | G | 6 | a0001c0001t0011g0190 a0001c0001t0011g0205 a0001c0001t0011g0216 others(3): Show |
6 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-14426C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486490 | |||||||
| chr9:76486501 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-289-14415C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486501 | |||||||
| chr9:76486894 | G | C | 1 | a0001c0001t0040g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-14022G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486894 | |||||||
| chr9:76486916 | A | AAAAC | 126 | a0001c0001t0002g0060 a0001c0001t0003g0003 a0001c0001t0003g0006 others(123): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-289-13976_-289-13 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76486916 | ||||||
| chr9:76486916 | AAAAC | A | 3 | a0002c0002t0001g0230 a0002c0002t0001g0278 a0002c0002t0001g0283 |
3 | HG00438.hp1 HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-289-13976_-289-13 others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76486916 | ||||||
| chr9:76486940 | C | A | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-13976C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486940 | |||||||
| chr9:76486947 | A | G | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-13969A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486947 | |||||||
| chr9:76486962 | G | A | 11 | a0001c0001t0011g0190 a0001c0001t0011g0205 a0001c0001t0011g0216 others(8): Show |
11 | HG02040.hp2 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-289-13954G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76486962 | |||||||
| chr9:76487175 | A | G | 1 | a0001c0001t0008g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-289-13741A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487175 | |||||||
| chr9:76487203 | C | G | 1 | a0001c0001t0008g0167 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-289-13713C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487203 | |||||||
| chr9:76487233 | C | T | 74 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(71): Show |
76 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-289-13683C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487233 | |||||||
| chr9:76487549 | G | A | 1 | a0001c0001t0010g0208 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-289-13367G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487549 | |||||||
| chr9:76487550 | C | T | 74 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(71): Show |
76 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-289-13366C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487550 | |||||||
| chr9:76487580 | T | C | 74 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(71): Show |
76 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-289-13336T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487580 | |||||||
| chr9:76487656 | T | C | 2 | a0001c0001t0004g0193 a0001c0001t0004g0203 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-289-13260T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487656 | |||||||
| chr9:76487680 | C | A | 1 | a0002c0002t0009g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-289-13236C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487680 | |||||||
| chr9:76487687 | G | C | 4 | a0002c0002t0001g0288 a0002c0002t0001g0289 a0002c0002t0001g0290 others(1): Show |
4 | HG03927.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-13229G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487687 | |||||||
| chr9:76487688 | G | T | 4 | a0002c0002t0001g0288 a0002c0002t0001g0289 a0002c0002t0001g0290 others(1): Show |
4 | HG03927.hp2 HG04184.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-13228G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487688 | |||||||
| chr9:76487900 | A | C | 2 | a0001c0001t0011g0226 a0001c0001t0011g0228 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-289-13016A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76487900 | |||||||
| chr9:76488000 | C | G | 10 | a0001c0001t0004g0018 a0001c0001t0004g0179 a0001c0001t0004g0196 others(7): Show |
11 | HG00639.hp1 HG01175.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.-289-12916C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488000 | |||||||
| chr9:76488027 | C | T | 25 | a0001c0001t0004g0018 a0001c0001t0004g0132 a0001c0001t0004g0179 others(22): Show |
26 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-289-12889C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488027 | |||||||
| chr9:76488132 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-12784C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488132 | |||||||
| chr9:76488445 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-12471C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488445 | |||||||
| chr9:76488446 | G | A | 2 | a0001c0001t0004g0196 a0001c0001t0004g0262 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-289-12470G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488446 | |||||||
| chr9:76488450 | T | C | 194 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(191): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-289-12466T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488450 | |||||||
| chr9:76488541 | A | G | 1 | a0001c0001t0026g0326 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-289-12375A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488541 | |||||||
| chr9:76488579 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-289-12337G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488579 | |||||||
| chr9:76488728 | T | A | 1 | a0001c0001t0022g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-289-12188T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488728 | |||||||
| chr9:76488786 | A | C | 52 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(49): Show |
53 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-289-12130A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488786 | |||||||
| chr9:76488786 | A | T | 23 | a0001c0001t0005g0016 a0001c0001t0005g0070 a0001c0001t0005g0072 others(20): Show |
24 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-289-12130A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488786 | |||||||
| chr9:76488792 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-12124C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488792 | |||||||
| chr9:76488793 | G | A | 1 | a0001c0001t0003g0327 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-289-12123G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488793 | |||||||
| chr9:76488879 | C | T | 1 | a0002c0006t0009g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-289-12037C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488879 | |||||||
| chr9:76488953 | T | A | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11963T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488953 | |||||||
| chr9:76488954 | T | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0132 a0001c0001t0004g0179 others(21): Show |
25 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-289-11962T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76488954 | |||||||
| chr9:76489003 | AC | A | 66 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(63): Show |
68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-11912delC | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489003 | |||||||
| chr9:76489005 | T | A | 66 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(63): Show |
68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-11911T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489005 | |||||||
| chr9:76489166 | C | T | 10 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(7): Show |
13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-11750C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489166 | |||||||
| chr9:76489192 | C | T | 21 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(18): Show |
24 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-289-11724C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489192 | |||||||
| chr9:76489254 | T | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11662T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489254 | |||||||
| chr9:76489283 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-289-11633C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489283 | |||||||
| chr9:76489301 | G | C | 8 | a0001c0001t0007g0017 a0001c0001t0007g0038 a0001c0001t0007g0076 others(5): Show |
9 | HG01255.hp1 HG02451.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-289-11615G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489301 | |||||||
| chr9:76489348 | C | T | 66 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(63): Show |
68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-11568C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489348 | |||||||
| chr9:76489456 | G | A | 1 | a0002c0002t0001g0254 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-289-11460G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489456 | |||||||
| chr9:76489549 | C | T | 5 | a0001c0001t0018g0086 a0001c0001t0018g0087 a0001c0001t0018g0088 others(2): Show |
5 | HG02280.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-289-11367C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489549 | |||||||
| chr9:76489683 | G | C | 81 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(78): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-289-11233G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489683 | |||||||
| chr9:76489734 | C | T | 21 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(18): Show |
24 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-289-11182C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489734 | |||||||
| chr9:76489744 | T | TC | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11166dupC | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76489744 | ||||||
| chr9:76489769 | A | G | 10 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(7): Show |
13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-11147A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489769 | |||||||
| chr9:76489891 | T | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-11025T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489891 | |||||||
| chr9:76489892 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-289-11024G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489892 | |||||||
| chr9:76489898 | G | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-11018G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489898 | |||||||
| chr9:76489902 | A | G | 2 | a0001c0001t0002g0105 a0001c0001t0002g0129 |
2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-289-11014A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489902 | |||||||
| chr9:76489957 | T | C | 299 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(296): Show |
330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-289-10959T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76489957 | |||||||
| chr9:76490088 | C | T | 1 | a0001c0001t0020g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-289-10828C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490088 | |||||||
| chr9:76490121 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-289-10795C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490121 | |||||||
| chr9:76490192 | A | G | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-10724A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490192 | |||||||
| chr9:76490364 | C | G | 85 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(82): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.-289-10552C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490364 | |||||||
| chr9:76490401 | T | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-10515T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490401 | |||||||
| chr9:76490445 | C | T | 21 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(18): Show |
24 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-289-10471C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490445 | |||||||
| chr9:76490648 | G | A | 1 | a0001c0001t0038g0143 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-289-10268G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490648 | |||||||
| chr9:76490668 | A | T | 1 | a0001c0001t0005g0150 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-289-10248A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490668 | |||||||
| chr9:76490742 | A | G | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-10174A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490742 | |||||||
| chr9:76490746 | T | C | 4 | a0002c0002t0001g0229 a0002c0002t0001g0231 a0002c0002t0001g0233 others(1): Show |
4 | NA18947.hp2 NA18982.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-10170T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490746 | |||||||
| chr9:76490762 | A | ACT | 298 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(295): Show |
329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-289-10153_-289-10 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76490762 | ||||||
| chr9:76490934 | T | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-9982T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490934 | |||||||
| chr9:76490941 | G | A | 24 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(21): Show |
27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-9975G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76490941 | |||||||
| chr9:76491116 | CTTCT | C | 3 | a0001c0001t0008g0044 a0001c0001t0022g0082 a0001c0001t0022g0083 |
3 | HG02109.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-289-9797_-289-979 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491116 | ||||||
| chr9:76491158 | C | CCT | 10 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(7): Show |
13 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-289-9749_-289-974 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491158 | ||||||
| chr9:76491177 | G | T | 18 | a0001c0001t0006g0207 a0002c0002t0001g0020 a0002c0002t0001g0118 others(15): Show |
19 | HG00438.hp1 HG00544.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-9739G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491177 | |||||||
| chr9:76491183 | TTCTC | T | 24 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(21): Show |
27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-9727_-289-972 others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491183 | ||||||
| chr9:76491220 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-289-9696T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491220 | |||||||
| chr9:76491258 | T | G | 1 | a0001c0001t0005g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-289-9658T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491258 | |||||||
| chr9:76491346 | T | A | 3 | a0003c0003t0017g0186 a0003c0003t0017g0222 a0003c0003t0017g0236 |
3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-9570T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491346 | |||||||
| chr9:76491357 | T | C | 3 | a0001c0001t0014g0036 a0001c0001t0014g0171 a0001c0001t0040g0047 |
3 | HG02280.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-289-9559T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491357 | |||||||
| chr9:76491509 | GT | G | 83 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(80): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-289-9402delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76491509 | ||||||
| chr9:76491736 | C | G | 100 | a0001c0001t0003g0327 a0001c0001t0006g0207 a0002c0002t0001g0002 others(97): Show |
110 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-289-9180C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491736 | |||||||
| chr9:76491741 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-9175C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491741 | |||||||
| chr9:76491797 | G | A | 154 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(151): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-289-9119G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491797 | |||||||
| chr9:76491829 | A | G | 66 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(63): Show |
68 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-289-9087A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491829 | |||||||
| chr9:76491835 | C | T | 154 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(151): Show |
167 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.-289-9081C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491835 | |||||||
| chr9:76491940 | A | G | 4 | a0001c0001t0003g0006 a0001c0001t0003g0022 a0001c0001t0003g0224 others(1): Show |
7 | HG00408.hp1 HG00544.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-289-8976A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491940 | |||||||
| chr9:76491994 | C | T | 1 | a0001c0001t0020g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-289-8922C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491994 | |||||||
| chr9:76491998 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-289-8918G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76491998 | |||||||
| chr9:76492023 | A | G | 1 | a0001c0001t0034g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-8893A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492023 | |||||||
| chr9:76492025 | C | G | 1 | a0001c0001t0006g0307 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-289-8891C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492025 | |||||||
| chr9:76492032 | C | T | 1 | a0001c0001t0005g0016 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-289-8884C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492032 | |||||||
| chr9:76492051 | A | C | 24 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(21): Show |
27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-8865A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492051 | |||||||
| chr9:76492102 | G | A | 14 | a0001c0001t0011g0190 a0001c0001t0011g0205 a0001c0001t0011g0216 others(11): Show |
14 | HG02040.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-289-8814G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492102 | |||||||
| chr9:76492198 | C | T | 1 | a0001c0001t0010g0215 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-289-8718C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492198 | |||||||
| chr9:76492279 | C | A | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-8637C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492279 | |||||||
| chr9:76492593 | C | T | 1 | a0001c0001t0003g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-289-8323C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492593 | |||||||
| chr9:76492660 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-289-8256G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492660 | |||||||
| chr9:76492661 | C | T | 2 | a0001c0001t0023g0176 a0001c0001t0023g0177 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-8255C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492661 | |||||||
| chr9:76492679 | T | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-8237T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492679 | |||||||
| chr9:76492706 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-8210C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492706 | |||||||
| chr9:76492707 | A | G | 299 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(296): Show |
330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-289-8209A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492707 | |||||||
| chr9:76492709 | T | A | 1 | a0001c0001t0006g0309 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-8207T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492709 | |||||||
| chr9:76492710 | C | A | 1 | a0001c0001t0006g0309 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-8206C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492710 | |||||||
| chr9:76492770 | C | T | 42 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(39): Show |
43 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-289-8146C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492770 | |||||||
| chr9:76492774 | A | AT | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-8138dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76492774 | ||||||
| chr9:76492833 | T | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-8083T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492833 | |||||||
| chr9:76492879 | G | A | 1 | a0001c0001t0006g0309 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-8037G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492879 | |||||||
| chr9:76492898 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-289-8018G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76492898 | |||||||
| chr9:76493031 | C | T | 25 | a0001c0001t0004g0018 a0001c0001t0004g0132 a0001c0001t0004g0179 others(22): Show |
26 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-289-7885C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493031 | |||||||
| chr9:76493046 | T | A | 1 | a0003c0003t0017g0186 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-289-7870T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493046 | |||||||
| chr9:76493072 | C | T | 24 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(21): Show |
27 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-7844C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493072 | |||||||
| chr9:76493158 | C | A | 3 | a0003c0003t0017g0186 a0003c0003t0017g0222 a0003c0003t0017g0236 |
3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-7758C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493158 | |||||||
| chr9:76493199 | T | G | 3 | a0001c0001t0002g0295 a0001c0001t0002g0296 a0001c0001t0002g0297 |
3 | HG02056.hp1 NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-289-7717T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493199 | |||||||
| chr9:76493248 | A | AT | 23 | a0001c0001t0005g0016 a0001c0001t0005g0070 a0001c0001t0005g0072 others(20): Show |
24 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-289-7667dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76493248 | ||||||
| chr9:76493283 | G | T | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-7633G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493283 | |||||||
| chr9:76493338 | C | T | 1 | a0001c0001t0035g0194 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-289-7578C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493338 | |||||||
| chr9:76493368 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-289-7548T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493368 | |||||||
| chr9:76493454 | A | G | 87 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(84): Show |
91 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.-289-7462A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493454 | |||||||
| chr9:76493466 | G | A | 153 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(150): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-289-7450G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493466 | |||||||
| chr9:76493513 | A | G | 1 | a0001c0001t0005g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-289-7403A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493513 | |||||||
| chr9:76493598 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-289-7318G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493598 | |||||||
| chr9:76493686 | C | A | 1 | a0001c0001t0040g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-7230C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493686 | |||||||
| chr9:76493689 | T | G | 1 | a0001c0001t0040g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-7227T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493689 | |||||||
| chr9:76493737 | A | G | 77 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(74): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.-289-7179A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493737 | |||||||
| chr9:76493823 | C | T | 3 | a0001c0001t0008g0044 a0001c0001t0022g0082 a0001c0001t0022g0083 |
3 | HG02109.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-289-7093C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493823 | |||||||
| chr9:76493836 | T | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-7080T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493836 | |||||||
| chr9:76493850 | A | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-7066A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493850 | |||||||
| chr9:76493882 | A | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-7034A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493882 | |||||||
| chr9:76493907 | T | C | 2 | a0001c0001t0004g0193 a0001c0001t0004g0203 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-289-7009T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76493907 | |||||||
| chr9:76494069 | C | T | 1 | a0001c0001t0004g0198 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-289-6847C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494069 | |||||||
| chr9:76494095 | C | A | 1 | a0001c0001t0008g0050 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-289-6821C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494095 | |||||||
| chr9:76494095 | C | T | 1 | a0002c0002t0001g0285 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-289-6821C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494095 | |||||||
| chr9:76494126 | G | A | 2 | a0002c0002t0001g0282 a0002c0004t0001g0281 |
2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-289-6790G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494126 | |||||||
| chr9:76494194 | A | G | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-6722A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494194 | |||||||
| chr9:76494216 | G | A | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-6700G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494216 | |||||||
| chr9:76494242 | G | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-6674G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494242 | |||||||
| chr9:76494289 | A | G | 42 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(39): Show |
43 | HG00639.hp1 HG00642.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-289-6627A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494289 | |||||||
| chr9:76494444 | G | A | 2 | a0002c0002t0001g0258 a0002c0002t0001g0259 |
2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-289-6472G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494444 | |||||||
| chr9:76494565 | G | A | 65 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(62): Show |
67 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.-289-6351G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494565 | |||||||
| chr9:76494618 | G | T | 7 | a0001c0001t0011g0190 a0001c0001t0011g0205 a0001c0001t0011g0216 others(4): Show |
7 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-289-6298G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494618 | |||||||
| chr9:76494647 | C | T | 6 | a0001c0001t0011g0190 a0001c0001t0011g0205 a0001c0001t0011g0216 others(3): Show |
6 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-6269C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494647 | |||||||
| chr9:76494656 | G | A | 2 | a0001c0001t0005g0072 a0001c0001t0005g0095 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-289-6260G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494656 | |||||||
| chr9:76494788 | C | T | 3 | a0001c0001t0006g0314 a0001c0001t0006g0315 a0001c0001t0006g0316 |
3 | NA18962.hp1 NA18965.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-289-6128C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494788 | |||||||
| chr9:76494807 | A | G | 1 | a0004c0009t0003g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-289-6109A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494807 | |||||||
| chr9:76494826 | C | T | 81 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(78): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-289-6090C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494826 | |||||||
| chr9:76494867 | C | T | 1 | a0001c0001t0026g0326 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-289-6049C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494867 | |||||||
| chr9:76494959 | A | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-5957A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76494959 | |||||||
| chr9:76495034 | G | A | 1 | a0001c0001t0040g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-289-5882G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495034 | |||||||
| chr9:76495082 | G | A | 81 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(78): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-289-5834G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495082 | |||||||
| chr9:76495115 | C | T | 2 | a0001c0001t0023g0176 a0001c0001t0023g0177 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-5801C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495115 | |||||||
| chr9:76495156 | A | G | 23 | a0001c0001t0005g0016 a0001c0001t0005g0070 a0001c0001t0005g0072 others(20): Show |
24 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-289-5760A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495156 | |||||||
| chr9:76495162 | C | T | 103 | a0001c0001t0003g0327 a0001c0001t0006g0013 a0001c0001t0006g0178 others(100): Show |
116 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-289-5754C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495162 | |||||||
| chr9:76495227 | G | A | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-5689G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495227 | |||||||
| chr9:76495244 | A | G | 298 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(295): Show |
329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-289-5672A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495244 | |||||||
| chr9:76495268 | T | A | 1 | a0001c0001t0012g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-289-5648T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495268 | |||||||
| chr9:76495320 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-289-5596T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495320 | |||||||
| chr9:76495338 | T | G | 3 | a0001c0001t0014g0036 a0001c0001t0014g0171 a0001c0001t0040g0047 |
3 | HG02280.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-289-5578T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495338 | |||||||
| chr9:76495528 | G | A | 7 | a0001c0001t0003g0011 a0001c0001t0003g0053 a0001c0001t0003g0058 others(4): Show |
8 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-289-5388G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495528 | |||||||
| chr9:76495565 | T | C | 1 | a0001c0001t0003g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-289-5351T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495565 | |||||||
| chr9:76495733 | G | A | 2 | a0001c0001t0004g0298 a0001c0001t0004g0303 |
2 | HG01167.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.-289-5183G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495733 | |||||||
| chr9:76495852 | T | G | 1 | a0001c0001t0005g0317 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-289-5064T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76495852 | |||||||
| chr9:76496085 | T | A | 2 | a0001c0001t0020g0028 a0001c0001t0020g0032 |
2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-289-4831T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496085 | |||||||
| chr9:76496164 | G | C | 1 | a0001c0001t0006g0309 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-289-4752G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496164 | |||||||
| chr9:76496278 | G | C | 1 | a0001c0001t0002g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-289-4638G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496278 | |||||||
| chr9:76496331 | C | G | 3 | a0002c0002t0001g0063 a0002c0002t0001g0249 a0002c0002t0001g0260 |
3 | HG01168.hp1 HG01981.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-289-4585C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496331 | |||||||
| chr9:76496346 | G | A | 2 | a0001c0001t0021g0318 a0001c0001t0021g0319 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-289-4570G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496346 | |||||||
| chr9:76496450 | T | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-4466T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496450 | |||||||
| chr9:76496476 | T | C | 1 | a0001c0001t0003g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-289-4440T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496476 | |||||||
| chr9:76496495 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-289-4421C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496495 | |||||||
| chr9:76496535 | A | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-4381A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496535 | |||||||
| chr9:76496600 | CTT | C | 83 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(80): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-289-4313_-289-431 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76496600 | ||||||
| chr9:76496612 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-289-4304A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496612 | |||||||
| chr9:76496759 | A | C | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-4157A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496759 | |||||||
| chr9:76496870 | A | G | 25 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(22): Show |
28 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.-289-4046A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496870 | |||||||
| chr9:76496995 | A | G | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3921A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76496995 | |||||||
| chr9:76497004 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-289-3912G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497004 | |||||||
| chr9:76497049 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-289-3867T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497049 | |||||||
| chr9:76497172 | C | G | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3744C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497172 | |||||||
| chr9:76497284 | C | T | 153 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(150): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-289-3632C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497284 | |||||||
| chr9:76497358 | G | A | 3 | a0003c0003t0017g0186 a0003c0003t0017g0222 a0003c0003t0017g0236 |
3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-3558G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497358 | |||||||
| chr9:76497510 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3406C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497510 | |||||||
| chr9:76497706 | A | C | 1 | a0001c0001t0034g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-3210A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497706 | |||||||
| chr9:76497772 | A | C | 191 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(188): Show |
209 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-289-3144A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497772 | |||||||
| chr9:76497785 | C | T | 152 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(149): Show |
165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.-289-3131C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497785 | |||||||
| chr9:76497854 | C | G | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3062C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497854 | |||||||
| chr9:76497901 | CAA | C | 25 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(22): Show |
28 | HG01243.hp2 HG01255.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.-289-3014_-289-301 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497901 | |||||||
| chr9:76497908 | T | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-3008T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76497908 | |||||||
| chr9:76497980 | AT | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(80): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-289-2934delT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76497980 | ||||||
| chr9:76498118 | A | C | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-2798A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498118 | |||||||
| chr9:76498158 | T | A | 1 | a0002c0002t0001g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-289-2758T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498158 | |||||||
| chr9:76498171 | G | A | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-2745G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498171 | |||||||
| chr9:76498227 | C | T | 17 | a0001c0001t0006g0024 a0001c0001t0006g0300 a0001c0001t0006g0301 others(14): Show |
19 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-289-2689C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498227 | |||||||
| chr9:76498389 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-289-2527C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498389 | |||||||
| chr9:76498581 | A | T | 195 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(192): Show |
213 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-289-2335A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498581 | |||||||
| chr9:76498614 | A | C | 100 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(97): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-289-2302A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498614 | |||||||
| chr9:76498638 | G | T | 298 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(295): Show |
329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-289-2278G>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498638 | |||||||
| chr9:76498641 | C | T | 2 | a0001c0001t0007g0009 a0001c0001t0007g0322 |
4 | HG01243.hp2 HG02257.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-2275C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498641 | |||||||
| chr9:76498773 | CA | C | 14 | a0001c0001t0005g0113 a0001c0001t0007g0009 a0001c0001t0007g0017 others(11): Show |
17 | HG01070.hp2 HG01243.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.-289-2126delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76498773 | ||||||
| chr9:76498786 | A | AG | 99 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(96): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-289-2130_-289-212 others(5): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498786 | |||||||
| chr9:76498786 | A | G | 1 | a0001c0001t0006g0301 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-289-2130A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498786 | |||||||
| chr9:76498787 | A | AG | 103 | a0001c0001t0003g0327 a0001c0001t0006g0013 a0001c0001t0006g0178 others(100): Show |
116 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.-289-2129_-289-212 others(5): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498787 | |||||||
| chr9:76498790 | A | AG | 6 | a0001c0001t0011g0190 a0001c0001t0011g0205 a0001c0001t0011g0216 others(3): Show |
6 | HG02040.hp2 HG02055.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-289-2125dupG | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76498790 | ||||||
| chr9:76498790 | A | G | 19 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(16): Show |
22 | HG01243.hp2 HG01255.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-289-2126A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498790 | |||||||
| chr9:76498923 | G | A | 315 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(312): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.-289-1993G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76498923 | |||||||
| chr9:76499020 | A | G | 2 | a0001c0001t0023g0176 a0001c0001t0023g0177 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-289-1896A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499020 | |||||||
| chr9:76499050 | A | AT | 107 | a0001c0001t0003g0081 a0001c0001t0003g0327 a0001c0001t0004g0189 others(104): Show |
120 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.-289-1856dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76499050 | ||||||
| chr9:76499050 | A | ATT | 192 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(189): Show |
210 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.-289-1857_-289-185 others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76499050 | ||||||
| chr9:76499309 | G | A | 3 | a0003c0003t0017g0186 a0003c0003t0017g0222 a0003c0003t0017g0236 |
3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-1607G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499309 | |||||||
| chr9:76499316 | T | C | 298 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(295): Show |
329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-289-1600T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499316 | |||||||
| chr9:76499416 | C | T | 71 | a0001c0001t0003g0042 a0001c0001t0003g0328 a0001c0001t0004g0018 others(68): Show |
73 | HG00639.hp1 HG00642.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.-289-1500C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499416 | |||||||
| chr9:76499443 | C | T | 4 | a0001c0001t0014g0036 a0001c0001t0014g0171 a0001c0001t0014g0174 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-1473C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499443 | |||||||
| chr9:76499468 | T | C | 299 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(296): Show |
330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-289-1448T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499468 | |||||||
| chr9:76499605 | C | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0263 |
2 | HG00609.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-289-1311C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499605 | |||||||
| chr9:76499743 | C | T | 1 | a0001c0001t0020g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-289-1173C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76499743 | |||||||
| chr9:76500138 | T | A | 4 | a0001c0001t0014g0036 a0001c0001t0014g0171 a0001c0001t0014g0174 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-289-778T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500138 | |||||||
| chr9:76500140 | A | AT | 98 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(95): Show |
110 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-289-766dupT | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr9 | 76500140 | ||||||
| chr9:76500148 | T | G | 3 | a0001c0001t0008g0044 a0001c0001t0022g0082 a0001c0001t0022g0083 |
3 | HG02109.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-289-768T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500148 | |||||||
| chr9:76500189 | A | G | 1 | a0001c0001t0002g0140 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-289-727A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500189 | |||||||
| chr9:76500241 | T | C | 1 | a0001c0001t0006g0321 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-289-675T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500241 | |||||||
| chr9:76500261 | T | C | 9 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(6): Show |
12 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-289-655T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500261 | |||||||
| chr9:76500322 | T | C | 4 | a0001c0001t0011g0190 a0001c0001t0011g0226 a0001c0001t0011g0227 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-289-594T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500322 | |||||||
| chr9:76500577 | G | A | 1 | a0001c0001t0034g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-289-339G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500577 | |||||||
| chr9:76500653 | T | G | 1 | a0001c0001t0003g0328 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-289-263T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500653 | |||||||
| chr9:76500682 | C | T | 1 | a0002c0002t0001g0244 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-289-234C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500682 | |||||||
| chr9:76500729 | C | A | 2 | a0002c0002t0009g0267 a0002c0002t0009g0268 |
2 | HG01106.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-289-187C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500729 | |||||||
| chr9:76500731 | A | G | 3 | a0003c0003t0017g0186 a0003c0003t0017g0222 a0003c0003t0017g0236 |
3 | HG02055.hp1 HG03471.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-289-185A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500731 | |||||||
| chr9:76500808 | T | G | 24 | a0001c0001t0002g0112 a0001c0001t0002g0127 a0001c0001t0002g0149 others(21): Show |
27 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.-289-108T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500808 | |||||||
| chr9:76500813 | A | G | 100 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(97): Show |
112 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-289-103A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 2/3 | chr9 | 76500813 | |||||||
| chr9:76501192 | C | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(100): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-144+131C>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501192 | |||||||
| chr9:76501249 | T | A | 30 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(27): Show |
33 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-144+188T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501249 | |||||||
| chr9:76501274 | G | C | 70 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0007 others(67): Show |
79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-144+213G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501274 | |||||||
| chr9:76501278 | C | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0178 a0001c0001t0006g0207 |
4 | NA18963.hp2 NA18975.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.-144+217C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501278 | |||||||
| chr9:76501358 | C | T | 132 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(129): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-144+297C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501358 | |||||||
| chr9:76501402 | G | A | 1 | a0002c0002t0001g0258 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-144+341G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501402 | |||||||
| chr9:76501429 | A | G | 102 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(99): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-144+368A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501429 | |||||||
| chr9:76501452 | C | T | 102 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(99): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-144+391C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501452 | |||||||
| chr9:76501497 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0032g0135 |
2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-144+436G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501497 | |||||||
| chr9:76501512 | A | C | 1 | a0001c0001t0002g0134 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-144+451A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501512 | |||||||
| chr9:76501516 | T | C | 1 | a0001c0001t0018g0086 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-144+455T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501516 | |||||||
| chr9:76501637 | G | A | 1 | a0002c0002t0001g0225 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-144+576G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501637 | |||||||
| chr9:76501712 | C | G | 2 | a0001c0001t0002g0110 a0001c0001t0002g0123 |
2 | HG00140.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-143-527C>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501712 | |||||||
| chr9:76501714 | T | G | 2 | a0001c0001t0021g0318 a0001c0001t0021g0319 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-143-525T>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501714 | |||||||
| chr9:76501820 | GA | G | 298 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(295): Show |
329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.-143-417delA | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76501820 | ||||||
| chr9:76501839 | T | C | 22 | a0001c0001t0006g0013 a0001c0001t0006g0024 a0001c0001t0006g0178 others(19): Show |
25 | HG01123.hp2 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.-143-400T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501839 | |||||||
| chr9:76501906 | G | A | 1 | a0001c0001t0045g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-143-333G>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76501906 | |||||||
| chr9:76502059 | A | C | 314 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(311): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.-143-180A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502059 | |||||||
| chr9:76502061 | T | C | 132 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(129): Show |
149 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-143-178T>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502061 | |||||||
| chr9:76502105 | C | T | 30 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(27): Show |
33 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-143-134C>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502105 | |||||||
| chr9:76502155 | A | G | 30 | a0001c0001t0007g0009 a0001c0001t0007g0017 a0001c0001t0007g0038 others(27): Show |
33 | HG01243.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-143-84A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502155 | |||||||
| chr9:76502169 | CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0005g0016 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-143-68_-143-53del others(16): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502169 | ||||||
| chr9:76502173 | CTCTCTGT others(5): Show |
C | 7 | a0001c0001t0008g0049 a0001c0001t0008g0050 a0001c0001t0008g0051 others(4): Show |
7 | HG00642.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-143-64_-143-53del others(12): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502173 | ||||||
| chr9:76502175 | CTCTGTAT others(5): Show |
C | 3 | a0001c0001t0002g0114 a0001c0001t0002g0119 a0001c0001t0030g0116 |
3 | HG00408.hp2 NA18965.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-143-62_-143-51del others(12): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502175 | ||||||
| chr9:76502177 | CTGTATA | C | 95 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(92): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-143-60_-143-55del others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502177 | ||||||
| chr9:76502179 | G | C | 21 | a0001c0001t0005g0070 a0001c0001t0005g0072 a0001c0001t0005g0089 others(18): Show |
21 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-143-60G>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502179 | |||||||
| chr9:76502179 | GTATA | G | 80 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0010 others(77): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-143-38_-143-35del others(4): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | ||||||
| chr9:76502179 | GTATATA | G | 43 | a0001c0001t0003g0081 a0001c0001t0003g0327 a0001c0001t0003g0328 others(40): Show |
46 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.-143-40_-143-35del others(6): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | ||||||
| chr9:76502179 | GTATATAT others(1): Show |
G | 57 | a0001c0001t0003g0042 a0001c0001t0004g0018 a0001c0001t0004g0132 others(54): Show |
61 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-143-42_-143-35del others(8): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | ||||||
| chr9:76502179 | GTATATAT others(3): Show |
G | 2 | a0001c0001t0002g0109 a0001c0001t0002g0133 |
2 | HG01081.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-143-44_-143-35del others(10): Show |
GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr9 | 76502179 | ||||||
| chr9:76502181 | A | C | 22 | a0001c0001t0005g0070 a0001c0001t0005g0072 a0001c0001t0005g0089 others(19): Show |
22 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-143-58A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502181 | |||||||
| chr9:76502183 | A | C | 23 | a0001c0001t0005g0070 a0001c0001t0005g0072 a0001c0001t0005g0089 others(20): Show |
23 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-143-56A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502183 | |||||||
| chr9:76502185 | A | C | 117 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(114): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-143-54A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502185 | |||||||
| chr9:76502185 | A | G | 1 | a0001c0001t0024g0162 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-143-54A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502185 | |||||||
| chr9:76502187 | A | C | 97 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(94): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-143-52A>C | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502187 | |||||||
| chr9:76502187 | A | G | 29 | a0001c0001t0005g0016 a0001c0001t0005g0070 a0001c0001t0005g0072 others(26): Show |
30 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-143-52A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502187 | |||||||
| chr9:76502189 | A | G | 100 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0014 others(97): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-143-50A>G | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502189 | |||||||
| chr9:76502201 | A | T | 1 | a0001c0001t0003g0077 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-143-38A>T | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502201 | |||||||
| chr9:76502205 | T | A | 1 | a0001c0001t0003g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-143-34T>A | GCNT1 | ENSG00000187210.14 | transcript | ENST00000376730.5 | protein_coding | 3/3 | chr9 | 76502205 |