Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57452 |
| ensemblid | ENSG00000100626.17 |
| hgncid | 23233 |
| symbol | GALNT16 |
| name | polypeptide N-acetylgalactosaminyltransferase 16 |
| refseq_nuc | NM_001168368.2 |
| refseq_prot | NP_001161840.1 |
| ensembl_nuc | ENST00000448469.8 |
| ensembl_prot | ENSP00000402970.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 69260158 |
| end | 69354466 |
| strand | + |
| ver | v1.2 |
| region | chr14:69260158-69354466 |
| region5000 | chr14:69255158-69359466 |
| regionname0 | GALNT16_chr14_69260158_69354466 |
| regionname5000 | GALNT16_chr14_69255158_69359466 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 558 | 227 | 64 | 32 | 84 | 8 | 37 | 61 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0002 | 0/0 | 558 | 46 | 7 | 12 | 13 | 6 | 8 | 8 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0003 | 0/0 | 558 | 22 | 18 | 4 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0004 | 0/0 | 558 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0005 | 0/0 | 558 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0006 | 0/0 | 558 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0007 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0008 | 0/0 | 558 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| a0009 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | MRKIR others(553): Show |
chr14 | 69255158 | 69359466 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1674 | 183 | 57 | 29 | 61 | 7 | 27 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0003 | 0/0 | 1674 | 31 | 1 | 2 | 22 | 0 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0005 | 0/0 | 1674 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0007 | 0/0 | 1674 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0008 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0009 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0015 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0016 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0001c0017 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0002c0002 | 0/0 | 1674 | 45 | 7 | 11 | 13 | 6 | 8 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0002c0011 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0003c0004 | 0/0 | 1674 | 22 | 18 | 4 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0004c0006 | 0/0 | 1674 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0005c0013 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0005c0014 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0006c0010 | 0/0 | 1674 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0007c0019 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0008c0018 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 | ||
| a0009c0012 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | ATGAG others(1669): Show |
chr14 | 69255158 | 69359466 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4108 | 96 | 19 | 16 | 46 | 3 | 11 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0002 | 0/1 | 4108 | 30 | 12 | 4 | 6 | 1 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0003 | 0/0 | 4108 | 15 | 5 | 4 | 5 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0004 | 0/0 | 4108 | 11 | 0 | 3 | 0 | 3 | 5 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0005 | 0/0 | 4108 | 5 | 3 | 1 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0007 | 0/0 | 4106 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4101): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0008 | 0/0 | 4108 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0010 | 0/0 | 4108 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0012 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0013 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0014 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0015 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0016 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0017 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0018 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0019 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0020 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0021 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0024 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0025 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0026 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0027 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0001t0028 | 0/0 | 4054 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4049): Show |
chr14 | 69255158 | 69359466 |
| a0001c0003t0001 | 0/0 | 4108 | 15 | 0 | 2 | 9 | 0 | 4 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0003t0002 | 0/0 | 4108 | 3 | 0 | 0 | 2 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0003t0003 | 0/0 | 4108 | 11 | 0 | 0 | 11 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0003t0022 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0003t0023 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0005t0006 | 0/0 | 4108 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0007t0001 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0007t0004 | 0/0 | 4108 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0008t0002 | 0/0 | 4108 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0009t0001 | 0/0 | 4108 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0015t0003 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0016t0006 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0001c0017t0001 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0002c0002t0001 | 0/0 | 4108 | 29 | 3 | 6 | 11 | 3 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0002c0002t0002 | 0/0 | 4108 | 11 | 3 | 3 | 1 | 2 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0002c0002t0003 | 0/0 | 4108 | 2 | 0 | 0 | 1 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0002c0002t0004 | 0/0 | 4108 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0002c0002t0011 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0002c0011t0002 | 0/0 | 4108 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0003c0004t0001 | 0/0 | 4108 | 14 | 13 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0003c0004t0002 | 0/0 | 4108 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0003c0004t0009 | 0/0 | 4108 | 4 | 2 | 2 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0003c0004t0011 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0004c0006t0003 | 0/0 | 4108 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0005c0013t0001 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0005c0014t0001 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0006c0010t0002 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0006c0010t0004 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0007c0019t0008 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0008c0018t0002 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| a0009c0012t0001 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | CTCCT others(4103): Show |
chr14 | 69255158 | 69359466 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0259 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0008g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0010g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0012g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0014g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0015g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0016g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0017g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0018g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0019g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0020g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0021g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0024g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0025g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0026g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0027g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0028g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0022g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0023g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0005t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0005t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0005t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0005t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0007t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0008t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0008t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0009t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0009t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0015t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0016t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0017t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0011t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0004c0006t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0004c0006t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0004c0006t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0004c0006t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0005c0013t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0005c0014t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0006c0010t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0006c0010t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0007c0019t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0008c0018t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0009c0012t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0252 | EUR | GBR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0240 | EUR | GBR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0253 | EUR | FIN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00673 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0255 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01069 | hp1 | a0002 | c0002 | t0004 | g0265 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01071 | hp2 | a0002 | c0002 | t0004 | g0266 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0260 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01081 | hp1 | a0002 | c0011 | t0002 | g0263 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01081 | hp2 | a0003 | c0004 | t0009 | g0148 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0133 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0297 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0238 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0291 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0216 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0292 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0258 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01433 | hp2 | a0003 | c0004 | t0002 | g0201 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01496 | hp1 | a0003 | c0004 | t0009 | g0149 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01496 | hp2 | a0001 | c0007 | t0004 | g0250 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01515 | hp1 | a0001 | c0007 | t0001 | g0262 | EUR | IBS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0034 | EUR | IBS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0254 | EUR | IBS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0033 | EUR | IBS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01884 | hp2 | a0003 | c0004 | t0001 | g0159 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0264 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0163 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0009 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0228 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0113 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02135 | hp1 | a0001 | c0001 | t0019 | g0165 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0010 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0285 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | CDX | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0094 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0198 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02258 | hp2 | a0003 | c0004 | t0001 | g0040 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02280 | hp1 | a0001 | c0003 | t0023 | g0021 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02451 | hp2 | a0001 | c0005 | t0006 | g0138 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0295 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02615 | hp1 | a0003 | c0004 | t0001 | g0039 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02622 | hp1 | a0001 | c0005 | t0006 | g0139 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0128 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0204 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02683 | hp1 | a0001 | c0003 | t0022 | g0066 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02717 | hp1 | a0002 | c0002 | t0011 | g0020 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02717 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02723 | hp1 | a0003 | c0004 | t0001 | g0271 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0050 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0023 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02809 | hp2 | a0001 | c0001 | t0021 | g0075 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0290 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02896 | hp1 | a0001 | c0016 | t0006 | g0154 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0146 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02965 | hp1 | a0003 | c0004 | t0002 | g0289 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02970 | hp1 | a0001 | c0005 | t0006 | g0175 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02976 | hp1 | a0003 | c0004 | t0009 | g0145 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0140 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03041 | hp1 | a0001 | c0005 | t0006 | g0081 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03139 | hp2 | a0007 | c0019 | t0008 | g0151 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0245 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03225 | hp1 | a0003 | c0004 | t0011 | g0024 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0143 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0272 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0015 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0177 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03540 | hp1 | a0003 | c0004 | t0002 | g0027 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0225 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0022 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0299 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03654 | hp2 | a0001 | c0008 | t0002 | g0188 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0251 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03688 | hp2 | a0001 | c0009 | t0001 | g0281 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0296 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0269 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0294 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03831 | hp2 | a0001 | c0001 | t0024 | g0097 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03927 | hp1 | a0008 | c0018 | t0002 | g0293 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0099 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03942 | hp2 | a0001 | c0008 | t0002 | g0189 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0056 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0089 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04184 | hp2 | a0001 | c0001 | t0028 | g0109 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0067 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04204 | hp1 | a0006 | c0010 | t0002 | g0055 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0232 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04228 | hp1 | a0006 | c0010 | t0004 | g0173 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0274 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18747 | hp1 | a0001 | c0003 | t0003 | g0029 | EAS | CHB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0280 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18941 | hp2 | a0001 | c0001 | t0020 | g0192 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18945 | hp2 | a0004 | c0006 | t0003 | g0220 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18957 | hp1 | a0001 | c0003 | t0003 | g0117 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18957 | hp2 | a0001 | c0017 | t0001 | g0270 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18963 | hp1 | a0001 | c0003 | t0003 | g0031 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0152 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18975 | hp1 | a0001 | c0003 | t0003 | g0122 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0213 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18982 | hp2 | a0001 | c0003 | t0003 | g0098 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0157 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0070 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18995 | hp1 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19007 | hp1 | a0001 | c0003 | t0003 | g0221 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19007 | hp2 | a0004 | c0006 | t0003 | g0112 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19010 | hp1 | a0004 | c0006 | t0003 | g0222 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19030 | hp1 | a0001 | c0001 | t0015 | g0057 | AFR | LWK | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0160 | AFR | LWK | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19043 | hp2 | a0003 | c0004 | t0009 | g0212 | AFR | LWK | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19056 | hp1 | a0001 | c0003 | t0003 | g0103 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19068 | hp1 | a0009 | c0012 | t0001 | g0119 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19077 | hp1 | a0004 | c0006 | t0003 | g0223 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0108 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19087 | hp1 | a0001 | c0001 | t0018 | g0134 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19240 | hp1 | a0003 | c0004 | t0001 | g0137 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20129 | hp1 | a0003 | c0004 | t0001 | g0233 | AFR | ASW | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | ASW | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0256 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0249 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20905 | hp1 | a0001 | c0001 | t0026 | g0298 | SAS | GIH | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20905 | hp2 | a0001 | c0009 | t0001 | g0065 | SAS | GIH | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02109 | hp1 | a0001 | c0015 | t0003 | g0287 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0277 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02486 | hp1 | a0005 | c0014 | t0001 | g0008 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02559 | hp1 | a0005 | c0013 | t0001 | g0283 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | USA | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | USA | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18955 | hp1 | a0001 | c0001 | t0025 | g0184 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | USA | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20300 | hp2 | a0001 | c0001 | t0027 | g0077 | AFR | USA | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0207 | REF | REF | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0259 | REF | REF | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69260462 | C | T | 1 | a0007 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.172C>T | p.Leu58Phe | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/15 | 305/4108 | 172/1677 | 58/558 | chr14 | 69260462 | |||
| chr14:69324727 | C | T | 1 | a0004 | 4 | NA18945.hp2 NA19007.hp2 NA19010.hp1 others(1): Show |
missense_variant | MODERATE | c.371C>T | p.Ala124Val | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 3/15 | 504/4108 | 371/1677 | 124/558 | chr14 | 69324727 | |||
| chr14:69324735 | G | A | 1 | a0009 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.379G>A | p.Val127Ile | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 3/15 | 512/4108 | 379/1677 | 127/558 | chr14 | 69324735 | |||
| chr14:69325369 | A | G | 1 | a0006 | 2 | HG04204.hp1 HG04228.hp1 |
missense_variant | MODERATE | c.467A>G | p.Gln156Arg | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/15 | 600/4108 | 467/1677 | 156/558 | chr14 | 69325369 | |||
| chr14:69326021 | C | T | 1 | a0008 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.562C>T | p.Arg188Trp | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/15 | 695/4108 | 562/1677 | 188/558 | chr14 | 69326021 | |||
| chr14:69328482 | G | A | 2 | a0002 a0009 |
47 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(44): Show |
missense_variant | MODERATE | c.601G>A | p.Val201Met | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/15 | 734/4108 | 601/1677 | 201/558 | chr14 | 69328482 | |||
| chr14:69338695 | G | A | 1 | a0005 | 2 | HG02486.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.1012G>A | p.Val338Ile | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/15 | 1145/4108 | 1012/1677 | 338/558 | chr14 | 69338695 | |||
| chr14:69347952 | C | T | 1 | a0003 | 22 | HG01081.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
missense_variant | MODERATE | c.1489C>T | p.Pro497Ser | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/15 | 1622/4108 | 1489/1677 | 497/558 | chr14 | 69347952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69260404 | G | A | 2 | a0001c0007 a0002c0011 |
3 | HG01081.hp1 HG01496.hp2 HG01515.hp1 |
synonymous_variant | LOW | c.114G>A | p.Arg38Arg | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/15 | 247/4108 | 114/1677 | 38/558 | chr14 | 69260404 | |||
| chr14:69328451 | G | A | 1 | a0007c0019 | 1 | HG03139.hp2 | splice_region_variant&synonymous_variant | LOW | c.570G>A | p.Gly190Gly | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/15 | 703/4108 | 570/1677 | 190/558 | chr14 | 69328451 | |||
| chr14:69333089 | C | T | 2 | a0001c0003 a0001c0009 |
33 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(30): Show |
synonymous_variant | LOW | c.783C>T | p.Phe261Phe | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 8/15 | 916/4108 | 783/1677 | 261/558 | chr14 | 69333089 | |||
| chr14:69339584 | G | A | 2 | a0001c0015 a0001c0016 |
2 | HG02109.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.1152G>A | p.Glu384Glu | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/15 | 1285/4108 | 1152/1677 | 384/558 | chr14 | 69339584 | |||
| chr14:69339614 | C | T | 1 | a0005c0014 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.1182C>T | p.Phe394Phe | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/15 | 1315/4108 | 1182/1677 | 394/558 | chr14 | 69339614 | |||
| chr14:69347052 | G | A | 1 | a0001c0009 | 2 | HG03688.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.1284G>A | p.Lys428Lys | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 13/15 | 1417/4108 | 1284/1677 | 428/558 | chr14 | 69347052 | |||
| chr14:69347960 | C | G | 1 | a0001c0017 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.1497C>G | p.Ser499Ser | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/15 | 1630/4108 | 1497/1677 | 499/558 | chr14 | 69347960 | |||
| chr14:69352129 | C | T | 2 | a0001c0005 a0001c0016 |
5 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.1638C>T | p.Asp546Asp | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1771/4108 | 1638/1677 | 546/558 | chr14 | 69352129 | |||
| chr14:69352138 | C | G | 1 | a0001c0008 | 2 | HG03654.hp2 HG03942.hp2 |
synonymous_variant | LOW | c.1647C>G | p.Ala549Ala | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1780/4108 | 1647/1677 | 549/558 | chr14 | 69352138 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69260251 | G | A | 4 | a0001c0001t0010 a0001c0001t0012 a0002c0002t0011 others(1): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-40G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/15 | 40 | chr14 | 69260251 | ||||||
| chr14:69352174 | G | A | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0013 others(3): Show |
21 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 6 | chr14 | 69352174 | ||||||
| chr14:69352347 | C | T | 1 | a0001c0001t0028 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 179 | chr14 | 69352347 | ||||||
| chr14:69352353 | G | A | 1 | a0001c0001t0014 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*185G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 185 | chr14 | 69352353 | ||||||
| chr14:69352353 | G | C | 1 | a0001c0001t0015 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*185G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 185 | chr14 | 69352353 | ||||||
| chr14:69352383 | C | T | 1 | a0001c0001t0027 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 215 | chr14 | 69352383 | ||||||
| chr14:69352384 | G | A | 4 | a0001c0001t0004 a0001c0007t0004 a0002c0002t0004 others(1): Show |
15 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*216G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 216 | chr14 | 69352384 | ||||||
| chr14:69352400 | A | C | 1 | a0003c0004t0009 | 4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*232A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 232 | chr14 | 69352400 | ||||||
| chr14:69352481 | G | A | 1 | a0001c0001t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 313 | chr14 | 69352481 | ||||||
| chr14:69352489 | G | A | 1 | a0001c0001t0017 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 321 | chr14 | 69352489 | ||||||
| chr14:69352593 | A | G | 9 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0025 others(6): Show |
37 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*425A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 425 | chr14 | 69352593 | ||||||
| chr14:69352611 | GGA | G | 1 | a0001c0001t0007 | 5 | HG02109.hp2 HG02886.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*447_*448delAG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 447 | INFO_REALIGN_3_PRIME | chr14 | 69352611 | |||||
| chr14:69352668 | G | A | 1 | a0001c0001t0017 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*500G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 500 | chr14 | 69352668 | ||||||
| chr14:69352970 | G | A | 2 | a0001c0001t0018 a0001c0001t0025 |
2 | NA18955.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*802G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 802 | chr14 | 69352970 | ||||||
| chr14:69353123 | A | G | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(27): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*955A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 955 | chr14 | 69353123 | ||||||
| chr14:69353209 | C | T | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(15): Show |
64 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1041C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1041 | chr14 | 69353209 | ||||||
| chr14:69353244 | TTCAACCT others(47): Show |
T | 1 | a0001c0001t0028 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1102_*1155delCGCT others(50): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1102 | INFO_REALIGN_3_PRIME | chr14 | 69353244 | |||||
| chr14:69353533 | T | C | 2 | a0001c0001t0008 a0007c0019t0008 |
4 | HG01175.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1365T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1365 | chr14 | 69353533 | ||||||
| chr14:69353697 | G | A | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0013 others(4): Show |
22 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1529G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1529 | chr14 | 69353697 | ||||||
| chr14:69353851 | C | T | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0024 others(3): Show |
21 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1683C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1683 | chr14 | 69353851 | ||||||
| chr14:69353986 | G | A | 1 | a0001c0001t0019 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1818G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1818 | chr14 | 69353986 | ||||||
| chr14:69353995 | T | C | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(28): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1827T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1827 | chr14 | 69353995 | ||||||
| chr14:69354063 | G | A | 1 | a0001c0001t0017 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1895G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1895 | chr14 | 69354063 | ||||||
| chr14:69354127 | A | C | 1 | a0001c0003t0022 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1959A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 1959 | chr14 | 69354127 | ||||||
| chr14:69354229 | C | A | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2061C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 2061 | chr14 | 69354229 | ||||||
| chr14:69354290 | C | T | 1 | a0001c0003t0023 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2122C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 2122 | chr14 | 69354290 | ||||||
| chr14:69354342 | T | C | 1 | a0001c0001t0021 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2174T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 2174 | chr14 | 69354342 | ||||||
| chr14:69354348 | C | T | 1 | a0001c0001t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2180C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 2180 | chr14 | 69354348 | ||||||
| chr14:69354439 | C | A | 1 | a0001c0001t0026 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2271C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 15/15 | 2271 | chr14 | 69354439 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:69260477 | C | A | 23 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0018 others(20): Show |
24 | HG00099.hp1 HG00741.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.177+10C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69260477 | |||||||
| chr14:69260495 | C | A | 2 | a0001c0001t0002g0028 a0001c0003t0003g0029 |
2 | HG02738.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.177+28C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69260495 | |||||||
| chr14:69260569 | C | G | 11 | a0001c0001t0005g0296 a0001c0001t0026g0298 a0001c0003t0001g0295 others(8): Show |
11 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+102C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69260569 | |||||||
| chr14:69260806 | T | TGCCCCGG others(20): Show |
3 | a0001c0001t0003g0030 a0001c0001t0003g0032 a0001c0003t0003g0031 |
3 | NA18963.hp1 NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.177+342_177+368dup others(27): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69260806 | ||||||
| chr14:69260856 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0002g0286 a0001c0001t0002g0288 others(3): Show |
7 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+389C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69260856 | |||||||
| chr14:69260873 | G | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0037 others(2): Show |
5 | HG00280.hp2 HG00738.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+406G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69260873 | |||||||
| chr14:69260956 | G | C | 1 | a0002c0002t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.177+489G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69260956 | |||||||
| chr14:69261101 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0037 others(2): Show |
5 | HG00280.hp2 HG00738.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+634C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69261101 | |||||||
| chr14:69261142 | G | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0018 others(12): Show |
16 | HG00099.hp1 HG00741.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+675G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69261142 | |||||||
| chr14:69261486 | C | T | 3 | a0001c0001t0002g0284 a0001c0001t0014g0285 a0005c0013t0001g0283 |
3 | HG02145.hp2 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.177+1019C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69261486 | |||||||
| chr14:69261752 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.177+1285G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69261752 | |||||||
| chr14:69261755 | C | T | 1 | a0001c0009t0001g0281 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.177+1288C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69261755 | |||||||
| chr14:69261770 | A | G | 6 | a0001c0001t0001g0018 a0002c0002t0001g0001 a0002c0002t0001g0016 others(3): Show |
7 | HG00099.hp1 HG00741.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+1303A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69261770 | |||||||
| chr14:69261846 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0037 others(2): Show |
5 | HG00280.hp2 HG00738.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+1379G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69261846 | |||||||
| chr14:69262042 | G | T | 4 | a0001c0001t0001g0278 a0001c0001t0003g0279 a0001c0001t0007g0277 others(1): Show |
4 | HG01192.hp1 HG02109.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+1575G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262042 | |||||||
| chr14:69262075 | G | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0002g0007 others(7): Show |
11 | HG00099.hp1 HG00741.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.177+1608G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262075 | |||||||
| chr14:69262130 | G | C | 3 | a0001c0001t0001g0041 a0003c0004t0001g0039 a0003c0004t0001g0040 |
3 | HG02258.hp2 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.177+1663G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262130 | |||||||
| chr14:69262174 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0002g0276 a0001c0001t0002g0286 others(4): Show |
8 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+1707A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262174 | |||||||
| chr14:69262181 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0045 others(66): Show |
70 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.177+1714G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262181 | |||||||
| chr14:69262199 | C | T | 3 | a0001c0001t0002g0284 a0001c0001t0014g0285 a0005c0013t0001g0283 |
3 | HG02145.hp2 HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.177+1732C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262199 | |||||||
| chr14:69262278 | C | T | 2 | a0001c0001t0002g0275 a0001c0001t0007g0274 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.177+1811C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262278 | |||||||
| chr14:69262390 | G | T | 5 | a0001c0001t0001g0018 a0002c0002t0001g0001 a0002c0002t0001g0016 others(2): Show |
6 | HG00099.hp1 HG00741.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+1923G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262390 | |||||||
| chr14:69262414 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+1947C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262414 | |||||||
| chr14:69262503 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+2036G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262503 | |||||||
| chr14:69262690 | G | A | 41 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(38): Show |
43 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.177+2223G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262690 | |||||||
| chr14:69262709 | AC | A | 6 | a0001c0001t0001g0005 a0001c0001t0002g0276 a0001c0001t0002g0288 others(3): Show |
7 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+2249delC | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69262709 | ||||||
| chr14:69262715 | C | A | 35 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(32): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.177+2248C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262715 | |||||||
| chr14:69262820 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0002g0042 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.177+2353G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69262820 | |||||||
| chr14:69262883 | CT | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.177+2430delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69262883 | ||||||
| chr14:69263253 | A | T | 1 | a0001c0001t0003g0037 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.177+2786A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263253 | |||||||
| chr14:69263529 | C | T | 1 | a0002c0002t0001g0246 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.177+3062C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263529 | |||||||
| chr14:69263627 | C | T | 5 | a0001c0001t0002g0276 a0001c0001t0002g0286 a0001c0001t0002g0288 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+3160C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263627 | |||||||
| chr14:69263745 | T | C | 1 | a0001c0001t0007g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.177+3278T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263745 | |||||||
| chr14:69263768 | A | T | 5 | a0001c0001t0002g0276 a0001c0001t0002g0286 a0001c0001t0002g0288 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+3301A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263768 | |||||||
| chr14:69263841 | C | T | 1 | a0003c0004t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.177+3374C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263841 | |||||||
| chr14:69263861 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0002g0042 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.177+3394C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263861 | |||||||
| chr14:69263867 | G | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.177+3400G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263867 | |||||||
| chr14:69263899 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0002g0095 a0001c0001t0002g0096 others(6): Show |
10 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.177+3432A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263899 | |||||||
| chr14:69263901 | C | T | 1 | a0001c0001t0017g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.177+3434C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69263901 | |||||||
| chr14:69264014 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 |
3 | HG02280.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.177+3547T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69264014 | |||||||
| chr14:69264155 | C | T | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(5): Show |
8 | HG00738.hp1 HG01123.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+3688C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69264155 | |||||||
| chr14:69264513 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0002g0276 a0001c0001t0002g0286 others(4): Show |
8 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+4046A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69264513 | |||||||
| chr14:69264571 | G | A | 1 | a0001c0001t0018g0134 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.177+4104G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69264571 | |||||||
| chr14:69264671 | GATTTTGT others(4): Show |
G | 1 | a0001c0001t0001g0135 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.177+4206_177+4216d others(13): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264671 | ||||||
| chr14:69264780 | C | CTTTCT | 4 | a0001c0001t0002g0276 a0001c0001t0002g0288 a0003c0004t0001g0290 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+4322_177+4326d others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264780 | ||||||
| chr14:69264819 | C | CTTTTTT | 28 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(25): Show |
28 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.177+4358_177+4363d others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(1): Show |
41 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(38): Show |
43 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.177+4356_177+4363d others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(7): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0045 others(11): Show |
16 | HG00099.hp1 HG00741.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.177+4363_177+4364i others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(8): Show |
39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0035 others(36): Show |
40 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.177+4363_177+4364i others(17): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(9): Show |
17 | a0001c0001t0001g0144 a0001c0001t0002g0007 a0001c0001t0002g0085 others(14): Show |
17 | HG01069.hp2 HG01192.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.177+4363_177+4364i others(18): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(10): Show |
17 | a0001c0001t0001g0011 a0001c0001t0001g0150 a0001c0001t0001g0153 others(14): Show |
17 | HG01081.hp2 HG01496.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.177+4363_177+4364i others(19): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(11): Show |
73 | a0001c0001t0001g0135 a0001c0001t0001g0162 a0001c0001t0001g0164 others(70): Show |
73 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.177+4363_177+4364i others(20): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(12): Show |
26 | a0001c0001t0001g0041 a0001c0001t0001g0218 a0001c0001t0001g0219 others(23): Show |
26 | HG00408.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.177+4363_177+4364i others(21): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(13): Show |
6 | a0001c0001t0001g0239 a0001c0001t0001g0241 a0001c0001t0001g0243 others(3): Show |
6 | HG00140.hp2 HG01258.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+4363_177+4364i others(22): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0010g0023 a0001c0001t0012g0022 |
2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.177+4363_177+4364i others(23): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(15): Show |
1 | a0003c0004t0011g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.177+4363_177+4364i others(24): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0010g0025 a0001c0001t0010g0026 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.177+4363_177+4364i others(25): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69264819 | ||||||
| chr14:69264819 | C | T | 1 | a0001c0001t0007g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.177+4352C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69264819 | |||||||
| chr14:69265107 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.177+4640C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265107 | |||||||
| chr14:69265158 | G | A | 1 | a0003c0004t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.177+4691G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265158 | |||||||
| chr14:69265164 | TCCTGGGC others(10): Show |
T | 1 | a0003c0004t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.177+4702_177+4718d others(19): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69265164 | ||||||
| chr14:69265210 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(52): Show |
56 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.177+4743G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265210 | |||||||
| chr14:69265402 | A | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.177+4935A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265402 | |||||||
| chr14:69265471 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0002g0276 a0001c0001t0002g0286 others(4): Show |
8 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+5004A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265471 | |||||||
| chr14:69265597 | T | C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+5130T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265597 | |||||||
| chr14:69265602 | G | A | 1 | a0003c0004t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.177+5135G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265602 | |||||||
| chr14:69265648 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+5181C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265648 | |||||||
| chr14:69265800 | T | C | 1 | a0002c0002t0002g0292 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.177+5333T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265800 | |||||||
| chr14:69265820 | C | T | 1 | a0001c0003t0001g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.177+5353C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265820 | |||||||
| chr14:69265842 | T | G | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+5375T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265842 | |||||||
| chr14:69265844 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(23): Show |
28 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.177+5377T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265844 | |||||||
| chr14:69265871 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+5404C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69265871 | |||||||
| chr14:69266082 | T | C | 4 | a0001c0001t0002g0276 a0001c0001t0002g0288 a0003c0004t0001g0290 others(1): Show |
4 | HG01891.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+5615T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266082 | |||||||
| chr14:69266127 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0002g0007 others(6): Show |
10 | HG00099.hp1 HG00741.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+5660T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266127 | |||||||
| chr14:69266205 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+5738G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266205 | |||||||
| chr14:69266501 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0002g0007 a0005c0014t0001g0008 |
3 | HG02486.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.177+6034C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266501 | |||||||
| chr14:69266626 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(23): Show |
28 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.177+6159C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266626 | |||||||
| chr14:69266791 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+6324C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266791 | |||||||
| chr14:69266937 | A | C | 1 | a0001c0001t0003g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.177+6470A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266937 | |||||||
| chr14:69266969 | T | C | 1 | a0001c0001t0007g0277 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.177+6502T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69266969 | |||||||
| chr14:69267112 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+6645G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267112 | |||||||
| chr14:69267268 | C | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.177+6801C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267268 | |||||||
| chr14:69267447 | G | A | 1 | a0001c0001t0008g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.177+6980G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267447 | |||||||
| chr14:69267583 | G | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(31): Show |
36 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.177+7116G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267583 | |||||||
| chr14:69267781 | C | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0045 others(65): Show |
69 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.177+7314C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267781 | |||||||
| chr14:69267832 | C | T | 2 | a0001c0001t0001g0083 a0001c0003t0001g0214 |
2 | HG00673.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.177+7365C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267832 | |||||||
| chr14:69267835 | C | T | 1 | a0002c0002t0003g0213 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.177+7368C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267835 | |||||||
| chr14:69267867 | T | C | 3 | a0001c0001t0003g0158 a0001c0003t0003g0157 a0002c0002t0001g0156 |
3 | NA18986.hp1 NA19011.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.177+7400T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267867 | |||||||
| chr14:69267883 | C | A | 1 | a0001c0001t0001g0011 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.177+7416C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267883 | |||||||
| chr14:69267974 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.177+7507C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69267974 | |||||||
| chr14:69268468 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 |
3 | HG02280.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.177+8001G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69268468 | |||||||
| chr14:69268475 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+8008C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69268475 | |||||||
| chr14:69268605 | G | A | 4 | a0003c0004t0002g0027 a0003c0004t0009g0145 a0003c0004t0009g0148 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+8138G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69268605 | |||||||
| chr14:69268672 | TG | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(52): Show |
56 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.177+8209delG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69268672 | ||||||
| chr14:69268911 | G | C | 4 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 others(1): Show |
4 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+8444G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69268911 | |||||||
| chr14:69269033 | G | A | 3 | a0003c0004t0001g0159 a0003c0004t0001g0160 a0003c0004t0001g0216 |
3 | HG01243.hp1 HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.177+8566G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269033 | |||||||
| chr14:69269380 | C | CGT | 276 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.177+8925_177+8926d others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69269380 | ||||||
| chr14:69269487 | G | A | 2 | a0001c0001t0003g0161 a0001c0003t0023g0021 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.177+9020G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269487 | |||||||
| chr14:69269498 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(63): Show |
67 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.177+9031G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269498 | |||||||
| chr14:69269502 | T | TTGTG | 11 | a0001c0001t0005g0296 a0001c0001t0026g0298 a0001c0003t0001g0295 others(8): Show |
11 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+9044_177+9047d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69269502 | ||||||
| chr14:69269525 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.177+9058C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269525 | |||||||
| chr14:69269756 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(21): Show |
26 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.177+9289G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269756 | |||||||
| chr14:69269778 | A | G | 7 | a0001c0001t0001g0041 a0001c0001t0002g0275 a0001c0001t0007g0274 others(4): Show |
7 | HG01175.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+9311A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269778 | |||||||
| chr14:69269802 | T | TTG | 5 | a0001c0001t0002g0276 a0001c0001t0002g0286 a0001c0001t0002g0288 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+9341_177+9342d others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69269802 | ||||||
| chr14:69269802 | T | TTGTGTG | 6 | a0001c0001t0001g0045 a0001c0001t0001g0144 a0001c0001t0005g0046 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+9337_177+9342d others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69269802 | ||||||
| chr14:69269802 | T | TTGTGTGT others(1): Show |
7 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(4): Show |
7 | HG02717.hp2 HG02922.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+9342_177+9343i others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69269802 | ||||||
| chr14:69269802 | T | TTGTGTGT others(3): Show |
4 | a0001c0001t0001g0005 a0001c0001t0003g0019 a0001c0003t0023g0021 others(1): Show |
5 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+9342_177+9343i others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69269802 | ||||||
| chr14:69269808 | GTT | G | 9 | a0001c0001t0001g0006 a0001c0001t0002g0007 a0001c0001t0002g0284 others(6): Show |
9 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+9343_177+9344d others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69269808 | ||||||
| chr14:69269810 | T | G | 29 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0018 others(26): Show |
31 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.177+9343T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269810 | |||||||
| chr14:69269818 | G | A | 46 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(43): Show |
48 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.177+9351G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269818 | |||||||
| chr14:69269840 | G | A | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(34): Show |
39 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.177+9373G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269840 | |||||||
| chr14:69269892 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.177+9425A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269892 | |||||||
| chr14:69269894 | G | A | 1 | a0003c0004t0001g0143 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+9427G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69269894 | |||||||
| chr14:69270520 | G | A | 1 | a0002c0002t0001g0100 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.177+10053G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69270520 | |||||||
| chr14:69270543 | C | A | 1 | a0002c0002t0001g0069 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.177+10076C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69270543 | |||||||
| chr14:69270728 | C | T | 11 | a0001c0001t0005g0296 a0001c0001t0026g0298 a0001c0003t0001g0295 others(8): Show |
11 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+10261C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69270728 | |||||||
| chr14:69270774 | G | A | 2 | a0001c0001t0001g0150 a0007c0019t0008g0151 |
2 | HG01934.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.177+10307G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69270774 | |||||||
| chr14:69270951 | C | T | 2 | a0001c0003t0001g0067 a0001c0003t0022g0066 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.177+10484C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69270951 | |||||||
| chr14:69270955 | T | TGAA | 276 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.177+10490_177+1049 others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69270955 | ||||||
| chr14:69271165 | G | A | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+10698G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271165 | |||||||
| chr14:69271344 | G | C | 1 | a0002c0002t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.177+10877G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271344 | |||||||
| chr14:69271362 | G | A | 173 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0101 others(170): Show |
175 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.177+10895G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271362 | |||||||
| chr14:69271415 | G | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0047 others(65): Show |
69 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.177+10948G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271415 | |||||||
| chr14:69271471 | C | T | 9 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0005g0046 others(6): Show |
9 | HG01175.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+11004C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271471 | |||||||
| chr14:69271543 | A | T | 1 | a0001c0009t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.177+11076A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271543 | |||||||
| chr14:69271567 | C | A | 1 | a0001c0001t0004g0272 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.177+11100C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271567 | |||||||
| chr14:69271567 | C | T | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+11100C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271567 | |||||||
| chr14:69271574 | A | C | 1 | a0001c0003t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.177+11107A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271574 | |||||||
| chr14:69271583 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+11116C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271583 | |||||||
| chr14:69271603 | G | C | 70 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(67): Show |
72 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.177+11136G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271603 | |||||||
| chr14:69271842 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.177+11375C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271842 | |||||||
| chr14:69271843 | G | A | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.177+11376G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69271843 | |||||||
| chr14:69272111 | G | A | 101 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0135 others(98): Show |
101 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.177+11644G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272111 | |||||||
| chr14:69272180 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0043 others(67): Show |
72 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.177+11713G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272180 | |||||||
| chr14:69272319 | T | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(269): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.177+11852T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272319 | |||||||
| chr14:69272336 | C | A | 1 | a0003c0004t0001g0159 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.177+11869C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272336 | |||||||
| chr14:69272648 | C | T | 46 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(43): Show |
48 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.177+12181C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272648 | |||||||
| chr14:69272746 | A | G | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+12279A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272746 | |||||||
| chr14:69272767 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0002g0007 others(6): Show |
10 | HG00099.hp1 HG00741.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+12300C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272767 | |||||||
| chr14:69272768 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0043 others(67): Show |
72 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.177+12301G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272768 | |||||||
| chr14:69272965 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.177+12498A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69272965 | |||||||
| chr14:69273022 | G | A | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+12555G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273022 | |||||||
| chr14:69273176 | G | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0037 others(3): Show |
6 | HG00280.hp2 HG00738.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+12709G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273176 | |||||||
| chr14:69273229 | TG | T | 46 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(43): Show |
48 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.177+12765delG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69273229 | ||||||
| chr14:69273263 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0002g0286 a0001c0015t0003g0287 others(2): Show |
6 | HG01243.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+12796G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273263 | |||||||
| chr14:69273343 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.177+12876A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273343 | |||||||
| chr14:69273350 | A | G | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.177+12883A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273350 | |||||||
| chr14:69273475 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0209 others(4): Show |
7 | HG00280.hp2 HG00738.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+13008A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273475 | |||||||
| chr14:69273766 | T | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(273): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.177+13299T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273766 | |||||||
| chr14:69273811 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+13344G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273811 | |||||||
| chr14:69273820 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+13353T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273820 | |||||||
| chr14:69273827 | G | A | 2 | a0001c0001t0003g0226 a0001c0001t0016g0225 |
2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.177+13360G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273827 | |||||||
| chr14:69273848 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.177+13381A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273848 | |||||||
| chr14:69273867 | A | G | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.177+13400A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273867 | |||||||
| chr14:69273894 | C | G | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+13427C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69273894 | |||||||
| chr14:69274131 | G | A | 2 | a0001c0001t0001g0101 a0005c0013t0001g0283 |
2 | HG02559.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.177+13664G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69274131 | |||||||
| chr14:69274169 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.177+13702C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69274169 | |||||||
| chr14:69274170 | A | C | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+13703A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69274170 | |||||||
| chr14:69274287 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+13820T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69274287 | |||||||
| chr14:69274311 | T | C | 5 | a0001c0001t0002g0276 a0001c0001t0002g0288 a0001c0001t0017g0245 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+13844T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69274311 | |||||||
| chr14:69274541 | T | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(85): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.177+14074T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69274541 | |||||||
| chr14:69274726 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.177+14259G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69274726 | |||||||
| chr14:69275047 | A | G | 2 | a0001c0001t0026g0298 a0002c0002t0002g0299 |
2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.177+14580A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275047 | |||||||
| chr14:69275109 | C | T | 44 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(41): Show |
46 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.177+14642C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275109 | |||||||
| chr14:69275143 | G | A | 5 | a0001c0001t0007g0140 a0001c0001t0008g0094 a0001c0005t0006g0138 others(2): Show |
5 | HG02257.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+14676G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275143 | |||||||
| chr14:69275202 | G | A | 1 | a0001c0003t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.177+14735G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275202 | |||||||
| chr14:69275341 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.177+14874T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275341 | |||||||
| chr14:69275371 | G | GTA | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0037 others(3): Show |
6 | HG00280.hp2 HG00738.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+14916_177+1491 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69275371 | ||||||
| chr14:69275427 | G | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0002c0002t0001g0001 others(4): Show |
8 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+14960G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275427 | |||||||
| chr14:69275435 | T | C | 3 | a0001c0001t0001g0239 a0001c0001t0002g0227 a0001c0001t0002g0240 |
3 | HG00140.hp2 HG01258.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.177+14968T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275435 | |||||||
| chr14:69275597 | C | T | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+15130C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275597 | |||||||
| chr14:69275604 | C | A | 1 | a0001c0005t0006g0175 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.177+15137C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275604 | |||||||
| chr14:69275648 | G | C | 1 | a0001c0001t0002g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.177+15181G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275648 | |||||||
| chr14:69275912 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.177+15445A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275912 | |||||||
| chr14:69275923 | G | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.177+15456G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69275923 | |||||||
| chr14:69276051 | G | C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+15584G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276051 | |||||||
| chr14:69276121 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+15654C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276121 | |||||||
| chr14:69276151 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0049 others(58): Show |
62 | HG00558.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.177+15684G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276151 | |||||||
| chr14:69276165 | A | G | 2 | a0002c0002t0001g0297 a0002c0002t0001g0301 |
2 | HG01069.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.177+15698A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276165 | |||||||
| chr14:69276203 | T | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(8): Show |
11 | HG00280.hp2 HG00738.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.177+15736T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276203 | |||||||
| chr14:69276260 | G | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.177+15793G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276260 | |||||||
| chr14:69276410 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+15943C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276410 | |||||||
| chr14:69276417 | G | A | 11 | a0001c0001t0005g0296 a0001c0001t0026g0298 a0001c0003t0001g0295 others(8): Show |
11 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+15950G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276417 | |||||||
| chr14:69276457 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0002g0286 a0001c0001t0005g0046 others(2): Show |
5 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+15990C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276457 | |||||||
| chr14:69276458 | G | A | 97 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0162 others(94): Show |
97 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.177+15991G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276458 | |||||||
| chr14:69276533 | T | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+16066T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276533 | |||||||
| chr14:69276581 | T | C | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+16114T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276581 | |||||||
| chr14:69276680 | CA | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0036 others(228): Show |
234 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.177+16226delA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69276680 | ||||||
| chr14:69276680 | CAA | C | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+16225_177+1622 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69276680 | ||||||
| chr14:69276738 | G | T | 1 | a0001c0001t0005g0296 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.177+16271G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276738 | |||||||
| chr14:69276795 | A | T | 2 | a0003c0004t0001g0290 a0003c0004t0002g0289 |
2 | HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.177+16328A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276795 | |||||||
| chr14:69276863 | G | A | 45 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(42): Show |
47 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.177+16396G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276863 | |||||||
| chr14:69276876 | T | C | 1 | a0001c0001t0007g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.177+16409T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69276876 | |||||||
| chr14:69277204 | C | G | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+16737C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277204 | |||||||
| chr14:69277218 | T | G | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+16751T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277218 | |||||||
| chr14:69277245 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+16778T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277245 | |||||||
| chr14:69277343 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.177+16876G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277343 | |||||||
| chr14:69277494 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.177+17027A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277494 | |||||||
| chr14:69277630 | A | T | 5 | a0001c0001t0001g0041 a0001c0001t0008g0238 a0003c0004t0001g0009 others(2): Show |
5 | HG01175.hp2 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+17163A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277630 | |||||||
| chr14:69277731 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+17264A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277731 | |||||||
| chr14:69277796 | C | T | 5 | a0001c0001t0002g0276 a0001c0001t0002g0288 a0001c0001t0017g0245 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+17329C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277796 | |||||||
| chr14:69277909 | C | T | 1 | a0001c0001t0008g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.177+17442C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69277909 | |||||||
| chr14:69278008 | C | CT | 8 | a0001c0001t0001g0045 a0001c0001t0001g0126 a0001c0001t0001g0209 others(5): Show |
8 | HG02074.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+17558dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69278008 | ||||||
| chr14:69278008 | CT | C | 10 | a0001c0001t0001g0049 a0001c0001t0001g0178 a0001c0001t0001g0241 others(7): Show |
10 | HG01175.hp2 HG02698.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.177+17558delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69278008 | ||||||
| chr14:69278031 | C | T | 6 | a0001c0001t0001g0045 a0001c0001t0002g0286 a0001c0001t0003g0161 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+17564C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278031 | |||||||
| chr14:69278067 | G | A | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+17600G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278067 | |||||||
| chr14:69278168 | C | T | 12 | a0001c0001t0001g0101 a0001c0001t0001g0115 a0001c0001t0001g0116 others(9): Show |
12 | HG00438.hp1 HG00621.hp2 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.177+17701C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278168 | |||||||
| chr14:69278170 | G | A | 3 | a0001c0001t0010g0023 a0001c0001t0010g0026 a0001c0001t0012g0022 |
3 | HG02572.hp1 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.177+17703G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278170 | |||||||
| chr14:69278225 | T | G | 100 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0162 others(97): Show |
100 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+17758T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278225 | |||||||
| chr14:69278308 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(2): Show |
5 | HG02145.hp1 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+17841A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278308 | |||||||
| chr14:69278440 | G | C | 1 | a0001c0003t0001g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.177+17973G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278440 | |||||||
| chr14:69278586 | A | G | 100 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0162 others(97): Show |
100 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.177+18119A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278586 | |||||||
| chr14:69278697 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0002g0286 others(4): Show |
8 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+18230C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278697 | |||||||
| chr14:69278932 | A | AT | 41 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(38): Show |
43 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.177+18481dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69278932 | ||||||
| chr14:69278932 | AT | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(26): Show |
31 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.177+18481delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69278932 | ||||||
| chr14:69278949 | G | A | 1 | a0001c0001t0026g0298 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.177+18482G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69278949 | |||||||
| chr14:69279042 | C | T | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+18575C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279042 | |||||||
| chr14:69279054 | C | T | 2 | a0001c0001t0002g0273 a0001c0001t0004g0272 |
2 | HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+18587C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279054 | |||||||
| chr14:69279080 | C | T | 44 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0114 others(41): Show |
46 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.177+18613C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279080 | |||||||
| chr14:69279081 | G | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.177+18614G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279081 | |||||||
| chr14:69279119 | A | G | 1 | a0005c0013t0001g0283 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.177+18652A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279119 | |||||||
| chr14:69279226 | C | G | 6 | a0001c0001t0010g0023 a0001c0001t0010g0025 a0001c0001t0010g0026 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.177+18759C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279226 | |||||||
| chr14:69279232 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0002g0286 others(6): Show |
10 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.177+18765A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279232 | |||||||
| chr14:69279262 | T | G | 1 | a0001c0001t0010g0026 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.177+18795T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279262 | |||||||
| chr14:69279403 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.177+18936G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279403 | |||||||
| chr14:69279532 | G | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(133): Show |
140 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.177+19065G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279532 | |||||||
| chr14:69279558 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0002g0013 a0001c0001t0002g0014 others(4): Show |
7 | HG02145.hp1 HG02717.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+19091A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279558 | |||||||
| chr14:69279628 | A | G | 260 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(257): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.177+19161A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279628 | |||||||
| chr14:69279639 | G | A | 215 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0043 others(212): Show |
218 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.177+19172G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279639 | |||||||
| chr14:69279714 | G | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(122): Show |
126 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.177+19247G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279714 | |||||||
| chr14:69279804 | T | G | 12 | a0001c0001t0002g0276 a0001c0001t0005g0296 a0001c0001t0026g0298 others(9): Show |
12 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+19337T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279804 | |||||||
| chr14:69279898 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0047 others(7): Show |
11 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+19431C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279898 | |||||||
| chr14:69280007 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0083 others(110): Show |
114 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.177+19540T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280007 | |||||||
| chr14:69280033 | A | G | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0019 others(14): Show |
17 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.177+19566A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280033 | |||||||
| chr14:69280036 | A | G | 4 | a0001c0001t0002g0275 a0001c0001t0007g0274 a0003c0004t0001g0143 others(1): Show |
4 | HG02895.hp2 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+19569A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280036 | |||||||
| chr14:69280092 | C | T | 2 | a0001c0001t0026g0298 a0002c0002t0002g0299 |
2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.177+19625C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280092 | |||||||
| chr14:69280174 | C | T | 192 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(189): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.177+19707C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280174 | |||||||
| chr14:69280202 | C | T | 3 | a0001c0001t0002g0275 a0001c0001t0007g0274 a0003c0004t0002g0027 |
3 | HG02895.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.177+19735C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280202 | |||||||
| chr14:69280245 | CT | C | 15 | a0001c0001t0001g0045 a0001c0001t0001g0141 a0001c0001t0001g0142 others(12): Show |
15 | HG01081.hp2 HG01496.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+19779delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280245 | |||||||
| chr14:69280329 | G | A | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(173): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.177+19862G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280329 | |||||||
| chr14:69280415 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0141 a0001c0001t0001g0142 others(10): Show |
13 | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.177+19948A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280415 | |||||||
| chr14:69280456 | C | T | 1 | a0003c0004t0001g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.177+19989C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280456 | |||||||
| chr14:69280517 | A | G | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(131): Show |
135 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.177+20050A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280517 | |||||||
| chr14:69280563 | A | G | 2 | a0001c0003t0001g0061 a0002c0002t0001g0062 |
2 | HG00741.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.177+20096A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280563 | |||||||
| chr14:69280616 | C | T | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(4): Show |
7 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+20149C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280616 | |||||||
| chr14:69280714 | T | C | 3 | a0001c0003t0001g0105 a0002c0002t0001g0004 a0002c0002t0002g0106 |
4 | HG02165.hp2 HG02523.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+20247T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280714 | |||||||
| chr14:69280767 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.177+20300T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280767 | |||||||
| chr14:69280799 | C | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(5): Show |
8 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+20332C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69280799 | |||||||
| chr14:69281009 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.177+20542C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281009 | |||||||
| chr14:69281017 | G | A | 5 | a0001c0001t0002g0286 a0001c0001t0003g0161 a0001c0001t0014g0285 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+20550G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281017 | |||||||
| chr14:69281108 | C | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+20641C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281108 | |||||||
| chr14:69281116 | A | T | 1 | a0003c0004t0002g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.177+20649A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281116 | |||||||
| chr14:69281148 | T | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0178 others(33): Show |
36 | HG01069.hp2 HG01081.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.177+20681T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281148 | |||||||
| chr14:69281393 | C | T | 1 | a0003c0004t0001g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.177+20926C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281393 | |||||||
| chr14:69281414 | C | T | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.177+20947C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281414 | |||||||
| chr14:69281577 | G | A | 5 | a0001c0001t0002g0286 a0001c0001t0003g0161 a0001c0001t0014g0285 others(2): Show |
5 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+21110G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281577 | |||||||
| chr14:69281611 | TG | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(7): Show |
10 | HG02145.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+21146delG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69281611 | ||||||
| chr14:69281824 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+21357C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281824 | |||||||
| chr14:69281841 | G | A | 20 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0206 others(17): Show |
20 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.177+21374G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281841 | |||||||
| chr14:69281915 | A | G | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(4): Show |
7 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+21448A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281915 | |||||||
| chr14:69281961 | T | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+21494T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281961 | |||||||
| chr14:69281993 | A | T | 2 | a0001c0001t0001g0006 a0005c0014t0001g0008 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.177+21526A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69281993 | |||||||
| chr14:69282087 | C | T | 1 | a0001c0003t0001g0214 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.177+21620C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282087 | |||||||
| chr14:69282149 | G | A | 20 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0206 others(17): Show |
20 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.177+21682G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282149 | |||||||
| chr14:69282169 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.177+21702C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282169 | |||||||
| chr14:69282324 | G | T | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(4): Show |
7 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+21857G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282324 | |||||||
| chr14:69282328 | T | C | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(4): Show |
7 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+21861T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282328 | |||||||
| chr14:69282380 | C | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.177+21913C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282380 | |||||||
| chr14:69282383 | G | A | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.177+21916G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282383 | |||||||
| chr14:69282650 | C | CTATT | 69 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0102 others(66): Show |
70 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.177+22213_177+2221 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69282650 | ||||||
| chr14:69282650 | C | CTATTTAT others(1): Show |
85 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0043 others(82): Show |
87 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.177+22209_177+2221 others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69282650 | ||||||
| chr14:69282650 | C | CTATTTAT others(5): Show |
5 | a0001c0001t0001g0051 a0001c0001t0003g0037 a0001c0001t0010g0026 others(2): Show |
5 | HG00738.hp2 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+22205_177+2221 others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69282650 | ||||||
| chr14:69282650 | CTATTTAT others(5): Show |
C | 42 | a0001c0001t0001g0011 a0001c0001t0001g0178 a0001c0001t0001g0180 others(39): Show |
42 | HG01069.hp2 HG01081.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.177+22205_177+2221 others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69282650 | ||||||
| chr14:69282755 | T | A | 42 | a0001c0001t0001g0011 a0001c0001t0001g0178 a0001c0001t0001g0180 others(39): Show |
42 | HG01069.hp2 HG01081.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.177+22288T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282755 | |||||||
| chr14:69282801 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(192): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.177+22334A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282801 | |||||||
| chr14:69282973 | T | C | 2 | a0001c0008t0002g0188 a0001c0008t0002g0189 |
2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.177+22506T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282973 | |||||||
| chr14:69282981 | A | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+22514A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69282981 | |||||||
| chr14:69283274 | G | C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+22807G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69283274 | |||||||
| chr14:69283461 | G | A | 26 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.177+22994G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69283461 | |||||||
| chr14:69283473 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(7): Show |
10 | HG02145.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+23006C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69283473 | |||||||
| chr14:69283785 | C | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(145): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.177+23318C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69283785 | |||||||
| chr14:69283987 | A | G | 8 | a0001c0001t0002g0276 a0001c0001t0005g0296 a0001c0001t0007g0274 others(5): Show |
8 | HG01346.hp1 HG02698.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+23520A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69283987 | |||||||
| chr14:69284078 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.177+23611C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284078 | |||||||
| chr14:69284248 | G | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+23781G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284248 | |||||||
| chr14:69284323 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0058 a0001c0001t0001g0060 others(2): Show |
5 | HG00558.hp2 HG02135.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+23856C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284323 | |||||||
| chr14:69284429 | C | T | 2 | a0001c0001t0014g0285 a0005c0013t0001g0283 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.177+23962C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284429 | |||||||
| chr14:69284532 | A | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(12): Show |
15 | HG02145.hp1 HG02145.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+24065A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284532 | |||||||
| chr14:69284565 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(143): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.177+24098G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284565 | |||||||
| chr14:69284605 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(7): Show |
10 | HG02145.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+24138G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284605 | |||||||
| chr14:69284656 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.177+24189A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284656 | |||||||
| chr14:69284734 | A | C | 4 | a0001c0001t0001g0080 a0001c0001t0003g0079 a0001c0001t0005g0082 others(1): Show |
4 | HG02615.hp2 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.177+24267A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284734 | |||||||
| chr14:69284736 | C | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(7): Show |
10 | HG02145.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.177+24269C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284736 | |||||||
| chr14:69284813 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(159): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.177+24346T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284813 | |||||||
| chr14:69284923 | G | A | 26 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(23): Show |
26 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.177+24456G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284923 | |||||||
| chr14:69285038 | C | CTT | 57 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 others(54): Show |
59 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.177+24572_177+2457 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69285038 | ||||||
| chr14:69285040 | C | CG | 9 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(6): Show |
9 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.177+24573_177+2457 others(5): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285040 | |||||||
| chr14:69285040 | C | CT | 112 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0045 others(109): Show |
113 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.177+24591dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69285040 | ||||||
| chr14:69285040 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.177+24573C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285040 | |||||||
| chr14:69285040 | CT | C | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0032 others(5): Show |
8 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+24591delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69285040 | ||||||
| chr14:69285041 | T | G | 23 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0206 others(20): Show |
23 | HG01069.hp2 HG01081.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.177+24574T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285041 | |||||||
| chr14:69285063 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+24596C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285063 | |||||||
| chr14:69285101 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.177+24634C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285101 | |||||||
| chr14:69285102 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(191): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.177+24635A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285102 | |||||||
| chr14:69285109 | C | A | 2 | a0003c0004t0001g0290 a0003c0004t0002g0289 |
2 | HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.177+24642C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285109 | |||||||
| chr14:69285173 | T | TG | 73 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(70): Show |
75 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.177+24709dupG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69285173 | ||||||
| chr14:69285185 | C | T | 1 | a0001c0001t0002g0288 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.177+24718C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285185 | |||||||
| chr14:69285442 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(163): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.177+24975G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285442 | |||||||
| chr14:69285444 | CAT | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(163): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.177+24978_177+2497 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285444 | |||||||
| chr14:69285462 | C | CA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
11 | HG00558.hp1 HG01361.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+24996dupA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69285462 | ||||||
| chr14:69285530 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0206 others(18): Show |
21 | HG01069.hp2 HG01175.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.177+25063C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285530 | |||||||
| chr14:69285659 | G | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+25192G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285659 | |||||||
| chr14:69285669 | G | A | 1 | a0001c0003t0003g0031 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.177+25202G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285669 | |||||||
| chr14:69285703 | C | T | 244 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.177+25236C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285703 | |||||||
| chr14:69285784 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(126): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.177+25317G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285784 | |||||||
| chr14:69285886 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(176): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.177+25419C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285886 | |||||||
| chr14:69285951 | C | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(66): Show |
71 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.177+25484C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285951 | |||||||
| chr14:69285985 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.177+25518G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285985 | |||||||
| chr14:69286058 | C | A | 25 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(22): Show |
25 | HG00558.hp2 HG00642.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.177+25591C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286058 | |||||||
| chr14:69286076 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.177+25609T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286076 | |||||||
| chr14:69286135 | G | A | 174 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(171): Show |
177 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.177+25668G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286135 | |||||||
| chr14:69286154 | A | G | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(4): Show |
7 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+25687A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286154 | |||||||
| chr14:69286249 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(66): Show |
71 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.177+25782G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286249 | |||||||
| chr14:69286267 | A | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0083 others(78): Show |
82 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.177+25800A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286267 | |||||||
| chr14:69286304 | C | CT | 172 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0035 others(169): Show |
175 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.177+25852dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69286304 | ||||||
| chr14:69286476 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.177+26009G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286476 | |||||||
| chr14:69286652 | T | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.177+26185T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286652 | |||||||
| chr14:69286877 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+26410C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286877 | |||||||
| chr14:69286949 | C | A | 1 | a0002c0002t0001g0301 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.177+26482C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286949 | |||||||
| chr14:69286975 | C | T | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0010g0023 others(4): Show |
7 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.177+26508C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286975 | |||||||
| chr14:69287004 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(4): Show |
7 | HG02486.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+26537C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287004 | |||||||
| chr14:69287039 | A | C | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.177+26572A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287039 | |||||||
| chr14:69287055 | C | A | 108 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(105): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.177+26588C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287055 | |||||||
| chr14:69287366 | C | T | 3 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0286 |
3 | HG02486.hp2 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+26899C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287366 | |||||||
| chr14:69287461 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+26994G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287461 | |||||||
| chr14:69287480 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+27013G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287480 | |||||||
| chr14:69287575 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+27108C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287575 | |||||||
| chr14:69287595 | C | T | 2 | a0001c0001t0001g0005 a0001c0015t0003g0287 |
3 | HG01243.hp2 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.177+27128C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287595 | |||||||
| chr14:69287727 | G | A | 1 | a0002c0002t0001g0190 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.177+27260G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287727 | |||||||
| chr14:69287751 | T | C | 3 | a0001c0003t0003g0221 a0004c0006t0003g0220 a0004c0006t0003g0222 |
3 | NA18945.hp2 NA19007.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.177+27284T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287751 | |||||||
| chr14:69287785 | A | G | 104 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(101): Show |
106 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.177+27318A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69287785 | |||||||
| chr14:69288056 | G | A | 251 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(248): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.177+27589G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288056 | |||||||
| chr14:69288160 | G | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.177+27693G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288160 | |||||||
| chr14:69288205 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(140): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.177+27738T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288205 | |||||||
| chr14:69288454 | C | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.177+27987C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288454 | |||||||
| chr14:69288496 | A | G | 1 | a0001c0001t0015g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.177+28029A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288496 | |||||||
| chr14:69288603 | C | T | 1 | a0003c0004t0002g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.177+28136C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288603 | |||||||
| chr14:69288637 | G | C | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.177+28170G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288637 | |||||||
| chr14:69288716 | A | G | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+28249A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288716 | |||||||
| chr14:69288720 | T | A | 3 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0286 |
3 | HG02486.hp2 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.177+28253T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288720 | |||||||
| chr14:69288737 | C | G | 95 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(92): Show |
97 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.177+28270C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288737 | |||||||
| chr14:69288753 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(217): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.177+28286A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288753 | |||||||
| chr14:69288767 | A | G | 1 | a0001c0001t0013g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.177+28300A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288767 | |||||||
| chr14:69288884 | C | A | 71 | a0001c0001t0001g0043 a0001c0001t0001g0083 a0001c0001t0001g0102 others(68): Show |
71 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.177+28417C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69288884 | |||||||
| chr14:69289104 | T | C | 33 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0178 others(30): Show |
33 | HG01069.hp2 HG01081.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.177+28637T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289104 | |||||||
| chr14:69289144 | C | T | 74 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(71): Show |
76 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.177+28677C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289144 | |||||||
| chr14:69289279 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0002g0042 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.177+28812C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289279 | |||||||
| chr14:69289281 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.177+28814C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289281 | |||||||
| chr14:69289338 | A | G | 9 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0003g0236 others(6): Show |
9 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.177+28871A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289338 | |||||||
| chr14:69289497 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.177+29030C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289497 | |||||||
| chr14:69289566 | G | T | 1 | a0003c0004t0001g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.177+29099G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289566 | |||||||
| chr14:69289592 | T | C | 74 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(71): Show |
76 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.177+29125T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289592 | |||||||
| chr14:69289630 | T | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(11): Show |
14 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.177+29163T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289630 | |||||||
| chr14:69289918 | T | A | 74 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(71): Show |
76 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.177+29451T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289918 | |||||||
| chr14:69289939 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.177+29472G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69289939 | |||||||
| chr14:69290413 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.177+29946T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290413 | |||||||
| chr14:69290472 | T | C | 108 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(105): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.177+30005T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290472 | |||||||
| chr14:69290501 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.177+30034G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290501 | |||||||
| chr14:69290749 | T | G | 1 | a0001c0001t0014g0285 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.178-29962T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290749 | |||||||
| chr14:69290786 | C | A | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.178-29925C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290786 | |||||||
| chr14:69290795 | C | T | 1 | a0003c0004t0002g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.178-29916C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290795 | |||||||
| chr14:69290823 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.178-29888A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290823 | |||||||
| chr14:69290961 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-29750G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69290961 | |||||||
| chr14:69291256 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.178-29455T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69291256 | |||||||
| chr14:69291438 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-29273C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69291438 | |||||||
| chr14:69291545 | T | A | 71 | a0001c0001t0001g0043 a0001c0001t0001g0083 a0001c0001t0001g0102 others(68): Show |
71 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.178-29166T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69291545 | |||||||
| chr14:69291707 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.178-29004T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69291707 | |||||||
| chr14:69291820 | C | T | 2 | a0003c0004t0001g0290 a0003c0004t0002g0289 |
2 | HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.178-28891C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69291820 | |||||||
| chr14:69292040 | T | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(13): Show |
16 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-28671T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292040 | |||||||
| chr14:69292059 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-28652T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292059 | |||||||
| chr14:69292186 | C | T | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-28525C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292186 | |||||||
| chr14:69292234 | A | T | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-28477A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292234 | |||||||
| chr14:69292274 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-28437C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292274 | |||||||
| chr14:69292435 | C | T | 2 | a0001c0001t0026g0298 a0002c0002t0002g0299 |
2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.178-28276C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292435 | |||||||
| chr14:69292568 | C | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.178-28143C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292568 | |||||||
| chr14:69292747 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-27964G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292747 | |||||||
| chr14:69292812 | G | A | 3 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0286 |
3 | HG02486.hp2 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.178-27899G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69292812 | |||||||
| chr14:69293078 | G | GT | 155 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(152): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.178-27624dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69293078 | ||||||
| chr14:69293300 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 others(56): Show |
61 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.178-27411G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69293300 | |||||||
| chr14:69293652 | A | G | 156 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(153): Show |
158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.178-27059A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69293652 | |||||||
| chr14:69293677 | T | C | 137 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0043 others(134): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.178-27034T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69293677 | |||||||
| chr14:69293859 | G | C | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.178-26852G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69293859 | |||||||
| chr14:69293896 | CT | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(13): Show |
16 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-26802delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69293896 | ||||||
| chr14:69294035 | T | C | 156 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(153): Show |
158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.178-26676T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294035 | |||||||
| chr14:69294080 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.178-26631G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294080 | |||||||
| chr14:69294128 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.178-26583T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294128 | |||||||
| chr14:69294131 | A | C | 1 | a0006c0010t0002g0055 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.178-26580A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294131 | |||||||
| chr14:69294139 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.178-26572T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294139 | |||||||
| chr14:69294232 | T | C | 137 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0043 others(134): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.178-26479T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294232 | |||||||
| chr14:69294289 | G | A | 2 | a0001c0001t0001g0202 a0003c0004t0002g0201 |
2 | HG01433.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.178-26422G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294289 | |||||||
| chr14:69294403 | G | A | 1 | a0001c0001t0024g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178-26308G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294403 | |||||||
| chr14:69294411 | G | A | 1 | a0001c0003t0001g0152 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.178-26300G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294411 | |||||||
| chr14:69294413 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01243.hp1 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-26298G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294413 | |||||||
| chr14:69294683 | A | G | 2 | a0003c0004t0001g0015 a0005c0013t0001g0283 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.178-26028A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294683 | |||||||
| chr14:69294801 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.178-25910T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294801 | |||||||
| chr14:69294806 | A | G | 66 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0101 others(63): Show |
68 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.178-25905A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294806 | |||||||
| chr14:69294874 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-25837G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294874 | |||||||
| chr14:69294911 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-25800T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294911 | |||||||
| chr14:69294957 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.178-25754T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294957 | |||||||
| chr14:69295048 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-25663T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295048 | |||||||
| chr14:69295136 | G | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-25575G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295136 | |||||||
| chr14:69295277 | T | C | 1 | a0001c0001t0002g0275 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178-25434T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295277 | |||||||
| chr14:69295414 | C | CA | 10 | a0001c0001t0001g0072 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG00621.hp2 HG02145.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-25277dupA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69295414 | ||||||
| chr14:69295414 | C | CAA | 47 | a0001c0001t0001g0101 a0001c0001t0001g0114 a0001c0001t0001g0115 others(44): Show |
49 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.178-25278_178-2527 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69295414 | ||||||
| chr14:69295414 | C | CAAA | 81 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0083 others(78): Show |
81 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.178-25279_178-2527 others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69295414 | ||||||
| chr14:69295414 | C | CAAAA | 20 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0141 others(17): Show |
20 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.178-25280_178-2527 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69295414 | ||||||
| chr14:69295414 | CA | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0144 others(23): Show |
26 | HG01081.hp2 HG01192.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.178-25277delA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69295414 | ||||||
| chr14:69295481 | A | T | 6 | a0001c0001t0004g0269 a0001c0003t0002g0251 a0002c0002t0001g0247 others(3): Show |
6 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-25230A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295481 | |||||||
| chr14:69295494 | C | T | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178-25217C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295494 | |||||||
| chr14:69295596 | T | G | 1 | a0001c0001t0002g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.178-25115T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295596 | |||||||
| chr14:69295653 | G | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(92): Show |
97 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.178-25058G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295653 | |||||||
| chr14:69295672 | A | T | 1 | a0001c0001t0003g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.178-25039A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295672 | |||||||
| chr14:69295675 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-25036G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295675 | |||||||
| chr14:69295682 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.178-25029T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295682 | |||||||
| chr14:69295715 | A | G | 257 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(254): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.178-24996A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295715 | |||||||
| chr14:69295786 | A | AT | 127 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(124): Show |
129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.178-24916dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69295786 | ||||||
| chr14:69296217 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(234): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.178-24494T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296217 | |||||||
| chr14:69296320 | A | G | 175 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0035 others(172): Show |
178 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.178-24391A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296320 | |||||||
| chr14:69296459 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0047 others(72): Show |
77 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.178-24252C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296459 | |||||||
| chr14:69296583 | C | T | 1 | a0003c0004t0002g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.178-24128C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296583 | |||||||
| chr14:69296697 | CAAAAT | C | 50 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.178-24009_178-2400 others(9): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296697 | ||||||
| chr14:69296720 | CAGATAGA others(4): Show |
C | 3 | a0001c0001t0002g0286 a0001c0003t0001g0163 a0002c0002t0001g0100 |
3 | HG02015.hp2 HG02486.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.178-23982_178-2397 others(15): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296720 | ||||||
| chr14:69296720 | CAGATAGA others(8): Show |
C | 37 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0118 others(34): Show |
38 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.178-23982_178-2396 others(19): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296720 | ||||||
| chr14:69296720 | CAGATAGA others(12): Show |
C | 1 | a0001c0001t0001g0126 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.178-23982_178-2396 others(23): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296720 | ||||||
| chr14:69296721 | AGATAGAT | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0115 others(4): Show |
7 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-23982_178-2397 others(11): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296721 | ||||||
| chr14:69296728 | T | TGATA | 21 | a0001c0001t0001g0041 a0001c0001t0001g0200 a0001c0001t0001g0243 others(18): Show |
21 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.178-23944_178-2394 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296728 | ||||||
| chr14:69296728 | T | TGATAGAT others(1): Show |
8 | a0001c0001t0003g0032 a0001c0001t0007g0140 a0001c0005t0006g0175 others(5): Show |
8 | HG01081.hp2 HG01496.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-23948_178-2394 others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296728 | ||||||
| chr14:69296728 | T | TGATAGAT others(1): Show |
57 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0043 others(54): Show |
59 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.178-23976_178-2397 others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296728 | ||||||
| chr14:69296728 | T | TGATAGAT others(9): Show |
1 | a0001c0003t0001g0244 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.178-23976_178-2397 others(20): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296728 | ||||||
| chr14:69296728 | TGATA | T | 17 | a0001c0001t0001g0045 a0001c0001t0001g0063 a0001c0001t0001g0064 others(14): Show |
17 | HG01255.hp2 HG01496.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.178-23944_178-2394 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296728 | ||||||
| chr14:69296728 | TGATAGAT others(1): Show |
T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0047 others(43): Show |
46 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.178-23948_178-2394 others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296728 | ||||||
| chr14:69296728 | TGATAGAT others(5): Show |
T | 4 | a0001c0001t0003g0037 a0001c0003t0001g0067 a0001c0003t0022g0066 others(1): Show |
4 | HG00738.hp2 HG02683.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-23952_178-2394 others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296728 | ||||||
| chr14:69296732 | A | AGATC | 11 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0003g0104 others(8): Show |
11 | HG01361.hp1 HG02074.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.178-23976_178-2397 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296732 | ||||||
| chr14:69296736 | A | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(54): Show |
58 | HG00673.hp1 HG00738.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.178-23975A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296736 | |||||||
| chr14:69296767 | TAGACAGA others(23): Show |
T | 1 | a0002c0002t0001g0237 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.178-23943_178-2391 others(34): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296767 | |||||||
| chr14:69296771 | C | G | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0032 others(3): Show |
6 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-23940C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296771 | |||||||
| chr14:69296771 | C | T | 104 | a0001c0001t0001g0005 a0001c0001t0001g0083 a0001c0001t0001g0086 others(101): Show |
106 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.178-23940C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296771 | |||||||
| chr14:69296777 | GATGATAG others(30): Show |
G | 1 | a0001c0001t0002g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.178-23932_178-2389 others(41): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296777 | ||||||
| chr14:69296779 | TGATAG | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(51): Show |
55 | HG00673.hp1 HG00738.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.178-23931_178-2392 others(9): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296779 | |||||||
| chr14:69296782 | T | G | 1 | a0003c0004t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.178-23929T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296782 | |||||||
| chr14:69296784 | G | T | 1 | a0003c0004t0002g0201 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.178-23927G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296784 | |||||||
| chr14:69296788 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(41): Show |
45 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-23923T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296788 | |||||||
| chr14:69296788 | TAGAC | T | 41 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(38): Show |
42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.178-23915_178-2391 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296788 | ||||||
| chr14:69296792 | C | T | 44 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(41): Show |
45 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-23919C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296792 | |||||||
| chr14:69296794 | GACAGATA others(5): Show |
G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0131 others(4): Show |
7 | HG00733.hp2 HG01074.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-23915_178-2390 others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296794 | ||||||
| chr14:69296795 | AC | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(41): Show |
45 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-23915delC | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296795 | |||||||
| chr14:69296796 | C | T | 12 | a0001c0001t0001g0135 a0001c0001t0001g0203 a0001c0001t0001g0205 others(9): Show |
12 | HG00673.hp1 HG01192.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-23915C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296796 | |||||||
| chr14:69296797 | A | AGAT | 12 | a0001c0001t0001g0135 a0001c0001t0001g0203 a0001c0001t0001g0205 others(9): Show |
12 | HG00673.hp1 HG01192.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-23913_178-2391 others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296797 | ||||||
| chr14:69296797 | A | T | 44 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(41): Show |
45 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.178-23914A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296797 | |||||||
| chr14:69296798 | GATAGAGC others(1): Show |
G | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0084 others(3): Show |
6 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-23911_178-2390 others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296798 | ||||||
| chr14:69296798 | GATAGAGC others(5): Show |
G | 6 | a0001c0001t0003g0032 a0001c0001t0010g0023 a0001c0001t0010g0025 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-23911_178-2390 others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296798 | ||||||
| chr14:69296805 | C | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(54): Show |
58 | HG00673.hp1 HG00738.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.178-23906C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296805 | |||||||
| chr14:69296805 | C | CTAGA | 10 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0068 others(7): Show |
10 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-23868_178-2386 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296805 | ||||||
| chr14:69296805 | C | CTAGATAG others(1): Show |
4 | a0001c0001t0007g0274 a0002c0002t0001g0136 a0002c0002t0001g0261 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-23872_178-2386 others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296805 | ||||||
| chr14:69296805 | CTAGA | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0063 others(34): Show |
37 | HG00558.hp2 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.178-23868_178-2386 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296805 | ||||||
| chr14:69296805 | CTAGATAG others(1): Show |
C | 14 | a0001c0001t0001g0114 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
15 | HG00609.hp2 HG01081.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-23872_178-2386 others(12): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296805 | ||||||
| chr14:69296805 | CTAGATAG others(5): Show |
C | 42 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0115 others(39): Show |
42 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.178-23876_178-2386 others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296805 | ||||||
| chr14:69296805 | CTAGATAG others(9): Show |
C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0043 others(67): Show |
72 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.178-23880_178-2386 others(20): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296805 | ||||||
| chr14:69296805 | CTAGATAG others(13): Show |
C | 1 | a0001c0001t0017g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178-23884_178-2386 others(24): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69296805 | ||||||
| chr14:69296809 | A | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0129 others(10): Show |
13 | HG00280.hp2 HG00733.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.178-23902A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296809 | |||||||
| chr14:69296810 | T | C | 57 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(54): Show |
58 | HG00673.hp1 HG00738.hp1 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.178-23901T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296810 | |||||||
| chr14:69296813 | A | C | 6 | a0001c0001t0003g0032 a0001c0001t0010g0023 a0001c0001t0010g0025 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-23898A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296813 | |||||||
| chr14:69296814 | T | C | 56 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(53): Show |
57 | HG00673.hp1 HG00738.hp1 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.178-23897T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296814 | |||||||
| chr14:69296817 | A | C | 1 | a0001c0001t0002g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.178-23894A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296817 | |||||||
| chr14:69296821 | A | AGC | 56 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0087 others(53): Show |
57 | HG00673.hp1 HG00738.hp1 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.178-23890_178-2388 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296821 | |||||||
| chr14:69296821 | A | C | 1 | a0002c0002t0001g0237 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.178-23890A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296821 | |||||||
| chr14:69296905 | A | T | 50 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.178-23806A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296905 | |||||||
| chr14:69296996 | A | G | 1 | a0001c0001t0004g0264 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.178-23715A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296996 | |||||||
| chr14:69297004 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0007c0019t0008g0151 |
3 | HG03139.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.178-23707G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297004 | |||||||
| chr14:69297259 | G | A | 1 | a0003c0004t0002g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.178-23452G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297259 | |||||||
| chr14:69297299 | A | G | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0200 others(9): Show |
12 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-23412A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297299 | |||||||
| chr14:69297356 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0007 others(2): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-23355C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297356 | |||||||
| chr14:69297405 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.178-23306T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297405 | |||||||
| chr14:69297522 | A | G | 1 | a0001c0001t0003g0037 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.178-23189A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297522 | |||||||
| chr14:69297572 | T | A | 1 | a0001c0001t0003g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.178-23139T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297572 | |||||||
| chr14:69297631 | C | CA | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(205): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.178-23069dupA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69297631 | ||||||
| chr14:69297631 | C | CAA | 14 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0123 others(11): Show |
14 | HG00140.hp2 HG01884.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-23070_178-2306 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69297631 | ||||||
| chr14:69297631 | C | CAAA | 6 | a0001c0001t0001g0200 a0001c0001t0007g0140 a0003c0004t0009g0145 others(3): Show |
6 | HG01081.hp2 HG01496.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-23071_178-2306 others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69297631 | ||||||
| chr14:69297631 | CAA | C | 11 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0003g0236 others(8): Show |
11 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-23070_178-2306 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69297631 | ||||||
| chr14:69297641 | A | C | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.178-23070A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297641 | |||||||
| chr14:69297736 | C | T | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-22975C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297736 | |||||||
| chr14:69297741 | G | GT | 50 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.178-22967dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69297741 | ||||||
| chr14:69297817 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178-22894G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69297817 | |||||||
| chr14:69298008 | A | G | 2 | a0003c0004t0001g0015 a0005c0013t0001g0283 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.178-22703A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298008 | |||||||
| chr14:69298053 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.178-22658G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298053 | |||||||
| chr14:69298097 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.178-22614C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298097 | |||||||
| chr14:69298341 | C | G | 50 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.178-22370C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298341 | |||||||
| chr14:69298360 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(124): Show |
130 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.178-22351G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298360 | |||||||
| chr14:69298369 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-22342G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298369 | |||||||
| chr14:69298425 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(125): Show |
131 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.178-22286G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298425 | |||||||
| chr14:69298460 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.178-22251G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298460 | |||||||
| chr14:69298818 | G | A | 1 | a0003c0004t0011g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.178-21893G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298818 | |||||||
| chr14:69298819 | G | C | 1 | a0003c0004t0011g0024 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.178-21892G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298819 | |||||||
| chr14:69298927 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.178-21784A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69298927 | |||||||
| chr14:69299134 | A | G | 2 | a0001c0001t0002g0288 a0001c0001t0014g0285 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.178-21577A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299134 | |||||||
| chr14:69299298 | T | C | 5 | a0001c0001t0007g0140 a0003c0004t0009g0145 a0003c0004t0009g0148 others(2): Show |
5 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-21413T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299298 | |||||||
| chr14:69299342 | G | C | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178-21369G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299342 | |||||||
| chr14:69299362 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.178-21349G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299362 | |||||||
| chr14:69299443 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.178-21268G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299443 | |||||||
| chr14:69299738 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(126): Show |
132 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.178-20973A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299738 | |||||||
| chr14:69299754 | G | A | 26 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0141 others(23): Show |
26 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.178-20957G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299754 | |||||||
| chr14:69299913 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.178-20798C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299913 | |||||||
| chr14:69299914 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0276 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-20797G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69299914 | |||||||
| chr14:69300045 | C | T | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-20666C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69300045 | |||||||
| chr14:69300501 | C | T | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0243 others(10): Show |
13 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-20210C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69300501 | |||||||
| chr14:69300602 | G | T | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.178-20109G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69300602 | |||||||
| chr14:69300674 | C | T | 1 | a0001c0009t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.178-20037C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69300674 | |||||||
| chr14:69301102 | A | AG | 65 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0083 others(62): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.178-19607dupG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69301102 | ||||||
| chr14:69301103 | G | A | 4 | a0001c0001t0002g0284 a0001c0001t0003g0226 a0001c0001t0016g0225 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-19608G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301103 | |||||||
| chr14:69301103 | G | GC | 67 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-19608_178-1960 others(5): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301103 | |||||||
| chr14:69301168 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(64): Show |
70 | HG00099.hp1 HG00558.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.178-19543A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301168 | |||||||
| chr14:69301176 | A | G | 65 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0083 others(62): Show |
66 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.178-19535A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301176 | |||||||
| chr14:69301197 | C | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(255): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.178-19514C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301197 | |||||||
| chr14:69301299 | A | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(277): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.178-19412A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301299 | |||||||
| chr14:69301377 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 |
3 | HG02280.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.178-19334G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301377 | |||||||
| chr14:69301714 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0021g0075 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-18997C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301714 | |||||||
| chr14:69301814 | C | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-18897C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301814 | |||||||
| chr14:69301900 | G | C | 4 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0001c0001t0015g0057 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-18811G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301900 | |||||||
| chr14:69301908 | T | G | 2 | a0001c0001t0001g0002 a0001c0003t0002g0070 |
3 | NA18971.hp2 NA18990.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.178-18803T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301908 | |||||||
| chr14:69301946 | G | T | 33 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(30): Show |
33 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.178-18765G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301946 | |||||||
| chr14:69301947 | C | G | 1 | a0002c0002t0001g0237 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.178-18764C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301947 | |||||||
| chr14:69301969 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.178-18742C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301969 | |||||||
| chr14:69302108 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.178-18603C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302108 | |||||||
| chr14:69302232 | G | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-18479G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302232 | |||||||
| chr14:69302300 | A | G | 2 | a0001c0001t0002g0288 a0001c0001t0014g0285 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.178-18411A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302300 | |||||||
| chr14:69302328 | A | T | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-18383A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302328 | |||||||
| chr14:69302441 | ATT | A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.178-18264_178-1826 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69302441 | ||||||
| chr14:69302518 | T | A | 55 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.178-18193T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302518 | |||||||
| chr14:69302566 | G | A | 2 | a0002c0002t0002g0253 a0002c0002t0002g0254 |
2 | HG00280.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.178-18145G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302566 | |||||||
| chr14:69302666 | A | G | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-18045A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302666 | |||||||
| chr14:69302884 | C | T | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-17827C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69302884 | |||||||
| chr14:69303131 | G | C | 1 | a0001c0001t0003g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.178-17580G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69303131 | |||||||
| chr14:69303652 | CT | C | 67 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-17057delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69303652 | ||||||
| chr14:69303723 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(186): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.178-16988C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69303723 | |||||||
| chr14:69303852 | G | A | 67 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-16859G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69303852 | |||||||
| chr14:69303853 | G | A | 2 | a0001c0001t0001g0005 a0001c0015t0003g0287 |
3 | HG01243.hp2 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.178-16858G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69303853 | |||||||
| chr14:69303973 | T | C | 66 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(63): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.178-16738T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69303973 | |||||||
| chr14:69304166 | A | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01192.hp1 HG01243.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-16545A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304166 | |||||||
| chr14:69304222 | C | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.178-16489C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304222 | |||||||
| chr14:69304247 | T | C | 1 | a0003c0004t0002g0289 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.178-16464T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304247 | |||||||
| chr14:69304392 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0007t0001g0262 others(4): Show |
7 | HG00280.hp1 HG01081.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-16319C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304392 | |||||||
| chr14:69304413 | G | C | 157 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0047 others(154): Show |
159 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.178-16298G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304413 | |||||||
| chr14:69304496 | T | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(65): Show |
71 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.178-16215T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304496 | |||||||
| chr14:69304580 | C | G | 61 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0083 others(58): Show |
62 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.178-16131C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304580 | |||||||
| chr14:69304860 | C | T | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-15851C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304860 | |||||||
| chr14:69305024 | A | AT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(118): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.178-15680dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69305024 | ||||||
| chr14:69305037 | C | T | 1 | a0002c0002t0001g0069 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.178-15674C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305037 | |||||||
| chr14:69305045 | C | T | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-15666C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305045 | |||||||
| chr14:69305109 | T | G | 66 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(63): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.178-15602T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305109 | |||||||
| chr14:69305119 | C | T | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-15592C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305119 | |||||||
| chr14:69305132 | C | CT | 75 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0043 others(72): Show |
76 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.178-15565dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69305132 | ||||||
| chr14:69305132 | CT | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(121): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.178-15565delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69305132 | ||||||
| chr14:69305169 | CT | C | 67 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0083 others(64): Show |
68 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.178-15525delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69305169 | ||||||
| chr14:69305219 | G | A | 52 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(49): Show |
53 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.178-15492G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305219 | |||||||
| chr14:69305232 | C | T | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178-15479C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305232 | |||||||
| chr14:69305392 | A | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(67): Show |
73 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.178-15319A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305392 | |||||||
| chr14:69305413 | T | A | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-15298T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305413 | |||||||
| chr14:69305605 | G | T | 1 | a0001c0001t0004g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.178-15106G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305605 | |||||||
| chr14:69305719 | T | G | 77 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0043 others(74): Show |
78 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.178-14992T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305719 | |||||||
| chr14:69305742 | G | T | 129 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0043 others(126): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.178-14969G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305742 | |||||||
| chr14:69305830 | G | A | 1 | a0008c0018t0002g0293 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.178-14881G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305830 | |||||||
| chr14:69305846 | C | G | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178-14865C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305846 | |||||||
| chr14:69305981 | T | A | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-14730T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305981 | |||||||
| chr14:69306181 | A | G | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-14530A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306181 | |||||||
| chr14:69306309 | T | G | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-14402T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306309 | |||||||
| chr14:69306353 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 |
3 | HG02280.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.178-14358G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306353 | |||||||
| chr14:69306370 | C | T | 5 | a0001c0001t0007g0140 a0001c0005t0006g0138 a0001c0005t0006g0139 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-14341C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306370 | |||||||
| chr14:69306374 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.178-14337T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306374 | |||||||
| chr14:69306449 | A | G | 2 | a0001c0003t0001g0061 a0002c0002t0001g0062 |
2 | HG00741.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.178-14262A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306449 | |||||||
| chr14:69306505 | G | A | 66 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(63): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.178-14206G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306505 | |||||||
| chr14:69306557 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.178-14154C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306557 | |||||||
| chr14:69306700 | A | G | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-14011A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69306700 | |||||||
| chr14:69307074 | A | C | 52 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(49): Show |
53 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.178-13637A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307074 | |||||||
| chr14:69307198 | C | T | 1 | a0001c0009t0001g0281 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.178-13513C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307198 | |||||||
| chr14:69307206 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0001g0197 a0001c0001t0001g0215 others(1): Show |
4 | HG01071.hp1 HG01928.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-13505C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307206 | |||||||
| chr14:69307268 | C | T | 50 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.178-13443C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307268 | |||||||
| chr14:69307269 | G | A | 66 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(63): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.178-13442G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307269 | |||||||
| chr14:69307291 | C | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(65): Show |
71 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.178-13420C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307291 | |||||||
| chr14:69307557 | A | G | 52 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(49): Show |
53 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.178-13154A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307557 | |||||||
| chr14:69307610 | G | A | 1 | a0003c0004t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.178-13101G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307610 | |||||||
| chr14:69307702 | C | T | 52 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(49): Show |
53 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.178-13009C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307702 | |||||||
| chr14:69307802 | G | A | 1 | a0002c0002t0001g0300 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.178-12909G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307802 | |||||||
| chr14:69307829 | G | A | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-12882G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307829 | |||||||
| chr14:69307884 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.178-12827G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307884 | |||||||
| chr14:69307961 | G | A | 1 | a0001c0001t0004g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.178-12750G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307961 | |||||||
| chr14:69308104 | G | A | 50 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(47): Show |
51 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.178-12607G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308104 | |||||||
| chr14:69308282 | T | C | 112 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(109): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.178-12429T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308282 | |||||||
| chr14:69308299 | A | T | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-12412A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308299 | |||||||
| chr14:69308313 | T | G | 1 | a0002c0002t0001g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.178-12398T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308313 | |||||||
| chr14:69308391 | G | A | 3 | a0001c0001t0014g0285 a0002c0002t0002g0146 a0002c0002t0002g0147 |
3 | HG02145.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-12320G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308391 | |||||||
| chr14:69308437 | A | T | 1 | a0001c0003t0003g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.178-12274A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308437 | |||||||
| chr14:69308458 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.178-12253A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308458 | |||||||
| chr14:69308561 | G | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.178-12150G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308561 | |||||||
| chr14:69308676 | A | T | 4 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0001c0001t0015g0057 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-12035A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308676 | |||||||
| chr14:69308761 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.178-11950A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308761 | |||||||
| chr14:69308936 | T | A | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-11775T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308936 | |||||||
| chr14:69309099 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178-11612T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69309099 | |||||||
| chr14:69309142 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.178-11569C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69309142 | |||||||
| chr14:69309143 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.178-11568A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69309143 | |||||||
| chr14:69309274 | T | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0032 others(3): Show |
6 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-11437T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69309274 | |||||||
| chr14:69309316 | T | A | 165 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(162): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.178-11395T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69309316 | |||||||
| chr14:69309524 | C | G | 1 | a0001c0001t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.178-11187C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69309524 | |||||||
| chr14:69309705 | T | C | 1 | a0002c0002t0001g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.178-11006T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69309705 | |||||||
| chr14:69310165 | T | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0032 others(3): Show |
6 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-10546T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310165 | |||||||
| chr14:69310173 | T | G | 1 | a0003c0004t0001g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.178-10538T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310173 | |||||||
| chr14:69310262 | T | C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0172 a0001c0001t0001g0219 |
3 | HG00558.hp1 NA18997.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.178-10449T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310262 | |||||||
| chr14:69310288 | G | GT | 68 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(65): Show |
69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.178-10414dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69310288 | ||||||
| chr14:69310321 | C | T | 14 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0058 others(11): Show |
14 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.178-10390C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310321 | |||||||
| chr14:69310480 | A | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0001g0203 others(12): Show |
15 | HG01192.hp1 HG01243.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-10231A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310480 | |||||||
| chr14:69310499 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(230): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.178-10212A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310499 | |||||||
| chr14:69310609 | A | C | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-10102A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310609 | |||||||
| chr14:69310641 | C | A | 33 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(30): Show |
33 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.178-10070C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310641 | |||||||
| chr14:69310777 | C | T | 5 | a0001c0001t0001g0182 a0002c0002t0001g0004 a0002c0002t0001g0186 others(2): Show |
6 | HG00621.hp1 HG02132.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-9934C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310777 | |||||||
| chr14:69310856 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.178-9855G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69310856 | |||||||
| chr14:69311051 | A | G | 1 | a0002c0002t0002g0232 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-9660A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311051 | |||||||
| chr14:69311107 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.178-9604G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311107 | |||||||
| chr14:69311138 | T | C | 164 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(161): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.178-9573T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311138 | |||||||
| chr14:69311177 | G | A | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-9534G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311177 | |||||||
| chr14:69311306 | C | G | 2 | a0002c0002t0001g0136 a0002c0002t0001g0261 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.178-9405C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311306 | |||||||
| chr14:69311653 | C | T | 67 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-9058C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311653 | |||||||
| chr14:69311690 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0003t0001g0168 |
3 | HG00438.hp2 NA18998.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.178-9021G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311690 | |||||||
| chr14:69311732 | T | C | 67 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-8979T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311732 | |||||||
| chr14:69311883 | C | T | 2 | a0001c0008t0002g0188 a0001c0008t0002g0189 |
2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.178-8828C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311883 | |||||||
| chr14:69311896 | C | CT | 13 | a0001c0001t0001g0011 a0001c0001t0001g0202 a0001c0001t0003g0019 others(10): Show |
13 | HG01192.hp1 HG01243.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-8807dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69311896 | ||||||
| chr14:69311904 | T | C | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-8807T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311904 | |||||||
| chr14:69311924 | CA | C | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-8786delA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311924 | |||||||
| chr14:69311929 | G | T | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-8782G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311929 | |||||||
| chr14:69311952 | C | T | 4 | a0001c0001t0001g0080 a0001c0001t0003g0079 a0001c0001t0005g0082 others(1): Show |
4 | HG02615.hp2 HG03041.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-8759C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69311952 | |||||||
| chr14:69312008 | G | A | 1 | a0001c0001t0007g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.178-8703G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312008 | |||||||
| chr14:69312014 | C | G | 164 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0036 others(161): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.178-8697C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312014 | |||||||
| chr14:69312038 | TA | T | 7 | a0001c0001t0001g0166 a0001c0001t0001g0178 a0001c0001t0001g0218 others(4): Show |
7 | HG02074.hp1 HG03486.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-8656delA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312038 | ||||||
| chr14:69312053 | AAATCTGT others(10): Show |
A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0032 others(3): Show |
6 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-8656_178-8640d others(19): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312053 | ||||||
| chr14:69312054 | AATCTG | A | 67 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-8656_178-8652d others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312054 | |||||||
| chr14:69312054 | AATCTGTC others(5): Show |
A | 1 | a0001c0001t0002g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178-8652_178-8641d others(14): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312054 | ||||||
| chr14:69312055 | A | G | 1 | a0002c0011t0002g0263 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.178-8656A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312055 | |||||||
| chr14:69312055 | ATCT | A | 3 | a0001c0001t0001g0006 a0001c0001t0002g0007 a0001c0003t0023g0021 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.178-8655_178-8653d others(5): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312055 | |||||||
| chr14:69312055 | ATCTG | A | 50 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0058 others(47): Show |
50 | HG00558.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.178-8652_178-8649d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312055 | ||||||
| chr14:69312059 | G | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0047 a0001c0001t0001g0049 others(40): Show |
44 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.178-8652G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312059 | |||||||
| chr14:69312059 | G | GTCTA | 25 | a0001c0001t0001g0202 a0001c0001t0001g0230 a0001c0001t0001g0231 others(22): Show |
26 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.178-8610_178-8607d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312059 | ||||||
| chr14:69312059 | G | GTCTATCT others(1): Show |
3 | a0001c0001t0001g0206 a0002c0002t0001g0294 a0003c0004t0009g0149 |
3 | HG01496.hp1 HG03831.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.178-8614_178-8607d others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312059 | ||||||
| chr14:69312059 | GTCTA | G | 14 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
14 | HG00738.hp1 HG01123.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.178-8610_178-8607d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312059 | ||||||
| chr14:69312059 | GTCTATCT others(5): Show |
G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
11 | HG00558.hp1 HG01361.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-8618_178-8607d others(14): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69312059 | ||||||
| chr14:69312063 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0203 a0001c0001t0001g0205 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-8648A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312063 | |||||||
| chr14:69312072 | T | C | 4 | a0001c0001t0001g0166 a0001c0001t0001g0218 a0001c0001t0020g0192 others(1): Show |
4 | HG02074.hp1 NA18941.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-8639T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312072 | |||||||
| chr14:69312076 | T | C | 63 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(60): Show |
64 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.178-8635T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312076 | |||||||
| chr14:69312173 | C | G | 3 | a0001c0001t0002g0284 a0001c0001t0003g0226 a0001c0001t0016g0225 |
3 | HG02630.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.178-8538C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312173 | |||||||
| chr14:69312259 | A | T | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-8452A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312259 | |||||||
| chr14:69312260 | T | A | 1 | a0001c0001t0002g0275 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178-8451T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312260 | |||||||
| chr14:69312348 | C | T | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-8363C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312348 | |||||||
| chr14:69312394 | C | T | 1 | a0001c0001t0003g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.178-8317C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312394 | |||||||
| chr14:69312510 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.178-8201A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312510 | |||||||
| chr14:69312652 | C | G | 6 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0211 others(3): Show |
6 | HG01255.hp1 HG01943.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-8059C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312652 | |||||||
| chr14:69312744 | A | G | 34 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(31): Show |
34 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.178-7967A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312744 | |||||||
| chr14:69312801 | C | G | 1 | a0002c0002t0001g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.178-7910C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312801 | |||||||
| chr14:69312947 | G | A | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-7764G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312947 | |||||||
| chr14:69312981 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178-7730G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69312981 | |||||||
| chr14:69313117 | G | T | 3 | a0001c0001t0002g0284 a0001c0001t0003g0226 a0001c0001t0016g0225 |
3 | HG02630.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.178-7594G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313117 | |||||||
| chr14:69313122 | C | A | 15 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0276 others(12): Show |
15 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.178-7589C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313122 | |||||||
| chr14:69313135 | G | A | 33 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(30): Show |
33 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.178-7576G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313135 | |||||||
| chr14:69313238 | A | G | 4 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0001c0001t0015g0057 others(1): Show |
4 | HG03139.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-7473A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313238 | |||||||
| chr14:69313292 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.178-7419C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313292 | |||||||
| chr14:69313370 | G | A | 1 | a0001c0001t0016g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.178-7341G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313370 | |||||||
| chr14:69313443 | G | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.178-7268G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313443 | |||||||
| chr14:69313507 | A | G | 1 | a0003c0004t0009g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.178-7204A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313507 | |||||||
| chr14:69313514 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.178-7197G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313514 | |||||||
| chr14:69313619 | G | GTCATCAG others(153): Show |
32 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(29): Show |
33 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.178-6953_178-6952i others(162): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69313619 | ||||||
| chr14:69313960 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 |
3 | HG02280.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.178-6751C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313960 | |||||||
| chr14:69313961 | C | T | 67 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0135 others(64): Show |
68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-6750C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69313961 | |||||||
| chr14:69314036 | C | G | 1 | a0001c0001t0026g0298 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.178-6675C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69314036 | |||||||
| chr14:69314059 | G | C | 68 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0102 others(65): Show |
69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.178-6652G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69314059 | |||||||
| chr14:69314306 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.178-6405A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69314306 | |||||||
| chr14:69314624 | C | T | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-6087C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69314624 | |||||||
| chr14:69314678 | G | A | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-6033G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69314678 | |||||||
| chr14:69314869 | C | A | 12 | a0001c0001t0001g0074 a0001c0001t0001g0078 a0001c0001t0001g0080 others(9): Show |
12 | HG01891.hp2 HG02615.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.178-5842C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69314869 | |||||||
| chr14:69314881 | A | G | 1 | a0001c0001t0004g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.178-5830A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69314881 | |||||||
| chr14:69315046 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.178-5665G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315046 | |||||||
| chr14:69315205 | C | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-5506C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315205 | |||||||
| chr14:69315255 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.178-5456C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315255 | |||||||
| chr14:69315284 | A | C | 51 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.178-5427A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315284 | |||||||
| chr14:69315294 | A | G | 69 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0102 others(66): Show |
70 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.178-5417A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315294 | |||||||
| chr14:69315640 | T | C | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-5071T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315640 | |||||||
| chr14:69315658 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.178-5053T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315658 | |||||||
| chr14:69315810 | A | T | 88 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0124 others(85): Show |
89 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.178-4901A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315810 | |||||||
| chr14:69315811 | A | T | 21 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0166 others(18): Show |
21 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.178-4900A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315811 | |||||||
| chr14:69315852 | C | T | 2 | a0001c0003t0001g0105 a0002c0002t0002g0106 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.178-4859C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315852 | |||||||
| chr14:69315862 | T | A | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178-4849T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315862 | |||||||
| chr14:69315900 | T | C | 1 | a0001c0001t0002g0240 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.178-4811T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315900 | |||||||
| chr14:69315927 | C | A | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-4784C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69315927 | |||||||
| chr14:69316091 | T | C | 69 | a0001c0001t0001g0043 a0001c0001t0001g0102 a0001c0001t0001g0124 others(66): Show |
70 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.178-4620T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316091 | |||||||
| chr14:69316206 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0243 others(7): Show |
10 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-4505C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316206 | |||||||
| chr14:69316352 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-4359G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316352 | |||||||
| chr14:69316597 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0003t0001g0168 |
3 | HG00438.hp2 NA18998.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.178-4114G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316597 | |||||||
| chr14:69316620 | G | A | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0243 others(7): Show |
10 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-4091G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316620 | |||||||
| chr14:69316737 | G | T | 1 | a0001c0001t0024g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.178-3974G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316737 | |||||||
| chr14:69316746 | C | A | 2 | a0001c0001t0004g0269 a0001c0003t0002g0251 |
2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.178-3965C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316746 | |||||||
| chr14:69316774 | T | TG | 20 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0074 others(17): Show |
20 | HG00280.hp1 HG01891.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.178-3936dupG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69316774 | ||||||
| chr14:69316774 | T | TGG | 8 | a0001c0001t0001g0060 a0001c0001t0002g0076 a0001c0001t0002g0284 others(5): Show |
8 | HG00558.hp2 HG00741.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-3936_178-3935i others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69316774 | ||||||
| chr14:69316774 | T | TGGG | 7 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0002g0275 others(4): Show |
7 | HG00738.hp2 HG02895.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-3936_178-3935i others(5): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69316774 | ||||||
| chr14:69316776 | A | G | 40 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(37): Show |
40 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.178-3935A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316776 | |||||||
| chr14:69316779 | G | GGC | 49 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(46): Show |
50 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.178-3931_178-3930i others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69316779 | ||||||
| chr14:69316780 | G | GGT | 76 | a0001c0001t0001g0043 a0001c0001t0001g0078 a0001c0001t0001g0080 others(73): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.178-3930_178-3929i others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69316780 | ||||||
| chr14:69316782 | G | GGGC | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
75 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.178-3927_178-3926i others(5): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69316782 | ||||||
| chr14:69316799 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0005g0046 a0001c0001t0007g0044 |
3 | HG02280.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.178-3912C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69316799 | |||||||
| chr14:69317188 | A | C | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-3523A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317188 | |||||||
| chr14:69317320 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0021g0075 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.178-3391C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317320 | |||||||
| chr14:69317390 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0002g0095 others(6): Show |
9 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-3321C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317390 | |||||||
| chr14:69317442 | C | T | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-3269C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317442 | |||||||
| chr14:69317461 | T | C | 33 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(30): Show |
33 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.178-3250T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317461 | |||||||
| chr14:69317696 | G | A | 30 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(27): Show |
30 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.178-3015G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317696 | |||||||
| chr14:69317771 | T | C | 30 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0049 others(27): Show |
30 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.178-2940T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317771 | |||||||
| chr14:69317790 | G | A | 1 | a0001c0001t0015g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.178-2921G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317790 | |||||||
| chr14:69317797 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178-2914A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317797 | |||||||
| chr14:69317845 | A | T | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-2866A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317845 | |||||||
| chr14:69317861 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.178-2850C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317861 | |||||||
| chr14:69317910 | G | T | 2 | a0001c0001t0001g0144 a0001c0001t0002g0275 |
2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.178-2801G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317910 | |||||||
| chr14:69317942 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0032 others(3): Show |
6 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-2769C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69317942 | |||||||
| chr14:69318086 | A | G | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-2625A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69318086 | |||||||
| chr14:69318479 | A | ATGAATGC others(17): Show |
1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-2223_178-2200d others(26): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69318479 | ||||||
| chr14:69318482 | A | C | 80 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0078 others(77): Show |
81 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.178-2229A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69318482 | |||||||
| chr14:69318890 | G | A | 1 | a0002c0002t0001g0069 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.178-1821G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69318890 | |||||||
| chr14:69318966 | C | T | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-1745C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69318966 | |||||||
| chr14:69318982 | C | T | 74 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0078 others(71): Show |
75 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.178-1729C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69318982 | |||||||
| chr14:69319012 | T | G | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-1699T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319012 | |||||||
| chr14:69319021 | C | T | 1 | a0001c0001t0015g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.178-1690C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319021 | |||||||
| chr14:69319310 | T | A | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-1401T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319310 | |||||||
| chr14:69319346 | A | G | 15 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0058 others(12): Show |
15 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.178-1365A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319346 | |||||||
| chr14:69319516 | C | T | 2 | a0001c0001t0002g0107 a0001c0001t0028g0109 |
2 | HG03017.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.178-1195C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319516 | |||||||
| chr14:69319517 | G | A | 1 | a0001c0007t0001g0262 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.178-1194G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319517 | |||||||
| chr14:69319552 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.178-1159A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319552 | |||||||
| chr14:69319574 | A | G | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-1137A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319574 | |||||||
| chr14:69319726 | C | T | 1 | a0001c0001t0004g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.178-985C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319726 | |||||||
| chr14:69319874 | G | A | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.178-837G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69319874 | |||||||
| chr14:69320086 | C | CCG | 83 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0043 others(80): Show |
84 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.178-624_178-623ins others(2): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69320086 | ||||||
| chr14:69320091 | C | G | 49 | a0001c0001t0001g0083 a0001c0001t0001g0101 a0001c0001t0001g0114 others(46): Show |
50 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.178-620C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320091 | |||||||
| chr14:69320093 | A | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.178-618A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320093 | |||||||
| chr14:69320284 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(64): Show |
70 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.178-427C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320284 | |||||||
| chr14:69320326 | C | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0003g0032 others(5): Show |
8 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-385C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320326 | |||||||
| chr14:69320355 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.178-356C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320355 | |||||||
| chr14:69320356 | G | A | 6 | a0001c0001t0001g0144 a0001c0001t0002g0275 a0001c0001t0002g0284 others(3): Show |
6 | HG02486.hp2 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-355G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320356 | |||||||
| chr14:69320488 | AAAAAAAA others(12): Show |
A | 2 | a0001c0001t0002g0288 a0001c0001t0014g0285 |
2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.178-205_178-187del others(19): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69320488 | ||||||
| chr14:69320496 | G | GA | 76 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0078 others(73): Show |
77 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.178-205dupA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69320496 | ||||||
| chr14:69320507 | GAAAAAAA others(3): Show |
G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(62): Show |
68 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.178-192_178-183del others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr14 | 69320507 | ||||||
| chr14:69320529 | C | T | 1 | a0001c0017t0001g0270 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.178-182C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320529 | |||||||
| chr14:69320872 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00280.hp2 | splice_region_variant&intron_variant | LOW | c.335+4C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69320872 | |||||||
| chr14:69320923 | G | A | 21 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0013 others(18): Show |
21 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.335+55G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69320923 | |||||||
| chr14:69321032 | T | C | 46 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0047 others(43): Show |
46 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.335+164T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321032 | |||||||
| chr14:69321069 | T | A | 1 | a0001c0001t0019g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.335+201T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321069 | |||||||
| chr14:69321154 | G | T | 2 | a0003c0004t0001g0290 a0003c0004t0002g0289 |
2 | HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.335+286G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321154 | |||||||
| chr14:69321233 | A | T | 1 | a0001c0001t0002g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.335+365A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321233 | |||||||
| chr14:69321477 | G | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.335+609G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321477 | |||||||
| chr14:69321519 | C | A | 1 | a0001c0003t0002g0251 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.335+651C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321519 | |||||||
| chr14:69321548 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.335+680T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321548 | |||||||
| chr14:69321564 | G | A | 17 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0013 others(14): Show |
17 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.335+696G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321564 | |||||||
| chr14:69321681 | A | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0007g0274 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.335+813A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321681 | |||||||
| chr14:69321689 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.335+821C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321689 | |||||||
| chr14:69321690 | G | A | 1 | a0001c0001t0014g0285 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.335+822G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321690 | |||||||
| chr14:69321871 | G | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.335+1003G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321871 | |||||||
| chr14:69321880 | A | G | 135 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0051 others(132): Show |
137 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.335+1012A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321880 | |||||||
| chr14:69322186 | A | G | 87 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(84): Show |
88 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.335+1318A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322186 | |||||||
| chr14:69322198 | T | C | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+1330T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322198 | |||||||
| chr14:69322212 | C | A | 86 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(83): Show |
87 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.335+1344C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322212 | |||||||
| chr14:69322213 | C | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0083 others(45): Show |
49 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.335+1345C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322213 | |||||||
| chr14:69322419 | C | A | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.335+1551C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322419 | |||||||
| chr14:69322472 | G | A | 2 | a0001c0003t0001g0105 a0002c0002t0002g0106 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.335+1604G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322472 | |||||||
| chr14:69322527 | A | T | 2 | a0003c0004t0001g0290 a0003c0004t0002g0289 |
2 | HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.335+1659A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322527 | |||||||
| chr14:69322535 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0002g0007 a0001c0003t0023g0021 |
3 | HG02280.hp1 HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.335+1667G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322535 | |||||||
| chr14:69322558 | G | A | 2 | a0003c0004t0001g0290 a0003c0004t0002g0289 |
2 | HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.335+1690G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322558 | |||||||
| chr14:69322853 | C | T | 45 | a0001c0001t0001g0074 a0001c0001t0001g0083 a0001c0001t0001g0101 others(42): Show |
46 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.336-1839C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322853 | |||||||
| chr14:69322866 | G | A | 1 | a0001c0003t0002g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.336-1826G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322866 | |||||||
| chr14:69322881 | G | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.336-1811G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322881 | |||||||
| chr14:69322922 | CG | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0164 a0001c0001t0008g0094 |
3 | HG01255.hp1 HG02257.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.336-1766delG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322922 | ||||||
| chr14:69322923 | G | C | 1 | a0002c0002t0002g0299 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.336-1769G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322923 | |||||||
| chr14:69322924 | GGGTGTGT others(6): Show |
G | 1 | a0001c0001t0008g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.336-1766_336-1754d others(15): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322924 | ||||||
| chr14:69322925 | G | GGGGTGTG others(9): Show |
2 | a0001c0001t0001g0045 a0001c0001t0007g0044 |
2 | HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.336-1766_336-1765i others(18): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322925 | G | GGGTGTGT others(6): Show |
1 | a0001c0001t0005g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.336-1766_336-1765i others(15): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322925 | G | GGT | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0004g0249 others(2): Show |
5 | HG01255.hp2 HG01346.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.336-1711_336-1710d others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322925 | G | GGTGTGT | 3 | a0001c0001t0001g0036 a0001c0001t0004g0033 a0002c0002t0002g0253 |
3 | HG00280.hp1 HG01361.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.336-1715_336-1710d others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322925 | G | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0083 others(45): Show |
49 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.336-1767G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322925 | |||||||
| chr14:69322925 | GGTGT | G | 8 | a0001c0001t0004g0255 a0001c0001t0004g0258 a0001c0003t0001g0260 others(5): Show |
8 | HG00733.hp1 HG01074.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.336-1713_336-1710d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322925 | GGTGTGT | G | 3 | a0001c0001t0001g0035 a0001c0001t0003g0032 a0002c0002t0001g0256 |
3 | HG00280.hp2 NA19088.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.336-1715_336-1710d others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322925 | GGTGTGTG others(11): Show |
G | 1 | a0001c0001t0001g0243 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.336-1727_336-1710d others(20): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322925 | GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0001g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.336-1729_336-1710d others(22): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322925 | ||||||
| chr14:69322926 | GT | G | 55 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0102 others(52): Show |
56 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.336-1765delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322926 | |||||||
| chr14:69322926 | GTGTGT | G | 10 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0206 others(7): Show |
10 | HG01123.hp2 HG02132.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.336-1765_336-1761d others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322926 | |||||||
| chr14:69322926 | GTGTGTGT | G | 5 | a0001c0001t0001g0178 a0001c0001t0001g0231 a0001c0001t0003g0079 others(2): Show |
5 | HG03927.hp2 HG06807.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-1765_336-1759d others(9): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322926 | |||||||
| chr14:69322927 | T | G | 1 | a0001c0001t0025g0184 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.336-1765T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322927 | |||||||
| chr14:69322931 | T | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0150 |
2 | HG01934.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.336-1761T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322931 | |||||||
| chr14:69322939 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.336-1753T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322939 | |||||||
| chr14:69322960 | GTGTGTGT others(35): Show |
G | 4 | a0002c0002t0001g0111 a0004c0006t0003g0112 a0004c0006t0003g0220 others(1): Show |
4 | HG00408.hp2 NA18945.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.336-1729_336-1688d others(44): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322960 | ||||||
| chr14:69322962 | GTGTGTGT others(33): Show |
G | 5 | a0001c0001t0001g0127 a0001c0001t0002g0107 a0002c0002t0001g0100 others(2): Show |
5 | HG03017.hp2 NA18997.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.336-1727_336-1688d others(42): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322962 | ||||||
| chr14:69322964 | GTGTGTGT others(27): Show |
G | 2 | a0001c0003t0001g0105 a0002c0002t0002g0106 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.336-1727_336-1694d others(36): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322964 | |||||||
| chr14:69322964 | GTGTGTGT others(31): Show |
G | 38 | a0001c0001t0001g0074 a0001c0001t0001g0083 a0001c0001t0001g0101 others(35): Show |
39 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.336-1725_336-1688d others(40): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322964 | ||||||
| chr14:69322965 | TGTGTGTG others(11): Show |
T | 1 | a0003c0004t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.336-1725_336-1708d others(20): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322965 | ||||||
| chr14:69322966 | GTGTGTGT others(29): Show |
G | 6 | a0001c0001t0001g0114 a0001c0001t0002g0286 a0001c0001t0004g0269 others(3): Show |
6 | HG00609.hp2 HG02486.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.336-1723_336-1688d others(38): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322966 | ||||||
| chr14:69322968 | GTGTGTGT others(27): Show |
G | 5 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0002g0110 others(2): Show |
5 | HG01192.hp2 HG02129.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.336-1721_336-1688d others(36): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322968 | ||||||
| chr14:69322969 | TGTGTGTG others(7): Show |
T | 5 | a0001c0001t0001g0041 a0001c0005t0006g0175 a0001c0016t0006g0154 others(2): Show |
5 | HG02486.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.336-1721_336-1708d others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322969 | ||||||
| chr14:69322970 | GTGTGTGT others(25): Show |
G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0071 others(32): Show |
37 | HG00099.hp1 HG00558.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.336-1719_336-1688d others(34): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322970 | ||||||
| chr14:69322971 | T | C | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.336-1721T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322971 | |||||||
| chr14:69322971 | TGTGTGTG others(13): Show |
T | 1 | a0003c0004t0009g0212 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.336-1719_336-1700d others(22): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322971 | ||||||
| chr14:69322972 | GTGTGTGT others(23): Show |
G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0087 others(12): Show |
16 | HG01243.hp1 HG01243.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.336-1717_336-1688d others(32): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322972 | ||||||
| chr14:69322973 | T | C | 2 | a0001c0001t0001g0243 a0006c0010t0004g0173 |
2 | HG03486.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.336-1719T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322973 | |||||||
| chr14:69322974 | GTGTGTGT others(21): Show |
G | 16 | a0001c0001t0001g0091 a0001c0001t0002g0095 a0001c0001t0005g0296 others(13): Show |
16 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.336-1715_336-1688d others(30): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322974 | ||||||
| chr14:69322975 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0006c0010t0004g0173 |
3 | HG03486.hp2 HG04228.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.336-1717T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322975 | |||||||
| chr14:69322975 | TGTGTGTG others(9): Show |
T | 3 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 |
3 | HG01081.hp2 HG01496.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.336-1715_336-1700d others(18): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322975 | ||||||
| chr14:69322976 | GTGTGTGC others(19): Show |
G | 12 | a0001c0001t0001g0068 a0001c0001t0001g0123 a0001c0001t0002g0096 others(9): Show |
12 | HG00741.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.336-1713_336-1688d others(28): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322976 | ||||||
| chr14:69322977 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0006c0010t0004g0173 |
3 | HG03486.hp2 HG04228.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.336-1715T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322977 | |||||||
| chr14:69322978 | GTGTGCGC others(17): Show |
G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0058 others(8): Show |
11 | HG00558.hp2 HG00738.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.336-1711_336-1688d others(26): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322978 | ||||||
| chr14:69322979 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0006c0010t0004g0173 |
3 | HG03486.hp2 HG04228.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.336-1713T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322979 | |||||||
| chr14:69322980 | GTGCGCGC others(15): Show |
G | 6 | a0001c0001t0002g0013 a0001c0001t0007g0274 a0001c0001t0010g0025 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.336-1708_336-1687d others(24): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322980 | ||||||
| chr14:69322981 | T | C | 5 | a0001c0001t0001g0243 a0001c0001t0001g0278 a0001c0003t0002g0251 others(2): Show |
5 | HG03139.hp2 HG03486.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.336-1711T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322981 | |||||||
| chr14:69322982 | GCGCGCGC others(1): Show |
G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0195 a0001c0001t0001g0199 others(5): Show |
8 | HG01123.hp2 HG02132.hp1 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.336-1698_336-1691d others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322982 | ||||||
| chr14:69322982 | GCGCGCGC others(13): Show |
G | 8 | a0001c0001t0001g0047 a0001c0001t0002g0014 a0001c0001t0003g0226 others(5): Show |
8 | HG00140.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.336-1709_336-1690d others(22): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322982 | |||||||
| chr14:69322983 | C | T | 59 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0080 others(56): Show |
60 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.336-1709C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322983 | |||||||
| chr14:69322984 | GCGCGCA | G | 32 | a0001c0001t0001g0043 a0001c0001t0001g0124 a0001c0001t0001g0150 others(29): Show |
32 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.336-1702_336-1697d others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322984 | ||||||
| chr14:69322985 | C | T | 41 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0135 others(38): Show |
41 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.336-1707C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322985 | |||||||
| chr14:69322986 | GCGCA | G | 25 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0080 others(22): Show |
25 | HG00140.hp2 HG00408.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.336-1702_336-1699d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322986 | ||||||
| chr14:69322986 | GCGCACGC others(5): Show |
G | 1 | a0001c0001t0010g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.336-1701_336-1690d others(14): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322986 | ||||||
| chr14:69322987 | C | T | 13 | a0001c0001t0001g0167 a0001c0001t0001g0169 a0001c0001t0001g0174 others(10): Show |
13 | HG00609.hp1 HG01928.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.336-1705C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322987 | |||||||
| chr14:69322988 | GCA | G | 15 | a0001c0001t0001g0174 a0001c0001t0001g0218 a0001c0001t0001g0241 others(12): Show |
15 | HG00438.hp2 HG00609.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.336-1702_336-1701d others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr14 | 69322988 | ||||||
| chr14:69322989 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.336-1703C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322989 | |||||||
| chr14:69322990 | A | G | 20 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0045 others(17): Show |
20 | HG00280.hp2 HG01257.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.336-1702A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322990 | |||||||
| chr14:69322999 | C | T | 1 | a0001c0001t0010g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.336-1693C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322999 | |||||||
| chr14:69323001 | C | T | 1 | a0001c0001t0010g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.336-1691C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323001 | |||||||
| chr14:69323002 | A | G | 1 | a0001c0001t0010g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.336-1690A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323002 | |||||||
| chr14:69323003 | T | C | 52 | a0001c0001t0001g0058 a0001c0001t0001g0074 a0001c0001t0001g0083 others(49): Show |
53 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.336-1689T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323003 | |||||||
| chr14:69323006 | A | G | 1 | a0001c0001t0024g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.336-1686A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323006 | |||||||
| chr14:69323010 | G | A | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.336-1682G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323010 | |||||||
| chr14:69323038 | T | G | 108 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0047 others(105): Show |
109 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.336-1654T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323038 | |||||||
| chr14:69323319 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.336-1373C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323319 | |||||||
| chr14:69323323 | T | G | 1 | a0001c0001t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.336-1369T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323323 | |||||||
| chr14:69323659 | C | T | 2 | a0001c0001t0001g0268 a0001c0003t0001g0260 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.336-1033C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323659 | |||||||
| chr14:69323672 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(65): Show |
71 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.336-1020C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323672 | |||||||
| chr14:69323763 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(83): Show |
89 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.336-929T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323763 | |||||||
| chr14:69323953 | A | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(202): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.336-739A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323953 | |||||||
| chr14:69324061 | G | T | 126 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0047 others(123): Show |
127 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.336-631G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324061 | |||||||
| chr14:69324247 | T | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.336-445T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324247 | |||||||
| chr14:69324346 | C | T | 3 | a0001c0001t0027g0077 a0003c0004t0001g0290 a0003c0004t0002g0289 |
3 | HG02818.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.336-346C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324346 | |||||||
| chr14:69324358 | G | A | 5 | a0001c0001t0001g0144 a0001c0001t0002g0275 a0001c0001t0014g0285 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.336-334G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324358 | |||||||
| chr14:69324390 | T | C | 217 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0043 others(214): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.336-302T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324390 | |||||||
| chr14:69324396 | T | C | 225 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0043 others(222): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.336-296T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324396 | |||||||
| chr14:69324496 | G | C | 63 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0051 others(60): Show |
64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.336-196G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324496 | |||||||
| chr14:69324550 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0206 a0001c0001t0001g0230 others(1): Show |
4 | NA18954.hp2 NA18968.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.336-142C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324550 | |||||||
| chr14:69324591 | T | A | 153 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0047 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.336-101T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324591 | |||||||
| chr14:69324814 | A | G | 2 | a0001c0001t0001g0005 a0001c0015t0003g0287 |
3 | HG01243.hp2 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.434+24A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 3/14 | chr14 | 69324814 | |||||||
| chr14:69325166 | C | G | 3 | a0001c0016t0006g0154 a0002c0002t0002g0146 a0002c0002t0002g0147 |
3 | HG02896.hp1 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.435-171C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 3/14 | chr14 | 69325166 | |||||||
| chr14:69325217 | A | G | 2 | a0001c0001t0014g0285 a0006c0010t0004g0173 |
2 | HG02145.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.435-120A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 3/14 | chr14 | 69325217 | |||||||
| chr14:69325220 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0248 |
2 | HG01258.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.435-117G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 3/14 | chr14 | 69325220 | |||||||
| chr14:69325284 | T | A | 1 | a0001c0001t0013g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.435-53T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 3/14 | chr14 | 69325284 | |||||||
| chr14:69325427 | G | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0129 a0001c0001t0016g0225 others(1): Show |
4 | HG02647.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+23G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325427 | |||||||
| chr14:69325447 | C | T | 1 | a0001c0003t0003g0031 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.502+43C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325447 | |||||||
| chr14:69325521 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0215 a0001c0001t0001g0234 |
3 | HG01071.hp1 HG01993.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.502+117C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325521 | |||||||
| chr14:69325530 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.502+126T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325530 | |||||||
| chr14:69325612 | G | A | 4 | a0003c0004t0009g0145 a0003c0004t0009g0148 a0003c0004t0009g0149 others(1): Show |
4 | HG01081.hp2 HG01496.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+208G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325612 | |||||||
| chr14:69325616 | T | A | 27 | a0001c0001t0001g0047 a0001c0001t0001g0074 a0001c0001t0002g0013 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(24): Show |
intron_variant | MODIFIER | c.502+212T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325616 | |||||||
| chr14:69325684 | A | G | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.503-278A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325684 | |||||||
| chr14:69325779 | C | T | 8 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0208 others(5): Show |
8 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(5): Show |
intron_variant | MODIFIER | c.503-183C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325779 | |||||||
| chr14:69325842 | C | G | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0047 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(8): Show |
intron_variant | MODIFIER | c.503-120C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325842 | |||||||
| chr14:69325852 | A | G | 28 | a0001c0001t0001g0041 a0001c0001t0001g0074 a0001c0001t0001g0078 others(25): Show |
28 | HG01074.hp1 HG01175.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.503-110A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325852 | |||||||
| chr14:69325883 | G | A | 2 | a0001c0001t0004g0099 a0001c0001t0004g0269 |
2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.503-79G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 4/14 | chr14 | 69325883 | |||||||
| chr14:69326183 | C | T | 15 | a0001c0001t0003g0019 a0001c0001t0008g0094 a0001c0001t0008g0238 others(12): Show |
15 | HG01081.hp2 HG01175.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.568+156C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326183 | |||||||
| chr14:69326312 | G | A | 1 | a0004c0006t0003g0223 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.568+285G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326312 | |||||||
| chr14:69326431 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.568+404T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326431 | |||||||
| chr14:69326505 | T | G | 1 | a0001c0003t0022g0066 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.568+478T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326505 | |||||||
| chr14:69326758 | G | A | 118 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(115): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.568+731G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326758 | |||||||
| chr14:69326798 | T | C | 12 | a0001c0001t0001g0041 a0001c0001t0001g0078 a0001c0001t0001g0080 others(9): Show |
12 | HG01175.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.568+771T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326798 | |||||||
| chr14:69326890 | C | T | 5 | a0003c0004t0001g0009 a0003c0004t0001g0015 a0003c0004t0001g0040 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.568+863C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326890 | |||||||
| chr14:69326907 | G | T | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.568+880G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69326907 | |||||||
| chr14:69327179 | C | T | 1 | a0001c0001t0016g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.568+1152C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327179 | |||||||
| chr14:69327209 | G | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(106): Show |
111 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.568+1182G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327209 | |||||||
| chr14:69327255 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.569-1195C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327255 | |||||||
| chr14:69327559 | A | G | 15 | a0001c0001t0002g0042 a0001c0001t0003g0019 a0001c0001t0014g0285 others(12): Show |
15 | HG01081.hp2 HG01496.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.569-891A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327559 | |||||||
| chr14:69327695 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.569-755G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327695 | |||||||
| chr14:69327834 | C | T | 30 | a0001c0001t0013g0010 a0002c0002t0001g0001 a0002c0002t0001g0004 others(27): Show |
32 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.569-616C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327834 | |||||||
| chr14:69327841 | C | T | 1 | a0001c0001t0008g0128 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.569-609C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327841 | |||||||
| chr14:69327904 | G | A | 1 | a0001c0003t0001g0163 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.569-546G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69327904 | |||||||
| chr14:69328236 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.569-214G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69328236 | |||||||
| chr14:69328308 | C | G | 1 | a0001c0003t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.569-142C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 5/14 | chr14 | 69328308 | |||||||
| chr14:69328579 | A | G | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.690+8A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69328579 | |||||||
| chr14:69328859 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0191 others(2): Show |
5 | HG00558.hp2 HG02129.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+288G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69328859 | |||||||
| chr14:69329125 | G | A | 41 | a0001c0001t0001g0124 a0001c0001t0001g0248 a0001c0001t0002g0007 others(38): Show |
41 | HG00438.hp2 HG00673.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.690+554G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69329125 | |||||||
| chr14:69329141 | T | G | 1 | a0001c0001t0002g0013 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.690+570T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69329141 | |||||||
| chr14:69329548 | G | T | 1 | a0002c0002t0011g0020 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.690+977G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69329548 | |||||||
| chr14:69329645 | G | A | 1 | a0003c0004t0001g0290 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.690+1074G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69329645 | |||||||
| chr14:69329759 | G | T | 1 | a0001c0003t0003g0224 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.690+1188G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69329759 | |||||||
| chr14:69329935 | T | C | 10 | a0001c0001t0001g0278 a0003c0004t0001g0039 a0003c0004t0001g0137 others(7): Show |
10 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.690+1364T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69329935 | |||||||
| chr14:69329967 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0007 |
2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.690+1396G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69329967 | |||||||
| chr14:69330159 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.691-1305A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330159 | |||||||
| chr14:69330299 | C | T | 2 | a0001c0001t0012g0022 a0007c0019t0008g0151 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.691-1165C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330299 | |||||||
| chr14:69330320 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.691-1144G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330320 | |||||||
| chr14:69330369 | G | T | 1 | a0002c0002t0001g0301 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.691-1095G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330369 | |||||||
| chr14:69330590 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(249): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.691-874T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330590 | |||||||
| chr14:69330715 | G | A | 3 | a0003c0004t0001g0009 a0003c0004t0001g0015 a0003c0004t0001g0290 |
3 | HG02055.hp1 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.691-749G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330715 | |||||||
| chr14:69330740 | A | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0041 a0001c0001t0001g0074 others(19): Show |
22 | HG01884.hp1 HG02135.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.691-724A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330740 | |||||||
| chr14:69330899 | C | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0011 others(163): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.691-565C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330899 | |||||||
| chr14:69330902 | G | T | 10 | a0001c0001t0001g0045 a0001c0001t0003g0037 a0001c0001t0003g0161 others(7): Show |
10 | HG00280.hp1 HG00738.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.691-562G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69330902 | |||||||
| chr14:69330919 | TG | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0114 others(16): Show |
20 | HG00438.hp1 HG00609.hp2 NA18941.hp1 others(17): Show |
intron_variant | MODIFIER | c.691-543delG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr14 | 69330919 | ||||||
| chr14:69331247 | G | A | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.691-217G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69331247 | |||||||
| chr14:69331448 | C | A | 4 | a0001c0001t0002g0131 a0001c0001t0002g0288 a0001c0001t0003g0226 others(1): Show |
4 | HG01074.hp1 HG01891.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-16C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 6/14 | chr14 | 69331448 | |||||||
| chr14:69331566 | C | T | 1 | a0002c0002t0011g0020 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.778+15C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69331566 | |||||||
| chr14:69331567 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(113): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.778+16G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69331567 | |||||||
| chr14:69332051 | G | A | 1 | a0001c0001t0012g0022 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.778+500G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332051 | |||||||
| chr14:69332303 | C | A | 1 | a0002c0002t0001g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.778+752C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332303 | |||||||
| chr14:69332331 | C | A | 3 | a0001c0001t0003g0037 a0001c0001t0003g0161 a0001c0001t0003g0279 |
3 | HG00738.hp2 HG01192.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.779-754C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332331 | |||||||
| chr14:69332374 | AC | A | 65 | a0001c0001t0001g0051 a0001c0001t0001g0229 a0001c0001t0002g0013 others(62): Show |
67 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.779-710delC | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332374 | |||||||
| chr14:69332522 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.779-563G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332522 | |||||||
| chr14:69332602 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.779-483T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332602 | |||||||
| chr14:69332644 | C | T | 1 | a0002c0002t0001g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.779-441C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332644 | |||||||
| chr14:69332729 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0218 |
2 | NA18948.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.779-356C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332729 | |||||||
| chr14:69332826 | C | CT | 129 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(126): Show |
130 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.779-242dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr14 | 69332826 | ||||||
| chr14:69332828 | T | TC | 75 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0124 others(72): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.779-257_779-256ins others(1): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332828 | |||||||
| chr14:69332829 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.779-256T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 7/14 | chr14 | 69332829 | |||||||
| chr14:69333175 | A | G | 165 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0018 others(162): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
splice_region_variant&intron_variant | LOW | c.863+6A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 8/14 | chr14 | 69333175 | |||||||
| chr14:69333227 | A | G | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.863+58A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 8/14 | chr14 | 69333227 | |||||||
| chr14:69333297 | T | C | 130 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0058 others(127): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.863+128T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 8/14 | chr14 | 69333297 | |||||||
| chr14:69333949 | G | GGCTGGGA | 36 | a0001c0001t0001g0124 a0001c0001t0001g0248 a0001c0001t0002g0092 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.967+351_967+357dup others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 69333949 | ||||||
| chr14:69334220 | G | A | 1 | a0003c0004t0001g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.967+620G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334220 | |||||||
| chr14:69334337 | C | G | 1 | a0006c0010t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.967+737C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334337 | |||||||
| chr14:69334337 | C | T | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.967+737C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334337 | |||||||
| chr14:69334466 | A | G | 1 | a0001c0001t0004g0272 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.967+866A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334466 | |||||||
| chr14:69334528 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.967+928G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334528 | |||||||
| chr14:69334666 | G | C | 38 | a0001c0001t0001g0124 a0001c0001t0001g0248 a0001c0001t0002g0092 others(35): Show |
38 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.967+1066G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334666 | |||||||
| chr14:69334711 | T | A | 1 | a0001c0003t0001g0210 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.967+1111T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334711 | |||||||
| chr14:69334816 | T | A | 36 | a0001c0001t0001g0124 a0001c0001t0001g0248 a0001c0001t0012g0022 others(33): Show |
36 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.967+1216T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69334816 | |||||||
| chr14:69335004 | G | A | 1 | a0001c0001t0013g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.967+1404G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335004 | |||||||
| chr14:69335147 | C | A | 79 | a0001c0001t0001g0018 a0001c0001t0002g0013 a0001c0001t0002g0014 others(76): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.967+1547C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335147 | |||||||
| chr14:69335240 | C | T | 1 | a0001c0017t0001g0270 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.967+1640C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335240 | |||||||
| chr14:69335271 | A | G | 37 | a0001c0001t0001g0124 a0001c0001t0001g0248 a0001c0001t0003g0158 others(34): Show |
37 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.967+1671A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335271 | |||||||
| chr14:69335549 | CAG | C | 7 | a0003c0004t0001g0009 a0003c0004t0001g0015 a0003c0004t0001g0040 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+1953_967+1954d others(4): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 69335549 | ||||||
| chr14:69335656 | G | A | 2 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.967+2056G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335656 | |||||||
| chr14:69335712 | C | T | 12 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(9): Show |
12 | HG00558.hp2 HG01123.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.967+2112C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335712 | |||||||
| chr14:69335741 | A | G | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00558.hp2 HG01123.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.967+2141A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335741 | |||||||
| chr14:69335754 | C | T | 1 | a0001c0003t0003g0029 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.967+2154C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335754 | |||||||
| chr14:69335992 | T | C | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.967+2392T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69335992 | |||||||
| chr14:69336048 | C | T | 2 | a0001c0015t0003g0287 a0001c0016t0006g0154 |
2 | HG02109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.967+2448C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336048 | |||||||
| chr14:69336167 | G | T | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2484G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336167 | |||||||
| chr14:69336179 | T | C | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2472T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336179 | |||||||
| chr14:69336212 | C | T | 3 | a0001c0003t0001g0050 a0001c0003t0001g0067 a0001c0003t0022g0066 |
3 | HG02683.hp1 HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.968-2439C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336212 | |||||||
| chr14:69336271 | G | A | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2380G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336271 | |||||||
| chr14:69336272 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.968-2379G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336272 | |||||||
| chr14:69336299 | G | A | 1 | a0001c0003t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.968-2352G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336299 | |||||||
| chr14:69336345 | C | T | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2306C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336345 | |||||||
| chr14:69336348 | G | A | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2303G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336348 | |||||||
| chr14:69336355 | A | G | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2296A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336355 | |||||||
| chr14:69336376 | G | T | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2275G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336376 | |||||||
| chr14:69336391 | C | T | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2260C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336391 | |||||||
| chr14:69336416 | T | C | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-2235T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336416 | |||||||
| chr14:69336432 | G | A | 1 | a0003c0004t0001g0143 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.968-2219G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336432 | |||||||
| chr14:69336457 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(1): Show |
4 | HG01123.hp1 HG01928.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.968-2194A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336457 | |||||||
| chr14:69336483 | G | A | 80 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0060 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.968-2168G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336483 | |||||||
| chr14:69336549 | T | A | 1 | a0001c0001t0003g0158 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.968-2102T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336549 | |||||||
| chr14:69336550 | C | T | 1 | a0001c0001t0003g0158 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.968-2101C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336550 | |||||||
| chr14:69336696 | T | TTTTA | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-1951_968-1948d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 69336696 | ||||||
| chr14:69336722 | A | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0124 others(84): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.968-1929A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336722 | |||||||
| chr14:69336774 | A | T | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-1877A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336774 | |||||||
| chr14:69336816 | C | T | 6 | a0001c0001t0001g0121 a0001c0001t0002g0273 a0001c0001t0018g0134 others(3): Show |
6 | HG00621.hp2 HG03927.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.968-1835C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336816 | |||||||
| chr14:69336834 | T | TCTC | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-1815_968-1814i others(5): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 69336834 | ||||||
| chr14:69336852 | A | G | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-1799A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336852 | |||||||
| chr14:69336867 | G | A | 2 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.968-1784G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336867 | |||||||
| chr14:69336871 | C | A | 2 | a0001c0001t0004g0255 a0001c0001t0004g0264 |
2 | HG00733.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.968-1780C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336871 | |||||||
| chr14:69336915 | C | CG | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-1732dupG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr14 | 69336915 | ||||||
| chr14:69336934 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0002g0007 |
2 | HG02572.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.968-1717C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336934 | |||||||
| chr14:69336969 | T | C | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-1682T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69336969 | |||||||
| chr14:69337007 | G | A | 100 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(97): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.968-1644G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337007 | |||||||
| chr14:69337064 | C | T | 181 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0035 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.968-1587C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337064 | |||||||
| chr14:69337277 | A | G | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-1374A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337277 | |||||||
| chr14:69337403 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0203 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.968-1248G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337403 | |||||||
| chr14:69337540 | G | T | 12 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(9): Show |
12 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.968-1111G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337540 | |||||||
| chr14:69337686 | G | T | 12 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(9): Show |
12 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.968-965G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337686 | |||||||
| chr14:69337727 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.968-924C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337727 | |||||||
| chr14:69337772 | G | C | 104 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(101): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.968-879G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337772 | |||||||
| chr14:69337962 | A | G | 1 | a0001c0001t0003g0104 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.968-689A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337962 | |||||||
| chr14:69337977 | A | G | 4 | a0001c0001t0001g0080 a0001c0005t0006g0175 a0001c0015t0003g0287 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-674A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337977 | |||||||
| chr14:69337996 | C | T | 1 | a0001c0003t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.968-655C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69337996 | |||||||
| chr14:69338025 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0125 others(3): Show |
7 | HG00438.hp1 NA18941.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.968-626C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69338025 | |||||||
| chr14:69338072 | A | G | 1 | a0002c0002t0002g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.968-579A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69338072 | |||||||
| chr14:69338207 | C | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0129 a0001c0001t0002g0013 others(65): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.968-444C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69338207 | |||||||
| chr14:69338294 | C | G | 1 | a0001c0001t0002g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.968-357C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69338294 | |||||||
| chr14:69338306 | T | G | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.968-345T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69338306 | |||||||
| chr14:69338346 | A | G | 14 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(11): Show |
14 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-305A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69338346 | |||||||
| chr14:69338399 | T | C | 13 | a0001c0001t0002g0131 a0001c0001t0002g0288 a0001c0001t0003g0226 others(10): Show |
13 | HG01074.hp1 HG01243.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.968-252T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 9/14 | chr14 | 69338399 | |||||||
| chr14:69339018 | G | A | 6 | a0001c0001t0002g0014 a0001c0001t0002g0132 a0001c0001t0010g0023 others(3): Show |
6 | HG00733.hp2 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1094+241G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/14 | chr14 | 69339018 | |||||||
| chr14:69339079 | T | G | 15 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0086 others(12): Show |
15 | HG00099.hp2 HG00558.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.1094+302T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/14 | chr14 | 69339079 | |||||||
| chr14:69339134 | C | T | 1 | a0001c0001t0015g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1094+357C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/14 | chr14 | 69339134 | |||||||
| chr14:69339308 | C | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0018 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1095-219C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/14 | chr14 | 69339308 | |||||||
| chr14:69339338 | A | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0129 a0001c0001t0002g0013 others(65): Show |
70 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.1095-189A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/14 | chr14 | 69339338 | |||||||
| chr14:69339434 | C | T | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1095-93C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/14 | chr14 | 69339434 | |||||||
| chr14:69339837 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1187+218G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69339837 | |||||||
| chr14:69339991 | A | G | 2 | a0001c0001t0001g0080 a0001c0005t0006g0175 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1187+372A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69339991 | |||||||
| chr14:69340039 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1187+420T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69340039 | |||||||
| chr14:69340180 | C | G | 5 | a0003c0004t0001g0009 a0003c0004t0001g0015 a0003c0004t0001g0040 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1187+561C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69340180 | |||||||
| chr14:69340426 | T | C | 1 | a0001c0001t0002g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1187+807T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69340426 | |||||||
| chr14:69340486 | A | AT | 9 | a0001c0001t0001g0091 a0001c0001t0001g0174 a0001c0001t0001g0202 others(6): Show |
9 | HG01258.hp2 HG01928.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187+882dupT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 69340486 | ||||||
| chr14:69340486 | AT | A | 96 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0058 others(93): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.1187+882delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 69340486 | ||||||
| chr14:69340533 | G | A | 15 | a0001c0001t0001g0006 a0001c0001t0002g0007 a0001c0001t0002g0131 others(12): Show |
15 | HG01074.hp1 HG01243.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1187+914G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69340533 | |||||||
| chr14:69340602 | G | A | 79 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0129 others(76): Show |
81 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1187+983G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69340602 | |||||||
| chr14:69340810 | G | C | 2 | a0001c0001t0012g0022 a0007c0019t0008g0151 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1188-871G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69340810 | |||||||
| chr14:69340888 | CA | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0129 others(76): Show |
81 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1188-790delA | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr14 | 69340888 | ||||||
| chr14:69340931 | A | G | 1 | a0001c0001t0028g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1188-750A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69340931 | |||||||
| chr14:69341013 | G | A | 1 | a0001c0001t0008g0094 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1188-668G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69341013 | |||||||
| chr14:69341171 | T | G | 1 | a0001c0001t0012g0022 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1188-510T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69341171 | |||||||
| chr14:69341244 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0199 a0001c0001t0001g0208 |
3 | HG00280.hp2 HG01123.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1188-437C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69341244 | |||||||
| chr14:69341471 | T | C | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1188-210T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69341471 | |||||||
| chr14:69341592 | T | A | 1 | a0007c0019t0008g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1188-89T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69341592 | |||||||
| chr14:69341600 | G | C | 1 | a0001c0001t0007g0274 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1188-81G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69341600 | |||||||
| chr14:69341671 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1188-10C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 11/14 | chr14 | 69341671 | |||||||
| chr14:69341910 | G | C | 70 | a0001c0001t0001g0018 a0001c0001t0001g0124 a0001c0001t0001g0129 others(67): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1271+146G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69341910 | |||||||
| chr14:69342409 | G | A | 122 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0001g0087 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.1271+645G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342409 | |||||||
| chr14:69342426 | G | A | 89 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0086 others(86): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.1271+662G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342426 | |||||||
| chr14:69342474 | A | AAGGG | 11 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0002g0085 others(8): Show |
11 | HG01074.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1271+742_1271+745d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(5): Show |
9 | a0001c0001t0001g0129 a0001c0001t0002g0007 a0001c0001t0002g0096 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1271+717_1271+718i others(14): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(9): Show |
20 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(17): Show |
21 | HG00099.hp2 HG00408.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1271+717_1271+718i others(18): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(13): Show |
33 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0002g0092 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1271+717_1271+718i others(22): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(17): Show |
5 | a0001c0001t0002g0028 a0001c0001t0002g0095 a0001c0001t0002g0110 others(2): Show |
5 | HG02129.hp2 HG02258.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271+717_1271+718i others(26): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(21): Show |
5 | a0001c0001t0002g0014 a0001c0001t0002g0088 a0001c0001t0010g0023 others(2): Show |
5 | HG01993.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271+717_1271+718i others(30): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(41): Show |
1 | a0001c0001t0002g0132 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1271+717_1271+718i others(50): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(45): Show |
1 | a0002c0002t0001g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1271+717_1271+718i others(54): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(1): Show |
9 | a0001c0001t0012g0022 a0003c0004t0001g0009 a0003c0004t0001g0015 others(6): Show |
9 | HG01081.hp2 HG01433.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1271+738_1271+745d others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | A | AAGGGAGG others(5): Show |
3 | a0003c0004t0001g0040 a0003c0004t0002g0027 a0003c0004t0011g0024 |
3 | HG02258.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1271+734_1271+745d others(14): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | AAGGG | A | 46 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0047 others(43): Show |
47 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1271+742_1271+745d others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342474 | AAGGGAGG others(1): Show |
A | 3 | a0001c0005t0006g0175 a0001c0016t0006g0154 a0003c0004t0001g0233 |
3 | HG02896.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1271+738_1271+745d others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342474 | ||||||
| chr14:69342478 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1271+714G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342478 | |||||||
| chr14:69342478 | G | C | 1 | a0001c0001t0005g0296 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1271+714G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342478 | |||||||
| chr14:69342478 | G | GAGGA | 6 | a0001c0001t0001g0278 a0001c0001t0002g0013 a0001c0001t0002g0076 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271+717_1271+718i others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342478 | ||||||
| chr14:69342478 | G | GAGGAAGG others(1): Show |
6 | a0002c0002t0001g0136 a0002c0002t0001g0185 a0002c0002t0001g0246 others(3): Show |
6 | HG00609.hp1 HG00621.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271+717_1271+718i others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342478 | ||||||
| chr14:69342482 | G | A | 37 | a0001c0001t0001g0124 a0001c0001t0001g0248 a0001c0001t0002g0194 others(34): Show |
37 | HG00438.hp2 HG00741.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.1271+718G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342482 | |||||||
| chr14:69342482 | G | C | 6 | a0001c0001t0001g0278 a0001c0001t0002g0013 a0001c0001t0002g0076 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1271+718G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342482 | |||||||
| chr14:69342486 | G | C | 37 | a0001c0001t0001g0124 a0001c0001t0001g0248 a0001c0001t0002g0194 others(34): Show |
37 | HG00438.hp2 HG00741.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.1271+722G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342486 | |||||||
| chr14:69342498 | G | GAGGGAGG others(44): Show |
1 | a0001c0001t0001g0125 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1271+743_1271+744i others(53): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342498 | ||||||
| chr14:69342510 | A | G | 123 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0086 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1271+746A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342510 | |||||||
| chr14:69342515 | A | AG | 57 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(54): Show |
57 | HG00099.hp2 HG00438.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1271+755dupG | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342515 | ||||||
| chr14:69342529 | GGAAAA | G | 67 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0129 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1271+777_1271+781d others(7): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69342529 | ||||||
| chr14:69342682 | A | G | 1 | a0002c0002t0002g0146 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1271+918A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342682 | |||||||
| chr14:69342768 | G | A | 1 | a0001c0001t0014g0285 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1271+1004G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342768 | |||||||
| chr14:69342904 | A | G | 70 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0086 others(67): Show |
70 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.1271+1140A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342904 | |||||||
| chr14:69342907 | G | A | 66 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0129 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1271+1143G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342907 | |||||||
| chr14:69342982 | A | G | 55 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(52): Show |
55 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.1271+1218A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342982 | |||||||
| chr14:69343066 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1271+1302T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69343066 | |||||||
| chr14:69343364 | T | A | 195 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0035 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1271+1600T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69343364 | |||||||
| chr14:69343465 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1271+1701C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69343465 | |||||||
| chr14:69343562 | A | G | 2 | a0001c0005t0006g0175 a0001c0016t0006g0154 |
2 | HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1271+1798A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69343562 | |||||||
| chr14:69343637 | G | T | 54 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(51): Show |
54 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1271+1873G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69343637 | |||||||
| chr14:69343976 | C | CTCATTCC others(22): Show |
1 | a0001c0001t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1271+2214_1271+224 others(33): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69343976 | ||||||
| chr14:69344043 | G | A | 54 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(51): Show |
54 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1271+2279G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69344043 | |||||||
| chr14:69344164 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1271+2400C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69344164 | |||||||
| chr14:69344191 | T | A | 13 | a0001c0001t0001g0101 a0001c0001t0001g0127 a0001c0001t0001g0169 others(10): Show |
13 | HG00673.hp1 HG02135.hp2 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.1271+2427T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69344191 | |||||||
| chr14:69344218 | G | T | 2 | a0002c0002t0002g0146 a0002c0002t0002g0147 |
2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1271+2454G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69344218 | |||||||
| chr14:69344304 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0203 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1271+2540C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69344304 | |||||||
| chr14:69345012 | G | A | 53 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(50): Show |
53 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1272-2028G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345012 | |||||||
| chr14:69345366 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0203 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1272-1674C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345366 | |||||||
| chr14:69345547 | A | C | 1 | a0001c0003t0001g0295 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1272-1493A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345547 | |||||||
| chr14:69345562 | G | A | 160 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1272-1478G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345562 | |||||||
| chr14:69345649 | G | T | 53 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(50): Show |
53 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1272-1391G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345649 | |||||||
| chr14:69345691 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1272-1349C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345691 | |||||||
| chr14:69345703 | A | AGT | 13 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0074 others(10): Show |
13 | HG00558.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1272-1304_1272-130 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGT | 8 | a0001c0001t0001g0043 a0001c0001t0002g0131 a0001c0001t0002g0288 others(5): Show |
8 | HG01074.hp1 HG01175.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1272-1306_1272-130 others(8): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGT | 4 | a0001c0001t0001g0006 a0001c0003t0002g0108 a0003c0004t0002g0027 others(1): Show |
4 | HG02886.hp1 HG02965.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1308_1272-130 others(10): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(3): Show |
10 | a0001c0001t0001g0101 a0001c0001t0001g0127 a0001c0001t0001g0169 others(7): Show |
10 | HG00099.hp2 HG01433.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1272-1312_1272-130 others(14): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(5): Show |
9 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0123 others(6): Show |
9 | HG01123.hp1 HG01943.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1272-1314_1272-130 others(16): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(7): Show |
21 | a0001c0001t0001g0045 a0001c0001t0001g0153 a0001c0001t0001g0248 others(18): Show |
21 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1272-1316_1272-130 others(18): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(9): Show |
11 | a0001c0001t0001g0068 a0001c0001t0003g0158 a0001c0001t0003g0236 others(8): Show |
11 | HG00673.hp1 HG00741.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1272-1318_1272-130 others(20): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(11): Show |
26 | a0001c0001t0001g0051 a0001c0001t0001g0164 a0001c0001t0001g0200 others(23): Show |
27 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.1272-1320_1272-130 others(22): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(13): Show |
20 | a0001c0001t0001g0018 a0001c0001t0001g0129 a0001c0001t0002g0110 others(17): Show |
21 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1272-1322_1272-130 others(24): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(15): Show |
19 | a0001c0001t0001g0072 a0001c0001t0001g0124 a0001c0001t0001g0215 others(16): Show |
19 | HG00140.hp2 HG00408.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1272-1324_1272-130 others(26): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(17): Show |
6 | a0001c0001t0002g0132 a0001c0017t0001g0270 a0002c0002t0001g0156 others(3): Show |
6 | HG00733.hp2 HG02922.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272-1326_1272-130 others(28): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(19): Show |
6 | a0001c0001t0001g0071 a0001c0001t0002g0076 a0001c0001t0002g0275 others(3): Show |
6 | HG00408.hp2 HG01361.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1272-1328_1272-130 others(30): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(21): Show |
3 | a0001c0001t0002g0014 a0001c0001t0002g0085 a0001c0001t0017g0245 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1272-1330_1272-130 others(32): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | A | AGTGTGTG others(23): Show |
1 | a0001c0001t0008g0128 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1272-1332_1272-130 others(34): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345703 | AGT | A | 4 | a0001c0001t0001g0080 a0001c0001t0002g0286 a0001c0005t0006g0175 others(1): Show |
4 | HG02486.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1272-1304_1272-130 others(6): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345703 | ||||||
| chr14:69345761 | T | G | 1 | a0001c0001t0015g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1272-1279T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345761 | |||||||
| chr14:69345882 | AATTTT | A | 22 | a0003c0004t0001g0009 a0003c0004t0001g0012 a0003c0004t0001g0015 others(19): Show |
22 | HG01081.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1272-1148_1272-114 others(9): Show |
GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69345882 | ||||||
| chr14:69345925 | A | G | 1 | a0001c0001t0005g0296 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1272-1115A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69345925 | |||||||
| chr14:69346019 | G | T | 2 | a0001c0001t0002g0131 a0001c0001t0002g0288 |
2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1272-1021G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346019 | |||||||
| chr14:69346039 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1272-1001C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346039 | |||||||
| chr14:69346054 | AT | A | 54 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(51): Show |
54 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1272-973delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr14 | 69346054 | ||||||
| chr14:69346213 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1272-827T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346213 | |||||||
| chr14:69346392 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1272-648T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346392 | |||||||
| chr14:69346653 | A | G | 112 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0068 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1272-387A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346653 | |||||||
| chr14:69346683 | G | C | 1 | a0001c0001t0015g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1272-357G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346683 | |||||||
| chr14:69346795 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1272-245G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346795 | |||||||
| chr14:69346933 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1272-107C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346933 | |||||||
| chr14:69346961 | A | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0086 others(59): Show |
62 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1272-79A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69346961 | |||||||
| chr14:69347246 | G | A | 22 | a0003c0004t0001g0009 a0003c0004t0001g0012 a0003c0004t0001g0015 others(19): Show |
22 | HG01081.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1413+65G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 13/14 | chr14 | 69347246 | |||||||
| chr14:69347430 | G | C | 6 | a0001c0001t0001g0006 a0001c0001t0003g0226 a0001c0001t0007g0044 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1413+249G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 13/14 | chr14 | 69347430 | |||||||
| chr14:69347807 | C | G | 6 | a0001c0001t0001g0006 a0001c0001t0003g0226 a0001c0001t0007g0044 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-70C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 13/14 | chr14 | 69347807 | |||||||
| chr14:69348136 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0203 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1539+134C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69348136 | |||||||
| chr14:69348739 | G | A | 2 | a0001c0003t0003g0098 a0001c0003t0003g0221 |
2 | NA18982.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1539+737G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69348739 | |||||||
| chr14:69348858 | C | A | 2 | a0001c0008t0002g0188 a0001c0008t0002g0189 |
2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1539+856C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69348858 | |||||||
| chr14:69349034 | G | C | 22 | a0003c0004t0001g0009 a0003c0004t0001g0012 a0003c0004t0001g0015 others(19): Show |
22 | HG01081.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1539+1032G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349034 | |||||||
| chr14:69349073 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0007g0140 |
2 | HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1539+1071G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349073 | |||||||
| chr14:69349165 | G | A | 47 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(44): Show |
47 | HG00099.hp2 HG00741.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.1539+1163G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349165 | |||||||
| chr14:69349263 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1539+1261G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349263 | |||||||
| chr14:69349333 | G | A | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1539+1331G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349333 | |||||||
| chr14:69349362 | C | G | 1 | a0001c0001t0001g0235 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1539+1360C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349362 | |||||||
| chr14:69349536 | C | T | 22 | a0003c0004t0001g0009 a0003c0004t0001g0012 a0003c0004t0001g0015 others(19): Show |
22 | HG01081.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1539+1534C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349536 | |||||||
| chr14:69349563 | A | G | 32 | a0001c0001t0003g0037 a0001c0001t0003g0079 a0001c0001t0003g0161 others(29): Show |
32 | HG00738.hp2 HG01081.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1539+1561A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349563 | |||||||
| chr14:69349627 | G | A | 79 | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0068 others(76): Show |
81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1539+1625G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349627 | |||||||
| chr14:69349683 | C | T | 22 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(19): Show |
22 | HG00099.hp2 HG00673.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1539+1681C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349683 | |||||||
| chr14:69349909 | C | T | 194 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0035 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1539+1907C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349909 | |||||||
| chr14:69349914 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1539+1912A>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349914 | |||||||
| chr14:69349935 | T | C | 87 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(84): Show |
87 | HG00099.hp2 HG00673.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.1539+1933T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349935 | |||||||
| chr14:69349951 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1539+1949T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349951 | |||||||
| chr14:69349992 | T | A | 1 | a0001c0003t0002g0070 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1539+1990T>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69349992 | |||||||
| chr14:69350014 | C | T | 22 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(19): Show |
22 | HG00099.hp2 HG00673.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1539+2012C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350014 | |||||||
| chr14:69350035 | A | C | 2 | a0001c0005t0006g0175 a0001c0016t0006g0154 |
2 | HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1540-1996A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350035 | |||||||
| chr14:69350073 | G | A | 1 | a0003c0004t0009g0145 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1540-1958G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350073 | |||||||
| chr14:69350104 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0203 a0001c0001t0001g0205 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1540-1927C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350104 | |||||||
| chr14:69350166 | C | T | 1 | a0001c0001t0014g0285 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1540-1865C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350166 | |||||||
| chr14:69350285 | C | A | 32 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(29): Show |
32 | HG00099.hp2 HG00673.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1540-1746C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350285 | |||||||
| chr14:69350448 | T | C | 25 | a0001c0001t0008g0094 a0001c0001t0008g0238 a0001c0001t0021g0075 others(22): Show |
25 | HG01081.hp2 HG01175.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1540-1583T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350448 | |||||||
| chr14:69350585 | C | T | 1 | a0001c0001t0005g0296 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1540-1446C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350585 | |||||||
| chr14:69350592 | G | T | 1 | a0001c0001t0001g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1540-1439G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350592 | |||||||
| chr14:69350736 | C | T | 1 | a0001c0003t0001g0295 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1540-1295C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350736 | |||||||
| chr14:69350839 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1540-1192T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350839 | |||||||
| chr14:69350958 | A | G | 1 | a0001c0003t0023g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1540-1073A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350958 | |||||||
| chr14:69350995 | C | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0144 others(78): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1540-1036C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350995 | |||||||
| chr14:69351013 | G | A | 26 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0047 others(23): Show |
27 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.1540-1018G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351013 | |||||||
| chr14:69351050 | G | A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0203 a0001c0001t0001g0205 others(5): Show |
8 | HG02109.hp2 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1540-981G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351050 | |||||||
| chr14:69351074 | C | G | 6 | a0001c0001t0012g0022 a0001c0005t0006g0081 a0001c0005t0006g0138 others(3): Show |
6 | HG02451.hp2 HG02622.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-957C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351074 | |||||||
| chr14:69351133 | A | G | 69 | a0001c0001t0001g0043 a0001c0001t0001g0121 a0001c0001t0001g0144 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1540-898A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351133 | |||||||
| chr14:69351262 | G | T | 2 | a0001c0003t0001g0168 a0001c0003t0001g0228 |
2 | HG00438.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.1540-769G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351262 | |||||||
| chr14:69351317 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1540-714G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351317 | |||||||
| chr14:69351580 | G | A | 56 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(53): Show |
56 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1540-451G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351580 | |||||||
| chr14:69351721 | T | G | 1 | a0001c0001t0028g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1540-310T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351721 | |||||||
| chr14:69351742 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1540-289G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351742 | |||||||
| chr14:69351771 | G | T | 5 | a0001c0001t0001g0051 a0002c0002t0001g0016 a0002c0002t0001g0257 others(2): Show |
5 | HG02698.hp1 HG03017.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1540-260G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351771 | |||||||
| chr14:69351832 | A | G | 54 | a0001c0001t0003g0019 a0001c0001t0003g0030 a0001c0001t0003g0032 others(51): Show |
55 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1540-199A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351832 | |||||||
| chr14:69351841 | G | A | 1 | a0001c0001t0017g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1540-190G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351841 | |||||||
| chr14:69351882 | C | A | 56 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(53): Show |
56 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1540-149C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351882 | |||||||
| chr14:69351945 | G | A | 1 | a0001c0001t0017g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1540-86G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69351945 | |||||||
| chr14:69352002 | C | T | 1 | a0001c0001t0015g0057 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1540-29C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69352002 | |||||||
| chr14:69352007 | C | T | 1 | a0001c0001t0017g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1540-24C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69352007 | |||||||
| chr14:69352012 | C | G | 1 | a0001c0001t0017g0245 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1540-19C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69352012 |