| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002 | 0/0 | 558 | 46 | 7 | 12 | 13 | 6 | 8 | 8 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0003 | 0/0 | 558 | 22 | 18 | 4 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0004 | 0/0 | 558 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0005 | 0/0 | 558 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0006 | 0/0 | 558 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0007 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0008 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0009 | 0/0 | 558 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1677 | 183 | 57 | 29 | 61 | 7 | 27 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0002 | 0/0 | 1677 | 45 | 7 | 11 | 13 | 6 | 8 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0003 | 0/0 | 1677 | 31 | 1 | 2 | 22 | 0 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0004 | 0/0 | 1677 | 22 | 18 | 4 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0005 | 0/0 | 1677 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0006 | 0/0 | 1677 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0007 | 0/0 | 1677 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0008 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0009 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0010 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0011 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0012 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0013 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0014 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0015 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0016 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0017 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0018 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| c0019 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 2432 | 161 | 37 | 25 | 68 | 7 | 23 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0002 | 0/1 | 2432 | 52 | 17 | 9 | 9 | 3 | 13 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0003 | 0/0 | 2432 | 33 | 6 | 4 | 21 | 1 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0004 | 0/0 | 2432 | 15 | 0 | 6 | 0 | 3 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0005 | 0/0 | 2432 | 5 | 3 | 1 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0006 | 0/0 | 2432 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0007 | 0/0 | 2430 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0008 | 0/0 | 2432 | 4 | 3 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0009 | 0/0 | 2432 | 4 | 2 | 2 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0010 | 0/0 | 2432 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0011 | 0/0 | 2432 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0012 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0013 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0014 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0015 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0016 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0017 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0018 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0019 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0020 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0021 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0022 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0023 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0024 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0025 | 0/0 | 2432 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0026 | 0/0 | 2432 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0027 | 0/0 | 2432 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| t0028 | 0/0 | 2378 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1677 | 183 | 57 | 29 | 61 | 7 | 27 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0003 | 0/0 | 1677 | 31 | 1 | 2 | 22 | 0 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0005 | 0/0 | 1677 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0007 | 0/0 | 1677 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0008 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0009 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0015 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0016 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0017 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0002 | 0/0 | 1677 | 45 | 7 | 11 | 13 | 6 | 8 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0011 | 0/0 | 1677 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0003c0004 | 0/0 | 1677 | 22 | 18 | 4 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0004c0006 | 0/0 | 1677 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0005c0013 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0005c0014 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0006c0010 | 0/0 | 1677 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0007c0019 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0008c0012 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0009c0018 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | 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 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0002 | 0/1 | 4108 | 30 | 12 | 4 | 6 | 1 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0003 | 0/0 | 4108 | 15 | 5 | 4 | 5 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0004 | 0/0 | 4108 | 11 | 0 | 3 | 0 | 3 | 5 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0005 | 0/0 | 4108 | 5 | 3 | 1 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0007 | 0/0 | 4106 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0008 | 0/0 | 4108 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0010 | 0/0 | 4108 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0012 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0013 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0014 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0015 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0016 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0017 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0018 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0019 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0020 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0021 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0024 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0025 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0026 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0027 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0001t0028 | 0/0 | 4054 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0003t0001 | 0/0 | 4108 | 15 | 0 | 2 | 9 | 0 | 4 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0003t0002 | 0/0 | 4108 | 3 | 0 | 0 | 2 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0003t0003 | 0/0 | 4108 | 11 | 0 | 0 | 11 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0003t0022 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0003t0023 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0005t0006 | 0/0 | 4108 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0007t0001 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0007t0004 | 0/0 | 4108 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0008t0002 | 0/0 | 4108 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0009t0001 | 0/0 | 4108 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0015t0003 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0016t0006 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0001c0017t0001 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0002t0001 | 0/0 | 4108 | 29 | 3 | 6 | 11 | 3 | 6 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0002t0002 | 0/0 | 4108 | 11 | 3 | 3 | 1 | 2 | 2 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0002t0003 | 0/0 | 4108 | 2 | 0 | 0 | 1 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0002t0004 | 0/0 | 4108 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0002t0011 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0002c0011t0002 | 0/0 | 4108 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0003c0004t0001 | 0/0 | 4108 | 14 | 13 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0003c0004t0002 | 0/0 | 4108 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0003c0004t0009 | 0/0 | 4108 | 4 | 2 | 2 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0003c0004t0011 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0004c0006t0003 | 0/0 | 4108 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0005c0013t0001 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0005c0014t0001 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0006c0010t0002 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0006c0010t0004 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0007c0019t0008 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0008c0012t0001 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| a0009c0018t0002 | 0/0 | 4108 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | copy fasta | chr14 | 69255158 | 69359466 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0009 | 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 |
| a0001c0001t0001g0053 | 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 |
| a0001c0001t0001g0070 | 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 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0092 | 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 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0117 | 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 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0143 | 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 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0168 | 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 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0221 | 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 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0269 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0012 | 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 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0091 | 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 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0112 | 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 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0157 | 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 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0002g0278 | 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 |
| a0001c0001t0002g0290 | 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 |
| a0001c0001t0003g0052 | 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 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0002 | 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 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0263 | 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 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0004g0274 | 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 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0005g0298 | 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 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0007g0282 | 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 |
| a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0008g0240 | 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 |
| a0001c0001t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0014g0287 | 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 |
| a0001c0001t0016g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0017g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0019g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0020g0194 | 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 |
| a0001c0001t0025g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0001t0026g0300 | 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 |
| a0001c0001t0028g0111 | 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 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0001g0246 | 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 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0002g0253 | 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 |
| a0001c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0003t0003g0199 | 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 |
| a0001c0003t0003g0226 | 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 |
| a0001c0005t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0005t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0005t0006g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0007t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0007t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0008t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0008t0002g0191 | 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 |
| a0001c0009t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0015t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0016t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0001c0017t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0017 | 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 |
| a0002c0002t0001g0088 | 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 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0014 | 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 |
| a0002c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0002c0002t0004g0268 | 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 |
| a0002c0011t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0013 | 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 |
| a0003c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0001g0292 | 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 |
| a0003c0004t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0003c0004t0009g0214 | 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 |
| a0004c0006t0003g0114 | 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 |
| a0004c0006t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0005c0013t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0005c0014t0001g0006 | 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 |
| a0006c0010t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0007c0019t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0008c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| a0009c0018t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | g0015 | EUR | GBR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0262 | 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 | g0242 | EUR | GBR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0257 | 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 | g0219 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0169 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | 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 | g0187 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00673 | hp1 | a0001 | c0003 | t0003 | g0199 | 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 | g0258 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0090 | 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 | g0014 | 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 | g0267 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0303 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01071 | hp2 | a0002 | c0002 | t0004 | g0268 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0135 | 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 | g0261 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01081 | hp2 | a0003 | c0004 | t0009 | g0150 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0132 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0266 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0240 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01243 | hp1 | a0003 | c0004 | t0001 | g0218 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0166 | 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 | g0138 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0294 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0070 | 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 | g0204 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01496 | hp1 | a0003 | c0004 | t0009 | g0151 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01496 | hp2 | a0001 | c0007 | t0004 | g0252 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01515 | hp1 | a0001 | c0007 | t0001 | g0254 | 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 | g0255 | 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 | g0161 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0290 | 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 | g0176 | 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 | g0152 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0213 | 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 | g0091 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0007 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0249 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0115 | EAS | KHV | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02135 | hp1 | a0001 | c0001 | t0019 | g0167 | 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 | g0008 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0287 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0155 | 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 | g0200 | 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 | g0140 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0184 | 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 | g0005 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0297 | 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 | g0141 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0130 | 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 | g0207 | 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 | g0125 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0302 | 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 | g0010 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02723 | hp1 | a0003 | c0004 | t0001 | g0273 | 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 | g0292 | 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 | g0004 | 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 | g0206 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02896 | hp1 | a0001 | c0016 | t0006 | g0156 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0148 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02965 | hp1 | a0003 | c0004 | t0002 | g0291 | 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 | g0177 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02976 | hp1 | a0003 | c0004 | t0009 | g0147 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0142 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0109 | 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 | g0096 | AFR | GWD | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03139 | hp2 | a0007 | c0019 | t0008 | g0153 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03209 | hp2 | a0001 | c0001 | t0017 | g0247 | 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 | g0145 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0274 | 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 | g0013 | 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 | g0095 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0244 | 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 | g0178 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0149 | AFR | ESN | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0163 | 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 | g0228 | 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 | g0301 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03654 | hp2 | a0001 | c0008 | t0002 | g0190 | 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 | g0253 | 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 | g0283 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0298 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0271 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0296 | 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 | a0009 | c0018 | t0002 | g0295 | 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 | g0250 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG03942 | hp2 | a0001 | c0008 | t0002 | g0191 | 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 | g0088 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04184 | hp2 | a0001 | c0001 | t0028 | g0111 | SAS | BEB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0195 | 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 | g0234 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04228 | hp1 | a0006 | c0010 | t0004 | g0175 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0275 | SAS | STU | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0276 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0280 | 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 | g0282 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18941 | hp2 | a0001 | c0001 | t0020 | g0194 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0118 | 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 | g0223 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18957 | hp1 | a0001 | c0003 | t0003 | g0119 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18957 | hp2 | a0001 | c0017 | t0001 | g0272 | 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 | g0193 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | 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 | g0154 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18975 | hp1 | a0001 | c0003 | t0003 | g0124 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18981 | hp2 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0168 | 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 | g0107 | 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 | g0159 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18990 | hp2 | a0001 | c0003 | t0002 | g0071 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0231 | 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 | g0226 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0171 | 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 | g0170 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0108 | 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 | g0172 | 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 | g0216 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19007 | hp1 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19007 | hp2 | a0004 | c0006 | t0003 | g0114 | 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 | g0158 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0182 | 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 | g0162 | AFR | LWK | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19043 | hp2 | a0003 | c0004 | t0009 | g0214 | 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 | g0243 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19068 | hp1 | a0008 | c0012 | t0001 | g0121 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19077 | hp1 | a0004 | c0006 | t0003 | g0225 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0110 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19087 | hp1 | a0001 | c0001 | t0018 | g0136 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0164 | 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 | g0139 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20129 | hp1 | a0003 | c0004 | t0001 | g0235 | AFR | ASW | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | ASW | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0265 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0251 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0016 | EUR | TSI | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| NA20905 | hp1 | a0001 | c0001 | t0026 | g0300 | 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 | g0089 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02109 | hp1 | a0001 | c0015 | t0003 | g0289 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0279 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02486 | hp1 | a0005 | c0014 | t0001 | g0006 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02559 | hp1 | a0005 | c0013 | t0001 | g0285 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0278 | 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 | g0185 | 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 | g0236 | 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 | hp1 | a0001 | c0001 | t0002 | g0210 | REF | REF | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0269 | REF | REF | GALNT16_chr14_69255158_69359466 | GALNT16 | chr14 | 69255158 | 69359466 |
| 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 | a0008 | 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 | a0009 | 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 | a0002a0008 | 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 |
| 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 | a0001c0007a0002c0011 | 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 | a0001c0003a0001c0009 | 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 | a0001c0015a0001c0016 | 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 | a0001c0005a0001c0016 | 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 |
| 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 | a0001c0001t0010a0001c0001t0012a0002c0002t0011others(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 | a0001c0001t0004a0001c0001t0005a0001c0001t0013others(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 | a0001c0001t0004a0001c0007t0004a0002c0002t0004others(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 | a0001c0001t0003a0001c0001t0012a0001c0001t0025others(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 | a0001c0001t0018a0001c0001t0025 | 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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(27): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): 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 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(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 | a0001c0001t0008a0007c0019t0008 | 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 | a0001c0001t0004a0001c0001t0005a0001c0001t0013others(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 | a0001c0001t0004a0001c0001t0005a0001c0001t0024others(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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(28): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): 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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): 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 |
| 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 | 24 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0018others(21): 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 | a0001c0001t0002g0028a0001c0003t0003g0029 | 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 | a0001c0001t0005g0298a0001c0001t0026g0300a0001c0003t0001g0297others(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 | a0001c0001t0003g0030a0001c0001t0003g0032a0001c0003t0003g0031 | 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 | a0001c0001t0001g0003a0001c0001t0002g0288a0001c0001t0002g0290others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0037others(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 | a0002c0002t0001g0293 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0037others(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 | 16 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0018others(13): 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 | a0001c0001t0002g0286a0001c0001t0014g0287a0005c0013t0001g0285 | 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 | a0001c0001t0001g0284 | 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 | a0001c0009t0001g0283 | 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 | 7 | a0001c0001t0001g0018a0002c0002t0001g0015a0002c0002t0001g0016others(4): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0037others(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 | a0001c0001t0001g0280a0001c0001t0003g0281a0001c0001t0007g0279others(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 | 11 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0002g0005others(8): 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 | a0001c0001t0001g0041a0003c0004t0001g0039a0003c0004t0001g0040 | 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 | a0001c0001t0001g0003a0001c0001t0002g0278a0001c0001t0002g0288others(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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0045others(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 | a0001c0001t0002g0286a0001c0001t0014g0287a0005c0013t0001g0285 | 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 | a0001c0001t0002g0277a0001c0001t0007g0276 | 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 | 6 | a0001c0001t0001g0018a0002c0002t0001g0015a0002c0002t0001g0016others(3): 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | 42 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(39): 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 | a0001c0001t0001g0003a0001c0001t0002g0278a0001c0001t0002g0290others(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 | 36 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(33): 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 | a0001c0001t0001g0043a0001c0001t0002g0042 | 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 | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): 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 | a0002c0002t0001g0248 | 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 | a0001c0001t0002g0278a0001c0001t0002g0288a0001c0001t0002g0290others(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 | a0001c0001t0007g0276 | 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 | a0001c0001t0002g0278a0001c0001t0002g0288a0001c0001t0002g0290others(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 | a0003c0004t0001g0007 | 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 | a0001c0001t0001g0043a0001c0001t0002g0042 | 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 | a0001c0001t0004g0033a0001c0001t0004g0034 | 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 | a0001c0001t0001g0003a0001c0001t0002g0095a0001c0001t0002g0096others(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 | a0001c0001t0017g0247 | 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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044 | 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 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(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 | a0001c0001t0001g0003a0001c0001t0002g0278a0001c0001t0002g0288others(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 | a0001c0001t0018g0136 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0002g0278a0001c0001t0002g0290a0003c0004t0001g0292others(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 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0053others(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 |
42 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(39): 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 |
15 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0045others(12): 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 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0035others(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 | a0001c0001t0001g0146a0001c0001t0002g0005a0001c0001t0002g0085others(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 | a0001c0001t0001g0009a0001c0001t0001g0152a0001c0001t0001g0155others(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 |
74 | a0001c0001t0001g0137a0001c0001t0001g0164a0001c0001t0001g0166others(71): Show | 74 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(71): 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 | a0001c0001t0001g0041a0001c0001t0001g0220a0001c0001t0001g0221others(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 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0245others(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 | a0001c0001t0010g0023a0001c0001t0012g0022 | 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 | a0001c0001t0010g0025a0001c0001t0010g0026 | 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 | a0001c0001t0007g0282 | 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 | a0001c0001t0001g0217 | 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 | a0003c0004t0001g0007 | 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 | a0003c0004t0001g0007 | 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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0047others(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 | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): 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 | a0001c0001t0001g0003a0001c0001t0002g0278a0001c0001t0002g0288others(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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0003c0004t0001g0007 | 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 | a0001c0001t0002g0288 | 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 | a0002c0002t0002g0294 | 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 | a0001c0003t0001g0246 | 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 | a0001c0001t0002g0157 | 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 | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(24): 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 | a0001c0001t0001g0009a0001c0001t0002g0011a0001c0001t0002g0012others(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 | a0001c0001t0002g0278a0001c0001t0002g0290a0003c0004t0001g0292others(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 | 10 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0002g0005others(7): 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0004a0001c0001t0002g0005a0005c0014t0001g0006 | 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 | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(24): 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | a0001c0001t0007g0279 | 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): 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 | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(32): 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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0045others(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 | a0001c0001t0001g0083a0001c0003t0001g0216 | 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 | a0002c0002t0003g0215 | 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 | a0001c0001t0003g0160a0001c0003t0003g0159a0002c0002t0001g0158 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044 | 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 | a0001c0001t0002g0288 | 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 | a0003c0004t0002g0027a0003c0004t0009g0147a0003c0004t0009g0150others(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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0047others(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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044others(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 | a0003c0004t0001g0161a0003c0004t0001g0162a0003c0004t0001g0218 | 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 | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): 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 | a0001c0001t0003g0163a0001c0003t0023g0021 | 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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0047others(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 | a0001c0001t0005g0298a0001c0001t0026g0300a0001c0003t0001g0297others(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 | 39 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(36): 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 | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(22): 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 | a0001c0001t0001g0041a0001c0001t0002g0277a0001c0001t0007g0276others(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 | a0001c0001t0002g0278a0001c0001t0002g0288a0001c0001t0002g0290others(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 | a0001c0001t0001g0045a0001c0001t0001g0146a0001c0001t0005g0046others(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 | a0001c0001t0001g0009a0001c0001t0002g0011a0001c0001t0002g0012others(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 | a0001c0001t0001g0003a0001c0001t0003g0019a0001c0003t0023g0021others(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 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0001t0002g0286others(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 | 30 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0018others(27): 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 | 47 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(44): 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 | 38 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(35): 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 | a0001c0001t0001g0213 | 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 | a0003c0004t0001g0145 | 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 | a0001c0001t0005g0298a0001c0001t0026g0300a0001c0003t0001g0297others(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 | a0001c0001t0001g0152a0007c0019t0008g0153 | 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 | a0001c0003t0001g0067a0001c0003t0022g0066 | 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 | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0002c0002t0001g0249 | 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 | 175 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0101others(172): Show | 176 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(173): 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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0047others(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 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0005g0046others(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 | a0001c0001t0004g0274 | 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0001c0003t0001g0212 | 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 | a0001c0001t0001g0146 | 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 | 71 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(68): 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 | a0001c0001t0001g0128 | 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 | a0006c0010t0004g0175 | 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 | 102 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0137others(99): Show | 102 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(99): 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0043others(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 | 275 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): 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 | a0003c0004t0001g0161 | 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 | 47 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(44): 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | 10 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0002g0005others(7): 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0043others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0037others(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 | 47 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(44): 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 | a0001c0001t0001g0003a0001c0001t0002g0288a0001c0015t0003g0289others(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 | a0001c0001t0001g0127 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0211others(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 | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | a0001c0001t0001g0009a0001c0001t0002g0011a0001c0001t0002g0012others(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 | a0001c0001t0003g0227a0001c0001t0016g0228 | 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 | 2 | a0001c0001t0001g0209a0001c0001t0002g0210 | 2 | NA20752.hp1 homoSapiens_chm13v2.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 | a0007c0019t0008g0153 | 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | a0001c0001t0001g0101a0005c0013t0001g0285 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0002g0278a0001c0001t0002g0290a0001c0001t0017g0247others(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 | 89 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(86): 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 | a0001c0001t0026g0300a0002c0002t0002g0301 | 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 | 45 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(42): 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 | a0001c0001t0007g0142a0001c0001t0008g0094a0001c0005t0006g0140others(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 | a0001c0003t0001g0212 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0037others(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 | 8 | a0001c0001t0001g0018a0001c0001t0001g0047a0002c0002t0001g0015others(5): 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 | a0001c0001t0001g0241a0001c0001t0002g0229a0001c0001t0002g0242 | 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0001c0005t0006g0177 | 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 | a0001c0001t0002g0286 | 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 | a0001c0001t0001g0126 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0001g0009a0001c0001t0002g0011a0001c0001t0002g0012others(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 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0049others(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 | a0002c0002t0001g0299a0002c0002t0001g0303 | 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 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044others(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 | a0001c0001t0005g0298a0001c0001t0026g0300a0001c0003t0001g0297others(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 | a0001c0001t0001g0045a0001c0001t0002g0288a0001c0001t0005g0046others(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 | 98 | a0001c0001t0001g0137a0001c0001t0001g0152a0001c0001t0001g0164others(95): Show | 98 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(95): 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | 233 | a0001c0001t0001g0001a0001c0001t0001g0035a0001c0001t0001g0036others(230): Show | 235 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(232): 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0001c0001t0005g0298 | 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 | a0003c0004t0001g0292a0003c0004t0002g0291 | 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 | 46 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(43): 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | a0001c0001t0001g0009a0001c0001t0002g0011a0001c0001t0002g0012others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0041a0001c0001t0008g0240a0003c0004t0001g0007others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0002g0278a0001c0001t0002g0290a0001c0001t0017g0247others(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 | a0001c0001t0001g0045a0001c0001t0001g0128a0001c0001t0001g0211others(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 | a0001c0001t0001g0049a0001c0001t0001g0180a0001c0001t0001g0243others(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 | a0001c0001t0001g0045a0001c0001t0002g0288a0001c0001t0003g0163others(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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | a0001c0001t0001g0101a0001c0001t0001g0117a0001c0001t0001g0118others(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 | a0001c0001t0010g0023a0001c0001t0010g0026a0001c0001t0012g0022 | 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 | 101 | a0001c0001t0001g0137a0001c0001t0001g0152a0001c0001t0001g0164others(98): Show | 101 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(98): 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 | a0001c0001t0001g0009a0001c0001t0002g0011a0001c0001t0002g0012others(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 | 101 | a0001c0001t0001g0137a0001c0001t0001g0152a0001c0001t0001g0164others(98): Show | 101 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(98): 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 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0002g0288others(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 | 42 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(39): 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 | 30 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(27): 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 | a0001c0001t0026g0300 | 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0001c0001t0002g0275a0001c0001t0004g0274 | 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 | 45 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0116others(42): 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0005c0013t0001g0285 | 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 | a0001c0001t0010g0023a0001c0001t0010g0025a0001c0001t0010g0026others(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 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0002g0288others(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 | a0001c0001t0001g0146 | 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 | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(135): 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 | a0001c0001t0001g0009a0001c0001t0002g0011a0001c0001t0002g0012others(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 | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(260): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.177+19161A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279628 | ||||||
| chr14:69279639
|
G | A | 217 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0043others(214): Show | 219 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.177+19172G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69279639 | ||||||
| chr14:69279714
|
G | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(123): Show | 127 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(124): 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 | a0001c0001t0002g0278a0001c0001t0005g0298a0001c0001t0026g0300others(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 | 11 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0047others(8): 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 | 114 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0083others(111): Show | 115 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(112): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0019others(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 | a0001c0001t0002g0277a0001c0001t0007g0276a0003c0004t0001g0145others(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 | a0001c0001t0026g0300a0002c0002t0002g0301 | 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 | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): 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 | a0001c0001t0002g0277a0001c0001t0007g0276a0003c0004t0002g0027 | 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 | a0001c0001t0001g0045a0001c0001t0001g0143a0001c0001t0001g0144others(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 | 178 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(175): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): 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 | a0001c0001t0001g0004a0001c0001t0001g0143a0001c0001t0001g0144others(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 | a0003c0004t0001g0013 | 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 | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(132): Show | 136 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(133): 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 | a0001c0003t0001g0061a0002c0002t0001g0062 | 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | 4 | a0001c0003t0001g0105a0002c0002t0001g0107a0002c0002t0001g0108others(1): Show | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | a0001c0001t0001g0208 | 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 | a0001c0001t0002g0288a0001c0001t0003g0163a0001c0001t0014g0287others(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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0001g0180others(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 | a0007c0019t0008g0153 | 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 | a0001c0001t0002g0288a0001c0001t0003g0163a0001c0001t0014g0287others(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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0208others(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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | a0001c0001t0001g0004a0005c0014t0001g0006 | 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 | a0001c0003t0001g0216 | 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 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0208others(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 | 214 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): 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 | a0007c0019t0008g0153 | 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 | 71 | a0001c0001t0001g0068a0001c0001t0001g0083a0001c0001t0001g0102others(68): Show | 71 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(68): 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 |
86 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0043others(83): 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 | a0001c0001t0001g0051a0001c0001t0003g0037a0001c0001t0010g0026others(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 | a0001c0001t0001g0009a0001c0001t0001g0180a0001c0001t0001g0182others(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 | a0001c0001t0001g0009a0001c0001t0001g0180a0001c0001t0001g0182others(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 | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(194): Show | 199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): 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 | a0001c0008t0002g0190a0001c0008t0002g0191 | 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0053others(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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(147): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): 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 | a0001c0001t0002g0278a0001c0001t0005g0298a0001c0001t0007g0276others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0060others(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 | a0001c0001t0014g0287a0005c0013t0001g0285 | 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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): 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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(193): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): 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 | a0001c0001t0001g0080a0001c0001t0003g0079a0001c0001t0005g0082others(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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(161): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.177+24346T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284813 | ||||||
| chr14:69284889
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.177+24422T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69284889 | ||||||
| chr14:69284923
|
G | A | 26 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0053others(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 | 58 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0047others(55): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | 113 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0045others(110): Show | 114 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(111): 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 | 60 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0047others(57): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0032others(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 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0208others(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 | a0001c0001t0002g0012 | 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 | a0001c0001t0001g0202 | 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 | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(193): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): 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 | a0003c0004t0001g0292a0003c0004t0002g0291 | 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 | 74 | a0001c0001t0001g0004a0001c0001t0001g0035a0001c0001t0001g0036others(71): 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 | a0001c0001t0002g0290 | 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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(165): 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 | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(165): 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 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0072others(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 | a0001c0001t0001g0180a0001c0001t0001g0182a0001c0001t0001g0208others(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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.177+25236C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285703 | ||||||
| chr14:69285784
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(128): 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 | ||||||
| chr14:69285826
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.177+25359T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69285826 | ||||||
| chr14:69285886
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(178): 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 | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(67): 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0053others(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 | a0001c0001t0001g0202 | 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 | 176 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0036others(173): Show | 178 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(175): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(67): 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 | 82 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0083others(79): Show | 83 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.177+25800A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69286267 | ||||||
| chr14:69286304
|
C | CT | 174 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0035others(171): Show | 176 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(173): 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 | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): 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 | a0001c0001t0002g0288 | 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 | a0002c0002t0001g0303 | 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0010g0023others(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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | a0006c0010t0004g0175 | 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 | 109 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(106): 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 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0288 | 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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | a0001c0001t0001g0003a0001c0015t0003g0289 | 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 | a0002c0002t0001g0192 | 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 | a0001c0003t0003g0224a0004c0006t0003g0222a0004c0006t0003g0223 | 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 | 105 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(102): 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 | 254 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(251): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(142): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): 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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | a0006c0010t0004g0175 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0288 | 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 | 96 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(93): 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 | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(220): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): 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 | a0001c0001t0013g0008 | 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 | 72 | a0001c0001t0001g0043a0001c0001t0001g0083a0001c0001t0001g0102others(69): Show | 72 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(69): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0180others(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 | 75 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(72): 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 | a0001c0001t0001g0043a0001c0001t0002g0042 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0003g0238others(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 | a0001c0001t0001g0202 | 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 | 75 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(72): 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | 75 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(72): 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0157 | 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 | 109 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(106): 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0014g0287 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0202 | 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 | 72 | a0001c0001t0001g0043a0001c0001t0001g0083a0001c0001t0001g0102others(69): Show | 72 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(69): 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 | a0001c0001t0002g0288 | 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 | a0003c0004t0001g0292a0003c0004t0002g0291 | 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | a0001c0001t0001g0202 | 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 | a0001c0001t0026g0300a0002c0002t0002g0301 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0288 | 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 | 157 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(154): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): 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 | 60 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0047others(57): 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 | 158 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(155): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.178-27059A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69293652 | ||||||
| chr14:69293677
|
T | C | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0043others(136): Show | 140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): 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 | a0001c0001t0002g0095a0001c0001t0002g0096 | 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | 158 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(155): Show | 159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): 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 | a0001c0001t0001g0152 | 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 | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.178-26572T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69294139 | ||||||
| chr14:69294232
|
T | C | 139 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0043others(136): Show | 140 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(137): 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 | a0001c0001t0001g0203a0003c0004t0002g0204 | 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 | a0001c0003t0001g0154 | 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | a0003c0004t0001g0013a0005c0013t0001g0285 | 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 | a0001c0001t0002g0012 | 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 | 67 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0101others(64): 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0157 | 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 | a0001c0001t0001g0202 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0002g0277 | 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 | a0001c0001t0001g0072a0001c0001t0001g0122a0001c0001t0001g0123others(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 | 48 | a0001c0001t0001g0101a0001c0001t0001g0116a0001c0001t0001g0117others(45): 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 | 82 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0083others(79): Show | 82 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(79): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0143others(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 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0146others(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 | a0001c0001t0004g0271a0001c0003t0002g0253a0002c0002t0001g0249others(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 | a0001c0001t0002g0109 | 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 | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(93): 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 | a0001c0001t0001g0202 | 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 | 260 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(257): Show | 262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.178-24996A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69295715 | ||||||
| chr14:69295786
|
A | AT | 129 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(126): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): 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 | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(237): Show | 243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.178-24494T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296217 | ||||||
| chr14:69296320
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0035others(174): Show | 179 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.178-24391A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69296320 | ||||||
| chr14:69296459
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0047others(73): 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0002g0288a0001c0003t0001g0165a0002c0002t0001g0100 | 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 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0120others(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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0117others(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 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0245others(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 | a0001c0001t0003g0032a0001c0001t0007g0142a0001c0005t0006g0177others(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 |
59 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0043others(56): Show | 60 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(57): 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 | a0001c0003t0001g0246 | 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 | a0001c0001t0001g0045a0001c0001t0001g0063a0001c0001t0001g0064others(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 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0047others(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 | a0001c0001t0003g0037a0001c0003t0001g0067a0001c0003t0022g0066others(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 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0003g0104others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0002c0002t0001g0239 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0032others(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 | a0001c0001t0001g0003a0001c0001t0001g0083a0001c0001t0001g0086others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0003c0004t0002g0204 | 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 | a0003c0004t0002g0204 | 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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0002g0131others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0137a0001c0001t0001g0205a0001c0001t0001g0206others(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 | a0001c0001t0001g0137a0001c0001t0001g0205a0001c0001t0001g0206others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0084others(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 | a0001c0001t0003g0032a0001c0001t0010g0023a0001c0001t0010g0025others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0068others(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 | a0001c0001t0007g0276a0002c0002t0001g0138a0002c0002t0001g0256others(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 | a0001c0001t0001g0004a0001c0001t0001g0060a0001c0001t0001g0063others(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 | a0001c0001t0001g0116a0001c0001t0001g0143a0001c0001t0001g0144others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0117others(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 | 72 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0043others(69): Show | 73 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(70): 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 | a0001c0001t0017g0247 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0133others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0003g0032a0001c0001t0010g0023a0001c0001t0010g0025others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0002c0002t0001g0239 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0001g0245a0001c0001t0001g0280a0007c0019t0008g0153 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0202others(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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0005others(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 | 211 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(208): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): 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 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0125others(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 | a0001c0001t0001g0202a0001c0001t0007g0142a0003c0004t0009g0147others(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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0003g0238others(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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0003c0004t0001g0013a0005c0013t0001g0285 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 129 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(126): Show | 131 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(128): 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 | a0001c0001t0001g0202 | 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 | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(127): Show | 132 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(129): 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 | a0001c0001t0002g0275 | 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 | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): 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 | a0001c0001t0002g0290a0001c0001t0014g0287 | 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 | a0001c0001t0007g0142a0003c0004t0009g0147a0003c0004t0009g0150others(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 | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(128): Show | 133 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(130): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0143others(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 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0278others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0245others(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 | a0001c0001t0002g0288 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0083others(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 | a0001c0001t0002g0286a0001c0001t0003g0227a0001c0001t0016g0228others(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 | 69 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): 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 | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(65): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0083others(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 | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(258): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.178-19514C>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69301197 | ||||||
| chr14:69301299
|
A | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(280): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): 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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044 | 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 | a0001c0001t0002g0076a0001c0001t0021g0075 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0001g0245a0001c0001t0001g0280a0001c0001t0015g0057others(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 | a0001c0001t0001g0001a0001c0003t0002g0071 | 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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | a0002c0002t0001g0239 | 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 | a0001c0001t0001g0195 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0002g0290a0001c0001t0014g0287 | 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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0002c0002t0002g0255a0002c0002t0002g0257 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 69 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): 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 | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.178-16988C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69303723 | ||||||
| chr14:69303852
|
G | A | 69 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): 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 | a0001c0001t0001g0003a0001c0015t0003g0289 | 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 | 68 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(65): Show | 68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(68): 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 | a0003c0004t0002g0291 | 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0007t0001g0254others(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 | 159 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0047others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.178-16298G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69304413 | ||||||
| chr14:69304496
|
T | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(66): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0083others(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 | a0007c0019t0008g0153 | 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 | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(119): 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 | a0006c0010t0004g0175 | 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 | 68 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(65): Show | 68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 77 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0043others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(74): 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 | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(122): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0083others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0007c0019t0008g0153 | 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 | 71 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(68): 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0004g0002 | 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 | 79 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0043others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.178-14992T>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69305719 | ||||||
| chr14:69305742
|
G | T | 131 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0043others(128): Show | 132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): 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 | a0009c0018t0002g0295 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044 | 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 | a0001c0001t0007g0142a0001c0005t0006g0140a0001c0005t0006g0141others(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 | a0001c0001t0002g0288 | 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 | a0001c0003t0001g0061a0002c0002t0001g0062 | 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 | 68 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(65): Show | 68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): 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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0009t0001g0283 | 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 | a0001c0001t0001g0176a0001c0001t0001g0198a0001c0001t0001g0217others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 68 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(65): Show | 68 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.178-13442G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69307269 | ||||||
| chr14:69307291
|
C | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(66): 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0003c0004t0001g0218 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0002c0002t0001g0302 | 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 114 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0036others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(111): 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0014g0287a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.178-12253A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69308458 | ||||||
| chr14:69308561
|
G | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): 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 | a0001c0001t0001g0245a0001c0001t0001g0280a0001c0001t0015g0057others(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 | a0001c0001t0001g0166 | 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 | a0006c0010t0004g0175 | 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 | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0032others(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 | 167 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0036others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(165): 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 | a0001c0001t0001g0284 | 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 | a0002c0002t0001g0249 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0032others(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 | a0003c0004t0001g0207 | 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 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0221 | 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 | 70 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(67): Show | 70 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(67): 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 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0058others(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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0001g0205others(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 | 236 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | 6 | a0001c0001t0001g0184a0002c0002t0001g0107a0002c0002t0001g0108others(3): 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 | a0001c0001t0002g0288 | 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 | a0002c0002t0002g0234 | 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 | a0001c0001t0001g0237 | 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 | 166 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0036others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): 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 | a0006c0010t0004g0175 | 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 | a0002c0002t0001g0138a0002c0002t0001g0256 | 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 | 69 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0003t0001g0169 | 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 | 69 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): 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 | a0001c0008t0002g0190a0001c0008t0002g0191 | 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 | a0001c0001t0001g0009a0001c0001t0001g0203a0001c0001t0003g0019others(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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | a0001c0001t0001g0080a0001c0001t0003g0079a0001c0001t0005g0082others(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 | 166 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0036others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): 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 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0001g0220others(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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0032others(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 | 69 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): 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 | a0001c0001t0002g0135 | 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 | a0002c0011t0002g0261 | 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 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0003t0023g0021 | 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 | a0001c0001t0001g0018a0001c0001t0001g0053a0001c0001t0001g0058others(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 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0049others(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 | 26 | a0001c0001t0001g0203a0001c0001t0001g0232a0001c0001t0001g0233others(23): 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 | a0001c0001t0001g0208a0002c0002t0001g0296a0003c0004t0009g0151 | 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 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0092others(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 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0072others(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 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0206others(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 | a0001c0001t0001g0168a0001c0001t0001g0220a0001c0001t0020g0194others(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 | 65 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(62): Show | 65 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(62): 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 | a0001c0001t0002g0286a0001c0001t0003g0227a0001c0001t0016g0228 | 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0002g0277 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0213others(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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | a0002c0002t0001g0266 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0002g0277 | 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 | a0001c0001t0002g0286a0001c0001t0003g0227a0001c0001t0016g0228 | 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 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0278others(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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | a0001c0001t0001g0245a0001c0001t0001g0280a0001c0001t0015g0057others(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 | a0001c0001t0001g0220 | 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 | a0001c0001t0016g0228 | 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 | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(65): 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 | a0003c0004t0009g0151 | 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 | a0001c0001t0001g0168 | 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 |
33 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(30): 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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044 | 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 | 69 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0137others(66): Show | 69 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(66): 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 | a0001c0001t0026g0300 | 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 | 70 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0102others(67): Show | 70 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(67): 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 | a0001c0001t0002g0277 | 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0080others(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 | a0001c0001t0004g0002 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0002c0002t0001g0187 | 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 71 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0102others(68): Show | 71 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(68): 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0001g0116 | 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 | 90 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0126others(87): Show | 90 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(87): 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0168others(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 | a0001c0003t0001g0105a0002c0002t0002g0106 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0002g0242 | 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 | a0006c0010t0004g0175 | 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 | 71 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0126others(68): Show | 71 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(68): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0245others(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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0003t0001g0169 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0245others(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 | a0001c0001t0004g0271a0001c0003t0002g0253 | 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 | a0001c0001t0001g0018a0001c0001t0001g0058a0001c0001t0001g0074others(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 | a0001c0001t0001g0060a0001c0001t0002g0076a0001c0001t0002g0286others(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 | a0001c0001t0001g0049a0001c0001t0001g0068a0001c0001t0002g0277others(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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 78 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0080others(75): Show | 78 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(75): 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 | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(70): 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 | a0001c0001t0001g0045a0001c0001t0005g0046a0001c0001t0007g0044 | 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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | a0001c0001t0002g0076a0001c0001t0021g0075 | 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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0002g0095others(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 | a0006c0010t0004g0175 | 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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0049others(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 | a0001c0001t0002g0135 | 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0001g0146a0001c0001t0002g0277 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0032others(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 | a0006c0010t0004g0175 | 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 | a0006c0010t0004g0175 | 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 | 82 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0078others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): 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 | a0006c0010t0004g0175 | 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 | 76 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0078others(73): Show | 76 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(73): 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 | a0006c0010t0004g0175 | 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0001g0049a0001c0001t0001g0053a0001c0001t0001g0058others(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 | a0001c0001t0002g0109a0001c0001t0028g0111 | 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 | a0001c0007t0001g0254 | 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 | a0001c0001t0002g0109 | 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0004g0002 | 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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | 85 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0043others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(82): 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 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0116others(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 | 268 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.178-618A>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 1/14 | chr14 | 69320093 | ||||||
| chr14:69320284
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(65): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0003g0032others(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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0146a0001c0001t0002g0277a0001c0001t0002g0286others(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 | a0001c0001t0002g0290a0001c0001t0014g0287 | 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 | 78 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0078others(75): Show | 78 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(75): 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 | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(63): 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 | a0001c0017t0001g0272 | 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0002g0011others(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 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0047others(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 | a0001c0001t0019g0167 | 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 | a0003c0004t0001g0292a0003c0004t0002g0291 | 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 | a0001c0001t0002g0012 | 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 | 269 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): 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 | a0001c0003t0002g0253 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0002g0011others(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 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0007g0276others(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 | a0001c0001t0002g0229 | 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 | a0001c0001t0014g0287 | 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 | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.335+1003G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321871 | ||||||
| chr14:69321880
|
A | G | 137 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0051others(134): Show | 138 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.335+1012A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69321880 | ||||||
| chr14:69322186
|
A | G | 89 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0053others(86): Show | 89 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(86): 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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | 88 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0053others(85): Show | 88 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(85): 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 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0083others(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 | a0007c0019t0008g0153 | 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 | a0001c0003t0001g0105a0002c0002t0002g0106 | 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 | a0003c0004t0001g0292a0003c0004t0002g0291 | 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 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0003t0023g0021 | 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 | a0003c0004t0001g0292a0003c0004t0002g0291 | 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 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0101others(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 | a0001c0003t0002g0110 | 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 | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): 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 | a0001c0001t0001g0049a0001c0001t0001g0166a0001c0001t0008g0094 | 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 | a0002c0002t0002g0301 | 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 | a0001c0001t0008g0240 | 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 | a0001c0001t0001g0045a0001c0001t0007g0044 | 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 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0004g0251others(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 | a0001c0001t0001g0036a0001c0001t0004g0033a0002c0002t0002g0257 | 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 | a0001c0001t0001g0004a0001c0001t0001g0074a0001c0001t0001g0083others(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 | a0001c0001t0004g0258a0001c0001t0004g0263a0001c0003t0001g0260others(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 | a0001c0001t0001g0035a0001c0001t0003g0032a0002c0002t0001g0265 | 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0280 | 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 | 57 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0102others(54): Show | 57 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.336-1765delT | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322926 | ||||||
| chr14:69322926
|
GTGTGT | G | 10 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0001g0208others(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 | a0001c0001t0001g0180a0001c0001t0001g0232a0001c0001t0003g0079others(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 | a0001c0001t0025g0185 | 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 | a0001c0001t0001g0102a0001c0001t0001g0152 | 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 | a0002c0002t0001g0113a0004c0006t0003g0114a0004c0006t0003g0223others(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 | a0001c0001t0001g0129a0001c0001t0002g0109a0002c0002t0001g0100others(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 | a0001c0003t0001g0105a0002c0002t0002g0106 | 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 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0101others(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 | a0003c0004t0001g0007 | 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 | a0001c0001t0001g0116a0001c0001t0002g0288a0001c0001t0004g0271others(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 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0002g0112others(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 | a0001c0001t0001g0041a0001c0005t0006g0177a0001c0016t0006g0156others(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 | 36 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0070others(33): 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 | a0006c0010t0004g0175 | 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 | a0003c0004t0009g0214 | 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 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0087others(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 | a0001c0001t0001g0245a0006c0010t0004g0175 | 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 | a0001c0001t0001g0092a0001c0001t0002g0096a0001c0001t0005g0298others(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 | a0001c0001t0001g0245a0001c0001t0001g0280a0006c0010t0004g0175 | 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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151 | 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 | a0001c0001t0001g0068a0001c0001t0001g0125a0001c0001t0002g0095others(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 | a0001c0001t0001g0245a0001c0001t0001g0280a0006c0010t0004g0175 | 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 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0058others(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 | a0001c0001t0001g0245a0001c0001t0001g0280a0006c0010t0004g0175 | 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 | a0001c0001t0002g0011a0001c0001t0007g0276a0001c0001t0010g0025others(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 | a0001c0001t0001g0245a0001c0001t0001g0280a0001c0003t0002g0253others(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 | a0001c0001t0001g0051a0001c0001t0001g0196a0001c0001t0001g0201others(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 | a0001c0001t0001g0047a0001c0001t0002g0012a0001c0001t0003g0227others(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 | 61 | a0001c0001t0001g0053a0001c0001t0001g0078a0001c0001t0001g0080others(58): Show | 61 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(58): 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 | a0001c0001t0001g0043a0001c0001t0001g0126a0001c0001t0001g0152others(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 | 42 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0137others(39): Show | 42 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(39): 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 | a0001c0001t0001g0053a0001c0001t0001g0078a0001c0001t0001g0080others(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 | 14 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0176others(11): Show | 14 | HG00609.hp1 HG01928.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.336-1705C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69322987 | ||||||
| chr14:69322988
|
GCA | G | 16 | a0001c0001t0001g0176a0001c0001t0001g0220a0001c0001t0001g0243others(13): Show | 16 | HG00438.hp2 HG00609.hp1 HG01928.hp2 others(13): 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(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 | a0001c0001t0001g0058a0001c0001t0001g0074a0001c0001t0001g0083others(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 | a0006c0010t0004g0175 | 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 | 110 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0047others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(107): 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 | a0001c0001t0002g0012 | 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 | a0001c0001t0004g0258 | 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 | a0001c0001t0001g0270a0001c0003t0001g0260 | 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 | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(66): 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 | 87 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(84): 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 | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.336-739A>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69323953 | ||||||
| chr14:69324061
|
G | T | 128 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0047others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.336-631G>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324061 | ||||||
| chr14:69324247
|
T | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(267): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): 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 | a0001c0001t0027g0077a0003c0004t0001g0292a0003c0004t0002g0291 | 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 | a0001c0001t0001g0146a0001c0001t0002g0277a0001c0001t0014g0287others(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 | 220 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0043others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.336-302T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324390 | ||||||
| chr14:69324396
|
T | C | 228 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0043others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.336-296T>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 2/14 | chr14 | 69324396 | ||||||
| chr14:69324496
|
G | C | 64 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0051others(61): 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 | a0001c0001t0001g0182a0001c0001t0001g0208a0001c0001t0001g0232others(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 | 156 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0047others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0001c0001t0001g0003a0001c0015t0003g0289 | 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 | a0001c0016t0006g0156a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0014g0287a0006c0010t0004g0175 | 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 | a0001c0001t0001g0241a0001c0001t0001g0250 | 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 | a0001c0001t0013g0008 | 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 | a0001c0001t0001g0074a0001c0001t0001g0134a0001c0001t0016g0228others(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 | a0001c0001t0001g0198a0001c0001t0001g0217a0001c0001t0001g0236 | 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 | a0001c0001t0001g0186 | 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 | a0003c0004t0009g0147a0003c0004t0009g0150a0003c0004t0009g0151others(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 | a0001c0001t0001g0047a0001c0001t0001g0074a0001c0001t0002g0011others(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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0209others(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 | 12 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0047others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(9): 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 | a0001c0001t0001g0041a0001c0001t0001g0074a0001c0001t0001g0078others(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 | a0001c0001t0004g0099a0001c0001t0004g0271 | 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 | a0001c0001t0003g0019a0001c0001t0008g0094a0001c0001t0008g0240others(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 | a0004c0006t0003g0225 | 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 | 120 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(117): 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 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0001g0080others(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 | a0003c0004t0001g0007a0003c0004t0001g0013a0003c0004t0001g0040others(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 | 266 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): 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 | a0001c0001t0016g0228 | 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 | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(107): Show | 112 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(109): 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 | a0001c0001t0002g0042a0001c0001t0003g0019a0001c0001t0014g0287others(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 | 32 | a0001c0001t0013g0008a0002c0002t0001g0015a0002c0002t0001g0016others(29): 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 | a0001c0001t0008g0130 | 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 | a0001c0003t0001g0165 | 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 | a0001c0001t0001g0133 | 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 | a0001c0003t0001g0212 | 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 | a0007c0019t0008g0153 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0193others(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 | a0001c0001t0001g0126a0001c0001t0001g0250a0001c0001t0002g0005others(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 | a0001c0001t0002g0011 | 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 | a0003c0004t0001g0292 | 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 | a0001c0003t0003g0226 | 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 | a0001c0001t0001g0280a0003c0004t0001g0039a0003c0004t0001g0139others(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 | a0001c0001t0001g0004a0001c0001t0002g0005 | 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0012g0022a0007c0019t0008g0153 | 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 | a0001c0001t0001g0168 | 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 | a0002c0002t0001g0303 | 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 | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): 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 | a0003c0004t0001g0007a0003c0004t0001g0013a0003c0004t0001g0292 | 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 | a0001c0001t0001g0009a0001c0001t0001g0041a0001c0001t0001g0074others(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 | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(164): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): 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 | a0001c0001t0001g0045a0001c0001t0003g0037a0001c0001t0003g0163others(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 | a0001c0001t0001g0001a0001c0001t0001g0049a0001c0001t0001g0116others(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 | a0001c0001t0002g0135a0001c0001t0002g0290a0001c0001t0003g0227others(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 | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(114): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): 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 | a0002c0002t0001g0017 | 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 | a0001c0001t0003g0037a0001c0001t0003g0163a0001c0001t0003g0281 | 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 | 67 | a0001c0001t0001g0051a0001c0001t0001g0231a0001c0001t0002g0011others(64): 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 | a0001c0001t0001g0078a0001c0001t0001g0143a0001c0001t0001g0144 | 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 | a0001c0001t0002g0157 | 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 | a0002c0002t0001g0259 | 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 | a0001c0001t0001g0168a0001c0001t0001g0220 | 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 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(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 | 78 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0126others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): 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 | a0001c0001t0001g0245 | 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 | 168 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0018others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): 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 | 133 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0058others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): 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 | a0001c0001t0001g0126a0001c0001t0001g0250a0001c0001t0002g0090others(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 | a0003c0004t0001g0207 | 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 | a0006c0010t0004g0175 | 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 | a0001c0001t0004g0274 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0126a0001c0001t0001g0250a0001c0001t0002g0090others(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 | a0001c0003t0001g0212 | 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 | a0001c0001t0001g0126a0001c0001t0001g0250a0001c0001t0012g0022others(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 | a0001c0001t0013g0008 | 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 | 82 | a0001c0001t0001g0018a0001c0001t0002g0011a0001c0001t0002g0012others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): 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 | a0001c0017t0001g0272 | 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 | a0001c0001t0001g0126a0001c0001t0001g0250a0001c0001t0003g0160others(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 | a0003c0004t0001g0007a0003c0004t0001g0013a0003c0004t0001g0040others(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 | a0001c0001t0004g0258a0001c0001t0004g0264 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0015t0003g0289a0001c0016t0006g0156 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0003t0001g0050a0001c0003t0001g0067a0001c0003t0022g0066 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0003c0004t0001g0145 | 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 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(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 | 83 | a0001c0001t0001g0018a0001c0001t0001g0058a0001c0001t0001g0060others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): 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 | a0001c0001t0003g0160 | 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 | a0001c0001t0003g0160 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | 90 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0126others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0123a0001c0001t0002g0275a0001c0001t0018g0136others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0004g0258a0001c0001t0004g0264 | 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 | a0001c0001t0004g0258a0001c0001t0004g0264 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0004a0001c0001t0002g0005 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(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 | 184 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0035others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0074a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(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 | a0001c0001t0001g0080a0001c0005t0006g0177a0001c0015t0003g0289others(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 | a0001c0001t0001g0001a0001c0001t0001g0117a0001c0001t0001g0127others(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 | a0002c0002t0002g0200 | 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 | 71 | a0001c0001t0001g0018a0001c0001t0001g0134a0001c0001t0002g0011others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(68): 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 | a0001c0001t0002g0005 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | a0001c0001t0002g0135a0001c0001t0002g0290a0001c0001t0003g0227others(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 | a0001c0001t0002g0012a0001c0001t0002g0131a0001c0001t0010g0023others(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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0086others(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 | 200 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0018others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1095-219C>T | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 10/14 | chr14 | 69339308 | ||||||
| chr14:69339338
|
A | T | 71 | a0001c0001t0001g0018a0001c0001t0001g0134a0001c0001t0002g0011others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(68): 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0080a0001c0005t0006g0177 | 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 | a0003c0004t0001g0007a0003c0004t0001g0013a0003c0004t0001g0040others(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 | a0001c0001t0002g0005 | 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 | a0001c0001t0001g0092a0001c0001t0001g0176a0001c0001t0001g0203others(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 | 99 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0058others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): 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 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0001t0002g0135others(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 | 82 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(79): 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 | a0001c0001t0012g0022a0007c0019t0008g0153 | 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 | 82 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(79): 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 | a0001c0001t0028g0111 | 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 | a0001c0001t0001g0035a0001c0001t0001g0201a0001c0001t0001g0209 | 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 | a0007c0019t0008g0153 | 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 | a0007c0019t0008g0153 | 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 | a0001c0001t0007g0276 | 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 | 73 | a0001c0001t0001g0018a0001c0001t0001g0126a0001c0001t0001g0134others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1271+146G>C | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69341910 | ||||||
| chr14:69342409
|
G | A | 125 | a0001c0001t0001g0018a0001c0001t0001g0086a0001c0001t0001g0087others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1271+645G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 12/14 | chr14 | 69342409 | ||||||
| chr14:69342426
|
G | A | 92 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0086others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): 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 | a0001c0001t0001g0004a0001c0001t0001g0146a0001c0001t0002g0085others(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 | a0001c0001t0001g0134a0001c0001t0002g0005a0001c0001t0002g0095others(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 |
21 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(18): 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 |
35 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0002g0090others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): 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 | a0001c0001t0002g0028a0001c0001t0002g0096a0001c0001t0002g0112others(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 | a0001c0001t0002g0012a0001c0001t0002g0091a0001c0001t0010g0023others(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 | a0001c0001t0002g0131 | 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 | a0002c0002t0001g0259 | 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 | a0001c0001t0012g0022a0003c0004t0001g0007a0003c0004t0001g0013others(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 | a0003c0004t0001g0040a0003c0004t0002g0027a0003c0004t0011g0024 | 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0047others(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 | a0001c0005t0006g0177a0001c0016t0006g0156a0003c0004t0001g0235 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0005g0298 | 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 | a0001c0001t0001g0280a0001c0001t0002g0011a0001c0001t0002g0076others(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 | a0002c0002t0001g0138a0002c0002t0001g0187a0002c0002t0001g0248others(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 | a0001c0001t0001g0126a0001c0001t0001g0250a0001c0001t0002g0197others(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 | a0001c0001t0001g0280a0001c0001t0002g0011a0001c0001t0002g0076others(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 | a0001c0001t0001g0126a0001c0001t0001g0250a0001c0001t0002g0197others(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 | a0001c0001t0001g0127 | 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 | 126 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0086others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): 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 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(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 | 70 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0134others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): 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 | a0002c0002t0002g0148 | 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 | a0001c0001t0014g0287 | 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 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(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 | 69 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0134others(66): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0002g0091 | 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 | 198 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0035others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): 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 | a0001c0001t0001g0250 | 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 | a0001c0005t0006g0177a0001c0016t0006g0156 | 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0002g0244 | 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 | a0001c0001t0001g0101a0001c0001t0001g0129a0001c0001t0001g0171others(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 | a0002c0002t0002g0148a0002c0002t0002g0149 | 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 | a0001c0001t0001g0074a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0074a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0003t0001g0297 | 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 | 163 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0045others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0003g0227 | 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 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0074others(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 | a0001c0001t0001g0043a0001c0001t0002g0135a0001c0001t0002g0290others(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 | a0001c0001t0001g0004a0001c0003t0002g0110a0003c0004t0002g0027others(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 | a0001c0001t0001g0101a0001c0001t0001g0129a0001c0001t0001g0171others(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 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0125others(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 |
22 | a0001c0001t0001g0045a0001c0001t0001g0155a0001c0001t0001g0250others(19): Show | 22 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(19): 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 | a0001c0001t0001g0068a0001c0001t0003g0160a0001c0001t0003g0238others(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 |
27 | a0001c0001t0001g0051a0001c0001t0001g0166a0001c0001t0001g0202others(24): 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 |
21 | a0001c0001t0001g0018a0001c0001t0001g0134a0001c0001t0002g0112others(18): 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 | a0001c0001t0001g0072a0001c0001t0001g0126a0001c0001t0001g0217others(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 | a0001c0001t0002g0131a0001c0017t0001g0272a0002c0002t0001g0158others(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 | a0001c0001t0001g0070a0001c0001t0002g0076a0001c0001t0002g0277others(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 | a0001c0001t0002g0012a0001c0001t0002g0085a0001c0001t0017g0247 | 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 | a0001c0001t0008g0130 | 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 | a0001c0001t0001g0080a0001c0001t0002g0288a0001c0005t0006g0177others(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 | a0003c0004t0001g0007a0003c0004t0001g0010a0003c0004t0001g0013others(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 | a0001c0001t0005g0298 | 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 | a0001c0001t0002g0135a0001c0001t0002g0290 | 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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0189 | 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 | 115 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0068others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(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 | a0003c0004t0001g0007a0003c0004t0001g0010a0003c0004t0001g0013others(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 | a0001c0001t0001g0004a0001c0001t0003g0227a0001c0001t0007g0044others(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 | a0001c0001t0001g0004a0001c0001t0003g0227a0001c0001t0007g0044others(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 | a0001c0001t0001g0074a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0003t0003g0098a0001c0003t0003g0224 | 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 | a0001c0008t0002g0190a0001c0008t0002g0191 | 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 | a0003c0004t0001g0007a0003c0004t0001g0010a0003c0004t0001g0013others(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 | a0001c0001t0001g0004a0001c0001t0007g0142 | 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0237 | 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 | a0003c0004t0001g0007a0003c0004t0001g0010a0003c0004t0001g0013others(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 | a0001c0001t0003g0037a0001c0001t0003g0079a0001c0001t0003g0163others(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 | 82 | a0001c0001t0001g0018a0001c0001t0001g0051a0001c0001t0001g0068others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): 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 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(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 | 197 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0035others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(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 | a0001c0001t0001g0120 | 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 | a0001c0003t0002g0071 | 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 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(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 | a0001c0005t0006g0177a0001c0016t0006g0156 | 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 | a0003c0004t0009g0147 | 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 | a0001c0001t0001g0074a0001c0001t0001g0205a0001c0001t0001g0206 | 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 | a0001c0001t0014g0287 | 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 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(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 | a0001c0001t0008g0094a0001c0001t0008g0240a0001c0001t0021g0075others(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 | a0001c0001t0005g0298 | 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 | a0001c0001t0001g0220 | 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 | a0001c0003t0001g0297 | 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 | a0001c0001t0001g0003 | 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 | ||||||
| chr14:69350981
|
G | A | 1 | a0001c0001t0002g0210 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1540-1050G>A | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69350981 | ||||||
| chr14:69350995
|
C | G | 82 | a0001c0001t0001g0004a0001c0001t0001g0043a0001c0001t0001g0146others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): 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 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0047others(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 | a0001c0001t0001g0074a0001c0001t0001g0205a0001c0001t0001g0206others(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 | a0001c0001t0012g0022a0001c0005t0006g0081a0001c0005t0006g0140others(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 | 70 | a0001c0001t0001g0043a0001c0001t0001g0123a0001c0001t0001g0146others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): 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 | a0001c0003t0001g0169a0001c0003t0001g0230 | 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 | 57 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(54): 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 | a0001c0001t0028g0111 | 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 | a0001c0001t0001g0051a0002c0002t0001g0017a0002c0002t0001g0259others(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 | a0001c0001t0003g0019a0001c0001t0003g0030a0001c0001t0003g0032others(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 | a0001c0001t0017g0247 | 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 | 57 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0012others(54): Show | 57 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(54): 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 | a0001c0001t0017g0247 | 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 | a0001c0001t0017g0247 | 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 | a0001c0001t0017g0247 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1540-19C>G | GALNT16 | ENSG00000100626.17 | transcript | ENST00000448469.8 | protein_coding | 14/14 | chr14 | 69352012 |