Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2651 |
|---|---|
| ensemblid | ENSG00000111846.20 |
| hgncid | 4204 |
| symbol | GCNT2 |
| name | glucosaminyl (N-acetyl) transferase 2 (I blood group) |
| refseq_nuc | NM_001491.3 |
| refseq_prot | NP_001482.1 |
| ensembl_nuc | ENST00000316170.9 |
| ensembl_prot | ENSP00000314844.3 |
| mane_status | MANE Plus Clinical |
| chr | chr6 |
| start | 10555809 |
| end | 10629368 |
| strand | + |
| ver | v1.2 |
| region | chr6:10555809-10629368 |
| region5000 | chr6:10550809-10634368 |
| regionname0 | GCNT2_chr6_10555809_10629368 |
| regionname5000 | GCNT2_chr6_10550809_10634368 |
| 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 | 400 | 338 | 81 | 64 | 143 | 12 | 36 | 109 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0002 | 0/0 | 400 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0003 | 0/0 | 400 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0004 | 0/0 | 73 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0005 | 0/0 | 400 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| 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 | 1203 | 321 | 73 | 60 | 142 | 10 | 34 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0002 | 0/0 | 1203 | 12 | 4 | 4 | 1 | 2 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0003 | 0/0 | 1203 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0004 | 0/0 | 1203 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0005 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0006 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0008 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| c0009 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| 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 | 1/1 | 3377 | 266 | 57 | 52 | 116 | 11 | 28 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0002 | 0/0 | 3377 | 44 | 1 | 7 | 27 | 1 | 8 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0003 | 0/0 | 3381 | 7 | 5 | 1 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0004 | 0/0 | 3377 | 5 | 5 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0005 | 0/0 | 3381 | 3 | 1 | 2 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0006 | 0/0 | 3381 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0007 | 0/0 | 3381 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0008 | 0/0 | 3377 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0009 | 0/0 | 3377 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0010 | 0/0 | 3381 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0011 | 0/0 | 3381 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0012 | 0/0 | 3377 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0013 | 0/0 | 3381 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0014 | 0/0 | 3377 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0015 | 0/0 | 3377 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0016 | 0/0 | 3377 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0017 | 0/0 | 3377 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0018 | 0/0 | 3377 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| t0019 | 0/0 | 3377 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| 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 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| 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 | 1203 | 321 | 73 | 60 | 142 | 10 | 34 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0002 | 0/0 | 1203 | 12 | 4 | 4 | 1 | 2 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0004 | 0/0 | 1203 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0006 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0002c0003 | 0/0 | 1203 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0003c0008 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0004c0009 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0005c0005 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4579 | 250 | 52 | 48 | 114 | 10 | 24 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0002 | 0/0 | 4579 | 43 | 1 | 7 | 27 | 0 | 8 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0003 | 0/0 | 4583 | 4 | 2 | 1 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0004 | 0/0 | 4579 | 5 | 5 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0005 | 0/0 | 4583 | 3 | 1 | 2 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0006 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0007 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0008 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0009 | 0/0 | 4579 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0010 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0012 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0013 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0014 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0015 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0016 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0017 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0001t0019 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0002t0001 | 0/0 | 4579 | 10 | 3 | 4 | 1 | 1 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0002t0002 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0002t0003 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0004t0003 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0004t0018 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0006t0001 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0001c0007t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0002c0003t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0002c0003t0010 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0002c0003t0011 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0003c0008t0001 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0004c0009t0001 | 0/0 | 4598 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| a0005c0005t0001 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | copy fasta | chr6 | 10550809 | 10634368 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0009g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0009g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0010g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0014g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0015g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0016g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0017g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0019g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0004t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0004t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0004t0018g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0006t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0007t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0002c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0002c0003t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0002c0003t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0003c0008t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0004c0009t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0005c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0297 | EUR | GBR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0289 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0326 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0046 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0301 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0281 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0283 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0290 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0246 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0303 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CDX | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0334 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02572 | hp1 | a0002 | c0003 | t0011 | g0264 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02717 | hp1 | a0001 | c0004 | t0018 | g0329 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02738 | hp2 | a0001 | c0001 | t0019 | g0107 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02895 | hp1 | a0001 | c0007 | t0001 | g0011 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0269 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0243 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03017 | hp2 | a0001 | c0006 | t0001 | g0060 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0330 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0299 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0291 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03195 | hp2 | a0001 | c0004 | t0003 | g0328 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0012 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03239 | hp1 | a0005 | c0005 | t0001 | g0319 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03579 | hp1 | a0002 | c0003 | t0010 | g0270 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03927 | hp1 | a0003 | c0008 | t0001 | g0037 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19005 | hp1 | a0001 | c0001 | t0017 | g0143 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0335 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19080 | hp1 | a0004 | c0009 | t0001 | g0081 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0331 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ASW | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0309 | AFR | ASW | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | GIH | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0130 | REF | REF | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10556431
|
T | C | 1 | a0002 | 3 | HG02572.hp1 HG02970.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.8T>C | p.Leu3Ser | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 623/4579 | 8/1203 | 3/400 | chr6 | 10556431 | ||
| chr6:10556488
|
T | C | 1 | a0005 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.65T>C | p.Phe22Ser | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 680/4579 | 65/1203 | 22/400 | chr6 | 10556488 | ||
| chr6:10556581
|
A | ATGGAAAA others(12): Show |
1 | a0004 | 1 | NA19080.hp1 | frameshift_variant | HIGH | c.169_187dupCGTTTCCT others(11): Show |
p.Lys63fs | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 803/4579 | 188/1203 | 63/400 | INFO_REALIGN_3_PRIME | chr6 | 10556581 | |
| chr6:10556940
|
A | G | 1 | a0003 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.517A>G | p.Arg173Gly | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 1132/4579 | 517/1203 | 173/400 | chr6 | 10556940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10556639
|
C | T | 1 | a0001c0002 | 12 | HG00140.hp1 HG00323.hp1 HG01099.hp2 others(9): Show |
synonymous_variant | LOW | c.216C>T | p.Cys72Cys | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 831/4579 | 216/1203 | 72/400 | chr6 | 10556639 | ||
| chr6:10556753
|
G | A | 1 | a0001c0006 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.330G>A | p.Arg110Arg | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 945/4579 | 330/1203 | 110/400 | chr6 | 10556753 | ||
| chr6:10557053
|
T | G | 1 | a0001c0007 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.630T>G | p.Gly210Gly | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 1245/4579 | 630/1203 | 210/400 | chr6 | 10557053 | ||
| chr6:10557110
|
T | C | 1 | a0001c0004 | 3 | HG02717.hp1 HG03130.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.687T>C | p.Tyr229Tyr | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 1302/4579 | 687/1203 | 229/400 | chr6 | 10557110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10556106
|
G | C | 2 | a0001c0001t0004a0001c0001t0006 | 7 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-318G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 318 | chr6 | 10556106 | |||||
| chr6:10626660
|
C | G | 2 | a0001c0001t0010a0002c0003t0010 | 2 | HG03579.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*53C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 53 | chr6 | 10626660 | |||||
| chr6:10626688
|
G | A | 1 | a0002c0003t0011 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 81 | chr6 | 10626688 | |||||
| chr6:10626712
|
C | T | 4 | a0001c0001t0003a0001c0001t0019a0001c0002t0003others(1): Show | 8 | HG01358.hp1 HG01891.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 105 | chr6 | 10626712 | |||||
| chr6:10626821
|
A | G | 1 | a0001c0004t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 214 | chr6 | 10626821 | |||||
| chr6:10626832
|
G | A | 1 | a0001c0001t0007 | 2 | HG02717.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*225G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 225 | chr6 | 10626832 | |||||
| chr6:10627005
|
T | A | 1 | a0001c0001t0008 | 2 | HG02055.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*398T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 398 | chr6 | 10627005 | |||||
| chr6:10627125
|
T | G | 1 | a0001c0001t0012 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 518 | chr6 | 10627125 | |||||
| chr6:10627278
|
C | T | 6 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(3): Show | 10 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*671C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 671 | chr6 | 10627278 | |||||
| chr6:10627289
|
G | C | 4 | a0001c0001t0003a0001c0001t0013a0001c0002t0003others(1): Show | 8 | HG01358.hp1 HG01891.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*682G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 682 | chr6 | 10627289 | |||||
| chr6:10627375
|
G | A | 1 | a0001c0001t0014 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 768 | chr6 | 10627375 | |||||
| chr6:10627546
|
G | T | 2 | a0001c0001t0005a0001c0001t0006 | 5 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 939 | chr6 | 10627546 | |||||
| chr6:10627628
|
C | CTTCA | 10 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(7): Show | 18 | HG00735.hp2 HG01109.hp1 HG01358.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1025dupTTCA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1026 | INFO_REALIGN_3_PRIME | chr6 | 10627628 | ||||
| chr6:10627681
|
A | G | 1 | a0001c0001t0017 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1074A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1074 | chr6 | 10627681 | |||||
| chr6:10627781
|
T | C | 2 | a0001c0001t0002a0001c0002t0002 | 44 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1174T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1174 | chr6 | 10627781 | |||||
| chr6:10627924
|
G | A | 1 | a0001c0001t0009 | 2 | HG01081.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1317G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1317 | chr6 | 10627924 | |||||
| chr6:10628004
|
A | G | 1 | a0001c0001t0016 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1397A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1397 | chr6 | 10628004 | |||||
| chr6:10628340
|
T | G | 5 | a0001c0001t0003a0001c0001t0010a0001c0002t0003others(2): Show | 9 | HG01358.hp1 HG01891.hp2 HG02738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1733T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1733 | chr6 | 10628340 | |||||
| chr6:10628878
|
C | T | 1 | a0001c0001t0013 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2271C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2271 | chr6 | 10628878 | |||||
| chr6:10629059
|
G | C | 1 | a0002c0003t0011 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2452G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2452 | chr6 | 10629059 | |||||
| chr6:10629127
|
C | A | 6 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(3): Show | 10 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2520C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2520 | chr6 | 10629127 | |||||
| chr6:10629333
|
T | C | 1 | a0001c0001t0015 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2726 | chr6 | 10629333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10557463
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.919+121C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557463 | ||||||
| chr6:10557493
|
CT | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 87 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.919+163delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10557493 | |||||
| chr6:10557542
|
C | T | 1 | a0001c0001t0001g0341 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.919+200C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557542 | ||||||
| chr6:10557668
|
T | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+326T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557668 | ||||||
| chr6:10557691
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 108 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.919+349A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557691 | ||||||
| chr6:10557691
|
A | T | 5 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0001t0001g0338others(2): Show | 5 | HG01346.hp1 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+349A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557691 | ||||||
| chr6:10557753
|
A | G | 4 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(1): Show | 4 | HG01496.hp2 HG02109.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+411A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557753 | ||||||
| chr6:10557856
|
C | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.919+514C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557856 | ||||||
| chr6:10558035
|
C | T | 5 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(2): Show | 5 | HG02622.hp2 HG03540.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+693C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558035 | ||||||
| chr6:10558329
|
A | C | 1 | a0001c0001t0001g0307 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.919+987A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558329 | ||||||
| chr6:10558374
|
A | G | 3 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | NA18955.hp1 NA18992.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.919+1032A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558374 | ||||||
| chr6:10558473
|
C | G | 8 | a0001c0001t0001g0302a0001c0001t0001g0304a0001c0001t0001g0305others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+1131C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558473 | ||||||
| chr6:10559072
|
C | CT | 47 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0082others(44): Show | 48 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.919+1747dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10559072 | |||||
| chr6:10559072
|
CT | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 9 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+1747delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10559072 | |||||
| chr6:10559221
|
C | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+1879C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559221 | ||||||
| chr6:10559306
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0306 | 2 | HG03579.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.919+1964C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559306 | ||||||
| chr6:10559718
|
G | A | 9 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(6): Show | 9 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+2376G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559718 | ||||||
| chr6:10559719
|
A | G | 9 | a0001c0001t0001g0308a0001c0001t0001g0310a0001c0001t0001g0311others(6): Show | 9 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+2377A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559719 | ||||||
| chr6:10559767
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.919+2425T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559767 | ||||||
| chr6:10560088
|
C | G | 1 | a0001c0001t0001g0253 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.919+2746C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560088 | ||||||
| chr6:10560113
|
G | C | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+2771G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560113 | ||||||
| chr6:10560119
|
C | T | 36 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(33): Show | 36 | HG00741.hp1 HG01071.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.919+2777C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560119 | ||||||
| chr6:10560299
|
AG | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 106 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.919+2961delG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10560299 | |||||
| chr6:10560343
|
G | A | 8 | a0001c0001t0004g0274a0001c0001t0004g0275a0001c0001t0004g0276others(5): Show | 9 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+3001G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560343 | ||||||
| chr6:10560402
|
T | C | 8 | a0001c0001t0001g0302a0001c0001t0001g0304a0001c0001t0001g0305others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+3060T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560402 | ||||||
| chr6:10560498
|
T | C | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+3156T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560498 | ||||||
| chr6:10560603
|
A | C | 1 | a0001c0001t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.919+3261A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560603 | ||||||
| chr6:10560671
|
C | A | 1 | a0001c0001t0009g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+3329C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560671 | ||||||
| chr6:10560869
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0010g0309 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.919+3527T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560869 | ||||||
| chr6:10561009
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.919+3667C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561009 | ||||||
| chr6:10561037
|
G | A | 11 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(8): Show | 11 | HG00735.hp2 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+3695G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561037 | ||||||
| chr6:10561126
|
G | A | 2 | a0001c0002t0001g0278a0001c0002t0001g0279 | 2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.919+3784G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561126 | ||||||
| chr6:10561173
|
C | CT | 6 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(3): Show | 6 | HG00438.hp2 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+3840dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10561173 | |||||
| chr6:10561232
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.919+3890G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561232 | ||||||
| chr6:10561399
|
C | T | 8 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(5): Show | 8 | HG00735.hp2 HG01884.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+4057C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561399 | ||||||
| chr6:10561403
|
A | G | 11 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0320others(8): Show | 11 | HG00735.hp2 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+4061A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561403 | ||||||
| chr6:10561565
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.919+4223C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561565 | ||||||
| chr6:10561594
|
C | T | 1 | a0001c0001t0014g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+4252C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561594 | ||||||
| chr6:10561634
|
G | A | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+4292G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561634 | ||||||
| chr6:10561656
|
C | G | 3 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0009g0246 | 3 | HG01978.hp2 HG02698.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.919+4314C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561656 | ||||||
| chr6:10561862
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.919+4520G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561862 | ||||||
| chr6:10561952
|
T | G | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.919+4610T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561952 | ||||||
| chr6:10561960
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.919+4618A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561960 | ||||||
| chr6:10561964
|
G | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.919+4622G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561964 | ||||||
| chr6:10562019
|
C | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 106 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.919+4677C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562019 | ||||||
| chr6:10562096
|
G | T | 3 | a0001c0004t0003g0328a0001c0004t0003g0330a0001c0004t0018g0329 | 3 | HG02717.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.919+4754G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562096 | ||||||
| chr6:10562154
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 106 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.919+4812G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562154 | ||||||
| chr6:10562228
|
C | T | 1 | a0001c0001t0005g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.919+4886C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562228 | ||||||
| chr6:10562242
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG00280.hp1 HG01070.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.919+4900C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562242 | ||||||
| chr6:10562301
|
C | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(20): Show | 23 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.919+4959C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562301 | ||||||
| chr6:10562466
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.919+5124C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562466 | ||||||
| chr6:10562496
|
T | G | 13 | a0001c0001t0001g0280a0001c0001t0001g0308a0001c0001t0001g0310others(10): Show | 13 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+5154T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562496 | ||||||
| chr6:10562656
|
G | GA | 40 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0098others(37): Show | 40 | HG00735.hp1 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.919+5335dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
G | GAA | 8 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0304others(5): Show | 8 | HG02055.hp2 HG02071.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+5334_919+5335d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
GA | G | 16 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0233others(13): Show | 16 | HG01192.hp1 HG01891.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+5335delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
GAA | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(10): Show | 13 | HG01256.hp1 HG01346.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+5334_919+5335d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
GAAA | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0013others(76): Show | 80 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.919+5333_919+5335d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562668
|
A | C | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0265others(6): Show | 9 | HG01358.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+5326A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562668 | ||||||
| chr6:10562669
|
A | C | 3 | a0001c0004t0003g0328a0001c0004t0003g0330a0001c0004t0018g0329 | 3 | HG02717.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.919+5327A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562669 | ||||||
| chr6:10562670
|
A | C | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | NA18980.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.919+5328A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562670 | ||||||
| chr6:10562673
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.919+5331A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562673 | ||||||
| chr6:10562675
|
A | C | 1 | a0001c0001t0009g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+5333A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562675 | ||||||
| chr6:10562678
|
C | A | 2 | a0001c0001t0001g0094a0001c0002t0001g0281 | 2 | HG01192.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.919+5336C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562678 | ||||||
| chr6:10562687
|
A | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 15 | HG00408.hp1 HG00558.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+5345A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562687 | ||||||
| chr6:10563166
|
A | G | 1 | a0001c0001t0004g0277 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.919+5824A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563166 | ||||||
| chr6:10563232
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919+5890G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563232 | ||||||
| chr6:10563276
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.919+5934A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563276 | ||||||
| chr6:10563410
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 100 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.919+6068A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563410 | ||||||
| chr6:10563436
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.919+6094G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563436 | ||||||
| chr6:10563510
|
G | C | 17 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0302others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+6168G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563510 | ||||||
| chr6:10563665
|
CCAGGAGG others(9): Show |
C | 1 | a0001c0001t0001g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919+6327_919+6342d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563665 | |||||
| chr6:10563749
|
GAAAA | G | 3 | a0002c0003t0001g0269a0002c0003t0010g0270a0002c0003t0011g0264 | 3 | HG02572.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.919+6410_919+6413d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563749 | |||||
| chr6:10563749
|
GAAAAAAG others(3): Show |
G | 1 | a0001c0001t0001g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.919+6414_919+6423d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563749 | |||||
| chr6:10563756
|
GA | G | 29 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0109others(26): Show | 29 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.919+6436delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563756
|
GAA | G | 17 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0121others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+6435_919+6436d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563756
|
GAAA | G | 9 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0223others(6): Show | 9 | HG00140.hp2 HG02809.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+6434_919+6436d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563756
|
GAAAAA | G | 7 | a0001c0001t0001g0225a0001c0001t0001g0292a0001c0001t0001g0293others(4): Show | 7 | HG02451.hp2 HG02615.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+6432_919+6436d others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563756
|
GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.919+6427_919+6436d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563760
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.919+6418A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563760 | ||||||
| chr6:10563763
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.919+6421A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563763 | ||||||
| chr6:10563766
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0317 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.919+6426_919+6438d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563766 | |||||
| chr6:10563767
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0010g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919+6427_919+6440d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563767 | |||||
| chr6:10563768
|
AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0085others(2): Show | 5 | HG00558.hp1 HG00673.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6428_919+6438d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563768 | |||||
| chr6:10563768
|
AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0002g0042a0005c0005t0001g0319 | 2 | HG03239.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.919+6428_919+6440d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563768 | |||||
| chr6:10563769
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0002g0074a0001c0002t0001g0283 | 2 | HG01884.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.919+6429_919+6438d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563769
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0018a0001c0001t0001g0075a0001c0002t0001g0297 | 3 | HG00140.hp1 HG01517.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.919+6429_919+6440d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563769
|
AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0306a0001c0001t0001g0308 | 2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.919+6429_919+6442d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563769
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+6429_919+6444d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563770
|
AAAAAAAA others(4): Show |
A | 16 | a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 16 | HG01099.hp2 HG02056.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+6430_919+6440d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | |||||
| chr6:10563770
|
AAAAAAAA others(6): Show |
A | 3 | a0001c0001t0001g0041a0001c0001t0008g0335a0001c0002t0001g0281 | 3 | HG01192.hp2 NA19030.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.919+6430_919+6442d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | |||||
| chr6:10563770
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0004t0003g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+6430_919+6444d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | |||||
| chr6:10563771
|
A | AAT | 6 | a0001c0001t0001g0211a0001c0001t0001g0259a0001c0001t0001g0336others(3): Show | 6 | HG00544.hp2 HG01934.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+6430_919+6431i others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
A | AATATATA others(3): Show |
1 | a0001c0002t0002g0289 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.919+6430_919+6431i others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.919+6430_919+6431i others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
A | AT | 6 | a0001c0001t0001g0092a0001c0001t0001g0123a0001c0001t0002g0220others(3): Show | 6 | HG02300.hp1 NA18980.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+6429_919+6430i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563771 | ||||||
| chr6:10563771
|
A | T | 3 | a0001c0001t0001g0227a0001c0001t0001g0339a0001c0002t0001g0296 | 3 | HG00597.hp2 HG01975.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.919+6429A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563771 | ||||||
| chr6:10563771
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0002g0051 | 3 | HG01256.hp1 HG02083.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.919+6431_919+6440d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
AAAAAAAA others(5): Show |
A | 9 | a0001c0001t0001g0002a0001c0001t0001g0069a0001c0001t0001g0070others(6): Show | 10 | HG00741.hp1 HG01081.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+6431_919+6442d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
AAAAAAAA others(7): Show |
A | 4 | a0001c0001t0001g0089a0001c0001t0001g0302a0001c0004t0003g0328others(1): Show | 4 | HG02717.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+6431_919+6444d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0310a0001c0001t0003g0300 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.919+6431_919+6446d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563772
|
AAAAAAAT others(2): Show |
A | 6 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG01071.hp2 HG01934.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+6432_919+6440d others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563772
|
AAAAAAAT others(4): Show |
A | 27 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(24): Show | 27 | HG00323.hp2 HG01081.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+6432_919+6442d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563772
|
AAAAAAAT others(6): Show |
A | 4 | a0001c0001t0007g0016a0001c0001t0014g0331a0002c0003t0001g0269others(1): Show | 4 | HG02717.hp2 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+6432_919+6444d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563772
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+6432_919+6446d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563773
|
A | AT | 8 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(5): Show | 8 | HG02083.hp1 HG02155.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+6431_919+6432i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | ||||||
| chr6:10563773
|
A | ATAT | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0190others(2): Show | 5 | NA18956.hp2 NA18981.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6431_919+6432i others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | ||||||
| chr6:10563773
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.919+6431_919+6432i others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | ||||||
| chr6:10563773
|
A | T | 25 | a0001c0001t0001g0092a0001c0001t0001g0119a0001c0001t0001g0120others(22): Show | 25 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.919+6431A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | ||||||
| chr6:10563773
|
AAAAAATA others(3): Show |
A | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0090others(2): Show | 5 | HG02630.hp2 HG03540.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+6433_919+6442d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563773
|
AAAAAATA others(5): Show |
A | 3 | a0001c0001t0001g0265a0001c0001t0003g0312a0002c0003t0011g0264 | 3 | HG02559.hp2 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.919+6433_919+6444d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563773
|
AAAAAATA others(7): Show |
A | 1 | a0001c0001t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.919+6433_919+6446d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563773
|
AAAAAATA others(9): Show |
A | 1 | a0001c0001t0004g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.919+6433_919+6448d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563774
|
AAAAATAT others(4): Show |
A | 18 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0024others(15): Show | 18 | HG00408.hp1 HG01099.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+6434_919+6444d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | |||||
| chr6:10563774
|
AAAAATAT others(6): Show |
A | 3 | a0001c0001t0001g0035a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01496.hp2 HG03710.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.919+6434_919+6446d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | |||||
| chr6:10563774
|
AAAAATAT others(8): Show |
A | 5 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0004g0275others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6434_919+6448d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | |||||
| chr6:10563775
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.919+6434_919+6435i others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563775 | |||||
| chr6:10563775
|
A | AT | 13 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(10): Show | 13 | HG01516.hp1 HG02080.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+6433_919+6434i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | ATAT | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0257others(1): Show | 4 | HG02273.hp1 HG02615.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+6433_919+6434i others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | ATATAT | 3 | a0001c0001t0001g0156a0001c0001t0001g0240a0001c0001t0002g0157 | 3 | HG02698.hp2 HG03239.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.919+6433_919+6434i others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.919+6433_919+6434i others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0092others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.919+6433A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | ||||||
| chr6:10563775
|
AAAATATA others(7): Show |
A | 3 | a0001c0001t0001g0086a0001c0001t0004g0274a0001c0001t0006g0001 | 4 | HG02258.hp1 HG02486.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+6435_919+6448d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563775 | |||||
| chr6:10563776
|
AAATATAT others(6): Show |
A | 1 | a0001c0001t0001g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.919+6436_919+6448d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563776 | |||||
| chr6:10563777
|
A | AAATATAT others(28): Show |
1 | a0001c0001t0001g0126 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.919+6436_919+6437i others(37): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563777 | |||||
| chr6:10563777
|
A | AT | 5 | a0001c0001t0001g0096a0001c0001t0001g0142a0001c0001t0017g0143others(2): Show | 5 | HG01361.hp2 HG02071.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6435_919+6436i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563777 | ||||||
| chr6:10563777
|
A | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.919+6435A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563777 | ||||||
| chr6:10563777
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0001g0313 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.919+6456_919+6467d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563777 | |||||
| chr6:10563778
|
AT | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG00621.hp2 HG01358.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+6437delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563778 | ||||||
| chr6:10563779
|
T | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0125a0001c0001t0001g0321 | 3 | HG01123.hp1 HG03516.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.919+6437T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563779 | ||||||
| chr6:10563781
|
T | A | 1 | a0001c0001t0001g0321 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.919+6439T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563781 | ||||||
| chr6:10563899
|
G | A | 2 | a0001c0001t0001g0341a0001c0001t0002g0129 | 2 | NA18981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.919+6557G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563899 | ||||||
| chr6:10563981
|
G | T | 1 | a0001c0001t0017g0143 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.919+6639G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563981 | ||||||
| chr6:10564171
|
T | C | 8 | a0001c0001t0004g0274a0001c0001t0004g0275a0001c0001t0004g0276others(5): Show | 9 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+6829T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564171 | ||||||
| chr6:10564367
|
T | C | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+7025T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564367 | ||||||
| chr6:10564440
|
C | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.919+7098C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564440 | ||||||
| chr6:10564453
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.919+7111G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564453 | ||||||
| chr6:10564526
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0012g0243 | 3 | HG02258.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.919+7184G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564526 | ||||||
| chr6:10564642
|
T | G | 2 | a0001c0001t0001g0317a0005c0005t0001g0319 | 2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.919+7300T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564642 | ||||||
| chr6:10564761
|
G | C | 1 | a0001c0001t0001g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919+7419G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564761 | ||||||
| chr6:10565067
|
G | A | 7 | a0001c0001t0001g0302a0001c0001t0001g0304a0001c0001t0001g0305others(4): Show | 7 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+7725G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565067 | ||||||
| chr6:10565104
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.919+7762A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565104 | ||||||
| chr6:10565123
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+7781A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565123 | ||||||
| chr6:10565170
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919+7828G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565170 | ||||||
| chr6:10565383
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0002g0141 | 2 | NA19084.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.919+8041A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565383 | ||||||
| chr6:10565383
|
AAGGGAAA others(4): Show |
A | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 101 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.919+8054_919+8064d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10565383 | |||||
| chr6:10565564
|
A | G | 2 | a0001c0001t0004g0268a0001c0001t0015g0299 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.919+8222A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565564 | ||||||
| chr6:10565708
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 172 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.919+8366C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565708 | ||||||
| chr6:10565776
|
C | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.919+8434C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565776 | ||||||
| chr6:10565845
|
T | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0091a0001c0001t0001g0158others(27): Show | 31 | HG00323.hp1 HG01109.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.919+8503T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565845 | ||||||
| chr6:10565898
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.919+8556C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565898 | ||||||
| chr6:10565959
|
A | G | 5 | a0001c0001t0001g0266a0001c0001t0001g0280a0001c0001t0001g0311others(2): Show | 5 | HG02976.hp1 HG03041.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+8617A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565959 | ||||||
| chr6:10566052
|
C | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+8710C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566052 | ||||||
| chr6:10566053
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.919+8711G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566053 | ||||||
| chr6:10566074
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.919+8732G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566074 | ||||||
| chr6:10566089
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.919+8747C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566089 | ||||||
| chr6:10566110
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.919+8768G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566110 | ||||||
| chr6:10566141
|
C | T | 15 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0265others(12): Show | 15 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+8799C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566141 | ||||||
| chr6:10566258
|
C | T | 47 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(44): Show | 47 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.919+8916C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566258 | ||||||
| chr6:10566361
|
C | A | 5 | a0001c0001t0001g0294a0001c0001t0004g0274a0001c0001t0004g0275others(2): Show | 6 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+9019C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566361 | ||||||
| chr6:10566422
|
C | T | 178 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(175): Show | 178 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.919+9080C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566422 | ||||||
| chr6:10566436
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.919+9094T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566436 | ||||||
| chr6:10566442
|
T | G | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | NA18980.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.919+9100T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566442 | ||||||
| chr6:10566585
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.919+9243C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566585 | ||||||
| chr6:10566586
|
G | A | 1 | a0001c0002t0001g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.919+9244G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566586 | ||||||
| chr6:10566623
|
T | A | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 188 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.919+9281T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566623 | ||||||
| chr6:10566713
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.919+9371G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566713 | ||||||
| chr6:10566798
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.919+9456C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566798 | ||||||
| chr6:10566882
|
C | T | 203 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(200): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.919+9540C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566882 | ||||||
| chr6:10566883
|
C | T | 8 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0306others(5): Show | 8 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+9541C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566883 | ||||||
| chr6:10567055
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+9713A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567055 | ||||||
| chr6:10567172
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0178others(5): Show | 8 | HG00597.hp2 HG00621.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+9830G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567172 | ||||||
| chr6:10567244
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+9902G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567244 | ||||||
| chr6:10567300
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.919+9958T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567300 | ||||||
| chr6:10567387
|
A | G | 224 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(221): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.919+10045A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567387 | ||||||
| chr6:10567679
|
A | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.919+10337A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567679 | ||||||
| chr6:10567694
|
C | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.919+10352C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567694 | ||||||
| chr6:10567821
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.919+10479A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567821 | ||||||
| chr6:10568068
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+10726C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568068 | ||||||
| chr6:10568120
|
T | G | 8 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0306others(5): Show | 8 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+10778T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568120 | ||||||
| chr6:10568151
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0008g0335 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+10809C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568151 | ||||||
| chr6:10568219
|
T | C | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.919+10877T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568219 | ||||||
| chr6:10568313
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.919+10971T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568313 | ||||||
| chr6:10568414
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.919+11072A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568414 | ||||||
| chr6:10568598
|
A | G | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+11256A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568598 | ||||||
| chr6:10568616
|
A | G | 1 | a0001c0001t0002g0023 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.919+11274A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568616 | ||||||
| chr6:10568622
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.919+11280T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568622 | ||||||
| chr6:10568753
|
C | A | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+11411C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568753 | ||||||
| chr6:10568765
|
T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(211): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.919+11423T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568765 | ||||||
| chr6:10568869
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.919+11527G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568869 | ||||||
| chr6:10568881
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+11539A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568881 | ||||||
| chr6:10568929
|
G | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(197): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.919+11587G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568929 | ||||||
| chr6:10569037
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0008g0335 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+11695G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569037 | ||||||
| chr6:10569129
|
G | C | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 179 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.919+11787G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569129 | ||||||
| chr6:10569156
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0321a0001c0001t0005g0326 | 3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.919+11814T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569156 | ||||||
| chr6:10569235
|
C | CCA | 25 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0039others(22): Show | 26 | HG00438.hp2 HG00673.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.919+11931_919+1193 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACA | 6 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0082others(3): Show | 6 | HG00558.hp1 HG03209.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+11929_919+1193 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(1): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0125a0001c0001t0001g0136others(2): Show | 5 | HG00642.hp1 HG01123.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+11925_919+1193 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(3): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG00639.hp1 HG00738.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+11923_919+1193 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(7): Show |
3 | a0001c0001t0001g0122a0001c0001t0001g0314a0001c0001t0002g0110 | 3 | HG03041.hp2 HG06807.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.919+11919_919+1193 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(9): Show |
3 | a0001c0001t0001g0226a0001c0001t0001g0245a0001c0001t0001g0249 | 3 | HG02080.hp1 HG02572.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.919+11917_919+1193 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(11): Show |
11 | a0001c0001t0001g0095a0001c0001t0001g0118a0001c0001t0001g0171others(8): Show | 11 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+11915_919+1193 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(13): Show |
23 | a0001c0001t0001g0067a0001c0001t0001g0093a0001c0001t0001g0135others(20): Show | 23 | HG00558.hp2 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.919+11913_919+1193 others(24): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(15): Show |
31 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0112others(28): Show | 31 | HG00323.hp2 HG00621.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.919+11911_919+1193 others(26): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(17): Show |
19 | a0001c0001t0001g0043a0001c0001t0001g0070a0001c0001t0001g0104others(16): Show | 19 | HG00408.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.919+11909_919+1193 others(28): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(19): Show |
14 | a0001c0001t0001g0015a0001c0001t0001g0096a0001c0001t0001g0128others(11): Show | 14 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+11907_919+1193 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(21): Show |
16 | a0001c0001t0001g0098a0001c0001t0001g0113a0001c0001t0001g0116others(13): Show | 16 | HG01346.hp1 HG01975.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+11905_919+1193 others(32): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(23): Show |
13 | a0001c0001t0001g0075a0001c0001t0001g0103a0001c0001t0001g0124others(10): Show | 13 | HG00280.hp2 HG01074.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+11903_919+1193 others(34): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(25): Show |
16 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0092others(13): Show | 16 | HG00597.hp2 HG01074.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+11901_919+1193 others(36): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(27): Show |
6 | a0001c0001t0001g0127a0001c0001t0001g0153a0001c0001t0001g0173others(3): Show | 6 | HG00735.hp1 NA18968.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+11899_919+1193 others(38): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(29): Show |
9 | a0001c0001t0001g0029a0001c0001t0001g0115a0001c0001t0001g0126others(6): Show | 9 | HG02155.hp2 HG02280.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+11897_919+1193 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(31): Show |
3 | a0001c0001t0001g0230a0001c0001t0001g0252a0001c0001t0001g0259 | 3 | HG02129.hp1 HG02273.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.919+11895_919+1193 others(42): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(33): Show |
3 | a0001c0001t0001g0167a0001c0001t0002g0221a0001c0002t0001g0297 | 3 | HG00140.hp1 HG01175.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(44): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(35): Show |
1 | a0001c0001t0002g0160 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.919+11932_919+1193 others(46): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(37): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0192 | 2 | NA18956.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(48): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(39): Show |
1 | a0001c0001t0002g0074 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(50): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(41): Show |
1 | a0001c0001t0001g0342 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(52): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
CCACA | C | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(7): Show | 10 | HG00408.hp1 HG01928.hp2 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+11929_919+1193 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
CCACACA | C | 8 | a0001c0001t0001g0069a0001c0001t0001g0294a0001c0001t0004g0274others(5): Show | 9 | HG00741.hp1 HG01361.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+11927_919+1193 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
CCACACAC others(3): Show |
C | 1 | a0001c0001t0008g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.919+11923_919+1193 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569245
|
A | ACACC | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+11906_919+1190 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569245 | |||||
| chr6:10569271
|
ACACC | A | 3 | a0001c0001t0001g0273a0001c0001t0001g0321a0001c0001t0005g0326 | 3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.919+11931_919+1193 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569271 | |||||
| chr6:10569273
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0001g0260 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(34): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569273 | |||||
| chr6:10569273
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0001g0313 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569273 | |||||
| chr6:10569274
|
C | CACACACA others(8): Show |
1 | a0001c0001t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.919+11932_919+1193 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(18): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0101 | 2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(29): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(20): Show |
1 | a0001c0001t0001g0183 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(31): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(22): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0193 | 2 | HG03017.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(33): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(28): Show |
1 | a0001c0001t0001g0161 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(39): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(32): Show |
1 | a0001c0001t0001g0056 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(43): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(34): Show |
1 | a0001c0001t0001g0094 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.919+11932_919+1193 others(45): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | ||||||
| chr6:10569275
|
C | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.919+11933C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569275 | ||||||
| chr6:10569276
|
C | A | 8 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0101others(5): Show | 8 | HG02056.hp2 HG03017.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+11934C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569276 | ||||||
| chr6:10569290
|
G | C | 2 | a0001c0001t0002g0117a0001c0001t0002g0221 | 2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.919+11948G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569290 | ||||||
| chr6:10569466
|
C | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0120a0001c0001t0001g0127others(2): Show | 5 | HG00621.hp2 HG02080.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+12124C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569466 | ||||||
| chr6:10569531
|
T | C | 20 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(17): Show | 20 | HG00597.hp2 HG00621.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.919+12189T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569531 | ||||||
| chr6:10569564
|
T | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0311others(4): Show | 7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12222T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569564 | ||||||
| chr6:10569571
|
T | C | 14 | a0001c0001t0001g0104a0001c0001t0001g0153a0001c0001t0001g0171others(11): Show | 14 | HG00741.hp2 HG01993.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+12229T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569571 | ||||||
| chr6:10569644
|
C | A | 3 | a0001c0001t0001g0090a0001c0001t0005g0045a0001c0001t0007g0016 | 3 | HG02630.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.919+12302C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569644 | ||||||
| chr6:10569824
|
T | TCTTC | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 177 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.919+12502_919+1250 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569824 | |||||
| chr6:10569847
|
T | TCCTTTCT others(5): Show |
7 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0311others(4): Show | 7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12505_919+1250 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569847 | ||||||
| chr6:10569848
|
T | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0144others(9): Show | 12 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+12506T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569848 | ||||||
| chr6:10569849
|
C | T | 7 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0311others(4): Show | 7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12507C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569849 | ||||||
| chr6:10569851
|
C | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0144others(9): Show | 12 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+12509C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569851 | ||||||
| chr6:10569853
|
T | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0144others(9): Show | 12 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+12511T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569853 | ||||||
| chr6:10569854
|
T | C | 2 | a0001c0001t0001g0306a0001c0001t0015g0299 | 2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.919+12512T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569854 | ||||||
| chr6:10569861
|
C | T | 10 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0181others(7): Show | 10 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+12519C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569861 | ||||||
| chr6:10569863
|
T | C | 10 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0181others(7): Show | 10 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+12521T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569863 | ||||||
| chr6:10569865
|
C | CTT | 7 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0311others(4): Show | 7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12525_919+1252 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569865 | |||||
| chr6:10569875
|
TTC | T | 4 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0317others(1): Show | 4 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+12537_919+1253 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569875 | |||||
| chr6:10569877
|
C | CCTT | 7 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0311others(4): Show | 7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12535_919+1253 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569877 | ||||||
| chr6:10569878
|
T | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0311others(4): Show | 7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12536T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569878 | ||||||
| chr6:10569882
|
T | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0273a0001c0001t0001g0311others(4): Show | 7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12540T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569882 | ||||||
| chr6:10569885
|
T | C | 1 | a0001c0002t0001g0278 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.919+12543T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569885 | ||||||
| chr6:10569887
|
TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0001g0308a0001c0001t0008g0335 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+12546_919+1255 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569887 | ||||||
| chr6:10569935
|
T | C | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+12593T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569935 | ||||||
| chr6:10569947
|
TCTTC | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.919+12621_919+1262 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569947 | |||||
| chr6:10569963
|
CCTTT | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+12628_919+1263 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569963 | |||||
| chr6:10569991
|
A | T | 6 | a0001c0001t0001g0185a0001c0001t0001g0195a0001c0001t0001g0218others(3): Show | 6 | HG01516.hp2 HG01517.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+12649A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569991 | ||||||
| chr6:10569995
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.919+12653A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569995 | ||||||
| chr6:10570135
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.919+12793A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570135 | ||||||
| chr6:10570176
|
T | C | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.919+12834T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570176 | ||||||
| chr6:10570177
|
C | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0165 | 3 | HG01256.hp2 HG01258.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.919+12835C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570177 | ||||||
| chr6:10570312
|
T | C | 7 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0315others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12970T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570312 | ||||||
| chr6:10570444
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.919+13102A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570444 | ||||||
| chr6:10570534
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.919+13192C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570534 | ||||||
| chr6:10570552
|
C | T | 2 | a0001c0001t0003g0312a0001c0001t0010g0309 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.919+13210C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570552 | ||||||
| chr6:10570785
|
A | G | 4 | a0001c0001t0002g0117a0001c0001t0002g0221a0001c0001t0002g0236others(1): Show | 4 | NA18980.hp1 NA18990.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+13443A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570785 | ||||||
| chr6:10570877
|
T | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG01071.hp2 HG01346.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+13535T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570877 | ||||||
| chr6:10570895
|
G | C | 204 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.919+13553G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570895 | ||||||
| chr6:10570909
|
G | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+13567G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570909 | ||||||
| chr6:10571027
|
A | G | 185 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(182): Show | 185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.919+13685A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571027 | ||||||
| chr6:10571158
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919+13816A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571158 | ||||||
| chr6:10571186
|
T | C | 1 | a0001c0001t0010g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919+13844T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571186 | ||||||
| chr6:10571259
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.919+13917A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571259 | ||||||
| chr6:10571326
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0215 | 2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.919+13984T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571326 | ||||||
| chr6:10571342
|
AATT | A | 10 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+14016_919+1401 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10571342 | |||||
| chr6:10571420
|
C | T | 194 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.919+14078C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571420 | ||||||
| chr6:10571513
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.919+14171C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571513 | ||||||
| chr6:10571579
|
C | G | 2 | a0001c0001t0002g0210a0001c0001t0002g0220 | 2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.919+14237C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571579 | ||||||
| chr6:10571593
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+14251C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571593 | ||||||
| chr6:10571628
|
C | T | 3 | a0001c0001t0002g0009a0001c0001t0002g0014a0001c0001t0002g0152 | 3 | NA18971.hp1 NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.919+14286C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571628 | ||||||
| chr6:10571639
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.919+14297C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571639 | ||||||
| chr6:10571643
|
G | A | 1 | a0001c0001t0014g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+14301G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571643 | ||||||
| chr6:10571758
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.919+14416C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571758 | ||||||
| chr6:10571759
|
G | A | 209 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.919+14417G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571759 | ||||||
| chr6:10571837
|
G | A | 10 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+14495G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571837 | ||||||
| chr6:10571890
|
C | T | 9 | a0001c0001t0001g0310a0001c0001t0001g0313a0001c0001t0001g0314others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+14548C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571890 | ||||||
| chr6:10571918
|
A | G | 6 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+14576A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571918 | ||||||
| chr6:10571946
|
C | CACTGATA others(38): Show |
3 | a0001c0001t0001g0090a0001c0001t0005g0045a0001c0001t0007g0016 | 3 | HG02630.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.919+14606_919+1465 others(49): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10571946 | |||||
| chr6:10572087
|
C | T | 9 | a0001c0001t0001g0310a0001c0001t0001g0313a0001c0001t0001g0314others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+14745C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572087 | ||||||
| chr6:10572225
|
C | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0014g0331 | 3 | HG02622.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+14883C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572225 | ||||||
| chr6:10572332
|
C | A | 11 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0273others(8): Show | 11 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+14990C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572332 | ||||||
| chr6:10572382
|
C | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.919+15040C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572382 | ||||||
| chr6:10572452
|
T | A | 11 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0273others(8): Show | 11 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+15110T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572452 | ||||||
| chr6:10572452
|
T | G | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.919+15110T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572452 | ||||||
| chr6:10572459
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.919+15117C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572459 | ||||||
| chr6:10572496
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0014g0331 | 3 | HG02622.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+15154G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572496 | ||||||
| chr6:10572514
|
T | C | 209 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.919+15172T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572514 | ||||||
| chr6:10572548
|
T | C | 12 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(9): Show | 13 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+15206T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572548 | ||||||
| chr6:10572606
|
C | T | 10 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+15264C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572606 | ||||||
| chr6:10572754
|
A | G | 15 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(12): Show | 15 | HG01192.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+15412A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572754 | ||||||
| chr6:10572805
|
C | T | 175 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(172): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.919+15463C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572805 | ||||||
| chr6:10572962
|
G | T | 207 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.919+15620G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572962 | ||||||
| chr6:10573006
|
G | A | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+15664G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573006 | ||||||
| chr6:10573038
|
G | T | 2 | a0001c0001t0004g0274a0001c0001t0006g0001 | 3 | HG02258.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.919+15696G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573038 | ||||||
| chr6:10573168
|
G | GATC | 189 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(186): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.919+15827_919+1582 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10573168 | |||||
| chr6:10573192
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.919+15850C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573192 | ||||||
| chr6:10573211
|
C | T | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+15869C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573211 | ||||||
| chr6:10573237
|
C | A | 2 | a0001c0001t0003g0312a0001c0001t0010g0309 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.919+15895C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573237 | ||||||
| chr6:10573318
|
A | G | 1 | a0001c0001t0015g0299 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.919+15976A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573318 | ||||||
| chr6:10573350
|
A | ATTGTTG | 211 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.919+16014_919+1601 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10573350 | |||||
| chr6:10573531
|
C | A | 17 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(14): Show | 17 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+16189C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573531 | ||||||
| chr6:10573574
|
A | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+16232A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573574 | ||||||
| chr6:10573613
|
A | G | 3 | a0001c0001t0001g0273a0001c0001t0001g0321a0001c0001t0005g0326 | 3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.919+16271A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573613 | ||||||
| chr6:10573677
|
A | G | 196 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.919+16335A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573677 | ||||||
| chr6:10573704
|
T | C | 1 | a0001c0001t0014g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+16362T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573704 | ||||||
| chr6:10573720
|
C | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+16378C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573720 | ||||||
| chr6:10573885
|
C | A | 187 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(184): Show | 188 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.919+16543C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573885 | ||||||
| chr6:10573971
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0106 | 2 | NA19055.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.919+16629A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573971 | ||||||
| chr6:10574079
|
T | C | 187 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(184): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.919+16737T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574079 | ||||||
| chr6:10574099
|
T | C | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+16757T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574099 | ||||||
| chr6:10574101
|
T | C | 1 | a0001c0001t0015g0299 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.919+16759T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574101 | ||||||
| chr6:10574111
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+16769G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574111 | ||||||
| chr6:10574164
|
G | T | 196 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(193): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.919+16822G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574164 | ||||||
| chr6:10574215
|
C | A | 190 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(187): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.919+16873C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574215 | ||||||
| chr6:10574229
|
G | T | 6 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0142others(3): Show | 6 | HG00544.hp2 HG02155.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+16887G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574229 | ||||||
| chr6:10574343
|
C | T | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+17001C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574343 | ||||||
| chr6:10574395
|
G | T | 2 | a0001c0001t0001g0306a0001c0001t0001g0311 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.919+17053G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574395 | ||||||
| chr6:10574398
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0163 | 2 | NA18939.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.919+17056A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574398 | ||||||
| chr6:10574408
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0002g0229 | 2 | HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.919+17066A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574408 | ||||||
| chr6:10574489
|
G | A | 9 | a0001c0001t0001g0294a0001c0001t0004g0274a0001c0001t0004g0275others(6): Show | 10 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+17147G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574489 | ||||||
| chr6:10574570
|
C | G | 1 | a0001c0001t0001g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919+17228C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574570 | ||||||
| chr6:10574673
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0008g0335 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+17331T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574673 | ||||||
| chr6:10574716
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.919+17374T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574716 | ||||||
| chr6:10574728
|
AT | A | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+17395delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10574728 | |||||
| chr6:10574787
|
C | G | 10 | a0001c0001t0001g0095a0001c0001t0001g0310a0001c0001t0001g0313others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+17445C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574787 | ||||||
| chr6:10574791
|
C | G | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17449C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574791 | ||||||
| chr6:10574796
|
C | A | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17454C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574796 | ||||||
| chr6:10574797
|
A | G | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17455A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574797 | ||||||
| chr6:10574799
|
T | A | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17457T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574799 | ||||||
| chr6:10574802
|
C | T | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17460C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574802 | ||||||
| chr6:10574808
|
T | C | 14 | a0001c0001t0001g0095a0001c0001t0001g0310a0001c0001t0001g0313others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+17466T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574808 | ||||||
| chr6:10574810
|
A | C | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17468A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574810 | ||||||
| chr6:10574813
|
T | C | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17471T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574813 | ||||||
| chr6:10574814
|
G | A | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17472G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574814 | ||||||
| chr6:10574815
|
T | G | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17473T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574815 | ||||||
| chr6:10574816
|
G | C | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17474G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574816 | ||||||
| chr6:10574819
|
A | G | 1 | a0001c0001t0005g0301 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17477A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574819 | ||||||
| chr6:10574861
|
C | G | 1 | a0002c0003t0010g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.919+17519C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574861 | ||||||
| chr6:10574898
|
T | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.919+17556T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574898 | ||||||
| chr6:10574914
|
G | C | 2 | a0001c0001t0001g0090a0001c0001t0007g0016 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+17572G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574914 | ||||||
| chr6:10574991
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.919+17649C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574991 | ||||||
| chr6:10575009
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.919+17667T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575009 | ||||||
| chr6:10575015
|
C | T | 2 | a0001c0001t0004g0276a0001c0002t0001g0283 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.919+17673C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575015 | ||||||
| chr6:10575113
|
T | C | 11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+17771T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575113 | ||||||
| chr6:10575142
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.919+17800G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575142 | ||||||
| chr6:10575261
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0226 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.919+17919T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575261 | ||||||
| chr6:10575307
|
A | T | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+17965A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575307 | ||||||
| chr6:10575358
|
A | AT | 6 | a0001c0001t0001g0047a0001c0001t0001g0089a0001c0001t0001g0145others(3): Show | 6 | HG00438.hp2 HG04184.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+18035dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | |||||
| chr6:10575358
|
A | ATT | 7 | a0001c0001t0001g0006a0001c0001t0001g0022a0001c0001t0001g0026others(4): Show | 7 | HG00408.hp1 HG01928.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+18034_919+1803 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | |||||
| chr6:10575358
|
A | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0109a0001c0001t0001g0133others(2): Show | 5 | HG02040.hp2 NA18969.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+18016A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575358 | ||||||
| chr6:10575358
|
AT | A | 19 | a0001c0001t0001g0091a0001c0001t0001g0114a0001c0001t0001g0181others(16): Show | 20 | HG00280.hp2 HG00558.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.919+18035delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | |||||
| chr6:10575454
|
T | C | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.919+18112T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575454 | ||||||
| chr6:10575464
|
A | G | 22 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0265others(19): Show | 22 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.919+18122A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575464 | ||||||
| chr6:10575576
|
G | A | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+18234G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575576 | ||||||
| chr6:10575672
|
CT | C | 54 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(51): Show | 55 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.919+18333delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575672 | |||||
| chr6:10575762
|
C | T | 11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+18420C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575762 | ||||||
| chr6:10575908
|
C | T | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+18566C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575908 | ||||||
| chr6:10575939
|
C | CT | 24 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(21): Show | 25 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.919+18597_919+1859 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575939 | ||||||
| chr6:10576076
|
T | G | 11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+18734T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576076 | ||||||
| chr6:10576089
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+18747C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576089 | ||||||
| chr6:10576090
|
G | A | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+18748G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576090 | ||||||
| chr6:10576150
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.919+18808G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576150 | ||||||
| chr6:10576162
|
G | A | 1 | a0001c0001t0005g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.919+18820G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576162 | ||||||
| chr6:10576254
|
AAAG | A | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+18916_919+1891 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576254 | |||||
| chr6:10576366
|
A | G | 1 | a0001c0001t0014g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+19024A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576366 | ||||||
| chr6:10576401
|
T | C | 26 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(23): Show | 27 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+19059T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576401 | ||||||
| chr6:10576451
|
G | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19109G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576451 | ||||||
| chr6:10576471
|
G | T | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19129G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576471 | ||||||
| chr6:10576479
|
C | T | 8 | a0001c0001t0001g0092a0001c0001t0001g0109a0001c0001t0001g0133others(5): Show | 8 | HG02040.hp2 NA18949.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+19137C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576479 | ||||||
| chr6:10576553
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.919+19211G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576553 | ||||||
| chr6:10576571
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+19229G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576571 | ||||||
| chr6:10576611
|
G | A | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+19269G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576611 | ||||||
| chr6:10576645
|
A | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.919+19303A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576645 | ||||||
| chr6:10576653
|
T | C | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19311T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576653 | ||||||
| chr6:10576654
|
T | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+19312T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576654 | ||||||
| chr6:10576671
|
CAGAA | C | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19333_919+1933 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576671 | |||||
| chr6:10576675
|
A | C | 1 | a0001c0001t0001g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.919+19333A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576675 | ||||||
| chr6:10576697
|
G | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0014g0331 | 3 | HG02622.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+19355G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576697 | ||||||
| chr6:10576707
|
TAGAA | T | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19370_919+1937 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576707 | |||||
| chr6:10576730
|
A | G | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19388A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576730 | ||||||
| chr6:10576796
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0003g0032 | 2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.919+19454G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576796 | ||||||
| chr6:10576804
|
T | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+19462T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576804 | ||||||
| chr6:10576920
|
CAATAAT | C | 12 | a0001c0001t0001g0181a0001c0001t0001g0271a0001c0001t0001g0272others(9): Show | 13 | HG00280.hp2 HG01192.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+19593_919+1959 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576920 | |||||
| chr6:10576967
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.919+19625C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576967 | ||||||
| chr6:10577014
|
G | C | 15 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0310others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+19672G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577014 | ||||||
| chr6:10577140
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.919+19798C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577140 | ||||||
| chr6:10577155
|
C | T | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19813C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577155 | ||||||
| chr6:10577231
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.919+19889G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577231 | ||||||
| chr6:10577304
|
T | C | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19962T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577304 | ||||||
| chr6:10577355
|
C | T | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+20013C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577355 | ||||||
| chr6:10577394
|
A | G | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20052A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577394 | ||||||
| chr6:10577589
|
G | A | 1 | a0001c0001t0015g0299 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.919+20247G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577589 | ||||||
| chr6:10577634
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.919+20292G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577634 | ||||||
| chr6:10577635
|
G | C | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20293G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577635 | ||||||
| chr6:10577725
|
G | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20383G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577725 | ||||||
| chr6:10577730
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0186a0001c0001t0001g0194 | 3 | NA18951.hp2 NA18974.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.919+20388G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577730 | ||||||
| chr6:10577789
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.919+20447C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577789 | ||||||
| chr6:10577885
|
TTCG | T | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+20545_919+2054 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10577885 | |||||
| chr6:10577960
|
C | T | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20618C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577960 | ||||||
| chr6:10577990
|
G | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+20648G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577990 | ||||||
| chr6:10578066
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.919+20724T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578066 | ||||||
| chr6:10578074
|
A | G | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20732A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578074 | ||||||
| chr6:10578167
|
G | C | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+20825G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578167 | ||||||
| chr6:10578345
|
C | G | 5 | a0001c0001t0001g0097a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG00673.hp1 NA18981.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+21003C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578345 | ||||||
| chr6:10578391
|
T | TA | 11 | a0001c0001t0001g0027a0001c0001t0001g0227a0001c0001t0001g0310others(8): Show | 11 | HG00597.hp2 HG02109.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+21065dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578391 | |||||
| chr6:10578391
|
TA | T | 28 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(25): Show | 29 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.919+21065delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578391 | |||||
| chr6:10578445
|
C | CT | 43 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0034others(40): Show | 43 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.919+21124dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578445
|
C | CTT | 24 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0265others(21): Show | 24 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.919+21123_919+2112 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578445
|
C | CTTT | 13 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(10): Show | 13 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+21122_919+2112 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578445
|
C | CTTTT | 7 | a0001c0001t0001g0090a0001c0001t0001g0306a0001c0001t0001g0308others(4): Show | 7 | HG01175.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+21121_919+2112 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578547
|
T | C | 205 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(202): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.919+21205T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578547 | ||||||
| chr6:10578548
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.919+21206G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578548 | ||||||
| chr6:10578592
|
A | G | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21250A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578592 | ||||||
| chr6:10578634
|
G | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21292G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578634 | ||||||
| chr6:10578648
|
G | A | 10 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+21306G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578648 | ||||||
| chr6:10578692
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0008g0335 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+21350T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578692 | ||||||
| chr6:10578726
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0008g0335 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+21384G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578726 | ||||||
| chr6:10578746
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.919+21404C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578746 | ||||||
| chr6:10578759
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.919+21417C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578759 | ||||||
| chr6:10578778
|
G | T | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21436G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578778 | ||||||
| chr6:10578787
|
T | C | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21445T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578787 | ||||||
| chr6:10578800
|
A | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+21458A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578800 | ||||||
| chr6:10578821
|
T | TTTGTTG | 2 | a0001c0001t0004g0274a0001c0001t0006g0001 | 3 | HG02258.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.919+21491_919+2149 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578821 | |||||
| chr6:10578903
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0003g0300 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.919+21561G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578903 | ||||||
| chr6:10578991
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.919+21649G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578991 | ||||||
| chr6:10579066
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+21724C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579066 | ||||||
| chr6:10579139
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.919+21797C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579139 | ||||||
| chr6:10579222
|
C | T | 3 | a0001c0001t0015g0299a0001c0004t0003g0328a0001c0004t0003g0330 | 3 | HG03130.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.919+21880C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579222 | ||||||
| chr6:10579344
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.919+22002T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579344 | ||||||
| chr6:10579453
|
C | T | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+22111C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579453 | ||||||
| chr6:10579611
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+22269C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579611 | ||||||
| chr6:10579643
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.919+22301C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579643 | ||||||
| chr6:10579730
|
G | C | 337 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(334): Show | 339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.919+22388G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579730 | ||||||
| chr6:10579731
|
G | A | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+22389G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579731 | ||||||
| chr6:10579743
|
A | G | 13 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+22401A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579743 | ||||||
| chr6:10579757
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.919+22415A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579757 | ||||||
| chr6:10579780
|
C | T | 6 | a0001c0001t0001g0252a0001c0001t0001g0265a0001c0001t0001g0267others(3): Show | 6 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+22438C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579780 | ||||||
| chr6:10579803
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.919+22461G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579803 | ||||||
| chr6:10579826
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0233 | 2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.919+22484C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579826 | ||||||
| chr6:10579826
|
C | CA | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(121): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.919+22506dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | |||||
| chr6:10579826
|
C | CAA | 24 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0024others(21): Show | 24 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.919+22505_919+2250 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | |||||
| chr6:10579826
|
C | CAAACA | 9 | a0001c0001t0001g0310a0001c0001t0001g0313a0001c0001t0001g0314others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+22487_919+2248 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | |||||
| chr6:10579827
|
A | AAAC | 23 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0140others(20): Show | 23 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.919+22487_919+2248 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579827 | |||||
| chr6:10579829
|
A | AC | 4 | a0001c0001t0001g0035a0001c0001t0001g0158a0001c0001t0001g0318others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+22487_919+2248 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579829 | ||||||
| chr6:10579829
|
A | ACAAAC | 3 | a0001c0001t0001g0090a0001c0001t0005g0045a0001c0001t0007g0016 | 3 | HG02630.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.919+22487_919+2248 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579829 | ||||||
| chr6:10579830
|
A | C | 11 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(8): Show | 12 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+22488A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579830 | ||||||
| chr6:10579831
|
A | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0308a0001c0001t0003g0312others(2): Show | 5 | HG01243.hp1 NA19030.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+22489A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579831 | ||||||
| chr6:10579832
|
A | C | 1 | a0001c0001t0014g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+22490A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579832 | ||||||
| chr6:10579834
|
A | C | 11 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(8): Show | 12 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+22492A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579834 | ||||||
| chr6:10579835
|
A | C | 3 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0008g0335 | 3 | HG03579.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+22493A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579835 | ||||||
| chr6:10579837
|
A | C | 2 | a0001c0001t0001g0302a0001c0001t0003g0300 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.919+22495A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579837 | ||||||
| chr6:10579839
|
A | C | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.919+22497A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579839 | ||||||
| chr6:10579840
|
A | C | 4 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+22498A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579840 | ||||||
| chr6:10579841
|
A | ACC | 11 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0294others(8): Show | 12 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+22499_919+2250 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579841 | ||||||
| chr6:10579841
|
A | C | 36 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(33): Show | 36 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.919+22499A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579841 | ||||||
| chr6:10579886
|
G | T | 15 | a0001c0001t0001g0091a0001c0001t0001g0271a0001c0001t0001g0272others(12): Show | 16 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+22544G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579886 | ||||||
| chr6:10579900
|
A | G | 7 | a0001c0001t0001g0294a0001c0001t0004g0274a0001c0001t0004g0275others(4): Show | 8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+22558A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579900 | ||||||
| chr6:10580061
|
C | T | 52 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(49): Show | 53 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.919+22719C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580061 | ||||||
| chr6:10580219
|
A | G | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0311others(5): Show | 8 | HG02630.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+22877A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580219 | ||||||
| chr6:10580252
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+22910G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580252 | ||||||
| chr6:10580271
|
A | G | 18 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0140others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+22929A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580271 | ||||||
| chr6:10580274
|
G | GGGGGGT | 13 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0310others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+22935_919+2293 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10580274 | |||||
| chr6:10580375
|
C | T | 1 | a0005c0005t0001g0319 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.919+23033C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580375 | ||||||
| chr6:10580394
|
A | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.919+23052A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580394 | ||||||
| chr6:10580435
|
C | T | 48 | a0001c0001t0001g0067a0001c0001t0001g0090a0001c0001t0001g0095others(45): Show | 49 | HG00735.hp2 HG01099.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.919+23093C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580435 | ||||||
| chr6:10580501
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.919+23159C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580501 | ||||||
| chr6:10580592
|
G | A | 4 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0317others(1): Show | 4 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+23250G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580592 | ||||||
| chr6:10580615
|
T | TA | 15 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(12): Show | 15 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.919+23285dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10580615 | |||||
| chr6:10580615
|
TA | T | 10 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0155others(7): Show | 10 | HG01175.hp2 HG01361.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+23285delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10580615 | |||||
| chr6:10580668
|
G | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+23326G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580668 | ||||||
| chr6:10580677
|
T | G | 50 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(47): Show | 51 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.919+23335T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580677 | ||||||
| chr6:10580723
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+23381C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580723 | ||||||
| chr6:10580840
|
G | C | 17 | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0272others(14): Show | 18 | HG01192.hp1 HG01361.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+23498G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580840 | ||||||
| chr6:10580872
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.919+23530T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580872 | ||||||
| chr6:10580919
|
G | C | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.919+23577G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580919 | ||||||
| chr6:10580935
|
G | C | 1 | a0001c0001t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.919+23593G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580935 | ||||||
| chr6:10580956
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+23614G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580956 | ||||||
| chr6:10580972
|
A | G | 10 | a0001c0001t0001g0095a0001c0001t0001g0310a0001c0001t0001g0313others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+23630A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580972 | ||||||
| chr6:10581064
|
C | T | 7 | a0001c0001t0001g0294a0001c0001t0004g0274a0001c0001t0004g0275others(4): Show | 8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+23722C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581064 | ||||||
| chr6:10581099
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+23757A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581099 | ||||||
| chr6:10581263
|
A | T | 1 | a0001c0001t0001g0249 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.919+23921A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581263 | ||||||
| chr6:10581263
|
ATTTATTT | A | 3 | a0001c0002t0001g0281a0001c0002t0001g0282a0001c0002t0001g0295 | 3 | HG01099.hp2 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.919+23939_919+2394 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581263 | |||||
| chr6:10581291
|
A | C | 7 | a0001c0001t0001g0294a0001c0001t0004g0274a0001c0001t0004g0275others(4): Show | 8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+23949A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581291 | ||||||
| chr6:10581309
|
T | C | 16 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0265others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+23967T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581309 | ||||||
| chr6:10581337
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.919+23995C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581337 | ||||||
| chr6:10581565
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24223C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581565 | ||||||
| chr6:10581727
|
CA | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0154a0001c0001t0001g0174others(3): Show | 6 | HG00544.hp1 HG00558.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+24388delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581727 | |||||
| chr6:10581733
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.919+24391G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581733 | ||||||
| chr6:10581763
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24421G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581763 | ||||||
| chr6:10581793
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.919+24451A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581793 | ||||||
| chr6:10581803
|
T | G | 3 | a0001c0001t0015g0299a0001c0004t0003g0328a0001c0004t0003g0330 | 3 | HG03130.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.919+24461T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581803 | ||||||
| chr6:10581931
|
A | AGT | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24597_919+2459 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581931 | |||||
| chr6:10581961
|
AAT | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24631_919+2463 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581961 | |||||
| chr6:10582010
|
G | GTA | 5 | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0001g0302others(2): Show | 5 | HG02523.hp2 HG02896.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+24674_919+2467 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582010 | |||||
| chr6:10582016
|
ATG | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0255 | 3 | HG01074.hp2 HG02155.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.919+24676_919+2467 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582016 | |||||
| chr6:10582018
|
G | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.919+24676G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582018 | ||||||
| chr6:10582043
|
T | TATATATT others(3): Show |
3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24705_919+2470 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582043 | |||||
| chr6:10582059
|
CAT | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24718_919+2471 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582059 | ||||||
| chr6:10582095
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0004g0268a0001c0001t0005g0045others(1): Show | 4 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+24753T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582095 | ||||||
| chr6:10582113
|
T | TATAC | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24772_919+2477 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582113 | |||||
| chr6:10582116
|
A | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24774A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582116 | ||||||
| chr6:10582118
|
A | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24776A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582118 | ||||||
| chr6:10582120
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24778C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582120 | ||||||
| chr6:10582125
|
A | T | 36 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(33): Show | 36 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.919+24783A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582125 | ||||||
| chr6:10582172
|
T | TTATATAA others(36): Show |
3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24839_919+2484 others(47): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582172 | |||||
| chr6:10582177
|
T | G | 14 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(11): Show | 14 | HG00408.hp1 HG01928.hp2 NA18946.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+24835T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582177 | ||||||
| chr6:10582221
|
ATTATATA others(1): Show |
A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24880_919+2488 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582221 | ||||||
| chr6:10582231
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24889T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582231 | ||||||
| chr6:10582231
|
T | TTTAAATA others(29): Show |
1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.919+24903_919+2493 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582231 | |||||
| chr6:10582233
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24891T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582233 | ||||||
| chr6:10582241
|
TAAAA | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24900_919+2490 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582241 | ||||||
| chr6:10582242
|
A | AAAATATA others(28): Show |
10 | a0001c0001t0001g0049a0001c0001t0001g0116a0001c0001t0001g0294others(7): Show | 11 | HG01346.hp2 HG01361.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+24916_919+2495 others(39): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582242 | |||||
| chr6:10582277
|
T | TA | 11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+24938dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582277 | |||||
| chr6:10582280
|
A | ATATAT | 24 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0140others(21): Show | 24 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.919+24939_919+2494 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582280 | |||||
| chr6:10582285
|
TATA | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24947_919+2494 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582285 | |||||
| chr6:10582288
|
A | AATATATA others(30): Show |
11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+24950_919+2495 others(41): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582288 | |||||
| chr6:10582289
|
ATAT | A | 3 | a0001c0001t0015g0299a0001c0004t0003g0328a0001c0004t0003g0330 | 3 | HG03130.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.919+24950_919+2495 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582289 | |||||
| chr6:10582292
|
T | A | 1 | a0001c0001t0010g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919+24950T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582292 | ||||||
| chr6:10582303
|
T | TTAATATA others(29): Show |
1 | a0001c0001t0002g0117 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.919+24998_919+2503 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582303 | |||||
| chr6:10582303
|
TTAATATA others(29): Show |
T | 17 | a0001c0001t0001g0095a0001c0001t0001g0140a0001c0001t0001g0265others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+24998_919+2503 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582303 | |||||
| chr6:10582339
|
A | ATATT | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24999_919+2500 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582339 | |||||
| chr6:10582346
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0007g0016 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25004A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582346 | ||||||
| chr6:10582351
|
A | T | 2 | a0001c0001t0001g0090a0001c0001t0007g0016 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25009A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582351 | ||||||
| chr6:10582359
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0007g0016 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25017A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582359 | ||||||
| chr6:10582367
|
T | A | 2 | a0001c0001t0001g0090a0001c0001t0007g0016 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25025T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582367 | ||||||
| chr6:10582371
|
C | G | 2 | a0001c0001t0001g0090a0001c0001t0007g0016 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25029C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582371 | ||||||
| chr6:10582373
|
ATAATT | A | 16 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(13): Show | 16 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+25036_919+2504 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582373 | |||||
| chr6:10582375
|
A | AT | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25033_919+2503 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582375 | ||||||
| chr6:10582378
|
T | TTAATATT others(24): Show |
4 | a0001c0001t0001g0204a0001c0001t0001g0280a0001c0001t0002g0129others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+25060_919+2509 others(35): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582378 | |||||
| chr6:10582378
|
T | TTAATATT others(86): Show |
7 | a0001c0001t0001g0294a0001c0001t0004g0274a0001c0001t0004g0275others(4): Show | 8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+25090_919+2509 others(97): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582378 | |||||
| chr6:10582385
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25043T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582385 | ||||||
| chr6:10582388
|
T | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25046T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582388 | ||||||
| chr6:10582390
|
ATATACT | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25049_919+2505 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582390 | ||||||
| chr6:10582400
|
A | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25058A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582400 | ||||||
| chr6:10582406
|
AGTATAAT others(3): Show |
A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25065_919+2507 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582406 | ||||||
| chr6:10582419
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25077T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582419 | ||||||
| chr6:10582426
|
CTATAAT | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25086_919+2509 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582426 | |||||
| chr6:10582438
|
A | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25096A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582438 | ||||||
| chr6:10582441
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25099T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582441 | ||||||
| chr6:10582443
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25101T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582443 | ||||||
| chr6:10582453
|
T | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25111T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582453 | ||||||
| chr6:10582456
|
A | G | 1 | a0001c0001t0002g0117 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.919+25114A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582456 | ||||||
| chr6:10582456
|
ATAATAAA others(1): Show |
A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25115_919+2512 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582456 | ||||||
| chr6:10582462
|
A | T | 1 | a0001c0001t0003g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.919+25120A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582462 | ||||||
| chr6:10582463
|
ATATAATA others(5): Show |
A | 5 | a0001c0001t0001g0211a0001c0001t0001g0245a0001c0001t0001g0266others(2): Show | 5 | HG00544.hp2 HG02698.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+25145_919+2515 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582463 | |||||
| chr6:10582466
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25124T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582466 | ||||||
| chr6:10582475
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25133C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582475 | ||||||
| chr6:10582480
|
A | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25138A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582480 | ||||||
| chr6:10582481
|
T | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25139T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582481 | ||||||
| chr6:10582481
|
TATATACT others(10): Show |
T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+25145_919+2516 others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582481 | |||||
| chr6:10582482
|
ATATAC | A | 22 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0140others(19): Show | 22 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.919+25145_919+2514 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582482 | |||||
| chr6:10582486
|
AC | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25145delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582486 | ||||||
| chr6:10582487
|
C | A | 19 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(16): Show | 20 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+25145C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582487 | ||||||
| chr6:10582491
|
A | AATACATC | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25152_919+2515 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582491 | |||||
| chr6:10582498
|
A | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25156A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582498 | ||||||
| chr6:10582501
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+25159A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582501 | ||||||
| chr6:10582503
|
A | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25161A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582503 | ||||||
| chr6:10582519
|
T | TAC | 10 | a0001c0001t0001g0091a0001c0001t0001g0294a0001c0001t0001g0318others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+25178_919+2517 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582519 | |||||
| chr6:10582522
|
T | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25180T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582522 | ||||||
| chr6:10582522
|
T | C | 10 | a0001c0001t0001g0091a0001c0001t0001g0294a0001c0001t0001g0318others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+25180T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582522 | ||||||
| chr6:10582526
|
C | T | 19 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(16): Show | 20 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+25184C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582526 | ||||||
| chr6:10582528
|
TCA | T | 10 | a0001c0001t0001g0091a0001c0001t0001g0294a0001c0001t0001g0318others(7): Show | 11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+25187_919+2518 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582528 | ||||||
| chr6:10582531
|
T | TATATAAT others(14): Show |
9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25193_919+2519 others(25): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582531 | |||||
| chr6:10582536
|
T | A | 21 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(18): Show | 22 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.919+25194T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582536 | ||||||
| chr6:10582536
|
T | TATATA | 26 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0140others(23): Show | 26 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.919+25195_919+2519 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582536 | |||||
| chr6:10582546
|
G | A | 49 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(46): Show | 50 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.919+25204G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582546 | ||||||
| chr6:10582550
|
A | T | 2 | a0001c0001t0001g0321a0001c0001t0005g0326 | 2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919+25208A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582550 | ||||||
| chr6:10582552
|
T | TATA | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25211_919+2521 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582552 | |||||
| chr6:10582572
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0092a0001c0001t0001g0109others(6): Show | 9 | HG02040.hp2 NA18949.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25230A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582572 | ||||||
| chr6:10582583
|
C | T | 4 | a0001c0001t0001g0302a0001c0001t0003g0300a0001c0001t0008g0335others(1): Show | 4 | HG02896.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+25241C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582583 | ||||||
| chr6:10582613
|
A | AAT | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25280_919+2528 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582613 | |||||
| chr6:10582617
|
T | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0033others(16): Show | 20 | HG00323.hp1 HG00558.hp1 HG03490.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+25275T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582617 | ||||||
| chr6:10582624
|
T | A | 190 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(187): Show | 191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.919+25282T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582624 | ||||||
| chr6:10582721
|
C | CT | 7 | a0001c0001t0001g0083a0001c0001t0001g0153a0001c0001t0001g0155others(4): Show | 7 | HG00735.hp2 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+25388dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582721 | |||||
| chr6:10582730
|
TC | T | 33 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(30): Show | 33 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.919+25390delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582730 | |||||
| chr6:10582770
|
G | C | 19 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(16): Show | 19 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.919+25428G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582770 | ||||||
| chr6:10582804
|
AAAC | A | 47 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(44): Show | 48 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.919+25477_919+2547 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582804 | |||||
| chr6:10582897
|
A | G | 11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+25555A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582897 | ||||||
| chr6:10583009
|
G | T | 1 | a0001c0001t0001g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.919+25667G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583009 | ||||||
| chr6:10583112
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0187a0001c0001t0001g0197 | 3 | NA18951.hp1 NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.919+25770G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583112 | ||||||
| chr6:10583229
|
C | T | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0302others(5): Show | 8 | HG01192.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+25887C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583229 | ||||||
| chr6:10583268
|
A | C | 8 | a0001c0001t0001g0280a0001c0001t0001g0294a0001c0001t0004g0274others(5): Show | 9 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+25926A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583268 | ||||||
| chr6:10583356
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.919+26014C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583356 | ||||||
| chr6:10583370
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+26028G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583370 | ||||||
| chr6:10583432
|
C | T | 1 | a0001c0001t0004g0268 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+26090C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583432 | ||||||
| chr6:10583468
|
C | T | 2 | a0001c0001t0001g0317a0005c0005t0001g0319 | 2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.919+26126C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583468 | ||||||
| chr6:10583492
|
T | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+26150T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583492 | ||||||
| chr6:10583543
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+26201G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583543 | ||||||
| chr6:10583868
|
C | G | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+26526C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583868 | ||||||
| chr6:10583922
|
A | G | 21 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+26580A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583922 | ||||||
| chr6:10583943
|
C | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+26601C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583943 | ||||||
| chr6:10583960
|
G | C | 28 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095others(25): Show | 29 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.919+26618G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583960 | ||||||
| chr6:10583991
|
A | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0267 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.919+26649A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583991 | ||||||
| chr6:10584047
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+26705G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584047 | ||||||
| chr6:10584084
|
T | C | 28 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095others(25): Show | 29 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.919+26742T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584084 | ||||||
| chr6:10584113
|
C | T | 9 | a0001c0001t0001g0280a0001c0001t0001g0294a0001c0001t0004g0274others(6): Show | 10 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+26771C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584113 | ||||||
| chr6:10584129
|
C | A | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.919+26787C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584129 | ||||||
| chr6:10584170
|
A | C | 2 | a0001c0001t0001g0321a0001c0001t0005g0326 | 2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919+26828A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584170 | ||||||
| chr6:10584211
|
A | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0192 | 2 | NA18956.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.919+26869A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584211 | ||||||
| chr6:10584232
|
A | C | 18 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0126others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+26890A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584232 | ||||||
| chr6:10584234
|
T | C | 8 | a0001c0001t0001g0280a0001c0001t0001g0294a0001c0001t0004g0274others(5): Show | 9 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+26892T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584234 | ||||||
| chr6:10584438
|
G | A | 146 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(143): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.919+27096G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584438 | ||||||
| chr6:10584624
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+27282G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584624 | ||||||
| chr6:10584673
|
C | T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+27331C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584673 | ||||||
| chr6:10584735
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+27393C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584735 | ||||||
| chr6:10584917
|
C | T | 47 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(44): Show | 48 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.919+27575C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584917 | ||||||
| chr6:10584956
|
G | C | 199 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(196): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.919+27614G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584956 | ||||||
| chr6:10584977
|
T | C | 39 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(36): Show | 40 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.919+27635T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584977 | ||||||
| chr6:10585028
|
AGTCAGTG others(3): Show |
A | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.919+27689_919+2769 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | |||||
| chr6:10585028
|
AGTCAGTG others(9): Show |
A | 14 | a0001c0001t0001g0095a0001c0001t0001g0310a0001c0001t0001g0313others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+27689_919+2770 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | |||||
| chr6:10585028
|
AGTCAGTG others(11): Show |
A | 2 | a0001c0001t0001g0090a0001c0001t0001g0308 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.919+27689_919+2770 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | |||||
| chr6:10585032
|
A | AGT | 8 | a0001c0001t0001g0086a0001c0001t0001g0125a0001c0001t0001g0144others(5): Show | 8 | HG00735.hp1 HG01123.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+27736_919+2773 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
A | AGTGT | 9 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0180others(6): Show | 9 | HG01243.hp2 HG03017.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+27734_919+2773 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGT | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 123 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.919+27736_919+2773 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGT | A | 58 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0064others(55): Show | 58 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.919+27734_919+2773 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGT | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0015others(20): Show | 23 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.919+27732_919+2773 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.919+27728_919+2773 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(7): Show |
A | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0321others(1): Show | 4 | HG00735.hp2 HG03516.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+27724_919+2773 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0002g0166 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.919+27722_919+2773 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(11): Show |
A | 4 | a0001c0001t0001g0109a0001c0001t0001g0302a0001c0001t0003g0300others(1): Show | 4 | HG02896.hp2 HG06807.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+27720_919+2773 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585052
|
TGTGTGTG others(21): Show |
T | 8 | a0001c0001t0001g0280a0001c0001t0001g0294a0001c0001t0004g0274others(5): Show | 9 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+27712_919+2773 others(32): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585052 | |||||
| chr6:10585064
|
TGTGTGTG others(9): Show |
T | 3 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0311 | 3 | HG02109.hp2 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.919+27724_919+2773 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585064 | |||||
| chr6:10585066
|
TGTGTGTG others(7): Show |
T | 4 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0004t0003g0328others(1): Show | 4 | HG02622.hp1 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+27726_919+2773 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585066 | |||||
| chr6:10585066
|
TGTGTGTG others(9): Show |
T | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+27726_919+2774 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585066 | |||||
| chr6:10585068
|
TGTGTGTG others(5): Show |
T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+27728_919+2773 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585068 | |||||
| chr6:10585070
|
TGTGTGTG others(3): Show |
T | 3 | a0001c0001t0001g0266a0001c0001t0003g0238a0001c0001t0014g0331 | 3 | HG01358.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+27730_919+2773 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585070 | |||||
| chr6:10585074
|
TGTGTGC | T | 3 | a0001c0001t0001g0185a0001c0001t0001g0195a0001c0001t0001g0257 | 3 | HG02273.hp1 HG02293.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.919+27734_919+2773 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585074 | |||||
| chr6:10585076
|
T | C | 2 | a0001c0001t0001g0006a0001c0001t0002g0023 | 2 | HG01928.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.919+27734T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585076 | ||||||
| chr6:10585078
|
T | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0022others(37): Show | 40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.919+27736T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585078 | ||||||
| chr6:10585078
|
TGC | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0002g0205 | 3 | HG01516.hp2 HG01517.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.919+27741_919+2774 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585078 | |||||
| chr6:10585078
|
TGCGC | T | 18 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0126others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+27739_919+2774 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585078 | |||||
| chr6:10585081
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+27739G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585081 | ||||||
| chr6:10585083
|
G | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+27741G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585083 | ||||||
| chr6:10585162
|
T | A | 21 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+27820T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585162 | ||||||
| chr6:10585193
|
G | T | 21 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+27851G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585193 | ||||||
| chr6:10585261
|
C | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+27919C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585261 | ||||||
| chr6:10585368
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.919+28026G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585368 | ||||||
| chr6:10585419
|
G | T | 2 | a0001c0001t0001g0147a0001c0001t0002g0229 | 2 | HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.919+28077G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585419 | ||||||
| chr6:10585443
|
G | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0179 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.919+28101G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585443 | ||||||
| chr6:10585471
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.919+28129C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585471 | ||||||
| chr6:10585618
|
C | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+28276C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585618 | ||||||
| chr6:10585619
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0007g0016 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+28277G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585619 | ||||||
| chr6:10585747
|
A | G | 21 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+28405A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585747 | ||||||
| chr6:10585773
|
A | C | 51 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(48): Show | 52 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.919+28431A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585773 | ||||||
| chr6:10585874
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.919+28532C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585874 | ||||||
| chr6:10585878
|
C | T | 2 | a0001c0001t0001g0321a0001c0001t0005g0326 | 2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919+28536C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585878 | ||||||
| chr6:10585879
|
G | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+28537G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585879 | ||||||
| chr6:10585880
|
G | A | 18 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0126others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+28538G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585880 | ||||||
| chr6:10586199
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.919+28857A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586199 | ||||||
| chr6:10586378
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0002g0221 | 2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.919+29036A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586378 | ||||||
| chr6:10586386
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0002g0248 | 2 | HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.919+29044C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586386 | ||||||
| chr6:10586494
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919+29152G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586494 | ||||||
| chr6:10586696
|
A | G | 7 | a0001c0001t0001g0280a0001c0001t0001g0294a0001c0001t0004g0275others(4): Show | 8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+29354A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586696 | ||||||
| chr6:10586805
|
C | G | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(327): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.919+29463C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586805 | ||||||
| chr6:10586823
|
A | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+29481A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586823 | ||||||
| chr6:10587120
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0128 | 2 | HG00621.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.919+29778G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587120 | ||||||
| chr6:10587156
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.919+29814A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587156 | ||||||
| chr6:10587188
|
G | A | 13 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0001g0053others(10): Show | 13 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+29846G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587188 | ||||||
| chr6:10587280
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.919+29938C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587280 | ||||||
| chr6:10587416
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0067others(10): Show | 13 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+30074C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587416 | ||||||
| chr6:10587463
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0316 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.919+30121T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587463 | ||||||
| chr6:10587603
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.919+30261A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587603 | ||||||
| chr6:10587781
|
T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0266a0001c0001t0001g0293others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+30439T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587781 | ||||||
| chr6:10587857
|
A | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0256 | 2 | HG00438.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.919+30515A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587857 | ||||||
| chr6:10588199
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.919+30857A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588199 | ||||||
| chr6:10588237
|
T | C | 11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+30895T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588237 | ||||||
| chr6:10588288
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.919+30946A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588288 | ||||||
| chr6:10588374
|
TC | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+31034delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588374 | |||||
| chr6:10588397
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.919+31055C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588397 | ||||||
| chr6:10588710
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.919+31368G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588710 | ||||||
| chr6:10588713
|
A | G | 11 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0308others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+31371A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588713 | ||||||
| chr6:10588785
|
A | ATG | 4 | a0001c0001t0009g0046a0001c0001t0009g0246a0001c0001t0010g0309others(1): Show | 4 | HG01081.hp1 HG01978.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+31466_919+3146 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | |||||
| chr6:10588785
|
ATG | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(172): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.919+31466_919+3146 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | |||||
| chr6:10588785
|
ATGTG | A | 11 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(8): Show | 11 | HG00140.hp1 HG00597.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+31464_919+3146 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | |||||
| chr6:10588831
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.919+31489A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588831 | ||||||
| chr6:10588831
|
ATGTGTGT others(4): Show |
A | 4 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+31504_919+3151 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588831 | |||||
| chr6:10588890
|
C | CGTGTGTG others(4): Show |
196 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.919+31552_919+3156 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588890 | |||||
| chr6:10588925
|
G | T | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | NA18980.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.919+31583G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588925 | ||||||
| chr6:10588983
|
T | C | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+31641T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588983 | ||||||
| chr6:10589078
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02280.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.919+31736G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589078 | ||||||
| chr6:10589102
|
AGT | A | 161 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(158): Show | 161 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.919+31770_919+3177 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589102 | |||||
| chr6:10589113
|
GGT | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283 | 3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.919+31780_919+3178 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589113 | |||||
| chr6:10589156
|
GTGCGTGT others(26): Show |
G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+31817_919+3184 others(37): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589156 | |||||
| chr6:10589188
|
C | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(329): Show | 334 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.919+31846C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589188 | ||||||
| chr6:10589292
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.919+31950G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589292 | ||||||
| chr6:10589306
|
GGTGTGTT others(51): Show |
G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+31987_920-3196 others(62): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589306 | |||||
| chr6:10589398
|
G | C | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.920-31953G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589398 | ||||||
| chr6:10589421
|
T | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-31930T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589421 | ||||||
| chr6:10589425
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.920-31926T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589425 | ||||||
| chr6:10589469
|
G | C | 1 | a0001c0001t0005g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.920-31882G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589469 | ||||||
| chr6:10589786
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.920-31565T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589786 | ||||||
| chr6:10589808
|
TATACTC | T | 3 | a0001c0001t0001g0321a0001c0001t0004g0274a0001c0001t0012g0243 | 3 | HG02970.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.920-31541_920-3153 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589808 | |||||
| chr6:10590086
|
T | C | 1 | a0001c0001t0010g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920-31265T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590086 | ||||||
| chr6:10590242
|
T | C | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-31109T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590242 | ||||||
| chr6:10590362
|
C | T | 7 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0115others(4): Show | 7 | HG02080.hp2 HG02155.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-30989C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590362 | ||||||
| chr6:10590397
|
C | CA | 33 | a0001c0001t0001g0027a0001c0001t0001g0056a0001c0001t0001g0062others(30): Show | 33 | HG00140.hp1 HG00408.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.920-30938dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10590397 | |||||
| chr6:10590559
|
A | AT | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.920-30779dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10590559 | |||||
| chr6:10590673
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.920-30678C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590673 | ||||||
| chr6:10590711
|
G | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-30640G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590711 | ||||||
| chr6:10590798
|
C | T | 147 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(144): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.920-30553C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590798 | ||||||
| chr6:10590848
|
G | A | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 150 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.920-30503G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590848 | ||||||
| chr6:10590918
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-30433G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590918 | ||||||
| chr6:10591101
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.920-30250C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591101 | ||||||
| chr6:10591278
|
A | T | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.920-30073A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591278 | ||||||
| chr6:10591293
|
C | A | 1 | a0001c0001t0001g0255 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.920-30058C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591293 | ||||||
| chr6:10591396
|
C | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-29955C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591396 | ||||||
| chr6:10591469
|
T | G | 22 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0140others(19): Show | 22 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-29882T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591469 | ||||||
| chr6:10591598
|
G | T | 1 | a0001c0001t0002g0157 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.920-29753G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591598 | ||||||
| chr6:10591732
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.920-29619T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591732 | ||||||
| chr6:10591762
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.920-29589A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591762 | ||||||
| chr6:10591901
|
C | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-29450C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591901 | ||||||
| chr6:10591928
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.920-29423A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591928 | ||||||
| chr6:10592095
|
A | AAACGTCA others(8): Show |
9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-29255_920-2924 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10592095 | |||||
| chr6:10592113
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.920-29238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592113 | ||||||
| chr6:10592162
|
A | G | 31 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(28): Show | 31 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.920-29189A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592162 | ||||||
| chr6:10592571
|
G | C | 1 | a0001c0001t0001g0333 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.920-28780G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592571 | ||||||
| chr6:10592753
|
A | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.920-28598A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592753 | ||||||
| chr6:10592922
|
T | C | 3 | a0001c0001t0001g0310a0001c0001t0005g0045a0001c0001t0015g0299 | 3 | HG02622.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.920-28429T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592922 | ||||||
| chr6:10593018
|
G | A | 8 | a0001c0001t0001g0293a0001c0001t0001g0308a0001c0001t0001g0323others(5): Show | 8 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-28333G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593018 | ||||||
| chr6:10593033
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28318G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593033 | ||||||
| chr6:10593051
|
G | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28300G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593051 | ||||||
| chr6:10593226
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28125G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593226 | ||||||
| chr6:10593230
|
T | C | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.920-28121T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593230 | ||||||
| chr6:10593250
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.920-28101C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593250 | ||||||
| chr6:10593346
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28005G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593346 | ||||||
| chr6:10593383
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.920-27968A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593383 | ||||||
| chr6:10593417
|
A | C | 1 | a0001c0001t0010g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920-27934A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593417 | ||||||
| chr6:10593525
|
A | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27826A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593525 | ||||||
| chr6:10593534
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.920-27817C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593534 | ||||||
| chr6:10593568
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920-27783G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593568 | ||||||
| chr6:10593595
|
T | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27756T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593595 | ||||||
| chr6:10593670
|
T | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27681T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593670 | ||||||
| chr6:10593730
|
A | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27621A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593730 | ||||||
| chr6:10593776
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.920-27575G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593776 | ||||||
| chr6:10593864
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG00408.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.920-27487G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593864 | ||||||
| chr6:10593877
|
C | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27474C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593877 | ||||||
| chr6:10593885
|
C | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27466C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593885 | ||||||
| chr6:10593902
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.920-27449G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593902 | ||||||
| chr6:10594027
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27324G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594027 | ||||||
| chr6:10594249
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.920-27102G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594249 | ||||||
| chr6:10594513
|
T | C | 4 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-26838T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594513 | ||||||
| chr6:10594575
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283 | 3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-26776G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594575 | ||||||
| chr6:10594615
|
G | C | 1 | a0001c0001t0001g0015 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.920-26736G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594615 | ||||||
| chr6:10594647
|
T | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26704T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594647 | ||||||
| chr6:10594685
|
C | T | 5 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0271others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-26666C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594685 | ||||||
| chr6:10594832
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26519G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594832 | ||||||
| chr6:10594852
|
C | CTT | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26490_920-2648 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10594852 | |||||
| chr6:10594889
|
A | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283 | 3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-26462A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594889 | ||||||
| chr6:10594940
|
GGCTCAA | G | 8 | a0001c0001t0001g0293a0001c0001t0001g0308a0001c0001t0001g0323others(5): Show | 8 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-26408_920-2640 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10594940 | |||||
| chr6:10595266
|
C | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26085C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595266 | ||||||
| chr6:10595427
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.920-25924G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595427 | ||||||
| chr6:10595558
|
T | TGA | 35 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0091others(32): Show | 35 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-25792_920-2579 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10595558 | |||||
| chr6:10595558
|
T | TGC | 4 | a0001c0001t0001g0140a0001c0001t0001g0318a0001c0001t0001g0320others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-25792_920-2579 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10595558 | |||||
| chr6:10595565
|
C | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25786C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595565 | ||||||
| chr6:10595592
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.920-25759T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595592 | ||||||
| chr6:10595606
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0002g0160 | 2 | NA18968.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.920-25745G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595606 | ||||||
| chr6:10595672
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283 | 3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-25679C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595672 | ||||||
| chr6:10595681
|
G | GA | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25662dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10595681 | |||||
| chr6:10595759
|
T | G | 1 | a0001c0001t0001g0062 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.920-25592T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595759 | ||||||
| chr6:10595773
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.920-25578G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595773 | ||||||
| chr6:10595804
|
G | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25547G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595804 | ||||||
| chr6:10595850
|
A | G | 4 | a0001c0001t0001g0302a0001c0001t0003g0300a0001c0001t0008g0303others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-25501A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595850 | ||||||
| chr6:10595940
|
A | G | 4 | a0001c0001t0001g0302a0001c0001t0003g0300a0001c0001t0008g0303others(1): Show | 4 | HG02055.hp2 HG02896.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-25411A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595940 | ||||||
| chr6:10595949
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(7): Show | 10 | HG00408.hp1 HG02300.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-25402G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595949 | ||||||
| chr6:10595990
|
A | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25361A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595990 | ||||||
| chr6:10596114
|
C | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25237C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596114 | ||||||
| chr6:10596281
|
T | C | 3 | a0001c0001t0002g0009a0001c0001t0002g0014a0001c0001t0002g0152 | 3 | NA18971.hp1 NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.920-25070T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596281 | ||||||
| chr6:10596320
|
A | G | 107 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0031others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.920-25031A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596320 | ||||||
| chr6:10596373
|
T | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.920-24978T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596373 | ||||||
| chr6:10596387
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 190 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.920-24964G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596387 | ||||||
| chr6:10596453
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920-24898G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596453 | ||||||
| chr6:10596504
|
G | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24847G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596504 | ||||||
| chr6:10596520
|
C | CA | 16 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0067others(13): Show | 16 | HG00140.hp1 HG00323.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.920-24819dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10596520 | |||||
| chr6:10596555
|
G | A | 9 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0308others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24796G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596555 | ||||||
| chr6:10596669
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0215 | 2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.920-24682C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596669 | ||||||
| chr6:10596734
|
T | TA | 12 | a0001c0001t0001g0038a0001c0001t0001g0056a0001c0001t0001g0067others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-24605dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10596734 | |||||
| chr6:10596799
|
CCTTCAGC others(5): Show |
C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24549_920-2453 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10596799 | |||||
| chr6:10596897
|
A | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24454A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596897 | ||||||
| chr6:10596997
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.920-24354T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596997 | ||||||
| chr6:10597153
|
C | CT | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.920-24178dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | |||||
| chr6:10597153
|
C | CTT | 15 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0116others(12): Show | 15 | HG01070.hp2 HG01175.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-24179_920-2417 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | |||||
| chr6:10597153
|
CT | C | 29 | a0001c0001t0001g0062a0001c0001t0001g0091a0001c0001t0001g0095others(26): Show | 29 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.920-24178delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | |||||
| chr6:10597386
|
C | T | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-23965C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597386 | ||||||
| chr6:10597447
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0159a0001c0001t0001g0226 | 3 | HG02572.hp2 HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.920-23904G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597447 | ||||||
| chr6:10597613
|
T | TTTG | 15 | a0001c0001t0001g0140a0001c0001t0001g0265a0001c0001t0001g0266others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-23723_920-2372 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597613 | |||||
| chr6:10597672
|
G | A | 1 | a0001c0001t0004g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.920-23679G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597672 | ||||||
| chr6:10597700
|
A | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-23651A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597700 | ||||||
| chr6:10597715
|
T | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-23636T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597715 | ||||||
| chr6:10597842
|
C | T | 2 | a0001c0001t0002g0054a0003c0008t0001g0037 | 2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.920-23509C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597842 | ||||||
| chr6:10597853
|
T | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 179 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.920-23498T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597853 | ||||||
| chr6:10597903
|
C | A | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-23448C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597903 | ||||||
| chr6:10597920
|
CT | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0086others(3): Show | 6 | HG01975.hp2 HG02896.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-23424delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597920 | |||||
| chr6:10598102
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.920-23249G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598102 | ||||||
| chr6:10598109
|
C | T | 1 | a0001c0001t0003g0300 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.920-23242C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598109 | ||||||
| chr6:10598404
|
G | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22947G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598404 | ||||||
| chr6:10598620
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-22731A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598620 | ||||||
| chr6:10598636
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.920-22715C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598636 | ||||||
| chr6:10598672
|
C | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22679C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598672 | ||||||
| chr6:10598865
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22486G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598865 | ||||||
| chr6:10598966
|
T | C | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22385T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598966 | ||||||
| chr6:10598973
|
G | C | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.920-22378G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598973 | ||||||
| chr6:10599046
|
T | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22305T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599046 | ||||||
| chr6:10599065
|
C | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22286C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599065 | ||||||
| chr6:10599087
|
G | A | 9 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0189others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22264G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599087 | ||||||
| chr6:10599089
|
C | T | 1 | a0001c0002t0003g0290 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.920-22262C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599089 | ||||||
| chr6:10599238
|
G | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.920-22113G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599238 | ||||||
| chr6:10599263
|
C | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(172): Show | 176 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.920-22088C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599263 | ||||||
| chr6:10599280
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.920-22071A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599280 | ||||||
| chr6:10599301
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(172): Show | 176 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.920-22050G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599301 | ||||||
| chr6:10599367
|
A | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0271others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-21984A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599367 | ||||||
| chr6:10599382
|
A | G | 19 | a0001c0001t0001g0056a0001c0001t0001g0067a0001c0001t0001g0090others(16): Show | 19 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-21969A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599382 | ||||||
| chr6:10599510
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.920-21841G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599510 | ||||||
| chr6:10599681
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.920-21670T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599681 | ||||||
| chr6:10600021
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0266a0001c0001t0001g0267others(16): Show | 19 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-21330G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600021 | ||||||
| chr6:10600119
|
T | C | 4 | a0001c0001t0001g0315a0001c0001t0001g0322a0001c0001t0004g0276others(1): Show | 4 | HG01109.hp1 HG01496.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-21232T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600119 | ||||||
| chr6:10600421
|
C | G | 5 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0271others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-20930C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600421 | ||||||
| chr6:10600606
|
C | T | 8 | a0001c0001t0001g0097a0001c0001t0001g0101a0001c0001t0001g0132others(5): Show | 8 | HG00621.hp1 HG00673.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-20745C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600606 | ||||||
| chr6:10600647
|
C | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-20704C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600647 | ||||||
| chr6:10600665
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.920-20686C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600665 | ||||||
| chr6:10600675
|
T | G | 167 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.920-20676T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600675 | ||||||
| chr6:10600760
|
T | TTTTA | 4 | a0001c0001t0001g0040a0001c0001t0002g0044a0001c0001t0002g0188others(1): Show | 4 | HG00558.hp1 HG03195.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-20570_920-2056 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10600760 | |||||
| chr6:10601171
|
A | G | 1 | a0001c0001t0008g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.920-20180A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601171 | ||||||
| chr6:10601289
|
C | G | 1 | a0001c0001t0007g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.920-20062C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601289 | ||||||
| chr6:10601433
|
G | C | 53 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0095others(50): Show | 53 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.920-19918G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601433 | ||||||
| chr6:10601463
|
G | T | 28 | a0001c0001t0001g0090a0001c0001t0001g0140a0001c0001t0001g0292others(25): Show | 28 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.920-19888G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601463 | ||||||
| chr6:10601465
|
A | G | 12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-19886A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601465 | ||||||
| chr6:10601471
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.920-19880G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601471 | ||||||
| chr6:10601486
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.920-19865C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601486 | ||||||
| chr6:10601674
|
G | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0215 | 2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.920-19677G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601674 | ||||||
| chr6:10601680
|
G | A | 12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-19671G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601680 | ||||||
| chr6:10601769
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.920-19582C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601769 | ||||||
| chr6:10601821
|
G | A | 2 | a0001c0001t0007g0016a0002c0003t0011g0264 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-19530G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601821 | ||||||
| chr6:10601939
|
T | TTAAAAA | 3 | a0001c0001t0001g0293a0001c0001t0007g0291a0001c0002t0001g0279 | 3 | HG02257.hp2 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.920-19412_920-1941 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601939 | ||||||
| chr6:10601940
|
C | A | 5 | a0001c0001t0001g0280a0001c0001t0001g0293a0001c0001t0007g0291others(2): Show | 5 | HG01361.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-19411C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601940 | ||||||
| chr6:10601940
|
CAAGAA | C | 16 | a0001c0001t0001g0311a0001c0001t0001g0315a0001c0001t0001g0322others(13): Show | 16 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.920-19408_920-1940 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601940 | |||||
| chr6:10601940
|
CAAGAAAA others(10): Show |
C | 2 | a0001c0001t0007g0016a0002c0003t0011g0264 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-19408_920-1939 others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601940 | |||||
| chr6:10601943
|
G | A | 5 | a0001c0001t0001g0280a0001c0001t0001g0293a0001c0001t0007g0291others(2): Show | 5 | HG01361.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-19408G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601943 | ||||||
| chr6:10601943
|
G | GA | 6 | a0001c0001t0001g0027a0001c0001t0001g0105a0001c0001t0001g0136others(3): Show | 6 | HG00642.hp1 HG02293.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-19391dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | |||||
| chr6:10601943
|
GA | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.920-19391delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | |||||
| chr6:10601943
|
GAA | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0163a0001c0001t0001g0228others(4): Show | 7 | NA18612.hp1 NA18955.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.920-19392_920-1939 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | |||||
| chr6:10601951
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920-19391_920-1938 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601951 | |||||
| chr6:10601954
|
A | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0209 | 2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.920-19397A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601954 | ||||||
| chr6:10601960
|
A | C | 1 | a0001c0002t0001g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-19391A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601960 | ||||||
| chr6:10601961
|
C | A | 35 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0140others(32): Show | 35 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.920-19390C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601961 | ||||||
| chr6:10602000
|
T | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0001t0001g0231 | 3 | NA18945.hp1 NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.920-19351T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602000 | ||||||
| chr6:10602054
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.920-19297C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602054 | ||||||
| chr6:10602179
|
C | G | 1 | a0001c0001t0002g0196 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.920-19172C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602179 | ||||||
| chr6:10602237
|
C | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0105others(2): Show | 5 | NA18951.hp1 NA18973.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-19114C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602237 | ||||||
| chr6:10602250
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.920-19101G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602250 | ||||||
| chr6:10602326
|
A | G | 10 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0271others(7): Show | 10 | HG01109.hp1 HG01496.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-19025A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602326 | ||||||
| chr6:10602391
|
C | A | 2 | a0001c0001t0004g0274a0001c0001t0012g0243 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-18960C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602391 | ||||||
| chr6:10602638
|
CAAATAGG others(5): Show |
C | 12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-18708_920-1869 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10602638 | |||||
| chr6:10602762
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.920-18589G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602762 | ||||||
| chr6:10602971
|
A | C | 1 | a0001c0001t0001g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.920-18380A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602971 | ||||||
| chr6:10603424
|
A | G | 31 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(28): Show | 31 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.920-17927A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603424 | ||||||
| chr6:10603504
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-17847A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603504 | ||||||
| chr6:10603545
|
T | A | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-17806T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603545 | ||||||
| chr6:10603690
|
A | AT | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-17657dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603690 | |||||
| chr6:10603817
|
C | CT | 21 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 21 | HG00735.hp2 HG00741.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.920-17512dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | |||||
| chr6:10603817
|
CT | C | 46 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0043others(43): Show | 46 | HG00323.hp1 HG00558.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.920-17512delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | |||||
| chr6:10603817
|
CTTTTT | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.920-17516_920-1751 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | |||||
| chr6:10603887
|
GTTGT | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-17441_920-1743 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603887 | |||||
| chr6:10603887
|
GTTGTTTG others(1): Show |
G | 5 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0206others(2): Show | 5 | HG01081.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-17445_920-1743 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603887 | |||||
| chr6:10603964
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-17387T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603964 | ||||||
| chr6:10603985
|
G | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.920-17366G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603985 | ||||||
| chr6:10603989
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.920-17362C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603989 | ||||||
| chr6:10603990
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-17361G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603990 | ||||||
| chr6:10603997
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-17354A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603997 | ||||||
| chr6:10603998
|
C | T | 1 | a0001c0001t0001g0340 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.920-17353C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603998 | ||||||
| chr6:10603999
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.920-17352G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603999 | ||||||
| chr6:10604052
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.920-17299C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604052 | ||||||
| chr6:10604098
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.920-17253T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604098 | ||||||
| chr6:10604139
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.920-17212C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604139 | ||||||
| chr6:10604195
|
C | A | 1 | a0001c0001t0002g0009 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.920-17156C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604195 | ||||||
| chr6:10604263
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.920-17088T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604263 | ||||||
| chr6:10604364
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-16987A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604364 | ||||||
| chr6:10604387
|
A | C | 1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.920-16964A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604387 | ||||||
| chr6:10604438
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-16913T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604438 | ||||||
| chr6:10604574
|
C | T | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-16777C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604574 | ||||||
| chr6:10604873
|
G | A | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-16478G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604873 | ||||||
| chr6:10604877
|
A | AAAAAG | 4 | a0001c0001t0001g0239a0001c0001t0007g0016a0001c0001t0013g0012others(1): Show | 4 | HG02572.hp1 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-16473_920-1647 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10604877 | |||||
| chr6:10604877
|
A | AAAAG | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.920-16473_920-1647 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10604877 | |||||
| chr6:10604877
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.920-16474A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604877 | ||||||
| chr6:10604879
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-16472G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604879 | ||||||
| chr6:10605147
|
TAAAACAA | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0187a0001c0001t0001g0197 | 3 | NA18951.hp1 NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.920-16190_920-1618 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605147 | |||||
| chr6:10605169
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0271others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-16182G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605169 | ||||||
| chr6:10605208
|
A | AT | 31 | a0001c0001t0001g0040a0001c0001t0001g0069a0001c0001t0001g0091others(28): Show | 31 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.920-16118dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATT | 14 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0001t0001g0322others(11): Show | 14 | HG00735.hp2 HG01358.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.920-16119_920-1611 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATTT | 7 | a0001c0001t0001g0140a0001c0001t0001g0302a0001c0001t0001g0311others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-16120_920-1611 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATTTT | 9 | a0001c0001t0001g0260a0001c0001t0001g0288a0001c0001t0001g0310others(6): Show | 9 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-16121_920-1611 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATTTTT | 14 | a0001c0001t0001g0013a0001c0001t0001g0088a0001c0001t0001g0103others(11): Show | 14 | HG01070.hp2 HG01361.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-16122_920-1611 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
AT | A | 8 | a0001c0001t0001g0172a0001c0001t0001g0192a0001c0001t0001g0267others(5): Show | 9 | HG02109.hp2 HG02135.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-16118delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
ATT | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(30): Show | 33 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.920-16119_920-1611 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
ATTT | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0015others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-16120_920-1611 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
ATTTT | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0104a0001c0001t0001g0118others(8): Show | 11 | HG02040.hp1 HG02735.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.920-16121_920-1611 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605266
|
A | G | 1 | a0001c0001t0003g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.920-16085A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605266 | ||||||
| chr6:10605365
|
C | T | 2 | a0001c0001t0007g0016a0002c0003t0011g0264 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-15986C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605365 | ||||||
| chr6:10605372
|
C | CT | 6 | a0001c0001t0001g0088a0001c0001t0001g0315a0001c0001t0002g0025others(3): Show | 6 | HG01496.hp2 HG01952.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-15965dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605372 | |||||
| chr6:10605372
|
CT | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-15965delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605372 | |||||
| chr6:10605438
|
G | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-15913G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605438 | ||||||
| chr6:10605518
|
T | C | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.920-15833T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605518 | ||||||
| chr6:10605573
|
C | G | 1 | a0001c0001t0001g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.920-15778C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605573 | ||||||
| chr6:10605653
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.920-15698G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605653 | ||||||
| chr6:10605675
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920-15676G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605675 | ||||||
| chr6:10605764
|
G | C | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.920-15587G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605764 | ||||||
| chr6:10605931
|
C | G | 1 | a0001c0002t0001g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-15420C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605931 | ||||||
| chr6:10605946
|
C | T | 6 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG00408.hp1 HG02300.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-15405C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605946 | ||||||
| chr6:10605988
|
C | G | 1 | a0001c0001t0005g0326 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920-15363C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605988 | ||||||
| chr6:10606043
|
G | A | 2 | a0001c0001t0004g0274a0001c0001t0012g0243 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-15308G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606043 | ||||||
| chr6:10606165
|
AT | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283 | 3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-15184delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606165 | |||||
| chr6:10606204
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.920-15147A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606204 | ||||||
| chr6:10606207
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.920-15144C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606207 | ||||||
| chr6:10606266
|
G | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-15085G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606266 | ||||||
| chr6:10606271
|
C | T | 3 | a0001c0001t0001g0336a0001c0001t0001g0338a0001c0001t0001g0340 | 3 | HG01346.hp1 HG01952.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.920-15080C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606271 | ||||||
| chr6:10606351
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-15000T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606351 | ||||||
| chr6:10606378
|
G | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-14973G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606378 | ||||||
| chr6:10606432
|
A | G | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-14919A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606432 | ||||||
| chr6:10606485
|
G | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0177a0001c0001t0001g0247 | 3 | HG01261.hp1 HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-14866G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606485 | ||||||
| chr6:10606487
|
CACA | C | 30 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 30 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.920-14859_920-1485 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606487 | |||||
| chr6:10606591
|
A | C | 1 | a0001c0001t0007g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.920-14760A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606591 | ||||||
| chr6:10606603
|
C | CTTCCATT others(19): Show |
14 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0140others(11): Show | 14 | HG00621.hp1 HG01081.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-14701_920-1467 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(45): Show |
52 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(49): Show | 53 | HG00738.hp2 HG01071.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.920-14727_920-1467 others(56): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(71): Show |
56 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0069others(53): Show | 57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(82): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(97): Show |
52 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0017others(49): Show | 52 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(108): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(123): Show |
7 | a0001c0001t0002g0009a0001c0001t0002g0014a0001c0001t0002g0079others(4): Show | 7 | HG02135.hp1 HG03239.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(134): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(149): Show |
4 | a0001c0001t0001g0311a0001c0001t0001g0318a0001c0001t0001g0320others(1): Show | 4 | HG02818.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(160): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(175): Show |
6 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0001t0001g0321others(3): Show | 6 | HG01884.hp2 HG02630.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(186): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(201): Show |
1 | a0002c0003t0010g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.920-14676_920-1467 others(212): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(227): Show |
1 | a0001c0001t0003g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.920-14676_920-1467 others(238): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(253): Show |
1 | a0001c0001t0003g0238 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.920-14676_920-1467 others(264): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(331): Show |
1 | a0001c0004t0003g0328 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.920-14676_920-1467 others(342): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(357): Show |
1 | a0001c0004t0003g0330 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.920-14676_920-1467 others(368): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
CTTCCATT others(19): Show |
C | 9 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0056others(6): Show | 9 | HG00140.hp1 HG00639.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-14701_920-1467 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606614
|
G | GAAATTTA others(45): Show |
1 | a0001c0001t0001g0070 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.920-14686_920-1468 others(56): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606614 | |||||
| chr6:10606742
|
T | TAAAG | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-14606_920-1460 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606742 | |||||
| chr6:10606778
|
C | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0061 | 2 | HG01256.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.920-14573C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606778 | ||||||
| chr6:10606897
|
C | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.920-14454C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606897 | ||||||
| chr6:10606929
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14422A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606929 | ||||||
| chr6:10607121
|
TA | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0001g0206 | 3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.920-14229delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607121 | ||||||
| chr6:10607136
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14215C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607136 | ||||||
| chr6:10607216
|
G | C | 9 | a0001c0001t0001g0118a0001c0001t0001g0121a0001c0001t0001g0127others(6): Show | 9 | HG01346.hp1 HG01952.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-14135G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607216 | ||||||
| chr6:10607262
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14089A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607262 | ||||||
| chr6:10607328
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14023A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607328 | ||||||
| chr6:10607434
|
C | T | 2 | a0001c0001t0008g0303a0001c0001t0008g0335 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.920-13917C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607434 | ||||||
| chr6:10607435
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13916G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607435 | ||||||
| chr6:10607541
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.920-13810C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607541 | ||||||
| chr6:10607683
|
CCTAACTT others(17): Show |
C | 16 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0069others(13): Show | 16 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.920-13665_920-1364 others(28): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10607683 | |||||
| chr6:10607688
|
C | T | 2 | a0001c0001t0002g0117a0001c0001t0002g0221 | 2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.920-13663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607688 | ||||||
| chr6:10607699
|
T | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13652T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607699 | ||||||
| chr6:10607848
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.920-13503T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607848 | ||||||
| chr6:10607860
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13491A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607860 | ||||||
| chr6:10607866
|
G | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13485G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607866 | ||||||
| chr6:10607897
|
G | A | 2 | a0001c0001t0007g0016a0002c0003t0011g0264 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-13454G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607897 | ||||||
| chr6:10607908
|
A | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13443A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607908 | ||||||
| chr6:10607909
|
G | A | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-13442G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607909 | ||||||
| chr6:10608014
|
T | A | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-13337T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608014 | ||||||
| chr6:10608073
|
C | CT | 24 | a0001c0001t0001g0041a0001c0001t0001g0140a0001c0001t0001g0154others(21): Show | 24 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.920-13257dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10608073 | |||||
| chr6:10608073
|
CT | C | 15 | a0001c0001t0001g0095a0001c0001t0001g0104a0001c0001t0001g0137others(12): Show | 15 | HG00735.hp2 HG01169.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-13257delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10608073 | |||||
| chr6:10608227
|
G | A | 2 | a0001c0001t0007g0016a0002c0003t0011g0264 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-13124G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608227 | ||||||
| chr6:10608239
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13112G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608239 | ||||||
| chr6:10608359
|
T | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12992T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608359 | ||||||
| chr6:10608645
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.920-12706G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608645 | ||||||
| chr6:10608710
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.920-12641A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608710 | ||||||
| chr6:10609077
|
A | T | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.920-12274A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609077 | ||||||
| chr6:10609206
|
G | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12145G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609206 | ||||||
| chr6:10609212
|
C | T | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12139C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609212 | ||||||
| chr6:10609277
|
A | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12074A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609277 | ||||||
| chr6:10609292
|
A | G | 7 | a0001c0001t0001g0140a0001c0001t0001g0310a0001c0001t0003g0300others(4): Show | 7 | HG01243.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-12059A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609292 | ||||||
| chr6:10609356
|
T | G | 12 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-11995T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609356 | ||||||
| chr6:10609376
|
T | C | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-11975T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609376 | ||||||
| chr6:10609585
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.920-11766G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609585 | ||||||
| chr6:10609617
|
G | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.920-11734G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609617 | ||||||
| chr6:10609780
|
A | AG | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-11567dupG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10609780 | |||||
| chr6:10609786
|
A | G | 2 | a0001c0001t0007g0016a0002c0003t0011g0264 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-11565A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609786 | ||||||
| chr6:10609856
|
C | G | 47 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(44): Show | 47 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.920-11495C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609856 | ||||||
| chr6:10609877
|
C | G | 35 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-11474C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609877 | ||||||
| chr6:10609896
|
TTTG | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.920-11451_920-1144 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10609896 | |||||
| chr6:10609904
|
A | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.920-11447A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609904 | ||||||
| chr6:10609907
|
G | T | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.920-11444G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609907 | ||||||
| chr6:10610078
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-11273G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610078 | ||||||
| chr6:10610319
|
C | T | 9 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0308others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-11032C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610319 | ||||||
| chr6:10610688
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.920-10663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610688 | ||||||
| chr6:10610773
|
T | C | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-10578T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610773 | ||||||
| chr6:10610804
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.920-10547T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610804 | ||||||
| chr6:10610812
|
T | A | 3 | a0001c0001t0001g0311a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.920-10539T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610812 | ||||||
| chr6:10610854
|
G | A | 1 | a0001c0002t0001g0281 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.920-10497G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610854 | ||||||
| chr6:10610862
|
G | A | 3 | a0001c0001t0001g0149a0001c0001t0001g0177a0001c0001t0001g0247 | 3 | HG01261.hp1 HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-10489G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610862 | ||||||
| chr6:10611148
|
G | A | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-10203G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611148 | ||||||
| chr6:10611174
|
C | T | 8 | a0001c0001t0001g0088a0001c0001t0001g0103a0001c0001t0001g0167others(5): Show | 8 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-10177C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611174 | ||||||
| chr6:10611191
|
G | T | 1 | a0001c0001t0001g0255 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.920-10160G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611191 | ||||||
| chr6:10611259
|
CACTTGAA others(16): Show |
C | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.920-10090_920-1006 others(27): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611259 | |||||
| chr6:10611284
|
T | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.920-10067T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611284 | ||||||
| chr6:10611334
|
C | CT | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.920-10002dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611334 | |||||
| chr6:10611334
|
CTT | C | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-10003_920-1000 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611334 | |||||
| chr6:10611413
|
C | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.920-9938C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611413 | ||||||
| chr6:10611487
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0001t0001g0322others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-9864C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611487 | ||||||
| chr6:10611565
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0002g0044a0001c0001t0002g0188 | 3 | HG00558.hp1 NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.920-9786G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611565 | ||||||
| chr6:10611575
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920-9776C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611575 | ||||||
| chr6:10611576
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.920-9775G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611576 | ||||||
| chr6:10611624
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0302 | 2 | HG06807.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.920-9727C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611624 | ||||||
| chr6:10611728
|
AT | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-9615delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611728 | |||||
| chr6:10611979
|
T | G | 2 | a0001c0001t0002g0141a0001c0001t0002g0160 | 2 | NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.920-9372T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611979 | ||||||
| chr6:10612025
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.920-9326T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612025 | ||||||
| chr6:10612203
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.920-9148T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612203 | ||||||
| chr6:10612209
|
A | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0001t0001g0231 | 3 | NA18945.hp1 NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.920-9142A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612209 | ||||||
| chr6:10612217
|
C | G | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-9134C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612217 | ||||||
| chr6:10612241
|
C | T | 1 | a0001c0002t0001g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-9110C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612241 | ||||||
| chr6:10612384
|
C | T | 23 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0083others(20): Show | 23 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.920-8967C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612384 | ||||||
| chr6:10612453
|
A | G | 1 | a0001c0001t0007g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.920-8898A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612453 | ||||||
| chr6:10613128
|
A | G | 1 | a0001c0002t0001g0295 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.920-8223A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613128 | ||||||
| chr6:10613207
|
G | C | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-8144G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613207 | ||||||
| chr6:10613214
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-8137G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613214 | ||||||
| chr6:10613224
|
C | T | 84 | a0001c0001t0001g0010a0001c0001t0001g0031a0001c0001t0001g0033others(81): Show | 85 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.920-8127C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613224 | ||||||
| chr6:10613358
|
G | A | 6 | a0001c0001t0002g0023a0001c0001t0002g0042a0001c0001t0002g0079others(3): Show | 6 | HG01928.hp2 HG01993.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-7993G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613358 | ||||||
| chr6:10613378
|
C | CT | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-7963dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10613378 | |||||
| chr6:10613397
|
C | G | 6 | a0001c0001t0001g0010a0001c0001t0001g0122a0001c0001t0001g0159others(3): Show | 6 | HG01192.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-7954C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613397 | ||||||
| chr6:10613572
|
G | A | 52 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(49): Show | 52 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.920-7779G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613572 | ||||||
| chr6:10613885
|
C | T | 6 | a0001c0001t0002g0023a0001c0001t0002g0042a0001c0001t0002g0079others(3): Show | 6 | HG01928.hp2 HG01993.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-7466C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613885 | ||||||
| chr6:10613950
|
T | G | 1 | a0003c0008t0001g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.920-7401T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613950 | ||||||
| chr6:10614240
|
T | C | 1 | a0002c0003t0011g0264 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.920-7111T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614240 | ||||||
| chr6:10614246
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.920-7105C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614246 | ||||||
| chr6:10614261
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.920-7090T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614261 | ||||||
| chr6:10614486
|
G | C | 15 | a0001c0001t0001g0140a0001c0001t0001g0266a0001c0001t0001g0310others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-6865G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614486 | ||||||
| chr6:10614625
|
C | CA | 13 | a0001c0001t0001g0034a0001c0001t0001g0219a0001c0001t0001g0265others(10): Show | 13 | HG00323.hp1 HG00408.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.920-6706dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | |||||
| chr6:10614625
|
CA | C | 20 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0158others(17): Show | 20 | HG02055.hp2 HG02109.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-6706delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | |||||
| chr6:10614625
|
CAAA | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.920-6708_920-6706d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | |||||
| chr6:10614642
|
A | AG | 4 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0001t0001g0333others(1): Show | 4 | HG01884.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-6709_920-6708i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614642 | ||||||
| chr6:10614642
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.920-6709A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614642 | ||||||
| chr6:10614644
|
A | AAAAAAG | 10 | a0001c0001t0001g0140a0001c0001t0001g0315a0001c0001t0003g0312others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-6706_920-6705i others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614644 | |||||
| chr6:10614644
|
A | AAG | 9 | a0001c0001t0001g0018a0001c0001t0001g0213a0001c0001t0001g0260others(6): Show | 9 | HG01891.hp1 HG01978.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-6703_920-6702d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614644 | |||||
| chr6:10614644
|
A | AG | 20 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0167others(17): Show | 20 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-6707_920-6706i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614644 | ||||||
| chr6:10614644
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-6707A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614644 | ||||||
| chr6:10614691
|
GTAGAGAT others(3): Show |
G | 2 | a0001c0001t0001g0056a0001c0002t0001g0297 | 2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.920-6657_920-6648d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614691 | |||||
| chr6:10614844
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.920-6507C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614844 | ||||||
| chr6:10614845
|
G | T | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.920-6506G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614845 | ||||||
| chr6:10614846
|
C | T | 1 | a0001c0001t0005g0326 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920-6505C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614846 | ||||||
| chr6:10614869
|
G | A | 1 | a0003c0008t0001g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.920-6482G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614869 | ||||||
| chr6:10615035
|
C | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.920-6316C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615035 | ||||||
| chr6:10615472
|
A | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.920-5879A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615472 | ||||||
| chr6:10615567
|
T | TA | 3 | a0001c0001t0001g0008a0001c0001t0001g0199a0001c0001t0001g0258 | 3 | NA18969.hp2 NA19002.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.920-5783dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10615567 | |||||
| chr6:10615644
|
T | G | 47 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(44): Show | 47 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.920-5707T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615644 | ||||||
| chr6:10615697
|
CCACTCCA others(9): Show |
C | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-5651_920-5636d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10615697 | |||||
| chr6:10615705
|
TAGAC | T | 8 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0298others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-5642_920-5639d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10615705 | |||||
| chr6:10615876
|
G | A | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-5475G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615876 | ||||||
| chr6:10615904
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.920-5447G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615904 | ||||||
| chr6:10615921
|
C | G | 1 | a0002c0003t0011g0264 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.920-5430C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615921 | ||||||
| chr6:10615983
|
A | G | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-5368A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615983 | ||||||
| chr6:10615999
|
G | T | 1 | a0001c0001t0001g0322 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.920-5352G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615999 | ||||||
| chr6:10616073
|
G | A | 1 | a0001c0001t0001g0015 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.920-5278G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616073 | ||||||
| chr6:10616118
|
T | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0059others(8): Show | 12 | HG01071.hp2 HG01258.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.920-5233T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616118 | ||||||
| chr6:10616183
|
C | CGTTATAT others(95): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0242 | 2 | HG01070.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.920-5087_920-5086i others(104): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10616183 | |||||
| chr6:10616183
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0177a0001c0001t0001g0247 | 3 | HG01261.hp1 HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-5168C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616183 | ||||||
| chr6:10616265
|
T | C | 38 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.920-5086T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616265 | ||||||
| chr6:10616277
|
G | C | 1 | a0001c0001t0001g0256 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.920-5074G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616277 | ||||||
| chr6:10616435
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.920-4916C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616435 | ||||||
| chr6:10616583
|
G | C | 7 | a0001c0001t0003g0032a0001c0001t0003g0238a0001c0001t0007g0016others(4): Show | 7 | HG01358.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-4768G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616583 | ||||||
| chr6:10616598
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0002g0196 | 2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.920-4753C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616598 | ||||||
| chr6:10616744
|
A | C | 10 | a0001c0001t0001g0140a0001c0001t0001g0266a0001c0001t0001g0310others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-4607A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616744 | ||||||
| chr6:10617001
|
TG | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-4348delG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617001 | |||||
| chr6:10617020
|
G | A | 2 | a0001c0001t0004g0274a0001c0001t0012g0243 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-4331G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617020 | ||||||
| chr6:10617049
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.920-4302C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617049 | ||||||
| chr6:10617077
|
C | T | 1 | a0003c0008t0001g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.920-4274C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617077 | ||||||
| chr6:10617281
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0062 | 2 | NA19082.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.920-4070C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617281 | ||||||
| chr6:10617285
|
C | T | 1 | a0001c0001t0007g0291 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.920-4066C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617285 | ||||||
| chr6:10617354
|
C | G | 1 | a0001c0001t0002g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920-3997C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617354 | ||||||
| chr6:10617366
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.920-3985G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617366 | ||||||
| chr6:10617377
|
T | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.920-3974T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617377 | ||||||
| chr6:10617387
|
C | T | 1 | a0001c0001t0001g0112 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.920-3964C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617387 | ||||||
| chr6:10617411
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0047others(9): Show | 12 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-3940C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617411 | ||||||
| chr6:10617438
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.920-3913C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617438 | ||||||
| chr6:10617449
|
C | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283 | 3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-3902C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617449 | ||||||
| chr6:10617518
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.920-3833G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617518 | ||||||
| chr6:10617530
|
G | T | 2 | a0001c0001t0001g0322a0001c0001t0001g0333 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.920-3821G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617530 | ||||||
| chr6:10617640
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.920-3711C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617640 | ||||||
| chr6:10617709
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.920-3642C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617709 | ||||||
| chr6:10617743
|
A | ATTTTTTT others(4): Show |
1 | a0002c0003t0010g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.920-3605_920-3604i others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617743 | |||||
| chr6:10617747
|
C | T | 5 | a0001c0001t0003g0032a0001c0001t0003g0238a0001c0004t0003g0328others(2): Show | 5 | HG01358.hp1 HG02738.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-3604C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617747 | ||||||
| chr6:10617747
|
CTTCTTTT others(2): Show |
C | 26 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(23): Show | 26 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.920-3601_920-3593d others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617747 | |||||
| chr6:10617750
|
C | CT | 7 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0090others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-3579dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0140a0001c0001t0001g0266a0001c0001t0001g0310others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-3586_920-3579d others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(3): Show |
20 | a0001c0001t0001g0091a0001c0001t0001g0265a0001c0001t0001g0267others(17): Show | 20 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-3588_920-3579d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0287a0001c0001t0014g0331 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.920-3589_920-3579d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0095a0001c0001t0001g0307a0001c0001t0001g0321 | 3 | HG02486.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.920-3590_920-3579d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0005g0301a0001c0001t0010g0309 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.920-3591_920-3579d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0315a0001c0001t0008g0303 | 2 | HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.920-3592_920-3579d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0004g0276a0001c0001t0008g0335 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.920-3593_920-3579d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0004g0274a0001c0001t0012g0243 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-3594_920-3579d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | T | 12 | a0001c0001t0001g0311a0001c0001t0001g0318a0001c0001t0001g0320others(9): Show | 12 | HG00735.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.920-3601C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617750 | ||||||
| chr6:10617750
|
CT | C | 21 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0043others(18): Show | 21 | HG00323.hp1 HG00558.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.920-3579delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
CTT | C | 18 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0098others(15): Show | 18 | HG00140.hp2 HG01928.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.920-3580_920-3579d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
CTTT | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.920-3581_920-3579d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617751
|
T | C | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-3600T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617751 | ||||||
| chr6:10617753
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.920-3598T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617753 | ||||||
| chr6:10617756
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.920-3595T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617756 | ||||||
| chr6:10617775
|
C | G | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.920-3576C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617775 | ||||||
| chr6:10617807
|
T | C | 1 | a0001c0002t0001g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-3544T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617807 | ||||||
| chr6:10617864
|
T | C | 39 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-3487T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617864 | ||||||
| chr6:10617916
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-3435G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617916 | ||||||
| chr6:10617930
|
T | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0292a0001c0002t0001g0283 | 3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-3421T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617930 | ||||||
| chr6:10617993
|
G | A | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-3358G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617993 | ||||||
| chr6:10618060
|
C | A | 2 | a0001c0001t0002g0210a0001c0001t0002g0220 | 2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.920-3291C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618060 | ||||||
| chr6:10618217
|
C | T | 5 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0271others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-3134C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618217 | ||||||
| chr6:10618281
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-3070G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618281 | ||||||
| chr6:10618295
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.920-3056A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618295 | ||||||
| chr6:10618449
|
G | C | 2 | a0001c0001t0007g0016a0002c0003t0011g0264 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-2902G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618449 | ||||||
| chr6:10618630
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.920-2721G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618630 | ||||||
| chr6:10618753
|
C | CT | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.920-2595dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10618753 | |||||
| chr6:10618775
|
A | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 30 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.920-2576A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618775 | ||||||
| chr6:10618835
|
T | TCTTGAAT others(1): Show |
38 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.920-2504_920-2497d others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10618835 | |||||
| chr6:10618953
|
G | C | 2 | a0001c0001t0004g0276a0001c0001t0005g0301 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.920-2398G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618953 | ||||||
| chr6:10619010
|
C | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-2341C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619010 | ||||||
| chr6:10619030
|
A | G | 38 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 38 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.920-2321A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619030 | ||||||
| chr6:10619506
|
A | T | 39 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-1845A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619506 | ||||||
| chr6:10619521
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.920-1830T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619521 | ||||||
| chr6:10619606
|
G | A | 3 | a0001c0001t0001g0311a0001c0001t0001g0318a0001c0001t0001g0320 | 3 | HG02818.hp2 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.920-1745G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619606 | ||||||
| chr6:10619684
|
G | A | 1 | a0001c0001t0005g0326 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920-1667G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619684 | ||||||
| chr6:10619704
|
T | A | 39 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(36): Show | 39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-1647T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619704 | ||||||
| chr6:10619984
|
T | C | 33 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.920-1367T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619984 | ||||||
| chr6:10620407
|
A | ATT | 29 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(26): Show | 30 | HG01070.hp2 HG01109.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.920-933_920-932dup others(2): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10620407 | |||||
| chr6:10620428
|
A | T | 1 | a0001c0001t0002g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.920-923A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620428 | ||||||
| chr6:10620445
|
A | G | 30 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(27): Show | 31 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.920-906A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620445 | ||||||
| chr6:10620527
|
C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0140a0001c0001t0001g0310others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-824C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620527 | ||||||
| chr6:10620583
|
T | C | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(25): Show | 28 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.920-768T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620583 | ||||||
| chr6:10620613
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0019g0107 | 3 | HG02738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.920-738C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620613 | ||||||
| chr6:10620744
|
C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0140a0001c0001t0001g0310others(6): Show | 9 | HG01243.hp1 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-607C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620744 | ||||||
| chr6:10620921
|
A | C | 1 | a0001c0001t0001g0288 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.920-430A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620921 | ||||||
| chr6:10620940
|
A | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(24): Show | 27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.920-411A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620940 | ||||||
| chr6:10620993
|
C | G | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-358C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620993 | ||||||
| chr6:10621109
|
A | G | 2 | a0001c0001t0005g0301a0001c0001t0006g0001 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.920-242A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621109 | ||||||
| chr6:10621158
|
A | G | 2 | a0001c0001t0005g0301a0001c0001t0006g0001 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.920-193A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621158 | ||||||
| chr6:10621313
|
A | T | 3 | a0001c0004t0003g0328a0001c0004t0003g0330a0002c0003t0010g0270 | 3 | HG03130.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.920-38A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621313 | ||||||
| chr6:10621314
|
C | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-37C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621314 | ||||||
| chr6:10621458
|
C | G | 1 | a0001c0001t0001g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1012+15C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621458 | ||||||
| chr6:10621597
|
C | T | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1012+154C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621597 | ||||||
| chr6:10621634
|
T | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(46): Show | 50 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1012+191T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621634 | ||||||
| chr6:10621681
|
C | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0019g0107 | 3 | HG02738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1012+238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621681 | ||||||
| chr6:10621695
|
T | C | 36 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1012+252T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621695 | ||||||
| chr6:10621731
|
A | G | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(24): Show | 27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+288A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621731 | ||||||
| chr6:10621951
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1012+508G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621951 | ||||||
| chr6:10622095
|
A | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(24): Show | 27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+652A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622095 | ||||||
| chr6:10622171
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(24): Show | 27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+728T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622171 | ||||||
| chr6:10622231
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1012+788A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622231 | ||||||
| chr6:10622308
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(24): Show | 27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+865T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622308 | ||||||
| chr6:10622494
|
T | C | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(24): Show | 27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+1051T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622494 | ||||||
| chr6:10622579
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1012+1136A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622579 | ||||||
| chr6:10622742
|
C | CT | 12 | a0001c0001t0001g0091a0001c0001t0001g0183a0001c0001t0001g0226others(9): Show | 12 | HG01496.hp2 HG01934.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1012+1327dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CT | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1012+1327delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTT | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0104a0001c0001t0001g0121others(6): Show | 9 | HG01243.hp1 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+1326_1012+132 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTTTTTTT | C | 21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(18): Show | 21 | HG00735.hp2 HG01175.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1012+1321_1012+132 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0001g0135a0001c0001t0003g0032a0001c0001t0003g0238others(5): Show | 8 | HG01358.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1012+1318_1012+132 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0002t0001g0278a0001c0002t0001g0279a0001c0002t0001g0284 | 3 | HG01361.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1012+1317_1012+132 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622812
|
C | T | 17 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0078others(14): Show | 17 | HG00597.hp2 HG01346.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1012+1369C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622812 | ||||||
| chr6:10622813
|
G | A | 1 | a0001c0001t0002g0066 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1012+1370G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622813 | ||||||
| chr6:10622913
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1012+1470C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622913 | ||||||
| chr6:10623238
|
A | ATTTAC | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1012+1799_1012+180 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10623238 | |||||
| chr6:10623258
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0059others(8): Show | 12 | HG01071.hp2 HG01258.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1012+1815C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623258 | ||||||
| chr6:10623292
|
AT | A | 30 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(27): Show | 30 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1012+1864delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10623292 | |||||
| chr6:10623295
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1012+1852T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623295 | ||||||
| chr6:10623333
|
C | G | 1 | a0001c0001t0002g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1012+1890C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623333 | ||||||
| chr6:10623361
|
G | C | 1 | a0001c0001t0002g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1012+1918G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623361 | ||||||
| chr6:10623385
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0128 | 3 | HG00621.hp2 NA18939.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1012+1942G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623385 | ||||||
| chr6:10623535
|
C | G | 2 | a0001c0001t0005g0301a0001c0001t0006g0001 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1012+2092C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623535 | ||||||
| chr6:10623539
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0002g0044a0001c0001t0002g0188 | 3 | HG00558.hp1 NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1012+2096G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623539 | ||||||
| chr6:10623838
|
A | G | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(23): Show | 26 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1012+2395A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623838 | ||||||
| chr6:10624019
|
C | T | 27 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0088others(24): Show | 27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1013-2398C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624019 | ||||||
| chr6:10624253
|
C | G | 8 | a0001c0001t0003g0032a0001c0001t0003g0238a0001c0002t0001g0278others(5): Show | 8 | HG01358.hp1 HG01361.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1013-2164C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624253 | ||||||
| chr6:10624281
|
T | A | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1013-2136T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624281 | ||||||
| chr6:10624754
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1013-1663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624754 | ||||||
| chr6:10625029
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1013-1388G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625029 | ||||||
| chr6:10625030
|
C | A | 2 | a0001c0001t0005g0301a0001c0001t0006g0001 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1013-1387C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625030 | ||||||
| chr6:10625063
|
G | A | 2 | a0001c0002t0001g0278a0001c0002t0001g0279 | 2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1013-1354G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625063 | ||||||
| chr6:10625141
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | NA18977.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1013-1276C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625141 | ||||||
| chr6:10625225
|
T | C | 2 | a0001c0001t0005g0301a0001c0001t0006g0001 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1013-1192T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625225 | ||||||
| chr6:10625518
|
TA | T | 30 | a0001c0001t0001g0056a0001c0001t0001g0065a0001c0001t0001g0094others(27): Show | 30 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1013-885delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10625518 | |||||
| chr6:10625546
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1013-871G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625546 | ||||||
| chr6:10625567
|
T | G | 1 | a0001c0001t0013g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1013-850T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625567 | ||||||
| chr6:10625653
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1013-764C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625653 | ||||||
| chr6:10625722
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1013-695T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625722 | ||||||
| chr6:10625861
|
G | A | 3 | a0001c0002t0001g0278a0001c0002t0001g0279a0001c0002t0001g0284 | 3 | HG01361.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1013-556G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625861 | ||||||
| chr6:10625917
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0100 | 3 | NA18993.hp1 NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1013-500A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625917 | ||||||
| chr6:10625938
|
C | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0310a0001c0001t0005g0045others(8): Show | 12 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1013-479C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625938 | ||||||
| chr6:10625989
|
T | C | 4 | a0001c0001t0001g0124a0001c0001t0001g0266a0001c0001t0001g0311others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-428T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625989 | ||||||
| chr6:10626014
|
C | T | 8 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0308others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1013-403C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626014 | ||||||
| chr6:10626069
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1013-348G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626069 | ||||||
| chr6:10626139
|
T | C | 1 | a0001c0001t0010g0309 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1013-278T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626139 | ||||||
| chr6:10626179
|
C | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0310a0001c0001t0003g0032others(14): Show | 17 | HG01358.hp1 HG01891.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1013-238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626179 | ||||||
| chr6:10626331
|
G | A | 3 | a0001c0001t0007g0016a0001c0001t0007g0291a0002c0003t0011g0264 | 3 | HG02572.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1013-86G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626331 | ||||||
| chr6:10626382
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0134 | 2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1013-35T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626382 |