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_145649.5 |
| refseq_prot | NP_663624.1 |
| ensembl_nuc | ENST00000495262.7 |
| ensembl_prot | ENSP00000419411.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 10521351 |
| end | 10629368 |
| strand | + |
| ver | v1.2 |
| region | chr6:10521351-10629368 |
| region5000 | chr6:10516351-10634368 |
| regionname0 | GCNT2_chr6_10521351_10629368 |
| regionname5000 | GCNT2_chr6_10516351_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 | 402 | 323 | 86 | 59 | 132 | 8 | 36 | 98 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0002 | 0/0 | 89 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 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 | 1209 | 321 | 86 | 59 | 130 | 8 | 36 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| c0002 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| c0003 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| c0004 | 0/0 | 284 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 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 | 3297 | 233 | 55 | 40 | 105 | 7 | 24 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0002 | 0/0 | 3297 | 39 | 1 | 6 | 25 | 1 | 6 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0003 | 0/0 | 3297 | 11 | 6 | 4 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0004 | 0/0 | 3301 | 7 | 6 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0005 | 0/0 | 3301 | 3 | 1 | 2 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0006 | 0/0 | 3297 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0007 | 0/0 | 3297 | 3 | 0 | 1 | 0 | 0 | 2 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0008 | 0/0 | 3301 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0009 | 0/0 | 3297 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0010 | 0/0 | 3301 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0011 | 0/0 | 3230 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0012 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0013 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0014 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0015 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0016 | 0/0 | 3297 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0017 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0018 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0019 | 0/0 | 3297 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0020 | 0/0 | 3297 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0021 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0022 | 0/0 | 3297 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0023 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0024 | 0/0 | 3297 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0025 | 0/0 | 3297 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0026 | 0/0 | 3297 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0027 | 0/0 | 3234 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| t0028 | 0/0 | 2762 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 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 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 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 | 1209 | 321 | 86 | 59 | 130 | 8 | 36 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0002 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0003 | 0/0 | 1209 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0002c0004 | 0/0 | 284 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4505 | 231 | 55 | 40 | 103 | 7 | 24 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0002 | 0/0 | 4505 | 39 | 1 | 6 | 25 | 1 | 6 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0003 | 0/0 | 4505 | 11 | 6 | 4 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0004 | 0/0 | 4509 | 7 | 6 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0005 | 0/0 | 4509 | 3 | 1 | 2 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0006 | 0/0 | 4505 | 3 | 0 | 3 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0007 | 0/0 | 4505 | 3 | 0 | 1 | 0 | 0 | 2 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0008 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0009 | 0/0 | 4505 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0010 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0011 | 0/0 | 4438 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0012 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0013 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0014 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0015 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0016 | 0/0 | 4505 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0017 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0018 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0019 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0020 | 0/0 | 4505 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0021 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0022 | 0/0 | 4505 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0023 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0024 | 0/0 | 4505 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0025 | 0/0 | 4505 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0026 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0001t0027 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0002t0001 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0001c0003t0001 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 10634368 |
| a0002c0004t0028 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | copy fasta | chr6 | 10516351 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0007g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0007g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0014g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0016g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0018g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0019g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0020g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0021g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0022g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0023g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0024g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0025g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0026g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0027g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0002c0004t0028g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0280 | EUR | FIN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0288 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0245 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0295 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01081 | hp2 | a0001 | c0001 | t0022 | g0271 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0286 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01496 | hp1 | a0001 | c0001 | t0025 | g0217 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01978 | hp1 | a0001 | c0001 | t0016 | g0098 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0033 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02135 | hp2 | a0001 | c0001 | t0026 | g0051 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CDX | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0242 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02293 | hp2 | a0002 | c0004 | t0028 | g0324 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0067 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02572 | hp2 | a0001 | c0001 | t0023 | g0313 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0219 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02717 | hp2 | a0001 | c0001 | t0019 | g0127 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0253 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0152 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0108 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0322 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0316 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0315 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03239 | hp2 | a0001 | c0001 | t0024 | g0241 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0244 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0243 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03579 | hp1 | a0001 | c0001 | t0021 | g0064 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0311 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19005 | hp2 | a0001 | c0001 | t0018 | g0100 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0076 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ASW | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20129 | hp2 | a0001 | c0001 | t0027 | g0003 | AFR | ASW | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0240 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0088 | REF | REF | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0095 | REF | REF | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10529562
|
C | T | 1 | a0001c0003 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.651C>T | p.Pro217Pro | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/5 | 1186/4505 | 651/1209 | 217/402 | chr6 | 10529562 | ||
| chr6:10529709
|
C | T | 1 | a0001c0002 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.798C>T | p.Tyr266Tyr | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/5 | 1333/4505 | 798/1209 | 266/402 | chr6 | 10529709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10527516
|
C | T | 1 | a0001c0001t0026 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-426C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/5 | 1396 | chr6 | 10527516 | |||||
| chr6:10527583
|
G | A | 1 | a0001c0001t0012 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-359G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/5 | 1329 | chr6 | 10527583 | |||||
| chr6:10528682
|
A | G | 1 | a0001c0001t0025 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-230A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/5 | 230 | chr6 | 10528682 | |||||
| chr6:10528781
|
A | G | 7 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(4): Show | 21 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-131A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/5 | 131 | chr6 | 10528781 | |||||
| chr6:10528854
|
T | C | 6 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(3): Show | 18 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-58T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/5 | 58 | chr6 | 10528854 | |||||
| chr6:10528886
|
A | C | 2 | a0001c0001t0006a0001c0001t0022 | 4 | HG00639.hp2 HG00741.hp2 HG01081.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-26A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/5 | 26 | chr6 | 10528886 | |||||
| chr6:10626660
|
C | G | 2 | a0001c0001t0021a0001c0001t0027 | 2 | HG03579.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*53C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 53 | chr6 | 10626660 | |||||
| chr6:10626688
|
G | A | 1 | a0001c0001t0023 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 81 | chr6 | 10626688 | |||||
| chr6:10626712
|
C | T | 2 | a0001c0001t0004a0001c0001t0020 | 8 | HG01891.hp1 HG02647.hp1 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 105 | chr6 | 10626712 | |||||
| chr6:10626821
|
A | G | 1 | a0001c0001t0019 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 214 | chr6 | 10626821 | |||||
| chr6:10626832
|
G | A | 1 | a0001c0001t0008 | 2 | HG02717.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*225G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 225 | chr6 | 10626832 | |||||
| chr6:10627005
|
T | A | 1 | a0001c0001t0009 | 2 | HG02055.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*398T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 398 | chr6 | 10627005 | |||||
| chr6:10627125
|
T | G | 1 | a0001c0001t0013 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 518 | chr6 | 10627125 | |||||
| chr6:10627278
|
C | T | 6 | a0001c0001t0005a0001c0001t0008a0001c0001t0010others(3): Show | 10 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*671C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 671 | chr6 | 10627278 | |||||
| chr6:10627289
|
G | C | 2 | a0001c0001t0004a0001c0001t0014 | 8 | HG01891.hp1 HG02647.hp1 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*682G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 682 | chr6 | 10627289 | |||||
| chr6:10627375
|
G | A | 1 | a0001c0001t0015 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 768 | chr6 | 10627375 | |||||
| chr6:10627546
|
G | T | 2 | a0001c0001t0005a0001c0001t0010 | 5 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 939 | chr6 | 10627546 | |||||
| chr6:10627628
|
C | CTTCA | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(5): Show | 18 | HG00735.hp2 HG01109.hp1 HG01891.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1025dupTTCA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 1026 | INFO_REALIGN_3_PRIME | chr6 | 10627628 | ||||
| chr6:10627681
|
A | G | 1 | a0001c0001t0018 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1074A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 1074 | chr6 | 10627681 | |||||
| chr6:10627781
|
T | C | 3 | a0001c0001t0002a0001c0001t0024a0001c0001t0026 | 41 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1174T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 1174 | chr6 | 10627781 | |||||
| chr6:10627924
|
G | A | 2 | a0001c0001t0016a0001c0001t0022 | 2 | HG01081.hp2 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1317G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 1317 | chr6 | 10627924 | |||||
| chr6:10628004
|
A | G | 1 | a0001c0001t0017 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1397A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 1397 | chr6 | 10628004 | |||||
| chr6:10628340
|
T | G | 3 | a0001c0001t0004a0001c0001t0021a0001c0001t0027 | 9 | HG01891.hp1 HG02647.hp1 HG02738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1733T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 1733 | chr6 | 10628340 | |||||
| chr6:10628878
|
C | T | 1 | a0001c0001t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2271C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 2271 | chr6 | 10628878 | |||||
| chr6:10629059
|
G | C | 1 | a0001c0001t0023 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2452G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 2452 | chr6 | 10629059 | |||||
| chr6:10629127
|
C | A | 6 | a0001c0001t0005a0001c0001t0008a0001c0001t0010others(3): Show | 10 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2520C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 2520 | chr6 | 10629127 | |||||
| chr6:10629333
|
T | C | 1 | a0001c0001t0012 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10521465
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-469+48C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521465 | ||||||
| chr6:10521482
|
C | T | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-469+65C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521482 | ||||||
| chr6:10521484
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-469+67T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521484 | ||||||
| chr6:10521497
|
A | G | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-469+80A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521497 | ||||||
| chr6:10521507
|
C | T | 4 | a0001c0001t0001g0317a0001c0001t0004g0314a0001c0001t0004g0316others(1): Show | 4 | HG03098.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-469+90C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521507 | ||||||
| chr6:10521654
|
G | GT | 69 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(66): Show | 69 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-469+249dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10521654 | |||||
| chr6:10521655
|
T | G | 1 | a0001c0001t0001g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-469+238T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521655 | ||||||
| chr6:10521681
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0009g0006 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-469+264T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521681 | ||||||
| chr6:10521888
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0012g0008 | 3 | HG03139.hp1 NA18949.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-469+471G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10521888 | ||||||
| chr6:10521901
|
A | AT | 19 | a0001c0001t0001g0228a0001c0001t0003g0229a0001c0001t0003g0230others(16): Show | 19 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.-469+499dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10521901 | |||||
| chr6:10522013
|
G | C | 9 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(6): Show | 9 | HG02258.hp2 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-469+596G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522013 | ||||||
| chr6:10522039
|
A | C | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-469+622A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522039 | ||||||
| chr6:10522161
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-469+744T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522161 | ||||||
| chr6:10522168
|
G | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG00735.hp2 HG02615.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-469+751G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522168 | ||||||
| chr6:10522623
|
A | G | 1 | a0001c0001t0010g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-469+1206A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522623 | ||||||
| chr6:10522635
|
A | G | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-469+1218A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522635 | ||||||
| chr6:10522676
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-469+1259G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522676 | ||||||
| chr6:10522823
|
C | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(11): Show | 14 | HG00642.hp2 HG00735.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-469+1406C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522823 | ||||||
| chr6:10522840
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-469+1423C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522840 | ||||||
| chr6:10522965
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-469+1548C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10522965 | ||||||
| chr6:10523142
|
A | T | 18 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(15): Show | 18 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-469+1725A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523142 | ||||||
| chr6:10523347
|
A | G | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-469+1930A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523347 | ||||||
| chr6:10523431
|
G | GA | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00735.hp2 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-469+2031dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10523431 | |||||
| chr6:10523431
|
GA | G | 153 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(150): Show | 153 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-469+2031delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10523431 | |||||
| chr6:10523431
|
GAA | G | 24 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0225others(21): Show | 24 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-469+2030_-469+203 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10523431 | |||||
| chr6:10523465
|
T | C | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-469+2048T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523465 | ||||||
| chr6:10523500
|
G | C | 18 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(15): Show | 18 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-469+2083G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523500 | ||||||
| chr6:10523569
|
C | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-469+2152C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523569 | ||||||
| chr6:10523593
|
G | C | 195 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(192): Show | 195 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.-469+2176G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523593 | ||||||
| chr6:10523669
|
G | T | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG01346.hp2 HG03017.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.-469+2252G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523669 | ||||||
| chr6:10523960
|
G | A | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-469+2543G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10523960 | ||||||
| chr6:10523972
|
C | CA | 157 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0021others(154): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-469+2576dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10523972 | |||||
| chr6:10523972
|
C | CAA | 53 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(50): Show | 53 | HG00597.hp2 HG01123.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.-469+2575_-469+257 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10523972 | |||||
| chr6:10524198
|
G | A | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-469+2781G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524198 | ||||||
| chr6:10524250
|
G | C | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-469+2833G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524250 | ||||||
| chr6:10524251
|
C | CT | 21 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0128others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.-469+2851dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10524251 | |||||
| chr6:10524251
|
CT | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG00642.hp2 HG03139.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.-469+2851delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10524251 | |||||
| chr6:10524306
|
G | A | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-469+2889G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524306 | ||||||
| chr6:10524322
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-469+2905C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524322 | ||||||
| chr6:10524399
|
T | C | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-469+2982T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524399 | ||||||
| chr6:10524401
|
C | T | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-469+2984C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524401 | ||||||
| chr6:10524454
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0009g0033 | 3 | HG02055.hp1 HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-468-3020G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524454 | ||||||
| chr6:10524560
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG01934.hp2 HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-468-2914T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524560 | ||||||
| chr6:10524567
|
G | A | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-468-2907G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524567 | ||||||
| chr6:10524582
|
C | T | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-468-2892C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524582 | ||||||
| chr6:10524619
|
C | G | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-468-2855C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524619 | ||||||
| chr6:10524810
|
C | CAAAAGCA others(322): Show |
1 | a0001c0001t0001g0306 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-468-2649_-468-264 others(333): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10524810 | |||||
| chr6:10524810
|
C | CAAAAGCA others(325): Show |
1 | a0001c0001t0001g0308 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-468-2649_-468-264 others(336): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr6 | 10524810 | |||||
| chr6:10524817
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-468-2657A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524817 | ||||||
| chr6:10524847
|
G | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0302 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-468-2627G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524847 | ||||||
| chr6:10524886
|
G | A | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-468-2588G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524886 | ||||||
| chr6:10524887
|
C | T | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-468-2587C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524887 | ||||||
| chr6:10524904
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-468-2570C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10524904 | ||||||
| chr6:10525151
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-468-2323G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525151 | ||||||
| chr6:10525476
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-468-1998C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525476 | ||||||
| chr6:10525494
|
A | G | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-468-1980A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525494 | ||||||
| chr6:10525539
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | HG01071.hp1 HG01123.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-468-1935G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525539 | ||||||
| chr6:10525587
|
A | G | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-468-1887A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525587 | ||||||
| chr6:10525666
|
G | A | 10 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0063others(7): Show | 10 | HG01361.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-468-1808G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525666 | ||||||
| chr6:10525672
|
G | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00735.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-468-1802G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525672 | ||||||
| chr6:10525813
|
G | T | 2 | a0001c0001t0001g0300a0001c0001t0002g0301 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-468-1661G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525813 | ||||||
| chr6:10525850
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-468-1624G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525850 | ||||||
| chr6:10525856
|
A | G | 22 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(19): Show | 22 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-468-1618A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525856 | ||||||
| chr6:10525896
|
G | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0021g0064 | 3 | HG01361.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-468-1578G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525896 | ||||||
| chr6:10525898
|
A | G | 22 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(19): Show | 22 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-468-1576A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525898 | ||||||
| chr6:10525962
|
G | A | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-468-1512G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10525962 | ||||||
| chr6:10526007
|
C | T | 1 | a0001c0001t0005g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-468-1467C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526007 | ||||||
| chr6:10526012
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-468-1462T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526012 | ||||||
| chr6:10526140
|
T | A | 245 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(242): Show | 245 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(242): Show |
intron_variant | MODIFIER | c.-468-1334T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526140 | ||||||
| chr6:10526376
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-468-1098C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526376 | ||||||
| chr6:10526410
|
C | T | 1 | a0001c0002t0001g0207 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-468-1064C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526410 | ||||||
| chr6:10526565
|
C | G | 148 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0137others(145): Show | 148 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.-468-909C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526565 | ||||||
| chr6:10526813
|
G | A | 18 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(15): Show | 18 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-468-661G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526813 | ||||||
| chr6:10526815
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-468-659C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10526815 | ||||||
| chr6:10527047
|
A | C | 1 | a0001c0001t0001g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-468-427A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527047 | ||||||
| chr6:10527098
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-468-376G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527098 | ||||||
| chr6:10527118
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-468-356C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527118 | ||||||
| chr6:10527161
|
C | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0004g0069others(1): Show | 4 | HG02055.hp1 HG02280.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-468-313C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527161 | ||||||
| chr6:10527190
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-468-284G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527190 | ||||||
| chr6:10527288
|
G | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00735.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-468-186G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527288 | ||||||
| chr6:10527339
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0009g0033 | 3 | HG02055.hp1 HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-468-135C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527339 | ||||||
| chr6:10527403
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-468-71C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527403 | ||||||
| chr6:10527409
|
G | C | 3 | a0001c0001t0011g0001a0001c0001t0011g0002a0001c0001t0027g0003 | 3 | HG02976.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-468-65G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527409 | ||||||
| chr6:10527421
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0009g0006 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-468-53G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 1/4 | chr6 | 10527421 | ||||||
| chr6:10527700
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-282+40G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | chr6 | 10527700 | ||||||
| chr6:10527717
|
A | ATGTGTGT others(3): Show |
18 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(15): Show | 18 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-282+59_-282+60ins others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 10527717 | |||||
| chr6:10527745
|
T | C | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-282+85T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | chr6 | 10527745 | ||||||
| chr6:10527949
|
T | C | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-282+289T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | chr6 | 10527949 | ||||||
| chr6:10527985
|
T | C | 21 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(18): Show | 21 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-282+325T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | chr6 | 10527985 | ||||||
| chr6:10528023
|
A | G | 18 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0003g0231others(15): Show | 18 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-282+363A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | chr6 | 10528023 | ||||||
| chr6:10528201
|
A | G | 168 | a0001c0001t0001g0007a0001c0001t0001g0133a0001c0001t0001g0135others(165): Show | 168 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.-281-430A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | chr6 | 10528201 | ||||||
| chr6:10528561
|
T | C | 197 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(194): Show | 197 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.-281-70T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 2/4 | chr6 | 10528561 | ||||||
| chr6:10529902
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.925+66C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10529902 | ||||||
| chr6:10529940
|
C | A | 2 | a0001c0001t0001g0007a0001c0001t0009g0006 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.925+104C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10529940 | ||||||
| chr6:10529972
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.925+136C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10529972 | ||||||
| chr6:10530003
|
A | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG00741.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.925+167A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530003 | ||||||
| chr6:10530249
|
C | A | 1 | a0001c0001t0002g0161 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.925+413C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530249 | ||||||
| chr6:10530254
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.925+418A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530254 | ||||||
| chr6:10530257
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.925+421G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530257 | ||||||
| chr6:10530295
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.925+459G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530295 | ||||||
| chr6:10530352
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0015 | 2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.925+516G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530352 | ||||||
| chr6:10530410
|
G | A | 11 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(8): Show | 11 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.925+574G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530410 | ||||||
| chr6:10530559
|
T | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+723T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530559 | ||||||
| chr6:10530704
|
C | G | 23 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(20): Show | 23 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.925+868C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530704 | ||||||
| chr6:10530781
|
G | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00735.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+945G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530781 | ||||||
| chr6:10530881
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0004g0298 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.925+1045C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530881 | ||||||
| chr6:10530910
|
C | T | 1 | a0001c0001t0004g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.925+1074C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530910 | ||||||
| chr6:10530919
|
T | C | 1 | a0001c0001t0004g0316 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.925+1083T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530919 | ||||||
| chr6:10530954
|
T | C | 23 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(20): Show | 23 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.925+1118T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530954 | ||||||
| chr6:10530986
|
G | A | 1 | a0001c0001t0021g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.925+1150G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10530986 | ||||||
| chr6:10531010
|
C | T | 19 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(16): Show | 19 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.925+1174C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531010 | ||||||
| chr6:10531011
|
G | A | 136 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0137others(133): Show | 136 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.925+1175G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531011 | ||||||
| chr6:10531016
|
C | T | 2 | a0001c0001t0003g0232a0001c0001t0024g0241 | 2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.925+1180C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531016 | ||||||
| chr6:10531040
|
C | CA | 8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0162others(5): Show | 8 | HG02056.hp2 HG03239.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+1221dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531040 | |||||
| chr6:10531040
|
C | CAAAA | 22 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(19): Show | 22 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.925+1218_925+1221d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531040 | |||||
| chr6:10531040
|
CA | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0058others(6): Show | 9 | HG01516.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+1221delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531040 | |||||
| chr6:10531203
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.925+1367A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531203 | ||||||
| chr6:10531303
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0068a0001c0001t0017g0067 | 3 | HG02451.hp1 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.925+1467G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531303 | ||||||
| chr6:10531442
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0321 | 3 | HG01361.hp1 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.925+1606C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531442 | ||||||
| chr6:10531537
|
C | T | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.925+1701C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531537 | ||||||
| chr6:10531551
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.925+1715C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531551 | ||||||
| chr6:10531724
|
C | T | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+1888C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531724 | ||||||
| chr6:10531775
|
G | C | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0073others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+1939G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531775 | ||||||
| chr6:10531874
|
C | CT | 33 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0034others(30): Show | 33 | HG00438.hp2 HG00642.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.925+2058dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531874 | |||||
| chr6:10531874
|
C | CTT | 7 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG01256.hp1 HG01256.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+2057_925+2058d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531874 | |||||
| chr6:10531874
|
C | CTTT | 122 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0137others(119): Show | 122 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.925+2056_925+2058d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531874 | |||||
| chr6:10531874
|
C | CTTTT | 12 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(9): Show | 12 | HG01123.hp2 HG01175.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.925+2055_925+2058d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531874 | |||||
| chr6:10531874
|
CT | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0056others(3): Show | 6 | HG00408.hp2 HG01361.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+2058delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10531874 | |||||
| chr6:10531953
|
C | T | 19 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(16): Show | 19 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.925+2117C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10531953 | ||||||
| chr6:10532001
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.925+2165C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10532001 | ||||||
| chr6:10532158
|
G | A | 1 | a0001c0001t0003g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.925+2322G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10532158 | ||||||
| chr6:10532288
|
G | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00735.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+2452G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10532288 | ||||||
| chr6:10532688
|
T | C | 23 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(20): Show | 23 | HG00642.hp2 HG01074.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.925+2852T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10532688 | ||||||
| chr6:10532868
|
C | T | 1 | a0001c0001t0009g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.925+3032C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10532868 | ||||||
| chr6:10532914
|
C | CT | 27 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0022others(24): Show | 27 | HG00408.hp2 HG00438.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.925+3098dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10532914 | |||||
| chr6:10532914
|
C | CTT | 6 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0131others(3): Show | 6 | HG00735.hp2 HG01884.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+3097_925+3098d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10532914 | |||||
| chr6:10532914
|
CT | C | 156 | a0001c0001t0001g0025a0001c0001t0001g0057a0001c0001t0001g0058others(153): Show | 156 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.925+3098delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10532914 | |||||
| chr6:10533080
|
G | A | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.925+3244G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533080 | ||||||
| chr6:10533126
|
G | A | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.925+3290G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533126 | ||||||
| chr6:10533230
|
T | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(198): Show | 201 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.925+3394T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533230 | ||||||
| chr6:10533518
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0321 | 3 | HG01361.hp1 HG02257.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.925+3682T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533518 | ||||||
| chr6:10533597
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.925+3761G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533597 | ||||||
| chr6:10533702
|
T | A | 140 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0137others(137): Show | 140 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.925+3866T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533702 | ||||||
| chr6:10533759
|
C | T | 19 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(16): Show | 19 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.925+3923C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533759 | ||||||
| chr6:10533800
|
C | CA | 20 | a0001c0001t0001g0009a0001c0001t0001g0054a0001c0001t0001g0059others(17): Show | 20 | HG00597.hp1 HG00735.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.925+3990dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10533800 | |||||
| chr6:10533800
|
CA | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0053others(12): Show | 15 | HG00642.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.925+3990delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10533800 | |||||
| chr6:10533800
|
CAA | C | 17 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0133others(14): Show | 17 | HG00438.hp1 HG00621.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.925+3989_925+3990d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10533800 | |||||
| chr6:10533800
|
CAAA | C | 128 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0138others(125): Show | 128 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.925+3988_925+3990d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10533800 | |||||
| chr6:10533829
|
A | G | 140 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0137others(137): Show | 140 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.925+3993A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533829 | ||||||
| chr6:10533846
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00735.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+4010C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533846 | ||||||
| chr6:10533946
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.925+4110C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533946 | ||||||
| chr6:10533960
|
C | T | 1 | a0001c0001t0004g0314 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.925+4124C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10533960 | ||||||
| chr6:10534028
|
T | A | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(1): Show | 4 | HG01496.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+4192T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534028 | ||||||
| chr6:10534139
|
C | CTTTT | 4 | a0001c0001t0001g0007a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG02895.hp1 NA18956.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTT | 15 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(12): Show | 15 | HG01074.hp2 HG01192.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTT | 4 | a0001c0001t0003g0231a0001c0001t0010g0240a0001c0001t0010g0242others(1): Show | 4 | HG01175.hp2 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0301 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.925+4304_925+4305i others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0022g0271 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.925+4304_925+4305i others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(13): Show |
39 | a0001c0001t0001g0133a0001c0001t0001g0154a0001c0001t0001g0158others(36): Show | 39 | HG00642.hp2 HG01993.hp1 HG02071.hp2 others(36): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(14): Show |
34 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0147others(31): Show | 34 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(23): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(15): Show |
26 | a0001c0001t0001g0137a0001c0001t0001g0149a0001c0001t0001g0150others(23): Show | 26 | HG00639.hp2 HG01099.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(24): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(16): Show |
11 | a0001c0001t0001g0162a0001c0001t0001g0167a0001c0001t0001g0184others(8): Show | 11 | HG00621.hp1 HG01256.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(25): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(17): Show |
7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(4): Show | 7 | HG01258.hp1 HG01517.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(26): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(18): Show |
8 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG00741.hp2 HG01175.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(27): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(19): Show |
5 | a0001c0001t0001g0190a0001c0001t0001g0300a0001c0001t0002g0264others(2): Show | 5 | HG02293.hp1 HG02293.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+4304_925+4305i others(28): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.925+4304_925+4305i others(29): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0249a0001c0001t0002g0151a0001c0001t0005g0213 | 3 | HG01109.hp1 HG03130.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.925+4304_925+4305i others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0311 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.925+4304_925+4305i others(31): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0192 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.925+4304_925+4305i others(33): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.925+4304_925+4305i others(37): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534139
|
C | CTTTTTTT others(31): Show |
1 | a0001c0001t0001g0142 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.925+4304_925+4305i others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534139 | |||||
| chr6:10534141
|
C | CT | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(8): Show | 11 | HG00735.hp2 HG01243.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+4323dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534141 | |||||
| chr6:10534141
|
C | CTT | 6 | a0001c0001t0001g0029a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01361.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+4322_925+4323d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534141 | |||||
| chr6:10534141
|
C | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0133others(162): Show | 165 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.925+4305C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534141 | ||||||
| chr6:10534270
|
C | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0133others(162): Show | 165 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.925+4434C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534270 | ||||||
| chr6:10534288
|
C | A | 20 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(17): Show | 20 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.925+4452C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534288 | ||||||
| chr6:10534330
|
C | T | 12 | a0001c0001t0001g0256a0001c0001t0001g0260a0001c0001t0001g0262others(9): Show | 12 | HG00597.hp2 HG02056.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.925+4494C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534330 | ||||||
| chr6:10534422
|
C | T | 1 | a0001c0001t0007g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.925+4586C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534422 | ||||||
| chr6:10534509
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.925+4673T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534509 | ||||||
| chr6:10534578
|
G | C | 162 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0133others(159): Show | 162 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.925+4742G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534578 | ||||||
| chr6:10534621
|
A | G | 1 | a0001c0002t0001g0207 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.925+4785A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534621 | ||||||
| chr6:10534715
|
TAGTC | T | 9 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0087others(6): Show | 9 | HG00438.hp2 HG00558.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+4882_925+4885d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10534715 | |||||
| chr6:10534797
|
G | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0068a0001c0001t0004g0035others(1): Show | 4 | HG02451.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+4961G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534797 | ||||||
| chr6:10534949
|
T | G | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(12): Show | 15 | HG00735.hp2 HG01361.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.925+5113T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10534949 | ||||||
| chr6:10535000
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0009g0006 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.925+5164A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535000 | ||||||
| chr6:10535009
|
C | T | 19 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(16): Show | 19 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.925+5173C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535009 | ||||||
| chr6:10535140
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.925+5304C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535140 | ||||||
| chr6:10535146
|
T | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0091a0001c0001t0001g0159 | 3 | HG00673.hp2 HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.925+5310T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535146 | ||||||
| chr6:10535220
|
A | G | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.925+5384A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535220 | ||||||
| chr6:10535288
|
G | A | 19 | a0001c0001t0001g0025a0001c0001t0003g0229a0001c0001t0003g0230others(16): Show | 19 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.925+5452G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535288 | ||||||
| chr6:10535358
|
A | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(208): Show | 211 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.925+5522A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535358 | ||||||
| chr6:10535371
|
T | C | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+5535T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535371 | ||||||
| chr6:10535553
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.925+5717T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535553 | ||||||
| chr6:10535657
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0068a0001c0001t0004g0035others(1): Show | 4 | HG02451.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+5821C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535657 | ||||||
| chr6:10535831
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.925+5995G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535831 | ||||||
| chr6:10535846
|
C | G | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+6010C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535846 | ||||||
| chr6:10535899
|
C | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.925+6063C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535899 | ||||||
| chr6:10535900
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.925+6064G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535900 | ||||||
| chr6:10535915
|
G | A | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+6079G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10535915 | ||||||
| chr6:10536003
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.925+6167C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536003 | ||||||
| chr6:10536062
|
A | AT | 7 | a0001c0001t0001g0029a0001c0001t0001g0062a0001c0001t0001g0063others(4): Show | 7 | HG01361.hp1 HG01884.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+6227dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10536062 | |||||
| chr6:10536126
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0009g0006 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.925+6290C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536126 | ||||||
| chr6:10536139
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+6303T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536139 | ||||||
| chr6:10536227
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0068a0001c0001t0001g0317others(2): Show | 5 | HG02451.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+6391C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536227 | ||||||
| chr6:10536303
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.925+6467C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536303 | ||||||
| chr6:10536338
|
A | C | 4 | a0001c0001t0001g0215a0001c0001t0003g0239a0001c0001t0010g0240others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+6502A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536338 | ||||||
| chr6:10536358
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.925+6522T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536358 | ||||||
| chr6:10536359
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.925+6523T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536359 | ||||||
| chr6:10536609
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.925+6773C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536609 | ||||||
| chr6:10536656
|
T | C | 18 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(15): Show | 18 | HG00642.hp2 HG00735.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.925+6820T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536656 | ||||||
| chr6:10536706
|
C | CT | 40 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0062others(37): Show | 40 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.925+6885dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10536706 | |||||
| chr6:10536706
|
C | CTT | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(6): Show | 9 | HG00735.hp2 HG02615.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+6884_925+6885d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10536706 | |||||
| chr6:10536746
|
C | G | 1 | a0001c0001t0001g0053 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.925+6910C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536746 | ||||||
| chr6:10536893
|
G | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+7057G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536893 | ||||||
| chr6:10536923
|
G | A | 2 | a0001c0001t0004g0314a0001c0001t0004g0316 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.925+7087G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536923 | ||||||
| chr6:10536957
|
G | T | 1 | a0001c0001t0001g0113 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.925+7121G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536957 | ||||||
| chr6:10536991
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.925+7155C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10536991 | ||||||
| chr6:10537180
|
G | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+7344G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537180 | ||||||
| chr6:10537278
|
G | T | 1 | a0001c0001t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.925+7442G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537278 | ||||||
| chr6:10537402
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+7566T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537402 | ||||||
| chr6:10537425
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.925+7589G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537425 | ||||||
| chr6:10537426
|
TG | T | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+7594delG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537426 | |||||
| chr6:10537493
|
A | G | 186 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(183): Show | 186 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.925+7657A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537493 | ||||||
| chr6:10537498
|
T | C | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.925+7662T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537498 | ||||||
| chr6:10537544
|
T | C | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(1): Show | 4 | HG01496.hp1 HG03471.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+7708T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537544 | ||||||
| chr6:10537647
|
G | T | 1 | a0001c0001t0007g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.925+7811G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537647 | ||||||
| chr6:10537658
|
G | T | 2 | a0001c0001t0003g0233a0001c0001t0003g0238 | 2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.925+7822G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537658 | ||||||
| chr6:10537698
|
C | CA | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(9): Show | 12 | HG00408.hp2 HG00642.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.925+7890dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537698 | |||||
| chr6:10537698
|
CA | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0028others(58): Show | 61 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.925+7890delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537698 | |||||
| chr6:10537698
|
CAAAAAAA others(5): Show |
C | 11 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0001t0001g0172others(8): Show | 11 | HG01891.hp1 HG02056.hp2 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+7879_925+7890d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537698 | |||||
| chr6:10537698
|
CAAAAAAA others(6): Show |
C | 135 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0133others(132): Show | 135 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.925+7878_925+7890d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537698 | |||||
| chr6:10537712
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+7881_925+7895d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537712 | |||||
| chr6:10537715
|
AAAAAAAA others(5): Show |
A | 4 | a0001c0001t0001g0034a0001c0001t0001g0068a0001c0001t0004g0035others(1): Show | 4 | HG02451.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+7884_925+7895d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537715 | |||||
| chr6:10537716
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0317 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.925+7885_925+7895d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537716 | |||||
| chr6:10537717
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0011g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.925+7886_925+7895d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537717 | |||||
| chr6:10537719
|
A | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0063a0001c0001t0001g0132others(1): Show | 4 | HG01361.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+7883A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537719 | ||||||
| chr6:10537722
|
A | C | 2 | a0001c0001t0001g0249a0001c0001t0005g0213 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.925+7886A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537722 | ||||||
| chr6:10537725
|
AAC | A | 9 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0003g0229others(6): Show | 9 | HG00735.hp2 HG01175.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+7891_925+7892d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537725 | |||||
| chr6:10537726
|
AC | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(8): Show | 11 | HG00738.hp2 HG01516.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+7891delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537726 | ||||||
| chr6:10537727
|
C | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0092others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+7891C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537727 | ||||||
| chr6:10537733
|
AAAGAAAA others(2): Show |
A | 3 | a0001c0001t0007g0243a0001c0001t0007g0244a0001c0001t0007g0245 | 3 | HG00642.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.925+7900_925+7908d others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10537733 | |||||
| chr6:10537815
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.925+7979G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537815 | ||||||
| chr6:10537862
|
A | G | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+8026A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537862 | ||||||
| chr6:10537950
|
A | G | 172 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0036others(169): Show | 172 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.925+8114A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10537950 | ||||||
| chr6:10538133
|
C | T | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG00735.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+8297C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538133 | ||||||
| chr6:10538134
|
G | A | 22 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0085others(19): Show | 22 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.925+8298G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538134 | ||||||
| chr6:10538160
|
C | T | 8 | a0001c0001t0001g0085a0001c0001t0002g0283a0001c0001t0003g0229others(5): Show | 8 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+8324C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538160 | ||||||
| chr6:10538161
|
A | G | 195 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0034others(192): Show | 195 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.925+8325A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538161 | ||||||
| chr6:10538303
|
G | A | 1 | a0001c0001t0021g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.925+8467G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538303 | ||||||
| chr6:10538404
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.925+8568G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538404 | ||||||
| chr6:10538408
|
C | CA | 30 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0088others(27): Show | 30 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.925+8602dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538408 | |||||
| chr6:10538408
|
CA | C | 21 | a0001c0001t0001g0018a0001c0001t0001g0070a0001c0001t0001g0077others(18): Show | 21 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.925+8602delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538408 | |||||
| chr6:10538408
|
CAAAA | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0068others(19): Show | 22 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.925+8599_925+8602d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538408 | |||||
| chr6:10538431
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.925+8596_925+8597i others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538431 | |||||
| chr6:10538431
|
A | ATAT | 3 | a0001c0001t0001g0216a0001c0001t0001g0218a0001c0001t0025g0217 | 3 | HG01496.hp1 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.925+8595_925+8596i others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538431 | ||||||
| chr6:10538431
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0215 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.925+8595_925+8596i others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538431 | ||||||
| chr6:10538433
|
A | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0132others(11): Show | 14 | HG01496.hp1 HG02622.hp1 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.925+8597A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538433 | ||||||
| chr6:10538435
|
A | AAT | 9 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0259others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+8600_925+8601i others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538435 | |||||
| chr6:10538435
|
A | AATATATA others(3): Show |
1 | a0001c0001t0008g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.925+8600_925+8601i others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538435 | |||||
| chr6:10538435
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0029 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.925+8600_925+8601i others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538435 | |||||
| chr6:10538435
|
A | AT | 8 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0015others(5): Show | 8 | HG01891.hp2 HG02258.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+8599_925+8600i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538435 | ||||||
| chr6:10538435
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.925+8599_925+8600i others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538435 | ||||||
| chr6:10538435
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.925+8599_925+8600i others(23): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538435 | ||||||
| chr6:10538435
|
A | T | 33 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(30): Show | 33 | HG01175.hp2 HG01192.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.925+8599A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538435 | ||||||
| chr6:10538437
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0007 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.925+8602_925+8603i others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAAAAATA others(25): Show |
1 | a0001c0001t0019g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.925+8602_925+8603i others(34): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAAAATAT others(8): Show |
1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.925+8602_925+8603i others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0005g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.925+8602_925+8603i others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAAAATAT others(12): Show |
1 | a0001c0001t0009g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.925+8602_925+8603i others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAAAATAT others(32): Show |
1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+8602_925+8603i others(41): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.925+8602_925+8603i others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAATATAT others(8): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+8602_925+8603i others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAATATAT others(16): Show |
1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.925+8602_925+8603i others(25): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AAT | 9 | a0001c0001t0001g0036a0001c0001t0001g0074a0001c0001t0001g0166others(6): Show | 9 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+8620_925+8621d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10538437 | |||||
| chr6:10538437
|
A | AT | 22 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0084others(19): Show | 22 | HG00558.hp1 HG00642.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.925+8601_925+8602i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538437 | ||||||
| chr6:10538437
|
A | ATATAT | 3 | a0001c0001t0001g0206a0001c0001t0001g0292a0001c0001t0004g0069 | 3 | HG02615.hp2 HG02896.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.925+8601_925+8602i others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538437 | ||||||
| chr6:10538437
|
A | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 111 | HG00558.hp2 HG01074.hp1 HG01074.hp2 others(108): Show |
intron_variant | MODIFIER | c.925+8601A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538437 | ||||||
| chr6:10538439
|
T | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0052a0001c0001t0001g0142others(4): Show | 7 | HG00408.hp1 HG02080.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+8603T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538439 | ||||||
| chr6:10538441
|
T | A | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.925+8605T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538441 | ||||||
| chr6:10538480
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0009g0006 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.925+8644A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538480 | ||||||
| chr6:10538567
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.925+8731A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538567 | ||||||
| chr6:10538712
|
A | G | 170 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0001g0085others(167): Show | 170 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.925+8876A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538712 | ||||||
| chr6:10538843
|
C | G | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.925+9007C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10538843 | ||||||
| chr6:10539056
|
T | G | 191 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(188): Show | 191 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.925+9220T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539056 | ||||||
| chr6:10539087
|
C | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0249a0001c0001t0005g0213 | 3 | HG01109.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.925+9251C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539087 | ||||||
| chr6:10539180
|
C | CT | 31 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(28): Show | 31 | HG00621.hp2 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.925+9370dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
C | CTTTTT | 6 | a0001c0001t0001g0029a0001c0001t0001g0222a0001c0001t0001g0248others(3): Show | 6 | HG00642.hp2 HG02109.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.925+9366_925+9370d others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
C | CTTTTTT | 8 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0167others(5): Show | 8 | HG01256.hp1 HG01884.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+9365_925+9370d others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
C | CTTTTTTT | 34 | a0001c0001t0001g0139a0001c0001t0001g0142a0001c0001t0001g0154others(31): Show | 34 | HG00558.hp1 HG00639.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.925+9364_925+9370d others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
C | CTTTTTTT others(1): Show |
47 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0150others(44): Show | 47 | HG00597.hp2 HG00621.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.925+9363_925+9370d others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
C | CTTTTTTT others(2): Show |
26 | a0001c0001t0001g0039a0001c0001t0001g0137a0001c0001t0001g0140others(23): Show | 26 | HG00438.hp1 HG01099.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.925+9362_925+9370d others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
C | CTTTTTTT others(3): Show |
19 | a0001c0001t0001g0133a0001c0001t0001g0146a0001c0001t0001g0162others(16): Show | 19 | HG00323.hp2 HG01109.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.925+9361_925+9370d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0259a0001c0001t0001g0307 | 3 | HG02735.hp2 HG03927.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.925+9360_925+9370d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
CT | C | 10 | a0001c0001t0001g0073a0001c0001t0001g0317a0001c0001t0001g0320others(7): Show | 10 | HG01074.hp2 HG01175.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+9370delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539180
|
CTT | C | 17 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0068others(14): Show | 17 | HG02109.hp1 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.925+9369_925+9370d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539180 | |||||
| chr6:10539220
|
AC | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0068others(21): Show | 24 | HG01074.hp2 HG01175.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.925+9387delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539220 | |||||
| chr6:10539222
|
C | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0188others(1): Show | 4 | HG01175.hp1 HG01361.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+9386C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539222 | ||||||
| chr6:10539246
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0009g0006 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.925+9410G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539246 | ||||||
| chr6:10539262
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0081others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+9426C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539262 | ||||||
| chr6:10539278
|
C | A | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0281others(2): Show | 5 | HG00621.hp1 HG02080.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+9442C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539278 | ||||||
| chr6:10539282
|
T | C | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0281others(2): Show | 5 | HG00621.hp1 HG02080.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+9446T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539282 | ||||||
| chr6:10539283
|
G | A | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0281others(2): Show | 5 | HG00621.hp1 HG02080.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+9447G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539283 | ||||||
| chr6:10539298
|
C | T | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0281others(2): Show | 5 | HG00621.hp1 HG02080.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+9462C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539298 | ||||||
| chr6:10539313
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.925+9477C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539313 | ||||||
| chr6:10539432
|
G | A | 125 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0133others(122): Show | 125 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.925+9596G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539432 | ||||||
| chr6:10539459
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG01884.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+9623A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539459 | ||||||
| chr6:10539509
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.925+9673G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539509 | ||||||
| chr6:10539557
|
G | A | 1 | a0001c0001t0015g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.925+9721G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539557 | ||||||
| chr6:10539615
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.925+9779G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539615 | ||||||
| chr6:10539639
|
GGA | G | 162 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(159): Show | 162 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.925+9816_925+9817d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10539639 | |||||
| chr6:10539744
|
T | C | 138 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(135): Show | 138 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.925+9908T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539744 | ||||||
| chr6:10539805
|
G | T | 1 | a0001c0001t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.925+9969G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539805 | ||||||
| chr6:10539807
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.925+9971C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539807 | ||||||
| chr6:10539953
|
C | T | 1 | a0001c0001t0005g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.925+10117C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539953 | ||||||
| chr6:10539976
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.925+10140G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10539976 | ||||||
| chr6:10540002
|
C | T | 1 | a0001c0001t0019g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.925+10166C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540002 | ||||||
| chr6:10540037
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.925+10201C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540037 | ||||||
| chr6:10540077
|
C | CA | 66 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0055others(63): Show | 66 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.925+10250dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10540077 | |||||
| chr6:10540087
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.925+10251G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540087 | ||||||
| chr6:10540092
|
GAAAGGAA others(7): Show |
G | 1 | a0001c0001t0001g0034 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.925+10265_925+1027 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10540092 | |||||
| chr6:10540093
|
AAAGG | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG01496.hp1 HG02615.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+10268_925+1027 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10540093 | |||||
| chr6:10540335
|
C | T | 41 | a0001c0001t0001g0053a0001c0001t0001g0124a0001c0001t0001g0137others(38): Show | 41 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.925+10499C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540335 | ||||||
| chr6:10540342
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.925+10506T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540342 | ||||||
| chr6:10540389
|
G | GTTCTC | 152 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(149): Show | 152 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.925+10556_925+1055 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10540389 | |||||
| chr6:10540583
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.925+10747C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540583 | ||||||
| chr6:10540756
|
T | C | 1 | a0001c0001t0002g0296 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.925+10920T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540756 | ||||||
| chr6:10540870
|
T | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+11034T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540870 | ||||||
| chr6:10540882
|
G | A | 320 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(317): Show | 320 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.925+11046G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540882 | ||||||
| chr6:10540980
|
G | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(109): Show | 112 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.925+11144G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540980 | ||||||
| chr6:10541005
|
G | C | 2 | a0001c0001t0001g0215a0001c0001t0004g0069 | 2 | HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.925+11169G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541005 | ||||||
| chr6:10541186
|
G | A | 2 | a0001c0001t0007g0243a0001c0001t0007g0244 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.925+11350G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541186 | ||||||
| chr6:10541192
|
G | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0081a0001c0001t0001g0266others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.925+11356G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541192 | ||||||
| chr6:10541342
|
C | G | 1 | a0001c0001t0005g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.925+11506C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541342 | ||||||
| chr6:10541387
|
C | T | 1 | a0001c0001t0009g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.925+11551C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541387 | ||||||
| chr6:10541440
|
T | C | 51 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(48): Show | 51 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.925+11604T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541440 | ||||||
| chr6:10541450
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.925+11614T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541450 | ||||||
| chr6:10541517
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.925+11681G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541517 | ||||||
| chr6:10541550
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0075a0001c0001t0001g0139 | 3 | HG02735.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+11714C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541550 | ||||||
| chr6:10541595
|
G | T | 51 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(48): Show | 51 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.925+11759G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541595 | ||||||
| chr6:10541812
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+11976G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10541812 | ||||||
| chr6:10542141
|
A | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+12305A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542141 | ||||||
| chr6:10542167
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.925+12331A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542167 | ||||||
| chr6:10542208
|
G | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.925+12372G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542208 | ||||||
| chr6:10542217
|
GT | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+12384delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542217 | |||||
| chr6:10542228
|
C | G | 2 | a0001c0001t0001g0299a0001c0001t0004g0298 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.925+12392C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542228 | ||||||
| chr6:10542250
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.925+12414T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542250 | ||||||
| chr6:10542256
|
G | C | 40 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.925+12420G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542256 | ||||||
| chr6:10542294
|
A | C | 40 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.925+12458A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542294 | ||||||
| chr6:10542310
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+12474C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542310 | ||||||
| chr6:10542318
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0004g0298 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.925+12482C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542318 | ||||||
| chr6:10542415
|
T | TA | 58 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(55): Show | 58 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.925+12579_925+1258 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542415 | ||||||
| chr6:10542416
|
T | A | 58 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(55): Show | 58 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.925+12580T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542416 | ||||||
| chr6:10542455
|
G | T | 1 | a0001c0001t0003g0231 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.925+12619G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542455 | ||||||
| chr6:10542458
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.925+12622A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542458 | ||||||
| chr6:10542496
|
A | G | 8 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0143others(5): Show | 8 | HG03834.hp1 NA18946.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+12660A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542496 | ||||||
| chr6:10542498
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.925+12662A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542498 | ||||||
| chr6:10542521
|
C | G | 1 | a0001c0001t0009g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.925+12685C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542521 | ||||||
| chr6:10542532
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+12696A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542532 | ||||||
| chr6:10542543
|
G | A | 58 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(55): Show | 58 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.925+12707G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542543 | ||||||
| chr6:10542650
|
A | G | 67 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(64): Show | 67 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.925+12814A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542650 | ||||||
| chr6:10542661
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0075a0001c0001t0001g0139 | 3 | HG02735.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+12825G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542661 | ||||||
| chr6:10542668
|
C | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(17): Show | 20 | HG01496.hp1 HG02615.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.925+12832C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542668 | ||||||
| chr6:10542772
|
A | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG00735.hp2 HG01884.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+12936A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542772 | ||||||
| chr6:10542860
|
C | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+13024C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542860 | ||||||
| chr6:10542862
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.925+13026A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542862 | ||||||
| chr6:10542890
|
ATTCT | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0018others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+13057_925+1306 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542890 | |||||
| chr6:10542890
|
ATTCTTTT others(3): Show |
A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+13057_925+1306 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542890 | |||||
| chr6:10542893
|
C | CT | 32 | a0001c0001t0001g0036a0001c0001t0001g0057a0001c0001t0001g0058others(29): Show | 32 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.925+13082dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542893 | |||||
| chr6:10542893
|
C | CTT | 31 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 31 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.925+13081_925+1308 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542893 | |||||
| chr6:10542893
|
C | CTTTT | 6 | a0001c0001t0001g0075a0001c0001t0001g0081a0001c0001t0001g0125others(3): Show | 6 | HG00140.hp1 HG01099.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.925+13079_925+1308 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542893 | |||||
| chr6:10542893
|
C | CTTTTTT | 9 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0131others(6): Show | 9 | HG00735.hp2 HG01175.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+13077_925+1308 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542893 | |||||
| chr6:10542893
|
CT | C | 14 | a0001c0001t0001g0059a0001c0001t0001g0089a0001c0001t0001g0119others(11): Show | 14 | HG00558.hp2 HG01256.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.925+13082delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10542893 | |||||
| chr6:10542929
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0186 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.925+13093C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10542929 | ||||||
| chr6:10543011
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0183 | 3 | NA18955.hp2 NA18992.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.925+13175G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543011 | ||||||
| chr6:10543035
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0070a0001c0001t0001g0214others(1): Show | 4 | HG01928.hp2 HG02273.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+13199G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543035 | ||||||
| chr6:10543057
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.925+13221G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543057 | ||||||
| chr6:10543123
|
G | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(42): Show | 45 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.925+13287G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543123 | ||||||
| chr6:10543180
|
T | A | 40 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.925+13344T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543180 | ||||||
| chr6:10543195
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.925+13359A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543195 | ||||||
| chr6:10543216
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+13380T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543216 | ||||||
| chr6:10543243
|
G | A | 40 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.925+13407G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543243 | ||||||
| chr6:10543330
|
G | A | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.925+13494G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543330 | ||||||
| chr6:10543437
|
T | C | 58 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(55): Show | 58 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.925+13601T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543437 | ||||||
| chr6:10543564
|
T | C | 50 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(47): Show | 50 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.925+13728T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543564 | ||||||
| chr6:10543733
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+13897A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543733 | ||||||
| chr6:10543818
|
T | C | 71 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(68): Show | 71 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.925+13982T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543818 | ||||||
| chr6:10543910
|
A | G | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+14074A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543910 | ||||||
| chr6:10543930
|
A | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+14094A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10543930 | ||||||
| chr6:10544089
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0017g0067 | 3 | HG02451.hp1 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.925+14253G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544089 | ||||||
| chr6:10544207
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+14371G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544207 | ||||||
| chr6:10544292
|
C | T | 1 | a0001c0001t0009g0033 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.925+14456C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544292 | ||||||
| chr6:10544386
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0002g0153 | 2 | NA19067.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.925+14550C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544386 | ||||||
| chr6:10544446
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.925+14610C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544446 | ||||||
| chr6:10544489
|
C | T | 2 | a0001c0001t0007g0243a0001c0001t0007g0244 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.925+14653C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544489 | ||||||
| chr6:10544568
|
C | T | 1 | a0001c0001t0004g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.925+14732C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544568 | ||||||
| chr6:10544615
|
CATAAA | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.925+14793_925+1479 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544615 | |||||
| chr6:10544634
|
TTAAA | T | 8 | a0001c0001t0001g0068a0001c0001t0001g0205a0001c0001t0001g0317others(5): Show | 8 | HG00741.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+14820_925+1482 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544634 | |||||
| chr6:10544684
|
C | G | 17 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.925+14848C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544684 | ||||||
| chr6:10544715
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.925+14879G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544715 | ||||||
| chr6:10544754
|
G | C | 2 | a0001c0001t0003g0233a0001c0001t0003g0238 | 2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.925+14918G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544754 | ||||||
| chr6:10544760
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+14924G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544760 | ||||||
| chr6:10544806
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.925+14970G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544806 | ||||||
| chr6:10544822
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.925+14986G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544822 | ||||||
| chr6:10544869
|
C | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0075a0001c0001t0001g0139 | 3 | HG02735.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+15033C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544869 | ||||||
| chr6:10544920
|
T | C | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+15084T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544920 | ||||||
| chr6:10544940
|
T | C | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+15104T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544940 | ||||||
| chr6:10544941
|
GT | G | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+15106delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544941 | ||||||
| chr6:10544945
|
C | CAAAT | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0025others(78): Show | 81 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.925+15142_925+1514 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544945 | |||||
| chr6:10544945
|
C | CAAATAAA others(1): Show |
8 | a0001c0001t0001g0063a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG01361.hp1 HG01496.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+15138_925+1514 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544945 | |||||
| chr6:10544945
|
C | CAAATAAA others(5): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01099.hp1 HG02071.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.925+15134_925+1514 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544945 | |||||
| chr6:10544945
|
C | CAAATAAA others(9): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0319a0001c0001t0004g0035others(1): Show | 4 | HG02622.hp2 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+15130_925+1514 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544945 | |||||
| chr6:10544945
|
CAAAT | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073others(4): Show | 7 | HG01243.hp1 HG02735.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+15142_925+1514 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544945 | |||||
| chr6:10544945
|
CAAATAAA others(1): Show |
C | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0222others(2): Show | 5 | HG01884.hp1 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+15138_925+1514 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10544945 | |||||
| chr6:10544982
|
G | A | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+15146G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10544982 | ||||||
| chr6:10545049
|
A | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+15213A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545049 | ||||||
| chr6:10545213
|
G | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0111a0001c0001t0002g0254others(1): Show | 4 | HG00735.hp1 HG01978.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+15377G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545213 | ||||||
| chr6:10545286
|
C | G | 5 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0281others(2): Show | 5 | HG00621.hp1 HG02080.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+15450C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545286 | ||||||
| chr6:10545338
|
C | T | 2 | a0001c0001t0001g0299a0001c0001t0004g0298 | 2 | HG01891.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.925+15502C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545338 | ||||||
| chr6:10545452
|
G | A | 17 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 17 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.925+15616G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545452 | ||||||
| chr6:10545495
|
G | A | 64 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 64 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.925+15659G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545495 | ||||||
| chr6:10545513
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0075a0001c0001t0001g0139 | 3 | HG02735.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+15677T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545513 | ||||||
| chr6:10545568
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 64 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.925+15732C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545568 | ||||||
| chr6:10545638
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.925+15802C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545638 | ||||||
| chr6:10545749
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.925+15913G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545749 | ||||||
| chr6:10545959
|
T | G | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+16123T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545959 | ||||||
| chr6:10546050
|
C | T | 34 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(31): Show | 34 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.925+16214C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546050 | ||||||
| chr6:10546051
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.925+16215G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546051 | ||||||
| chr6:10546247
|
C | T | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+16411C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546247 | ||||||
| chr6:10546260
|
A | G | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0084others(17): Show | 20 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.925+16424A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546260 | ||||||
| chr6:10546289
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.925+16453C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546289 | ||||||
| chr6:10546398
|
A | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0075others(4): Show | 7 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+16562A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546398 | ||||||
| chr6:10546434
|
G | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG00735.hp2 HG01884.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+16598G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546434 | ||||||
| chr6:10546500
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+16664T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546500 | ||||||
| chr6:10546520
|
G | A | 130 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.925+16684G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546520 | ||||||
| chr6:10546568
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.925+16732A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546568 | ||||||
| chr6:10546573
|
T | C | 127 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(124): Show | 127 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.925+16737T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546573 | ||||||
| chr6:10546763
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0025 | 2 | HG01891.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.925+16927T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546763 | ||||||
| chr6:10546785
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+16949T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546785 | ||||||
| chr6:10546796
|
T | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.925+16960T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546796 | ||||||
| chr6:10546817
|
T | G | 2 | a0001c0001t0001g0043a0001c0001t0003g0229 | 2 | HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.925+16981T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10546817 | ||||||
| chr6:10547131
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.925+17295A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10547131 | ||||||
| chr6:10547337
|
C | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0302a0001c0001t0020g0152 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.925+17501C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10547337 | ||||||
| chr6:10547389
|
T | C | 3 | a0001c0001t0003g0239a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG02258.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.925+17553T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10547389 | ||||||
| chr6:10547461
|
A | G | 8 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG00735.hp2 HG01884.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+17625A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10547461 | ||||||
| chr6:10547534
|
G | C | 1 | a0001c0001t0001g0156 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.925+17698G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10547534 | ||||||
| chr6:10548110
|
C | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0075others(4): Show | 7 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+18274C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548110 | ||||||
| chr6:10548284
|
G | T | 121 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(118): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.925+18448G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548284 | ||||||
| chr6:10548359
|
A | G | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+18523A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548359 | ||||||
| chr6:10548657
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.925+18821C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548657 | ||||||
| chr6:10548693
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0075 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+18857C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548693 | ||||||
| chr6:10548694
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.925+18858G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548694 | ||||||
| chr6:10548716
|
T | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0075others(4): Show | 7 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+18880T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548716 | ||||||
| chr6:10548726
|
C | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 8 | HG02615.hp1 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+18890C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548726 | ||||||
| chr6:10548729
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0021g0064a0001c0001t0023g0313 | 3 | HG02572.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.925+18893A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548729 | ||||||
| chr6:10548750
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.925+18914C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548750 | ||||||
| chr6:10548765
|
C | CT | 10 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0068others(7): Show | 10 | HG01361.hp1 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+18942dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10548765 | |||||
| chr6:10548784
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.925+18948G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548784 | ||||||
| chr6:10548864
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.925+19028G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548864 | ||||||
| chr6:10548919
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(61): Show | 64 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.925+19083C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548919 | ||||||
| chr6:10548930
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.925+19094T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548930 | ||||||
| chr6:10548938
|
T | C | 1 | a0001c0001t0002g0254 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.925+19102T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548938 | ||||||
| chr6:10548948
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.925+19112G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548948 | ||||||
| chr6:10548961
|
G | A | 16 | a0001c0001t0001g0120a0001c0001t0001g0137a0001c0001t0001g0142others(13): Show | 16 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.925+19125G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10548961 | ||||||
| chr6:10549010
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.925+19174G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549010 | ||||||
| chr6:10549046
|
C | T | 11 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.925+19210C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549046 | ||||||
| chr6:10549103
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.925+19267T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549103 | ||||||
| chr6:10549197
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.925+19361C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549197 | ||||||
| chr6:10549335
|
T | A | 1 | a0001c0001t0003g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.925+19499T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549335 | ||||||
| chr6:10549346
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.925+19510A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549346 | ||||||
| chr6:10549419
|
G | A | 1 | a0001c0001t0004g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.925+19583G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549419 | ||||||
| chr6:10549552
|
A | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0075others(4): Show | 7 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+19716A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549552 | ||||||
| chr6:10549553
|
A | ATC | 3 | a0001c0001t0001g0081a0001c0001t0001g0139a0001c0001t0005g0026 | 3 | HG00735.hp2 HG01243.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.925+19727_925+1972 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10549553 | |||||
| chr6:10549563
|
C | CT | 18 | a0001c0001t0001g0019a0001c0001t0001g0087a0001c0001t0001g0120others(15): Show | 18 | HG00438.hp1 HG00438.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.925+19753dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10549563 | |||||
| chr6:10549563
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+19727C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549563 | ||||||
| chr6:10549563
|
CT | C | 34 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0015others(31): Show | 34 | HG01081.hp1 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.925+19753delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10549563 | |||||
| chr6:10549563
|
CTT | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.925+19752_925+1975 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10549563 | |||||
| chr6:10549563
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.925+19741_925+1975 others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10549563 | |||||
| chr6:10549564
|
T | TC | 6 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG01884.hp1 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+19728_925+1972 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549564 | ||||||
| chr6:10549565
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.925+19729T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549565 | ||||||
| chr6:10549566
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0015others(12): Show | 15 | HG01099.hp2 HG01256.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.925+19730T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549566 | ||||||
| chr6:10549567
|
T | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014others(79): Show | 82 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.925+19731T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549567 | ||||||
| chr6:10549568
|
T | C | 5 | a0001c0001t0001g0270a0001c0001t0001g0287a0001c0001t0002g0090others(2): Show | 5 | HG00558.hp2 HG01099.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+19732T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549568 | ||||||
| chr6:10549569
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.925+19733T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549569 | ||||||
| chr6:10549578
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.925+19742T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549578 | ||||||
| chr6:10549713
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.925+19877C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549713 | ||||||
| chr6:10549820
|
G | T | 1 | a0001c0001t0001g0010 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.925+19984G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549820 | ||||||
| chr6:10549916
|
A | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 103 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.925+20080A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549916 | ||||||
| chr6:10549959
|
G | C | 1 | a0001c0001t0001g0272 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.925+20123G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10549959 | ||||||
| chr6:10550013
|
T | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0075others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+20177T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550013 | ||||||
| chr6:10550107
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0117 | 2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.925+20271G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550107 | ||||||
| chr6:10550137
|
T | A | 1 | a0001c0001t0002g0296 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.925+20301T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550137 | ||||||
| chr6:10550285
|
C | G | 10 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+20449C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550285 | ||||||
| chr6:10550331
|
C | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG00735.hp2 HG01884.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+20495C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550331 | ||||||
| chr6:10550340
|
A | T | 10 | a0001c0001t0001g0266a0001c0001t0001g0318a0001c0001t0001g0319others(7): Show | 10 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.925+20504A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550340 | ||||||
| chr6:10550398
|
A | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(25): Show | 28 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.925+20562A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550398 | ||||||
| chr6:10550408
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.925+20572G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550408 | ||||||
| chr6:10550611
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.925+20775C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550611 | ||||||
| chr6:10550675
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0126 | 2 | NA18959.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.925+20839G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550675 | ||||||
| chr6:10550763
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+20927G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550763 | ||||||
| chr6:10550907
|
A | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0075others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+21071A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550907 | ||||||
| chr6:10550992
|
G | A | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(5): Show | 8 | HG01346.hp1 HG01934.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+21156G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10550992 | ||||||
| chr6:10551131
|
T | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0075others(5): Show | 8 | HG02451.hp1 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+21295T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551131 | ||||||
| chr6:10551375
|
T | C | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.925+21539T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551375 | ||||||
| chr6:10551382
|
C | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.925+21546C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551382 | ||||||
| chr6:10551388
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.925+21552C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551388 | ||||||
| chr6:10551389
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+21553C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551389 | ||||||
| chr6:10551396
|
G | C | 3 | a0001c0001t0003g0234a0001c0001t0011g0001a0001c0001t0027g0003 | 3 | HG02976.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+21560G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551396 | ||||||
| chr6:10551401
|
A | G | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0019g0127 | 3 | HG02717.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.925+21565A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551401 | ||||||
| chr6:10551427
|
ATTAT | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0017g0067 | 3 | HG02451.hp1 HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.925+21597_925+2160 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10551427 | |||||
| chr6:10551431
|
TTTA | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 16 | HG01169.hp2 HG01496.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.925+21608_925+2161 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10551431 | |||||
| chr6:10551451
|
AT | A | 105 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(102): Show | 105 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.925+21627delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10551451 | |||||
| chr6:10551457
|
T | A | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0074others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+21621T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551457 | ||||||
| chr6:10551481
|
C | T | 8 | a0001c0001t0001g0154a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | NA18945.hp2 NA18951.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+21645C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551481 | ||||||
| chr6:10551523
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0159 | 2 | HG00673.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.925+21687G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551523 | ||||||
| chr6:10551637
|
G | T | 2 | a0001c0001t0002g0200a0001c0001t0002g0203 | 2 | HG00408.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.925+21801G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551637 | ||||||
| chr6:10551734
|
C | T | 38 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(35): Show | 38 | HG00140.hp1 HG01099.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.925+21898C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551734 | ||||||
| chr6:10551779
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0317a0001c0001t0007g0243others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+21943C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551779 | ||||||
| chr6:10551781
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.925+21945C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551781 | ||||||
| chr6:10551848
|
C | G | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.925+22012C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551848 | ||||||
| chr6:10551858
|
A | G | 18 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 18 | HG01496.hp1 HG02572.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.925+22022A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551858 | ||||||
| chr6:10551861
|
G | A | 1 | a0001c0003t0001g0144 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.925+22025G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10551861 | ||||||
| chr6:10552300
|
TA | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0021others(41): Show | 44 | HG00140.hp1 HG01099.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.925+22480delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10552300 | |||||
| chr6:10552338
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.925+22502C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10552338 | ||||||
| chr6:10552440
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+22604G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10552440 | ||||||
| chr6:10552456
|
A | T | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0019g0127 | 3 | HG02717.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.925+22620A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10552456 | ||||||
| chr6:10552533
|
T | G | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+22697T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10552533 | ||||||
| chr6:10552732
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+22896G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10552732 | ||||||
| chr6:10552953
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.925+23117C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10552953 | ||||||
| chr6:10553060
|
G | A | 8 | a0001c0001t0001g0266a0001c0001t0003g0233a0001c0001t0003g0235others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+23224G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553060 | ||||||
| chr6:10553233
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.925+23397G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553233 | ||||||
| chr6:10553341
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.925+23505C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553341 | ||||||
| chr6:10553468
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.925+23632G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553468 | ||||||
| chr6:10553632
|
G | A | 20 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.925+23796G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553632 | ||||||
| chr6:10553710
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0221 | 3 | HG02818.hp1 HG02895.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.925+23874G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553710 | ||||||
| chr6:10553723
|
G | A | 12 | a0001c0001t0001g0029a0001c0001t0001g0068a0001c0001t0001g0131others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.925+23887G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553723 | ||||||
| chr6:10553755
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.925+23919G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553755 | ||||||
| chr6:10553815
|
C | G | 164 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(161): Show | 164 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.925+23979C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553815 | ||||||
| chr6:10553832
|
C | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0057others(18): Show | 21 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.925+23996C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553832 | ||||||
| chr6:10553932
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.925+24096A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10553932 | ||||||
| chr6:10554089
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.925+24253A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554089 | ||||||
| chr6:10554235
|
C | G | 2 | a0001c0001t0001g0216a0001c0001t0025g0217 | 2 | HG01496.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.925+24399C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554235 | ||||||
| chr6:10554377
|
C | T | 155 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(152): Show | 155 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.925+24541C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554377 | ||||||
| chr6:10554381
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.925+24545C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554381 | ||||||
| chr6:10554480
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.925+24644A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554480 | ||||||
| chr6:10554500
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.925+24664A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554500 | ||||||
| chr6:10554552
|
GTAAC | G | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0019g0127 | 3 | HG02717.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.925+24719_925+2472 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10554552 | |||||
| chr6:10554651
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0187 | 2 | NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.925+24815T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554651 | ||||||
| chr6:10554923
|
G | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0216others(8): Show | 11 | HG01496.hp1 HG02572.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.925+25087G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554923 | ||||||
| chr6:10554957
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0082others(1): Show | 4 | HG01192.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+25121C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554957 | ||||||
| chr6:10554994
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0302a0001c0001t0020g0152 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.925+25158A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10554994 | ||||||
| chr6:10555056
|
T | C | 87 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.925+25220T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10555056 | ||||||
| chr6:10555146
|
A | G | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+25310A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10555146 | ||||||
| chr6:10555359
|
T | C | 1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.925+25523T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10555359 | ||||||
| chr6:10555414
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.925+25578T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10555414 | ||||||
| chr6:10555516
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.925+25680G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10555516 | ||||||
| chr6:10555655
|
G | A | 24 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0024others(21): Show | 24 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.925+25819G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10555655 | ||||||
| chr6:10555749
|
G | T | 84 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.925+25913G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10555749 | ||||||
| chr6:10556106
|
G | C | 7 | a0001c0001t0001g0075a0001c0001t0001g0266a0001c0001t0003g0235others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+26270G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10556106 | ||||||
| chr6:10556431
|
T | C | 3 | a0001c0001t0001g0017a0001c0001t0021g0064a0001c0001t0023g0313 | 3 | HG02572.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.925+26595T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10556431 | ||||||
| chr6:10556488
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925+26652T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10556488 | ||||||
| chr6:10556581
|
A | ATGGAAAA others(12): Show |
1 | a0001c0001t0001g0084 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.925+26756_925+2677 others(23): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10556581 | |||||
| chr6:10556639
|
C | T | 11 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0125others(8): Show | 11 | HG00140.hp1 HG00323.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+26803C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10556639 | ||||||
| chr6:10556753
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.925+26917G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10556753 | ||||||
| chr6:10556940
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.925+27104A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10556940 | ||||||
| chr6:10557053
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.925+27217T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557053 | ||||||
| chr6:10557110
|
T | C | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0019g0127 | 3 | HG02717.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.925+27274T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557110 | ||||||
| chr6:10557463
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.925+27627C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557463 | ||||||
| chr6:10557493
|
CT | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(82): Show | 85 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.925+27669delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10557493 | |||||
| chr6:10557542
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.925+27706C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557542 | ||||||
| chr6:10557668
|
T | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0226 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.925+27832T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557668 | ||||||
| chr6:10557691
|
A | G | 106 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(103): Show | 106 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.925+27855A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557691 | ||||||
| chr6:10557691
|
A | T | 5 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | HG01346.hp1 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+27855A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557691 | ||||||
| chr6:10557753
|
A | G | 4 | a0001c0001t0001g0216a0001c0001t0003g0233a0001c0001t0003g0238others(1): Show | 4 | HG01496.hp1 HG02109.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+27917A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557753 | ||||||
| chr6:10557856
|
C | G | 164 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(161): Show | 164 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.925+28020C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10557856 | ||||||
| chr6:10558035
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0004g0035others(2): Show | 5 | HG02622.hp1 HG03540.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+28199C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10558035 | ||||||
| chr6:10558329
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.925+28493A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10558329 | ||||||
| chr6:10558374
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0183 | 3 | NA18955.hp2 NA18992.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.925+28538A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10558374 | ||||||
| chr6:10558473
|
C | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+28637C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10558473 | ||||||
| chr6:10559072
|
C | CT | 45 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0022others(42): Show | 45 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.925+29253dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10559072 | |||||
| chr6:10559072
|
CT | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0001g0226others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+29253delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10559072 | |||||
| chr6:10559221
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0226 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.925+29385C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10559221 | ||||||
| chr6:10559306
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0102a0001c0001t0001g0321 | 3 | HG02647.hp2 HG03579.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.925+29470C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10559306 | ||||||
| chr6:10559718
|
G | A | 9 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0216others(6): Show | 9 | HG01496.hp1 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+29882G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10559718 | ||||||
| chr6:10559719
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0216others(6): Show | 9 | HG01496.hp1 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+29883A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10559719 | ||||||
| chr6:10559767
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.925+29931T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10559767 | ||||||
| chr6:10560113
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+30277G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10560113 | ||||||
| chr6:10560119
|
C | T | 35 | a0001c0001t0001g0103a0001c0001t0001g0156a0001c0001t0001g0165others(32): Show | 35 | HG00741.hp2 HG01071.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.925+30283C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10560119 | ||||||
| chr6:10560299
|
AG | A | 104 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(101): Show | 104 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.925+30467delG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10560299 | |||||
| chr6:10560343
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0266a0001c0001t0003g0235others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+30507G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10560343 | ||||||
| chr6:10560402
|
T | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+30566T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10560402 | ||||||
| chr6:10560498
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+30662T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10560498 | ||||||
| chr6:10560671
|
C | A | 1 | a0001c0001t0022g0271 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.925+30835C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10560671 | ||||||
| chr6:10560869
|
T | C | 2 | a0001c0001t0011g0001a0001c0001t0027g0003 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.925+31033T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10560869 | ||||||
| chr6:10561009
|
C | T | 2 | a0001c0001t0007g0243a0001c0001t0007g0244 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.925+31173C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561009 | ||||||
| chr6:10561037
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0073others(8): Show | 11 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+31201G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561037 | ||||||
| chr6:10561126
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG01361.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.925+31290G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561126 | ||||||
| chr6:10561173
|
C | CT | 6 | a0001c0001t0001g0068a0001c0001t0001g0137a0001c0001t0001g0209others(3): Show | 6 | HG00438.hp1 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+31346dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10561173 | |||||
| chr6:10561232
|
G | A | 1 | a0001c0001t0007g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.925+31396G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561232 | ||||||
| chr6:10561399
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0075a0001c0001t0001g0131others(5): Show | 8 | HG00735.hp2 HG01884.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+31563C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561399 | ||||||
| chr6:10561403
|
A | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0073others(8): Show | 11 | HG00735.hp2 HG01192.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+31567A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561403 | ||||||
| chr6:10561565
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.925+31729C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561565 | ||||||
| chr6:10561594
|
C | T | 1 | a0001c0001t0015g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.925+31758C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561594 | ||||||
| chr6:10561634
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+31798G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561634 | ||||||
| chr6:10561656
|
C | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0016g0098 | 3 | HG01978.hp1 HG02698.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.925+31820C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561656 | ||||||
| chr6:10561862
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.925+32026G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561862 | ||||||
| chr6:10561952
|
T | G | 1 | a0001c0001t0011g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.925+32116T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561952 | ||||||
| chr6:10561960
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.925+32124A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561960 | ||||||
| chr6:10561964
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0018 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.925+32128G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10561964 | ||||||
| chr6:10562019
|
C | G | 104 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(101): Show | 104 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.925+32183C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562019 | ||||||
| chr6:10562096
|
G | T | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0019g0127 | 3 | HG02717.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.925+32260G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562096 | ||||||
| chr6:10562154
|
G | A | 104 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(101): Show | 104 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.925+32318G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562154 | ||||||
| chr6:10562228
|
C | T | 1 | a0001c0001t0005g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.925+32392C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562228 | ||||||
| chr6:10562242
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.925+32406C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562242 | ||||||
| chr6:10562301
|
C | G | 21 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0084others(18): Show | 21 | HG00558.hp2 HG00597.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.925+32465C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562301 | ||||||
| chr6:10562466
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.925+32630C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562466 | ||||||
| chr6:10562496
|
T | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0068others(10): Show | 13 | HG01496.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.925+32660T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562496 | ||||||
| chr6:10562656
|
G | GA | 37 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0046others(34): Show | 37 | HG00735.hp1 HG01109.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.925+32841dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
G | GAA | 8 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0057others(5): Show | 8 | HG02055.hp1 HG02071.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+32840_925+3284 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
GA | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0017others(13): Show | 16 | HG01192.hp2 HG01891.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.925+32841delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
GAA | G | 13 | a0001c0001t0001g0038a0001c0001t0001g0071a0001c0001t0001g0073others(10): Show | 13 | HG01256.hp2 HG01346.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.925+32840_925+3284 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562656
|
GAAA | G | 78 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 78 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.925+32839_925+3284 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | |||||
| chr6:10562668
|
A | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0068a0001c0001t0001g0074others(5): Show | 8 | HG02109.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+32832A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562668 | ||||||
| chr6:10562669
|
A | C | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0019g0127 | 3 | HG02717.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.925+32833A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562669 | ||||||
| chr6:10562670
|
A | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0246 | 2 | NA18980.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.925+32834A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562670 | ||||||
| chr6:10562673
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.925+32837A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562673 | ||||||
| chr6:10562675
|
A | C | 1 | a0001c0001t0022g0271 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.925+32839A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562675 | ||||||
| chr6:10562678
|
C | A | 2 | a0001c0001t0001g0142a0001c0001t0003g0230 | 2 | HG01192.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.925+32842C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562678 | ||||||
| chr6:10562687
|
A | C | 16 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0071others(13): Show | 16 | HG00408.hp1 HG00558.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.925+32851A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10562687 | ||||||
| chr6:10563166
|
A | G | 1 | a0001c0001t0003g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.925+33330A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563166 | ||||||
| chr6:10563232
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.925+33396G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563232 | ||||||
| chr6:10563276
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.925+33440A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563276 | ||||||
| chr6:10563410
|
A | G | 98 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.925+33574A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563410 | ||||||
| chr6:10563436
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.925+33600G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563436 | ||||||
| chr6:10563510
|
G | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0057others(15): Show | 18 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.925+33674G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563510 | ||||||
| chr6:10563665
|
CCAGGAGG others(9): Show |
C | 2 | a0001c0001t0001g0030a0001c0001t0001g0321 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.925+33833_925+3384 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563665 | |||||
| chr6:10563749
|
GAAAA | G | 3 | a0001c0001t0001g0017a0001c0001t0021g0064a0001c0001t0023g0313 | 3 | HG02572.hp2 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.925+33916_925+3391 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563749 | |||||
| chr6:10563749
|
GAAAAAAG others(3): Show |
G | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.925+33920_925+3392 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563749 | |||||
| chr6:10563756
|
GA | G | 26 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0068others(23): Show | 26 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.925+33942delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563756
|
GAA | G | 10 | a0001c0001t0001g0087a0001c0001t0001g0093a0001c0001t0001g0140others(7): Show | 10 | HG01071.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+33941_925+3394 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563756
|
GAAA | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0112a0001c0001t0001g0126others(5): Show | 8 | HG00140.hp2 HG02809.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+33940_925+3394 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563756
|
GAAAAA | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0027others(4): Show | 7 | HG02451.hp1 HG02615.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+33938_925+3394 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | |||||
| chr6:10563760
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.925+33924A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563760 | ||||||
| chr6:10563766
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0082 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.925+33932_925+3394 others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563766 | |||||
| chr6:10563767
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0027g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.925+33933_925+3394 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563767 | |||||
| chr6:10563768
|
AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0001g0091a0001c0001t0001g0171a0001c0001t0002g0090others(2): Show | 5 | HG00558.hp2 HG00673.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+33934_925+3394 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563768 | |||||
| chr6:10563768
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.925+33934_925+3394 others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563768 | |||||
| chr6:10563768
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.925+33934_925+3394 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563768 | |||||
| chr6:10563769
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0320a0001c0001t0002g0296 | 2 | HG01884.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.925+33935_925+3394 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563769
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0065a0001c0001t0001g0125a0001c0001t0001g0290 | 3 | HG00140.hp1 HG01517.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.925+33935_925+3394 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563769
|
AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0030a0001c0001t0011g0001 | 2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.925+33935_925+3394 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563769
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.925+33935_925+3395 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | |||||
| chr6:10563770
|
AAAAAAAA others(4): Show |
A | 18 | a0001c0001t0001g0028a0001c0001t0001g0089a0001c0001t0001g0099others(15): Show | 18 | HG01099.hp1 HG02056.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.925+33936_925+3394 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | |||||
| chr6:10563770
|
AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0003g0230a0001c0001t0009g0006 | 2 | HG01192.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.925+33936_925+3394 others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | |||||
| chr6:10563770
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0004g0314 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.925+33936_925+3395 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | |||||
| chr6:10563771
|
A | AATATATA others(3): Show |
1 | a0001c0001t0002g0280 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.925+33936_925+3393 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0055 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.925+33936_925+3393 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
A | AT | 4 | a0001c0001t0001g0129a0001c0001t0002g0153a0001c0001t0002g0223others(1): Show | 4 | HG02300.hp1 NA18980.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+33935_925+3393 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563771 | ||||||
| chr6:10563771
|
A | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0128a0001c0001t0001g0139 | 3 | HG00597.hp1 HG01975.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.925+33935A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563771 | ||||||
| chr6:10563771
|
AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0103a0001c0001t0001g0270a0001c0001t0002g0294 | 3 | HG01256.hp2 HG02083.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.925+33937_925+3394 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
AAAAAAAA others(5): Show |
A | 10 | a0001c0001t0001g0107a0001c0001t0001g0248a0001c0001t0001g0259others(7): Show | 10 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+33937_925+3394 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0001g0215a0001c0001t0004g0316a0001c0001t0019g0127 | 3 | HG02717.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.925+33937_925+3395 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563771
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0014a0001c0001t0004g0069 | 2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.925+33937_925+3395 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | |||||
| chr6:10563772
|
AAAAAAAT others(2): Show |
A | 6 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0267others(3): Show | 6 | HG01071.hp1 HG01934.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.925+33938_925+3394 others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563772
|
AAAAAAAT others(4): Show |
A | 28 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0053others(25): Show | 28 | HG00323.hp1 HG01081.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.925+33938_925+3394 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563772
|
AAAAAAAT others(6): Show |
A | 4 | a0001c0001t0001g0017a0001c0001t0008g0219a0001c0001t0015g0076others(1): Show | 4 | HG02717.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+33938_925+3395 others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563772
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+33938_925+3395 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | |||||
| chr6:10563773
|
A | AT | 7 | a0001c0001t0001g0106a0001c0001t0001g0177a0001c0001t0001g0195others(4): Show | 7 | HG02083.hp2 HG02155.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+33937_925+3393 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563773 | ||||||
| chr6:10563773
|
A | ATAT | 4 | a0001c0001t0001g0046a0001c0001t0001g0119a0001c0001t0001g0133others(1): Show | 4 | NA18956.hp1 NA18981.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+33937_925+3393 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563773 | ||||||
| chr6:10563773
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0032 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.925+33937_925+3393 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563773 | ||||||
| chr6:10563773
|
A | T | 23 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0059others(20): Show | 23 | HG00323.hp2 HG00597.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.925+33937A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563773 | ||||||
| chr6:10563773
|
AAAAAATA others(3): Show |
A | 5 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0214others(2): Show | 5 | HG02630.hp1 HG03540.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+33939_925+3394 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563773
|
AAAAAATA others(5): Show |
A | 3 | a0001c0001t0001g0247a0001c0001t0004g0035a0001c0001t0023g0313 | 3 | HG02559.hp2 HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.925+33939_925+3395 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563773
|
AAAAAATA others(7): Show |
A | 1 | a0001c0001t0003g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.925+33939_925+3395 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563773
|
AAAAAATA others(9): Show |
A | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.925+33939_925+3395 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | |||||
| chr6:10563774
|
AAAAATAT others(4): Show |
A | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0038others(15): Show | 18 | HG00408.hp1 HG01099.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.925+33940_925+3395 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | |||||
| chr6:10563774
|
AAAAATAT others(6): Show |
A | 3 | a0001c0001t0001g0216a0001c0001t0001g0300a0001c0001t0025g0217 | 3 | HG01496.hp1 HG03710.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.925+33940_925+3395 others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | |||||
| chr6:10563774
|
AAAAATAT others(8): Show |
A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0003g0235others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+33940_925+3395 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | |||||
| chr6:10563775
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.925+33940_925+3394 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563775 | |||||
| chr6:10563775
|
A | AT | 13 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0054others(10): Show | 13 | HG01516.hp1 HG02080.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.925+33939_925+3394 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | ATAT | 4 | a0001c0001t0001g0163a0001c0001t0001g0206a0001c0001t0001g0289others(1): Show | 4 | HG02273.hp2 HG02615.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+33939_925+3394 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | ATATAT | 4 | a0001c0001t0001g0045a0001c0001t0001g0196a0001c0001t0002g0197others(1): Show | 4 | HG02698.hp1 HG03239.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+33939_925+3394 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.925+33939_925+3394 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563775 | ||||||
| chr6:10563775
|
A | T | 66 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0032others(63): Show | 66 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.925+33939A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563775 | ||||||
| chr6:10563775
|
AAAATATA others(7): Show |
A | 3 | a0001c0001t0003g0239a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG02258.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.925+33941_925+3395 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563775 | |||||
| chr6:10563776
|
AAATATAT others(6): Show |
A | 1 | a0001c0001t0003g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.925+33942_925+3395 others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563776 | |||||
| chr6:10563777
|
A | AAATATAT others(28): Show |
1 | a0001c0001t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.925+33942_925+3394 others(39): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563777 | |||||
| chr6:10563777
|
A | AT | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0169others(2): Show | 5 | HG01361.hp1 HG02071.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.925+33941_925+3394 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563777 | ||||||
| chr6:10563777
|
A | T | 120 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(117): Show | 120 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.925+33941A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563777 | ||||||
| chr6:10563777
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0003g0238 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.925+33962_925+3397 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10563777 | |||||
| chr6:10563778
|
AT | A | 4 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0281others(1): Show | 4 | HG00621.hp1 HG02080.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+33943delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563778 | ||||||
| chr6:10563779
|
T | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0044 | 2 | HG01123.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.925+33943T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563779 | ||||||
| chr6:10563781
|
T | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0323 | 2 | HG02080.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.925+33945T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563781 | ||||||
| chr6:10563899
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0002g0193 | 2 | NA18981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.925+34063G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563899 | ||||||
| chr6:10563981
|
G | T | 1 | a0001c0001t0018g0100 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.925+34145G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10563981 | ||||||
| chr6:10564171
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0266a0001c0001t0003g0235others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+34335T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10564171 | ||||||
| chr6:10564367
|
T | C | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.925+34531T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10564367 | ||||||
| chr6:10564440
|
C | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+34604C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10564440 | ||||||
| chr6:10564453
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.925+34617G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10564453 | ||||||
| chr6:10564526
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0013g0108 | 3 | HG02258.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.925+34690G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10564526 | ||||||
| chr6:10564642
|
T | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0221 | 2 | HG01192.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.925+34806T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10564642 | ||||||
| chr6:10564761
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.925+34925G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10564761 | ||||||
| chr6:10565067
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+35231G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565067 | ||||||
| chr6:10565104
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.925+35268A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565104 | ||||||
| chr6:10565123
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+35287A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565123 | ||||||
| chr6:10565170
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.925+35334G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565170 | ||||||
| chr6:10565383
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0002g0047 | 2 | NA19084.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.925+35547A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565383 | ||||||
| chr6:10565383
|
AAGGGAAA others(4): Show |
A | 95 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(92): Show | 95 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.925+35560_925+3557 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10565383 | |||||
| chr6:10565564
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0012g0008 | 2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.925+35728A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565564 | ||||||
| chr6:10565708
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(164): Show | 167 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.925+35872C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565708 | ||||||
| chr6:10565776
|
C | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.925+35940C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565776 | ||||||
| chr6:10565845
|
T | C | 31 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0021others(28): Show | 31 | HG00323.hp2 HG01109.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.925+36009T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565845 | ||||||
| chr6:10565898
|
C | T | 1 | a0001c0001t0011g0002 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.925+36062C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565898 | ||||||
| chr6:10565959
|
A | G | 5 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0001t0003g0234others(2): Show | 5 | HG02976.hp1 HG03041.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+36123A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10565959 | ||||||
| chr6:10566052
|
C | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073others(3): Show | 6 | HG02622.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+36216C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566052 | ||||||
| chr6:10566053
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0004g0020 | 2 | HG02647.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.925+36217G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566053 | ||||||
| chr6:10566074
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.925+36238G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566074 | ||||||
| chr6:10566089
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0228 | 2 | NA19007.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.925+36253C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566089 | ||||||
| chr6:10566110
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.925+36274G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566110 | ||||||
| chr6:10566141
|
C | T | 15 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0062others(12): Show | 15 | HG00735.hp2 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.925+36305C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566141 | ||||||
| chr6:10566258
|
C | T | 46 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.925+36422C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566258 | ||||||
| chr6:10566361
|
C | A | 6 | a0001c0001t0001g0022a0001c0001t0003g0235a0001c0001t0003g0236others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.925+36525C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566361 | ||||||
| chr6:10566422
|
C | T | 166 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(163): Show | 166 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.925+36586C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566422 | ||||||
| chr6:10566436
|
T | C | 1 | a0001c0001t0002g0258 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.925+36600T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566436 | ||||||
| chr6:10566442
|
T | G | 2 | a0001c0001t0002g0153a0001c0001t0002g0246 | 2 | NA18980.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.925+36606T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566442 | ||||||
| chr6:10566585
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.925+36749C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566585 | ||||||
| chr6:10566623
|
T | A | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(173): Show | 176 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.925+36787T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566623 | ||||||
| chr6:10566713
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.925+36877G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566713 | ||||||
| chr6:10566798
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.925+36962C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566798 | ||||||
| chr6:10566882
|
C | T | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(187): Show | 190 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.925+37046C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566882 | ||||||
| chr6:10566883
|
C | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 9 | HG00735.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+37047C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10566883 | ||||||
| chr6:10567055
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.925+37219A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567055 | ||||||
| chr6:10567172
|
G | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0071a0001c0001t0001g0072others(5): Show | 8 | HG00597.hp1 HG00621.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.925+37336G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567172 | ||||||
| chr6:10567197
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.925+37361C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567197 | ||||||
| chr6:10567244
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.925+37408G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567244 | ||||||
| chr6:10567300
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.925+37464T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567300 | ||||||
| chr6:10567387
|
A | G | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(210): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.925+37551A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567387 | ||||||
| chr6:10567509
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.925+37673C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567509 | ||||||
| chr6:10567679
|
A | T | 185 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(182): Show | 185 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.925+37843A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567679 | ||||||
| chr6:10567694
|
C | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0187 | 2 | NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.925+37858C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567694 | ||||||
| chr6:10567821
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.925+37985A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10567821 | ||||||
| chr6:10568068
|
C | T | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+38232C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568068 | ||||||
| chr6:10568120
|
T | G | 9 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 9 | HG00735.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+38284T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568120 | ||||||
| chr6:10568151
|
C | T | 2 | a0001c0001t0009g0006a0001c0001t0011g0001 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.925+38315C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568151 | ||||||
| chr6:10568219
|
T | C | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.925+38383T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568219 | ||||||
| chr6:10568313
|
T | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0250 | 2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.925+38477T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568313 | ||||||
| chr6:10568598
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+38762A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568598 | ||||||
| chr6:10568616
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.925+38780A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568616 | ||||||
| chr6:10568622
|
T | A | 1 | a0001c0001t0003g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.925+38786T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568622 | ||||||
| chr6:10568753
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+38917C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568753 | ||||||
| chr6:10568765
|
T | C | 201 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.925+38929T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568765 | ||||||
| chr6:10568869
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.925+39033G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568869 | ||||||
| chr6:10568881
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+39045A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568881 | ||||||
| chr6:10568929
|
G | A | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(186): Show | 189 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.925+39093G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10568929 | ||||||
| chr6:10569037
|
G | A | 2 | a0001c0001t0009g0006a0001c0001t0011g0001 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.925+39201G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569037 | ||||||
| chr6:10569129
|
G | C | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(166): Show | 169 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.925+39293G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569129 | ||||||
| chr6:10569156
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0220a0001c0001t0005g0026 | 3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.925+39320T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569156 | ||||||
| chr6:10569217
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.925+39381T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569217 | ||||||
| chr6:10569235
|
C | CCA | 24 | a0001c0001t0001g0045a0001c0001t0001g0068a0001c0001t0001g0084others(21): Show | 24 | HG00438.hp1 HG00673.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.925+39437_925+3943 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACA | 6 | a0001c0001t0001g0109a0001c0001t0001g0156a0001c0001t0001g0165others(3): Show | 6 | HG00558.hp2 HG03209.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+39435_925+3943 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(1): Show |
4 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0092others(1): Show | 4 | HG00642.hp1 HG01123.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+39431_925+3943 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(3): Show |
6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0094others(3): Show | 6 | HG00639.hp1 HG00738.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.925+39429_925+3943 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(7): Show |
4 | a0001c0001t0001g0054a0001c0001t0001g0107a0001c0001t0002g0104others(1): Show | 4 | HG02132.hp2 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+39425_925+3943 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(9): Show |
3 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0323 | 3 | HG02080.hp1 HG02572.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.925+39423_925+3943 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(11): Show |
11 | a0001c0001t0001g0019a0001c0001t0001g0082a0001c0001t0001g0101others(8): Show | 11 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+39421_925+3943 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(13): Show |
20 | a0001c0001t0001g0060a0001c0001t0001g0087a0001c0001t0001g0140others(17): Show | 20 | HG00558.hp1 HG00642.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.925+39419_925+3943 others(24): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(15): Show |
28 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0055others(25): Show | 28 | HG00323.hp1 HG00621.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.925+39417_925+3943 others(26): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(17): Show |
16 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0061others(13): Show | 16 | HG00408.hp2 HG00738.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.925+39415_925+3943 others(28): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(19): Show |
14 | a0001c0001t0001g0041a0001c0001t0001g0048a0001c0001t0001g0053others(11): Show | 14 | HG00438.hp2 HG00621.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.925+39413_925+3943 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(21): Show |
15 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0059others(12): Show | 15 | HG01346.hp1 HG01975.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.925+39411_925+3943 others(32): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(23): Show |
12 | a0001c0001t0001g0049a0001c0001t0001g0105a0001c0001t0001g0146others(9): Show | 12 | HG01074.hp2 HG01361.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.925+39409_925+3943 others(34): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(25): Show |
16 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0031others(13): Show | 16 | HG00597.hp1 HG01074.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.925+39407_925+3943 others(36): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(27): Show |
7 | a0001c0001t0001g0187a0001c0001t0001g0252a0001c0001t0001g0281others(4): Show | 7 | HG00735.hp1 HG02132.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+39405_925+3943 others(38): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(29): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0039a0001c0001t0001g0072others(6): Show | 9 | HG02155.hp2 HG02280.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+39403_925+3943 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(31): Show |
2 | a0001c0001t0001g0070a0001c0001t0001g0110 | 2 | HG02129.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.925+39401_925+3943 others(42): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(33): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0145 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.925+39438_925+3943 others(44): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(35): Show |
1 | a0001c0001t0002g0303 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(46): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(37): Show |
2 | a0001c0001t0001g0155a0001c0001t0001g0182 | 2 | NA18956.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.925+39438_925+3943 others(48): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(39): Show |
1 | a0001c0001t0002g0296 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(50): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
C | CCACACAC others(41): Show |
1 | a0001c0001t0001g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(52): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
CCACA | C | 12 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0077others(9): Show | 12 | HG00408.hp1 HG01928.hp2 HG03486.hp2 others(9): Show |
intron_variant | MODIFIER | c.925+39435_925+3943 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
CCACACA | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG00741.hp2 HG01361.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+39433_925+3943 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569235
|
CCACACAC others(3): Show |
C | 1 | a0001c0001t0009g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.925+39429_925+3943 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | |||||
| chr6:10569245
|
A | ACACC | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+39412_925+3941 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569245 | |||||
| chr6:10569271
|
ACACC | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0220a0001c0001t0005g0026 | 3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.925+39437_925+3944 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569271 | |||||
| chr6:10569273
|
A | ACACACAC others(23): Show |
1 | a0001c0001t0001g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.925+39438_925+3943 others(34): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569273 | |||||
| chr6:10569273
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0003g0238 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569273 | |||||
| chr6:10569273
|
ACC | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0170a0001c0001t0001g0228others(1): Show | 4 | HG03540.hp2 NA19007.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+39441_925+3944 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569273 | |||||
| chr6:10569274
|
C | CACACACA others(8): Show |
1 | a0001c0001t0001g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.925+39438_925+3943 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(18): Show |
1 | a0001c0001t0001g0162 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.925+39438_925+3943 others(29): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(20): Show |
1 | a0001c0001t0001g0251 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.925+39438_925+3943 others(31): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(22): Show |
1 | a0001c0001t0001g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(33): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(24): Show |
1 | a0001c0001t0004g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(35): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(32): Show |
1 | a0001c0001t0001g0287 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.925+39438_925+3943 others(43): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(34): Show |
1 | a0001c0001t0001g0142 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(45): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569274
|
C | CACACACA others(38): Show |
1 | a0001c0001t0002g0151 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.925+39438_925+3943 others(49): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569274 | ||||||
| chr6:10569275
|
C | A | 135 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0019others(132): Show | 135 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.925+39439C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569275 | ||||||
| chr6:10569276
|
C | A | 6 | a0001c0001t0001g0106a0001c0001t0001g0111a0001c0001t0001g0142others(3): Show | 6 | HG02056.hp2 HG03017.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+39440C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569276 | ||||||
| chr6:10569290
|
G | C | 1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.925+39454G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569290 | ||||||
| chr6:10569466
|
C | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0274a0001c0001t0001g0281others(3): Show | 6 | HG00621.hp1 HG02080.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+39630C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569466 | ||||||
| chr6:10569531
|
T | C | 20 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0060others(17): Show | 20 | HG00597.hp1 HG00621.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.925+39695T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569531 | ||||||
| chr6:10569564
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+39728T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569564 | ||||||
| chr6:10569571
|
T | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0195a0001c0001t0001g0205others(7): Show | 10 | HG00741.hp1 HG01993.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+39735T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569571 | ||||||
| chr6:10569644
|
C | A | 3 | a0001c0001t0001g0226a0001c0001t0005g0040a0001c0001t0008g0219 | 3 | HG02630.hp1 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.925+39808C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569644 | ||||||
| chr6:10569824
|
T | TCTTC | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(165): Show | 168 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.925+40008_925+4001 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569824 | |||||
| chr6:10569844
|
CCTTTCT | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0321a0001c0001t0012g0008 | 3 | HG02647.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.925+40015_925+4002 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569844 | |||||
| chr6:10569847
|
T | TCCTTTCT others(5): Show |
7 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+40011_925+4001 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569847 | ||||||
| chr6:10569848
|
T | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0180others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+40012T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569848 | ||||||
| chr6:10569849
|
C | T | 7 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+40013C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569849 | ||||||
| chr6:10569851
|
C | T | 9 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0180others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+40015C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569851 | ||||||
| chr6:10569853
|
T | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0180others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+40017T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569853 | ||||||
| chr6:10569854
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0321a0001c0001t0012g0008 | 3 | HG02647.hp2 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.925+40018T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569854 | ||||||
| chr6:10569861
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+40025C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569861 | ||||||
| chr6:10569863
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+40027T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569863 | ||||||
| chr6:10569865
|
C | CTT | 7 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+40031_925+4003 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569865 | |||||
| chr6:10569875
|
TTC | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0221a0001c0001t0001g0247others(1): Show | 4 | HG01192.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.925+40043_925+4004 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569875 | |||||
| chr6:10569877
|
C | CCTT | 7 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+40041_925+4004 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569877 | ||||||
| chr6:10569878
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+40042T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569878 | ||||||
| chr6:10569882
|
T | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0220others(4): Show | 7 | HG00735.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.925+40046T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569882 | ||||||
| chr6:10569885
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.925+40049T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569885 | ||||||
| chr6:10569887
|
TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0009g0006a0001c0001t0011g0001 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.925+40052_925+4006 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569887 | ||||||
| chr6:10569935
|
T | C | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.925+40099T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569935 | ||||||
| chr6:10569947
|
TCTTC | T | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.925+40127_925+4013 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569947 | |||||
| chr6:10569963
|
CCTTT | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+40134_925+4013 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10569963 | |||||
| chr6:10569991
|
A | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0225a0001c0001t0001g0289others(3): Show | 6 | HG01516.hp2 HG01517.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+40155A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569991 | ||||||
| chr6:10569995
|
A | G | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(188): Show | 191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.925+40159A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10569995 | ||||||
| chr6:10570135
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.925+40299A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570135 | ||||||
| chr6:10570176
|
T | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.925+40340T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570176 | ||||||
| chr6:10570177
|
C | G | 3 | a0001c0001t0001g0138a0001c0001t0001g0167a0001c0001t0001g0186 | 3 | HG01256.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.925+40341C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570177 | ||||||
| chr6:10570312
|
T | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0057a0001c0001t0001g0058others(4): Show | 7 | HG01496.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+40476T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570312 | ||||||
| chr6:10570444
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.925+40608A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570444 | ||||||
| chr6:10570534
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.925+40698C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570534 | ||||||
| chr6:10570552
|
C | T | 2 | a0001c0001t0004g0035a0001c0001t0027g0003 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.925+40716C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570552 | ||||||
| chr6:10570785
|
A | G | 3 | a0001c0001t0002g0153a0001c0001t0002g0199a0001c0001t0002g0246 | 3 | NA18980.hp2 NA18990.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.925+40949A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570785 | ||||||
| chr6:10570877
|
T | C | 4 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(1): Show | 4 | HG01071.hp1 HG01346.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+41041T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570877 | ||||||
| chr6:10570895
|
G | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.925+41059G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570895 | ||||||
| chr6:10570909
|
G | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073others(3): Show | 6 | HG02622.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+41073G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10570909 | ||||||
| chr6:10571027
|
A | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(172): Show | 175 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.925+41191A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571027 | ||||||
| chr6:10571158
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.925+41322A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571158 | ||||||
| chr6:10571186
|
T | C | 1 | a0001c0001t0027g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.925+41350T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571186 | ||||||
| chr6:10571259
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.925+41423A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571259 | ||||||
| chr6:10571326
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.925+41490T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571326 | ||||||
| chr6:10571342
|
AATT | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+41522_925+4152 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10571342 | |||||
| chr6:10571420
|
C | T | 181 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.925+41584C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571420 | ||||||
| chr6:10571579
|
C | G | 2 | a0001c0001t0002g0160a0001c0001t0002g0223 | 2 | NA18992.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.925+41743C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571579 | ||||||
| chr6:10571593
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+41757C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571593 | ||||||
| chr6:10571628
|
C | T | 3 | a0001c0001t0002g0134a0001c0001t0002g0277a0001c0001t0002g0291 | 3 | NA18971.hp1 NA18983.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.925+41792C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571628 | ||||||
| chr6:10571639
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.925+41803C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571639 | ||||||
| chr6:10571643
|
G | A | 1 | a0001c0001t0015g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.925+41807G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571643 | ||||||
| chr6:10571758
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.925+41922C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571758 | ||||||
| chr6:10571759
|
G | A | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.925+41923G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571759 | ||||||
| chr6:10571829
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.925+41993G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571829 | ||||||
| chr6:10571837
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+42001G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571837 | ||||||
| chr6:10571890
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+42054C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571890 | ||||||
| chr6:10571918
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073others(3): Show | 6 | HG02622.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+42082A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10571918 | ||||||
| chr6:10571946
|
C | CACTGATA others(38): Show |
3 | a0001c0001t0001g0226a0001c0001t0005g0040a0001c0001t0008g0219 | 3 | HG02630.hp1 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.925+42112_925+4215 others(49): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10571946 | |||||
| chr6:10572087
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.925+42251C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572087 | ||||||
| chr6:10572225
|
C | T | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0015g0076 | 3 | HG02622.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.925+42389C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572225 | ||||||
| chr6:10572332
|
C | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0018others(9): Show | 12 | HG00735.hp2 HG02630.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.925+42496C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572332 | ||||||
| chr6:10572382
|
C | G | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.925+42546C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572382 | ||||||
| chr6:10572452
|
T | A | 12 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0018others(9): Show | 12 | HG00735.hp2 HG02630.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.925+42616T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572452 | ||||||
| chr6:10572452
|
T | G | 175 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.925+42616T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572452 | ||||||
| chr6:10572459
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.925+42623C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572459 | ||||||
| chr6:10572496
|
G | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0015g0076 | 3 | HG02622.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.925+42660G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572496 | ||||||
| chr6:10572514
|
T | C | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.925+42678T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572514 | ||||||
| chr6:10572548
|
T | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(10): Show | 13 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.925+42712T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572548 | ||||||
| chr6:10572606
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.925+42770C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572606 | ||||||
| chr6:10572754
|
A | G | 15 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0082others(12): Show | 15 | HG01192.hp2 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.925+42918A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572754 | ||||||
| chr6:10572805
|
C | T | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(160): Show | 163 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.925+42969C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572805 | ||||||
| chr6:10572962
|
G | T | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.925+43126G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572962 | ||||||
| chr6:10573006
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.925+43170G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573006 | ||||||
| chr6:10573038
|
G | T | 3 | a0001c0001t0003g0239a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG02258.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.925+43202G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573038 | ||||||
| chr6:10573168
|
G | GATC | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(175): Show | 178 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.925+43333_925+4333 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10573168 | |||||
| chr6:10573192
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.925+43356C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573192 | ||||||
| chr6:10573211
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+43375C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573211 | ||||||
| chr6:10573237
|
C | A | 2 | a0001c0001t0004g0035a0001c0001t0027g0003 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.925+43401C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573237 | ||||||
| chr6:10573318
|
A | G | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+43482A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573318 | ||||||
| chr6:10573350
|
A | ATTGTTG | 199 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.925+43520_925+4352 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10573350 | |||||
| chr6:10573531
|
C | A | 16 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0030others(13): Show | 16 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.925+43695C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573531 | ||||||
| chr6:10573574
|
A | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+43738A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573574 | ||||||
| chr6:10573613
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0220a0001c0001t0005g0026 | 3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.925+43777A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573613 | ||||||
| chr6:10573677
|
A | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.925+43841A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573677 | ||||||
| chr6:10573704
|
T | C | 1 | a0001c0001t0015g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.925+43868T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573704 | ||||||
| chr6:10573720
|
C | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.925+43884C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573720 | ||||||
| chr6:10573885
|
C | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(174): Show | 177 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.925+44049C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573885 | ||||||
| chr6:10573971
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.925+44135A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10573971 | ||||||
| chr6:10574079
|
T | C | 174 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.925+44243T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574079 | ||||||
| chr6:10574099
|
T | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+44263T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574099 | ||||||
| chr6:10574101
|
T | C | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.925+44265T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574101 | ||||||
| chr6:10574111
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.925+44275G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574111 | ||||||
| chr6:10574164
|
G | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.925+44328G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574164 | ||||||
| chr6:10574215
|
C | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.925+44379C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574215 | ||||||
| chr6:10574229
|
G | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG02155.hp1 NA18951.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.925+44393G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574229 | ||||||
| chr6:10574343
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+44507C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574343 | ||||||
| chr6:10574395
|
G | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0030a0001c0001t0001g0321 | 3 | HG02647.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.925+44559G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574395 | ||||||
| chr6:10574398
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0168a0001c0001t0001g0305 | 3 | HG02132.hp2 NA18939.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.925+44562A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574398 | ||||||
| chr6:10574408
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.925+44572A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574408 | ||||||
| chr6:10574489
|
G | A | 10 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(7): Show | 10 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.925+44653G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574489 | ||||||
| chr6:10574570
|
C | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0321 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.925+44734C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574570 | ||||||
| chr6:10574673
|
T | C | 2 | a0001c0001t0009g0006a0001c0001t0011g0001 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.925+44837T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574673 | ||||||
| chr6:10574716
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.925+44880T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574716 | ||||||
| chr6:10574728
|
AT | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+44901delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10574728 | |||||
| chr6:10574787
|
C | G | 10 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0131others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.925+44951C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574787 | ||||||
| chr6:10574791
|
C | G | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44955C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574791 | ||||||
| chr6:10574796
|
C | A | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44960C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574796 | ||||||
| chr6:10574797
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44961A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574797 | ||||||
| chr6:10574799
|
T | A | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44963T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574799 | ||||||
| chr6:10574802
|
C | T | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44966C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574802 | ||||||
| chr6:10574808
|
T | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0131others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.925+44972T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574808 | ||||||
| chr6:10574810
|
A | C | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44974A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574810 | ||||||
| chr6:10574813
|
T | C | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44977T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574813 | ||||||
| chr6:10574814
|
G | A | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44978G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574814 | ||||||
| chr6:10574815
|
T | G | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44979T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574815 | ||||||
| chr6:10574816
|
G | C | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44980G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574816 | ||||||
| chr6:10574819
|
A | G | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.925+44983A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574819 | ||||||
| chr6:10574861
|
C | G | 1 | a0001c0001t0021g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.925+45025C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574861 | ||||||
| chr6:10574898
|
T | C | 229 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(226): Show | 229 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.925+45062T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574898 | ||||||
| chr6:10574914
|
G | C | 2 | a0001c0001t0001g0226a0001c0001t0008g0219 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.925+45078G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574914 | ||||||
| chr6:10574991
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.925+45155C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574991 | ||||||
| chr6:10575015
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0320 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.925+45179C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575015 | ||||||
| chr6:10575113
|
T | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0075others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.925+45277T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575113 | ||||||
| chr6:10575142
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.925+45306G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575142 | ||||||
| chr6:10575261
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0107 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.925+45425T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575261 | ||||||
| chr6:10575307
|
A | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+45471A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575307 | ||||||
| chr6:10575358
|
A | ATT | 7 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0078others(4): Show | 7 | HG00408.hp1 HG01928.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+45540_925+4554 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | |||||
| chr6:10575358
|
A | T | 4 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0174others(1): Show | 4 | HG02040.hp1 HG02132.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+45522A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575358 | ||||||
| chr6:10575358
|
AT | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(15): Show | 18 | HG00558.hp1 HG01071.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.925+45541delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | |||||
| chr6:10575454
|
T | C | 196 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.925+45618T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575454 | ||||||
| chr6:10575464
|
A | G | 22 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0074others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.925+45628A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575464 | ||||||
| chr6:10575576
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.925+45740G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575576 | ||||||
| chr6:10575672
|
CT | C | 54 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(51): Show | 54 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.926-45676delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10575672 | |||||
| chr6:10575762
|
C | T | 10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0075others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-45589C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575762 | ||||||
| chr6:10575908
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-45443C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575908 | ||||||
| chr6:10575939
|
C | CT | 24 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(21): Show | 24 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.926-45412_926-4541 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10575939 | ||||||
| chr6:10576076
|
T | G | 10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0075others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-45275T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576076 | ||||||
| chr6:10576089
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.926-45262C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576089 | ||||||
| chr6:10576090
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-45261G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576090 | ||||||
| chr6:10576150
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.926-45201G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576150 | ||||||
| chr6:10576162
|
G | A | 1 | a0001c0001t0005g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.926-45189G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576162 | ||||||
| chr6:10576254
|
AAAG | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-45093_926-4509 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10576254 | |||||
| chr6:10576366
|
A | G | 1 | a0001c0001t0015g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.926-44985A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576366 | ||||||
| chr6:10576401
|
T | C | 26 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(23): Show | 26 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.926-44950T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576401 | ||||||
| chr6:10576451
|
G | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-44900G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576451 | ||||||
| chr6:10576471
|
G | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-44880G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576471 | ||||||
| chr6:10576479
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0121a0001c0001t0001g0174others(5): Show | 8 | HG02040.hp1 HG02132.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-44872C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576479 | ||||||
| chr6:10576553
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.926-44798G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576553 | ||||||
| chr6:10576571
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.926-44780G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576571 | ||||||
| chr6:10576611
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.926-44740G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576611 | ||||||
| chr6:10576645
|
A | G | 194 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.926-44706A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576645 | ||||||
| chr6:10576653
|
T | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-44698T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576653 | ||||||
| chr6:10576654
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-44697T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576654 | ||||||
| chr6:10576671
|
CAGAA | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-44676_926-4467 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10576671 | |||||
| chr6:10576675
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.926-44676A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576675 | ||||||
| chr6:10576697
|
G | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0015g0076 | 3 | HG02622.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.926-44654G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576697 | ||||||
| chr6:10576707
|
TAGAA | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-44639_926-4463 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10576707 | |||||
| chr6:10576730
|
A | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-44621A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576730 | ||||||
| chr6:10576796
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0004g0253 | 2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.926-44555G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576796 | ||||||
| chr6:10576804
|
T | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-44547T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576804 | ||||||
| chr6:10576920
|
CAATAAT | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(9): Show | 12 | HG01192.hp2 HG01361.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-44416_926-4441 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10576920 | |||||
| chr6:10576967
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.926-44384C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576967 | ||||||
| chr6:10577014
|
G | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0081others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.926-44337G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577014 | ||||||
| chr6:10577140
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.926-44211C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577140 | ||||||
| chr6:10577155
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-44196C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577155 | ||||||
| chr6:10577231
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.926-44120G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577231 | ||||||
| chr6:10577304
|
T | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-44047T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577304 | ||||||
| chr6:10577355
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-43996C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577355 | ||||||
| chr6:10577394
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-43957A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577394 | ||||||
| chr6:10577589
|
G | A | 1 | a0001c0001t0012g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.926-43762G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577589 | ||||||
| chr6:10577634
|
G | C | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.926-43717G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577634 | ||||||
| chr6:10577635
|
G | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-43716G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577635 | ||||||
| chr6:10577725
|
G | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-43626G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577725 | ||||||
| chr6:10577730
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0297 | 2 | NA18951.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.926-43621G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577730 | ||||||
| chr6:10577789
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.926-43562C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577789 | ||||||
| chr6:10577885
|
TTCG | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-43464_926-4346 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10577885 | |||||
| chr6:10577960
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-43391C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577960 | ||||||
| chr6:10577990
|
G | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-43361G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10577990 | ||||||
| chr6:10578066
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.926-43285T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578066 | ||||||
| chr6:10578074
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-43277A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578074 | ||||||
| chr6:10578167
|
G | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-43184G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578167 | ||||||
| chr6:10578345
|
C | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0185a0001c0001t0002g0193others(1): Show | 4 | HG00673.hp1 NA18981.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-43006C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578345 | ||||||
| chr6:10578391
|
T | TA | 11 | a0001c0001t0001g0014a0001c0001t0001g0128a0001c0001t0001g0214others(8): Show | 11 | HG00597.hp1 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-42944dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10578391 | |||||
| chr6:10578391
|
TA | T | 28 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0030others(25): Show | 28 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.926-42944delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10578391 | |||||
| chr6:10578445
|
C | CT | 41 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0044others(38): Show | 41 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.926-42885dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578445
|
C | CTT | 23 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0081others(20): Show | 23 | HG00735.hp2 HG01192.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.926-42886_926-4288 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578445
|
C | CTTT | 12 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0074others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-42887_926-4288 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578445
|
C | CTTTT | 8 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0075others(5): Show | 8 | HG01175.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-42888_926-4288 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | |||||
| chr6:10578547
|
T | C | 193 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.926-42804T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578547 | ||||||
| chr6:10578548
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.926-42803G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578548 | ||||||
| chr6:10578592
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-42759A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578592 | ||||||
| chr6:10578634
|
G | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-42717G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578634 | ||||||
| chr6:10578648
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-42703G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578648 | ||||||
| chr6:10578692
|
T | C | 2 | a0001c0001t0009g0006a0001c0001t0011g0001 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.926-42659T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578692 | ||||||
| chr6:10578726
|
G | A | 2 | a0001c0001t0009g0006a0001c0001t0011g0001 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.926-42625G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578726 | ||||||
| chr6:10578746
|
C | T | 1 | a0001c0001t0002g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.926-42605C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578746 | ||||||
| chr6:10578759
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.926-42592C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578759 | ||||||
| chr6:10578761
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.926-42590T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578761 | ||||||
| chr6:10578778
|
G | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-42573G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578778 | ||||||
| chr6:10578787
|
T | C | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-42564T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578787 | ||||||
| chr6:10578800
|
A | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-42551A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578800 | ||||||
| chr6:10578821
|
T | TTTGTTG | 3 | a0001c0001t0003g0239a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG02258.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.926-42518_926-4251 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10578821 | |||||
| chr6:10578903
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0004g0069 | 2 | HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.926-42448G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578903 | ||||||
| chr6:10578991
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.926-42360G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10578991 | ||||||
| chr6:10579066
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.926-42285C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579066 | ||||||
| chr6:10579139
|
C | G | 1 | a0001c0001t0001g0281 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.926-42212C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579139 | ||||||
| chr6:10579222
|
C | T | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0012g0008 | 3 | HG03130.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.926-42129C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579222 | ||||||
| chr6:10579344
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.926-42007T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579344 | ||||||
| chr6:10579453
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-41898C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579453 | ||||||
| chr6:10579611
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-41740C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579611 | ||||||
| chr6:10579643
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.926-41708C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579643 | ||||||
| chr6:10579730
|
G | C | 321 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(318): Show | 321 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.926-41621G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579730 | ||||||
| chr6:10579731
|
G | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-41620G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579731 | ||||||
| chr6:10579743
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(11): Show | 14 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-41608A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579743 | ||||||
| chr6:10579757
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.926-41594A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579757 | ||||||
| chr6:10579780
|
C | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0221a0001c0001t0001g0247others(2): Show | 5 | HG01192.hp2 HG02109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-41571C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579780 | ||||||
| chr6:10579803
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.926-41548G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579803 | ||||||
| chr6:10579826
|
C | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0123 | 2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.926-41525C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579826 | ||||||
| chr6:10579826
|
C | CA | 113 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(110): Show | 113 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.926-41503dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | |||||
| chr6:10579826
|
C | CAA | 23 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0061others(20): Show | 23 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.926-41504_926-4150 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | |||||
| chr6:10579826
|
C | CAAACA | 9 | a0001c0001t0001g0014a0001c0001t0001g0131a0001c0001t0001g0132others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-41522_926-4152 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | |||||
| chr6:10579827
|
A | AAAC | 21 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0074others(18): Show | 21 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.926-41522_926-4152 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10579827 | |||||
| chr6:10579829
|
A | AC | 4 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0163others(1): Show | 4 | HG02818.hp1 HG02895.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-41522_926-4152 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579829 | ||||||
| chr6:10579829
|
A | ACAAAC | 3 | a0001c0001t0001g0226a0001c0001t0005g0040a0001c0001t0008g0219 | 3 | HG02630.hp1 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.926-41522_926-4152 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579829 | ||||||
| chr6:10579830
|
A | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0062others(9): Show | 12 | HG00735.hp2 HG01361.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-41521A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579830 | ||||||
| chr6:10579831
|
A | C | 5 | a0001c0001t0001g0081a0001c0001t0004g0035a0001c0001t0009g0006others(2): Show | 5 | HG01243.hp1 NA19030.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-41520A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579831 | ||||||
| chr6:10579832
|
A | C | 1 | a0001c0001t0015g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.926-41519A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579832 | ||||||
| chr6:10579834
|
A | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0062others(9): Show | 12 | HG00735.hp2 HG01361.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-41517A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579834 | ||||||
| chr6:10579835
|
A | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0321a0001c0001t0009g0006others(1): Show | 4 | HG02647.hp2 HG03579.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-41516A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579835 | ||||||
| chr6:10579837
|
A | C | 2 | a0001c0001t0001g0215a0001c0001t0004g0069 | 2 | HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.926-41514A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579837 | ||||||
| chr6:10579839
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.926-41512A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579839 | ||||||
| chr6:10579840
|
A | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073others(1): Show | 4 | HG02818.hp1 HG02895.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-41511A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579840 | ||||||
| chr6:10579841
|
A | ACC | 12 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0062others(9): Show | 12 | HG00735.hp2 HG01361.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-41510_926-4150 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579841 | ||||||
| chr6:10579841
|
A | C | 34 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-41510A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579841 | ||||||
| chr6:10579886
|
G | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(13): Show | 16 | HG00735.hp2 HG01361.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.926-41465G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579886 | ||||||
| chr6:10579900
|
A | G | 8 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-41451A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579900 | ||||||
| chr6:10580061
|
C | T | 52 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(49): Show | 52 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.926-41290C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580061 | ||||||
| chr6:10580219
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0018others(5): Show | 8 | HG02630.hp1 HG02717.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-41132A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580219 | ||||||
| chr6:10580252
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-41099G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580252 | ||||||
| chr6:10580271
|
A | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.926-41080A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580271 | ||||||
| chr6:10580274
|
G | GGGGGGT | 13 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0081others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.926-41074_926-4107 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10580274 | |||||
| chr6:10580375
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.926-40976C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580375 | ||||||
| chr6:10580394
|
A | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0225 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.926-40957A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580394 | ||||||
| chr6:10580435
|
C | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(45): Show | 48 | HG00735.hp2 HG01099.hp1 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.926-40916C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580435 | ||||||
| chr6:10580592
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0221a0001c0001t0001g0247others(1): Show | 4 | HG01192.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-40759G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580592 | ||||||
| chr6:10580615
|
T | TA | 14 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0125others(11): Show | 14 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.926-40724dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10580615 | |||||
| chr6:10580615
|
TA | T | 8 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG01175.hp1 HG01361.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-40724delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10580615 | |||||
| chr6:10580668
|
G | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-40683G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580668 | ||||||
| chr6:10580677
|
T | G | 50 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(47): Show | 50 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.926-40674T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580677 | ||||||
| chr6:10580723
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-40628C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580723 | ||||||
| chr6:10580840
|
G | C | 18 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0063others(15): Show | 18 | HG01192.hp2 HG01361.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.926-40511G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580840 | ||||||
| chr6:10580872
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.926-40479T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580872 | ||||||
| chr6:10580919
|
G | C | 1 | a0001c0001t0011g0001 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.926-40432G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580919 | ||||||
| chr6:10580935
|
G | C | 1 | a0001c0001t0003g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.926-40416G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580935 | ||||||
| chr6:10580956
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-40395G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580956 | ||||||
| chr6:10580972
|
A | G | 10 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0131others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.926-40379A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10580972 | ||||||
| chr6:10581064
|
C | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-40287C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581064 | ||||||
| chr6:10581099
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.926-40252A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581099 | ||||||
| chr6:10581263
|
A | T | 1 | a0001c0001t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.926-40088A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581263 | ||||||
| chr6:10581263
|
ATTTATTT | A | 3 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0006g0286 | 3 | HG01099.hp1 HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.926-40070_926-4006 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10581263 | |||||
| chr6:10581291
|
A | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-40060A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581291 | ||||||
| chr6:10581309
|
T | C | 16 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0074others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.926-40042T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581309 | ||||||
| chr6:10581337
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.926-40014C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581337 | ||||||
| chr6:10581565
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39786C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581565 | ||||||
| chr6:10581727
|
CA | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0180a0001c0001t0001g0184others(2): Show | 5 | HG00558.hp1 HG02129.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-39621delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10581727 | |||||
| chr6:10581733
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.926-39618G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581733 | ||||||
| chr6:10581763
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39588G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581763 | ||||||
| chr6:10581803
|
T | G | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0012g0008 | 3 | HG03130.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.926-39548T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10581803 | ||||||
| chr6:10581931
|
A | AGT | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39412_926-3941 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10581931 | |||||
| chr6:10581961
|
AAT | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39378_926-3937 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10581961 | |||||
| chr6:10582010
|
G | GTA | 5 | a0001c0001t0001g0046a0001c0001t0001g0194a0001c0001t0001g0215others(2): Show | 5 | HG02523.hp1 HG02896.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.926-39335_926-3933 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582010 | |||||
| chr6:10582016
|
ATG | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0227a0001c0001t0003g0237 | 3 | HG01074.hp2 HG02155.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.926-39333_926-3933 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582016 | |||||
| chr6:10582018
|
G | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(128): Show | 131 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.926-39333G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582018 | ||||||
| chr6:10582043
|
T | TATATATT others(3): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39304_926-3930 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582043 | |||||
| chr6:10582059
|
CAT | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39291_926-3929 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582059 | ||||||
| chr6:10582095
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0226a0001c0001t0005g0040others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-39256T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582095 | ||||||
| chr6:10582113
|
T | TATAC | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39237_926-3923 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582113 | |||||
| chr6:10582116
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39235A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582116 | ||||||
| chr6:10582118
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39233A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582118 | ||||||
| chr6:10582120
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39231C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582120 | ||||||
| chr6:10582125
|
A | T | 35 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0030others(32): Show | 35 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.926-39226A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582125 | ||||||
| chr6:10582172
|
T | TTATATAA others(36): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39170_926-3916 others(47): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582172 | |||||
| chr6:10582177
|
T | G | 16 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0077others(13): Show | 16 | HG00408.hp1 HG01928.hp2 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.926-39174T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582177 | ||||||
| chr6:10582221
|
ATTATATA others(1): Show |
A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39129_926-3912 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582221 | ||||||
| chr6:10582231
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39120T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582231 | ||||||
| chr6:10582231
|
T | TTTAAATA others(29): Show |
1 | a0001c0001t0001g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.926-39106_926-3907 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582231 | |||||
| chr6:10582233
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39118T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582233 | ||||||
| chr6:10582241
|
TAAAA | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39109_926-3910 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582241 | ||||||
| chr6:10582242
|
A | AAAATATA others(28): Show |
11 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0062others(8): Show | 11 | HG01346.hp2 HG01361.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.926-39093_926-3905 others(39): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582242 | |||||
| chr6:10582254
|
A | C | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.926-39097A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582254 | ||||||
| chr6:10582277
|
T | TA | 10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0125others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-39071dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582277 | |||||
| chr6:10582280
|
A | ATATAT | 24 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0074others(21): Show | 24 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.926-39070_926-3906 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582280 | |||||
| chr6:10582285
|
TATA | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39062_926-3906 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582285 | |||||
| chr6:10582288
|
A | AATATATA others(30): Show |
10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0125others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-39059_926-3905 others(41): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582288 | |||||
| chr6:10582289
|
ATAT | A | 3 | a0001c0001t0004g0314a0001c0001t0004g0316a0001c0001t0012g0008 | 3 | HG03130.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.926-39059_926-3905 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582289 | |||||
| chr6:10582292
|
T | A | 1 | a0001c0001t0027g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.926-39059T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582292 | ||||||
| chr6:10582303
|
T | TTAATATA others(29): Show |
1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.926-39011_926-3897 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582303 | |||||
| chr6:10582303
|
TTAATATA others(29): Show |
T | 17 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0075others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.926-39011_926-3897 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582303 | |||||
| chr6:10582339
|
A | ATATT | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-39010_926-3900 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582339 | |||||
| chr6:10582346
|
A | T | 2 | a0001c0001t0001g0226a0001c0001t0008g0219 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.926-39005A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582346 | ||||||
| chr6:10582351
|
A | T | 2 | a0001c0001t0001g0226a0001c0001t0008g0219 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.926-39000A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582351 | ||||||
| chr6:10582359
|
A | C | 2 | a0001c0001t0001g0226a0001c0001t0008g0219 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.926-38992A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582359 | ||||||
| chr6:10582367
|
T | A | 2 | a0001c0001t0001g0226a0001c0001t0008g0219 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.926-38984T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582367 | ||||||
| chr6:10582371
|
C | G | 2 | a0001c0001t0001g0226a0001c0001t0008g0219 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.926-38980C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582371 | ||||||
| chr6:10582373
|
ATAATT | A | 15 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0074others(12): Show | 15 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.926-38973_926-3896 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582373 | |||||
| chr6:10582375
|
A | AT | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38976_926-3897 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582375 | ||||||
| chr6:10582378
|
T | TTAATATT others(24): Show |
4 | a0001c0001t0001g0149a0001c0001t0001g0299a0001c0001t0002g0193others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-38949_926-3891 others(35): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582378 | |||||
| chr6:10582378
|
T | TTAATATT others(86): Show |
8 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-38919_926-3891 others(97): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582378 | |||||
| chr6:10582385
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38966T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582385 | ||||||
| chr6:10582388
|
T | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38963T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582388 | ||||||
| chr6:10582390
|
ATATACT | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38960_926-3895 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582390 | ||||||
| chr6:10582400
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38951A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582400 | ||||||
| chr6:10582406
|
AGTATAAT others(3): Show |
A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38944_926-3893 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582406 | ||||||
| chr6:10582419
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38932T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582419 | ||||||
| chr6:10582426
|
CTATAAT | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38923_926-3891 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582426 | |||||
| chr6:10582438
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38913A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582438 | ||||||
| chr6:10582441
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38910T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582441 | ||||||
| chr6:10582443
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38908T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582443 | ||||||
| chr6:10582453
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38898T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582453 | ||||||
| chr6:10582456
|
A | G | 1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.926-38895A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582456 | ||||||
| chr6:10582456
|
ATAATAAA others(1): Show |
A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38894_926-3888 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582456 | ||||||
| chr6:10582462
|
A | T | 1 | a0001c0001t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.926-38889A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582462 | ||||||
| chr6:10582463
|
ATATAATA others(5): Show |
A | 5 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0001g0074others(2): Show | 5 | HG02647.hp2 HG02698.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.926-38864_926-3885 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582463 | |||||
| chr6:10582466
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38885T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582466 | ||||||
| chr6:10582475
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38876C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582475 | ||||||
| chr6:10582480
|
A | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38871A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582480 | ||||||
| chr6:10582481
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38870T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582481 | ||||||
| chr6:10582481
|
TATATACT others(10): Show |
T | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.926-38864_926-3884 others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582481 | |||||
| chr6:10582482
|
ATATAC | A | 22 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0075others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.926-38864_926-3886 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582482 | |||||
| chr6:10582486
|
AC | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38864delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582486 | ||||||
| chr6:10582487
|
C | A | 18 | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0001g0062others(15): Show | 18 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.926-38864C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582487 | ||||||
| chr6:10582491
|
A | AATACATC | 7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-38857_926-3885 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582491 | |||||
| chr6:10582498
|
A | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-38853A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582498 | ||||||
| chr6:10582501
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.926-38850A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582501 | ||||||
| chr6:10582503
|
A | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-38848A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582503 | ||||||
| chr6:10582519
|
T | TAC | 11 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-38831_926-3883 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582519 | |||||
| chr6:10582522
|
T | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-38829T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582522 | ||||||
| chr6:10582522
|
T | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-38829T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582522 | ||||||
| chr6:10582526
|
C | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(15): Show | 18 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.926-38825C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582526 | ||||||
| chr6:10582528
|
TCA | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-38822_926-3882 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582528 | ||||||
| chr6:10582531
|
T | TATATAAT others(14): Show |
7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-38816_926-3881 others(25): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582531 | |||||
| chr6:10582536
|
T | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0022others(17): Show | 20 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.926-38815T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582536 | ||||||
| chr6:10582536
|
T | TATATA | 27 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0030others(24): Show | 27 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.926-38814_926-3881 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582536 | |||||
| chr6:10582546
|
G | A | 49 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 49 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.926-38805G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582546 | ||||||
| chr6:10582550
|
A | T | 2 | a0001c0001t0001g0029a0001c0001t0005g0026 | 2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.926-38801A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582550 | ||||||
| chr6:10582552
|
T | TATA | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38798_926-3879 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582552 | |||||
| chr6:10582572
|
A | G | 9 | a0001c0001t0001g0004a0001c0001t0001g0071a0001c0001t0001g0121others(6): Show | 9 | HG02040.hp1 HG02132.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-38779A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582572 | ||||||
| chr6:10582583
|
C | T | 4 | a0001c0001t0001g0215a0001c0001t0004g0069a0001c0001t0009g0006others(1): Show | 4 | HG02896.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-38768C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582583 | ||||||
| chr6:10582613
|
A | AAT | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-38729_926-3872 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582613 | |||||
| chr6:10582617
|
T | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0089others(15): Show | 18 | HG00323.hp2 HG00558.hp2 HG03490.hp1 others(15): Show |
intron_variant | MODIFIER | c.926-38734T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582617 | ||||||
| chr6:10582624
|
T | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.926-38727T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582624 | ||||||
| chr6:10582721
|
C | CT | 7 | a0001c0001t0001g0029a0001c0001t0001g0159a0001c0001t0001g0188others(4): Show | 7 | HG00735.hp2 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-38621dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582721 | |||||
| chr6:10582730
|
TC | T | 32 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0030others(29): Show | 32 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.926-38619delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582730 | |||||
| chr6:10582770
|
G | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0030others(15): Show | 18 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.926-38581G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582770 | ||||||
| chr6:10582804
|
AAAC | A | 47 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 47 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.926-38532_926-3853 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10582804 | |||||
| chr6:10582897
|
A | G | 10 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0125others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-38454A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10582897 | ||||||
| chr6:10583009
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.926-38342G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583009 | ||||||
| chr6:10583112
|
G | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0177 | 3 | NA18951.hp1 NA18973.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.926-38239G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583112 | ||||||
| chr6:10583229
|
C | T | 8 | a0001c0001t0001g0082a0001c0001t0001g0215a0001c0001t0001g0221others(5): Show | 8 | HG01192.hp2 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-38122C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583229 | ||||||
| chr6:10583268
|
A | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-38083A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583268 | ||||||
| chr6:10583356
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.926-37995C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583356 | ||||||
| chr6:10583370
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.926-37981G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583370 | ||||||
| chr6:10583432
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.926-37919C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583432 | ||||||
| chr6:10583468
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0221 | 2 | HG01192.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.926-37883C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583468 | ||||||
| chr6:10583492
|
T | C | 11 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(8): Show | 11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.926-37859T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583492 | ||||||
| chr6:10583543
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-37808G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583543 | ||||||
| chr6:10583587
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.926-37764T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583587 | ||||||
| chr6:10583868
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.926-37483C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583868 | ||||||
| chr6:10583922
|
A | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.926-37429A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583922 | ||||||
| chr6:10583943
|
C | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-37408C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583943 | ||||||
| chr6:10583960
|
G | C | 29 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(26): Show | 29 | HG01243.hp1 HG01361.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.926-37391G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583960 | ||||||
| chr6:10583991
|
A | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.926-37360A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10583991 | ||||||
| chr6:10584047
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-37304G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584047 | ||||||
| chr6:10584084
|
T | C | 29 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(26): Show | 29 | HG01243.hp1 HG01361.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.926-37267T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584084 | ||||||
| chr6:10584113
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(8): Show | 11 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.926-37238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584113 | ||||||
| chr6:10584129
|
C | A | 1 | a0001c0001t0001g0012 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.926-37222C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584129 | ||||||
| chr6:10584170
|
A | C | 2 | a0001c0001t0001g0029a0001c0001t0005g0026 | 2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.926-37181A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584170 | ||||||
| chr6:10584211
|
A | C | 2 | a0001c0001t0001g0133a0001c0001t0001g0155 | 2 | NA18956.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.926-37140A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584211 | ||||||
| chr6:10584232
|
A | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0039others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.926-37119A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584232 | ||||||
| chr6:10584234
|
T | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-37117T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584234 | ||||||
| chr6:10584438
|
G | A | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(130): Show | 133 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.926-36913G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584438 | ||||||
| chr6:10584624
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.926-36727G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584624 | ||||||
| chr6:10584673
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-36678C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584673 | ||||||
| chr6:10584735
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.926-36616C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584735 | ||||||
| chr6:10584917
|
C | T | 46 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.926-36434C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584917 | ||||||
| chr6:10584956
|
G | C | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.926-36395G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584956 | ||||||
| chr6:10584977
|
T | C | 38 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.926-36374T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584977 | ||||||
| chr6:10585028
|
AGTCAGTG others(3): Show |
A | 1 | a0001c0001t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.926-36320_926-3631 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | |||||
| chr6:10585028
|
AGTCAGTG others(9): Show |
A | 14 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0131others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-36320_926-3630 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | |||||
| chr6:10585028
|
AGTCAGTG others(11): Show |
A | 2 | a0001c0001t0001g0226a0001c0001t0011g0001 | 2 | HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.926-36320_926-3630 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | |||||
| chr6:10585032
|
A | AGT | 8 | a0001c0001t0001g0044a0001c0001t0001g0066a0001c0001t0001g0115others(5): Show | 8 | HG00735.hp1 HG01123.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-36273_926-3627 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
A | AGTGT | 8 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0085others(5): Show | 8 | HG01243.hp2 HG03017.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-36275_926-3627 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGT | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(114): Show | 117 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.926-36273_926-3627 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGT | A | 55 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0054others(52): Show | 55 | HG00323.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.926-36275_926-3627 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGT | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0053others(17): Show | 20 | HG00639.hp1 HG01192.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.926-36277_926-3627 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0001g0265a0001c0001t0001g0302 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.926-36281_926-3627 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(7): Show |
A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0029others(1): Show | 4 | HG00735.hp2 HG03516.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-36285_926-3627 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0002g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.926-36287_926-3627 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585032
|
AGTGTGTG others(11): Show |
A | 3 | a0001c0001t0001g0215a0001c0001t0004g0069a0001c0001t0009g0006 | 3 | HG02896.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.926-36289_926-3627 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | |||||
| chr6:10585052
|
TGTGTGTG others(21): Show |
T | 9 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-36297_926-3627 others(32): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585052 | |||||
| chr6:10585064
|
TGTGTGTG others(9): Show |
T | 3 | a0001c0001t0001g0018a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG02109.hp2 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.926-36285_926-3627 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585064 | |||||
| chr6:10585066
|
TGTGTGTG others(7): Show |
T | 4 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0004g0314others(1): Show | 4 | HG02622.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-36283_926-3627 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585066 | |||||
| chr6:10585066
|
TGTGTGTG others(9): Show |
T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-36283_926-3626 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585066 | |||||
| chr6:10585068
|
TGTGTGTG others(5): Show |
T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-36281_926-3627 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585068 | |||||
| chr6:10585070
|
TGTGTGTG others(3): Show |
T | 2 | a0001c0001t0001g0074a0001c0001t0015g0076 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.926-36279_926-3627 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585070 | |||||
| chr6:10585074
|
TGTGTGC | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0308a0002c0004t0028g0324 | 3 | HG02273.hp2 HG02293.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.926-36275_926-3627 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585074 | |||||
| chr6:10585076
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0002g0293 | 2 | HG01928.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.926-36275T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585076 | ||||||
| chr6:10585078
|
T | C | 39 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.926-36273T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585078 | ||||||
| chr6:10585078
|
TGC | T | 3 | a0001c0001t0001g0140a0001c0001t0001g0225a0001c0001t0002g0136 | 3 | HG01516.hp2 HG01517.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.926-36268_926-3626 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585078 | |||||
| chr6:10585078
|
TGCGC | T | 18 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0039others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.926-36270_926-3626 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10585078 | |||||
| chr6:10585081
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.926-36270G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585081 | ||||||
| chr6:10585083
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0032others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-36268G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585083 | ||||||
| chr6:10585162
|
T | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.926-36189T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585162 | ||||||
| chr6:10585193
|
G | T | 21 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.926-36158G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585193 | ||||||
| chr6:10585261
|
C | G | 2 | a0001c0001t0001g0318a0001c0001t0001g0319 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.926-36090C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585261 | ||||||
| chr6:10585368
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.926-35983G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585368 | ||||||
| chr6:10585419
|
G | T | 1 | a0001c0001t0003g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.926-35932G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585419 | ||||||
| chr6:10585443
|
G | C | 2 | a0001c0001t0001g0147a0001c0001t0003g0232 | 2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.926-35908G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585443 | ||||||
| chr6:10585471
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.926-35880C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585471 | ||||||
| chr6:10585618
|
C | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-35733C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585618 | ||||||
| chr6:10585619
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0008g0219 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.926-35732G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585619 | ||||||
| chr6:10585747
|
A | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.926-35604A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585747 | ||||||
| chr6:10585773
|
A | C | 51 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(48): Show | 51 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.926-35578A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585773 | ||||||
| chr6:10585878
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0005g0026 | 2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.926-35473C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585878 | ||||||
| chr6:10585879
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.926-35472G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585879 | ||||||
| chr6:10585880
|
G | A | 18 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0039others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.926-35471G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10585880 | ||||||
| chr6:10586199
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.926-35152A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10586199 | ||||||
| chr6:10586378
|
A | G | 1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.926-34973A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10586378 | ||||||
| chr6:10586386
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0002g0083 | 2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.926-34965C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10586386 | ||||||
| chr6:10586494
|
G | A | 1 | a0001c0001t0002g0283 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.926-34857G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10586494 | ||||||
| chr6:10586696
|
A | G | 8 | a0001c0001t0001g0022a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG01361.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-34655A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10586696 | ||||||
| chr6:10586805
|
C | G | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(312): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.926-34546C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10586805 | ||||||
| chr6:10586823
|
A | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-34528A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10586823 | ||||||
| chr6:10587120
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0274 | 2 | HG00621.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.926-34231G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587120 | ||||||
| chr6:10587156
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.926-34195A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587156 | ||||||
| chr6:10587188
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0039others(10): Show | 13 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.926-34163G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587188 | ||||||
| chr6:10587280
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.926-34071C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587280 | ||||||
| chr6:10587416
|
C | T | 12 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0027others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-33935C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587416 | ||||||
| chr6:10587463
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0001g0216 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.926-33888T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587463 | ||||||
| chr6:10587603
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.926-33748A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587603 | ||||||
| chr6:10587781
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0074others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.926-33570T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587781 | ||||||
| chr6:10587857
|
A | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0170a0001c0001t0001g0228 | 3 | HG00438.hp2 NA19007.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.926-33494A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10587857 | ||||||
| chr6:10588199
|
A | C | 1 | a0001c0001t0002g0296 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.926-33152A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588199 | ||||||
| chr6:10588237
|
T | C | 10 | a0001c0001t0001g0032a0001c0001t0001g0074a0001c0001t0001g0125others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-33114T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588237 | ||||||
| chr6:10588288
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.926-33063A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588288 | ||||||
| chr6:10588374
|
TC | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-32975delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10588374 | |||||
| chr6:10588397
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.926-32954C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588397 | ||||||
| chr6:10588710
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.926-32641G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588710 | ||||||
| chr6:10588713
|
A | G | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0131others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.926-32638A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588713 | ||||||
| chr6:10588785
|
A | ATG | 4 | a0001c0001t0015g0076a0001c0001t0016g0098a0001c0001t0022g0271others(1): Show | 4 | HG01081.hp2 HG01978.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-32543_926-3254 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | |||||
| chr6:10588785
|
ATG | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(156): Show | 159 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.926-32543_926-3254 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | |||||
| chr6:10588785
|
ATGTG | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0125others(7): Show | 10 | HG00140.hp1 HG00597.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.926-32545_926-3254 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | |||||
| chr6:10588831
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.926-32520A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588831 | ||||||
| chr6:10588831
|
ATGTGTGT others(4): Show |
A | 4 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320others(1): Show | 4 | HG01884.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-32505_926-3249 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10588831 | |||||
| chr6:10588890
|
C | CGTGTGTG others(4): Show |
179 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(176): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.926-32457_926-3244 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10588890 | |||||
| chr6:10588925
|
G | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0246 | 2 | NA18980.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.926-32426G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588925 | ||||||
| chr6:10588983
|
T | C | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.926-32368T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10588983 | ||||||
| chr6:10589078
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0206 | 3 | HG02280.hp2 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.926-32273G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10589078 | ||||||
| chr6:10589102
|
AGT | A | 145 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(142): Show | 145 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.926-32239_926-3223 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10589102 | |||||
| chr6:10589113
|
GGT | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.926-32229_926-3222 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10589113 | |||||
| chr6:10589156
|
GTGCGTGT others(26): Show |
G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-32192_926-3216 others(37): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10589156 | |||||
| chr6:10589188
|
C | G | 315 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(312): Show | 315 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.926-32163C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10589188 | ||||||
| chr6:10589306
|
GGTGTGTT others(51): Show |
G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-32022_926-3196 others(62): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10589306 | |||||
| chr6:10589398
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.926-31953G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10589398 | ||||||
| chr6:10589421
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320others(1): Show | 4 | HG01884.hp2 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-31930T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10589421 | ||||||
| chr6:10589425
|
T | C | 1 | a0001c0001t0002g0264 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.926-31926T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10589425 | ||||||
| chr6:10589469
|
G | C | 1 | a0001c0001t0005g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.926-31882G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10589469 | ||||||
| chr6:10589786
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.926-31565T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10589786 | ||||||
| chr6:10589808
|
TATACTC | T | 3 | a0001c0001t0001g0029a0001c0001t0003g0239a0001c0001t0013g0108 | 3 | HG02970.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.926-31541_926-3153 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10589808 | |||||
| chr6:10590086
|
T | C | 1 | a0001c0001t0027g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.926-31265T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590086 | ||||||
| chr6:10590242
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0216a0001c0001t0001g0247others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-31109T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590242 | ||||||
| chr6:10590362
|
C | T | 6 | a0001c0001t0001g0133a0001c0001t0001g0137a0001c0001t0001g0155others(3): Show | 6 | HG02080.hp2 HG02155.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.926-30989C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590362 | ||||||
| chr6:10590397
|
C | CA | 32 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0019others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.926-30938dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10590397 | |||||
| chr6:10590559
|
A | AT | 155 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0016others(152): Show | 155 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.926-30779dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10590559 | |||||
| chr6:10590673
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.926-30678C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590673 | ||||||
| chr6:10590711
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-30640G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590711 | ||||||
| chr6:10590798
|
C | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0016others(128): Show | 131 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.926-30553C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590798 | ||||||
| chr6:10590848
|
G | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0016others(131): Show | 134 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.926-30503G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590848 | ||||||
| chr6:10590918
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-30433G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10590918 | ||||||
| chr6:10591101
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.926-30250C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591101 | ||||||
| chr6:10591278
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.926-30073A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591278 | ||||||
| chr6:10591293
|
C | A | 1 | a0001c0001t0001g0210 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.926-30058C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591293 | ||||||
| chr6:10591396
|
C | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-29955C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591396 | ||||||
| chr6:10591469
|
T | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 22 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.926-29882T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591469 | ||||||
| chr6:10591598
|
G | T | 1 | a0001c0001t0024g0241 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.926-29753G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591598 | ||||||
| chr6:10591732
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.926-29619T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591732 | ||||||
| chr6:10591901
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-29450C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591901 | ||||||
| chr6:10591928
|
A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.926-29423A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10591928 | ||||||
| chr6:10592095
|
A | AAACGTCA others(8): Show |
8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-29255_926-2924 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10592095 | |||||
| chr6:10592113
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.926-29238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10592113 | ||||||
| chr6:10592162
|
A | G | 30 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 30 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.926-29189A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10592162 | ||||||
| chr6:10592571
|
G | C | 1 | a0001c0001t0001g0317 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.926-28780G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10592571 | ||||||
| chr6:10592753
|
A | G | 152 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0016others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.926-28598A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10592753 | ||||||
| chr6:10592922
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0005g0040a0001c0001t0012g0008 | 3 | HG02622.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.926-28429T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10592922 | ||||||
| chr6:10593018
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-28333G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593018 | ||||||
| chr6:10593033
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-28318G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593033 | ||||||
| chr6:10593051
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-28300G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593051 | ||||||
| chr6:10593226
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-28125G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593226 | ||||||
| chr6:10593230
|
T | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.926-28121T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593230 | ||||||
| chr6:10593250
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.926-28101C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593250 | ||||||
| chr6:10593346
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-28005G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593346 | ||||||
| chr6:10593383
|
A | G | 182 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.926-27968A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593383 | ||||||
| chr6:10593417
|
A | C | 1 | a0001c0001t0027g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.926-27934A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593417 | ||||||
| chr6:10593525
|
A | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-27826A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593525 | ||||||
| chr6:10593534
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.926-27817C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593534 | ||||||
| chr6:10593568
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.926-27783G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593568 | ||||||
| chr6:10593595
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-27756T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593595 | ||||||
| chr6:10593670
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-27681T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593670 | ||||||
| chr6:10593730
|
A | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-27621A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593730 | ||||||
| chr6:10593864
|
G | A | 2 | a0001c0001t0002g0200a0001c0001t0002g0203 | 2 | HG00408.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.926-27487G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593864 | ||||||
| chr6:10593877
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-27474C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593877 | ||||||
| chr6:10593885
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-27466C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593885 | ||||||
| chr6:10593902
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.926-27449G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10593902 | ||||||
| chr6:10594027
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-27324G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594027 | ||||||
| chr6:10594513
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0216a0001c0001t0001g0247others(1): Show | 4 | HG02109.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-26838T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594513 | ||||||
| chr6:10594575
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.926-26776G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594575 | ||||||
| chr6:10594615
|
G | C | 1 | a0001c0001t0001g0053 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.926-26736G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594615 | ||||||
| chr6:10594647
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-26704T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594647 | ||||||
| chr6:10594685
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0318others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-26666C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594685 | ||||||
| chr6:10594832
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-26519G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594832 | ||||||
| chr6:10594852
|
C | CTT | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-26490_926-2648 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10594852 | |||||
| chr6:10594889
|
A | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.926-26462A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10594889 | ||||||
| chr6:10594940
|
GGCTCAA | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-26408_926-2640 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10594940 | |||||
| chr6:10595266
|
C | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-26085C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595266 | ||||||
| chr6:10595427
|
G | A | 2 | a0001c0001t0001g0265a0001c0001t0001g0302 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.926-25924G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595427 | ||||||
| chr6:10595558
|
T | TGA | 34 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0019others(31): Show | 34 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-25792_926-2579 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10595558 | |||||
| chr6:10595558
|
T | TGC | 4 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0081others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-25792_926-2579 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10595558 | |||||
| chr6:10595565
|
C | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-25786C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595565 | ||||||
| chr6:10595592
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.926-25759T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595592 | ||||||
| chr6:10595606
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0002g0303 | 2 | NA18968.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.926-25745G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595606 | ||||||
| chr6:10595672
|
C | T | 3 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.926-25679C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595672 | ||||||
| chr6:10595681
|
G | GA | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-25662dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10595681 | |||||
| chr6:10595759
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.926-25592T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595759 | ||||||
| chr6:10595773
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.926-25578G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595773 | ||||||
| chr6:10595804
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-25547G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595804 | ||||||
| chr6:10595850
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0004g0069a0001c0001t0009g0006others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-25501A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595850 | ||||||
| chr6:10595940
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0004g0069a0001c0001t0009g0006others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-25411A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595940 | ||||||
| chr6:10595949
|
G | A | 12 | a0001c0001t0001g0037a0001c0001t0001g0077a0001c0001t0001g0079others(9): Show | 12 | HG00408.hp1 HG02300.hp2 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-25402G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595949 | ||||||
| chr6:10595990
|
A | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-25361A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10595990 | ||||||
| chr6:10596114
|
C | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-25237C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596114 | ||||||
| chr6:10596281
|
T | C | 3 | a0001c0001t0002g0134a0001c0001t0002g0277a0001c0001t0002g0291 | 3 | NA18971.hp1 NA18983.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.926-25070T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596281 | ||||||
| chr6:10596320
|
A | G | 96 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0036others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.926-25031A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596320 | ||||||
| chr6:10596373
|
T | G | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(180): Show | 183 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.926-24978T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596373 | ||||||
| chr6:10596387
|
G | A | 186 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(183): Show | 186 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.926-24964G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596387 | ||||||
| chr6:10596504
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-24847G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596504 | ||||||
| chr6:10596520
|
C | CA | 15 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0050others(12): Show | 15 | HG00140.hp1 HG00323.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.926-24819dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10596520 | |||||
| chr6:10596555
|
G | A | 9 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0222others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-24796G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596555 | ||||||
| chr6:10596669
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.926-24682C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596669 | ||||||
| chr6:10596734
|
T | TA | 12 | a0001c0001t0001g0032a0001c0001t0001g0054a0001c0001t0001g0057others(9): Show | 12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-24605dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10596734 | |||||
| chr6:10596799
|
CCTTCAGC others(5): Show |
C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-24549_926-2453 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10596799 | |||||
| chr6:10596897
|
A | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-24454A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596897 | ||||||
| chr6:10596997
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.926-24354T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596997 | ||||||
| chr6:10597153
|
C | CT | 132 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0016others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.926-24178dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | |||||
| chr6:10597153
|
C | CTT | 12 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0070others(9): Show | 12 | HG01175.hp1 HG02056.hp2 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.926-24179_926-2417 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | |||||
| chr6:10597153
|
CT | C | 28 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0018others(25): Show | 28 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.926-24178delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | |||||
| chr6:10597386
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-23965C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597386 | ||||||
| chr6:10597447
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0107a0001c0001t0001g0206 | 3 | HG02572.hp1 HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.926-23904G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597447 | ||||||
| chr6:10597613
|
T | TTTG | 15 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0074others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.926-23723_926-2372 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10597613 | |||||
| chr6:10597672
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.926-23679G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597672 | ||||||
| chr6:10597700
|
A | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-23651A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597700 | ||||||
| chr6:10597715
|
T | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-23636T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597715 | ||||||
| chr6:10597842
|
C | T | 2 | a0001c0001t0001g0307a0001c0001t0002g0258 | 2 | HG03491.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.926-23509C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597842 | ||||||
| chr6:10597853
|
T | G | 165 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(162): Show | 165 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.926-23498T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597853 | ||||||
| chr6:10597903
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.926-23448C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597903 | ||||||
| chr6:10597920
|
CT | C | 5 | a0001c0001t0001g0068a0001c0001t0001g0130a0001c0001t0001g0163others(2): Show | 5 | HG01975.hp2 HG02896.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-23424delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10597920 | |||||
| chr6:10597959
|
G | T | 1 | a0001c0001t0003g0229 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.926-23392G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10597959 | ||||||
| chr6:10598102
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.926-23249G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598102 | ||||||
| chr6:10598109
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.926-23242C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598109 | ||||||
| chr6:10598404
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-22947G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598404 | ||||||
| chr6:10598620
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.926-22731A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598620 | ||||||
| chr6:10598636
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.926-22715C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598636 | ||||||
| chr6:10598672
|
C | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-22679C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598672 | ||||||
| chr6:10598865
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-22486G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598865 | ||||||
| chr6:10598966
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-22385T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598966 | ||||||
| chr6:10598973
|
G | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0012others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.926-22378G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10598973 | ||||||
| chr6:10599046
|
T | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-22305T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599046 | ||||||
| chr6:10599065
|
C | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-22286C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599065 | ||||||
| chr6:10599087
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0125a0001c0001t0001g0192others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-22264G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599087 | ||||||
| chr6:10599089
|
C | T | 1 | a0001c0001t0004g0298 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.926-22262C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599089 | ||||||
| chr6:10599238
|
G | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0116 | 2 | HG00642.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.926-22113G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599238 | ||||||
| chr6:10599263
|
C | T | 162 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(159): Show | 162 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.926-22088C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599263 | ||||||
| chr6:10599301
|
G | A | 162 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0013others(159): Show | 162 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.926-22050G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599301 | ||||||
| chr6:10599367
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0318others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-21984A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599367 | ||||||
| chr6:10599382
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0032others(15): Show | 18 | HG00140.hp1 HG01081.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.926-21969A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599382 | ||||||
| chr6:10599510
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.926-21841G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599510 | ||||||
| chr6:10599681
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.926-21670T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10599681 | ||||||
| chr6:10600021
|
G | A | 19 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0022others(16): Show | 19 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.926-21330G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10600021 | ||||||
| chr6:10600119
|
T | C | 4 | a0001c0001t0001g0266a0001c0001t0005g0213a0001c0001t0011g0002others(1): Show | 4 | HG01109.hp1 HG01496.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-21232T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10600119 | ||||||
| chr6:10600421
|
C | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0318others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-20930C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10600421 | ||||||
| chr6:10600606
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0096others(4): Show | 7 | HG00621.hp2 HG00673.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-20745C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10600606 | ||||||
| chr6:10600647
|
C | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(128): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.926-20704C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10600647 | ||||||
| chr6:10600665
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.926-20686C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10600665 | ||||||
| chr6:10600675
|
T | G | 155 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0016others(152): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.926-20676T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10600675 | ||||||
| chr6:10600760
|
T | TTTTA | 3 | a0001c0001t0001g0089a0001c0001t0002g0090a0001c0001t0008g0322 | 3 | HG00558.hp2 HG03195.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.926-20570_926-2056 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10600760 | |||||
| chr6:10601171
|
A | G | 1 | a0001c0001t0009g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.926-20180A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601171 | ||||||
| chr6:10601289
|
C | G | 1 | a0001c0001t0008g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.926-20062C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601289 | ||||||
| chr6:10601351
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.926-20000C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601351 | ||||||
| chr6:10601433
|
G | C | 53 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0018others(50): Show | 53 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.926-19918G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601433 | ||||||
| chr6:10601463
|
G | T | 28 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0023others(25): Show | 28 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.926-19888G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601463 | ||||||
| chr6:10601465
|
A | G | 12 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.926-19886A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601465 | ||||||
| chr6:10601471
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0073 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.926-19880G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601471 | ||||||
| chr6:10601486
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.926-19865C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601486 | ||||||
| chr6:10601674
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.926-19677G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601674 | ||||||
| chr6:10601680
|
G | A | 12 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.926-19671G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601680 | ||||||
| chr6:10601769
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.926-19582C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601769 | ||||||
| chr6:10601821
|
G | A | 2 | a0001c0001t0008g0219a0001c0001t0023g0313 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.926-19530G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601821 | ||||||
| chr6:10601939
|
T | TTAAAAA | 3 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0008g0322 | 3 | HG02257.hp2 HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.926-19412_926-1941 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601939 | ||||||
| chr6:10601940
|
C | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01361.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.926-19411C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601940 | ||||||
| chr6:10601940
|
CAAGAA | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0266a0001c0001t0003g0230others(14): Show | 17 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.926-19408_926-1940 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10601940 | |||||
| chr6:10601940
|
CAAGAAAA others(10): Show |
C | 2 | a0001c0001t0008g0219a0001c0001t0023g0313 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.926-19408_926-1939 others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10601940 | |||||
| chr6:10601943
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG01361.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.926-19408G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601943 | ||||||
| chr6:10601943
|
G | GA | 6 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0092others(3): Show | 6 | HG00642.hp1 HG02293.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.926-19391dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | |||||
| chr6:10601943
|
GA | G | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(203): Show | 206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.926-19391delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | |||||
| chr6:10601943
|
GAA | G | 7 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0093others(4): Show | 7 | NA18747.hp1 NA18955.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.926-19392_926-1939 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | |||||
| chr6:10601951
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0218 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.926-19391_926-1938 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10601951 | |||||
| chr6:10601954
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0255 | 2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.926-19397A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601954 | ||||||
| chr6:10601960
|
A | C | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.926-19391A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601960 | ||||||
| chr6:10601961
|
C | A | 35 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0018others(32): Show | 35 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.926-19390C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10601961 | ||||||
| chr6:10602000
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0284 | 2 | NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.926-19351T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602000 | ||||||
| chr6:10602179
|
C | G | 1 | a0001c0001t0002g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.926-19172C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602179 | ||||||
| chr6:10602237
|
C | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0154a0001c0001t0001g0172others(2): Show | 5 | NA18951.hp1 NA18973.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-19114C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602237 | ||||||
| chr6:10602250
|
G | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.926-19101G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602250 | ||||||
| chr6:10602326
|
A | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0266others(7): Show | 10 | HG01109.hp1 HG01496.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-19025A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602326 | ||||||
| chr6:10602391
|
C | A | 2 | a0001c0001t0003g0239a0001c0001t0013g0108 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.926-18960C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602391 | ||||||
| chr6:10602638
|
CAAATAGG others(5): Show |
C | 12 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.926-18708_926-1869 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10602638 | |||||
| chr6:10602762
|
G | C | 1 | a0001c0001t0001g0171 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.926-18589G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602762 | ||||||
| chr6:10602971
|
A | C | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.926-18380A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10602971 | ||||||
| chr6:10603424
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(27): Show | 30 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.926-17927A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603424 | ||||||
| chr6:10603504
|
A | G | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-17847A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603504 | ||||||
| chr6:10603545
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.926-17806T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603545 | ||||||
| chr6:10603690
|
A | AT | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-17657dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10603690 | |||||
| chr6:10603817
|
C | CT | 22 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(19): Show | 22 | HG00735.hp2 HG00741.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.926-17512dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | |||||
| chr6:10603817
|
CT | C | 42 | a0001c0001t0001g0070a0001c0001t0001g0089a0001c0001t0001g0124others(39): Show | 42 | HG00323.hp2 HG00558.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.926-17512delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | |||||
| chr6:10603817
|
CTTTTT | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(128): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.926-17516_926-1751 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | |||||
| chr6:10603887
|
GTTGT | G | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-17441_926-1743 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10603887 | |||||
| chr6:10603887
|
GTTGTTTG others(1): Show |
G | 5 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0105others(2): Show | 5 | HG01081.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.926-17445_926-1743 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10603887 | |||||
| chr6:10603964
|
T | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-17387T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603964 | ||||||
| chr6:10603985
|
G | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.926-17366G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603985 | ||||||
| chr6:10603989
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.926-17362C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603989 | ||||||
| chr6:10603990
|
G | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-17361G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603990 | ||||||
| chr6:10603997
|
A | G | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-17354A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603997 | ||||||
| chr6:10603998
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.926-17353C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603998 | ||||||
| chr6:10603999
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.926-17352G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603999 | ||||||
| chr6:10604052
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.926-17299C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604052 | ||||||
| chr6:10604098
|
T | C | 1 | a0001c0003t0001g0144 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.926-17253T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604098 | ||||||
| chr6:10604195
|
C | A | 1 | a0001c0001t0002g0277 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.926-17156C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604195 | ||||||
| chr6:10604263
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.926-17088T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604263 | ||||||
| chr6:10604364
|
A | G | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-16987A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604364 | ||||||
| chr6:10604387
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.926-16964A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604387 | ||||||
| chr6:10604438
|
T | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-16913T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604438 | ||||||
| chr6:10604574
|
C | T | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.926-16777C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604574 | ||||||
| chr6:10604873
|
G | A | 133 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.926-16478G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604873 | ||||||
| chr6:10604877
|
A | AAAAAG | 4 | a0001c0001t0001g0198a0001c0001t0008g0219a0001c0001t0014g0315others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-16473_926-1647 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10604877 | |||||
| chr6:10604877
|
A | AAAAG | 129 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.926-16473_926-1647 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10604877 | |||||
| chr6:10604877
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.926-16474A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604877 | ||||||
| chr6:10604879
|
G | A | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-16472G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10604879 | ||||||
| chr6:10605147
|
TAAAACAA | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0177 | 3 | NA18951.hp1 NA18973.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.926-16190_926-1618 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605147 | |||||
| chr6:10605169
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0318others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-16182G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605169 | ||||||
| chr6:10605208
|
A | AT | 29 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(26): Show | 29 | HG00408.hp1 HG00558.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.926-16118dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATT | 15 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0266others(12): Show | 15 | HG00735.hp2 HG01433.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.926-16119_926-1611 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATTT | 7 | a0001c0001t0001g0018a0001c0001t0001g0081a0001c0001t0001g0215others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.926-16120_926-1611 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATTTT | 10 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.926-16121_926-1611 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
A | ATTTTT | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0022others(9): Show | 12 | HG01361.hp2 HG01978.hp2 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.926-16122_926-1611 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
AT | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0130a0001c0001t0001g0150others(7): Show | 10 | HG02109.hp2 HG02135.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.926-16118delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
ATT | A | 31 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0077others(28): Show | 31 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.926-16119_926-1611 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
ATTT | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(88): Show | 91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.926-16120_926-1611 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605208
|
ATTTT | A | 9 | a0001c0001t0001g0072a0001c0001t0001g0101a0001c0001t0001g0119others(6): Show | 9 | HG02040.hp2 HG02735.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.926-16121_926-1611 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | |||||
| chr6:10605266
|
A | G | 1 | a0001c0001t0004g0035 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.926-16085A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605266 | ||||||
| chr6:10605365
|
C | T | 2 | a0001c0001t0008g0219a0001c0001t0023g0313 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.926-15986C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605365 | ||||||
| chr6:10605372
|
CT | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-15965delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10605372 | |||||
| chr6:10605438
|
G | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-15913G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605438 | ||||||
| chr6:10605518
|
T | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.926-15833T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605518 | ||||||
| chr6:10605573
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.926-15778C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605573 | ||||||
| chr6:10605653
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.926-15698G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605653 | ||||||
| chr6:10605764
|
G | C | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.926-15587G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605764 | ||||||
| chr6:10605931
|
C | G | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.926-15420C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605931 | ||||||
| chr6:10605946
|
C | T | 7 | a0001c0001t0002g0148a0001c0001t0002g0160a0001c0001t0002g0197others(4): Show | 7 | HG00408.hp1 HG02300.hp2 NA18992.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-15405C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605946 | ||||||
| chr6:10605988
|
C | G | 1 | a0001c0001t0005g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.926-15363C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605988 | ||||||
| chr6:10606043
|
G | A | 2 | a0001c0001t0003g0239a0001c0001t0013g0108 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.926-15308G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606043 | ||||||
| chr6:10606165
|
AT | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.926-15184delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606165 | |||||
| chr6:10606204
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.926-15147A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606204 | ||||||
| chr6:10606207
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.926-15144C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606207 | ||||||
| chr6:10606266
|
G | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-15085G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606266 | ||||||
| chr6:10606271
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0001g0202a0001c0001t0001g0211 | 3 | HG01346.hp1 HG01952.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.926-15080C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606271 | ||||||
| chr6:10606351
|
T | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-15000T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606351 | ||||||
| chr6:10606378
|
G | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-14973G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606378 | ||||||
| chr6:10606432
|
A | G | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-14919A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606432 | ||||||
| chr6:10606485
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.926-14866G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606485 | ||||||
| chr6:10606487
|
CACA | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(26): Show | 29 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.926-14859_926-1485 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606487 | |||||
| chr6:10606591
|
A | C | 1 | a0001c0001t0008g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.926-14760A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606591 | ||||||
| chr6:10606603
|
C | CTTCCATT others(19): Show |
14 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0019others(11): Show | 14 | HG00621.hp2 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.926-14701_926-1467 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(45): Show |
52 | a0001c0001t0001g0009a0001c0001t0001g0037a0001c0001t0001g0059others(49): Show | 52 | HG00738.hp1 HG01071.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.926-14727_926-1467 others(56): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(71): Show |
54 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0028others(51): Show | 54 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.926-14676_926-1467 others(82): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(97): Show |
46 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0015others(43): Show | 46 | HG00323.hp2 HG00558.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.926-14676_926-1467 others(108): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(123): Show |
7 | a0001c0001t0002g0134a0001c0001t0002g0277a0001c0001t0002g0291others(4): Show | 7 | HG02135.hp2 HG03239.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.926-14676_926-1467 others(134): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(149): Show |
4 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0073others(1): Show | 4 | HG02818.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-14676_926-1467 others(160): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(175): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0226others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.926-14676_926-1467 others(186): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(201): Show |
1 | a0001c0001t0021g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.926-14676_926-1467 others(212): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(227): Show |
2 | a0001c0001t0004g0020a0001c0001t0004g0253 | 2 | HG02647.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.926-14676_926-1467 others(238): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(331): Show |
1 | a0001c0001t0004g0316 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.926-14676_926-1467 others(342): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
C | CTTCCATT others(357): Show |
1 | a0001c0001t0004g0314 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.926-14676_926-1467 others(368): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606603
|
CTTCCATT others(19): Show |
C | 9 | a0001c0001t0001g0085a0001c0001t0001g0125a0001c0001t0001g0162others(6): Show | 9 | HG00140.hp1 HG00639.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.926-14701_926-1467 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | |||||
| chr6:10606614
|
G | GAAATTTA others(45): Show |
1 | a0001c0001t0001g0309 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.926-14686_926-1468 others(56): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606614 | |||||
| chr6:10606742
|
T | TAAAG | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(33): Show | 36 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.926-14606_926-1460 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10606742 | |||||
| chr6:10606778
|
C | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0279 | 2 | HG01256.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.926-14573C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606778 | ||||||
| chr6:10606897
|
C | G | 131 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(128): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.926-14454C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606897 | ||||||
| chr6:10606929
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-14422A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606929 | ||||||
| chr6:10607121
|
TA | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0105a0001c0001t0001g0117 | 3 | HG02055.hp2 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.926-14229delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607121 | ||||||
| chr6:10607136
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-14215C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607136 | ||||||
| chr6:10607216
|
G | C | 8 | a0001c0001t0001g0061a0001c0001t0001g0101a0001c0001t0001g0119others(5): Show | 8 | HG01346.hp1 HG01952.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-14135G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607216 | ||||||
| chr6:10607262
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-14089A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607262 | ||||||
| chr6:10607328
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-14023A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607328 | ||||||
| chr6:10607434
|
C | T | 2 | a0001c0001t0009g0006a0001c0001t0009g0033 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.926-13917C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607434 | ||||||
| chr6:10607435
|
G | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-13916G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607435 | ||||||
| chr6:10607541
|
C | T | 2 | a0001c0001t0007g0243a0001c0001t0007g0244 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.926-13810C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607541 | ||||||
| chr6:10607683
|
CCTAACTT others(17): Show |
C | 15 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0116others(12): Show | 15 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.926-13665_926-1364 others(28): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10607683 | |||||
| chr6:10607688
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.926-13663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607688 | ||||||
| chr6:10607699
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-13652T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607699 | ||||||
| chr6:10607848
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.926-13503T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607848 | ||||||
| chr6:10607860
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-13491A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607860 | ||||||
| chr6:10607866
|
G | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-13485G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607866 | ||||||
| chr6:10607897
|
G | A | 2 | a0001c0001t0008g0219a0001c0001t0023g0313 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.926-13454G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607897 | ||||||
| chr6:10607908
|
A | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-13443A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607908 | ||||||
| chr6:10607909
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(32): Show | 35 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.926-13442G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10607909 | ||||||
| chr6:10608014
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.926-13337T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10608014 | ||||||
| chr6:10608073
|
C | CT | 22 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0081others(19): Show | 22 | HG01109.hp1 HG01175.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.926-13257dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10608073 | |||||
| chr6:10608073
|
CT | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(12): Show | 15 | HG00735.hp2 HG01169.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.926-13257delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10608073 | |||||
| chr6:10608227
|
G | A | 2 | a0001c0001t0008g0219a0001c0001t0023g0313 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.926-13124G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10608227 | ||||||
| chr6:10608239
|
G | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-13112G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10608239 | ||||||
| chr6:10608359
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-12992T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10608359 | ||||||
| chr6:10608645
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.926-12706G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10608645 | ||||||
| chr6:10608710
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.926-12641A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10608710 | ||||||
| chr6:10609077
|
A | T | 1 | a0001c0001t0001g0060 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.926-12274A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609077 | ||||||
| chr6:10609206
|
G | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-12145G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609206 | ||||||
| chr6:10609212
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-12139C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609212 | ||||||
| chr6:10609277
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-12074A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609277 | ||||||
| chr6:10609292
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0081a0001c0001t0004g0035others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.926-12059A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609292 | ||||||
| chr6:10609356
|
T | G | 12 | a0001c0001t0001g0074a0001c0001t0001g0131a0001c0001t0001g0132others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.926-11995T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609356 | ||||||
| chr6:10609376
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-11975T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609376 | ||||||
| chr6:10609585
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.926-11766G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609585 | ||||||
| chr6:10609617
|
G | A | 135 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(132): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.926-11734G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609617 | ||||||
| chr6:10609780
|
A | AG | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-11567dupG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10609780 | |||||
| chr6:10609786
|
A | G | 2 | a0001c0001t0008g0219a0001c0001t0023g0313 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.926-11565A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609786 | ||||||
| chr6:10609856
|
C | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.926-11495C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609856 | ||||||
| chr6:10609877
|
C | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.926-11474C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609877 | ||||||
| chr6:10609896
|
TTTG | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.926-11451_926-1144 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10609896 | |||||
| chr6:10609904
|
A | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.926-11447A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609904 | ||||||
| chr6:10609907
|
G | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.926-11444G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609907 | ||||||
| chr6:10610078
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(33): Show | 36 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.926-11273G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610078 | ||||||
| chr6:10610161
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.926-11190A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610161 | ||||||
| chr6:10610319
|
C | T | 9 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0222others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-11032C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610319 | ||||||
| chr6:10610688
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.926-10663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610688 | ||||||
| chr6:10610773
|
T | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(33): Show | 36 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.926-10578T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610773 | ||||||
| chr6:10610812
|
T | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.926-10539T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610812 | ||||||
| chr6:10610854
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.926-10497G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610854 | ||||||
| chr6:10610862
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.926-10489G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10610862 | ||||||
| chr6:10611148
|
G | A | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.926-10203G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611148 | ||||||
| chr6:10611174
|
C | T | 6 | a0001c0001t0001g0045a0001c0001t0001g0070a0001c0001t0001g0141others(3): Show | 6 | HG01175.hp1 HG01361.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.926-10177C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611174 | ||||||
| chr6:10611191
|
G | T | 1 | a0001c0001t0001g0210 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.926-10160G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611191 | ||||||
| chr6:10611259
|
CACTTGAA others(16): Show |
C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.926-10090_926-1006 others(27): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10611259 | |||||
| chr6:10611284
|
T | A | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(180): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.926-10067T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611284 | ||||||
| chr6:10611334
|
C | CT | 131 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(128): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.926-10002dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10611334 | |||||
| chr6:10611334
|
CTT | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(32): Show | 35 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.926-10003_926-1000 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10611334 | |||||
| chr6:10611413
|
C | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.926-9938C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611413 | ||||||
| chr6:10611487
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0317others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-9864C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611487 | ||||||
| chr6:10611565
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0002g0090 | 2 | HG00558.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.926-9786G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611565 | ||||||
| chr6:10611575
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.926-9776C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611575 | ||||||
| chr6:10611576
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.926-9775G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611576 | ||||||
| chr6:10611624
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.926-9727C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611624 | ||||||
| chr6:10611722
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.926-9629T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611722 | ||||||
| chr6:10611728
|
AT | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(33): Show | 36 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.926-9615delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10611728 | |||||
| chr6:10611979
|
T | G | 3 | a0001c0001t0002g0047a0001c0001t0002g0151a0001c0001t0002g0303 | 3 | NA18977.hp1 NA18989.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.926-9372T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611979 | ||||||
| chr6:10612025
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.926-9326T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10612025 | ||||||
| chr6:10612203
|
T | G | 1 | a0001c0001t0003g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.926-9148T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10612203 | ||||||
| chr6:10612209
|
A | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0284 | 2 | NA18945.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.926-9142A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10612209 | ||||||
| chr6:10612217
|
C | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(33): Show | 36 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.926-9134C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10612217 | ||||||
| chr6:10612241
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.926-9110C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10612241 | ||||||
| chr6:10612384
|
C | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0084others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.926-8967C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10612384 | ||||||
| chr6:10612453
|
A | G | 1 | a0001c0001t0008g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.926-8898A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10612453 | ||||||
| chr6:10613128
|
A | G | 1 | a0001c0001t0006g0286 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.926-8223A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613128 | ||||||
| chr6:10613207
|
G | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(33): Show | 36 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.926-8144G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613207 | ||||||
| chr6:10613214
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(33): Show | 36 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.926-8137G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613214 | ||||||
| chr6:10613224
|
C | T | 81 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(78): Show | 81 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.926-8127C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613224 | ||||||
| chr6:10613358
|
G | A | 5 | a0001c0001t0002g0042a0001c0001t0002g0161a0001c0001t0002g0264others(2): Show | 5 | HG01928.hp2 HG01993.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-7993G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613358 | ||||||
| chr6:10613378
|
C | CT | 35 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0017others(32): Show | 35 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.926-7963dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10613378 | |||||
| chr6:10613397
|
C | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0082others(3): Show | 6 | HG01192.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.926-7954C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613397 | ||||||
| chr6:10613572
|
G | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(48): Show | 51 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.926-7779G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613572 | ||||||
| chr6:10613885
|
C | T | 5 | a0001c0001t0002g0042a0001c0001t0002g0161a0001c0001t0002g0264others(2): Show | 5 | HG01928.hp2 HG01993.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-7466C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613885 | ||||||
| chr6:10613950
|
T | G | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.926-7401T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10613950 | ||||||
| chr6:10614240
|
T | C | 1 | a0001c0001t0023g0313 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.926-7111T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614240 | ||||||
| chr6:10614246
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.926-7105C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614246 | ||||||
| chr6:10614261
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.926-7090T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614261 | ||||||
| chr6:10614476
|
T | A | 1 | a0001c0001t0002g0197 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.926-6875T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614476 | ||||||
| chr6:10614486
|
G | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0081others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.926-6865G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614486 | ||||||
| chr6:10614625
|
C | CA | 13 | a0001c0001t0001g0009a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | HG00323.hp2 HG00408.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.926-6706dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | |||||
| chr6:10614625
|
CA | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0024others(17): Show | 20 | HG02055.hp1 HG02109.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.926-6706delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | |||||
| chr6:10614625
|
CAAA | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.926-6708_926-6706d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | |||||
| chr6:10614642
|
A | AG | 4 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0317others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-6709_926-6708i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614642 | ||||||
| chr6:10614642
|
A | G | 1 | a0001c0001t0011g0002 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.926-6709A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614642 | ||||||
| chr6:10614644
|
A | AAAAAAG | 10 | a0001c0001t0001g0081a0001c0001t0001g0266a0001c0001t0003g0239others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.926-6706_926-6705i others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10614644 | |||||
| chr6:10614644
|
A | AAG | 10 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(7): Show | 10 | HG01891.hp2 HG01978.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.926-6703_926-6702d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10614644 | |||||
| chr6:10614644
|
A | AG | 18 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0022others(15): Show | 18 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.926-6707_926-6706i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614644 | ||||||
| chr6:10614644
|
A | G | 134 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0023others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-6707A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614644 | ||||||
| chr6:10614691
|
GTAGAGAT others(3): Show |
G | 2 | a0001c0001t0001g0125a0001c0001t0001g0287 | 2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.926-6657_926-6648d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10614691 | |||||
| chr6:10614845
|
G | T | 249 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(246): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.926-6506G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614845 | ||||||
| chr6:10614846
|
C | T | 1 | a0001c0001t0005g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.926-6505C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614846 | ||||||
| chr6:10614869
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.926-6482G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10614869 | ||||||
| chr6:10615035
|
C | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0027others(128): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.926-6316C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615035 | ||||||
| chr6:10615472
|
A | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.926-5879A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615472 | ||||||
| chr6:10615644
|
T | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(43): Show | 46 | HG00735.hp2 HG01175.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.926-5707T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615644 | ||||||
| chr6:10615697
|
CCACTCCA others(9): Show |
C | 35 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(32): Show | 35 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.926-5651_926-5636d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10615697 | |||||
| chr6:10615705
|
TAGAC | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0024others(5): Show | 8 | HG02109.hp1 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-5642_926-5639d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10615705 | |||||
| chr6:10615876
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(32): Show | 35 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.926-5475G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615876 | ||||||
| chr6:10615904
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.926-5447G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615904 | ||||||
| chr6:10615921
|
C | G | 1 | a0001c0001t0023g0313 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.926-5430C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615921 | ||||||
| chr6:10615983
|
A | G | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.926-5368A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615983 | ||||||
| chr6:10615999
|
G | T | 1 | a0001c0001t0011g0002 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.926-5352G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615999 | ||||||
| chr6:10616073
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.926-5278G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616073 | ||||||
| chr6:10616118
|
T | C | 12 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0140others(9): Show | 12 | HG01071.hp1 HG01258.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.926-5233T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616118 | ||||||
| chr6:10616183
|
C | CGTTATAT others(95): Show |
1 | a0001c0001t0001g0045 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.926-5087_926-5086i others(104): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10616183 | |||||
| chr6:10616183
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.926-5168C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616183 | ||||||
| chr6:10616265
|
T | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(34): Show | 37 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.926-5086T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616265 | ||||||
| chr6:10616277
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.926-5074G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616277 | ||||||
| chr6:10616583
|
G | C | 7 | a0001c0001t0004g0020a0001c0001t0004g0253a0001c0001t0004g0314others(4): Show | 7 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.926-4768G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616583 | ||||||
| chr6:10616598
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.926-4753C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616598 | ||||||
| chr6:10616744
|
A | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0081others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.926-4607A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10616744 | ||||||
| chr6:10617001
|
TG | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.926-4348delG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617001 | |||||
| chr6:10617020
|
G | A | 2 | a0001c0001t0003g0239a0001c0001t0013g0108 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.926-4331G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617020 | ||||||
| chr6:10617077
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.926-4274C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617077 | ||||||
| chr6:10617281
|
C | T | 2 | a0001c0001t0001g0165a0001c0003t0001g0144 | 2 | NA19082.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.926-4070C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617281 | ||||||
| chr6:10617285
|
C | T | 1 | a0001c0001t0008g0322 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.926-4066C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617285 | ||||||
| chr6:10617377
|
T | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.926-3974T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617377 | ||||||
| chr6:10617387
|
C | T | 1 | a0001c0001t0001g0088 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.926-3964C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617387 | ||||||
| chr6:10617411
|
C | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0055others(10): Show | 13 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.926-3940C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617411 | ||||||
| chr6:10617438
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.926-3913C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617438 | ||||||
| chr6:10617449
|
C | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.926-3902C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617449 | ||||||
| chr6:10617518
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.926-3833G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617518 | ||||||
| chr6:10617530
|
G | T | 2 | a0001c0001t0001g0317a0001c0001t0011g0002 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.926-3821G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617530 | ||||||
| chr6:10617640
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.926-3711C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617640 | ||||||
| chr6:10617743
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0004g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.926-3605_926-3604i others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617743 | |||||
| chr6:10617743
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0021g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.926-3605_926-3604i others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617743 | |||||
| chr6:10617747
|
C | T | 5 | a0001c0001t0004g0020a0001c0001t0004g0253a0001c0001t0004g0314others(2): Show | 5 | HG02647.hp1 HG02738.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.926-3604C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617747 | ||||||
| chr6:10617747
|
CTTCTTTT others(2): Show |
C | 25 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0017others(22): Show | 25 | HG01175.hp1 HG01361.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.926-3601_926-3593d others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617747 | |||||
| chr6:10617750
|
C | CT | 6 | a0001c0001t0001g0023a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.926-3579dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0074a0001c0001t0001g0081others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.926-3586_926-3579d others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(3): Show |
20 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0024others(17): Show | 20 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.926-3588_926-3579d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0021a0001c0001t0015g0076 | 2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.926-3589_926-3579d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0066 | 3 | HG02486.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.926-3590_926-3579d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0005g0213a0001c0001t0027g0003 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.926-3591_926-3579d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0009g0033a0001c0001t0025g0217 | 2 | HG01496.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.926-3592_926-3579d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0266a0001c0001t0009g0006 | 2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.926-3593_926-3579d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0003g0239a0001c0001t0013g0108 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.926-3594_926-3579d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0073others(9): Show | 12 | HG00735.hp2 HG02572.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.926-3601C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617750 | ||||||
| chr6:10617750
|
CT | C | 16 | a0001c0001t0001g0089a0001c0001t0001g0124a0001c0001t0001g0163others(13): Show | 16 | HG00323.hp2 HG00558.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.926-3579delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
CTT | C | 19 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0001t0001g0079others(16): Show | 19 | HG00140.hp2 HG01928.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.926-3580_926-3579d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617750
|
CTTT | C | 108 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(105): Show | 108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.926-3581_926-3579d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | |||||
| chr6:10617751
|
T | C | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.926-3600T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617751 | ||||||
| chr6:10617756
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.926-3595T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617756 | ||||||
| chr6:10617775
|
C | G | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.926-3576C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617775 | ||||||
| chr6:10617807
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.926-3544T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617807 | ||||||
| chr6:10617864
|
T | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.926-3487T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617864 | ||||||
| chr6:10617916
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.926-3435G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617916 | ||||||
| chr6:10617930
|
T | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0226a0001c0001t0001g0320 | 3 | HG01884.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.926-3421T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617930 | ||||||
| chr6:10617993
|
G | A | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.926-3358G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617993 | ||||||
| chr6:10618060
|
C | A | 2 | a0001c0001t0002g0160a0001c0001t0002g0223 | 2 | NA18992.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.926-3291C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10618060 | ||||||
| chr6:10618217
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0318others(2): Show | 5 | HG02486.hp2 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-3134C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10618217 | ||||||
| chr6:10618281
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.926-3070G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10618281 | ||||||
| chr6:10618449
|
G | C | 2 | a0001c0001t0008g0219a0001c0001t0023g0313 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.926-2902G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10618449 | ||||||
| chr6:10618630
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.926-2721G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10618630 | ||||||
| chr6:10618753
|
C | CT | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.926-2595dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10618753 | |||||
| chr6:10618775
|
A | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(26): Show | 29 | HG01175.hp1 HG01361.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.926-2576A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10618775 | ||||||
| chr6:10618835
|
T | TCTTGAAT others(1): Show |
37 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(34): Show | 37 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.926-2504_926-2497d others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10618835 | |||||
| chr6:10618953
|
G | C | 2 | a0001c0001t0001g0266a0001c0001t0005g0213 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.926-2398G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10618953 | ||||||
| chr6:10619010
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.926-2341C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619010 | ||||||
| chr6:10619030
|
A | G | 37 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(34): Show | 37 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.926-2321A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619030 | ||||||
| chr6:10619506
|
A | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.926-1845A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619506 | ||||||
| chr6:10619521
|
T | A | 1 | a0001c0001t0001g0021 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.926-1830T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619521 | ||||||
| chr6:10619606
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0073 | 3 | HG02818.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.926-1745G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619606 | ||||||
| chr6:10619684
|
G | A | 1 | a0001c0001t0005g0026 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.926-1667G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619684 | ||||||
| chr6:10619704
|
T | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(35): Show | 38 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.926-1647T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619704 | ||||||
| chr6:10619984
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0015others(28): Show | 31 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.926-1367T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10619984 | ||||||
| chr6:10620407
|
A | ATT | 28 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(25): Show | 28 | HG01109.hp1 HG01175.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.926-933_926-932dup others(2): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | 10620407 | |||||
| chr6:10620428
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.926-923A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620428 | ||||||
| chr6:10620445
|
A | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(26): Show | 29 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.926-906A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620445 | ||||||
| chr6:10620527
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-824C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620527 | ||||||
| chr6:10620583
|
T | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(23): Show | 26 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.926-768T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620583 | ||||||
| chr6:10620613
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0302a0001c0001t0020g0152 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.926-738C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620613 | ||||||
| chr6:10620744
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.926-607C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620744 | ||||||
| chr6:10620921
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.926-430A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620921 | ||||||
| chr6:10620940
|
A | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(22): Show | 25 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.926-411A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620940 | ||||||
| chr6:10620993
|
C | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.926-358C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10620993 | ||||||
| chr6:10621109
|
A | G | 3 | a0001c0001t0005g0213a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.926-242A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10621109 | ||||||
| chr6:10621158
|
A | G | 3 | a0001c0001t0005g0213a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.926-193A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10621158 | ||||||
| chr6:10621313
|
A | T | 4 | a0001c0001t0004g0020a0001c0001t0004g0314a0001c0001t0004g0316others(1): Show | 4 | HG02647.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-38A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10621313 | ||||||
| chr6:10621314
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.926-37C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10621314 | ||||||
| chr6:10621337
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.926-14T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10621337 | ||||||
| chr6:10621458
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1018+15C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10621458 | ||||||
| chr6:10621597
|
C | T | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1018+154C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10621597 | ||||||
| chr6:10621634
|
T | C | 49 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 49 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.1018+191T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10621634 | ||||||
| chr6:10621681
|
C | T | 3 | a0001c0001t0001g0265a0001c0001t0001g0302a0001c0001t0020g0152 | 3 | HG02738.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1018+238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10621681 | ||||||
| chr6:10621695
|
T | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00735.hp2 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1018+252T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10621695 | ||||||
| chr6:10621731
|
A | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(22): Show | 25 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1018+288A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10621731 | ||||||
| chr6:10621951
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1018+508G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10621951 | ||||||
| chr6:10622095
|
A | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(22): Show | 25 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1018+652A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622095 | ||||||
| chr6:10622171
|
T | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(22): Show | 25 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1018+728T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622171 | ||||||
| chr6:10622231
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1018+788A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622231 | ||||||
| chr6:10622308
|
T | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(22): Show | 25 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1018+865T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622308 | ||||||
| chr6:10622494
|
T | C | 25 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(22): Show | 25 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1018+1051T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622494 | ||||||
| chr6:10622579
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1018+1136A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622579 | ||||||
| chr6:10622742
|
C | CT | 12 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG01496.hp1 HG01934.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018+1327dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CT | C | 127 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0031others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1018+1327delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTT | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(4): Show | 7 | HG01243.hp1 HG02622.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1018+1326_1018+132 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTTTTTTT | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0022others(18): Show | 21 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.1018+1321_1018+132 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0001g0147a0001c0001t0004g0020a0001c0001t0004g0253others(5): Show | 8 | HG02572.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1018+1318_1018+132 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622742
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0299others(1): Show | 4 | HG01361.hp1 HG02257.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018+1317_1018+132 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | |||||
| chr6:10622812
|
C | T | 16 | a0001c0001t0001g0061a0001c0001t0001g0099a0001c0001t0001g0101others(13): Show | 16 | HG00597.hp1 HG01346.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1018+1369C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622812 | ||||||
| chr6:10622813
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1018+1370G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622813 | ||||||
| chr6:10622913
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1018+1470C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10622913 | ||||||
| chr6:10623184
|
A | G | 1 | a0001c0001t0003g0229 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1018+1741A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623184 | ||||||
| chr6:10623238
|
A | ATTTAC | 176 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0013others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1018+1799_1018+180 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10623238 | |||||
| chr6:10623258
|
C | T | 12 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0140others(9): Show | 12 | HG01071.hp1 HG01258.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018+1815C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623258 | ||||||
| chr6:10623292
|
AT | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(25): Show | 28 | HG00735.hp2 HG01175.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1018+1864delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10623292 | |||||
| chr6:10623295
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1018+1852T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623295 | ||||||
| chr6:10623333
|
C | G | 1 | a0001c0001t0002g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1018+1890C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623333 | ||||||
| chr6:10623361
|
G | C | 1 | a0001c0001t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1018+1918G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623361 | ||||||
| chr6:10623385
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0305 | 2 | HG00621.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1018+1942G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623385 | ||||||
| chr6:10623535
|
C | G | 3 | a0001c0001t0005g0213a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1018+2092C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623535 | ||||||
| chr6:10623539
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0002g0090 | 2 | HG00558.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1018+2096G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623539 | ||||||
| chr6:10623838
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(21): Show | 24 | HG01175.hp1 HG01361.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1018+2395A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10623838 | ||||||
| chr6:10624019
|
C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0018others(22): Show | 25 | HG00735.hp2 HG01175.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1019-2398C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10624019 | ||||||
| chr6:10624253
|
C | G | 9 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0299others(6): Show | 9 | HG01361.hp1 HG02257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1019-2164C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10624253 | ||||||
| chr6:10624281
|
T | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0031others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1019-2136T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10624281 | ||||||
| chr6:10625029
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1019-1388G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625029 | ||||||
| chr6:10625030
|
C | A | 3 | a0001c0001t0005g0213a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1019-1387C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625030 | ||||||
| chr6:10625063
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG01361.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1019-1354G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625063 | ||||||
| chr6:10625141
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0214 | 2 | NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1019-1276C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625141 | ||||||
| chr6:10625225
|
T | C | 3 | a0001c0001t0005g0213a0001c0001t0010g0240a0001c0001t0010g0242 | 3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1019-1192T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625225 | ||||||
| chr6:10625518
|
TA | T | 29 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0045others(26): Show | 29 | HG00738.hp2 HG01099.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1019-885delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 10625518 | |||||
| chr6:10625567
|
T | G | 1 | a0001c0001t0014g0315 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1019-850T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625567 | ||||||
| chr6:10625653
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1019-764C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625653 | ||||||
| chr6:10625722
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1019-695T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625722 | ||||||
| chr6:10625861
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0299 | 3 | HG01361.hp1 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1019-556G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625861 | ||||||
| chr6:10625917
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0275a0001c0001t0001g0282 | 3 | NA18993.hp2 NA19011.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1019-500A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625917 | ||||||
| chr6:10625938
|
C | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(10): Show | 13 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1019-479C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625938 | ||||||
| chr6:10625989
|
T | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0074a0001c0001t0001g0105others(1): Show | 4 | HG02451.hp1 HG03041.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-428T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10625989 | ||||||
| chr6:10626014
|
C | T | 8 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0222others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1019-403C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10626014 | ||||||
| chr6:10626069
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1019-348G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10626069 | ||||||
| chr6:10626139
|
T | C | 1 | a0001c0001t0027g0003 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1019-278T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10626139 | ||||||
| chr6:10626179
|
C | T | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(15): Show | 18 | HG01891.hp1 HG02572.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.1019-238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10626179 | ||||||
| chr6:10626331
|
G | A | 3 | a0001c0001t0008g0219a0001c0001t0008g0322a0001c0001t0023g0313 | 3 | HG02572.hp2 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1019-86G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10626331 | ||||||
| chr6:10626382
|
T | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0261 | 2 | NA18949.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1019-35T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10626382 |