Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MMGSW others(397): Show |
chr6 | 10516351 | 10634368 |
| a0002 | 0/0 | 89 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | MPNAS others(84): Show |
chr6 | 10516351 | 10634368 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1206 | 323 | 86 | 59 | 132 | 8 | 36 | GCNT2_chr6_10516351_10634368 | GCNT2 | ATGAT others(1201): Show |
chr6 | 10516351 | 10634368 | ||
| a0002c0002 | 0/0 | 281 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | GTGTT others(276): Show |
chr6 | 10516351 | 10634368 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4505 | 253 | 63 | 49 | 105 | 7 | 27 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0002 | 0/0 | 4505 | 41 | 1 | 6 | 26 | 1 | 7 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0003 | 0/0 | 4509 | 7 | 6 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4504): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0004 | 0/0 | 4509 | 5 | 3 | 2 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4504): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0005 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4504): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0006 | 0/0 | 4505 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0007 | 0/0 | 4505 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0008 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4504): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0009 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4504): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0010 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0011 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4504): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0012 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0013 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0014 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0015 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0016 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0001c0001t0017 | 0/0 | 4505 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | AAACA others(4500): Show |
chr6 | 10516351 | 10634368 |
| a0002c0002t0018 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | GTGTT others(3040): Show |
chr6 | 10516351 | 10634368 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0100 | 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 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 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 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0254 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0302 | 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 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0011g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0012g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0014g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0015g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0001c0001t0017g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| a0002c0002t0018g0322 | 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 | g0234 | EUR | GBR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | GBR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0320 | EUR | FIN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0063 | EUR | FIN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0260 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CDX | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02293 | hp2 | a0002 | c0002 | t0018 | g0322 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0164 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0182 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0165 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02738 | hp2 | a0001 | c0001 | t0017 | g0023 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0253 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0155 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0304 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0149 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | STU | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19005 | hp2 | a0001 | c0001 | t0015 | g0276 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0277 | AFR | YRI | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ASW | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | ASW | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0215 | REF | REF | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0254 | REF | REF | GCNT2_chr6_10516351_10634368 | GCNT2 | chr6 | 10516351 | 10634368 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10529562 | C | T | 1 | a0001c0001 | 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 | a0001c0001 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10527516 | C | T | 1 | a0001c0001t0002 | 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 | a0001c0001t0013 | 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 | a0001c0001t0001 | 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 | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(2): 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 | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(2): 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 | a0001c0001t0001 a0001c0001t0007 |
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 | 1 | a0001c0001t0008 | 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 | a0001c0001t0009 | 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 | a0001c0001t0003 a0001c0001t0017 |
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 | a0001c0001t0016 | 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 | a0001c0001t0005 | 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 | a0001c0001t0006 | 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 | a0001c0001t0010 | 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 | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(1): 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 | a0001c0001t0003 a0001c0001t0011 |
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 | a0001c0001t0012 | 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 | 1 | a0001c0001t0004 | 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 | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(3): 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 | a0001c0001t0015 | 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 | 1 | a0001c0001t0002 | 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 | 1 | a0001c0001t0007 | 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 | a0001c0001t0014 | 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 | 2 | a0001c0001t0003 a0001c0001t0008 |
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 | a0001c0001t0011 | 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 | a0001c0001t0009 | 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 | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(1): 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 | a0001c0001t0013 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 5/5 | 2726 | chr6 | 10629333 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10521465 | C | T | 1 | a0001c0001t0001g0025 | 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 | a0001c0001t0005g0181 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0179 others(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 | a0001c0001t0001g0214 a0001c0001t0003g0303 a0001c0001t0003g0319 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0169 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0205 a0001c0001t0001g0256 a0001c0001t0013g0155 |
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 | 18 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(15): 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 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(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 | a0001c0001t0004g0002 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0272 | 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 | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0160 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | 23 | a0001c0001t0001g0008 a0001c0001t0001g0120 a0001c0001t0001g0121 others(20): 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 | a0001c0001t0013g0155 | 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 | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): 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 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | 194 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(191): 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 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0083 others(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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0037 others(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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0005g0181 | 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 | a0001c0001t0013g0155 | 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 | 2 | a0001c0001t0001g0001 a0001c0001t0006g0166 |
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 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0001g0248 |
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 | a0001c0001t0005g0181 | 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0001g0307 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | a0001c0001t0005g0181 | 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 | a0001c0001t0005g0181 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0068 a0001c0001t0001g0071 others(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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0135 a0001c0001t0002g0010 |
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 | a0001c0001t0001g0195 | 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 | 21 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(18): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0008g0149 |
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 | 21 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(18): 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 | a0001c0001t0011g0304 | 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 | a0001c0001t0004g0146 | 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 | a0001c0001t0002g0236 | 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 | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0110 | 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 | a0001c0001t0001g0078 | 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 | 3 | a0001c0001t0001g0001 a0001c0001t0003g0167 a0001c0001t0006g0166 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0160 others(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 | 2 | a0001c0001t0001g0001 a0001c0001t0006g0166 |
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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0001t0008g0198 |
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 | a0001c0001t0001g0169 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0282 | 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 |
17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0148 a0001c0001t0001g0179 others(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 | 20 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): 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 | 17 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): 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 | 167 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(164): 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 | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): 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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0169 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0075 |
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 | a0001c0001t0002g0033 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0229 |
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 | a0001c0001t0002g0050 | 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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0308 a0001c0001t0001g0310 |
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 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0309 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | 22 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(19): 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0053 a0001c0001t0003g0080 |
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 | a0001c0001t0003g0150 | 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 | a0001c0001t0003g0303 | 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 | 22 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(19): 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 | a0001c0001t0008g0149 | 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 | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0194 a0001c0001t0002g0192 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0041 others(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 | 21 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(18): 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 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0014g0164 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0005g0181 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | 5 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0175 others(2): 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 | 32 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0001g0171 others(29): 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 | a0001c0001t0001g0064 a0001c0001t0001g0115 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | 22 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(19): 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 | a0001c0001t0006g0166 | 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 | a0001c0001t0001g0074 a0001c0001t0001g0099 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): 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 | a0001c0001t0005g0181 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): 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 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0199 others(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 | 14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0163 others(11): 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0320 | 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 | a0001c0001t0003g0319 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0186 others(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 | 3 | a0001c0001t0001g0184 a0001c0001t0004g0002 a0001c0001t0008g0198 |
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 | a0001c0001t0002g0010 | 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 | a0001c0001t0007g0011 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0123 a0001c0001t0001g0124 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0129 a0001c0001t0001g0130 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0140 a0001c0001t0002g0139 a0001c0001t0004g0141 |
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 | a0001c0001t0002g0142 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0151 others(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 | 164 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(161): 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 | 164 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(161): 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 | 19 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(16): 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 | a0001c0001t0001g0058 a0001c0001t0001g0085 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0006 | 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 | 161 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(158): 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 | a0001c0001t0001g0134 | 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 | 8 | a0001c0001t0001g0199 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG00438.hp2 HG00558.hp2 HG01071.hp2 others(5): 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 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0003g0150 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0169 a0001c0001t0006g0170 |
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 | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): 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 | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): 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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0003g0150 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0015 | 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0306 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0169 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0214 others(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 | a0001c0001t0002g0213 | 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 | 3 | a0001c0001t0001g0147 a0001c0001t0001g0197 a0001c0001t0004g0002 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0321 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | a0001c0001t0003g0303 a0001c0001t0003g0319 |
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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0301 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0180 |
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 | a0001c0001t0002g0213 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
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 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0231 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0148 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0003g0150 others(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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0140 a0001c0001t0004g0141 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0184 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(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 | 10 | a0001c0001t0001g0197 a0001c0001t0001g0244 a0001c0001t0001g0245 others(7): 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | 21 | a0001c0001t0001g0169 a0001c0001t0001g0183 a0001c0001t0001g0184 others(18): 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 | a0001c0001t0001g0184 a0001c0001t0001g0190 a0001c0001t0001g0191 others(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 | 194 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(191): 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 | a0001c0001t0008g0149 | 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 | a0001c0001t0001g0133 | 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 | 29 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0031 others(26): Show |
29 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(26): 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 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0049 others(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 | 21 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0001c0001t0001g0172 others(18): 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0147 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0001g0082 others(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 | a0001c0001t0005g0269 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0278 a0001c0001t0001g0279 others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0107 a0001c0001t0001g0144 others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0016g0165 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0004g0146 | 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 | a0001c0001t0006g0170 | 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0112 a0001c0001t0003g0167 |
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 | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(107): 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 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0169 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0175 | 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 | 169 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(166): 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 | a0001c0001t0005g0181 | 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 | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(186): 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 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0004g0141 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0151 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0125 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0179 a0001c0001t0001g0184 others(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 | 16 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0183 others(13): 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 | 23 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0183 others(20): 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 | a0001c0001t0001g0022 a0001c0001t0001g0130 a0001c0001t0001g0131 others(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 | a0001c0001t0001g0169 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0147 a0001c0001t0001g0169 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0012g0277 | 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 | a0001c0001t0001g0144 | 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 | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(158): 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0002g0048 | 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 | a0001c0001t0004g0280 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0016g0165 | 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 | a0001c0001t0001g0312 | 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 | 65 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(62): Show |
65 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(62): 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0312 | 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 | 150 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
319 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.925+11046G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10540882 | |||||||
| chr6:10540980 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): 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 | a0001c0001t0001g0147 a0001c0001t0003g0167 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | 12 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0148 others(9): 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 | a0001c0001t0004g0280 | 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 | a0001c0001t0006g0170 | 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 | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0226 a0001c0001t0001g0312 |
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 | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): 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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0053 a0001c0001t0003g0080 |
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 | a0001c0001t0001g0098 | 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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(36): 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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(36): 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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0053 a0001c0001t0003g0080 |
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 | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): 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 | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0316 | 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 | a0001c0001t0006g0170 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0312 |
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 | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): 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 | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): 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 | a0001c0001t0001g0126 a0001c0001t0001g0226 a0001c0001t0001g0312 |
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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0178 a0001c0001t0001g0308 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | 31 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(28): 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 | 30 | a0001c0001t0001g0081 a0001c0001t0001g0148 a0001c0001t0001g0157 others(27): 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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0179 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0227 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0209 a0001c0001t0001g0291 a0001c0001t0001g0296 others(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 | a0001c0001t0001g0147 | 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 | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(41): 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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(36): 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(36): 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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): 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 | 57 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(54): 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 | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0214 a0001c0001t0014g0164 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0006g0166 | 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 | a0001c0001t0001g0239 a0001c0001t0002g0050 |
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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | a0001c0001t0003g0150 | 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 | 16 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0140 others(13): 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 | a0001c0001t0001g0070 a0001c0001t0001g0148 a0001c0001t0001g0171 others(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 | 16 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0140 others(13): 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0226 a0001c0001t0001g0312 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): 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 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0180 a0001c0001t0001g0309 a0001c0001t0003g0150 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0097 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | 3 | a0001c0001t0001g0293 a0001c0001t0002g0305 a0001c0001t0007g0260 |
3 | HG00735.hp1 HG01978.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.925+15377G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10545213 | |||||||
| chr6:10545286 | C | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0053 a0001c0001t0003g0080 |
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 | 16 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0140 others(13): 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 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0226 a0001c0001t0001g0312 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | 33 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0089 others(30): 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0085 a0001c0001t0001g0097 others(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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): 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 | a0001c0001t0001g0075 | 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 | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(123): 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 | a0001c0001t0001g0186 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): 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 | a0001c0001t0001g0190 a0001c0001t0001g0220 |
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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0017g0023 |
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 | 2 | a0001c0001t0001g0197 a0001c0001t0004g0002 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(117): 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0312 |
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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0309 a0001c0001t0008g0149 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0062 others(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 | a0001c0001t0002g0221 | 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 | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): 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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0019 | 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 | a0001c0001t0002g0305 | 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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0012 | 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 | 10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0144 others(7): 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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0193 | 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 | 10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0144 others(7): 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 | a0001c0001t0003g0150 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0126 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0015 others(30): 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 | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(78): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0090 others(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 | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(78): 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 | a0001c0001t0001g0090 a0001c0001t0001g0115 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0046 | 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 | a0001c0001t0001g0256 | 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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(99): 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0246 |
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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0140 a0001c0001t0001g0151 others(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 | 9 | a0001c0001t0001g0081 a0001c0001t0001g0148 a0001c0001t0001g0180 others(6): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0200 a0001c0001t0001g0203 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0008g0198 |
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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0016g0165 |
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 | a0001c0001t0001g0174 a0001c0001t0001g0214 a0001c0001t0014g0164 |
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 | a0001c0001t0001g0143 a0001c0001t0001g0157 a0001c0001t0001g0158 others(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 | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(101): 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 | 6 | a0001c0001t0001g0001 a0001c0001t0001g0147 a0001c0001t0001g0175 others(3): 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 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0225 |
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 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
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 | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0053 others(34): 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0174 others(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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0074 | 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 | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(40): 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0016g0165 |
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 | a0001c0001t0013g0155 | 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 | 7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0147 others(4): 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 | a0001c0001t0002g0136 | 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 | 7 | a0001c0001t0001g0081 a0001c0001t0001g0183 a0001c0001t0001g0187 others(4): 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0270 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0002g0093 | 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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): 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 | 20 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0144 others(17): 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 | a0001c0001t0001g0046 | 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 | 10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0144 others(7): 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 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
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 | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0016g0165 |
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 | a0001c0001t0001g0114 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0186 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0207 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0017g0023 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | 6 | a0001c0001t0001g0081 a0001c0001t0001g0183 a0001c0001t0001g0187 others(3): 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 | a0001c0001t0001g0309 a0001c0001t0008g0149 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0016g0165 |
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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0312 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0001g0248 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0195 others(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 | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): 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 | a0001c0001t0001g0185 a0001c0001t0001g0316 a0001c0001t0001g0317 others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0227 a0001c0001t0001g0238 |
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 | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0147 others(5): 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 | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(41): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0272 a0001c0001t0001g0312 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0232 a0001c0001t0001g0315 |
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 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0185 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0027 others(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 | 8 | a0001c0001t0001g0081 a0001c0001t0001g0183 a0001c0001t0001g0187 others(5): 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 | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0147 others(5): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0007g0011 | 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 | a0001c0001t0001g0185 a0001c0001t0008g0198 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0002g0208 | 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 | a0001c0001t0012g0277 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0307 a0001c0001t0001g0318 a0001c0001t0007g0260 |
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 | a0001c0001t0001g0306 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(100): 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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0016g0165 |
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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(100): 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 | a0001c0001t0004g0280 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0085 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0177 others(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 | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(33): Show |
36 | HG00735.hp1 HG01109.hp1 HG01109.hp2 others(33): 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 | 7 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0313 others(4): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0043 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0174 others(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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0016g0165 |
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 | a0001c0001t0002g0050 a0001c0001t0002g0127 |
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 | a0001c0001t0001g0279 | 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 | a0001c0001t0007g0011 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0078 a0001c0001t0001g0209 a0001c0001t0001g0285 others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0200 | 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 | 17 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0140 others(14): 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 | a0001c0001t0001g0005 a0001c0001t0001g0315 |
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 | a0001c0001t0001g0309 a0001c0001t0008g0149 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0098 others(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 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0008g0198 | 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 | a0001c0001t0001g0047 a0001c0001t0001g0134 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0179 a0001c0001t0002g0104 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0234 a0001c0001t0001g0311 |
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 | a0001c0001t0001g0185 a0001c0001t0001g0315 |
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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0044 a0001c0001t0001g0058 others(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 | a0001c0001t0001g0193 a0001c0001t0006g0170 |
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 | a0001c0001t0003g0319 | 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 | a0001c0001t0002g0063 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0219 a0001c0001t0002g0050 a0001c0001t0002g0127 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0201 a0001c0001t0001g0203 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0240 a0001c0001t0002g0122 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0082 others(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 | a0001c0001t0001g0147 a0001c0001t0003g0303 a0001c0001t0016g0165 |
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 | a0001c0001t0001g0317 a0001c0001t0003g0167 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0309 a0001c0001t0005g0269 a0001c0001t0008g0149 others(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 | a0001c0001t0004g0141 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0088 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0001g0120 others(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 | a0001c0001t0001g0209 a0001c0001t0001g0272 a0001c0001t0001g0291 others(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 | a0001c0001t0001g0028 a0001c0001t0003g0150 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0135 a0001c0001t0001g0176 a0001c0001t0001g0177 |
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 | 4 | a0001c0001t0001g0001 a0001c0001t0001g0183 a0001c0001t0001g0187 others(1): 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0094 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0281 a0001c0001t0002g0067 others(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 | a0001c0001t0001g0211 | 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 | 65 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0026 others(62): Show |
65 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(62): 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 | 2 | a0001c0001t0001g0197 a0001c0001t0004g0002 |
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 | a0001c0001t0001g0195 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(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 | 119 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
119 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(116): 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0245 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0151 |
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 | a0001c0001t0001g0117 a0001c0001t0002g0007 |
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 | a0001c0001t0015g0276 | 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 | 8 | a0001c0001t0001g0081 a0001c0001t0001g0183 a0001c0001t0001g0187 others(5): 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 | a0001c0001t0011g0304 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0010g0253 |
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 | a0001c0001t0001g0207 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0317 | 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 | 7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0147 others(4): 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0279 a0001c0001t0002g0271 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0226 a0001c0001t0013g0155 |
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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
166 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(163): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0316 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0168 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0318 a0001c0001t0003g0156 |
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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0233 |
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 | a0001c0001t0001g0235 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | 5 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0001g0187 others(2): 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 | 165 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(162): Show |
165 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(162): 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 | a0001c0001t0002g0045 | 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 | a0001c0001t0002g0050 a0001c0001t0002g0127 |
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 | a0001c0001t0001g0232 | 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 | 175 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(172): Show |
175 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(172): 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0274 | 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 | 189 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(186): Show |
189 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(186): 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 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0201 a0001c0001t0001g0232 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0046 | 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 | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0001g0237 | 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 | 184 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(181): Show |
184 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(181): 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 | a0001c0001t0001g0114 a0001c0001t0001g0124 |
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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0185 a0001c0001t0006g0170 |
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 | 195 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): 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 | a0001c0001t0001g0211 a0001c0001t0001g0306 |
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 | a0001c0001t0004g0141 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0226 | 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 | 200 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0226 | 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 | 188 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(185): Show |
188 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(185): 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 | a0001c0001t0001g0185 a0001c0001t0006g0170 |
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 | 168 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(165): Show |
168 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(165): 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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0079 a0001c0001t0001g0108 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0245 a0001c0001t0001g0264 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0205 a0001c0001t0001g0228 others(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 | a0001c0001t0001g0195 a0001c0001t0001g0204 a0001c0001t0001g0249 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0258 a0001c0001t0001g0318 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0091 a0001c0001t0001g0101 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0029 others(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 |
27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0060 others(24): Show |
27 | HG00323.hp1 HG00621.hp2 HG01109.hp2 others(24): 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0094 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0124 a0001c0001t0001g0298 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0268 a0001c0001t0001g0296 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0234 |
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 | a0001c0001t0002g0048 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0100 |
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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0209 others(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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0132 others(5): 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 | a0001c0001t0006g0170 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0278 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0233 a0001c0001t0001g0316 others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0003g0156 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0002g0139 | 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 | 134 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(131): Show |
134 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(131): 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 | a0001c0001t0001g0021 a0001c0001t0001g0145 a0001c0001t0001g0239 others(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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0088 a0001c0001t0001g0200 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0272 a0001c0001t0004g0280 a0001c0001t0005g0269 |
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 | 167 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(164): Show |
167 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(164): 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 | a0001c0001t0001g0005 a0001c0001t0001g0315 a0001c0001t0013g0155 |
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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0315 a0001c0001t0013g0155 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0185 a0001c0001t0006g0170 |
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 | a0001c0001t0011g0304 | 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 | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0121 others(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 | 190 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): 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 | a0001c0001t0001g0311 | 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 | 192 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(189): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): 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 | a0001c0001t0001g0116 a0001c0001t0001g0123 a0001c0001t0001g0125 |
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 | 6 | a0001c0001t0001g0001 a0001c0001t0001g0176 a0001c0001t0001g0309 others(3): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0003g0167 | 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 | a0001c0001t0003g0150 a0001c0001t0008g0198 |
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 | a0001c0001t0002g0050 a0001c0001t0002g0096 a0001c0001t0002g0127 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0068 a0001c0001t0001g0092 others(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 | 191 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(188): Show |
191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): 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 | a0001c0001t0001g0148 a0001c0001t0001g0168 a0001c0001t0001g0180 others(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 | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(171): Show |
174 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(171): 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0008g0198 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 180 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): 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 | a0001c0001t0002g0236 a0001c0001t0002g0266 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0002g0032 a0001c0001t0002g0057 a0001c0001t0002g0111 |
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 | a0001c0001t0002g0118 | 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 | a0001c0001t0012g0277 | 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 | a0001c0001t0001g0064 | 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 | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0168 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0272 a0001c0001t0004g0280 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0012g0277 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0151 others(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 | 173 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): 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 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0001t0001g0151 others(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 | 174 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0012g0277 |
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 | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.925+42678T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572514 | |||||||
| chr6:10572548 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(9): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | 162 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(159): Show |
162 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.925+42969C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10572805 | |||||||
| chr6:10572962 | G | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(191): 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 | a0001c0001t0001g0226 | 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 | 2 | a0001c0001t0001g0197 a0001c0001t0004g0002 |
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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
177 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(174): 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 | a0001c0001t0001g0230 | 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0003g0150 a0001c0001t0008g0198 |
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 | a0001c0001t0013g0155 | 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 | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): 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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0144 a0001c0001t0001g0151 a0001c0001t0004g0146 |
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 | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): 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 | a0001c0001t0012g0277 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
176 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(173): 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 | a0001c0001t0001g0302 | 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 | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.925+44243T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574079 | |||||||
| chr6:10574099 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.925+44328G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10574164 | |||||||
| chr6:10574215 | C | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): 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 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0051 others(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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0005 a0001c0001t0001g0315 a0001c0001t0001g0316 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0119 a0001c0001t0001g0204 |
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 | a0001c0001t0001g0191 | 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 | 9 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(6): 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 | a0001c0001t0001g0005 a0001c0001t0001g0315 |
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 | a0001c0001t0001g0185 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0028 | 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0004g0141 | 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 | a0001c0001t0008g0149 | 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 | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): 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 | a0001c0001t0001g0272 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0081 a0001c0001t0001g0179 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0249 a0001c0001t0001g0258 |
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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0209 a0001c0001t0001g0286 a0001c0001t0001g0287 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0199 a0001c0001t0001g0224 others(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 | 17 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0036 others(14): 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 | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): 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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 23 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(20): 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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0175 | 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0312 | 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 | a0001c0001t0004g0280 | 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0012g0277 | 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 | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(22): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0038 a0001c0001t0001g0095 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0226 | 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 | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.926-44706A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10576645 | |||||||
| chr6:10576653 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0012g0277 |
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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0318 a0001c0001t0003g0212 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(8): 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0006 | 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0200 | 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0013g0155 | 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 | a0001c0001t0001g0009 | 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0001g0077 a0001c0001t0001g0088 |
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 | a0001c0001t0002g0136 | 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0222 | 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0117 a0001c0001t0001g0255 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0177 a0001c0001t0001g0195 others(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 | 27 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(24): 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(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 | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): 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 | a0001c0001t0001g0019 | 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(7): 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 | a0001c0001t0001g0185 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0185 a0001c0001t0006g0170 |
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 | a0001c0001t0002g0136 | 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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0005 | 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 2 | a0001c0001t0001g0197 a0001c0001t0004g0002 |
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 | a0001c0001t0001g0147 a0001c0001t0003g0167 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0013g0155 |
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 | a0001c0001t0001g0178 | 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0186 | 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 | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
320 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.926-41621G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10579730 | |||||||
| chr6:10579731 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(10): 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0075 | 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 | a0001c0001t0001g0229 a0001c0001t0001g0293 |
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 | 112 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(109): Show |
112 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(109): 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 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0168 others(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 | a0001c0001t0001g0272 a0001c0001t0004g0280 a0001c0001t0005g0269 |
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 | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(8): 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 | a0001c0001t0001g0006 a0001c0001t0001g0185 a0001c0001t0003g0150 others(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 | a0001c0001t0012g0277 | 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 | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(8): 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 | a0001c0001t0001g0005 a0001c0001t0001g0185 a0001c0001t0001g0315 others(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 | a0001c0001t0001g0147 a0001c0001t0003g0167 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 others(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 | 11 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(8): 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | 15 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0148 others(12): 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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(4): 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 | 51 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): 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 | a0001c0001t0001g0168 a0001c0001t0001g0226 a0001c0001t0001g0272 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0270 | 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 | a0001c0001t0001g0121 a0001c0001t0001g0128 |
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 | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0207 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 17 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0162 others(14): 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(4): 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0184 a0001c0001t0001g0193 |
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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(4): 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0312 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0072 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0013g0155 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0147 a0001c0001t0001g0265 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0001g0191 |
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 | 130 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
130 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(127): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0226 a0001c0001t0001g0272 a0001c0001t0004g0280 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 |
10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0107 others(7): 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0003g0303 a0001c0001t0003g0319 a0001c0001t0013g0155 |
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 | a0001c0001t0008g0198 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0272 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0272 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0272 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0272 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0272 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0053 a0001c0001t0001g0098 a0001c0001t0001g0188 others(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 |
7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(4): 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0003g0212 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0175 a0001c0001t0001g0315 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 17 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(14): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(7): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(7): 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 | 17 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(14): 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(7): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0089 others(16): 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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(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 | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(45): 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 | a0001c0001t0001g0151 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0038 a0001c0001t0001g0095 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0147 a0001c0001t0003g0167 a0001c0001t0006g0170 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0135 others(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 | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): 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 | a0001c0001t0001g0019 a0001c0001t0001g0131 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): 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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0180 others(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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(5): 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0207 a0001c0001t0001g0270 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(25): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | 28 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(25): 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 | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(7): 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0151 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0026 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(5): 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 | 132 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(129): Show |
132 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(129): 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0316 | 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 | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(42): 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 | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.926-36395G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10584956 | |||||||
| chr6:10584977 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(34): 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0101 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0100 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(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 | 54 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): 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 | 19 | a0001c0001t0001g0039 a0001c0001t0001g0058 a0001c0001t0001g0060 others(16): Show |
19 | HG00639.hp1 HG01192.hp2 HG02040.hp1 others(16): 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0205 a0001c0001t0001g0256 others(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 | a0001c0001t0002g0136 | 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 | a0001c0001t0001g0147 a0001c0001t0003g0167 a0001c0001t0006g0170 |
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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(5): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0316 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0003g0303 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0175 a0001c0001t0012g0277 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0002c0002t0018g0322 |
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 | a0001c0001t0001g0286 a0001c0001t0002g0118 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0021 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0128 a0001c0001t0002g0103 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0180 |
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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0194 |
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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0272 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(47): 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 | a0001c0001t0001g0151 a0001c0001t0004g0146 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0312 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0001g0268 a0001c0001t0002g0208 |
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 | a0001c0001t0002g0084 | 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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0162 others(4): 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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0020 a0001c0001t0001g0321 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0177 |
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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0175 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0217 a0001c0001t0001g0233 |
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 | a0001c0001t0002g0104 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0225 | 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 | 10 | a0001c0001t0001g0001 a0001c0001t0001g0140 a0001c0001t0001g0152 others(7): 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 | a0001c0001t0007g0011 a0001c0001t0007g0260 a0001c0001t0008g0198 others(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 | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 others(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 |
178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(175): 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 | a0001c0001t0002g0050 a0001c0001t0002g0127 |
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 | a0001c0001t0011g0304 | 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 | 2 | a0001c0001t0001g0001 a0001c0001t0001g0075 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
314 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(311): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 others(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 | a0001c0001t0002g0136 | 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 | a0001c0001t0004g0280 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0151 a0001c0001t0001g0197 a0001c0001t0010g0253 |
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 | a0001c0001t0008g0198 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0079 others(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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0002g0192 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(176): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0214 | 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 | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(148): 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 | a0001c0001t0001g0317 a0001c0001t0004g0280 a0001c0001t0013g0155 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(173): 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(178): 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 | a0001c0001t0008g0198 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0002g0289 a0001c0001t0002g0290 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 1 | a0001c0001t0001g0001 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0321 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0001g0312 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0140 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0065 a0001c0001t0002g0048 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0147 a0001c0001t0003g0167 a0001c0001t0006g0166 others(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 | a0001c0001t0001g0147 a0001c0001t0003g0167 a0001c0001t0006g0166 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0002g0032 a0001c0001t0002g0057 a0001c0001t0002g0111 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
182 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.926-24978T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10596373 | |||||||
| chr6:10596387 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
185 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(182): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0070 | 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 | 11 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0090 others(8): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0026 a0001c0001t0001g0062 others(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 | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(24): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0249 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0097 a0001c0001t0002g0045 |
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 | 164 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(161): 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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0061 a0001c0001t0001g0110 others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0003g0167 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(173): 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0143 others(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 | a0001c0001t0003g0080 | 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 | a0001c0001t0001g0264 a0001c0001t0001g0267 |
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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(158): 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 | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(158): 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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0001g0312 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0020 | 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 | a0001c0001t0001g0229 | 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 | 18 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0081 others(15): 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 | a0001c0001t0001g0081 a0001c0001t0001g0176 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0001g0312 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0060 others(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 | 130 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): 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 | a0001c0001t0001g0147 | 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 | 154 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): 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 | a0001c0001t0001g0222 a0001c0001t0002g0221 a0001c0001t0005g0181 |
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 | a0001c0001t0006g0170 | 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 | a0001c0001t0005g0269 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0089 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0168 a0001c0001t0001g0314 |
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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0234 | 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 | a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0005g0181 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0176 others(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 | a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0037 a0001c0001t0001g0168 a0001c0001t0001g0209 others(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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(200): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): 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 | a0001c0001t0001g0009 a0001c0001t0001g0102 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0242 |
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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0086 |
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 | a0001c0001t0002g0259 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0051 a0001c0001t0001g0056 others(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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): 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 | a0001c0001t0001g0081 a0001c0001t0001g0148 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0197 a0001c0001t0010g0253 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0054 | 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 | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(26): 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0316 | 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | 21 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0053 others(18): 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 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0081 others(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 | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0235 a0001c0001t0001g0246 a0001c0001t0001g0251 others(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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.926-17387T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603964 | |||||||
| chr6:10603985 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(128): Show |
131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): 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 | a0001c0001t0002g0210 | 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.926-17361G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10603990 | |||||||
| chr6:10603997 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0074 | 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 | a0001c0001t0002g0057 | 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 | a0001c0001t0002g0213 | 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0252 | 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0011g0304 | 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 | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(129): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): 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 | a0001c0001t0001g0108 a0001c0001t0005g0269 a0001c0001t0009g0182 others(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 | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(125): 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 | a0001c0001t0001g0086 | 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0001g0312 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0116 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0161 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0147 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0168 a0001c0001t0001g0186 others(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 | 11 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0053 others(8): 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 | 9 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0058 others(6): 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 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(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 | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): 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 | a0001c0001t0001g0052 a0001c0001t0001g0066 a0001c0001t0001g0077 others(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 | a0001c0001t0003g0150 | 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 | a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.926-15913G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10605438 | |||||||
| chr6:10605518 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0077 | 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 | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0002g0067 a0001c0001t0002g0087 a0001c0001t0002g0210 others(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 | a0001c0001t0004g0146 | 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 | a0001c0001t0001g0197 a0001c0001t0010g0253 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0054 | 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 | a0001c0001t0002g0210 | 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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0200 a0001c0001t0001g0283 a0001c0001t0001g0284 |
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 | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.926-15000T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606351 | |||||||
| chr6:10606378 | G | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.926-14973G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606378 | |||||||
| chr6:10606432 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0307 | 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 | 28 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(25): 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 | a0001c0001t0005g0269 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0148 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0027 others(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 |
53 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0029 others(50): 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 |
45 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0024 others(42): 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 | a0001c0001t0002g0010 a0001c0001t0002g0032 a0001c0001t0002g0057 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0168 a0001c0001t0001g0314 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0161 others(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 | a0001c0001t0008g0149 | 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 | a0001c0001t0003g0156 a0001c0001t0003g0212 |
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 | a0001c0001t0003g0303 | 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 | a0001c0001t0003g0319 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0083 a0001c0001t0001g0090 others(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 | a0001c0001t0001g0046 | 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 | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(32): 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 | a0001c0001t0001g0061 a0001c0001t0001g0115 |
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 | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.926-14454C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10606897 | |||||||
| chr6:10606929 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0235 a0001c0001t0001g0246 a0001c0001t0001g0300 |
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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0066 a0001c0001t0001g0077 a0001c0001t0001g0088 others(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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0006g0166 a0001c0001t0006g0170 |
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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0071 others(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 | a0001c0001t0002g0096 | 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0312 | 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(31): 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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0053 others(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 | a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0135 | 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0248 | 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0006 a0001c0001t0001g0317 a0001c0001t0003g0080 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0278 | 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 | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.926-11734G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609617 | |||||||
| chr6:10609780 | A | AG | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(30): 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 | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): 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 | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.926-11447A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609904 | |||||||
| chr6:10609907 | G | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.926-11444G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10609907 | |||||||
| chr6:10610078 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(32): 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0099 | 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 | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(32): 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 | a0001c0001t0001g0168 a0001c0001t0001g0314 a0001c0001t0001g0316 |
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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0307 | 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 | a0001c0001t0011g0304 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0082 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0099 | 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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): 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 | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.926-10067T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10611284 | |||||||
| chr6:10611334 | C | CT | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): 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 | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(31): 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 | 125 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): 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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0189 others(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 | a0001c0001t0001g0222 a0001c0001t0002g0221 |
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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0005 | 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 | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(32): 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 | a0001c0001t0002g0048 a0001c0001t0002g0139 a0001c0001t0002g0271 |
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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0188 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0086 |
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 | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(32): 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0099 others(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 | a0001c0001t0005g0269 | 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 | a0001c0001t0001g0089 | 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 | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(32): 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 | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(32): 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 | 80 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0028 others(77): 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 | a0001c0001t0002g0033 a0001c0001t0002g0118 a0001c0001t0002g0136 others(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 | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(31): 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 | a0001c0001t0001g0075 a0001c0001t0001g0207 a0001c0001t0001g0249 others(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 | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): 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 | a0001c0001t0002g0033 a0001c0001t0002g0118 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0009g0182 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0002g0067 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0175 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0128 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0144 others(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 | 123 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): 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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0176 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0129 others(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 | 17 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0130 others(14): 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 | 133 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): 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 | a0001c0001t0001g0090 a0001c0001t0001g0234 |
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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): 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 | a0001c0001t0004g0146 | 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 | a0001c0001t0001g0097 | 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 | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.926-6316C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615035 | |||||||
| chr6:10615472 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.926-5879A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10615472 | |||||||
| chr6:10615644 | T | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): 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 | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(31): 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 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0160 others(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 | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0022 others(31): 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0009g0182 | 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 | a0001c0001t0011g0304 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0321 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0094 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0307 | 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 | 36 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(33): 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0003g0156 a0001c0001t0003g0212 a0001c0001t0003g0303 others(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 | a0001c0001t0002g0259 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0175 a0001c0001t0001g0177 others(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 | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): 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 | a0001c0001t0001g0197 a0001c0001t0010g0253 |
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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0074 a0001c0001t0001g0079 |
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 | a0001c0001t0005g0181 | 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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.926-3974T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 3/4 | chr6 | 10617377 | |||||||
| chr6:10617411 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0020 others(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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0214 |
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 | a0001c0001t0002g0221 | 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 | a0001c0001t0003g0156 | 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 | a0001c0001t0008g0149 | 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 | a0001c0001t0003g0156 a0001c0001t0003g0212 a0001c0001t0003g0303 others(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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(21): 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 | a0001c0001t0001g0064 a0001c0001t0001g0079 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0175 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0160 a0001c0001t0012g0277 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0159 a0001c0001t0001g0313 |
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 | a0001c0001t0004g0141 a0001c0001t0008g0198 |
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 | a0001c0001t0001g0176 a0001c0001t0006g0166 |
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 | a0001c0001t0001g0081 a0001c0001t0006g0170 |
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 | a0001c0001t0001g0197 a0001c0001t0010g0253 |
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 | a0001c0001t0001g0168 a0001c0001t0001g0314 a0001c0001t0001g0316 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0202 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0031 others(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 | 107 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(104): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): 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 | a0001c0001t0011g0304 | 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 | a0001c0001t0001g0101 | 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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): 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 | a0001c0001t0001g0053 | 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 | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0179 a0001c0001t0001g0272 |
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 | a0001c0001t0011g0304 | 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 | a0001c0001t0002g0236 a0001c0001t0002g0266 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0001g0312 others(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 | a0001c0001t0001g0120 | 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 | a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0107 | 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 | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): 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 | 28 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(25): 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 |
36 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(33): 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 | a0001c0001t0001g0081 a0001c0001t0004g0141 |
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 | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): 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 | 36 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(33): 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 | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0168 a0001c0001t0001g0314 a0001c0001t0001g0316 |
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 | a0001c0001t0004g0146 | 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 | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(34): 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 | 30 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(27): 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 | 26 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(23): 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 | a0001c0001t0002g0210 | 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 | 27 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(24): 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 | a0001c0001t0001g0006 a0001c0001t0001g0308 a0001c0001t0001g0309 others(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 | 25 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(22): 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0017g0023 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0308 a0001c0001t0001g0309 others(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 | a0001c0001t0001g0186 | 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(21): 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(30): 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 | 2 | a0001c0001t0004g0002 a0001c0001t0004g0141 |
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 | 2 | a0001c0001t0004g0002 a0001c0001t0004g0141 |
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 | a0001c0001t0003g0156 a0001c0001t0003g0303 a0001c0001t0003g0319 others(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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(30): 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0054 | 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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(30): 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 | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(44): 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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0017g0023 |
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 | 33 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0022 others(30): 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(21): 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 | a0001c0001t0001g0148 | 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(21): 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(21): 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 | a0001c0001t0001g0041 | 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(21): 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(21): 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 | a0001c0001t0001g0009 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0081 a0001c0001t0001g0099 others(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 | 126 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(123): Show |
126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): 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 | a0001c0001t0001g0006 a0001c0001t0001g0247 a0001c0001t0001g0308 others(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 | 20 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(17): 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 | a0001c0001t0001g0062 a0001c0001t0003g0156 a0001c0001t0003g0212 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0066 a0001c0001t0001g0077 others(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 | a0001c0001t0002g0087 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0190 | 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 | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): 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 | a0001c0001t0001g0068 a0001c0001t0001g0094 a0001c0001t0001g0121 others(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 | 27 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(24): 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0002g0213 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0119 |
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 | 2 | a0001c0001t0004g0002 a0001c0001t0004g0141 |
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 | a0001c0001t0001g0222 a0001c0001t0002g0221 |
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 | 23 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(20): 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 | 24 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(21): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): 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 | a0001c0001t0001g0079 | 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 | 2 | a0001c0001t0004g0002 a0001c0001t0004g0141 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
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 | a0001c0001t0001g0209 a0001c0001t0001g0291 |
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 | 2 | a0001c0001t0004g0002 a0001c0001t0004g0141 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0028 others(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 | a0001c0001t0011g0304 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0053 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0294 |
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 | 12 | a0001c0001t0001g0005 a0001c0001t0001g0308 a0001c0001t0001g0309 others(9): 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 | a0001c0001t0001g0175 a0001c0001t0001g0246 a0001c0001t0001g0316 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0140 others(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 | a0001c0001t0002g0259 | 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 | a0001c0001t0008g0198 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0308 a0001c0001t0001g0309 others(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 | a0001c0001t0005g0181 a0001c0001t0005g0269 a0001c0001t0009g0182 |
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 | a0001c0001t0001g0065 a0001c0001t0001g0095 |
2 | NA18949.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1019-35T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000495262.7 | protein_coding | 4/4 | chr6 | 10626382 |