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_001491.3 |
| refseq_prot | NP_001482.1 |
| ensembl_nuc | ENST00000316170.9 |
| ensembl_prot | ENSP00000314844.3 |
| mane_status | MANE Plus Clinical |
| chr | chr6 |
| start | 10555809 |
| end | 10629368 |
| strand | + |
| ver | v1.2 |
| region | chr6:10555809-10629368 |
| region5000 | chr6:10550809-10634368 |
| regionname0 | GCNT2_chr6_10555809_10629368 |
| regionname5000 | GCNT2_chr6_10550809_10634368 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 400 | 338 | 81 | 64 | 143 | 12 | 36 | 109 | GCNT2_chr6_10550809_10634368 | GCNT2 | MPLSM others(395): Show |
chr6 | 10550809 | 10634368 |
| a0002 | 0/0 | 400 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | MPSSM others(395): Show |
chr6 | 10550809 | 10634368 |
| a0003 | 0/0 | 400 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | MPLSM others(395): Show |
chr6 | 10550809 | 10634368 |
| a0004 | 0/0 | 400 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | MPLSM others(395): Show |
chr6 | 10550809 | 10634368 |
| a0005 | 0/0 | 73 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | MPLSM others(68): Show |
chr6 | 10550809 | 10634368 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1200 | 321 | 73 | 60 | 142 | 10 | 34 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0001c0002 | 0/0 | 1200 | 12 | 4 | 4 | 1 | 2 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0001c0004 | 0/0 | 1200 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0001c0006 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0001c0007 | 0/0 | 1200 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0002c0003 | 0/0 | 1200 | 3 | 3 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0003c0005 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0004c0008 | 0/0 | 1200 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1195): Show |
chr6 | 10550809 | 10634368 | ||
| a0005c0009 | 0/0 | 1219 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ATGCC others(1214): Show |
chr6 | 10550809 | 10634368 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4579 | 250 | 52 | 48 | 114 | 10 | 24 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0002 | 0/0 | 4579 | 43 | 1 | 7 | 27 | 0 | 8 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0003 | 0/0 | 4583 | 4 | 2 | 1 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0004 | 0/0 | 4579 | 5 | 5 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0005 | 0/0 | 4583 | 3 | 1 | 2 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0006 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0007 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0008 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0009 | 0/0 | 4579 | 2 | 0 | 2 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0010 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0012 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0013 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0014 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0015 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0016 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0017 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0001t0019 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0002t0001 | 0/0 | 4579 | 10 | 3 | 4 | 1 | 1 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0002t0002 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0002t0003 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0004t0003 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0001c0004t0018 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0006t0001 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0001c0007t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0002c0003t0001 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0002c0003t0010 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0002c0003t0011 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4578): Show |
chr6 | 10550809 | 10634368 |
| a0003c0005t0001 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0004c0008t0001 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4574): Show |
chr6 | 10550809 | 10634368 |
| a0005c0009t0001 | 0/0 | 4598 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | ACTTG others(4593): Show |
chr6 | 10550809 | 10634368 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0008g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0009g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0009g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0012g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0013g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0014g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0015g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0016g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0017g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0001t0019g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0002t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0004t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0004t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0004t0018g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0001c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0002c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0002c0003t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0002c0003t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0003c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0004c0008t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| a0005c0009t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0292 | EUR | GBR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0290 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0325 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0047 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0302 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0286 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0247 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0304 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | CDX | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0333 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02572 | hp1 | a0002 | c0003 | t0011 | g0265 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02717 | hp1 | a0001 | c0004 | t0018 | g0329 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0284 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02738 | hp2 | a0001 | c0001 | t0019 | g0114 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02895 | hp1 | a0001 | c0007 | t0001 | g0017 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0270 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0244 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03017 | hp2 | a0001 | c0006 | t0001 | g0070 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0327 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0301 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0278 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0295 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03195 | hp2 | a0001 | c0004 | t0003 | g0328 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0010 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03239 | hp1 | a0003 | c0005 | t0001 | g0318 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03579 | hp1 | a0002 | c0003 | t0010 | g0271 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03927 | hp1 | a0004 | c0008 | t0001 | g0041 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19005 | hp1 | a0001 | c0001 | t0017 | g0192 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0334 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19080 | hp1 | a0005 | c0009 | t0001 | g0082 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0330 | AFR | YRI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ASW | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0308 | AFR | ASW | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | GIH | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | GIH | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | USA | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0125 | REF | REF | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 10634368 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0130 | REF | REF | GCNT2_chr6_10550809_10634368 | GCNT2 | chr6 | 10550809 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10556431 | T | C | 1 | a0002 | 3 | HG02572.hp1 HG02970.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.8T>C | p.Leu3Ser | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 623/4579 | 8/1203 | 3/400 | chr6 | 10556431 | |||
| chr6:10556488 | T | C | 1 | a0003 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.65T>C | p.Phe22Ser | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 680/4579 | 65/1203 | 22/400 | chr6 | 10556488 | |||
| chr6:10556581 | A | ATGGAAAA others(12): Show |
1 | a0005 | 1 | NA19080.hp1 | frameshift_variant | HIGH | c.169_187dupCGTTTCCT others(11): Show |
p.Lys63fs | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 803/4579 | 188/1203 | 63/400 | INFO_REALIGN_3_PRIME | chr6 | 10556581 | ||
| chr6:10556940 | A | G | 1 | a0004 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.517A>G | p.Arg173Gly | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 1132/4579 | 517/1203 | 173/400 | chr6 | 10556940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10556639 | C | T | 1 | a0001c0002 | 12 | HG00140.hp1 HG00323.hp1 HG01099.hp2 others(9): Show |
synonymous_variant | LOW | c.216C>T | p.Cys72Cys | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 831/4579 | 216/1203 | 72/400 | chr6 | 10556639 | |||
| chr6:10556753 | G | A | 1 | a0001c0006 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.330G>A | p.Arg110Arg | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 945/4579 | 330/1203 | 110/400 | chr6 | 10556753 | |||
| chr6:10557053 | T | G | 1 | a0001c0007 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.630T>G | p.Gly210Gly | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 1245/4579 | 630/1203 | 210/400 | chr6 | 10557053 | |||
| chr6:10557110 | T | C | 1 | a0001c0004 | 3 | HG02717.hp1 HG03130.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.687T>C | p.Tyr229Tyr | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 1302/4579 | 687/1203 | 229/400 | chr6 | 10557110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10556106 | G | C | 2 | a0001c0001t0004 a0001c0001t0006 |
7 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-318G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/3 | 318 | chr6 | 10556106 | ||||||
| chr6:10626660 | C | G | 2 | a0001c0001t0010 a0002c0003t0010 |
2 | HG03579.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*53C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 53 | chr6 | 10626660 | ||||||
| chr6:10626688 | G | A | 1 | a0002c0003t0011 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 81 | chr6 | 10626688 | ||||||
| chr6:10626712 | C | T | 4 | a0001c0001t0003 a0001c0001t0019 a0001c0002t0003 others(1): Show |
8 | HG01358.hp1 HG01891.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 105 | chr6 | 10626712 | ||||||
| chr6:10626821 | A | G | 1 | a0001c0004t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 214 | chr6 | 10626821 | ||||||
| chr6:10626832 | G | A | 1 | a0001c0001t0007 | 2 | HG02717.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*225G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 225 | chr6 | 10626832 | ||||||
| chr6:10627005 | T | A | 1 | a0001c0001t0008 | 2 | HG02055.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*398T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 398 | chr6 | 10627005 | ||||||
| chr6:10627125 | T | G | 1 | a0001c0001t0012 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 518 | chr6 | 10627125 | ||||||
| chr6:10627278 | C | T | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(3): Show |
10 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*671C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 671 | chr6 | 10627278 | ||||||
| chr6:10627289 | G | C | 4 | a0001c0001t0003 a0001c0001t0013 a0001c0002t0003 others(1): Show |
8 | HG01358.hp1 HG01891.hp2 HG02738.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*682G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 682 | chr6 | 10627289 | ||||||
| chr6:10627375 | G | A | 1 | a0001c0001t0014 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*768G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 768 | chr6 | 10627375 | ||||||
| chr6:10627546 | G | T | 2 | a0001c0001t0005 a0001c0001t0006 |
5 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*939G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 939 | chr6 | 10627546 | ||||||
| chr6:10627628 | C | CTTCA | 10 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(7): Show |
18 | HG00735.hp2 HG01109.hp1 HG01358.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1025dupTTCA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1026 | INFO_REALIGN_3_PRIME | chr6 | 10627628 | |||||
| chr6:10627681 | A | G | 1 | a0001c0001t0017 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1074A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1074 | chr6 | 10627681 | ||||||
| chr6:10627781 | T | C | 2 | a0001c0001t0002 a0001c0002t0002 |
44 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1174T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1174 | chr6 | 10627781 | ||||||
| chr6:10627924 | G | A | 1 | a0001c0001t0009 | 2 | HG01081.hp1 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1317G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1317 | chr6 | 10627924 | ||||||
| chr6:10628004 | A | G | 1 | a0001c0001t0016 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1397A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1397 | chr6 | 10628004 | ||||||
| chr6:10628340 | T | G | 5 | a0001c0001t0003 a0001c0001t0010 a0001c0002t0003 others(2): Show |
9 | HG01358.hp1 HG01891.hp2 HG02738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1733T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 1733 | chr6 | 10628340 | ||||||
| chr6:10628878 | C | T | 1 | a0001c0001t0013 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2271C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2271 | chr6 | 10628878 | ||||||
| chr6:10629059 | G | C | 1 | a0002c0003t0011 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2452G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2452 | chr6 | 10629059 | ||||||
| chr6:10629127 | C | A | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(3): Show |
10 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2520C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2520 | chr6 | 10629127 | ||||||
| chr6:10629333 | T | C | 1 | a0001c0001t0015 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 3/3 | 2726 | chr6 | 10629333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:10557463 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.919+121C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557463 | |||||||
| chr6:10557493 | CT | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
87 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.919+163delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10557493 | ||||||
| chr6:10557542 | C | T | 1 | a0001c0001t0001g0340 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.919+200C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557542 | |||||||
| chr6:10557668 | T | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+326T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557668 | |||||||
| chr6:10557691 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
108 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.919+349A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557691 | |||||||
| chr6:10557691 | A | T | 5 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(2): Show |
5 | HG01346.hp1 HG01934.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+349A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557691 | |||||||
| chr6:10557753 | A | G | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+411A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557753 | |||||||
| chr6:10557856 | C | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
165 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.919+514C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10557856 | |||||||
| chr6:10558035 | C | T | 5 | a0001c0001t0001g0307 a0001c0001t0001g0309 a0001c0001t0001g0310 others(2): Show |
5 | HG02622.hp2 HG03540.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+693C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558035 | |||||||
| chr6:10558329 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.919+987A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558329 | |||||||
| chr6:10558374 | A | G | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | NA18955.hp1 NA18992.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.919+1032A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558374 | |||||||
| chr6:10558473 | C | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0303 a0001c0001t0001g0305 others(4): Show |
8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+1131C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10558473 | |||||||
| chr6:10559072 | C | CT | 47 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0083 others(44): Show |
48 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.919+1747dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10559072 | ||||||
| chr6:10559072 | CT | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0092 others(5): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+1747delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10559072 | ||||||
| chr6:10559221 | C | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+1879C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559221 | |||||||
| chr6:10559306 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0305 |
2 | HG03579.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.919+1964C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559306 | |||||||
| chr6:10559718 | G | A | 9 | a0001c0001t0001g0307 a0001c0001t0001g0309 a0001c0001t0001g0310 others(6): Show |
9 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+2376G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559718 | |||||||
| chr6:10559719 | A | G | 9 | a0001c0001t0001g0307 a0001c0001t0001g0309 a0001c0001t0001g0310 others(6): Show |
9 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+2377A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559719 | |||||||
| chr6:10559767 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.919+2425T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10559767 | |||||||
| chr6:10560088 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.919+2746C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560088 | |||||||
| chr6:10560113 | G | C | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+2771G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560113 | |||||||
| chr6:10560119 | C | T | 36 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(33): Show |
36 | HG00741.hp1 HG01071.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.919+2777C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560119 | |||||||
| chr6:10560299 | AG | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
106 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.919+2961delG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10560299 | ||||||
| chr6:10560343 | G | A | 8 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0277 others(5): Show |
9 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+3001G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560343 | |||||||
| chr6:10560402 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0303 a0001c0001t0001g0305 others(4): Show |
8 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+3060T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560402 | |||||||
| chr6:10560498 | T | C | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+3156T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560498 | |||||||
| chr6:10560603 | A | C | 1 | a0001c0001t0001g0253 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.919+3261A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560603 | |||||||
| chr6:10560671 | C | A | 1 | a0001c0001t0009g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+3329C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560671 | |||||||
| chr6:10560869 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0010g0308 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.919+3527T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10560869 | |||||||
| chr6:10561009 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.919+3667C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561009 | |||||||
| chr6:10561037 | G | A | 11 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0319 others(8): Show |
11 | HG00735.hp2 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+3695G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561037 | |||||||
| chr6:10561126 | G | A | 2 | a0001c0002t0001g0279 a0001c0002t0001g0280 |
2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.919+3784G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561126 | |||||||
| chr6:10561173 | C | CT | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG00438.hp2 HG02080.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+3840dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10561173 | ||||||
| chr6:10561232 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.919+3890G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561232 | |||||||
| chr6:10561399 | C | T | 8 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00735.hp2 HG01884.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+4057C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561399 | |||||||
| chr6:10561403 | A | G | 11 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0319 others(8): Show |
11 | HG00735.hp2 HG01192.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+4061A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561403 | |||||||
| chr6:10561565 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.919+4223C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561565 | |||||||
| chr6:10561594 | C | T | 1 | a0001c0001t0014g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+4252C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561594 | |||||||
| chr6:10561634 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+4292G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561634 | |||||||
| chr6:10561656 | C | G | 3 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0009g0247 |
3 | HG01978.hp2 HG02698.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.919+4314C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561656 | |||||||
| chr6:10561862 | G | C | 1 | a0001c0001t0001g0004 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.919+4520G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561862 | |||||||
| chr6:10561952 | T | G | 1 | a0001c0001t0001g0307 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.919+4610T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561952 | |||||||
| chr6:10561960 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.919+4618A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561960 | |||||||
| chr6:10561964 | G | A | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.919+4622G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10561964 | |||||||
| chr6:10562019 | C | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(101): Show |
106 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.919+4677C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562019 | |||||||
| chr6:10562096 | G | T | 3 | a0001c0004t0003g0327 a0001c0004t0003g0328 a0001c0004t0018g0329 |
3 | HG02717.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.919+4754G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562096 | |||||||
| chr6:10562154 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(101): Show |
106 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.919+4812G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562154 | |||||||
| chr6:10562228 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.919+4886C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562228 | |||||||
| chr6:10562242 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG00280.hp1 HG01070.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.919+4900C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562242 | |||||||
| chr6:10562301 | C | G | 23 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
23 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.919+4959C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562301 | |||||||
| chr6:10562466 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.919+5124C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562466 | |||||||
| chr6:10562496 | T | G | 13 | a0001c0001t0001g0281 a0001c0001t0001g0307 a0001c0001t0001g0309 others(10): Show |
13 | HG01496.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+5154T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562496 | |||||||
| chr6:10562656 | G | GA | 39 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0100 others(36): Show |
39 | HG00735.hp1 HG01109.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.919+5335dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | ||||||
| chr6:10562656 | G | GAA | 7 | a0001c0001t0001g0002 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
8 | HG02055.hp2 HG02071.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+5334_919+5335d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | ||||||
| chr6:10562656 | GA | G | 16 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0234 others(13): Show |
16 | HG01192.hp1 HG01891.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+5335delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | ||||||
| chr6:10562656 | GAA | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(10): Show |
13 | HG01256.hp1 HG01346.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+5334_919+5335d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | ||||||
| chr6:10562656 | GAAA | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
80 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.919+5333_919+5335d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10562656 | ||||||
| chr6:10562668 | A | C | 9 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0266 others(6): Show |
9 | HG01358.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+5326A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562668 | |||||||
| chr6:10562669 | A | C | 3 | a0001c0004t0003g0327 a0001c0004t0003g0328 a0001c0004t0018g0329 |
3 | HG02717.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.919+5327A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562669 | |||||||
| chr6:10562670 | A | C | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | NA18980.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.919+5328A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562670 | |||||||
| chr6:10562673 | A | C | 1 | a0001c0001t0001g0236 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.919+5331A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562673 | |||||||
| chr6:10562675 | A | C | 1 | a0001c0001t0009g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+5333A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562675 | |||||||
| chr6:10562678 | C | A | 2 | a0001c0001t0001g0110 a0001c0002t0001g0294 |
2 | HG01192.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.919+5336C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562678 | |||||||
| chr6:10562687 | A | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG00408.hp1 HG00558.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+5345A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10562687 | |||||||
| chr6:10563166 | A | G | 1 | a0001c0001t0004g0278 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.919+5824A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563166 | |||||||
| chr6:10563232 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919+5890G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563232 | |||||||
| chr6:10563276 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.919+5934A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563276 | |||||||
| chr6:10563410 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
100 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.919+6068A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563410 | |||||||
| chr6:10563436 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.919+6094G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563436 | |||||||
| chr6:10563510 | G | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0272 a0001c0001t0001g0273 others(13): Show |
17 | HG00735.hp2 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+6168G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563510 | |||||||
| chr6:10563665 | CCAGGAGG others(9): Show |
C | 1 | a0001c0001t0001g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919+6327_919+6342d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563665 | ||||||
| chr6:10563749 | GAAAA | G | 3 | a0002c0003t0001g0270 a0002c0003t0010g0271 a0002c0003t0011g0265 |
3 | HG02572.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.919+6410_919+6413d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563749 | ||||||
| chr6:10563749 | GAAAAAAG others(3): Show |
G | 1 | a0001c0001t0001g0299 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.919+6414_919+6423d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563749 | ||||||
| chr6:10563756 | GA | G | 29 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(26): Show |
29 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.919+6436delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | ||||||
| chr6:10563756 | GAA | G | 17 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(14): Show |
17 | HG01070.hp1 HG01071.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+6435_919+6436d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | ||||||
| chr6:10563756 | GAAA | G | 9 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0226 others(6): Show |
9 | HG00140.hp2 HG02809.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+6434_919+6436d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | ||||||
| chr6:10563756 | GAAAAA | G | 7 | a0001c0001t0001g0229 a0001c0001t0001g0296 a0001c0001t0001g0297 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+6432_919+6436d others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | ||||||
| chr6:10563756 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0001g0044 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.919+6427_919+6436d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563756 | ||||||
| chr6:10563760 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.919+6418A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563760 | |||||||
| chr6:10563763 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.919+6421A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563763 | |||||||
| chr6:10563766 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0316 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.919+6426_919+6438d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563766 | ||||||
| chr6:10563767 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0010g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919+6427_919+6440d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563767 | ||||||
| chr6:10563768 | AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0072 a0001c0001t0001g0083 others(2): Show |
5 | HG00558.hp1 HG00673.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6428_919+6438d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563768 | ||||||
| chr6:10563768 | AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0002g0038 a0003c0005t0001g0318 |
2 | HG03239.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.919+6428_919+6440d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563768 | ||||||
| chr6:10563769 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0002g0056 a0001c0002t0001g0282 |
2 | HG01884.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.919+6429_919+6438d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | ||||||
| chr6:10563769 | AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0002t0001g0292 |
3 | HG00140.hp1 HG01517.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.919+6429_919+6440d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | ||||||
| chr6:10563769 | AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0307 |
2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.919+6429_919+6442d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | ||||||
| chr6:10563769 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+6429_919+6444d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563769 | ||||||
| chr6:10563770 | AAAAAAAA others(4): Show |
A | 16 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0037 others(13): Show |
16 | HG01099.hp2 HG02056.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+6430_919+6440d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | ||||||
| chr6:10563770 | AAAAAAAA others(6): Show |
A | 3 | a0001c0001t0001g0043 a0001c0001t0008g0334 a0001c0002t0001g0294 |
3 | HG01192.hp2 NA19030.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.919+6430_919+6442d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | ||||||
| chr6:10563770 | AAAAAAAA others(8): Show |
A | 1 | a0001c0004t0003g0327 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+6430_919+6444d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563770 | ||||||
| chr6:10563771 | A | AAT | 6 | a0001c0001t0001g0185 a0001c0001t0001g0257 a0001c0001t0001g0335 others(3): Show |
6 | HG00544.hp2 HG01934.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+6430_919+6431i others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | ||||||
| chr6:10563771 | A | AATATATA others(3): Show |
1 | a0001c0002t0002g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.919+6430_919+6431i others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | ||||||
| chr6:10563771 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0107 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.919+6430_919+6431i others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | ||||||
| chr6:10563771 | A | AT | 6 | a0001c0001t0001g0093 a0001c0001t0001g0108 a0001c0001t0002g0134 others(3): Show |
6 | HG02300.hp1 NA18980.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+6429_919+6430i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563771 | |||||||
| chr6:10563771 | A | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0336 a0001c0002t0001g0284 |
3 | HG00597.hp2 HG01975.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.919+6429A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563771 | |||||||
| chr6:10563771 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0066 a0001c0001t0002g0052 |
3 | HG01256.hp1 HG02083.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.919+6431_919+6440d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | ||||||
| chr6:10563771 | AAAAAAAA others(5): Show |
A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0074 a0001c0001t0001g0075 others(6): Show |
10 | HG00741.hp1 HG01081.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+6431_919+6442d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | ||||||
| chr6:10563771 | AAAAAAAA others(7): Show |
A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0303 a0001c0004t0003g0328 others(1): Show |
4 | HG02717.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+6431_919+6444d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | ||||||
| chr6:10563771 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0309 a0001c0001t0003g0300 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.919+6431_919+6446d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563771 | ||||||
| chr6:10563772 | AAAAAAAT others(2): Show |
A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0062 others(3): Show |
6 | HG01071.hp2 HG01934.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+6432_919+6440d others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | ||||||
| chr6:10563772 | AAAAAAAT others(4): Show |
A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(24): Show |
27 | HG00323.hp2 HG01081.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+6432_919+6442d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | ||||||
| chr6:10563772 | AAAAAAAT others(6): Show |
A | 4 | a0001c0001t0007g0019 a0001c0001t0014g0330 a0002c0003t0001g0270 others(1): Show |
4 | HG02717.hp2 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+6432_919+6444d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | ||||||
| chr6:10563772 | AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+6432_919+6446d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563772 | ||||||
| chr6:10563773 | A | AT | 8 | a0001c0001t0001g0153 a0001c0001t0001g0161 a0001c0001t0001g0172 others(5): Show |
8 | HG02083.hp1 HG02155.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+6431_919+6432i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | |||||||
| chr6:10563773 | A | ATAT | 5 | a0001c0001t0001g0100 a0001c0001t0001g0104 a0001c0001t0001g0157 others(2): Show |
5 | NA18956.hp2 NA18981.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6431_919+6432i others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | |||||||
| chr6:10563773 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.919+6431_919+6432i others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | |||||||
| chr6:10563773 | A | T | 25 | a0001c0001t0001g0093 a0001c0001t0001g0106 a0001c0001t0001g0107 others(22): Show |
25 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.919+6431A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563773 | |||||||
| chr6:10563773 | AAAAAATA others(3): Show |
A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0091 others(2): Show |
5 | HG02630.hp2 HG03540.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+6433_919+6442d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | ||||||
| chr6:10563773 | AAAAAATA others(5): Show |
A | 3 | a0001c0001t0001g0266 a0001c0001t0003g0311 a0002c0003t0011g0265 |
3 | HG02559.hp2 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.919+6433_919+6444d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | ||||||
| chr6:10563773 | AAAAAATA others(7): Show |
A | 1 | a0001c0001t0001g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.919+6433_919+6446d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | ||||||
| chr6:10563773 | AAAAAATA others(9): Show |
A | 1 | a0001c0001t0004g0277 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.919+6433_919+6448d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563773 | ||||||
| chr6:10563774 | AAAAATAT others(4): Show |
A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0029 others(15): Show |
18 | HG00408.hp1 HG01099.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+6434_919+6444d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | ||||||
| chr6:10563774 | AAAAATAT others(6): Show |
A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG01496.hp2 HG03710.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.919+6434_919+6446d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | ||||||
| chr6:10563774 | AAAAATAT others(8): Show |
A | 4 | a0001c0001t0001g0002 a0001c0001t0004g0275 a0001c0001t0004g0278 others(1): Show |
5 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6434_919+6448d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563774 | ||||||
| chr6:10563775 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.919+6434_919+6435i others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563775 | ||||||
| chr6:10563775 | A | AT | 13 | a0001c0001t0001g0163 a0001c0001t0001g0169 a0001c0001t0001g0174 others(10): Show |
13 | HG01516.hp1 HG02080.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+6433_919+6434i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | |||||||
| chr6:10563775 | A | ATAT | 4 | a0001c0001t0001g0127 a0001c0001t0001g0171 a0001c0001t0001g0260 others(1): Show |
4 | HG02273.hp1 HG02615.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+6433_919+6434i others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | |||||||
| chr6:10563775 | A | ATATAT | 3 | a0001c0001t0001g0131 a0001c0001t0001g0241 a0001c0001t0002g0170 |
3 | HG02698.hp2 HG03239.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.919+6433_919+6434i others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | |||||||
| chr6:10563775 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.919+6433_919+6434i others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | |||||||
| chr6:10563775 | A | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0093 others(73): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.919+6433A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563775 | |||||||
| chr6:10563775 | AAAATATA others(7): Show |
A | 3 | a0001c0001t0001g0088 a0001c0001t0004g0276 a0001c0001t0006g0001 |
4 | HG02258.hp1 HG02486.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+6435_919+6448d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563775 | ||||||
| chr6:10563776 | AAATATAT others(6): Show |
A | 1 | a0001c0001t0001g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.919+6436_919+6448d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563776 | ||||||
| chr6:10563777 | A | AAATATAT others(28): Show |
1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.919+6436_919+6437i others(37): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563777 | ||||||
| chr6:10563777 | A | AT | 5 | a0001c0001t0001g0095 a0001c0001t0001g0186 a0001c0001t0017g0192 others(2): Show |
5 | HG01361.hp2 HG02071.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+6435_919+6436i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563777 | |||||||
| chr6:10563777 | A | T | 136 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.919+6435A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563777 | |||||||
| chr6:10563777 | AATATATA others(5): Show |
A | 1 | a0001c0001t0001g0315 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.919+6456_919+6467d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10563777 | ||||||
| chr6:10563778 | AT | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0142 a0001c0001t0001g0152 others(1): Show |
4 | HG00621.hp2 HG01358.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+6437delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563778 | |||||||
| chr6:10563779 | T | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0180 a0001c0001t0001g0320 |
3 | HG01123.hp1 HG03516.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.919+6437T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563779 | |||||||
| chr6:10563781 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.919+6439T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563781 | |||||||
| chr6:10563899 | G | A | 2 | a0001c0001t0001g0340 a0001c0001t0002g0126 |
2 | NA18981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.919+6557G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563899 | |||||||
| chr6:10563981 | G | T | 1 | a0001c0001t0017g0192 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.919+6639G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10563981 | |||||||
| chr6:10564171 | T | C | 8 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0277 others(5): Show |
9 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+6829T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564171 | |||||||
| chr6:10564367 | T | C | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+7025T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564367 | |||||||
| chr6:10564440 | C | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0319 |
2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.919+7098C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564440 | |||||||
| chr6:10564453 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0319 |
2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.919+7111G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564453 | |||||||
| chr6:10564526 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0012g0244 |
3 | HG02258.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.919+7184G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564526 | |||||||
| chr6:10564642 | T | G | 2 | a0001c0001t0001g0316 a0003c0005t0001g0318 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.919+7300T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564642 | |||||||
| chr6:10564761 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919+7419G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10564761 | |||||||
| chr6:10565067 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0303 a0001c0001t0001g0305 others(3): Show |
7 | HG01109.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+7725G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565067 | |||||||
| chr6:10565104 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.919+7762A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565104 | |||||||
| chr6:10565123 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+7781A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565123 | |||||||
| chr6:10565170 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919+7828G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565170 | |||||||
| chr6:10565383 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0002g0191 |
2 | NA19084.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.919+8041A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565383 | |||||||
| chr6:10565383 | AAGGGAAA others(4): Show |
A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
101 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.919+8054_919+8064d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10565383 | ||||||
| chr6:10565564 | A | G | 2 | a0001c0001t0004g0269 a0001c0001t0015g0301 |
2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.919+8222A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565564 | |||||||
| chr6:10565708 | C | T | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
171 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.919+8366C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565708 | |||||||
| chr6:10565776 | C | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.919+8434C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565776 | |||||||
| chr6:10565845 | T | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0127 others(27): Show |
31 | HG00323.hp1 HG01109.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.919+8503T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565845 | |||||||
| chr6:10565898 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.919+8556C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565898 | |||||||
| chr6:10565959 | A | G | 5 | a0001c0001t0001g0268 a0001c0001t0001g0281 a0001c0001t0001g0310 others(2): Show |
5 | HG02976.hp1 HG03041.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+8617A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10565959 | |||||||
| chr6:10566052 | C | T | 6 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+8710C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566052 | |||||||
| chr6:10566053 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.919+8711G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566053 | |||||||
| chr6:10566074 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.919+8732G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566074 | |||||||
| chr6:10566089 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.919+8747C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566089 | |||||||
| chr6:10566110 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.919+8768G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566110 | |||||||
| chr6:10566141 | C | T | 15 | a0001c0001t0001g0096 a0001c0001t0001g0184 a0001c0001t0001g0266 others(12): Show |
15 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+8799C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566141 | |||||||
| chr6:10566258 | C | T | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(44): Show |
47 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.919+8916C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566258 | |||||||
| chr6:10566361 | C | A | 5 | a0001c0001t0001g0298 a0001c0001t0004g0275 a0001c0001t0004g0276 others(2): Show |
6 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+9019C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566361 | |||||||
| chr6:10566422 | C | T | 177 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(174): Show |
177 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.919+9080C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566422 | |||||||
| chr6:10566436 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.919+9094T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566436 | |||||||
| chr6:10566442 | T | G | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | NA18980.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.919+9100T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566442 | |||||||
| chr6:10566585 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.919+9243C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566585 | |||||||
| chr6:10566586 | G | A | 1 | a0001c0002t0001g0291 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.919+9244G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566586 | |||||||
| chr6:10566623 | T | A | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
187 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.919+9281T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566623 | |||||||
| chr6:10566713 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.919+9371G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566713 | |||||||
| chr6:10566798 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.919+9456C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566798 | |||||||
| chr6:10566882 | C | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(199): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.919+9540C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566882 | |||||||
| chr6:10566883 | C | T | 8 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0305 others(5): Show |
8 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+9541C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10566883 | |||||||
| chr6:10567055 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+9713A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567055 | |||||||
| chr6:10567172 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0133 others(5): Show |
8 | HG00597.hp2 HG00621.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+9830G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567172 | |||||||
| chr6:10567244 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.919+9902G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567244 | |||||||
| chr6:10567300 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.919+9958T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567300 | |||||||
| chr6:10567387 | A | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.919+10045A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567387 | |||||||
| chr6:10567679 | A | T | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.919+10337A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567679 | |||||||
| chr6:10567694 | C | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.919+10352C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567694 | |||||||
| chr6:10567821 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.919+10479A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10567821 | |||||||
| chr6:10568068 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+10726C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568068 | |||||||
| chr6:10568120 | T | G | 8 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0305 others(5): Show |
8 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+10778T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568120 | |||||||
| chr6:10568151 | C | T | 2 | a0001c0001t0001g0307 a0001c0001t0008g0334 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+10809C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568151 | |||||||
| chr6:10568219 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.919+10877T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568219 | |||||||
| chr6:10568313 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.919+10971T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568313 | |||||||
| chr6:10568414 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.919+11072A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568414 | |||||||
| chr6:10568598 | A | G | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+11256A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568598 | |||||||
| chr6:10568616 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.919+11274A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568616 | |||||||
| chr6:10568622 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.919+11280T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568622 | |||||||
| chr6:10568753 | C | A | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+11411C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568753 | |||||||
| chr6:10568765 | T | C | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.919+11423T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568765 | |||||||
| chr6:10568869 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.919+11527G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568869 | |||||||
| chr6:10568881 | A | G | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+11539A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568881 | |||||||
| chr6:10568929 | G | A | 199 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.919+11587G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10568929 | |||||||
| chr6:10569037 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0008g0334 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+11695G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569037 | |||||||
| chr6:10569129 | G | C | 178 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.919+11787G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569129 | |||||||
| chr6:10569156 | T | C | 3 | a0001c0001t0001g0274 a0001c0001t0001g0320 a0001c0001t0005g0325 |
3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.919+11814T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569156 | |||||||
| chr6:10569235 | C | CCA | 25 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0037 others(22): Show |
26 | HG00438.hp2 HG00673.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.919+11931_919+1193 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACA | 6 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0081 others(3): Show |
6 | HG00558.hp1 HG03209.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+11929_919+1193 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(1): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG00642.hp1 HG01123.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+11925_919+1193 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(3): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
6 | HG00639.hp1 HG00738.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+11923_919+1193 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(7): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0314 a0001c0001t0002g0098 |
3 | HG03041.hp2 HG06807.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.919+11919_919+1193 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(9): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0246 a0001c0001t0001g0251 |
3 | HG02080.hp1 HG02572.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.919+11917_919+1193 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(11): Show |
11 | a0001c0001t0001g0096 a0001c0001t0001g0120 a0001c0001t0001g0202 others(8): Show |
11 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+11915_919+1193 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(13): Show |
23 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0167 others(20): Show |
23 | HG00558.hp2 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.919+11913_919+1193 others(24): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(15): Show |
30 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0106 others(27): Show |
30 | HG00323.hp2 HG00621.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.919+11911_919+1193 others(26): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(17): Show |
19 | a0001c0001t0001g0044 a0001c0001t0001g0075 a0001c0001t0001g0119 others(16): Show |
19 | HG00408.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.919+11909_919+1193 others(28): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(19): Show |
14 | a0001c0001t0001g0016 a0001c0001t0001g0095 a0001c0001t0001g0152 others(11): Show |
14 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+11907_919+1193 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(21): Show |
16 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0122 others(13): Show |
16 | HG01346.hp1 HG01975.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+11905_919+1193 others(32): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(23): Show |
13 | a0001c0001t0001g0058 a0001c0001t0001g0103 a0001c0001t0001g0118 others(10): Show |
13 | HG00280.hp2 HG01074.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+11903_919+1193 others(34): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(25): Show |
16 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0093 others(13): Show |
16 | HG00597.hp2 HG01074.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+11901_919+1193 others(36): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(27): Show |
6 | a0001c0001t0001g0142 a0001c0001t0001g0205 a0001c0001t0001g0211 others(3): Show |
6 | HG00735.hp1 NA18968.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+11899_919+1193 others(38): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(29): Show |
9 | a0001c0001t0001g0028 a0001c0001t0001g0100 a0001c0001t0001g0141 others(6): Show |
9 | HG02155.hp2 HG02280.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+11897_919+1193 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(31): Show |
3 | a0001c0001t0001g0231 a0001c0001t0001g0253 a0001c0001t0001g0257 |
3 | HG02129.hp1 HG02273.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.919+11895_919+1193 others(42): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(33): Show |
3 | a0001c0001t0001g0193 a0001c0001t0002g0140 a0001c0002t0001g0292 |
3 | HG00140.hp1 HG01175.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(44): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(35): Show |
1 | a0001c0001t0002g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.919+11932_919+1193 others(46): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(37): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0188 |
2 | NA18956.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(48): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(39): Show |
1 | a0001c0001t0002g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(50): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | C | CCACACAC others(41): Show |
1 | a0001c0001t0001g0341 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(52): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | CCACA | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(7): Show |
10 | HG00408.hp1 HG01928.hp2 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+11929_919+1193 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | CCACACA | C | 8 | a0001c0001t0001g0074 a0001c0001t0001g0298 a0001c0001t0004g0275 others(5): Show |
9 | HG00741.hp1 HG01361.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+11927_919+1193 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569235 | CCACACAC others(3): Show |
C | 1 | a0001c0001t0008g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.919+11923_919+1193 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569235 | ||||||
| chr6:10569245 | A | ACACC | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+11906_919+1190 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569245 | ||||||
| chr6:10569271 | ACACC | A | 3 | a0001c0001t0001g0274 a0001c0001t0001g0320 a0001c0001t0005g0325 |
3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.919+11931_919+1193 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569271 | ||||||
| chr6:10569273 | A | ACACACAC others(23): Show |
1 | a0001c0001t0001g0261 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(34): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569273 | ||||||
| chr6:10569273 | A | ACACACAC others(7): Show |
1 | a0001c0001t0001g0315 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569273 | ||||||
| chr6:10569274 | C | CACACACA others(8): Show |
1 | a0001c0001t0001g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.919+11932_919+1193 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | |||||||
| chr6:10569274 | C | CACACACA others(18): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(29): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | |||||||
| chr6:10569274 | C | CACACACA others(20): Show |
1 | a0001c0001t0001g0173 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(31): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | |||||||
| chr6:10569274 | C | CACACACA others(22): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG03017.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.919+11932_919+1193 others(33): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | |||||||
| chr6:10569274 | C | CACACACA others(28): Show |
1 | a0001c0001t0001g0174 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(39): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | |||||||
| chr6:10569274 | C | CACACACA others(32): Show |
1 | a0001c0001t0001g0077 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.919+11932_919+1193 others(43): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | |||||||
| chr6:10569274 | C | CACACACA others(34): Show |
1 | a0001c0001t0001g0110 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.919+11932_919+1193 others(45): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569274 | |||||||
| chr6:10569275 | C | A | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.919+11933C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569275 | |||||||
| chr6:10569276 | C | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0110 a0001c0001t0001g0111 others(5): Show |
8 | HG02056.hp2 HG03017.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+11934C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569276 | |||||||
| chr6:10569290 | G | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0140 |
2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.919+11948G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569290 | |||||||
| chr6:10569466 | C | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0001t0001g0142 others(2): Show |
5 | HG00621.hp2 HG02080.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+12124C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569466 | |||||||
| chr6:10569531 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0029 others(17): Show |
20 | HG00597.hp2 HG00621.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.919+12189T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569531 | |||||||
| chr6:10569564 | T | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0310 others(4): Show |
7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12222T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569564 | |||||||
| chr6:10569571 | T | C | 14 | a0001c0001t0001g0119 a0001c0001t0001g0202 a0001c0001t0001g0203 others(11): Show |
14 | HG00741.hp2 HG01993.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+12229T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569571 | |||||||
| chr6:10569644 | C | A | 3 | a0001c0001t0001g0091 a0001c0001t0005g0046 a0001c0001t0007g0019 |
3 | HG02630.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.919+12302C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569644 | |||||||
| chr6:10569824 | T | TCTTC | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
176 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.919+12502_919+1250 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569824 | ||||||
| chr6:10569847 | T | TCCTTTCT others(5): Show |
7 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0310 others(4): Show |
7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12505_919+1250 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569847 | |||||||
| chr6:10569848 | T | C | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0149 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+12506T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569848 | |||||||
| chr6:10569849 | C | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0310 others(4): Show |
7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12507C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569849 | |||||||
| chr6:10569851 | C | T | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0149 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+12509C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569851 | |||||||
| chr6:10569853 | T | C | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0149 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+12511T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569853 | |||||||
| chr6:10569854 | T | C | 2 | a0001c0001t0001g0305 a0001c0001t0015g0301 |
2 | HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.919+12512T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569854 | |||||||
| chr6:10569861 | C | T | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0149 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+12519C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569861 | |||||||
| chr6:10569863 | T | C | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0149 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+12521T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569863 | |||||||
| chr6:10569865 | C | CTT | 7 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0310 others(4): Show |
7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12525_919+1252 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569865 | ||||||
| chr6:10569875 | TTC | T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0316 others(1): Show |
4 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+12537_919+1253 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569875 | ||||||
| chr6:10569877 | C | CCTT | 7 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0310 others(4): Show |
7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12535_919+1253 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569877 | |||||||
| chr6:10569878 | T | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0310 others(4): Show |
7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12536T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569878 | |||||||
| chr6:10569882 | T | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0274 a0001c0001t0001g0310 others(4): Show |
7 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12540T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569882 | |||||||
| chr6:10569885 | T | C | 1 | a0001c0002t0001g0279 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.919+12543T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569885 | |||||||
| chr6:10569887 | TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0001g0307 a0001c0001t0008g0334 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+12546_919+1255 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569887 | |||||||
| chr6:10569935 | T | C | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+12593T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569935 | |||||||
| chr6:10569947 | TCTTC | T | 188 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.919+12621_919+1262 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569947 | ||||||
| chr6:10569963 | CCTTT | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+12628_919+1263 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10569963 | ||||||
| chr6:10569991 | A | T | 6 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0217 others(3): Show |
6 | HG01516.hp2 HG01517.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+12649A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569991 | |||||||
| chr6:10569995 | A | G | 201 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.919+12653A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10569995 | |||||||
| chr6:10570135 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.919+12793A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570135 | |||||||
| chr6:10570176 | T | C | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.919+12834T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570176 | |||||||
| chr6:10570177 | C | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG01256.hp2 HG01258.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.919+12835C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570177 | |||||||
| chr6:10570312 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0312 a0001c0001t0008g0304 others(3): Show |
7 | HG01496.hp2 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+12970T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570312 | |||||||
| chr6:10570444 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.919+13102A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570444 | |||||||
| chr6:10570534 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.919+13192C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570534 | |||||||
| chr6:10570552 | C | T | 2 | a0001c0001t0003g0311 a0001c0001t0010g0308 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.919+13210C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570552 | |||||||
| chr6:10570785 | A | G | 4 | a0001c0001t0002g0117 a0001c0001t0002g0140 a0001c0001t0002g0237 others(1): Show |
4 | NA18980.hp1 NA18990.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+13443A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570785 | |||||||
| chr6:10570877 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0062 others(1): Show |
4 | HG01071.hp2 HG01346.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+13535T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570877 | |||||||
| chr6:10570895 | G | C | 203 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.919+13553G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570895 | |||||||
| chr6:10570909 | G | T | 6 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+13567G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10570909 | |||||||
| chr6:10571027 | A | G | 184 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.919+13685A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571027 | |||||||
| chr6:10571158 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919+13816A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571158 | |||||||
| chr6:10571186 | T | C | 1 | a0001c0001t0010g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919+13844T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571186 | |||||||
| chr6:10571259 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.919+13917A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571259 | |||||||
| chr6:10571326 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0214 |
2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.919+13984T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571326 | |||||||
| chr6:10571342 | AATT | A | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(7): Show |
10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+14016_919+1401 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10571342 | ||||||
| chr6:10571420 | C | T | 193 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(190): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.919+14078C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571420 | |||||||
| chr6:10571513 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.919+14171C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571513 | |||||||
| chr6:10571579 | C | G | 2 | a0001c0001t0002g0134 a0001c0001t0002g0136 |
2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.919+14237C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571579 | |||||||
| chr6:10571593 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+14251C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571593 | |||||||
| chr6:10571628 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 |
3 | NA18971.hp1 NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.919+14286C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571628 | |||||||
| chr6:10571639 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.919+14297C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571639 | |||||||
| chr6:10571643 | G | A | 1 | a0001c0001t0014g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+14301G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571643 | |||||||
| chr6:10571758 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.919+14416C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571758 | |||||||
| chr6:10571759 | G | A | 208 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(205): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.919+14417G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571759 | |||||||
| chr6:10571837 | G | A | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(7): Show |
10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+14495G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571837 | |||||||
| chr6:10571890 | C | T | 9 | a0001c0001t0001g0309 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+14548C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571890 | |||||||
| chr6:10571918 | A | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+14576A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10571918 | |||||||
| chr6:10571946 | C | CACTGATA others(38): Show |
3 | a0001c0001t0001g0091 a0001c0001t0005g0046 a0001c0001t0007g0019 |
3 | HG02630.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.919+14606_919+1465 others(49): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10571946 | ||||||
| chr6:10572087 | C | T | 9 | a0001c0001t0001g0309 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+14745C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572087 | |||||||
| chr6:10572225 | C | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0014g0330 |
3 | HG02622.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+14883C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572225 | |||||||
| chr6:10572332 | C | A | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0274 others(8): Show |
11 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+14990C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572332 | |||||||
| chr6:10572382 | C | G | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.919+15040C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572382 | |||||||
| chr6:10572452 | T | A | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0274 others(8): Show |
11 | HG00735.hp2 HG02630.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+15110T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572452 | |||||||
| chr6:10572452 | T | G | 188 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.919+15110T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572452 | |||||||
| chr6:10572459 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.919+15117C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572459 | |||||||
| chr6:10572496 | G | A | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0014g0330 |
3 | HG02622.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+15154G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572496 | |||||||
| chr6:10572514 | T | C | 208 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(205): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.919+15172T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572514 | |||||||
| chr6:10572548 | T | C | 12 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(9): Show |
13 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+15206T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572548 | |||||||
| chr6:10572606 | C | T | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(7): Show |
10 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+15264C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572606 | |||||||
| chr6:10572754 | A | G | 15 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(12): Show |
15 | HG01192.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+15412A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572754 | |||||||
| chr6:10572805 | C | T | 174 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(171): Show |
174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.919+15463C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572805 | |||||||
| chr6:10572962 | G | T | 206 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(203): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.919+15620G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10572962 | |||||||
| chr6:10573006 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+15664G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573006 | |||||||
| chr6:10573038 | G | T | 2 | a0001c0001t0004g0276 a0001c0001t0006g0001 |
3 | HG02258.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.919+15696G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573038 | |||||||
| chr6:10573168 | G | GATC | 188 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(185): Show |
189 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.919+15827_919+1582 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10573168 | ||||||
| chr6:10573192 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.919+15850C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573192 | |||||||
| chr6:10573211 | C | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+15869C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573211 | |||||||
| chr6:10573237 | C | A | 2 | a0001c0001t0003g0311 a0001c0001t0010g0308 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.919+15895C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573237 | |||||||
| chr6:10573318 | A | G | 1 | a0001c0001t0015g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.919+15976A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573318 | |||||||
| chr6:10573350 | A | ATTGTTG | 210 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(207): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.919+16014_919+1601 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10573350 | ||||||
| chr6:10573531 | C | A | 17 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(14): Show |
17 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+16189C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573531 | |||||||
| chr6:10573574 | A | T | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(9): Show |
12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+16232A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573574 | |||||||
| chr6:10573613 | A | G | 3 | a0001c0001t0001g0274 a0001c0001t0001g0320 a0001c0001t0005g0325 |
3 | HG00735.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.919+16271A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573613 | |||||||
| chr6:10573677 | A | G | 195 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.919+16335A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573677 | |||||||
| chr6:10573704 | T | C | 1 | a0001c0001t0014g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+16362T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573704 | |||||||
| chr6:10573720 | C | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+16378C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573720 | |||||||
| chr6:10573885 | C | A | 186 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(183): Show |
187 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.919+16543C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573885 | |||||||
| chr6:10573971 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0116 |
2 | NA19055.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.919+16629A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10573971 | |||||||
| chr6:10574079 | T | C | 186 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.919+16737T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574079 | |||||||
| chr6:10574099 | T | C | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+16757T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574099 | |||||||
| chr6:10574101 | T | C | 1 | a0001c0001t0015g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.919+16759T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574101 | |||||||
| chr6:10574111 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+16769G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574111 | |||||||
| chr6:10574164 | G | T | 195 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.919+16822G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574164 | |||||||
| chr6:10574215 | C | A | 189 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(186): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.919+16873C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574215 | |||||||
| chr6:10574229 | G | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0185 others(3): Show |
6 | HG00544.hp2 HG02155.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+16887G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574229 | |||||||
| chr6:10574343 | C | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+17001C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574343 | |||||||
| chr6:10574395 | G | T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0310 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.919+17053G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574395 | |||||||
| chr6:10574398 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0169 |
2 | NA18939.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.919+17056A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574398 | |||||||
| chr6:10574408 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0002g0230 |
2 | HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.919+17066A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574408 | |||||||
| chr6:10574489 | G | A | 9 | a0001c0001t0001g0298 a0001c0001t0004g0275 a0001c0001t0004g0276 others(6): Show |
10 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+17147G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574489 | |||||||
| chr6:10574570 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.919+17228C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574570 | |||||||
| chr6:10574673 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0008g0334 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+17331T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574673 | |||||||
| chr6:10574716 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.919+17374T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574716 | |||||||
| chr6:10574728 | AT | A | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+17395delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10574728 | ||||||
| chr6:10574787 | C | G | 10 | a0001c0001t0001g0096 a0001c0001t0001g0309 a0001c0001t0001g0313 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+17445C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574787 | |||||||
| chr6:10574791 | C | G | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17449C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574791 | |||||||
| chr6:10574796 | C | A | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17454C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574796 | |||||||
| chr6:10574797 | A | G | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17455A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574797 | |||||||
| chr6:10574799 | T | A | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17457T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574799 | |||||||
| chr6:10574802 | C | T | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17460C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574802 | |||||||
| chr6:10574808 | T | C | 14 | a0001c0001t0001g0096 a0001c0001t0001g0309 a0001c0001t0001g0313 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+17466T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574808 | |||||||
| chr6:10574810 | A | C | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17468A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574810 | |||||||
| chr6:10574813 | T | C | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17471T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574813 | |||||||
| chr6:10574814 | G | A | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17472G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574814 | |||||||
| chr6:10574815 | T | G | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17473T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574815 | |||||||
| chr6:10574816 | G | C | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17474G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574816 | |||||||
| chr6:10574819 | A | G | 1 | a0001c0001t0005g0302 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.919+17477A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574819 | |||||||
| chr6:10574861 | C | G | 1 | a0002c0003t0010g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.919+17519C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574861 | |||||||
| chr6:10574898 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.919+17556T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574898 | |||||||
| chr6:10574914 | G | C | 2 | a0001c0001t0001g0091 a0001c0001t0007g0019 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+17572G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574914 | |||||||
| chr6:10574991 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.919+17649C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10574991 | |||||||
| chr6:10575009 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.919+17667T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575009 | |||||||
| chr6:10575015 | C | T | 2 | a0001c0001t0004g0277 a0001c0002t0001g0282 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.919+17673C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575015 | |||||||
| chr6:10575113 | T | C | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(8): Show |
11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+17771T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575113 | |||||||
| chr6:10575142 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.919+17800G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575142 | |||||||
| chr6:10575261 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0132 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.919+17919T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575261 | |||||||
| chr6:10575307 | A | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+17965A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575307 | |||||||
| chr6:10575358 | A | AT | 6 | a0001c0001t0001g0048 a0001c0001t0001g0087 a0001c0001t0001g0207 others(3): Show |
6 | HG00438.hp2 HG04184.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+18035dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | ||||||
| chr6:10575358 | A | ATT | 7 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0023 others(4): Show |
7 | HG00408.hp1 HG01928.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+18034_919+1803 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | ||||||
| chr6:10575358 | A | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0151 others(2): Show |
5 | HG02040.hp2 NA18969.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+18016A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575358 | |||||||
| chr6:10575358 | AT | A | 19 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0149 others(16): Show |
20 | HG00280.hp2 HG00558.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.919+18035delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575358 | ||||||
| chr6:10575454 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.919+18112T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575454 | |||||||
| chr6:10575464 | A | G | 22 | a0001c0001t0001g0096 a0001c0001t0001g0184 a0001c0001t0001g0266 others(19): Show |
22 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.919+18122A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575464 | |||||||
| chr6:10575576 | G | A | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+18234G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575576 | |||||||
| chr6:10575672 | CT | C | 54 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(51): Show |
55 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.919+18333delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10575672 | ||||||
| chr6:10575762 | C | T | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(8): Show |
11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+18420C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575762 | |||||||
| chr6:10575908 | C | T | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+18566C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575908 | |||||||
| chr6:10575939 | C | CT | 24 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(21): Show |
25 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.919+18597_919+1859 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10575939 | |||||||
| chr6:10576076 | T | G | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(8): Show |
11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+18734T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576076 | |||||||
| chr6:10576089 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+18747C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576089 | |||||||
| chr6:10576090 | G | A | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+18748G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576090 | |||||||
| chr6:10576150 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.919+18808G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576150 | |||||||
| chr6:10576162 | G | A | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.919+18820G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576162 | |||||||
| chr6:10576254 | AAAG | A | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+18916_919+1891 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576254 | ||||||
| chr6:10576366 | A | G | 1 | a0001c0001t0014g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+19024A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576366 | |||||||
| chr6:10576401 | T | C | 26 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(23): Show |
27 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+19059T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576401 | |||||||
| chr6:10576451 | G | A | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19109G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576451 | |||||||
| chr6:10576471 | G | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19129G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576471 | |||||||
| chr6:10576479 | C | T | 8 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0151 others(5): Show |
8 | HG02040.hp2 NA18949.hp2 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+19137C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576479 | |||||||
| chr6:10576553 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.919+19211G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576553 | |||||||
| chr6:10576571 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+19229G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576571 | |||||||
| chr6:10576611 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+19269G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576611 | |||||||
| chr6:10576645 | A | G | 206 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.919+19303A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576645 | |||||||
| chr6:10576653 | T | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19311T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576653 | |||||||
| chr6:10576654 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+19312T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576654 | |||||||
| chr6:10576671 | CAGAA | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19333_919+1933 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576671 | ||||||
| chr6:10576675 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.919+19333A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576675 | |||||||
| chr6:10576697 | G | C | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0014g0330 |
3 | HG02622.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+19355G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576697 | |||||||
| chr6:10576707 | TAGAA | T | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+19370_919+1937 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576707 | ||||||
| chr6:10576730 | A | G | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19388A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576730 | |||||||
| chr6:10576796 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0003g0033 |
2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.919+19454G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576796 | |||||||
| chr6:10576804 | T | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+19462T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576804 | |||||||
| chr6:10576920 | CAATAAT | C | 12 | a0001c0001t0001g0149 a0001c0001t0001g0272 a0001c0001t0001g0273 others(9): Show |
13 | HG00280.hp2 HG01192.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+19593_919+1959 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10576920 | ||||||
| chr6:10576967 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.919+19625C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10576967 | |||||||
| chr6:10577014 | G | C | 15 | a0001c0001t0001g0096 a0001c0001t0001g0184 a0001c0001t0001g0309 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+19672G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577014 | |||||||
| chr6:10577140 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.919+19798C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577140 | |||||||
| chr6:10577155 | C | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19813C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577155 | |||||||
| chr6:10577231 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.919+19889G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577231 | |||||||
| chr6:10577304 | T | C | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+19962T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577304 | |||||||
| chr6:10577355 | C | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+20013C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577355 | |||||||
| chr6:10577394 | A | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20052A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577394 | |||||||
| chr6:10577589 | G | A | 1 | a0001c0001t0015g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.919+20247G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577589 | |||||||
| chr6:10577634 | G | C | 1 | a0001c0001t0001g0169 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.919+20292G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577634 | |||||||
| chr6:10577635 | G | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20293G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577635 | |||||||
| chr6:10577725 | G | A | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20383G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577725 | |||||||
| chr6:10577730 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0153 a0001c0001t0001g0162 |
3 | NA18951.hp2 NA18974.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.919+20388G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577730 | |||||||
| chr6:10577789 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.919+20447C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577789 | |||||||
| chr6:10577885 | TTCG | T | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+20545_919+2054 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10577885 | ||||||
| chr6:10577960 | C | T | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20618C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577960 | |||||||
| chr6:10577990 | G | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+20648G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10577990 | |||||||
| chr6:10578066 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.919+20724T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578066 | |||||||
| chr6:10578074 | A | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+20732A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578074 | |||||||
| chr6:10578167 | G | C | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+20825G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578167 | |||||||
| chr6:10578345 | C | G | 5 | a0001c0001t0001g0112 a0001c0001t0001g0340 a0001c0001t0001g0341 others(2): Show |
5 | HG00673.hp1 NA18981.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+21003C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578345 | |||||||
| chr6:10578391 | T | TA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0133 a0001c0001t0001g0309 others(8): Show |
11 | HG00597.hp2 HG02109.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+21065dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578391 | ||||||
| chr6:10578391 | TA | T | 28 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(25): Show |
29 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.919+21065delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578391 | ||||||
| chr6:10578445 | C | CT | 43 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0035 others(40): Show |
43 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.919+21124dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | ||||||
| chr6:10578445 | C | CTT | 24 | a0001c0001t0001g0096 a0001c0001t0001g0184 a0001c0001t0001g0266 others(21): Show |
24 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.919+21123_919+2112 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | ||||||
| chr6:10578445 | C | CTTT | 13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(10): Show |
13 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+21122_919+2112 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | ||||||
| chr6:10578445 | C | CTTTT | 7 | a0001c0001t0001g0091 a0001c0001t0001g0305 a0001c0001t0001g0307 others(4): Show |
7 | HG01175.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+21121_919+2112 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578445 | ||||||
| chr6:10578547 | T | C | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.919+21205T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578547 | |||||||
| chr6:10578548 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.919+21206G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578548 | |||||||
| chr6:10578592 | A | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21250A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578592 | |||||||
| chr6:10578634 | G | A | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21292G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578634 | |||||||
| chr6:10578648 | G | A | 10 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+21306G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578648 | |||||||
| chr6:10578692 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0008g0334 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+21350T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578692 | |||||||
| chr6:10578726 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0008g0334 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+21384G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578726 | |||||||
| chr6:10578746 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.919+21404C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578746 | |||||||
| chr6:10578759 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.919+21417C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578759 | |||||||
| chr6:10578778 | G | T | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21436G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578778 | |||||||
| chr6:10578787 | T | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+21445T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578787 | |||||||
| chr6:10578800 | A | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+21458A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578800 | |||||||
| chr6:10578821 | T | TTTGTTG | 2 | a0001c0001t0004g0276 a0001c0001t0006g0001 |
3 | HG02258.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.919+21491_919+2149 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10578821 | ||||||
| chr6:10578903 | G | A | 2 | a0001c0001t0001g0303 a0001c0001t0003g0300 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.919+21561G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578903 | |||||||
| chr6:10578991 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.919+21649G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10578991 | |||||||
| chr6:10579066 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+21724C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579066 | |||||||
| chr6:10579139 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.919+21797C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579139 | |||||||
| chr6:10579222 | C | T | 3 | a0001c0001t0015g0301 a0001c0004t0003g0327 a0001c0004t0003g0328 |
3 | HG03130.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.919+21880C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579222 | |||||||
| chr6:10579344 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.919+22002T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579344 | |||||||
| chr6:10579453 | C | T | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+22111C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579453 | |||||||
| chr6:10579611 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+22269C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579611 | |||||||
| chr6:10579643 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.919+22301C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579643 | |||||||
| chr6:10579730 | G | C | 335 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(332): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.919+22388G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579730 | |||||||
| chr6:10579731 | G | A | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+22389G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579731 | |||||||
| chr6:10579743 | A | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(10): Show |
14 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+22401A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579743 | |||||||
| chr6:10579757 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.919+22415A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579757 | |||||||
| chr6:10579780 | C | T | 6 | a0001c0001t0001g0253 a0001c0001t0001g0266 a0001c0001t0001g0267 others(3): Show |
6 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+22438C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579780 | |||||||
| chr6:10579803 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.919+22461G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579803 | |||||||
| chr6:10579826 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0235 |
2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.919+22484C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579826 | |||||||
| chr6:10579826 | C | CA | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.919+22506dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | ||||||
| chr6:10579826 | C | CAA | 24 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0029 others(21): Show |
24 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.919+22505_919+2250 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | ||||||
| chr6:10579826 | C | CAAACA | 9 | a0001c0001t0001g0309 a0001c0001t0001g0313 a0001c0001t0001g0314 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+22487_919+2248 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579826 | ||||||
| chr6:10579827 | A | AAAC | 23 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0184 others(20): Show |
23 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.919+22487_919+2248 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10579827 | ||||||
| chr6:10579829 | A | AC | 4 | a0001c0001t0001g0042 a0001c0001t0001g0127 a0001c0001t0001g0317 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+22487_919+2248 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579829 | |||||||
| chr6:10579829 | A | ACAAAC | 3 | a0001c0001t0001g0091 a0001c0001t0005g0046 a0001c0001t0007g0019 |
3 | HG02630.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.919+22487_919+2248 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579829 | |||||||
| chr6:10579830 | A | C | 11 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(8): Show |
12 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+22488A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579830 | |||||||
| chr6:10579831 | A | C | 5 | a0001c0001t0001g0184 a0001c0001t0001g0307 a0001c0001t0003g0311 others(2): Show |
5 | HG01243.hp1 NA19030.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+22489A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579831 | |||||||
| chr6:10579832 | A | C | 1 | a0001c0001t0014g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.919+22490A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579832 | |||||||
| chr6:10579834 | A | C | 11 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(8): Show |
12 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+22492A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579834 | |||||||
| chr6:10579835 | A | C | 3 | a0001c0001t0001g0305 a0001c0001t0001g0307 a0001c0001t0008g0334 |
3 | HG03579.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.919+22493A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579835 | |||||||
| chr6:10579837 | A | C | 2 | a0001c0001t0001g0303 a0001c0001t0003g0300 |
2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.919+22495A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579837 | |||||||
| chr6:10579839 | A | C | 2 | a0001c0001t0001g0317 a0001c0001t0001g0319 |
2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.919+22497A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579839 | |||||||
| chr6:10579840 | A | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+22498A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579840 | |||||||
| chr6:10579841 | A | ACC | 11 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0298 others(8): Show |
12 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+22499_919+2250 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579841 | |||||||
| chr6:10579841 | A | C | 36 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(33): Show |
36 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.919+22499A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579841 | |||||||
| chr6:10579886 | G | T | 15 | a0001c0001t0001g0092 a0001c0001t0001g0272 a0001c0001t0001g0273 others(12): Show |
16 | HG00735.hp2 HG01361.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+22544G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579886 | |||||||
| chr6:10579900 | A | G | 7 | a0001c0001t0001g0298 a0001c0001t0004g0275 a0001c0001t0004g0276 others(4): Show |
8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+22558A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10579900 | |||||||
| chr6:10580061 | C | T | 52 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(49): Show |
53 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.919+22719C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580061 | |||||||
| chr6:10580219 | A | G | 8 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0310 others(5): Show |
8 | HG02630.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+22877A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580219 | |||||||
| chr6:10580252 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+22910G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580252 | |||||||
| chr6:10580271 | A | G | 18 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0184 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+22929A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580271 | |||||||
| chr6:10580274 | G | GGGGGGT | 13 | a0001c0001t0001g0096 a0001c0001t0001g0184 a0001c0001t0001g0309 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+22935_919+2293 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10580274 | ||||||
| chr6:10580375 | C | T | 1 | a0003c0005t0001g0318 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.919+23033C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580375 | |||||||
| chr6:10580394 | A | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.919+23052A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580394 | |||||||
| chr6:10580435 | C | T | 48 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0096 others(45): Show |
49 | HG00735.hp2 HG01099.hp2 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.919+23093C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580435 | |||||||
| chr6:10580501 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.919+23159C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580501 | |||||||
| chr6:10580592 | G | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0316 others(1): Show |
4 | HG01192.hp1 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+23250G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580592 | |||||||
| chr6:10580615 | T | TA | 15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(12): Show |
15 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.919+23285dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10580615 | ||||||
| chr6:10580615 | TA | T | 10 | a0001c0001t0001g0111 a0001c0001t0001g0118 a0001c0001t0001g0146 others(7): Show |
10 | HG01175.hp2 HG01361.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+23285delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10580615 | ||||||
| chr6:10580668 | G | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+23326G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580668 | |||||||
| chr6:10580677 | T | G | 50 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(47): Show |
51 | HG00140.hp1 HG00735.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.919+23335T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580677 | |||||||
| chr6:10580723 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+23381C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580723 | |||||||
| chr6:10580840 | G | C | 17 | a0001c0001t0001g0268 a0001c0001t0001g0272 a0001c0001t0001g0273 others(14): Show |
18 | HG01192.hp1 HG01361.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+23498G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580840 | |||||||
| chr6:10580872 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.919+23530T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580872 | |||||||
| chr6:10580919 | G | C | 1 | a0001c0001t0001g0307 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.919+23577G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580919 | |||||||
| chr6:10580935 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.919+23593G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580935 | |||||||
| chr6:10580956 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+23614G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580956 | |||||||
| chr6:10580972 | A | G | 10 | a0001c0001t0001g0096 a0001c0001t0001g0309 a0001c0001t0001g0313 others(7): Show |
10 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+23630A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10580972 | |||||||
| chr6:10581064 | C | T | 7 | a0001c0001t0001g0298 a0001c0001t0004g0275 a0001c0001t0004g0276 others(4): Show |
8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+23722C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581064 | |||||||
| chr6:10581099 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+23757A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581099 | |||||||
| chr6:10581263 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.919+23921A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581263 | |||||||
| chr6:10581263 | ATTTATTT | A | 3 | a0001c0002t0001g0283 a0001c0002t0001g0293 a0001c0002t0001g0294 |
3 | HG01099.hp2 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.919+23939_919+2394 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581263 | ||||||
| chr6:10581291 | A | C | 7 | a0001c0001t0001g0298 a0001c0001t0004g0275 a0001c0001t0004g0276 others(4): Show |
8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+23949A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581291 | |||||||
| chr6:10581309 | T | C | 16 | a0001c0001t0001g0096 a0001c0001t0001g0184 a0001c0001t0001g0266 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.919+23967T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581309 | |||||||
| chr6:10581337 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.919+23995C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581337 | |||||||
| chr6:10581565 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24223C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581565 | |||||||
| chr6:10581727 | CA | C | 6 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG00544.hp1 HG00558.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+24388delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581727 | ||||||
| chr6:10581733 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.919+24391G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581733 | |||||||
| chr6:10581763 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24421G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581763 | |||||||
| chr6:10581793 | A | C | 1 | a0001c0001t0001g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.919+24451A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581793 | |||||||
| chr6:10581803 | T | G | 3 | a0001c0001t0015g0301 a0001c0004t0003g0327 a0001c0004t0003g0328 |
3 | HG03130.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.919+24461T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10581803 | |||||||
| chr6:10581931 | A | AGT | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24597_919+2459 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581931 | ||||||
| chr6:10581961 | AAT | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24631_919+2463 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10581961 | ||||||
| chr6:10582010 | G | GTA | 5 | a0001c0001t0001g0104 a0001c0001t0001g0143 a0001c0001t0001g0303 others(2): Show |
5 | HG02523.hp2 HG02896.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+24674_919+2467 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582010 | ||||||
| chr6:10582016 | ATG | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0186 a0001c0001t0001g0256 |
3 | HG01074.hp2 HG02155.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.919+24676_919+2467 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582016 | ||||||
| chr6:10582018 | G | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.919+24676G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582018 | |||||||
| chr6:10582043 | T | TATATATT others(3): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24705_919+2470 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582043 | ||||||
| chr6:10582059 | CAT | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24718_919+2471 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582059 | |||||||
| chr6:10582095 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0004g0269 a0001c0001t0005g0046 others(1): Show |
4 | HG02630.hp2 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+24753T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582095 | |||||||
| chr6:10582113 | T | TATAC | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24772_919+2477 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582113 | ||||||
| chr6:10582116 | A | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24774A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582116 | |||||||
| chr6:10582118 | A | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24776A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582118 | |||||||
| chr6:10582120 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24778C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582120 | |||||||
| chr6:10582125 | A | T | 36 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(33): Show |
36 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.919+24783A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582125 | |||||||
| chr6:10582172 | T | TTATATAA others(36): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24839_919+2484 others(47): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582172 | ||||||
| chr6:10582177 | T | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(11): Show |
14 | HG00408.hp1 HG01928.hp2 NA18946.hp1 others(11): Show |
intron_variant | MODIFIER | c.919+24835T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582177 | |||||||
| chr6:10582221 | ATTATATA others(1): Show |
A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24880_919+2488 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582221 | |||||||
| chr6:10582231 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24889T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582231 | |||||||
| chr6:10582231 | T | TTTAAATA others(29): Show |
1 | a0001c0001t0001g0066 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.919+24903_919+2493 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582231 | ||||||
| chr6:10582233 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24891T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582233 | |||||||
| chr6:10582241 | TAAAA | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24900_919+2490 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582241 | |||||||
| chr6:10582242 | A | AAAATATA others(28): Show |
10 | a0001c0001t0001g0051 a0001c0001t0001g0104 a0001c0001t0001g0298 others(7): Show |
11 | HG01346.hp2 HG01361.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+24916_919+2495 others(39): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582242 | ||||||
| chr6:10582277 | T | TA | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(8): Show |
11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+24938dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582277 | ||||||
| chr6:10582280 | A | ATATAT | 24 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0184 others(21): Show |
24 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.919+24939_919+2494 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582280 | ||||||
| chr6:10582285 | TATA | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24947_919+2494 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582285 | ||||||
| chr6:10582288 | A | AATATATA others(30): Show |
11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(8): Show |
11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+24950_919+2495 others(41): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582288 | ||||||
| chr6:10582289 | ATAT | A | 3 | a0001c0001t0015g0301 a0001c0004t0003g0327 a0001c0004t0003g0328 |
3 | HG03130.hp2 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.919+24950_919+2495 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582289 | ||||||
| chr6:10582292 | T | A | 1 | a0001c0001t0010g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919+24950T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582292 | |||||||
| chr6:10582303 | T | TTAATATA others(29): Show |
1 | a0001c0001t0002g0117 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.919+24998_919+2503 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582303 | ||||||
| chr6:10582303 | TTAATATA others(29): Show |
T | 17 | a0001c0001t0001g0096 a0001c0001t0001g0184 a0001c0001t0001g0266 others(14): Show |
17 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.919+24998_919+2503 others(40): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582303 | ||||||
| chr6:10582339 | A | ATATT | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+24999_919+2500 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582339 | ||||||
| chr6:10582346 | A | T | 2 | a0001c0001t0001g0091 a0001c0001t0007g0019 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25004A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582346 | |||||||
| chr6:10582351 | A | T | 2 | a0001c0001t0001g0091 a0001c0001t0007g0019 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25009A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582351 | |||||||
| chr6:10582359 | A | C | 2 | a0001c0001t0001g0091 a0001c0001t0007g0019 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25017A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582359 | |||||||
| chr6:10582367 | T | A | 2 | a0001c0001t0001g0091 a0001c0001t0007g0019 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25025T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582367 | |||||||
| chr6:10582371 | C | G | 2 | a0001c0001t0001g0091 a0001c0001t0007g0019 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+25029C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582371 | |||||||
| chr6:10582373 | ATAATT | A | 16 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(13): Show |
16 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.919+25036_919+2504 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582373 | ||||||
| chr6:10582375 | A | AT | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25033_919+2503 others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582375 | |||||||
| chr6:10582378 | T | TTAATATT others(24): Show |
4 | a0001c0001t0001g0224 a0001c0001t0001g0281 a0001c0001t0002g0126 others(1): Show |
4 | HG02922.hp2 HG02976.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+25060_919+2509 others(35): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582378 | ||||||
| chr6:10582378 | T | TTAATATT others(86): Show |
7 | a0001c0001t0001g0298 a0001c0001t0004g0275 a0001c0001t0004g0276 others(4): Show |
8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+25090_919+2509 others(97): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582378 | ||||||
| chr6:10582385 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25043T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582385 | |||||||
| chr6:10582388 | T | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25046T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582388 | |||||||
| chr6:10582390 | ATATACT | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25049_919+2505 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582390 | |||||||
| chr6:10582400 | A | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25058A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582400 | |||||||
| chr6:10582406 | AGTATAAT others(3): Show |
A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25065_919+2507 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582406 | |||||||
| chr6:10582419 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25077T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582419 | |||||||
| chr6:10582426 | CTATAAT | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25086_919+2509 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582426 | ||||||
| chr6:10582438 | A | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25096A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582438 | |||||||
| chr6:10582441 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25099T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582441 | |||||||
| chr6:10582443 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25101T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582443 | |||||||
| chr6:10582453 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25111T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582453 | |||||||
| chr6:10582456 | A | G | 1 | a0001c0001t0002g0117 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.919+25114A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582456 | |||||||
| chr6:10582456 | ATAATAAA others(1): Show |
A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25115_919+2512 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582456 | |||||||
| chr6:10582462 | A | T | 1 | a0001c0001t0003g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.919+25120A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582462 | |||||||
| chr6:10582463 | ATATAATA others(5): Show |
A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0246 a0001c0001t0001g0268 others(2): Show |
5 | HG00544.hp2 HG02698.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+25145_919+2515 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582463 | ||||||
| chr6:10582466 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25124T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582466 | |||||||
| chr6:10582475 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25133C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582475 | |||||||
| chr6:10582480 | A | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25138A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582480 | |||||||
| chr6:10582481 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25139T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582481 | |||||||
| chr6:10582481 | TATATACT others(10): Show |
T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+25145_919+2516 others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582481 | ||||||
| chr6:10582482 | ATATAC | A | 22 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0184 others(19): Show |
22 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.919+25145_919+2514 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582482 | ||||||
| chr6:10582486 | AC | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25145delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582486 | |||||||
| chr6:10582487 | C | A | 19 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(16): Show |
20 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+25145C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582487 | |||||||
| chr6:10582491 | A | AATACATC | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25152_919+2515 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582491 | ||||||
| chr6:10582498 | A | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25156A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582498 | |||||||
| chr6:10582501 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+25159A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582501 | |||||||
| chr6:10582503 | A | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25161A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582503 | |||||||
| chr6:10582519 | T | TAC | 10 | a0001c0001t0001g0092 a0001c0001t0001g0298 a0001c0001t0001g0317 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+25178_919+2517 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582519 | ||||||
| chr6:10582522 | T | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25180T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582522 | |||||||
| chr6:10582522 | T | C | 10 | a0001c0001t0001g0092 a0001c0001t0001g0298 a0001c0001t0001g0317 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+25180T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582522 | |||||||
| chr6:10582526 | C | T | 19 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(16): Show |
20 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+25184C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582526 | |||||||
| chr6:10582528 | TCA | T | 10 | a0001c0001t0001g0092 a0001c0001t0001g0298 a0001c0001t0001g0317 others(7): Show |
11 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+25187_919+2518 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582528 | |||||||
| chr6:10582531 | T | TATATAAT others(14): Show |
9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25193_919+2519 others(25): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582531 | ||||||
| chr6:10582536 | T | A | 21 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(18): Show |
22 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.919+25194T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582536 | |||||||
| chr6:10582536 | T | TATATA | 26 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0184 others(23): Show |
26 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.919+25195_919+2519 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582536 | ||||||
| chr6:10582546 | G | A | 49 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(46): Show |
50 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.919+25204G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582546 | |||||||
| chr6:10582550 | A | T | 2 | a0001c0001t0001g0320 a0001c0001t0005g0325 |
2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919+25208A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582550 | |||||||
| chr6:10582552 | T | TATA | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25211_919+2521 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582552 | ||||||
| chr6:10582572 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0121 others(6): Show |
9 | HG02040.hp2 NA18949.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+25230A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582572 | |||||||
| chr6:10582583 | C | T | 4 | a0001c0001t0001g0303 a0001c0001t0003g0300 a0001c0001t0008g0334 others(1): Show |
4 | HG02896.hp2 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+25241C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582583 | |||||||
| chr6:10582613 | A | AAT | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+25280_919+2528 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582613 | ||||||
| chr6:10582617 | T | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0034 others(16): Show |
20 | HG00323.hp1 HG00558.hp1 HG03490.hp2 others(17): Show |
intron_variant | MODIFIER | c.919+25275T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582617 | |||||||
| chr6:10582624 | T | A | 189 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(186): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.919+25282T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582624 | |||||||
| chr6:10582721 | C | CT | 7 | a0001c0001t0001g0084 a0001c0001t0001g0211 a0001c0001t0001g0213 others(4): Show |
7 | HG00735.hp2 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+25388dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582721 | ||||||
| chr6:10582730 | TC | T | 33 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(30): Show |
33 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.919+25390delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582730 | ||||||
| chr6:10582770 | G | C | 19 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(16): Show |
19 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.919+25428G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582770 | |||||||
| chr6:10582804 | AAAC | A | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(44): Show |
48 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.919+25477_919+2547 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10582804 | ||||||
| chr6:10582897 | A | G | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(8): Show |
11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+25555A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10582897 | |||||||
| chr6:10583009 | G | T | 1 | a0001c0001t0001g0274 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.919+25667G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583009 | |||||||
| chr6:10583112 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0001g0219 |
3 | NA18951.hp1 NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.919+25770G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583112 | |||||||
| chr6:10583229 | C | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+25887C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583229 | |||||||
| chr6:10583268 | A | C | 8 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0004g0275 others(5): Show |
9 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+25926A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583268 | |||||||
| chr6:10583356 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.919+26014C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583356 | |||||||
| chr6:10583370 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+26028G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583370 | |||||||
| chr6:10583432 | C | T | 1 | a0001c0001t0004g0269 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.919+26090C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583432 | |||||||
| chr6:10583468 | C | T | 2 | a0001c0001t0001g0316 a0003c0005t0001g0318 |
2 | HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.919+26126C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583468 | |||||||
| chr6:10583492 | T | C | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(9): Show |
12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+26150T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583492 | |||||||
| chr6:10583543 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+26201G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583543 | |||||||
| chr6:10583868 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+26526C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583868 | |||||||
| chr6:10583922 | A | G | 21 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0096 others(18): Show |
21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+26580A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583922 | |||||||
| chr6:10583943 | C | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+26601C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583943 | |||||||
| chr6:10583960 | G | C | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0096 others(25): Show |
29 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.919+26618G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583960 | |||||||
| chr6:10583991 | A | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.919+26649A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10583991 | |||||||
| chr6:10584047 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+26705G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584047 | |||||||
| chr6:10584084 | T | C | 28 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0096 others(25): Show |
29 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.919+26742T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584084 | |||||||
| chr6:10584113 | C | T | 9 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0004g0275 others(6): Show |
10 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.919+26771C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584113 | |||||||
| chr6:10584129 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.919+26787C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584129 | |||||||
| chr6:10584170 | A | C | 2 | a0001c0001t0001g0320 a0001c0001t0005g0325 |
2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919+26828A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584170 | |||||||
| chr6:10584211 | A | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0188 |
2 | NA18956.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.919+26869A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584211 | |||||||
| chr6:10584232 | A | C | 18 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0141 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+26890A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584232 | |||||||
| chr6:10584234 | T | C | 8 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0004g0275 others(5): Show |
9 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+26892T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584234 | |||||||
| chr6:10584438 | G | A | 145 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(142): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.919+27096G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584438 | |||||||
| chr6:10584624 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+27282G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584624 | |||||||
| chr6:10584673 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+27331C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584673 | |||||||
| chr6:10584735 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.919+27393C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584735 | |||||||
| chr6:10584917 | C | T | 47 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(44): Show |
48 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.919+27575C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584917 | |||||||
| chr6:10584956 | G | C | 198 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(195): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.919+27614G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584956 | |||||||
| chr6:10584977 | T | C | 39 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(36): Show |
40 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.919+27635T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10584977 | |||||||
| chr6:10585028 | AGTCAGTG others(3): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.919+27689_919+2769 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | ||||||
| chr6:10585028 | AGTCAGTG others(9): Show |
A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0309 a0001c0001t0001g0313 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+27689_919+2770 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | ||||||
| chr6:10585028 | AGTCAGTG others(11): Show |
A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0307 |
2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.919+27689_919+2770 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585028 | ||||||
| chr6:10585032 | A | AGT | 8 | a0001c0001t0001g0088 a0001c0001t0001g0180 a0001c0001t0001g0200 others(5): Show |
8 | HG00735.hp1 HG01123.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.919+27736_919+2773 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | A | AGTGT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0138 others(6): Show |
9 | HG01243.hp2 HG03017.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+27734_919+2773 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | AGT | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.919+27736_919+2773 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | AGTGT | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0061 others(54): Show |
58 | HG00323.hp2 HG00544.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.919+27734_919+2773 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | AGTGTGT | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(19): Show |
22 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.919+27732_919+2773 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.919+27728_919+2773 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | AGTGTGTG others(7): Show |
A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0320 others(1): Show |
4 | HG00735.hp2 HG03516.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+27724_919+2773 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0002g0190 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.919+27722_919+2773 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585032 | AGTGTGTG others(11): Show |
A | 4 | a0001c0001t0001g0121 a0001c0001t0001g0303 a0001c0001t0003g0300 others(1): Show |
4 | HG02896.hp2 HG06807.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+27720_919+2773 others(22): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585032 | ||||||
| chr6:10585052 | TGTGTGTG others(21): Show |
T | 8 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0004g0275 others(5): Show |
9 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.919+27712_919+2773 others(32): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585052 | ||||||
| chr6:10585064 | TGTGTGTG others(9): Show |
T | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0310 |
3 | HG02109.hp2 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.919+27724_919+2773 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585064 | ||||||
| chr6:10585066 | TGTGTGTG others(7): Show |
T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0004t0003g0327 others(1): Show |
4 | HG02622.hp1 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+27726_919+2773 others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585066 | ||||||
| chr6:10585066 | TGTGTGTG others(9): Show |
T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+27726_919+2774 others(20): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585066 | ||||||
| chr6:10585068 | TGTGTGTG others(5): Show |
T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+27728_919+2773 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585068 | ||||||
| chr6:10585070 | TGTGTGTG others(3): Show |
T | 3 | a0001c0001t0001g0268 a0001c0001t0003g0239 a0001c0001t0014g0330 |
3 | HG01358.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.919+27730_919+2773 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585070 | ||||||
| chr6:10585074 | TGTGTGC | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0161 a0001c0001t0001g0260 |
3 | HG02273.hp1 HG02293.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.919+27734_919+2773 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585074 | ||||||
| chr6:10585076 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0002g0027 |
2 | HG01928.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.919+27734T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585076 | |||||||
| chr6:10585078 | T | C | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(37): Show |
40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.919+27736T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585078 | |||||||
| chr6:10585078 | TGC | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0002g0225 |
3 | HG01516.hp2 HG01517.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.919+27741_919+2774 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585078 | ||||||
| chr6:10585078 | TGCGC | T | 18 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0141 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+27739_919+2774 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10585078 | ||||||
| chr6:10585081 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.919+27739G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585081 | |||||||
| chr6:10585083 | G | A | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(9): Show |
12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+27741G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585083 | |||||||
| chr6:10585162 | T | A | 21 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0096 others(18): Show |
21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+27820T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585162 | |||||||
| chr6:10585193 | G | T | 21 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0096 others(18): Show |
21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+27851G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585193 | |||||||
| chr6:10585261 | C | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+27919C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585261 | |||||||
| chr6:10585368 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.919+28026G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585368 | |||||||
| chr6:10585419 | G | T | 2 | a0001c0001t0001g0148 a0001c0001t0002g0230 |
2 | HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.919+28077G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585419 | |||||||
| chr6:10585443 | G | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0167 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.919+28101G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585443 | |||||||
| chr6:10585471 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.919+28129C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585471 | |||||||
| chr6:10585618 | C | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+28276C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585618 | |||||||
| chr6:10585619 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0007g0019 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.919+28277G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585619 | |||||||
| chr6:10585747 | A | G | 21 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0096 others(18): Show |
21 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.919+28405A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585747 | |||||||
| chr6:10585773 | A | C | 51 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(48): Show |
52 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.919+28431A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585773 | |||||||
| chr6:10585874 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.919+28532C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585874 | |||||||
| chr6:10585878 | C | T | 2 | a0001c0001t0001g0320 a0001c0001t0005g0325 |
2 | HG00735.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.919+28536C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585878 | |||||||
| chr6:10585879 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.919+28537G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585879 | |||||||
| chr6:10585880 | G | A | 18 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0141 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.919+28538G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10585880 | |||||||
| chr6:10586199 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.919+28857A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586199 | |||||||
| chr6:10586378 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0140 |
2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.919+29036A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586378 | |||||||
| chr6:10586386 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0002g0249 |
2 | HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.919+29044C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586386 | |||||||
| chr6:10586494 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919+29152G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586494 | |||||||
| chr6:10586696 | A | G | 7 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0004g0275 others(4): Show |
8 | HG01361.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+29354A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586696 | |||||||
| chr6:10586805 | C | G | 328 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(325): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.919+29463C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586805 | |||||||
| chr6:10586823 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+29481A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10586823 | |||||||
| chr6:10587120 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0152 |
2 | HG00621.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.919+29778G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587120 | |||||||
| chr6:10587156 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.919+29814A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587156 | |||||||
| chr6:10587188 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0055 others(10): Show |
13 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+29846G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587188 | |||||||
| chr6:10587280 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.919+29938C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587280 | |||||||
| chr6:10587416 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(10): Show |
13 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.919+30074C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587416 | |||||||
| chr6:10587463 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0313 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.919+30121T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587463 | |||||||
| chr6:10587603 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.919+30261A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587603 | |||||||
| chr6:10587781 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0268 a0001c0001t0001g0297 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+30439T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587781 | |||||||
| chr6:10587857 | A | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0259 |
2 | HG00438.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.919+30515A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10587857 | |||||||
| chr6:10588199 | A | C | 1 | a0001c0001t0002g0056 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.919+30857A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588199 | |||||||
| chr6:10588237 | T | C | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(8): Show |
11 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+30895T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588237 | |||||||
| chr6:10588288 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.919+30946A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588288 | |||||||
| chr6:10588374 | TC | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+31034delC | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588374 | ||||||
| chr6:10588397 | C | T | 1 | a0001c0002t0001g0292 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.919+31055C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588397 | |||||||
| chr6:10588710 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.919+31368G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588710 | |||||||
| chr6:10588713 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0307 a0001c0001t0001g0314 others(7): Show |
11 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+31371A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588713 | |||||||
| chr6:10588785 | A | ATG | 4 | a0001c0001t0009g0047 a0001c0001t0009g0247 a0001c0001t0010g0308 others(1): Show |
4 | HG01081.hp1 HG01978.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+31466_919+3146 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | ||||||
| chr6:10588785 | ATG | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(171): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.919+31466_919+3146 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | ||||||
| chr6:10588785 | ATGTG | A | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0133 others(8): Show |
11 | HG00140.hp1 HG00597.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.919+31464_919+3146 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588785 | ||||||
| chr6:10588831 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.919+31489A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588831 | |||||||
| chr6:10588831 | ATGTGTGT others(4): Show |
A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+31504_919+3151 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588831 | ||||||
| chr6:10588890 | C | CGTGTGTG others(4): Show |
195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(192): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.919+31552_919+3156 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10588890 | ||||||
| chr6:10588925 | G | T | 2 | a0001c0001t0002g0237 a0001c0001t0002g0238 |
2 | NA18980.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.919+31583G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588925 | |||||||
| chr6:10588983 | T | C | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.919+31641T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10588983 | |||||||
| chr6:10589078 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0171 |
3 | HG02280.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.919+31736G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589078 | |||||||
| chr6:10589102 | AGT | A | 161 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(158): Show |
161 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.919+31770_919+3177 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589102 | ||||||
| chr6:10589113 | GGT | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 |
3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.919+31780_919+3178 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589113 | ||||||
| chr6:10589156 | GTGCGTGT others(26): Show |
G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+31817_919+3184 others(37): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589156 | ||||||
| chr6:10589188 | C | G | 330 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
333 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.919+31846C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589188 | |||||||
| chr6:10589292 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.919+31950G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589292 | |||||||
| chr6:10589306 | GGTGTGTT others(51): Show |
G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+31987_920-3196 others(62): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589306 | ||||||
| chr6:10589398 | G | C | 1 | a0001c0001t0001g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.920-31953G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589398 | |||||||
| chr6:10589421 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-31930T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589421 | |||||||
| chr6:10589425 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.920-31926T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589425 | |||||||
| chr6:10589469 | G | C | 1 | a0001c0001t0005g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.920-31882G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589469 | |||||||
| chr6:10589786 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.920-31565T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10589786 | |||||||
| chr6:10589808 | TATACTC | T | 3 | a0001c0001t0001g0320 a0001c0001t0004g0276 a0001c0001t0012g0244 |
3 | HG02970.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.920-31541_920-3153 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10589808 | ||||||
| chr6:10590086 | T | C | 1 | a0001c0001t0010g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920-31265T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590086 | |||||||
| chr6:10590242 | T | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-31109T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590242 | |||||||
| chr6:10590362 | C | T | 7 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0105 others(4): Show |
7 | HG02080.hp2 HG02155.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-30989C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590362 | |||||||
| chr6:10590397 | C | CA | 33 | a0001c0001t0001g0023 a0001c0001t0001g0059 a0001c0001t0001g0074 others(30): Show |
33 | HG00140.hp1 HG00408.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.920-30938dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10590397 | ||||||
| chr6:10590559 | A | AT | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.920-30779dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10590559 | ||||||
| chr6:10590673 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.920-30678C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590673 | |||||||
| chr6:10590711 | G | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-30640G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590711 | |||||||
| chr6:10590798 | C | T | 147 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0011 others(144): Show |
147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.920-30553C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590798 | |||||||
| chr6:10590848 | G | A | 150 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
150 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.920-30503G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590848 | |||||||
| chr6:10590918 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-30433G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10590918 | |||||||
| chr6:10591101 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.920-30250C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591101 | |||||||
| chr6:10591278 | A | T | 1 | a0001c0001t0001g0154 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.920-30073A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591278 | |||||||
| chr6:10591293 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.920-30058C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591293 | |||||||
| chr6:10591396 | C | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-29955C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591396 | |||||||
| chr6:10591469 | T | G | 22 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0184 others(19): Show |
22 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-29882T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591469 | |||||||
| chr6:10591598 | G | T | 1 | a0001c0001t0002g0170 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.920-29753G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591598 | |||||||
| chr6:10591732 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.920-29619T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591732 | |||||||
| chr6:10591762 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.920-29589A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591762 | |||||||
| chr6:10591901 | C | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-29450C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591901 | |||||||
| chr6:10591928 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.920-29423A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10591928 | |||||||
| chr6:10592095 | A | AAACGTCA others(8): Show |
9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-29255_920-2924 others(19): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10592095 | ||||||
| chr6:10592113 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.920-29238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592113 | |||||||
| chr6:10592162 | A | G | 31 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(28): Show |
31 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.920-29189A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592162 | |||||||
| chr6:10592571 | G | C | 1 | a0001c0001t0001g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.920-28780G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592571 | |||||||
| chr6:10592753 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.920-28598A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592753 | |||||||
| chr6:10592922 | T | C | 3 | a0001c0001t0001g0309 a0001c0001t0005g0046 a0001c0001t0015g0301 |
3 | HG02622.hp2 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.920-28429T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10592922 | |||||||
| chr6:10593018 | G | A | 8 | a0001c0001t0001g0297 a0001c0001t0001g0307 a0001c0001t0001g0322 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-28333G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593018 | |||||||
| chr6:10593033 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28318G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593033 | |||||||
| chr6:10593051 | G | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28300G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593051 | |||||||
| chr6:10593226 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28125G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593226 | |||||||
| chr6:10593230 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.920-28121T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593230 | |||||||
| chr6:10593250 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.920-28101C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593250 | |||||||
| chr6:10593346 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-28005G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593346 | |||||||
| chr6:10593383 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
198 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.920-27968A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593383 | |||||||
| chr6:10593417 | A | C | 1 | a0001c0001t0010g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920-27934A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593417 | |||||||
| chr6:10593525 | A | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27826A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593525 | |||||||
| chr6:10593534 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.920-27817C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593534 | |||||||
| chr6:10593568 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920-27783G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593568 | |||||||
| chr6:10593595 | T | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27756T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593595 | |||||||
| chr6:10593670 | T | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27681T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593670 | |||||||
| chr6:10593730 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27621A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593730 | |||||||
| chr6:10593776 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.920-27575G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593776 | |||||||
| chr6:10593864 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG00408.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.920-27487G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593864 | |||||||
| chr6:10593877 | C | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27474C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593877 | |||||||
| chr6:10593885 | C | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27466C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593885 | |||||||
| chr6:10593902 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.920-27449G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10593902 | |||||||
| chr6:10594027 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-27324G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594027 | |||||||
| chr6:10594249 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.920-27102G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594249 | |||||||
| chr6:10594513 | T | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-26838T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594513 | |||||||
| chr6:10594575 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 |
3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-26776G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594575 | |||||||
| chr6:10594615 | G | C | 1 | a0001c0001t0001g0016 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.920-26736G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594615 | |||||||
| chr6:10594647 | T | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26704T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594647 | |||||||
| chr6:10594685 | C | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0272 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-26666C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594685 | |||||||
| chr6:10594832 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26519G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594832 | |||||||
| chr6:10594852 | C | CTT | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26490_920-2648 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10594852 | ||||||
| chr6:10594889 | A | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 |
3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-26462A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10594889 | |||||||
| chr6:10594940 | GGCTCAA | G | 8 | a0001c0001t0001g0297 a0001c0001t0001g0307 a0001c0001t0001g0322 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-26408_920-2640 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10594940 | ||||||
| chr6:10595266 | C | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-26085C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595266 | |||||||
| chr6:10595427 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.920-25924G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595427 | |||||||
| chr6:10595558 | T | TGA | 35 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0092 others(32): Show |
35 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-25792_920-2579 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10595558 | ||||||
| chr6:10595558 | T | TGC | 4 | a0001c0001t0001g0184 a0001c0001t0001g0317 a0001c0001t0001g0319 others(1): Show |
4 | HG01243.hp1 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-25792_920-2579 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10595558 | ||||||
| chr6:10595565 | C | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25786C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595565 | |||||||
| chr6:10595592 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.920-25759T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595592 | |||||||
| chr6:10595606 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0002g0139 |
2 | NA18968.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.920-25745G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595606 | |||||||
| chr6:10595672 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 |
3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-25679C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595672 | |||||||
| chr6:10595681 | G | GA | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25662dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10595681 | ||||||
| chr6:10595759 | T | G | 1 | a0001c0001t0001g0059 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.920-25592T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595759 | |||||||
| chr6:10595773 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.920-25578G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595773 | |||||||
| chr6:10595804 | G | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25547G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595804 | |||||||
| chr6:10595850 | A | G | 4 | a0001c0001t0001g0303 a0001c0001t0003g0300 a0001c0001t0008g0304 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-25501A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595850 | |||||||
| chr6:10595940 | A | G | 4 | a0001c0001t0001g0303 a0001c0001t0003g0300 a0001c0001t0008g0304 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-25411A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595940 | |||||||
| chr6:10595949 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0022 others(7): Show |
10 | HG00408.hp1 HG02300.hp2 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.920-25402G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595949 | |||||||
| chr6:10595990 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25361A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10595990 | |||||||
| chr6:10596114 | C | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-25237C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596114 | |||||||
| chr6:10596281 | T | C | 3 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0210 |
3 | NA18971.hp1 NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.920-25070T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596281 | |||||||
| chr6:10596320 | A | G | 107 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0032 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.920-25031A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596320 | |||||||
| chr6:10596373 | T | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.920-24978T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596373 | |||||||
| chr6:10596387 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
189 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.920-24964G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596387 | |||||||
| chr6:10596453 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920-24898G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596453 | |||||||
| chr6:10596504 | G | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24847G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596504 | |||||||
| chr6:10596520 | C | CA | 16 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(13): Show |
16 | HG00140.hp1 HG00323.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.920-24819dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10596520 | ||||||
| chr6:10596555 | G | A | 9 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0307 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24796G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596555 | |||||||
| chr6:10596669 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0214 |
2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.920-24682C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596669 | |||||||
| chr6:10596734 | T | TA | 11 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0077 others(8): Show |
12 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-24605dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10596734 | ||||||
| chr6:10596799 | CCTTCAGC others(5): Show |
C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24549_920-2453 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10596799 | ||||||
| chr6:10596897 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-24454A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596897 | |||||||
| chr6:10596997 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.920-24354T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10596997 | |||||||
| chr6:10597153 | C | CT | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.920-24178dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | ||||||
| chr6:10597153 | C | CTT | 15 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
15 | HG01070.hp2 HG01175.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-24179_920-2417 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | ||||||
| chr6:10597153 | CT | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0092 others(25): Show |
29 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.920-24178delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597153 | ||||||
| chr6:10597386 | C | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-23965C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597386 | |||||||
| chr6:10597447 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0132 a0001c0001t0001g0171 |
3 | HG02572.hp2 HG02615.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.920-23904G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597447 | |||||||
| chr6:10597613 | T | TTTG | 15 | a0001c0001t0001g0184 a0001c0001t0001g0266 a0001c0001t0001g0267 others(12): Show |
15 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-23723_920-2372 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597613 | ||||||
| chr6:10597672 | G | A | 1 | a0001c0001t0004g0277 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.920-23679G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597672 | |||||||
| chr6:10597700 | A | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-23651A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597700 | |||||||
| chr6:10597715 | T | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-23636T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597715 | |||||||
| chr6:10597842 | C | T | 2 | a0001c0001t0002g0057 a0004c0008t0001g0041 |
2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.920-23509C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597842 | |||||||
| chr6:10597853 | T | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
179 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.920-23498T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597853 | |||||||
| chr6:10597903 | C | A | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-23448C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10597903 | |||||||
| chr6:10597920 | CT | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0068 a0001c0001t0001g0088 others(3): Show |
6 | HG01975.hp2 HG02896.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-23424delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10597920 | ||||||
| chr6:10598102 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.920-23249G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598102 | |||||||
| chr6:10598109 | C | T | 1 | a0001c0001t0003g0300 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.920-23242C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598109 | |||||||
| chr6:10598404 | G | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22947G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598404 | |||||||
| chr6:10598620 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-22731A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598620 | |||||||
| chr6:10598636 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.920-22715C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598636 | |||||||
| chr6:10598672 | C | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22679C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598672 | |||||||
| chr6:10598865 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22486G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598865 | |||||||
| chr6:10598966 | T | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22385T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598966 | |||||||
| chr6:10598973 | G | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.920-22378G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10598973 | |||||||
| chr6:10599046 | T | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22305T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599046 | |||||||
| chr6:10599065 | C | G | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22286C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599065 | |||||||
| chr6:10599087 | G | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0189 others(6): Show |
9 | HG00140.hp1 HG01099.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-22264G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599087 | |||||||
| chr6:10599089 | C | T | 1 | a0001c0002t0003g0286 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.920-22262C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599089 | |||||||
| chr6:10599238 | G | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.920-22113G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599238 | |||||||
| chr6:10599263 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(171): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.920-22088C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599263 | |||||||
| chr6:10599280 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.920-22071A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599280 | |||||||
| chr6:10599301 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(171): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.920-22050G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599301 | |||||||
| chr6:10599367 | A | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0272 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-21984A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599367 | |||||||
| chr6:10599382 | A | G | 19 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(16): Show |
19 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-21969A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599382 | |||||||
| chr6:10599510 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.920-21841G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599510 | |||||||
| chr6:10599681 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.920-21670T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10599681 | |||||||
| chr6:10600021 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0267 others(15): Show |
19 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-21330G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600021 | |||||||
| chr6:10600119 | T | C | 4 | a0001c0001t0001g0312 a0001c0001t0001g0321 a0001c0001t0004g0277 others(1): Show |
4 | HG01109.hp1 HG01496.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-21232T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600119 | |||||||
| chr6:10600421 | C | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0272 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-20930C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600421 | |||||||
| chr6:10600606 | C | T | 8 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0135 others(5): Show |
8 | HG00621.hp1 HG00673.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-20745C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600606 | |||||||
| chr6:10600647 | C | A | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-20704C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600647 | |||||||
| chr6:10600665 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.920-20686C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600665 | |||||||
| chr6:10600675 | T | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.920-20676T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10600675 | |||||||
| chr6:10600760 | T | TTTTA | 4 | a0001c0001t0001g0040 a0001c0001t0002g0045 a0001c0001t0002g0220 others(1): Show |
4 | HG00558.hp1 HG03195.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-20570_920-2056 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10600760 | ||||||
| chr6:10601171 | A | G | 1 | a0001c0001t0008g0334 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.920-20180A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601171 | |||||||
| chr6:10601289 | C | G | 1 | a0001c0001t0007g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.920-20062C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601289 | |||||||
| chr6:10601433 | G | C | 53 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0096 others(50): Show |
53 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.920-19918G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601433 | |||||||
| chr6:10601463 | G | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0184 a0001c0001t0001g0296 others(25): Show |
28 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.920-19888G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601463 | |||||||
| chr6:10601465 | A | G | 12 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-19886A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601465 | |||||||
| chr6:10601471 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0319 |
2 | HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.920-19880G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601471 | |||||||
| chr6:10601486 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.920-19865C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601486 | |||||||
| chr6:10601674 | G | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0214 |
2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.920-19677G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601674 | |||||||
| chr6:10601680 | G | A | 12 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-19671G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601680 | |||||||
| chr6:10601769 | C | T | 1 | a0001c0002t0001g0292 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.920-19582C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601769 | |||||||
| chr6:10601821 | G | A | 2 | a0001c0001t0007g0019 a0002c0003t0011g0265 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-19530G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601821 | |||||||
| chr6:10601939 | T | TTAAAAA | 3 | a0001c0001t0001g0297 a0001c0001t0007g0295 a0001c0002t0001g0280 |
3 | HG02257.hp2 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.920-19412_920-1941 others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601939 | |||||||
| chr6:10601940 | C | A | 5 | a0001c0001t0001g0281 a0001c0001t0001g0297 a0001c0001t0007g0295 others(2): Show |
5 | HG01361.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-19411C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601940 | |||||||
| chr6:10601940 | CAAGAA | C | 16 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0001g0321 others(13): Show |
16 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.920-19408_920-1940 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601940 | ||||||
| chr6:10601940 | CAAGAAAA others(10): Show |
C | 2 | a0001c0001t0007g0019 a0002c0003t0011g0265 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-19408_920-1939 others(21): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601940 | ||||||
| chr6:10601943 | G | A | 5 | a0001c0001t0001g0281 a0001c0001t0001g0297 a0001c0001t0007g0295 others(2): Show |
5 | HG01361.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-19408G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601943 | |||||||
| chr6:10601943 | G | GA | 6 | a0001c0001t0001g0023 a0001c0001t0001g0113 a0001c0001t0001g0178 others(3): Show |
6 | HG00642.hp1 HG02293.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-19391dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | ||||||
| chr6:10601943 | GA | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.920-19391delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | ||||||
| chr6:10601943 | GAA | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0169 a0001c0001t0001g0226 others(4): Show |
7 | NA18612.hp1 NA18955.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.920-19392_920-1939 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601943 | ||||||
| chr6:10601951 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920-19391_920-1938 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10601951 | ||||||
| chr6:10601954 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0175 |
2 | HG01123.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.920-19397A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601954 | |||||||
| chr6:10601960 | A | C | 1 | a0001c0002t0001g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-19391A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601960 | |||||||
| chr6:10601961 | C | A | 35 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0184 others(32): Show |
35 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.920-19390C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10601961 | |||||||
| chr6:10602000 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0212 a0001c0001t0001g0232 |
3 | NA18945.hp1 NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.920-19351T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602000 | |||||||
| chr6:10602054 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.920-19297C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602054 | |||||||
| chr6:10602179 | C | G | 1 | a0001c0001t0002g0158 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.920-19172C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602179 | |||||||
| chr6:10602237 | C | G | 5 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0113 others(2): Show |
5 | NA18951.hp1 NA18973.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-19114C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602237 | |||||||
| chr6:10602250 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.920-19101G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602250 | |||||||
| chr6:10602326 | A | G | 10 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0272 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-19025A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602326 | |||||||
| chr6:10602391 | C | A | 2 | a0001c0001t0004g0276 a0001c0001t0012g0244 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-18960C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602391 | |||||||
| chr6:10602638 | CAAATAGG others(5): Show |
C | 12 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-18708_920-1869 others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10602638 | ||||||
| chr6:10602762 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.920-18589G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602762 | |||||||
| chr6:10602971 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.920-18380A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10602971 | |||||||
| chr6:10603424 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
31 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.920-17927A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603424 | |||||||
| chr6:10603504 | A | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-17847A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603504 | |||||||
| chr6:10603545 | T | A | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-17806T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603545 | |||||||
| chr6:10603690 | A | AT | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-17657dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603690 | ||||||
| chr6:10603817 | C | CT | 20 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(17): Show |
21 | HG00735.hp2 HG00741.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.920-17512dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | ||||||
| chr6:10603817 | CT | C | 46 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0044 others(43): Show |
46 | HG00323.hp1 HG00558.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.920-17512delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | ||||||
| chr6:10603817 | CTTTTT | C | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.920-17516_920-1751 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603817 | ||||||
| chr6:10603887 | GTTGT | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-17441_920-1743 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603887 | ||||||
| chr6:10603887 | GTTGTTTG others(1): Show |
G | 5 | a0001c0001t0001g0103 a0001c0001t0001g0128 a0001c0001t0001g0141 others(2): Show |
5 | HG01081.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-17445_920-1743 others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10603887 | ||||||
| chr6:10603964 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-17387T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603964 | |||||||
| chr6:10603985 | G | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.920-17366G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603985 | |||||||
| chr6:10603989 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.920-17362C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603989 | |||||||
| chr6:10603990 | G | A | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-17361G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603990 | |||||||
| chr6:10603997 | A | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-17354A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603997 | |||||||
| chr6:10603998 | C | T | 1 | a0001c0001t0001g0339 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.920-17353C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603998 | |||||||
| chr6:10603999 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.920-17352G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10603999 | |||||||
| chr6:10604052 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.920-17299C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604052 | |||||||
| chr6:10604098 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.920-17253T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604098 | |||||||
| chr6:10604139 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.920-17212C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604139 | |||||||
| chr6:10604195 | C | A | 1 | a0001c0001t0002g0015 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.920-17156C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604195 | |||||||
| chr6:10604263 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.920-17088T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604263 | |||||||
| chr6:10604364 | A | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-16987A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604364 | |||||||
| chr6:10604387 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.920-16964A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604387 | |||||||
| chr6:10604438 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-16913T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604438 | |||||||
| chr6:10604574 | C | T | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-16777C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604574 | |||||||
| chr6:10604873 | G | A | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.920-16478G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604873 | |||||||
| chr6:10604877 | A | AAAAAG | 4 | a0001c0001t0001g0240 a0001c0001t0007g0019 a0001c0001t0013g0010 others(1): Show |
4 | HG02572.hp1 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-16473_920-1647 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10604877 | ||||||
| chr6:10604877 | A | AAAAG | 139 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.920-16473_920-1647 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10604877 | ||||||
| chr6:10604877 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.920-16474A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604877 | |||||||
| chr6:10604879 | G | A | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-16472G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10604879 | |||||||
| chr6:10605147 | TAAAACAA | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0187 a0001c0001t0001g0219 |
3 | NA18951.hp1 NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.920-16190_920-1618 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605147 | ||||||
| chr6:10605169 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0272 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-16182G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605169 | |||||||
| chr6:10605208 | A | AT | 31 | a0001c0001t0001g0040 a0001c0001t0001g0074 a0001c0001t0001g0092 others(28): Show |
31 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.920-16118dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | A | ATT | 14 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0001t0001g0321 others(11): Show |
14 | HG00735.hp2 HG01358.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.920-16119_920-1611 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | A | ATTT | 7 | a0001c0001t0001g0184 a0001c0001t0001g0303 a0001c0001t0001g0310 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-16120_920-1611 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | A | ATTTT | 9 | a0001c0001t0001g0261 a0001c0001t0001g0285 a0001c0001t0001g0309 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-16121_920-1611 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | A | ATTTTT | 13 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0089 others(10): Show |
14 | HG01070.hp2 HG01361.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-16122_920-1611 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | AT | A | 8 | a0001c0001t0001g0188 a0001c0001t0001g0203 a0001c0001t0001g0267 others(5): Show |
9 | HG02109.hp2 HG02135.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-16118delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | ATT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(30): Show |
33 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.920-16119_920-1611 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | ATTT | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.920-16120_920-1611 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605208 | ATTTT | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0119 a0001c0001t0001g0120 others(8): Show |
11 | HG02040.hp1 HG02735.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.920-16121_920-1611 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605208 | ||||||
| chr6:10605266 | A | G | 1 | a0001c0001t0003g0311 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.920-16085A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605266 | |||||||
| chr6:10605365 | C | T | 2 | a0001c0001t0007g0019 a0002c0003t0011g0265 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-15986C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605365 | |||||||
| chr6:10605372 | C | CT | 6 | a0001c0001t0001g0089 a0001c0001t0001g0312 a0001c0001t0002g0030 others(3): Show |
6 | HG01496.hp2 HG01952.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-15965dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605372 | ||||||
| chr6:10605372 | CT | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-15965delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10605372 | ||||||
| chr6:10605438 | G | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-15913G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605438 | |||||||
| chr6:10605518 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.920-15833T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605518 | |||||||
| chr6:10605573 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.920-15778C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605573 | |||||||
| chr6:10605653 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.920-15698G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605653 | |||||||
| chr6:10605675 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920-15676G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605675 | |||||||
| chr6:10605764 | G | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.920-15587G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605764 | |||||||
| chr6:10605931 | C | G | 1 | a0001c0002t0001g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-15420C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605931 | |||||||
| chr6:10605946 | C | T | 6 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0025 others(3): Show |
6 | HG00408.hp1 HG02300.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-15405C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605946 | |||||||
| chr6:10605988 | C | G | 1 | a0001c0001t0005g0325 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920-15363C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10605988 | |||||||
| chr6:10606043 | G | A | 2 | a0001c0001t0004g0276 a0001c0001t0012g0244 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-15308G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606043 | |||||||
| chr6:10606165 | AT | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 |
3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-15184delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606165 | ||||||
| chr6:10606204 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.920-15147A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606204 | |||||||
| chr6:10606207 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.920-15144C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606207 | |||||||
| chr6:10606266 | G | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-15085G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606266 | |||||||
| chr6:10606271 | C | T | 3 | a0001c0001t0001g0335 a0001c0001t0001g0337 a0001c0001t0001g0339 |
3 | HG01346.hp1 HG01952.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.920-15080C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606271 | |||||||
| chr6:10606351 | T | C | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-15000T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606351 | |||||||
| chr6:10606378 | G | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-14973G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606378 | |||||||
| chr6:10606432 | A | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.920-14919A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606432 | |||||||
| chr6:10606485 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0168 a0001c0001t0001g0248 |
3 | HG01261.hp1 HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-14866G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606485 | |||||||
| chr6:10606487 | CACA | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(26): Show |
30 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.920-14859_920-1485 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606487 | ||||||
| chr6:10606591 | A | C | 1 | a0001c0001t0007g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.920-14760A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606591 | |||||||
| chr6:10606603 | C | CTTCCATT others(19): Show |
14 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0135 others(11): Show |
14 | HG00621.hp1 HG01081.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-14701_920-1467 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(45): Show |
52 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0023 others(49): Show |
53 | HG00738.hp2 HG01071.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.920-14727_920-1467 others(56): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(71): Show |
56 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0064 others(53): Show |
57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(82): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(97): Show |
51 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
52 | HG00323.hp1 HG00558.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(108): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(123): Show |
7 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0080 others(4): Show |
7 | HG02135.hp1 HG03239.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(134): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(149): Show |
4 | a0001c0001t0001g0310 a0001c0001t0001g0317 a0001c0001t0001g0319 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(160): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(175): Show |
6 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0001t0001g0320 others(3): Show |
6 | HG01884.hp2 HG02630.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-14676_920-1467 others(186): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(201): Show |
1 | a0002c0003t0010g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.920-14676_920-1467 others(212): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(227): Show |
1 | a0001c0001t0003g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.920-14676_920-1467 others(238): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(253): Show |
1 | a0001c0001t0003g0239 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.920-14676_920-1467 others(264): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(331): Show |
1 | a0001c0004t0003g0328 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.920-14676_920-1467 others(342): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | C | CTTCCATT others(357): Show |
1 | a0001c0004t0003g0327 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.920-14676_920-1467 others(368): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606603 | CTTCCATT others(19): Show |
C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0077 others(6): Show |
9 | HG00140.hp1 HG00639.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-14701_920-1467 others(30): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606603 | ||||||
| chr6:10606614 | G | GAAATTTA others(45): Show |
1 | a0001c0001t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.920-14686_920-1468 others(56): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606614 | ||||||
| chr6:10606742 | T | TAAAG | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-14606_920-1460 others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10606742 | ||||||
| chr6:10606778 | C | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0054 |
2 | HG01256.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.920-14573C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606778 | |||||||
| chr6:10606897 | C | G | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.920-14454C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606897 | |||||||
| chr6:10606929 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14422A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10606929 | |||||||
| chr6:10607121 | TA | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0128 a0001c0001t0001g0141 |
3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.920-14229delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607121 | |||||||
| chr6:10607136 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14215C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607136 | |||||||
| chr6:10607216 | G | C | 9 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0142 others(6): Show |
9 | HG01346.hp1 HG01952.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-14135G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607216 | |||||||
| chr6:10607262 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14089A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607262 | |||||||
| chr6:10607328 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-14023A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607328 | |||||||
| chr6:10607434 | C | T | 2 | a0001c0001t0008g0304 a0001c0001t0008g0334 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.920-13917C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607434 | |||||||
| chr6:10607435 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13916G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607435 | |||||||
| chr6:10607541 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.920-13810C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607541 | |||||||
| chr6:10607683 | CCTAACTT others(17): Show |
C | 16 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0074 others(13): Show |
16 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.920-13665_920-1364 others(28): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10607683 | ||||||
| chr6:10607688 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0140 |
2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.920-13663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607688 | |||||||
| chr6:10607699 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13652T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607699 | |||||||
| chr6:10607848 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.920-13503T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607848 | |||||||
| chr6:10607860 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13491A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607860 | |||||||
| chr6:10607866 | G | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13485G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607866 | |||||||
| chr6:10607897 | G | A | 2 | a0001c0001t0007g0019 a0002c0003t0011g0265 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-13454G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607897 | |||||||
| chr6:10607908 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13443A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607908 | |||||||
| chr6:10607909 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-13442G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10607909 | |||||||
| chr6:10608014 | T | A | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.920-13337T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608014 | |||||||
| chr6:10608073 | C | CT | 24 | a0001c0001t0001g0043 a0001c0001t0001g0184 a0001c0001t0001g0193 others(21): Show |
24 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.920-13257dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10608073 | ||||||
| chr6:10608073 | CT | C | 15 | a0001c0001t0001g0096 a0001c0001t0001g0119 a0001c0001t0001g0177 others(12): Show |
15 | HG00735.hp2 HG01169.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-13257delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10608073 | ||||||
| chr6:10608227 | G | A | 2 | a0001c0001t0007g0019 a0002c0003t0011g0265 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-13124G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608227 | |||||||
| chr6:10608239 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-13112G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608239 | |||||||
| chr6:10608359 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12992T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608359 | |||||||
| chr6:10608645 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.920-12706G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608645 | |||||||
| chr6:10608710 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.920-12641A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10608710 | |||||||
| chr6:10609077 | A | T | 1 | a0001c0001t0001g0338 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.920-12274A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609077 | |||||||
| chr6:10609206 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12145G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609206 | |||||||
| chr6:10609212 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12139C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609212 | |||||||
| chr6:10609277 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-12074A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609277 | |||||||
| chr6:10609292 | A | G | 7 | a0001c0001t0001g0184 a0001c0001t0001g0309 a0001c0001t0003g0300 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-12059A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609292 | |||||||
| chr6:10609356 | T | G | 12 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-11995T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609356 | |||||||
| chr6:10609376 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-11975T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609376 | |||||||
| chr6:10609585 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.920-11766G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609585 | |||||||
| chr6:10609617 | G | A | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.920-11734G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609617 | |||||||
| chr6:10609780 | A | AG | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-11567dupG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10609780 | ||||||
| chr6:10609786 | A | G | 2 | a0001c0001t0007g0019 a0002c0003t0011g0265 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-11565A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609786 | |||||||
| chr6:10609856 | C | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
47 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.920-11495C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609856 | |||||||
| chr6:10609877 | C | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
35 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.920-11474C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609877 | |||||||
| chr6:10609896 | TTTG | T | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.920-11451_920-1144 others(7): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10609896 | ||||||
| chr6:10609904 | A | T | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.920-11447A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609904 | |||||||
| chr6:10609907 | G | T | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.920-11444G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10609907 | |||||||
| chr6:10610078 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-11273G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610078 | |||||||
| chr6:10610319 | C | T | 9 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0307 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-11032C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610319 | |||||||
| chr6:10610688 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.920-10663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610688 | |||||||
| chr6:10610773 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-10578T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610773 | |||||||
| chr6:10610804 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.920-10547T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610804 | |||||||
| chr6:10610812 | T | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.920-10539T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610812 | |||||||
| chr6:10610854 | G | A | 1 | a0001c0002t0001g0294 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.920-10497G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610854 | |||||||
| chr6:10610862 | G | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0168 a0001c0001t0001g0248 |
3 | HG01261.hp1 HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-10489G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10610862 | |||||||
| chr6:10611148 | G | A | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-10203G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611148 | |||||||
| chr6:10611174 | C | T | 8 | a0001c0001t0001g0089 a0001c0001t0001g0118 a0001c0001t0001g0146 others(5): Show |
8 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-10177C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611174 | |||||||
| chr6:10611191 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.920-10160G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611191 | |||||||
| chr6:10611259 | CACTTGAA others(16): Show |
C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.920-10090_920-1006 others(27): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611259 | ||||||
| chr6:10611284 | T | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.920-10067T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611284 | |||||||
| chr6:10611334 | C | CT | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.920-10002dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611334 | ||||||
| chr6:10611334 | CTT | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-10003_920-1000 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611334 | ||||||
| chr6:10611413 | C | G | 136 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.920-9938C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611413 | |||||||
| chr6:10611487 | C | T | 5 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0001t0001g0321 others(2): Show |
5 | HG01884.hp2 HG02630.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-9864C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611487 | |||||||
| chr6:10611565 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0002g0045 a0001c0001t0002g0220 |
3 | HG00558.hp1 NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.920-9786G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611565 | |||||||
| chr6:10611575 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.920-9776C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611575 | |||||||
| chr6:10611576 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.920-9775G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611576 | |||||||
| chr6:10611624 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0303 |
2 | HG06807.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.920-9727C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611624 | |||||||
| chr6:10611728 | AT | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-9615delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10611728 | ||||||
| chr6:10611979 | T | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0191 |
2 | NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.920-9372T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10611979 | |||||||
| chr6:10612025 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.920-9326T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612025 | |||||||
| chr6:10612203 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.920-9148T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612203 | |||||||
| chr6:10612209 | A | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0212 a0001c0001t0001g0232 |
3 | NA18945.hp1 NA18961.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.920-9142A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612209 | |||||||
| chr6:10612217 | C | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-9134C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612217 | |||||||
| chr6:10612241 | C | T | 1 | a0001c0002t0001g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-9110C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612241 | |||||||
| chr6:10612384 | C | T | 23 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(20): Show |
23 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.920-8967C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612384 | |||||||
| chr6:10612453 | A | G | 1 | a0001c0001t0007g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.920-8898A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10612453 | |||||||
| chr6:10613128 | A | G | 1 | a0001c0002t0001g0293 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.920-8223A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613128 | |||||||
| chr6:10613207 | G | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-8144G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613207 | |||||||
| chr6:10613214 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(33): Show |
37 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.920-8137G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613214 | |||||||
| chr6:10613224 | C | T | 84 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0034 others(81): Show |
85 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.920-8127C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613224 | |||||||
| chr6:10613358 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0038 a0001c0001t0002g0080 others(3): Show |
6 | HG01928.hp2 HG01993.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-7993G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613358 | |||||||
| chr6:10613378 | C | CT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-7963dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10613378 | ||||||
| chr6:10613397 | C | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0097 a0001c0001t0001g0132 others(3): Show |
6 | HG01192.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-7954C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613397 | |||||||
| chr6:10613572 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(48): Show |
52 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.920-7779G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613572 | |||||||
| chr6:10613885 | C | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0038 a0001c0001t0002g0080 others(3): Show |
6 | HG01928.hp2 HG01993.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-7466C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613885 | |||||||
| chr6:10613950 | T | G | 1 | a0004c0008t0001g0041 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.920-7401T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10613950 | |||||||
| chr6:10614240 | T | C | 1 | a0002c0003t0011g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.920-7111T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614240 | |||||||
| chr6:10614246 | C | T | 1 | a0001c0002t0001g0292 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.920-7105C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614246 | |||||||
| chr6:10614261 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.920-7090T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614261 | |||||||
| chr6:10614486 | G | C | 15 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0001t0001g0309 others(12): Show |
15 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-6865G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614486 | |||||||
| chr6:10614625 | C | CA | 13 | a0001c0001t0001g0035 a0001c0001t0001g0218 a0001c0001t0001g0266 others(10): Show |
13 | HG00323.hp1 HG00408.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.920-6706dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | ||||||
| chr6:10614625 | CA | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0127 others(17): Show |
20 | HG02055.hp2 HG02109.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-6706delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | ||||||
| chr6:10614625 | CAAA | C | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.920-6708_920-6706d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614625 | ||||||
| chr6:10614642 | A | AG | 4 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0001t0001g0332 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-6709_920-6708i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614642 | |||||||
| chr6:10614642 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.920-6709A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614642 | |||||||
| chr6:10614644 | A | AAAAAAG | 10 | a0001c0001t0001g0184 a0001c0001t0001g0312 a0001c0001t0003g0311 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-6706_920-6705i others(8): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614644 | ||||||
| chr6:10614644 | A | AAG | 9 | a0001c0001t0001g0013 a0001c0001t0001g0146 a0001c0001t0001g0261 others(6): Show |
9 | HG01891.hp1 HG01978.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-6703_920-6702d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614644 | ||||||
| chr6:10614644 | A | AG | 19 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0118 others(16): Show |
20 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-6707_920-6706i others(3): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614644 | |||||||
| chr6:10614644 | A | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.920-6707A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614644 | |||||||
| chr6:10614691 | GTAGAGAT others(3): Show |
G | 2 | a0001c0001t0001g0077 a0001c0002t0001g0292 |
2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.920-6657_920-6648d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10614691 | ||||||
| chr6:10614844 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.920-6507C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614844 | |||||||
| chr6:10614845 | G | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.920-6506G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614845 | |||||||
| chr6:10614846 | C | T | 1 | a0001c0001t0005g0325 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920-6505C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614846 | |||||||
| chr6:10614869 | G | A | 1 | a0004c0008t0001g0041 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.920-6482G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10614869 | |||||||
| chr6:10615035 | C | A | 140 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.920-6316C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615035 | |||||||
| chr6:10615472 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.920-5879A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615472 | |||||||
| chr6:10615567 | T | TA | 3 | a0001c0001t0001g0009 a0001c0001t0001g0196 a0001c0001t0001g0258 |
3 | NA18969.hp2 NA19002.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.920-5783dupA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10615567 | ||||||
| chr6:10615644 | T | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(43): Show |
47 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.920-5707T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615644 | |||||||
| chr6:10615697 | CCACTCCA others(9): Show |
C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-5651_920-5636d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10615697 | ||||||
| chr6:10615705 | TAGAC | T | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0299 others(5): Show |
8 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.920-5642_920-5639d others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10615705 | ||||||
| chr6:10615876 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-5475G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615876 | |||||||
| chr6:10615904 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.920-5447G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615904 | |||||||
| chr6:10615921 | C | G | 1 | a0002c0003t0011g0265 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.920-5430C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615921 | |||||||
| chr6:10615983 | A | G | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-5368A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615983 | |||||||
| chr6:10615999 | G | T | 1 | a0001c0001t0001g0321 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.920-5352G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10615999 | |||||||
| chr6:10616073 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.920-5278G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616073 | |||||||
| chr6:10616118 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0062 others(8): Show |
12 | HG01071.hp2 HG01258.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.920-5233T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616118 | |||||||
| chr6:10616183 | C | CGTTATAT others(95): Show |
2 | a0001c0001t0001g0241 a0001c0001t0001g0243 |
2 | HG01070.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.920-5087_920-5086i others(104): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10616183 | ||||||
| chr6:10616183 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0168 a0001c0001t0001g0248 |
3 | HG01261.hp1 HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.920-5168C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616183 | |||||||
| chr6:10616265 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
38 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.920-5086T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616265 | |||||||
| chr6:10616277 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.920-5074G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616277 | |||||||
| chr6:10616435 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.920-4916C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616435 | |||||||
| chr6:10616583 | G | C | 7 | a0001c0001t0003g0033 a0001c0001t0003g0239 a0001c0001t0007g0019 others(4): Show |
7 | HG01358.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-4768G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616583 | |||||||
| chr6:10616598 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0002g0158 |
2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.920-4753C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616598 | |||||||
| chr6:10616744 | A | C | 10 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0001t0001g0309 others(7): Show |
10 | HG01243.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-4607A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10616744 | |||||||
| chr6:10617001 | TG | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-4348delG | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617001 | ||||||
| chr6:10617020 | G | A | 2 | a0001c0001t0004g0276 a0001c0001t0012g0244 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-4331G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617020 | |||||||
| chr6:10617049 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.920-4302C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617049 | |||||||
| chr6:10617077 | C | T | 1 | a0004c0008t0001g0041 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.920-4274C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617077 | |||||||
| chr6:10617281 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0059 |
2 | NA19082.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.920-4070C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617281 | |||||||
| chr6:10617285 | C | T | 1 | a0001c0001t0007g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.920-4066C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617285 | |||||||
| chr6:10617354 | C | G | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.920-3997C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617354 | |||||||
| chr6:10617366 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.920-3985G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617366 | |||||||
| chr6:10617377 | T | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.920-3974T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617377 | |||||||
| chr6:10617411 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0048 others(9): Show |
12 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.920-3940C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617411 | |||||||
| chr6:10617438 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.920-3913C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617438 | |||||||
| chr6:10617449 | C | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 |
3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-3902C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617449 | |||||||
| chr6:10617518 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.920-3833G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617518 | |||||||
| chr6:10617530 | G | T | 2 | a0001c0001t0001g0321 a0001c0001t0001g0332 |
2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.920-3821G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617530 | |||||||
| chr6:10617640 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.920-3711C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617640 | |||||||
| chr6:10617709 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.920-3642C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617709 | |||||||
| chr6:10617743 | A | ATTTTTTT others(4): Show |
1 | a0002c0003t0010g0271 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.920-3605_920-3604i others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617743 | ||||||
| chr6:10617747 | C | T | 5 | a0001c0001t0003g0033 a0001c0001t0003g0239 a0001c0004t0003g0327 others(2): Show |
5 | HG01358.hp1 HG02738.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.920-3604C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617747 | |||||||
| chr6:10617747 | CTTCTTTT others(2): Show |
C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
26 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.920-3601_920-3593d others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617747 | ||||||
| chr6:10617750 | C | CT | 7 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0091 others(4): Show |
7 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-3579dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0001t0001g0309 others(5): Show |
8 | HG01243.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-3586_920-3579d others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(3): Show |
20 | a0001c0001t0001g0092 a0001c0001t0001g0266 a0001c0001t0001g0267 others(17): Show |
20 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.920-3588_920-3579d others(12): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0288 a0001c0001t0014g0330 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.920-3589_920-3579d others(13): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0096 a0001c0001t0001g0306 a0001c0001t0001g0320 |
3 | HG02486.hp2 HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.920-3590_920-3579d others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0005g0302 a0001c0001t0010g0308 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.920-3591_920-3579d others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0312 a0001c0001t0008g0304 |
2 | HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.920-3592_920-3579d others(16): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0004g0277 a0001c0001t0008g0334 |
2 | HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.920-3593_920-3579d others(17): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0004g0276 a0001c0001t0012g0244 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.920-3594_920-3579d others(18): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | C | T | 12 | a0001c0001t0001g0310 a0001c0001t0001g0317 a0001c0001t0001g0319 others(9): Show |
12 | HG00735.hp2 HG01358.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.920-3601C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617750 | |||||||
| chr6:10617750 | CT | C | 21 | a0001c0001t0001g0032 a0001c0001t0001g0040 a0001c0001t0001g0044 others(18): Show |
21 | HG00323.hp1 HG00558.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.920-3579delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | CTT | C | 18 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0099 others(15): Show |
18 | HG00140.hp2 HG01928.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.920-3580_920-3579d others(4): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617750 | CTTT | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.920-3581_920-3579d others(5): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10617750 | ||||||
| chr6:10617751 | T | C | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-3600T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617751 | |||||||
| chr6:10617753 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.920-3598T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617753 | |||||||
| chr6:10617756 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.920-3595T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617756 | |||||||
| chr6:10617775 | C | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.920-3576C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617775 | |||||||
| chr6:10617807 | T | C | 1 | a0001c0002t0001g0289 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-3544T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617807 | |||||||
| chr6:10617864 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-3487T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617864 | |||||||
| chr6:10617916 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-3435G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617916 | |||||||
| chr6:10617930 | T | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0296 a0001c0002t0001g0282 |
3 | HG01884.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.920-3421T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617930 | |||||||
| chr6:10617993 | G | A | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.920-3358G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10617993 | |||||||
| chr6:10618060 | C | A | 2 | a0001c0001t0002g0134 a0001c0001t0002g0136 |
2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.920-3291C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618060 | |||||||
| chr6:10618217 | C | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0272 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-3134C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618217 | |||||||
| chr6:10618281 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-3070G>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618281 | |||||||
| chr6:10618295 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.920-3056A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618295 | |||||||
| chr6:10618449 | G | C | 2 | a0001c0001t0007g0019 a0002c0003t0011g0265 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.920-2902G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618449 | |||||||
| chr6:10618630 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.920-2721G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618630 | |||||||
| chr6:10618753 | C | CT | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.920-2595dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10618753 | ||||||
| chr6:10618775 | A | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(26): Show |
30 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.920-2576A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618775 | |||||||
| chr6:10618835 | T | TCTTGAAT others(1): Show |
37 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
38 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.920-2504_920-2497d others(10): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10618835 | ||||||
| chr6:10618953 | G | C | 2 | a0001c0001t0004g0277 a0001c0001t0005g0302 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.920-2398G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10618953 | |||||||
| chr6:10619010 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-2341C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619010 | |||||||
| chr6:10619030 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
38 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.920-2321A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619030 | |||||||
| chr6:10619506 | A | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-1845A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619506 | |||||||
| chr6:10619521 | T | A | 1 | a0001c0001t0001g0288 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.920-1830T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619521 | |||||||
| chr6:10619606 | G | A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0317 a0001c0001t0001g0319 |
3 | HG02818.hp2 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.920-1745G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619606 | |||||||
| chr6:10619684 | G | A | 1 | a0001c0001t0005g0325 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.920-1667G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619684 | |||||||
| chr6:10619704 | T | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
39 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.920-1647T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619704 | |||||||
| chr6:10619984 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(29): Show |
33 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.920-1367T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10619984 | |||||||
| chr6:10620407 | A | ATT | 28 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(25): Show |
30 | HG01070.hp2 HG01109.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.920-933_920-932dup others(2): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 10620407 | ||||||
| chr6:10620428 | A | T | 1 | a0001c0001t0002g0021 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.920-923A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620428 | |||||||
| chr6:10620445 | A | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(26): Show |
31 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.920-906A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620445 | |||||||
| chr6:10620527 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0184 a0001c0001t0001g0309 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-824C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620527 | |||||||
| chr6:10620583 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(24): Show |
28 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.920-768T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620583 | |||||||
| chr6:10620613 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0019g0114 |
3 | HG02738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.920-738C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620613 | |||||||
| chr6:10620744 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0184 a0001c0001t0001g0309 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.920-607C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620744 | |||||||
| chr6:10620921 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.920-430A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620921 | |||||||
| chr6:10620940 | A | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(23): Show |
27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.920-411A>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620940 | |||||||
| chr6:10620993 | C | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-358C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10620993 | |||||||
| chr6:10621109 | A | G | 2 | a0001c0001t0005g0302 a0001c0001t0006g0001 |
3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.920-242A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621109 | |||||||
| chr6:10621158 | A | G | 2 | a0001c0001t0005g0302 a0001c0001t0006g0001 |
3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.920-193A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621158 | |||||||
| chr6:10621313 | A | T | 3 | a0001c0004t0003g0327 a0001c0004t0003g0328 a0002c0003t0010g0271 |
3 | HG03130.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.920-38A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621313 | |||||||
| chr6:10621314 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.920-37C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 1/2 | chr6 | 10621314 | |||||||
| chr6:10621458 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1012+15C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621458 | |||||||
| chr6:10621597 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1012+154C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621597 | |||||||
| chr6:10621634 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(45): Show |
50 | HG00735.hp2 HG01070.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1012+191T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621634 | |||||||
| chr6:10621681 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0019g0114 |
3 | HG02738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1012+238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621681 | |||||||
| chr6:10621695 | T | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
36 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1012+252T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621695 | |||||||
| chr6:10621731 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(23): Show |
27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+288A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621731 | |||||||
| chr6:10621951 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1012+508G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10621951 | |||||||
| chr6:10622095 | A | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(23): Show |
27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+652A>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622095 | |||||||
| chr6:10622171 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(23): Show |
27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+728T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622171 | |||||||
| chr6:10622231 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1012+788A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622231 | |||||||
| chr6:10622308 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(23): Show |
27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+865T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622308 | |||||||
| chr6:10622494 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(23): Show |
27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1012+1051T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622494 | |||||||
| chr6:10622579 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1012+1136A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622579 | |||||||
| chr6:10622742 | C | CT | 12 | a0001c0001t0001g0092 a0001c0001t0001g0132 a0001c0001t0001g0173 others(9): Show |
12 | HG01496.hp2 HG01934.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1012+1327dupT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | ||||||
| chr6:10622742 | CT | C | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1012+1327delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | ||||||
| chr6:10622742 | CTT | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0124 others(6): Show |
9 | HG01243.hp1 HG02622.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+1326_1012+132 others(6): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | ||||||
| chr6:10622742 | CTTTTTTT | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(17): Show |
21 | HG00735.hp2 HG01175.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1012+1321_1012+132 others(11): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | ||||||
| chr6:10622742 | CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0001g0167 a0001c0001t0003g0033 a0001c0001t0003g0239 others(5): Show |
8 | HG01358.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1012+1318_1012+132 others(14): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | ||||||
| chr6:10622742 | CTTTTTTT others(4): Show |
C | 3 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0289 |
3 | HG01361.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1012+1317_1012+132 others(15): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10622742 | ||||||
| chr6:10622812 | C | T | 17 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0079 others(14): Show |
17 | HG00597.hp2 HG01346.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1012+1369C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622812 | |||||||
| chr6:10622813 | G | A | 1 | a0001c0001t0002g0076 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1012+1370G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622813 | |||||||
| chr6:10622913 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1012+1470C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10622913 | |||||||
| chr6:10623238 | A | ATTTAC | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1012+1799_1012+180 others(9): Show |
GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10623238 | ||||||
| chr6:10623258 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0062 others(8): Show |
12 | HG01071.hp2 HG01258.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1012+1815C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623258 | |||||||
| chr6:10623292 | AT | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(26): Show |
30 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1012+1864delT | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10623292 | ||||||
| chr6:10623295 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1012+1852T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623295 | |||||||
| chr6:10623333 | C | G | 1 | a0001c0001t0002g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1012+1890C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623333 | |||||||
| chr6:10623361 | G | C | 1 | a0001c0001t0002g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1012+1918G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623361 | |||||||
| chr6:10623385 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0152 |
3 | HG00621.hp2 NA18939.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1012+1942G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623385 | |||||||
| chr6:10623535 | C | G | 2 | a0001c0001t0005g0302 a0001c0001t0006g0001 |
3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1012+2092C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623535 | |||||||
| chr6:10623539 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0002g0045 a0001c0001t0002g0220 |
3 | HG00558.hp1 NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1012+2096G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623539 | |||||||
| chr6:10623838 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(22): Show |
26 | HG01070.hp2 HG01175.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1012+2395A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10623838 | |||||||
| chr6:10624019 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(23): Show |
27 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1013-2398C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624019 | |||||||
| chr6:10624253 | C | G | 8 | a0001c0001t0003g0033 a0001c0001t0003g0239 a0001c0002t0001g0279 others(5): Show |
8 | HG01358.hp1 HG01361.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1013-2164C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624253 | |||||||
| chr6:10624281 | T | A | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1013-2136T>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624281 | |||||||
| chr6:10624754 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1013-1663C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10624754 | |||||||
| chr6:10625029 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1013-1388G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625029 | |||||||
| chr6:10625030 | C | A | 2 | a0001c0001t0005g0302 a0001c0001t0006g0001 |
3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1013-1387C>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625030 | |||||||
| chr6:10625063 | G | A | 2 | a0001c0002t0001g0279 a0001c0002t0001g0280 |
2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1013-1354G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625063 | |||||||
| chr6:10625141 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0023 |
2 | NA18977.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1013-1276C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625141 | |||||||
| chr6:10625225 | T | C | 2 | a0001c0001t0005g0302 a0001c0001t0006g0001 |
3 | HG01109.hp1 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1013-1192T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625225 | |||||||
| chr6:10625518 | TA | T | 30 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0103 others(27): Show |
30 | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1013-885delA | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 10625518 | ||||||
| chr6:10625546 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1013-871G>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625546 | |||||||
| chr6:10625567 | T | G | 1 | a0001c0001t0013g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1013-850T>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625567 | |||||||
| chr6:10625653 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1013-764C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625653 | |||||||
| chr6:10625722 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1013-695T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625722 | |||||||
| chr6:10625861 | G | A | 3 | a0001c0002t0001g0279 a0001c0002t0001g0280 a0001c0002t0001g0289 |
3 | HG01361.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1013-556G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625861 | |||||||
| chr6:10625917 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0102 a0001c0001t0001g0105 |
3 | NA18993.hp1 NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1013-500A>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625917 | |||||||
| chr6:10625938 | C | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0309 a0001c0001t0005g0046 others(8): Show |
12 | HG00735.hp2 HG01109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1013-479C>G | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625938 | |||||||
| chr6:10625989 | T | C | 4 | a0001c0001t0001g0103 a0001c0001t0001g0268 a0001c0001t0001g0310 others(1): Show |
4 | HG02451.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-428T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10625989 | |||||||
| chr6:10626014 | C | T | 8 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0307 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1013-403C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626014 | |||||||
| chr6:10626069 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1013-348G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626069 | |||||||
| chr6:10626139 | T | C | 1 | a0001c0001t0010g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1013-278T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626139 | |||||||
| chr6:10626179 | C | T | 17 | a0001c0001t0001g0012 a0001c0001t0001g0309 a0001c0001t0003g0033 others(14): Show |
17 | HG01358.hp1 HG01891.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.1013-238C>T | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626179 | |||||||
| chr6:10626331 | G | A | 3 | a0001c0001t0007g0019 a0001c0001t0007g0295 a0002c0003t0011g0265 |
3 | HG02572.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1013-86G>A | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626331 | |||||||
| chr6:10626382 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0160 |
2 | NA18949.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1013-35T>C | GCNT2 | ENSG00000111846.20 | transcript | ENST00000316170.9 | protein_coding | 2/2 | chr6 | 10626382 |