Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 146664 |
| ensemblid | ENSG00000167889.13 |
| hgncid | 24140 |
| symbol | MGAT5B |
| name | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B |
| refseq_nuc | NM_001199172.2 |
| refseq_prot | NP_001186101.1 |
| ensembl_nuc | ENST00000569840.7 |
| ensembl_prot | ENSP00000456037.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 76868404 |
| end | 76950393 |
| strand | + |
| ver | v1.2 |
| region | chr17:76868404-76950393 |
| region5000 | chr17:76863404-76955393 |
| regionname0 | MGAT5B_chr17_76868404_76950393 |
| regionname5000 | MGAT5B_chr17_76863404_76955393 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 792 | 146 | 25 | 39 | 51 | 9 | 20 | 25 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0002 | 0/0 | 792 | 120 | 43 | 24 | 36 | 3 | 14 | 24 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0003 | 0/0 | 792 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0004 | 0/0 | 792 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0005 | 0/0 | 792 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0006 | 0/0 | 792 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0007 | 0/0 | 792 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0008 | 0/0 | 792 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0009 | 0/0 | 792 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| a0010 | 0/0 | 792 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | MITVN others(787): Show |
chr17 | 76863404 | 76955393 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2376 | 37 | 8 | 13 | 5 | 4 | 6 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0003 | 0/1 | 2376 | 24 | 1 | 6 | 11 | 3 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0005 | 0/0 | 2376 | 12 | 5 | 3 | 1 | 0 | 3 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0007 | 0/0 | 2376 | 11 | 0 | 3 | 7 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0008 | 0/0 | 2376 | 9 | 0 | 2 | 7 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0010 | 0/0 | 2376 | 8 | 0 | 0 | 6 | 0 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0011 | 0/0 | 2376 | 8 | 0 | 2 | 5 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0013 | 0/0 | 2376 | 7 | 1 | 2 | 3 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0018 | 0/0 | 2376 | 5 | 0 | 5 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0023 | 0/0 | 2376 | 3 | 0 | 0 | 0 | 1 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0024 | 0/0 | 2376 | 3 | 1 | 0 | 0 | 0 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0025 | 0/0 | 2376 | 3 | 2 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0030 | 0/0 | 2376 | 2 | 1 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0031 | 0/0 | 2376 | 2 | 1 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0045 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0047 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0048 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0049 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0050 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0051 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0052 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0053 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0054 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0055 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0056 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0001c0057 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0002 | 0/0 | 2376 | 32 | 17 | 12 | 1 | 1 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0004 | 0/0 | 2376 | 13 | 0 | 3 | 10 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0006 | 0/0 | 2376 | 11 | 7 | 0 | 3 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0009 | 0/0 | 2376 | 8 | 1 | 0 | 5 | 0 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0012 | 0/0 | 2376 | 7 | 4 | 1 | 1 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0014 | 0/0 | 2376 | 6 | 1 | 0 | 4 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0015 | 0/0 | 2376 | 6 | 0 | 1 | 3 | 0 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0016 | 0/0 | 2376 | 5 | 1 | 2 | 2 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0017 | 0/0 | 2376 | 5 | 2 | 0 | 3 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0019 | 0/0 | 2376 | 4 | 1 | 2 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0020 | 0/0 | 2376 | 4 | 4 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0021 | 0/0 | 2376 | 4 | 0 | 0 | 0 | 0 | 4 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0022 | 0/0 | 2376 | 3 | 0 | 3 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0028 | 0/0 | 2376 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0029 | 0/0 | 2376 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0033 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0034 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0036 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0037 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0038 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0041 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0042 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0002c0043 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0003c0026 | 0/0 | 2376 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0003c0027 | 0/0 | 2376 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0003c0032 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0004c0035 | 0/0 | 2376 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0005c0044 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0006c0059 | 0/0 | 2376 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0007c0040 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0008c0039 | 0/0 | 2376 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0009c0058 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 | ||
| a0010c0046 | 0/0 | 2376 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | ATGAT others(2371): Show |
chr17 | 76863404 | 76955393 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 4548 | 3 | 0 | 0 | 2 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0003 | 1/0 | 4560 | 8 | 3 | 2 | 0 | 1 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0004 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0005 | 0/0 | 4559 | 6 | 0 | 5 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0006 | 0/0 | 4559 | 11 | 1 | 2 | 3 | 2 | 3 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0007 | 0/0 | 4560 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0008 | 0/0 | 4542 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4537): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0011 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4546): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0012 | 0/0 | 4559 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0027 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0001t0031 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0003t0001 | 0/0 | 4559 | 18 | 1 | 5 | 9 | 1 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0003t0013 | 0/0 | 4559 | 2 | 0 | 0 | 0 | 2 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0003t0021 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0003t0023 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0003t0024 | 0/1 | 4559 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0003t0029 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0005t0002 | 0/0 | 4548 | 2 | 0 | 1 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0001c0005t0003 | 0/0 | 4560 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0005t0004 | 0/0 | 4559 | 2 | 1 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0005t0007 | 0/0 | 4560 | 2 | 0 | 1 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0005t0008 | 0/0 | 4542 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4537): Show |
chr17 | 76863404 | 76955393 |
| a0001c0005t0009 | 0/0 | 4559 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0005t0015 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0007t0002 | 0/0 | 4548 | 8 | 0 | 1 | 6 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0001c0007t0003 | 0/0 | 4560 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0007t0018 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0001c0007t0019 | 0/0 | 4547 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4542): Show |
chr17 | 76863404 | 76955393 |
| a0001c0008t0001 | 0/0 | 4559 | 9 | 0 | 2 | 7 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0010t0003 | 0/0 | 4560 | 6 | 0 | 0 | 6 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0010t0007 | 0/0 | 4560 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0011t0002 | 0/0 | 4548 | 7 | 0 | 1 | 5 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0001c0011t0012 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0013t0001 | 0/0 | 4559 | 7 | 1 | 2 | 3 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0018t0004 | 0/0 | 4559 | 5 | 0 | 5 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0023t0004 | 0/0 | 4559 | 3 | 0 | 0 | 0 | 1 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0024t0001 | 0/0 | 4559 | 3 | 1 | 0 | 0 | 0 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0025t0010 | 0/0 | 4555 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4550): Show |
chr17 | 76863404 | 76955393 |
| a0001c0025t0014 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4550): Show |
chr17 | 76863404 | 76955393 |
| a0001c0030t0001 | 0/0 | 4559 | 2 | 1 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0031t0001 | 0/0 | 4559 | 2 | 1 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0045t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0047t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0048t0003 | 0/0 | 4560 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0049t0010 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4550): Show |
chr17 | 76863404 | 76955393 |
| a0001c0050t0033 | 0/0 | 4560 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0051t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0052t0003 | 0/0 | 4560 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0053t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0054t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0001c0055t0007 | 0/0 | 4560 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0001c0056t0008 | 0/0 | 4542 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4537): Show |
chr17 | 76863404 | 76955393 |
| a0001c0057t0004 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0002 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0003 | 0/0 | 4560 | 5 | 4 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0004 | 0/0 | 4559 | 4 | 4 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0005 | 0/0 | 4559 | 11 | 3 | 7 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0006 | 0/0 | 4559 | 3 | 2 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0008 | 0/0 | 4542 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4537): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0011 | 0/0 | 4551 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4546): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0016 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0020 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0025 | 0/0 | 4560 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0002t0028 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0004t0001 | 0/0 | 4559 | 13 | 0 | 3 | 10 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0006t0002 | 0/0 | 4548 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0002c0006t0004 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0006t0007 | 0/0 | 4560 | 3 | 2 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0006t0008 | 0/0 | 4542 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4537): Show |
chr17 | 76863404 | 76955393 |
| a0002c0006t0009 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0006t0032 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0009t0001 | 0/0 | 4559 | 8 | 1 | 0 | 5 | 0 | 2 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0012t0001 | 0/0 | 4559 | 7 | 4 | 1 | 1 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0014t0001 | 0/0 | 4559 | 5 | 0 | 0 | 4 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0014t0017 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0015t0003 | 0/0 | 4560 | 4 | 0 | 0 | 3 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0015t0005 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0015t0007 | 0/0 | 4560 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0016t0002 | 0/0 | 4548 | 4 | 0 | 2 | 2 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0002c0016t0007 | 0/0 | 4560 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0017t0002 | 0/0 | 4548 | 5 | 2 | 0 | 3 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0002c0019t0004 | 0/0 | 4559 | 4 | 1 | 2 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0020t0001 | 0/0 | 4559 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0020t0022 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0021t0001 | 0/0 | 4559 | 4 | 0 | 0 | 0 | 0 | 4 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0022t0003 | 0/0 | 4560 | 3 | 0 | 3 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0028t0004 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0028t0026 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0029t0001 | 0/0 | 4559 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0033t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0034t0014 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4550): Show |
chr17 | 76863404 | 76955393 |
| a0002c0036t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0037t0007 | 0/0 | 4560 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0002c0038t0001 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0041t0010 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4550): Show |
chr17 | 76863404 | 76955393 |
| a0002c0042t0004 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0002c0043t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0003c0026t0002 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0003c0026t0030 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0003c0027t0001 | 0/0 | 4559 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0003c0032t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0004c0035t0004 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0005c0044t0001 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0006c0059t0007 | 0/0 | 4560 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0007c0040t0002 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4543): Show |
chr17 | 76863404 | 76955393 |
| a0008c0039t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| a0009c0058t0003 | 0/0 | 4560 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4555): Show |
chr17 | 76863404 | 76955393 |
| a0010c0046t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | GCTCG others(4554): Show |
chr17 | 76863404 | 76955393 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0011g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0012g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0012g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0027g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0001t0031g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0013g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0013g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0021g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0023g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0024g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0003t0029g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0007g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0007g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0005t0015g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0018g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0007t0019g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0008t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0010t0007g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0011t0012g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0013t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0013t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0013t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0013t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0013t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0013t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0013t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0018t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0018t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0018t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0018t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0018t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0023t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0023t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0023t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0024t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0024t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0024t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0025t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0025t0010g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0025t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0030t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0030t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0031t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0031t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0045t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0047t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0048t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0049t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0050t0033g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0051t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0052t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0053t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0054t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0055t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0056t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0001c0057t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0008g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0016g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0020g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0025g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0002t0028g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0009g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0006t0032g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0009t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0012t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0012t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0012t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0012t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0012t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0012t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0012t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0014t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0014t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0014t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0014t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0014t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0014t0017g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0015t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0015t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0015t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0015t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0015t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0015t0007g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0016t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0016t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0016t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0016t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0016t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0017t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0017t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0017t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0017t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0017t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0019t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0019t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0019t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0019t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0020t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0020t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0020t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0020t0022g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0021t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0021t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0021t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0021t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0022t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0022t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0022t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0028t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0028t0026g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0029t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0029t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0033t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0034t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0036t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0037t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0038t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0041t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0042t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0002c0043t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0003c0026t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0003c0026t0030g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0003c0027t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0003c0027t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0003c0032t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0004c0035t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0005c0044t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0006c0059t0007g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0007c0040t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0008c0039t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0009c0058t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| a0010c0046t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0005 | g0164 | EUR | GBR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00099 | hp2 | a0001 | c0023 | t0004 | g0227 | EUR | GBR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0034 | EUR | GBR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00140 | hp2 | a0002 | c0019 | t0004 | g0242 | EUR | GBR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0125 | EUR | FIN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00280 | hp2 | a0002 | c0006 | t0007 | g0110 | EUR | FIN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00408 | hp1 | a0001 | c0051 | t0001 | g0171 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00408 | hp2 | a0001 | c0030 | t0001 | g0272 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00423 | hp1 | a0001 | c0010 | t0003 | g0130 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00423 | hp2 | a0001 | c0007 | t0002 | g0203 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00438 | hp1 | a0003 | c0026 | t0030 | g0269 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00438 | hp2 | a0002 | c0014 | t0001 | g0172 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00544 | hp1 | a0002 | c0015 | t0003 | g0150 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00544 | hp2 | a0002 | c0043 | t0001 | g0158 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00597 | hp1 | a0001 | c0003 | t0029 | g0051 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00597 | hp2 | a0002 | c0012 | t0001 | g0194 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00621 | hp1 | a0001 | c0003 | t0021 | g0225 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00621 | hp2 | a0002 | c0004 | t0001 | g0124 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00639 | hp1 | a0002 | c0002 | t0005 | g0081 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00639 | hp2 | a0002 | c0012 | t0001 | g0104 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00642 | hp1 | a0001 | c0001 | t0012 | g0014 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00642 | hp2 | a0001 | c0018 | t0004 | g0191 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00673 | hp1 | a0001 | c0007 | t0002 | g0127 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00673 | hp2 | a0002 | c0009 | t0001 | g0092 | EAS | CHS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00735 | hp1 | a0002 | c0002 | t0005 | g0089 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00735 | hp2 | a0001 | c0005 | t0007 | g0028 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0206 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00741 | hp1 | a0002 | c0004 | t0001 | g0075 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0083 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01069 | hp1 | a0002 | c0019 | t0004 | g0002 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01069 | hp2 | a0001 | c0056 | t0008 | g0108 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01071 | hp1 | a0002 | c0019 | t0004 | g0003 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01071 | hp2 | a0002 | c0002 | t0005 | g0086 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01074 | hp2 | a0001 | c0003 | t0023 | g0040 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01081 | hp2 | a0002 | c0015 | t0005 | g0080 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01099 | hp1 | a0001 | c0018 | t0004 | g0190 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01099 | hp2 | a0002 | c0002 | t0028 | g0259 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01106 | hp1 | a0002 | c0002 | t0008 | g0048 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01109 | hp1 | a0001 | c0005 | t0002 | g0019 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01109 | hp2 | a0001 | c0013 | t0001 | g0177 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01168 | hp1 | a0001 | c0001 | t0027 | g0220 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0094 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01175 | hp2 | a0001 | c0001 | t0012 | g0016 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01243 | hp1 | a0001 | c0011 | t0002 | g0033 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01243 | hp2 | a0001 | c0001 | t0031 | g0256 | AMR | PUR | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01255 | hp1 | a0001 | c0018 | t0004 | g0020 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01255 | hp2 | a0001 | c0025 | t0010 | g0229 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01256 | hp2 | a0002 | c0002 | t0020 | g0087 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01261 | hp1 | a0002 | c0002 | t0003 | g0084 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01261 | hp2 | a0001 | c0005 | t0015 | g0031 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0044 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01358 | hp2 | a0004 | c0035 | t0004 | g0155 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01361 | hp1 | a0001 | c0008 | t0001 | g0022 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01361 | hp2 | a0001 | c0018 | t0004 | g0226 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01433 | hp1 | a0001 | c0018 | t0004 | g0037 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0210 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01496 | hp1 | a0002 | c0022 | t0003 | g0082 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0042 | EUR | IBS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01516 | hp2 | a0001 | c0003 | t0013 | g0249 | EUR | IBS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0096 | EUR | IBS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01517 | hp2 | a0001 | c0003 | t0013 | g0251 | EUR | IBS | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01884 | hp1 | a0002 | c0028 | t0026 | g0060 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01884 | hp2 | a0002 | c0002 | t0003 | g0007 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01891 | hp2 | a0001 | c0048 | t0003 | g0143 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01928 | hp1 | a0001 | c0013 | t0001 | g0131 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01952 | hp1 | a0002 | c0016 | t0002 | g0079 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01952 | hp2 | a0002 | c0004 | t0001 | g0091 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01975 | hp1 | a0002 | c0016 | t0002 | g0085 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01975 | hp2 | a0002 | c0002 | t0005 | g0142 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01978 | hp1 | a0002 | c0002 | t0016 | g0098 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01978 | hp2 | a0002 | c0022 | t0003 | g0097 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01981 | hp1 | a0001 | c0007 | t0019 | g0180 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01981 | hp2 | a0002 | c0002 | t0005 | g0095 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01993 | hp1 | a0001 | c0052 | t0003 | g0137 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01993 | hp2 | a0002 | c0002 | t0005 | g0039 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02004 | hp1 | a0001 | c0007 | t0002 | g0136 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02004 | hp2 | a0002 | c0022 | t0003 | g0093 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02015 | hp2 | a0002 | c0009 | t0001 | g0197 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02027 | hp1 | a0001 | c0008 | t0001 | g0055 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02027 | hp2 | a0001 | c0010 | t0003 | g0128 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02040 | hp2 | a0001 | c0031 | t0001 | g0245 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02056 | hp2 | a0002 | c0009 | t0001 | g0148 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0183 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02071 | hp2 | a0001 | c0008 | t0001 | g0247 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02074 | hp1 | a0001 | c0010 | t0003 | g0133 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0215 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0134 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02080 | hp2 | a0002 | c0004 | t0001 | g0103 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02083 | hp1 | a0001 | c0007 | t0002 | g0216 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02129 | hp1 | a0001 | c0007 | t0002 | g0064 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02129 | hp2 | a0001 | c0050 | t0033 | g0179 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02132 | hp1 | a0002 | c0004 | t0001 | g0173 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02132 | hp2 | a0001 | c0010 | t0003 | g0132 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02145 | hp1 | a0001 | c0025 | t0014 | g0071 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0151 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | CDX | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | CDX | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02257 | hp1 | a0001 | c0053 | t0001 | g0032 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02257 | hp2 | a0002 | c0002 | t0004 | g0257 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02258 | hp1 | a0002 | c0002 | t0005 | g0238 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02280 | hp2 | a0002 | c0006 | t0007 | g0069 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02293 | hp1 | a0001 | c0007 | t0018 | g0176 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0090 | AMR | PEL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02451 | hp1 | a0002 | c0020 | t0001 | g0161 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02523 | hp1 | a0002 | c0004 | t0001 | g0077 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02523 | hp2 | a0001 | c0011 | t0002 | g0186 | EAS | KHV | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02615 | hp1 | a0001 | c0005 | t0004 | g0126 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02615 | hp2 | a0002 | c0002 | t0004 | g0240 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02622 | hp1 | a0002 | c0034 | t0014 | g0058 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02622 | hp2 | a0002 | c0006 | t0032 | g0070 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02630 | hp1 | a0002 | c0002 | t0005 | g0239 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02647 | hp1 | a0002 | c0016 | t0007 | g0063 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02647 | hp2 | a0002 | c0017 | t0002 | g0068 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02723 | hp1 | a0002 | c0009 | t0001 | g0122 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02723 | hp2 | a0002 | c0017 | t0002 | g0273 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02738 | hp1 | a0005 | c0044 | t0001 | g0213 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0204 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02809 | hp2 | a0002 | c0002 | t0011 | g0199 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02818 | hp1 | a0002 | c0012 | t0001 | g0147 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02818 | hp2 | a0002 | c0002 | t0006 | g0074 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02897 | hp1 | a0001 | c0024 | t0001 | g0141 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02897 | hp2 | a0002 | c0012 | t0001 | g0145 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02965 | hp1 | a0002 | c0006 | t0009 | g0001 | AFR | ESN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02965 | hp2 | a0002 | c0014 | t0017 | g0004 | AFR | ESN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02976 | hp1 | a0002 | c0012 | t0001 | g0271 | AFR | ESN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02976 | hp2 | a0002 | c0020 | t0001 | g0011 | AFR | ESN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03017 | hp1 | a0002 | c0037 | t0007 | g0166 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0233 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03041 | hp1 | a0001 | c0030 | t0001 | g0154 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03041 | hp2 | a0002 | c0020 | t0001 | g0008 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03139 | hp1 | a0002 | c0002 | t0004 | g0260 | AFR | ESN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03139 | hp2 | a0002 | c0006 | t0009 | g0001 | AFR | ESN | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03209 | hp1 | a0002 | c0012 | t0001 | g0012 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03209 | hp2 | a0002 | c0006 | t0008 | g0198 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03225 | hp1 | a0002 | c0033 | t0001 | g0059 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0065 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03239 | hp1 | a0001 | c0057 | t0004 | g0027 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03239 | hp2 | a0001 | c0024 | t0001 | g0078 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03453 | hp1 | a0002 | c0002 | t0025 | g0274 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03453 | hp2 | a0001 | c0005 | t0009 | g0170 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03486 | hp1 | a0002 | c0002 | t0004 | g0105 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03486 | hp2 | a0002 | c0002 | t0011 | g0057 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03491 | hp1 | a0002 | c0021 | t0001 | g0265 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03491 | hp2 | a0002 | c0014 | t0001 | g0121 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03492 | hp1 | a0002 | c0021 | t0001 | g0266 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03492 | hp2 | a0001 | c0005 | t0007 | g0045 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03540 | hp1 | a0001 | c0025 | t0010 | g0047 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0107 | AFR | GWD | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0010 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03579 | hp2 | a0002 | c0019 | t0004 | g0005 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03654 | hp1 | a0002 | c0042 | t0004 | g0168 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03654 | hp2 | a0002 | c0038 | t0001 | g0118 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0248 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03688 | hp2 | a0002 | c0015 | t0003 | g0169 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03710 | hp1 | a0001 | c0010 | t0007 | g0140 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03710 | hp2 | a0001 | c0010 | t0007 | g0255 | SAS | PJL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03831 | hp1 | a0002 | c0009 | t0001 | g0236 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03831 | hp2 | a0002 | c0012 | t0001 | g0159 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03834 | hp1 | a0002 | c0021 | t0001 | g0267 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03927 | hp1 | a0001 | c0023 | t0004 | g0182 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03927 | hp2 | a0001 | c0005 | t0004 | g0208 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03942 | hp1 | a0002 | c0021 | t0001 | g0167 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0254 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04115 | hp1 | a0001 | c0013 | t0001 | g0237 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04115 | hp2 | a0002 | c0002 | t0006 | g0185 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04184 | hp1 | a0001 | c0005 | t0003 | g0212 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04184 | hp2 | a0006 | c0059 | t0007 | g0046 | SAS | BEB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04199 | hp1 | a0001 | c0007 | t0002 | g0211 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0023 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04204 | hp1 | a0001 | c0024 | t0001 | g0026 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04204 | hp2 | a0002 | c0015 | t0007 | g0268 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04228 | hp1 | a0002 | c0009 | t0001 | g0120 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18522 | hp1 | a0002 | c0028 | t0004 | g0061 | AFR | YRI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18522 | hp2 | a0002 | c0020 | t0022 | g0153 | AFR | YRI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18612 | hp1 | a0001 | c0054 | t0001 | g0129 | EAS | CHB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18612 | hp2 | a0003 | c0027 | t0001 | g0234 | EAS | CHB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18906 | hp1 | a0002 | c0002 | t0006 | g0200 | AFR | YRI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18906 | hp2 | a0002 | c0041 | t0010 | g0062 | AFR | YRI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18941 | hp2 | a0001 | c0011 | t0002 | g0202 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18942 | hp1 | a0002 | c0009 | t0001 | g0119 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18942 | hp2 | a0007 | c0040 | t0002 | g0193 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18950 | hp1 | a0002 | c0017 | t0002 | g0195 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18950 | hp2 | a0002 | c0017 | t0002 | g0100 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18952 | hp1 | a0002 | c0006 | t0002 | g0196 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18952 | hp2 | a0002 | c0004 | t0001 | g0115 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18953 | hp1 | a0001 | c0007 | t0002 | g0201 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18953 | hp2 | a0001 | c0013 | t0001 | g0189 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18954 | hp1 | a0002 | c0015 | t0003 | g0109 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18954 | hp2 | a0002 | c0006 | t0002 | g0006 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18960 | hp1 | a0002 | c0036 | t0001 | g0232 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18960 | hp2 | a0002 | c0017 | t0002 | g0144 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18964 | hp1 | a0002 | c0004 | t0001 | g0114 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18965 | hp1 | a0002 | c0029 | t0001 | g0146 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18965 | hp2 | a0003 | c0026 | t0002 | g0263 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18966 | hp1 | a0003 | c0032 | t0001 | g0261 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18966 | hp2 | a0001 | c0008 | t0001 | g0056 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18971 | hp1 | a0003 | c0027 | t0001 | g0262 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18971 | hp2 | a0001 | c0008 | t0001 | g0277 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18975 | hp1 | a0001 | c0011 | t0002 | g0223 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18975 | hp2 | a0002 | c0004 | t0001 | g0052 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18977 | hp1 | a0002 | c0029 | t0001 | g0149 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18977 | hp2 | a0001 | c0013 | t0001 | g0250 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18979 | hp1 | a0002 | c0016 | t0002 | g0112 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18979 | hp2 | a0001 | c0005 | t0002 | g0235 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18983 | hp1 | a0001 | c0010 | t0003 | g0217 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18983 | hp2 | a0002 | c0009 | t0001 | g0113 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18995 | hp1 | a0008 | c0039 | t0001 | g0117 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18995 | hp2 | a0001 | c0013 | t0001 | g0152 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18998 | hp1 | a0002 | c0014 | t0001 | g0088 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA18998 | hp2 | a0002 | c0015 | t0003 | g0111 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19003 | hp1 | a0002 | c0004 | t0001 | g0102 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19007 | hp1 | a0001 | c0007 | t0003 | g0222 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19007 | hp2 | a0002 | c0016 | t0002 | g0116 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19011 | hp1 | a0002 | c0006 | t0002 | g0076 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19011 | hp2 | a0001 | c0045 | t0001 | g0231 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19012 | hp1 | a0001 | c0007 | t0002 | g0219 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19030 | hp1 | a0002 | c0006 | t0004 | g0241 | AFR | LWK | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19030 | hp2 | a0001 | c0049 | t0010 | g0067 | AFR | LWK | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19043 | hp1 | a0001 | c0031 | t0001 | g0252 | AFR | LWK | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19043 | hp2 | a0002 | c0006 | t0007 | g0072 | AFR | LWK | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19064 | hp1 | a0002 | c0004 | t0001 | g0139 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19064 | hp2 | a0001 | c0008 | t0001 | g0246 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19066 | hp1 | a0001 | c0008 | t0001 | g0230 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19066 | hp2 | a0001 | c0011 | t0002 | g0188 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19067 | hp1 | a0001 | c0011 | t0002 | g0276 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19067 | hp2 | a0001 | c0008 | t0001 | g0054 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19079 | hp1 | a0001 | c0010 | t0003 | g0218 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19079 | hp2 | a0002 | c0004 | t0001 | g0123 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19091 | hp1 | a0002 | c0014 | t0001 | g0066 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19091 | hp2 | a0002 | c0014 | t0001 | g0207 | EAS | JPT | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19240 | hp1 | a0001 | c0005 | t0009 | g0163 | AFR | YRI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | YRI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20129 | hp1 | a0001 | c0047 | t0001 | g0015 | AFR | ASW | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20129 | hp2 | a0002 | c0002 | t0008 | g0013 | AFR | ASW | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | TSI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20752 | hp2 | a0001 | c0011 | t0002 | g0184 | EUR | TSI | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0178 | SAS | GIH | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20905 | hp2 | a0001 | c0023 | t0004 | g0244 | SAS | GIH | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01123 | hp1 | a0001 | c0011 | t0012 | g0174 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG01123 | hp2 | a0001 | c0008 | t0001 | g0030 | AMR | CLM | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02109 | hp1 | a0001 | c0005 | t0009 | g0162 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG02109 | hp2 | a0002 | c0002 | t0005 | g0258 | AFR | ACB | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03471 | hp1 | a0001 | c0013 | t0001 | g0101 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| HG03471 | hp2 | a0001 | c0055 | t0007 | g0073 | AFR | MSL | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20300 | hp1 | a0009 | c0058 | t0003 | g0050 | AFR | USA | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA20300 | hp2 | a0001 | c0005 | t0008 | g0264 | AFR | USA | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0106 | AFR | LWK | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| NA21309 | hp2 | a0010 | c0046 | t0001 | g0224 | AFR | LWK | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0024 | g0275 | REF | REF | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0018 | REF | REF | MGAT5B_chr17_76863404_76955393 | MGAT5B | chr17 | 76863404 | 76955393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76872879 | A | G | 1 | a0006 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.97A>G | p.Thr33Ala | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/18 | 723/4560 | 97/2379 | 33/792 | chr17 | 76872879 | |||
| chr17:76882177 | G | A | 6 | a0002 a0003 a0004 others(3): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
missense_variant | MODERATE | c.208G>A | p.Val70Ile | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/18 | 834/4560 | 208/2379 | 70/792 | chr17 | 76882177 | |||
| chr17:76882291 | G | A | 1 | a0005 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.322G>A | p.Ala108Thr | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/18 | 948/4560 | 322/2379 | 108/792 | chr17 | 76882291 | |||
| chr17:76902556 | A | T | 1 | a0009 | 1 | NA20300.hp1 | missense_variant&splice_region_variant | MODERATE | c.331A>T | p.Met111Leu | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/18 | 957/4560 | 331/2379 | 111/792 | chr17 | 76902556 | |||
| chr17:76902571 | G | A | 1 | a0003 | 5 | HG00438.hp1 NA18612.hp2 NA18965.hp2 others(2): Show |
missense_variant | MODERATE | c.346G>A | p.Gly116Ser | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/18 | 972/4560 | 346/2379 | 116/792 | chr17 | 76902571 | |||
| chr17:76925011 | G | C | 1 | a0004 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1071G>C | p.Met357Ile | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/18 | 1697/4560 | 1071/2379 | 357/792 | chr17 | 76925011 | |||
| chr17:76925067 | G | A | 1 | a0008 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.1127G>A | p.Arg376Gln | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/18 | 1753/4560 | 1127/2379 | 376/792 | chr17 | 76925067 | |||
| chr17:76925069 | C | G | 1 | a0010 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1129C>G | p.His377Asp | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/18 | 1755/4560 | 1129/2379 | 377/792 | chr17 | 76925069 | |||
| chr17:76926626 | G | A | 1 | a0007 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.1187G>A | p.Gly396Glu | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/18 | 1813/4560 | 1187/2379 | 396/792 | chr17 | 76926626 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76902576 | C | T | 1 | a0001c0057 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.351C>T | p.Leu117Leu | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/18 | 977/4560 | 351/2379 | 117/792 | chr17 | 76902576 | |||
| chr17:76902606 | C | T | 2 | a0001c0055 a0001c0056 |
2 | HG01069.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.381C>T | p.Asn127Asn | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/18 | 1007/4560 | 381/2379 | 127/792 | chr17 | 76902606 | |||
| chr17:76904383 | G | A | 3 | a0002c0028 a0002c0033 a0002c0034 |
4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.651G>A | p.Thr217Thr | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/18 | 1277/4560 | 651/2379 | 217/792 | chr17 | 76904383 | |||
| chr17:76906053 | C | T | 1 | a0001c0054 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.891C>T | p.Ser297Ser | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/18 | 1517/4560 | 891/2379 | 297/792 | chr17 | 76906053 | |||
| chr17:76924975 | G | T | 1 | a0001c0053 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1035G>T | p.Gly345Gly | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/18 | 1661/4560 | 1035/2379 | 345/792 | chr17 | 76924975 | |||
| chr17:76924990 | G | C | 18 | a0001c0005 a0001c0013 a0001c0018 others(15): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
synonymous_variant | LOW | c.1050G>C | p.Arg350Arg | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/18 | 1676/4560 | 1050/2379 | 350/792 | chr17 | 76924990 | |||
| chr17:76925047 | C | T | 6 | a0001c0011 a0001c0051 a0001c0052 others(3): Show |
19 | HG00408.hp1 HG01123.hp1 HG01243.hp1 others(16): Show |
synonymous_variant | LOW | c.1107C>T | p.His369His | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/18 | 1733/4560 | 1107/2379 | 369/792 | chr17 | 76925047 | |||
| chr17:76926624 | C | T | 18 | a0001c0003 a0001c0007 a0001c0010 others(15): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
synonymous_variant | LOW | c.1185C>T | p.Phe395Phe | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/18 | 1811/4560 | 1185/2379 | 395/792 | chr17 | 76926624 | |||
| chr17:76932676 | C | T | 21 | a0001c0003 a0001c0010 a0001c0030 others(18): Show |
77 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
synonymous_variant | LOW | c.1323C>T | p.Phe441Phe | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 11/18 | 1949/4560 | 1323/2379 | 441/792 | chr17 | 76932676 | |||
| chr17:76932682 | C | T | 1 | a0001c0023 | 3 | HG00099.hp2 HG03927.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1329C>T | p.Ser443Ser | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 11/18 | 1955/4560 | 1329/2379 | 443/792 | chr17 | 76932682 | |||
| chr17:76940494 | G | A | 22 | a0001c0003 a0001c0013 a0001c0024 others(19): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
synonymous_variant | LOW | c.1677G>A | p.Pro559Pro | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 14/18 | 2303/4560 | 1677/2379 | 559/792 | chr17 | 76940494 | |||
| chr17:76946396 | C | T | 27 | a0001c0003 a0001c0008 a0001c0013 others(24): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(102): Show |
synonymous_variant | LOW | c.1869C>T | p.Tyr623Tyr | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/18 | 2495/4560 | 1869/2379 | 623/792 | chr17 | 76946396 | |||
| chr17:76947967 | C | T | 1 | a0001c0047 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2061C>T | p.His687His | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 17/18 | 2687/4560 | 2061/2379 | 687/792 | chr17 | 76947967 | |||
| chr17:76948069 | C | T | 6 | a0001c0018 a0001c0023 a0001c0057 others(3): Show |
15 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(12): Show |
synonymous_variant | LOW | c.2163C>T | p.Ser721Ser | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 17/18 | 2789/4560 | 2163/2379 | 721/792 | chr17 | 76948069 | |||
| chr17:76948754 | C | G | 4 | a0001c0025 a0001c0049 a0002c0034 others(1): Show |
6 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
synonymous_variant | LOW | c.2295C>G | p.Ala765Ala | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 2921/4560 | 2295/2379 | 765/792 | chr17 | 76948754 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76868539 | C | T | 1 | a0001c0050t0033 | 1 | HG02129.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-491C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/18 | chr17 | 76868539 | |||||||
| chr17:76868716 | G | T | 1 | a0002c0006t0032 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-314G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/18 | 314 | chr17 | 76868716 | ||||||
| chr17:76868922 | A | C | 1 | a0001c0001t0031 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/18 | 108 | chr17 | 76868922 | ||||||
| chr17:76868994 | C | T | 1 | a0003c0026t0030 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/18 | 36 | chr17 | 76868994 | ||||||
| chr17:76948852 | G | A | 25 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0031 others(22): Show |
46 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*14G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 14 | chr17 | 76948852 | ||||||
| chr17:76948942 | C | T | 1 | a0001c0003t0029 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 104 | chr17 | 76948942 | ||||||
| chr17:76948952 | G | A | 1 | a0002c0002t0016 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 114 | chr17 | 76948952 | ||||||
| chr17:76949038 | CCCAGGCA others(10): Show |
C | 5 | a0001c0001t0008 a0001c0005t0008 a0001c0056t0008 others(2): Show |
6 | HG01069.hp2 HG01106.hp1 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*202_*218delCAGGCA others(11): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 202 | INFO_REALIGN_3_PRIME | chr17 | 76949038 | |||||
| chr17:76949043 | G | A | 2 | a0001c0031t0001 a0002c0014t0017 |
2 | HG02965.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*205G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 205 | chr17 | 76949043 | ||||||
| chr17:76949048 | C | T | 1 | a0002c0020t0001 | 2 | HG02976.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*210C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 210 | chr17 | 76949048 | ||||||
| chr17:76949066 | G | A | 1 | a0002c0014t0017 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 228 | chr17 | 76949066 | ||||||
| chr17:76949073 | A | G | 49 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(46): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*235A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 235 | chr17 | 76949073 | ||||||
| chr17:76949075 | A | C | 82 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(79): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*237A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 237 | chr17 | 76949075 | ||||||
| chr17:76949425 | G | A | 7 | a0001c0001t0011 a0001c0025t0010 a0001c0025t0014 others(4): Show |
9 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*587G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 587 | chr17 | 76949425 | ||||||
| chr17:76949476 | CTTCCCTC others(5): Show |
C | 13 | a0001c0001t0002 a0001c0005t0002 a0001c0007t0002 others(10): Show |
38 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*644_*655delTCCCGA others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 644 | INFO_REALIGN_3_PRIME | chr17 | 76949476 | |||||
| chr17:76949570 | TTCTC | T | 2 | a0001c0001t0011 a0002c0002t0011 |
3 | HG02809.hp2 HG03225.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*737_*740delTCTC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 737 | INFO_REALIGN_3_PRIME | chr17 | 76949570 | |||||
| chr17:76949761 | T | C | 82 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(79): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*923T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 923 | chr17 | 76949761 | ||||||
| chr17:76949777 | T | C | 1 | a0001c0003t0021 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*939T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 939 | chr17 | 76949777 | ||||||
| chr17:76949809 | A | G | 28 | a0001c0003t0001 a0001c0003t0013 a0001c0003t0021 others(25): Show |
94 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*971A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 971 | chr17 | 76949809 | ||||||
| chr17:76949831 | C | T | 1 | a0001c0003t0023 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 993 | chr17 | 76949831 | ||||||
| chr17:76949860 | T | A | 2 | a0001c0001t0012 a0001c0011t0012 |
3 | HG00642.hp1 HG01123.hp1 HG01175.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1022T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1022 | chr17 | 76949860 | ||||||
| chr17:76949865 | T | A | 14 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0012 others(11): Show |
31 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1027T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1027 | chr17 | 76949865 | ||||||
| chr17:76949885 | A | C | 2 | a0001c0025t0014 a0002c0034t0014 |
2 | HG02145.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1047A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1047 | chr17 | 76949885 | ||||||
| chr17:76949896 | C | T | 23 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0031 others(20): Show |
42 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1058C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1058 | chr17 | 76949896 | ||||||
| chr17:76949911 | G | A | 1 | a0001c0007t0018 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1073G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1073 | chr17 | 76949911 | ||||||
| chr17:76949941 | A | C | 1 | a0001c0001t0027 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1103A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1103 | chr17 | 76949941 | ||||||
| chr17:76949970 | CCTT | C | 7 | a0001c0001t0011 a0001c0025t0010 a0001c0025t0014 others(4): Show |
9 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1135_*1137delTCT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1135 | INFO_REALIGN_3_PRIME | chr17 | 76949970 | |||||
| chr17:76949973 | T | C | 2 | a0001c0007t0002 a0002c0016t0002 |
2 | HG01952.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1135T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1135 | chr17 | 76949973 | ||||||
| chr17:76949978 | G | A | 16 | a0001c0001t0004 a0001c0001t0031 a0001c0005t0004 others(13): Show |
33 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1140 | chr17 | 76949978 | ||||||
| chr17:76950004 | C | G | 1 | a0002c0020t0022 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1166C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1166 | chr17 | 76950004 | ||||||
| chr17:76950013 | TC | T | 7 | a0001c0001t0011 a0001c0025t0010 a0001c0025t0014 others(4): Show |
9 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1182delC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1182 | INFO_REALIGN_3_PRIME | chr17 | 76950013 | |||||
| chr17:76950026 | C | T | 7 | a0001c0001t0011 a0001c0025t0010 a0001c0025t0014 others(4): Show |
9 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1188C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1188 | chr17 | 76950026 | ||||||
| chr17:76950056 | C | T | 2 | a0001c0005t0009 a0002c0006t0009 |
5 | HG02109.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1218C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1218 | chr17 | 76950056 | ||||||
| chr17:76950097 | C | T | 1 | a0002c0002t0028 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1259 | chr17 | 76950097 | ||||||
| chr17:76950161 | C | T | 1 | a0002c0028t0026 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1323C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1323 | chr17 | 76950161 | ||||||
| chr17:76950204 | T | C | 25 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(22): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1366T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1366 | chr17 | 76950204 | ||||||
| chr17:76950326 | CT | C | 74 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(71): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1496delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1496 | INFO_REALIGN_3_PRIME | chr17 | 76950326 | |||||
| chr17:76950384 | A | G | 7 | a0001c0001t0011 a0001c0025t0010 a0001c0025t0014 others(4): Show |
9 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1546A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 18/18 | 1546 | chr17 | 76950384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76869117 | G | C | 4 | a0002c0014t0017g0004 a0002c0019t0004g0002 a0002c0019t0004g0003 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+20G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869117 | |||||||
| chr17:76869137 | G | T | 1 | a0001c0008t0001g0277 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.68+40G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869137 | |||||||
| chr17:76869173 | G | T | 1 | a0001c0011t0002g0276 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.68+76G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869173 | |||||||
| chr17:76869373 | G | C | 1 | a0002c0006t0002g0006 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.68+276G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869373 | |||||||
| chr17:76869853 | T | G | 6 | a0002c0002t0003g0007 a0002c0002t0003g0009 a0002c0002t0003g0010 others(3): Show |
6 | HG01884.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+756T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869853 | |||||||
| chr17:76869871 | G | A | 1 | a0002c0002t0008g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68+774G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869871 | |||||||
| chr17:76869889 | G | T | 6 | a0002c0002t0003g0007 a0002c0002t0003g0009 a0002c0002t0003g0010 others(3): Show |
6 | HG01884.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.68+792G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869889 | |||||||
| chr17:76869924 | C | T | 2 | a0002c0002t0025g0274 a0002c0017t0002g0273 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.68+827C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869924 | |||||||
| chr17:76869928 | A | G | 244 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.68+831A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869928 | |||||||
| chr17:76869948 | G | A | 1 | a0006c0059t0007g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.68+851G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869948 | |||||||
| chr17:76869967 | G | A | 2 | a0002c0002t0025g0274 a0002c0017t0002g0273 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.68+870G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76869967 | |||||||
| chr17:76870013 | C | T | 1 | a0001c0030t0001g0272 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.68+916C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76870013 | |||||||
| chr17:76870176 | G | A | 1 | a0001c0025t0010g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.68+1079G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76870176 | |||||||
| chr17:76870349 | T | C | 219 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.68+1252T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76870349 | |||||||
| chr17:76870380 | G | A | 1 | a0002c0002t0008g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.68+1283G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76870380 | |||||||
| chr17:76870476 | C | CCTTCT | 221 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.68+1383_68+1384ins others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr17 | 76870476 | ||||||
| chr17:76870820 | GT | G | 16 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0003t0029g0051 others(13): Show |
17 | HG00597.hp1 HG01884.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+1727delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr17 | 76870820 | ||||||
| chr17:76871248 | G | A | 1 | a0001c0007t0002g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.69-1603G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871248 | |||||||
| chr17:76871252 | C | T | 16 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0003t0029g0051 others(13): Show |
17 | HG00597.hp1 HG01884.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.69-1599C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871252 | |||||||
| chr17:76871274 | A | G | 1 | a0002c0012t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.69-1577A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871274 | |||||||
| chr17:76871367 | C | T | 1 | a0002c0019t0004g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69-1484C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871367 | |||||||
| chr17:76871369 | C | T | 57 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0214 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.69-1482C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871369 | |||||||
| chr17:76871497 | C | G | 2 | a0001c0003t0001g0254 a0001c0010t0007g0255 |
2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.69-1354C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871497 | |||||||
| chr17:76871536 | T | C | 1 | a0001c0001t0011g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.69-1315T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871536 | |||||||
| chr17:76871628 | T | G | 1 | a0002c0014t0001g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.69-1223T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871628 | |||||||
| chr17:76871645 | A | G | 4 | a0002c0014t0017g0004 a0002c0019t0004g0002 a0002c0019t0004g0003 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-1206A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871645 | |||||||
| chr17:76871681 | G | A | 1 | a0002c0012t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.69-1170G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76871681 | |||||||
| chr17:76872022 | A | G | 157 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.69-829A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76872022 | |||||||
| chr17:76872203 | G | A | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.69-648G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76872203 | |||||||
| chr17:76872211 | C | T | 3 | a0002c0002t0006g0200 a0002c0002t0011g0199 a0002c0006t0008g0198 |
3 | HG02809.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.69-640C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76872211 | |||||||
| chr17:76872480 | G | C | 2 | a0002c0002t0025g0274 a0002c0017t0002g0273 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.69-371G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76872480 | |||||||
| chr17:76872754 | A | G | 5 | a0002c0006t0002g0196 a0002c0009t0001g0197 a0002c0012t0001g0194 others(2): Show |
5 | HG00597.hp2 HG02015.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-97A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 1/17 | chr17 | 76872754 | |||||||
| chr17:76872973 | T | G | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181+10T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76872973 | |||||||
| chr17:76873249 | G | T | 1 | a0001c0001t0003g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.181+286G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873249 | |||||||
| chr17:76873352 | T | C | 3 | a0001c0049t0010g0067 a0002c0006t0007g0069 a0002c0017t0002g0068 |
3 | HG02280.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.181+389T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873352 | |||||||
| chr17:76873472 | G | A | 1 | a0001c0030t0001g0272 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.181+509G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873472 | |||||||
| chr17:76873506 | C | T | 2 | a0001c0018t0004g0190 a0001c0018t0004g0191 |
2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.181+543C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873506 | |||||||
| chr17:76873559 | C | G | 1 | a0001c0005t0007g0045 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.181+596C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873559 | |||||||
| chr17:76873569 | C | T | 208 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(205): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.181+606C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873569 | |||||||
| chr17:76873584 | G | T | 2 | a0002c0016t0007g0063 a0002c0041t0010g0062 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.181+621G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873584 | |||||||
| chr17:76873659 | C | A | 3 | a0001c0049t0010g0067 a0002c0006t0007g0069 a0002c0017t0002g0068 |
3 | HG02280.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.181+696C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873659 | |||||||
| chr17:76873663 | C | CT | 33 | a0001c0001t0004g0160 a0001c0001t0006g0175 a0001c0001t0006g0178 others(30): Show |
33 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.181+701dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76873663 | ||||||
| chr17:76873787 | G | A | 2 | a0001c0055t0007g0073 a0002c0002t0006g0074 |
2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.181+824G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76873787 | |||||||
| chr17:76874169 | A | G | 5 | a0002c0002t0011g0057 a0002c0028t0004g0061 a0002c0028t0026g0060 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+1206A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76874169 | |||||||
| chr17:76874202 | C | T | 3 | a0001c0049t0010g0067 a0002c0006t0007g0069 a0002c0017t0002g0068 |
3 | HG02280.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.181+1239C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76874202 | |||||||
| chr17:76874437 | A | C | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181+1474A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76874437 | |||||||
| chr17:76874715 | A | C | 129 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.181+1752A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76874715 | |||||||
| chr17:76874796 | G | C | 129 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(126): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.181+1833G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76874796 | |||||||
| chr17:76874966 | T | C | 1 | a0001c0055t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.181+2003T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76874966 | |||||||
| chr17:76874969 | G | A | 96 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0214 others(93): Show |
97 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.181+2006G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76874969 | |||||||
| chr17:76875105 | C | G | 1 | a0002c0016t0007g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.181+2142C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875105 | |||||||
| chr17:76875371 | T | G | 62 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0214 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.181+2408T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875371 | |||||||
| chr17:76875494 | A | G | 2 | a0001c0008t0001g0055 a0001c0008t0001g0056 |
2 | HG02027.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.181+2531A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875494 | |||||||
| chr17:76875515 | A | C | 1 | a0002c0012t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.181+2552A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875515 | |||||||
| chr17:76875609 | A | G | 56 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0214 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.181+2646A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875609 | |||||||
| chr17:76875635 | C | T | 23 | a0001c0001t0006g0270 a0001c0001t0031g0256 a0001c0005t0008g0264 others(20): Show |
23 | HG00438.hp1 HG01099.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.181+2672C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875635 | |||||||
| chr17:76875653 | C | CT | 14 | a0001c0001t0005g0041 a0001c0001t0005g0043 a0001c0001t0006g0096 others(11): Show |
14 | HG00438.hp1 HG01081.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.181+2715dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76875653 | ||||||
| chr17:76875653 | C | CTT | 76 | a0001c0001t0003g0192 a0001c0001t0004g0160 a0001c0001t0005g0125 others(73): Show |
76 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.181+2714_181+2715d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76875653 | ||||||
| chr17:76875653 | C | CTTT | 35 | a0001c0001t0005g0053 a0001c0001t0006g0175 a0001c0001t0006g0178 others(32): Show |
35 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.181+2713_181+2715d others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76875653 | ||||||
| chr17:76875653 | C | CTTTT | 5 | a0001c0001t0003g0157 a0001c0001t0004g0156 a0001c0013t0001g0189 others(2): Show |
5 | HG00544.hp2 HG01358.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.181+2712_181+2715d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76875653 | ||||||
| chr17:76875653 | CTTTTTT | C | 6 | a0001c0001t0006g0248 a0001c0003t0013g0249 a0001c0003t0013g0251 others(3): Show |
6 | HG01516.hp2 HG01517.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+2710_181+2715d others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76875653 | ||||||
| chr17:76875653 | CTTTTTTT | C | 51 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0214 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.181+2709_181+2715d others(9): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76875653 | ||||||
| chr17:76875653 | CTTTTTTT others(4): Show |
C | 2 | a0001c0049t0010g0067 a0002c0017t0002g0068 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.181+2705_181+2715d others(13): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76875653 | ||||||
| chr17:76875773 | G | A | 8 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0003t0029g0051 others(5): Show |
8 | HG00597.hp1 HG02027.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+2810G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875773 | |||||||
| chr17:76875921 | C | T | 1 | a0002c0012t0001g0145 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.181+2958C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875921 | |||||||
| chr17:76875996 | G | A | 1 | a0002c0017t0002g0100 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.181+3033G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76875996 | |||||||
| chr17:76876092 | C | T | 3 | a0001c0049t0010g0067 a0002c0006t0007g0069 a0002c0017t0002g0068 |
3 | HG02280.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.181+3129C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76876092 | |||||||
| chr17:76876194 | G | A | 1 | a0001c0007t0002g0201 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.181+3231G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76876194 | |||||||
| chr17:76876459 | G | GA | 104 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(101): Show |
105 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.181+3512dupA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76876459 | ||||||
| chr17:76876459 | GA | G | 6 | a0001c0003t0001g0094 a0001c0003t0013g0251 a0001c0003t0023g0040 others(3): Show |
6 | HG01074.hp2 HG01168.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+3512delA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76876459 | ||||||
| chr17:76876496 | A | G | 60 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0214 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.181+3533A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76876496 | |||||||
| chr17:76876542 | G | A | 1 | a0001c0013t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.181+3579G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76876542 | |||||||
| chr17:76876582 | G | C | 1 | a0002c0002t0008g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.181+3619G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76876582 | |||||||
| chr17:76876823 | C | T | 11 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0003t0029g0051 others(8): Show |
11 | HG00597.hp1 HG02027.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.181+3860C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76876823 | |||||||
| chr17:76877063 | C | T | 1 | a0001c0031t0001g0245 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.181+4100C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877063 | |||||||
| chr17:76877097 | A | G | 2 | a0001c0003t0001g0187 a0001c0011t0002g0188 |
2 | HG02165.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.181+4134A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877097 | |||||||
| chr17:76877218 | G | A | 1 | a0001c0001t0031g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.181+4255G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877218 | |||||||
| chr17:76877249 | A | G | 1 | a0001c0023t0004g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.181+4286A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877249 | |||||||
| chr17:76877281 | C | A | 24 | a0001c0001t0006g0270 a0001c0001t0031g0256 a0001c0005t0008g0264 others(21): Show |
24 | HG00438.hp1 HG01099.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.181+4318C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877281 | |||||||
| chr17:76877329 | T | TA | 100 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(97): Show |
100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.181+4388dupA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76877329 | ||||||
| chr17:76877329 | T | TAA | 8 | a0001c0013t0001g0101 a0001c0049t0010g0067 a0002c0004t0001g0102 others(5): Show |
8 | HG02080.hp2 HG02818.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+4387_181+4388d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76877329 | ||||||
| chr17:76877486 | C | A | 99 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(96): Show |
99 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.181+4523C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877486 | |||||||
| chr17:76877541 | C | G | 10 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0003t0029g0051 others(7): Show |
10 | HG00597.hp1 HG00642.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.181+4578C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877541 | |||||||
| chr17:76877558 | G | A | 13 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0003t0029g0051 others(10): Show |
13 | HG00597.hp1 HG00642.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.182-4593G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877558 | |||||||
| chr17:76877569 | C | T | 1 | a0002c0002t0005g0142 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.182-4582C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877569 | |||||||
| chr17:76877570 | G | A | 1 | a0002c0002t0008g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.182-4581G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877570 | |||||||
| chr17:76877576 | C | T | 1 | a0001c0003t0001g0243 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.182-4575C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877576 | |||||||
| chr17:76877890 | C | T | 1 | a0001c0010t0007g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.182-4261C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877890 | |||||||
| chr17:76877955 | C | T | 1 | a0002c0004t0001g0139 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.182-4196C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76877955 | |||||||
| chr17:76878099 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.182-4052T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76878099 | |||||||
| chr17:76878462 | G | A | 2 | a0002c0004t0001g0077 a0002c0006t0002g0076 |
2 | HG02523.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.182-3689G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76878462 | |||||||
| chr17:76878539 | A | G | 134 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(131): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.182-3612A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76878539 | |||||||
| chr17:76878716 | C | G | 197 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(194): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.182-3435C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76878716 | |||||||
| chr17:76878887 | A | G | 227 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.182-3264A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76878887 | |||||||
| chr17:76878971 | A | G | 1 | a0001c0023t0004g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.182-3180A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76878971 | |||||||
| chr17:76878976 | G | A | 1 | a0002c0012t0001g0145 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.182-3175G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76878976 | |||||||
| chr17:76878981 | TGGAGTCC others(1): Show |
T | 18 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(15): Show |
18 | HG00642.hp2 HG01099.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.182-3167_182-3160d others(10): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76878981 | ||||||
| chr17:76879014 | T | C | 153 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(150): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.182-3137T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879014 | |||||||
| chr17:76879064 | A | G | 236 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.182-3087A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879064 | |||||||
| chr17:76879066 | G | A | 9 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(6): Show |
9 | HG00642.hp2 HG01099.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.182-3085G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879066 | |||||||
| chr17:76879089 | C | A | 70 | a0001c0001t0005g0053 a0001c0001t0005g0125 a0001c0001t0006g0049 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.182-3062C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879089 | |||||||
| chr17:76879094 | A | G | 13 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.182-3057A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879094 | |||||||
| chr17:76879248 | A | G | 245 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.182-2903A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879248 | |||||||
| chr17:76879299 | G | A | 1 | a0001c0055t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.182-2852G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879299 | |||||||
| chr17:76879352 | A | G | 186 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0214 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.182-2799A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879352 | |||||||
| chr17:76879413 | C | T | 65 | a0001c0001t0003g0192 a0001c0001t0004g0160 a0001c0001t0006g0134 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.182-2738C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879413 | |||||||
| chr17:76879421 | T | C | 5 | a0002c0002t0011g0057 a0002c0028t0004g0061 a0002c0028t0026g0060 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-2730T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879421 | |||||||
| chr17:76879501 | C | T | 1 | a0001c0003t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.182-2650C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879501 | |||||||
| chr17:76879544 | C | G | 99 | a0001c0001t0003g0157 a0001c0001t0005g0053 a0001c0001t0006g0049 others(96): Show |
100 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.182-2607C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879544 | |||||||
| chr17:76879550 | C | T | 1 | a0002c0002t0006g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.182-2601C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879550 | |||||||
| chr17:76879560 | C | T | 54 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(51): Show |
55 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.182-2591C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879560 | |||||||
| chr17:76879642 | G | A | 1 | a0002c0019t0004g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.182-2509G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879642 | |||||||
| chr17:76879925 | C | T | 1 | a0001c0025t0014g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.182-2226C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879925 | |||||||
| chr17:76879988 | C | T | 132 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(129): Show |
133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.182-2163C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879988 | |||||||
| chr17:76879992 | C | T | 7 | a0002c0002t0003g0106 a0002c0002t0004g0105 a0003c0026t0002g0263 others(4): Show |
7 | HG00438.hp1 HG03486.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-2159C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76879992 | |||||||
| chr17:76880109 | G | A | 1 | a0002c0004t0001g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.182-2042G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880109 | |||||||
| chr17:76880307 | T | C | 1 | a0001c0001t0005g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.182-1844T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880307 | |||||||
| chr17:76880355 | C | T | 1 | a0001c0003t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.182-1796C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880355 | |||||||
| chr17:76880546 | T | C | 112 | a0001c0001t0005g0125 a0001c0001t0006g0096 a0001c0003t0001g0094 others(109): Show |
113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.182-1605T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880546 | |||||||
| chr17:76880562 | T | C | 8 | a0002c0002t0011g0057 a0002c0002t0025g0274 a0002c0006t0007g0069 others(5): Show |
9 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-1589T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880562 | |||||||
| chr17:76880752 | T | C | 186 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0156 others(183): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.182-1399T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880752 | |||||||
| chr17:76880791 | C | T | 105 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0003g0106 others(102): Show |
106 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.182-1360C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880791 | |||||||
| chr17:76880812 | G | A | 105 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0003g0106 others(102): Show |
106 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.182-1339G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880812 | |||||||
| chr17:76880950 | T | C | 110 | a0001c0025t0014g0071 a0002c0002t0002g0253 a0002c0002t0003g0084 others(107): Show |
111 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.182-1201T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880950 | |||||||
| chr17:76880981 | C | T | 2 | a0001c0055t0007g0073 a0001c0056t0008g0108 |
2 | HG01069.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.182-1170C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76880981 | |||||||
| chr17:76881025 | G | T | 106 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0003g0106 others(103): Show |
107 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.182-1126G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881025 | |||||||
| chr17:76881226 | C | T | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.182-925C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881226 | |||||||
| chr17:76881272 | G | T | 153 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.182-879G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881272 | |||||||
| chr17:76881391 | T | C | 153 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.182-760T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881391 | |||||||
| chr17:76881470 | C | T | 3 | a0002c0002t0005g0238 a0002c0002t0005g0239 a0002c0017t0002g0273 |
3 | HG02258.hp1 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.182-681C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881470 | |||||||
| chr17:76881478 | C | T | 1 | a0001c0025t0014g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.182-673C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881478 | |||||||
| chr17:76881518 | G | A | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.182-633G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881518 | |||||||
| chr17:76881743 | T | C | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.182-408T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881743 | |||||||
| chr17:76881921 | C | T | 1 | a0001c0003t0023g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.182-230C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881921 | |||||||
| chr17:76881952 | G | A | 1 | a0001c0005t0004g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.182-199G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881952 | |||||||
| chr17:76881988 | A | G | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.182-163A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76881988 | |||||||
| chr17:76882046 | T | TG | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.182-100dupG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr17 | 76882046 | ||||||
| chr17:76882065 | C | G | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.182-86C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 2/17 | chr17 | 76882065 | |||||||
| chr17:76882308 | C | T | 1 | a0002c0002t0006g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.329+10C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882308 | |||||||
| chr17:76882338 | C | T | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.329+40C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882338 | |||||||
| chr17:76882366 | G | A | 11 | a0002c0002t0011g0057 a0002c0002t0025g0274 a0002c0006t0007g0069 others(8): Show |
12 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.329+68G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882366 | |||||||
| chr17:76882385 | T | C | 1 | a0002c0002t0006g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.329+87T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882385 | |||||||
| chr17:76882508 | G | A | 2 | a0002c0012t0001g0194 a0007c0040t0002g0193 |
2 | HG00597.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.329+210G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882508 | |||||||
| chr17:76882527 | A | G | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.329+229A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882527 | |||||||
| chr17:76882599 | G | A | 160 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0001t0006g0134 others(157): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.329+301G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882599 | |||||||
| chr17:76882632 | A | T | 1 | a0002c0014t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.329+334A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882632 | |||||||
| chr17:76882678 | C | T | 2 | a0001c0003t0013g0249 a0001c0003t0013g0251 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.329+380C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882678 | |||||||
| chr17:76882687 | G | A | 14 | a0002c0004t0001g0052 a0002c0004t0001g0114 a0002c0004t0001g0115 others(11): Show |
14 | HG00280.hp2 HG01358.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.329+389G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882687 | |||||||
| chr17:76882704 | CCT | C | 9 | a0002c0002t0011g0057 a0002c0002t0025g0274 a0002c0004t0001g0124 others(6): Show |
10 | HG00621.hp2 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.329+407_329+408del others(2): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882704 | |||||||
| chr17:76882704 | CCTT | C | 54 | a0002c0002t0005g0095 a0002c0002t0006g0185 a0002c0002t0008g0048 others(51): Show |
54 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.329+407_329+409del others(3): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882704 | |||||||
| chr17:76882704 | CCTTT | C | 87 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(84): Show |
87 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.329+407_329+410del others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882704 | |||||||
| chr17:76882705 | C | CT | 32 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0003g0214 others(29): Show |
32 | HG00738.hp2 HG01069.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.329+430dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76882705 | ||||||
| chr17:76882705 | CTTTTT | C | 9 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0005t0002g0235 others(6): Show |
9 | HG00642.hp2 HG01099.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.329+426_329+430del others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76882705 | ||||||
| chr17:76882728 | T | G | 150 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.329+430T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882728 | |||||||
| chr17:76882741 | G | A | 53 | a0002c0002t0006g0185 a0002c0002t0011g0199 a0002c0004t0001g0052 others(50): Show |
53 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.329+443G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882741 | |||||||
| chr17:76882771 | G | A | 150 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(147): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.329+473G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882771 | |||||||
| chr17:76882807 | T | C | 186 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(183): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.329+509T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882807 | |||||||
| chr17:76882825 | C | T | 3 | a0002c0002t0002g0253 a0002c0004t0001g0090 a0002c0004t0001g0091 |
3 | HG01952.hp2 HG02056.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.329+527C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882825 | |||||||
| chr17:76882861 | C | T | 7 | a0001c0001t0006g0134 a0001c0003t0001g0135 a0001c0003t0001g0183 others(4): Show |
7 | HG01928.hp1 HG02071.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.329+563C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882861 | |||||||
| chr17:76882869 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.329+571C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882869 | |||||||
| chr17:76882980 | G | A | 1 | a0001c0007t0002g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.329+682G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76882980 | |||||||
| chr17:76883015 | A | T | 1 | a0002c0002t0004g0260 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.329+717A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883015 | |||||||
| chr17:76883016 | T | A | 2 | a0001c0025t0014g0071 a0008c0039t0001g0117 |
2 | HG02145.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.329+718T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883016 | |||||||
| chr17:76883078 | A | G | 1 | a0001c0045t0001g0231 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.329+780A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883078 | |||||||
| chr17:76883127 | A | G | 44 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(41): Show |
44 | HG00408.hp2 HG00738.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.329+829A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883127 | |||||||
| chr17:76883138 | T | C | 188 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(185): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.329+840T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883138 | |||||||
| chr17:76883150 | A | G | 1 | a0002c0012t0001g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.329+852A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883150 | |||||||
| chr17:76883400 | A | G | 153 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.329+1102A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883400 | |||||||
| chr17:76883483 | C | T | 1 | a0001c0024t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.329+1185C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883483 | |||||||
| chr17:76883555 | C | G | 153 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.329+1257C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883555 | |||||||
| chr17:76883575 | A | G | 153 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.329+1277A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883575 | |||||||
| chr17:76883635 | C | T | 153 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.329+1337C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883635 | |||||||
| chr17:76883725 | C | T | 3 | a0002c0012t0001g0145 a0002c0012t0001g0147 a0002c0020t0022g0153 |
3 | HG02818.hp1 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.329+1427C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883725 | |||||||
| chr17:76883881 | T | C | 155 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(152): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.329+1583T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883881 | |||||||
| chr17:76883938 | G | A | 2 | a0002c0016t0007g0063 a0002c0041t0010g0062 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.329+1640G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883938 | |||||||
| chr17:76883957 | G | C | 2 | a0001c0001t0012g0016 a0001c0047t0001g0015 |
2 | HG01175.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.329+1659G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76883957 | |||||||
| chr17:76884073 | ATTTAC | A | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.329+1777_329+1781d others(7): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76884073 | ||||||
| chr17:76884173 | G | T | 1 | a0001c0008t0001g0230 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.329+1875G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76884173 | |||||||
| chr17:76884211 | C | G | 2 | a0001c0055t0007g0073 a0001c0056t0008g0108 |
2 | HG01069.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.329+1913C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76884211 | |||||||
| chr17:76884444 | T | TA | 3 | a0002c0012t0001g0145 a0002c0012t0001g0147 a0002c0020t0022g0153 |
3 | HG02818.hp1 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.329+2146_329+2147i others(3): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76884444 | |||||||
| chr17:76884445 | T | A | 154 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(151): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.329+2147T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76884445 | |||||||
| chr17:76884533 | G | A | 153 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.329+2235G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76884533 | |||||||
| chr17:76884602 | A | AT | 21 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(18): Show |
21 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.329+2323dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76884602 | ||||||
| chr17:76884602 | AT | A | 144 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(141): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.329+2323delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76884602 | ||||||
| chr17:76884602 | ATT | A | 16 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(13): Show |
16 | HG00642.hp2 HG01099.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.329+2322_329+2323d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76884602 | ||||||
| chr17:76884634 | C | T | 8 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01099.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+2336C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76884634 | |||||||
| chr17:76884981 | G | A | 19 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.329+2683G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76884981 | |||||||
| chr17:76885234 | G | A | 1 | a0002c0002t0003g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.329+2936G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885234 | |||||||
| chr17:76885267 | C | G | 2 | a0001c0055t0007g0073 a0001c0056t0008g0108 |
2 | HG01069.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.329+2969C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885267 | |||||||
| chr17:76885282 | C | G | 1 | a0002c0012t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.329+2984C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885282 | |||||||
| chr17:76885443 | A | G | 187 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(184): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.329+3145A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885443 | |||||||
| chr17:76885453 | G | C | 1 | a0002c0017t0002g0273 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.329+3155G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885453 | |||||||
| chr17:76885507 | T | C | 1 | a0001c0001t0011g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.329+3209T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885507 | |||||||
| chr17:76885564 | C | T | 2 | a0002c0014t0001g0066 a0002c0014t0001g0088 |
2 | NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.329+3266C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885564 | |||||||
| chr17:76885601 | G | C | 1 | a0001c0001t0006g0096 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.329+3303G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885601 | |||||||
| chr17:76885788 | C | T | 3 | a0002c0012t0001g0145 a0002c0012t0001g0147 a0002c0020t0022g0153 |
3 | HG02818.hp1 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.329+3490C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885788 | |||||||
| chr17:76885809 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.329+3511C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76885809 | |||||||
| chr17:76885951 | TA | T | 187 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(184): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.329+3661delA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76885951 | ||||||
| chr17:76886042 | G | A | 2 | a0002c0002t0005g0258 a0002c0012t0001g0271 |
2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.329+3744G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886042 | |||||||
| chr17:76886095 | C | A | 1 | a0002c0009t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.329+3797C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886095 | |||||||
| chr17:76886118 | C | T | 3 | a0001c0005t0009g0162 a0001c0005t0009g0163 a0001c0005t0009g0170 |
3 | HG02109.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.329+3820C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886118 | |||||||
| chr17:76886157 | G | A | 1 | a0001c0003t0001g0094 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.329+3859G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886157 | |||||||
| chr17:76886318 | A | G | 187 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(184): Show |
188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.329+4020A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886318 | |||||||
| chr17:76886364 | G | C | 37 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(34): Show |
38 | HG00642.hp2 HG01099.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.329+4066G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886364 | |||||||
| chr17:76886488 | G | A | 1 | a0002c0020t0022g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.329+4190G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886488 | |||||||
| chr17:76886491 | G | A | 1 | a0002c0014t0001g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.329+4193G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886491 | |||||||
| chr17:76886529 | G | A | 1 | a0001c0010t0007g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.329+4231G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886529 | |||||||
| chr17:76886714 | G | A | 1 | a0002c0017t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.329+4416G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886714 | |||||||
| chr17:76886956 | A | C | 19 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.329+4658A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886956 | |||||||
| chr17:76886976 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.329+4678G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76886976 | |||||||
| chr17:76887045 | C | CAAAACAA | 17 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(14): Show |
18 | HG00642.hp2 HG01099.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.329+4751_329+4757d others(9): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887045 | ||||||
| chr17:76887045 | C | CAAAACAA others(7): Show |
221 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.329+4757_329+4758i others(16): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887045 | ||||||
| chr17:76887051 | A | AAAAAACA others(6): Show |
1 | a0001c0003t0001g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.329+4757_329+4758i others(15): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887051 | ||||||
| chr17:76887256 | G | C | 1 | a0001c0001t0002g0209 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.329+4958G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887256 | |||||||
| chr17:76887318 | A | G | 185 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(182): Show |
186 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.329+5020A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887318 | |||||||
| chr17:76887449 | T | TCCTC | 3 | a0002c0002t0005g0238 a0002c0002t0005g0239 a0002c0017t0002g0273 |
3 | HG02258.hp1 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.329+5154_329+5155i others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887449 | ||||||
| chr17:76887453 | T | C | 3 | a0002c0002t0005g0238 a0002c0002t0005g0239 a0002c0017t0002g0273 |
3 | HG02258.hp1 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.329+5155T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887453 | |||||||
| chr17:76887485 | C | G | 1 | a0001c0001t0003g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.329+5187C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887485 | |||||||
| chr17:76887517 | CCCTCCCT others(9): Show |
C | 16 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(13): Show |
17 | HG00642.hp2 HG01099.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.329+5223_329+5238d others(18): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887517 | ||||||
| chr17:76887525 | C | T | 1 | a0002c0042t0004g0168 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.329+5227C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887525 | |||||||
| chr17:76887525 | CCCTCCCT others(1): Show |
C | 49 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(46): Show |
49 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.329+5231_329+5238d others(10): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887525 | ||||||
| chr17:76887529 | CCCTT | C | 119 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(116): Show |
119 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.329+5244_329+5247d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887529 | ||||||
| chr17:76887533 | T | C | 1 | a0002c0002t0016g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.329+5235T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887533 | |||||||
| chr17:76887559 | CT | C | 167 | a0001c0001t0002g0209 a0001c0001t0005g0053 a0001c0001t0006g0049 others(164): Show |
167 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.329+5275delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76887559 | ||||||
| chr17:76887663 | C | T | 8 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01099.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+5365C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887663 | |||||||
| chr17:76887714 | C | T | 8 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0054 others(5): Show |
8 | HG00642.hp2 HG01099.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+5416C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887714 | |||||||
| chr17:76887757 | A | G | 2 | a0001c0007t0002g0136 a0001c0052t0003g0137 |
2 | HG01993.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.329+5459A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887757 | |||||||
| chr17:76887846 | C | T | 2 | a0002c0002t0004g0240 a0002c0020t0001g0161 |
2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.329+5548C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887846 | |||||||
| chr17:76887885 | G | A | 2 | a0002c0014t0001g0066 a0002c0014t0001g0088 |
2 | NA18998.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.329+5587G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887885 | |||||||
| chr17:76887910 | C | T | 1 | a0001c0005t0008g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.329+5612C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887910 | |||||||
| chr17:76887920 | T | C | 2 | a0001c0001t0004g0156 a0002c0014t0001g0207 |
2 | HG02258.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.329+5622T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76887920 | |||||||
| chr17:76888201 | G | A | 3 | a0002c0012t0001g0145 a0002c0012t0001g0147 a0002c0020t0022g0153 |
3 | HG02818.hp1 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.329+5903G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888201 | |||||||
| chr17:76888375 | C | T | 3 | a0002c0002t0025g0274 a0002c0006t0007g0069 a0002c0006t0009g0001 |
4 | HG02280.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+6077C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888375 | |||||||
| chr17:76888399 | T | A | 1 | a0001c0003t0001g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.329+6101T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888399 | |||||||
| chr17:76888447 | T | C | 2 | a0002c0002t0008g0013 a0002c0020t0001g0008 |
2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.329+6149T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888447 | |||||||
| chr17:76888749 | T | C | 60 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(57): Show |
60 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.329+6451T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888749 | |||||||
| chr17:76888784 | G | A | 1 | a0002c0002t0011g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.329+6486G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888784 | |||||||
| chr17:76888806 | G | A | 5 | a0002c0002t0011g0057 a0002c0028t0004g0061 a0002c0028t0026g0060 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.329+6508G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888806 | |||||||
| chr17:76888812 | C | T | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.329+6514C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888812 | |||||||
| chr17:76888949 | G | T | 60 | a0001c0001t0007g0233 a0002c0002t0006g0185 a0002c0002t0006g0200 others(57): Show |
61 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.329+6651G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888949 | |||||||
| chr17:76888967 | C | T | 60 | a0001c0001t0007g0233 a0002c0002t0006g0185 a0002c0002t0006g0200 others(57): Show |
61 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.329+6669C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76888967 | |||||||
| chr17:76889054 | G | A | 153 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(150): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.329+6756G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889054 | |||||||
| chr17:76889094 | A | G | 60 | a0001c0001t0007g0233 a0002c0002t0006g0185 a0002c0002t0006g0200 others(57): Show |
61 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.329+6796A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889094 | |||||||
| chr17:76889120 | G | A | 27 | a0001c0001t0006g0134 a0001c0001t0006g0175 a0001c0001t0006g0178 others(24): Show |
27 | HG00408.hp2 HG00738.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.329+6822G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889120 | |||||||
| chr17:76889155 | G | A | 16 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0006g0270 others(13): Show |
16 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.329+6857G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889155 | |||||||
| chr17:76889198 | C | T | 189 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(186): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.329+6900C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889198 | |||||||
| chr17:76889276 | T | A | 1 | a0001c0003t0001g0206 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.329+6978T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889276 | |||||||
| chr17:76889513 | C | T | 56 | a0001c0001t0007g0233 a0002c0002t0006g0185 a0002c0002t0008g0048 others(53): Show |
56 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.329+7215C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889513 | |||||||
| chr17:76889567 | G | A | 140 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(137): Show |
141 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.329+7269G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889567 | |||||||
| chr17:76889609 | T | C | 6 | a0001c0005t0008g0264 a0001c0013t0001g0237 a0001c0025t0014g0071 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.329+7311T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889609 | |||||||
| chr17:76889664 | T | C | 4 | a0001c0001t0005g0210 a0001c0007t0002g0211 a0001c0011t0002g0184 others(1): Show |
4 | HG01433.hp2 HG03239.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.329+7366T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889664 | |||||||
| chr17:76889681 | AAAT | A | 25 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(22): Show |
25 | HG00642.hp2 HG01099.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.329+7392_329+7394d others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76889681 | ||||||
| chr17:76889807 | A | G | 159 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(156): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.329+7509A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889807 | |||||||
| chr17:76889865 | G | C | 1 | a0002c0002t0006g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.329+7567G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889865 | |||||||
| chr17:76889866 | C | T | 59 | a0001c0001t0007g0233 a0002c0002t0006g0185 a0002c0002t0008g0048 others(56): Show |
60 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.329+7568C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76889866 | |||||||
| chr17:76890021 | C | T | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.329+7723C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890021 | |||||||
| chr17:76890055 | C | G | 48 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(45): Show |
48 | HG00408.hp2 HG00738.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.329+7757C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890055 | |||||||
| chr17:76890156 | G | A | 155 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(152): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.329+7858G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890156 | |||||||
| chr17:76890175 | T | C | 3 | a0002c0002t0005g0238 a0002c0002t0005g0239 a0002c0017t0002g0273 |
3 | HG02258.hp1 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.329+7877T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890175 | |||||||
| chr17:76890240 | C | T | 1 | a0002c0002t0006g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.329+7942C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890240 | |||||||
| chr17:76890246 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.329+7948C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890246 | |||||||
| chr17:76890391 | T | A | 3 | a0002c0002t0025g0274 a0002c0006t0007g0069 a0002c0006t0009g0001 |
4 | HG02280.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+8093T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890391 | |||||||
| chr17:76890793 | G | A | 37 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0003g0106 others(34): Show |
37 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.329+8495G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890793 | |||||||
| chr17:76890914 | C | G | 1 | a0001c0010t0003g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.329+8616C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890914 | |||||||
| chr17:76890928 | A | G | 183 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(180): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.329+8630A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76890928 | |||||||
| chr17:76890961 | C | CT | 5 | a0001c0001t0012g0016 a0001c0003t0001g0151 a0001c0005t0004g0208 others(2): Show |
5 | HG01175.hp2 HG01433.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.329+8683dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76890961 | ||||||
| chr17:76890961 | CT | C | 5 | a0001c0003t0001g0099 a0001c0005t0002g0235 a0001c0005t0003g0212 others(2): Show |
5 | HG03927.hp1 HG04184.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.329+8683delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76890961 | ||||||
| chr17:76890961 | CTT | C | 64 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(61): Show |
64 | HG00099.hp1 HG00408.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.329+8682_329+8683d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76890961 | ||||||
| chr17:76890961 | CTTT | C | 117 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(114): Show |
118 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.329+8681_329+8683d others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76890961 | ||||||
| chr17:76891047 | C | T | 1 | a0002c0002t0011g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.329+8749C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76891047 | |||||||
| chr17:76891646 | G | C | 3 | a0002c0002t0025g0274 a0002c0006t0007g0069 a0002c0006t0009g0001 |
4 | HG02280.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+9348G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76891646 | |||||||
| chr17:76891675 | C | T | 1 | a0001c0007t0002g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.329+9377C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76891675 | |||||||
| chr17:76891694 | C | T | 133 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.329+9396C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76891694 | |||||||
| chr17:76891897 | T | C | 1 | a0001c0007t0002g0136 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.329+9599T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76891897 | |||||||
| chr17:76892029 | A | G | 188 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(185): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.329+9731A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892029 | |||||||
| chr17:76892077 | C | T | 123 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(120): Show |
123 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.329+9779C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892077 | |||||||
| chr17:76892115 | C | T | 1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.329+9817C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892115 | |||||||
| chr17:76892193 | A | G | 52 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(49): Show |
52 | HG00099.hp1 HG00408.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.329+9895A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892193 | |||||||
| chr17:76892284 | G | A | 1 | a0002c0002t0006g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.329+9986G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892284 | |||||||
| chr17:76892299 | C | T | 50 | a0001c0001t0004g0160 a0001c0001t0006g0134 a0001c0001t0006g0175 others(47): Show |
50 | HG00099.hp1 HG00408.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.329+10001C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892299 | |||||||
| chr17:76892324 | G | A | 1 | a0001c0001t0005g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.329+10026G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892324 | |||||||
| chr17:76892597 | A | G | 103 | a0001c0001t0007g0233 a0001c0005t0008g0264 a0001c0008t0001g0054 others(100): Show |
103 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.330-9958A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892597 | |||||||
| chr17:76892630 | A | G | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330-9925A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892630 | |||||||
| chr17:76892658 | C | T | 5 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0006g0270 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.330-9897C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892658 | |||||||
| chr17:76892675 | T | G | 1 | a0002c0002t0006g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.330-9880T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892675 | |||||||
| chr17:76892765 | C | T | 35 | a0001c0005t0008g0264 a0001c0013t0001g0237 a0002c0002t0002g0253 others(32): Show |
35 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.330-9790C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892765 | |||||||
| chr17:76892916 | C | T | 180 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(177): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.330-9639C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76892916 | |||||||
| chr17:76893046 | C | T | 1 | a0001c0010t0007g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.330-9509C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893046 | |||||||
| chr17:76893064 | C | T | 29 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0005g0039 others(26): Show |
29 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.330-9491C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893064 | |||||||
| chr17:76893162 | G | A | 180 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0004g0160 others(177): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.330-9393G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893162 | |||||||
| chr17:76893183 | G | A | 125 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(122): Show |
126 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.330-9372G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893183 | |||||||
| chr17:76893249 | G | A | 5 | a0002c0002t0011g0057 a0002c0028t0004g0061 a0002c0028t0026g0060 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.330-9306G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893249 | |||||||
| chr17:76893263 | C | T | 273 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0024 others(270): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.330-9292C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893263 | |||||||
| chr17:76893447 | C | T | 1 | a0002c0006t0008g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.330-9108C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893447 | |||||||
| chr17:76893838 | A | G | 129 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(126): Show |
130 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.330-8717A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893838 | |||||||
| chr17:76893863 | G | A | 1 | a0002c0006t0009g0001 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.330-8692G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893863 | |||||||
| chr17:76893887 | G | A | 30 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0005g0039 others(27): Show |
30 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.330-8668G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893887 | |||||||
| chr17:76893902 | C | T | 1 | a0002c0021t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.330-8653C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893902 | |||||||
| chr17:76893951 | C | A | 94 | a0001c0001t0007g0233 a0001c0005t0008g0264 a0001c0013t0001g0237 others(91): Show |
94 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.330-8604C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76893951 | |||||||
| chr17:76894070 | C | T | 35 | a0001c0005t0008g0264 a0001c0013t0001g0237 a0002c0002t0002g0253 others(32): Show |
35 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.330-8485C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894070 | |||||||
| chr17:76894103 | G | A | 126 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(123): Show |
127 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.330-8452G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894103 | |||||||
| chr17:76894195 | G | A | 2 | a0002c0006t0007g0069 a0002c0006t0009g0001 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.330-8360G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894195 | |||||||
| chr17:76894223 | C | G | 2 | a0002c0006t0007g0069 a0002c0006t0009g0001 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.330-8332C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894223 | |||||||
| chr17:76894253 | G | A | 1 | a0002c0022t0003g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.330-8302G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894253 | |||||||
| chr17:76894261 | G | C | 1 | a0002c0002t0006g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.330-8294G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894261 | |||||||
| chr17:76894387 | T | C | 2 | a0002c0006t0007g0069 a0002c0006t0009g0001 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.330-8168T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894387 | |||||||
| chr17:76894430 | G | C | 1 | a0002c0002t0004g0240 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.330-8125G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894430 | |||||||
| chr17:76894448 | G | C | 1 | a0002c0034t0014g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.330-8107G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894448 | |||||||
| chr17:76894577 | T | C | 153 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(150): Show |
154 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.330-7978T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894577 | |||||||
| chr17:76894578 | G | A | 146 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(143): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.330-7977G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894578 | |||||||
| chr17:76894586 | T | C | 1 | a0001c0054t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.330-7969T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894586 | |||||||
| chr17:76894660 | G | C | 156 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(153): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.330-7895G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894660 | |||||||
| chr17:76894687 | T | C | 2 | a0002c0014t0017g0004 a0002c0019t0004g0005 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.330-7868T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894687 | |||||||
| chr17:76894715 | C | T | 3 | a0002c0006t0007g0069 a0002c0006t0009g0001 a0002c0012t0001g0104 |
4 | HG00639.hp2 HG02280.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-7840C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894715 | |||||||
| chr17:76894716 | G | A | 1 | a0001c0045t0001g0231 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.330-7839G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894716 | |||||||
| chr17:76894818 | A | C | 1 | a0002c0002t0008g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.330-7737A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894818 | |||||||
| chr17:76894823 | A | C | 2 | a0002c0016t0007g0063 a0002c0041t0010g0062 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.330-7732A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894823 | |||||||
| chr17:76894917 | A | G | 156 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(153): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.330-7638A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76894917 | |||||||
| chr17:76895056 | T | A | 22 | a0001c0001t0004g0160 a0001c0001t0008g0107 a0001c0030t0001g0154 others(19): Show |
22 | HG00099.hp1 HG01099.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.330-7499T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895056 | |||||||
| chr17:76895058 | C | T | 31 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0005g0039 others(28): Show |
31 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.330-7497C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895058 | |||||||
| chr17:76895074 | C | T | 25 | a0001c0001t0004g0160 a0001c0001t0008g0107 a0001c0030t0001g0154 others(22): Show |
25 | HG00099.hp1 HG01069.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.330-7481C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895074 | |||||||
| chr17:76895301 | G | A | 36 | a0001c0005t0008g0264 a0001c0013t0001g0237 a0002c0002t0002g0253 others(33): Show |
36 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.330-7254G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895301 | |||||||
| chr17:76895301 | G | C | 1 | a0002c0017t0002g0100 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.330-7254G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895301 | |||||||
| chr17:76895382 | C | T | 7 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0055 others(4): Show |
7 | HG00642.hp2 HG01099.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-7173C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895382 | |||||||
| chr17:76895383 | A | T | 2 | a0002c0006t0007g0069 a0002c0006t0009g0001 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.330-7172A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895383 | |||||||
| chr17:76895475 | A | G | 2 | a0002c0012t0001g0271 a0002c0014t0017g0004 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.330-7080A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895475 | |||||||
| chr17:76895491 | G | A | 57 | a0001c0001t0007g0233 a0001c0013t0001g0250 a0002c0002t0003g0106 others(54): Show |
57 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.330-7064G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895491 | |||||||
| chr17:76895528 | A | G | 155 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.330-7027A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895528 | |||||||
| chr17:76895604 | G | T | 31 | a0002c0002t0002g0253 a0002c0002t0003g0084 a0002c0002t0005g0039 others(28): Show |
31 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.330-6951G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895604 | |||||||
| chr17:76895628 | T | A | 155 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.330-6927T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895628 | |||||||
| chr17:76895727 | G | T | 2 | a0002c0006t0007g0069 a0002c0006t0009g0001 |
3 | HG02280.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.330-6828G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895727 | |||||||
| chr17:76895812 | G | T | 28 | a0001c0001t0004g0160 a0001c0001t0008g0107 a0001c0030t0001g0154 others(25): Show |
28 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.330-6743G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895812 | |||||||
| chr17:76895908 | G | A | 2 | a0002c0002t0005g0238 a0007c0040t0002g0193 |
2 | HG02258.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.330-6647G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895908 | |||||||
| chr17:76895954 | G | A | 1 | a0001c0011t0002g0202 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.330-6601G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76895954 | |||||||
| chr17:76896018 | G | A | 2 | a0001c0001t0012g0016 a0001c0047t0001g0015 |
2 | HG01175.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.330-6537G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896018 | |||||||
| chr17:76896051 | G | A | 2 | a0001c0005t0008g0264 a0001c0013t0001g0237 |
2 | HG04115.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.330-6504G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896051 | |||||||
| chr17:76896089 | A | T | 60 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0005g0053 others(57): Show |
60 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.330-6466A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896089 | |||||||
| chr17:76896118 | C | T | 9 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0008t0001g0055 others(6): Show |
9 | HG00642.hp2 HG01099.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.330-6437C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896118 | |||||||
| chr17:76896149 | A | G | 52 | a0001c0001t0007g0233 a0001c0008t0001g0054 a0002c0002t0003g0106 others(49): Show |
52 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.330-6406A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896149 | |||||||
| chr17:76896454 | T | C | 58 | a0001c0001t0002g0209 a0001c0001t0003g0157 a0001c0001t0003g0192 others(55): Show |
59 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.330-6101T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896454 | |||||||
| chr17:76896466 | C | T | 55 | a0001c0001t0008g0107 a0001c0003t0001g0138 a0001c0005t0002g0235 others(52): Show |
55 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.330-6089C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896466 | |||||||
| chr17:76896658 | T | TG | 3 | a0001c0003t0001g0181 a0001c0003t0001g0187 a0001c0011t0002g0186 |
3 | HG02083.hp2 HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.330-5896dupG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76896658 | ||||||
| chr17:76896772 | A | C | 52 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0007t0019g0180 others(49): Show |
52 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.330-5783A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896772 | |||||||
| chr17:76896822 | C | T | 1 | a0001c0003t0029g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.330-5733C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896822 | |||||||
| chr17:76896945 | G | A | 70 | a0001c0001t0003g0214 a0001c0001t0004g0160 a0001c0001t0005g0053 others(67): Show |
71 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.330-5610G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76896945 | |||||||
| chr17:76897019 | A | G | 50 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(47): Show |
50 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.330-5536A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897019 | |||||||
| chr17:76897331 | C | G | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330-5224C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897331 | |||||||
| chr17:76897416 | A | T | 2 | a0002c0002t0025g0274 a0002c0017t0002g0273 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.330-5139A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897416 | |||||||
| chr17:76897496 | A | G | 9 | a0001c0001t0004g0160 a0001c0001t0006g0270 a0002c0002t0003g0009 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.330-5059A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897496 | |||||||
| chr17:76897504 | G | A | 189 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0003g0214 others(186): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.330-5051G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897504 | |||||||
| chr17:76897542 | G | C | 89 | a0001c0001t0003g0157 a0001c0001t0003g0214 a0001c0001t0004g0160 others(86): Show |
90 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.330-5013G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897542 | |||||||
| chr17:76897604 | A | G | 6 | a0001c0005t0009g0162 a0001c0005t0009g0163 a0001c0005t0009g0170 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-4951A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897604 | |||||||
| chr17:76897659 | CACTT | C | 8 | a0001c0005t0003g0212 a0001c0025t0014g0071 a0002c0002t0006g0185 others(5): Show |
8 | HG02145.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-4895_330-4892d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897659 | |||||||
| chr17:76897659 | CACTTTCT others(1): Show |
C | 5 | a0001c0005t0009g0162 a0001c0005t0009g0170 a0002c0002t0003g0106 others(2): Show |
5 | HG02109.hp1 HG03453.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.330-4895_330-4888d others(10): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897659 | |||||||
| chr17:76897659 | CACTTTCT others(5): Show |
C | 13 | a0001c0003t0001g0204 a0001c0005t0008g0264 a0001c0005t0009g0163 others(10): Show |
13 | HG00639.hp2 HG01069.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.330-4895_330-4884d others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897659 | |||||||
| chr17:76897659 | CACTTTCT others(9): Show |
C | 6 | a0002c0002t0006g0200 a0002c0002t0028g0259 a0002c0004t0001g0091 others(3): Show |
6 | HG01099.hp2 HG01952.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-4895_330-4880d others(18): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897659 | |||||||
| chr17:76897659 | CACTTTCT others(17): Show |
C | 2 | a0001c0030t0001g0154 a0002c0009t0001g0092 |
2 | HG00673.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.330-4895_330-4872d others(26): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897659 | |||||||
| chr17:76897660 | A | ACCTT | 9 | a0001c0001t0012g0016 a0001c0003t0001g0254 a0001c0003t0013g0249 others(6): Show |
9 | HG00408.hp1 HG01175.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.330-4894_330-4893i others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACCTTCTT others(1): Show |
16 | a0001c0001t0002g0205 a0001c0001t0005g0210 a0001c0003t0001g0243 others(13): Show |
16 | HG00423.hp2 HG00621.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.330-4894_330-4893i others(10): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACCTTCTT others(5): Show |
7 | a0001c0001t0027g0220 a0001c0007t0002g0136 a0001c0007t0002g0216 others(4): Show |
7 | HG01168.hp1 HG01255.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-4894_330-4893i others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACCTTCTT others(9): Show |
3 | a0001c0010t0003g0128 a0001c0010t0003g0217 a0001c0011t0002g0223 |
3 | HG02027.hp2 NA18975.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.330-4894_330-4893i others(18): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACCTTCTT others(13): Show |
1 | a0001c0007t0002g0219 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.330-4894_330-4893i others(22): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACCTTCTT others(17): Show |
5 | a0001c0001t0002g0209 a0001c0001t0006g0248 a0001c0007t0002g0064 others(2): Show |
5 | HG01952.hp1 HG02040.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.330-4894_330-4893i others(26): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACCTTCTT others(21): Show |
1 | a0001c0045t0001g0231 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.330-4894_330-4893i others(30): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACTTT | 10 | a0001c0001t0003g0036 a0001c0001t0004g0156 a0001c0001t0006g0034 others(7): Show |
10 | HG00140.hp1 HG00735.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.330-4830_330-4827d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACTTTCTT others(1): Show |
4 | a0001c0001t0005g0125 a0001c0005t0004g0126 a0001c0024t0001g0141 others(1): Show |
4 | HG00280.hp1 HG02615.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-4834_330-4827d others(10): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACTTTCTT others(5): Show |
4 | a0001c0003t0001g0035 a0001c0011t0002g0033 a0003c0027t0001g0262 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-4838_330-4827d others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | ACTTTCTT others(9): Show |
2 | a0001c0001t0012g0014 a0003c0026t0002g0263 |
2 | HG00642.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.330-4842_330-4827d others(18): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | A | T | 54 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0048t0003g0143 others(51): Show |
54 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.330-4895A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897660 | |||||||
| chr17:76897660 | ACTTT | A | 11 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0005g0021 others(8): Show |
11 | HG00099.hp2 HG01074.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.330-4830_330-4827d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | ACTTTCTT others(1): Show |
A | 4 | a0001c0008t0001g0230 a0001c0013t0001g0237 a0002c0014t0001g0207 others(1): Show |
4 | HG04115.hp1 NA18942.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-4834_330-4827d others(10): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | ACTTTCTT others(5): Show |
A | 4 | a0001c0001t0006g0025 a0002c0009t0001g0119 a0002c0009t0001g0120 others(1): Show |
4 | HG01496.hp2 HG02056.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-4838_330-4827d others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | ACTTTCTT others(9): Show |
A | 1 | a0001c0024t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.330-4842_330-4827d others(18): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897660 | ACTTTCTT others(13): Show |
A | 3 | a0001c0001t0003g0024 a0001c0001t0003g0029 a0001c0057t0004g0027 |
3 | HG02280.hp1 HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.330-4846_330-4827d others(22): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897660 | ||||||
| chr17:76897662 | T | C | 4 | a0001c0003t0029g0051 a0001c0007t0002g0127 a0001c0011t0002g0184 others(1): Show |
4 | HG00597.hp1 HG00673.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.330-4893T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897662 | |||||||
| chr17:76897664 | T | A | 1 | a0001c0001t0006g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.330-4891T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897664 | |||||||
| chr17:76897666 | T | C | 2 | a0001c0001t0003g0221 a0001c0023t0004g0227 |
2 | HG00099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.330-4889T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897666 | |||||||
| chr17:76897667 | T | C | 1 | a0001c0010t0003g0130 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.330-4888T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897667 | |||||||
| chr17:76897670 | T | C | 2 | a0001c0008t0001g0230 a0007c0040t0002g0193 |
2 | NA18942.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.330-4885T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897670 | |||||||
| chr17:76897680 | T | C | 1 | a0003c0027t0001g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.330-4875T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897680 | |||||||
| chr17:76897691 | TTCTTTCT others(33): Show |
T | 1 | a0002c0002t0005g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.330-4862_330-4823d others(42): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897691 | ||||||
| chr17:76897693 | CTTTCTTT others(27): Show |
C | 1 | a0002c0022t0003g0097 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.330-4854_330-4821d others(36): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897693 | ||||||
| chr17:76897695 | TTCTTTCT others(29): Show |
T | 2 | a0002c0016t0002g0085 a0002c0022t0003g0082 |
2 | HG01496.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.330-4858_330-4823d others(38): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897695 | ||||||
| chr17:76897699 | TTCTTTCT others(25): Show |
T | 2 | a0002c0002t0005g0039 a0002c0043t0001g0158 |
2 | HG00544.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.330-4854_330-4823d others(34): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897699 | ||||||
| chr17:76897703 | TTCTTTCT others(21): Show |
T | 25 | a0001c0001t0008g0107 a0002c0002t0003g0084 a0002c0002t0004g0257 others(22): Show |
25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.330-4850_330-4823d others(30): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897703 | ||||||
| chr17:76897707 | TTCTTTCT others(17): Show |
T | 16 | a0001c0003t0001g0044 a0002c0002t0002g0253 a0002c0002t0005g0258 others(13): Show |
16 | HG00544.hp1 HG00621.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.330-4846_330-4823d others(26): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897707 | ||||||
| chr17:76897710 | TTTCTTTC others(14): Show |
T | 1 | a0001c0001t0006g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.330-4842_330-4822d others(23): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897710 | ||||||
| chr17:76897727 | T | TTC | 35 | a0001c0001t0004g0160 a0001c0001t0005g0043 a0001c0001t0006g0134 others(32): Show |
35 | HG00438.hp2 HG00738.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.330-4827_330-4826i others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897727 | ||||||
| chr17:76897727 | T | TTCTTTC | 18 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0006g0049 others(15): Show |
18 | HG00280.hp2 HG00408.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.330-4827_330-4826i others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897727 | ||||||
| chr17:76897727 | T | TTCTTTCT others(3): Show |
11 | a0001c0001t0005g0053 a0001c0001t0006g0178 a0001c0001t0031g0256 others(8): Show |
11 | HG00738.hp1 HG01243.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.330-4827_330-4826i others(12): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897727 | ||||||
| chr17:76897727 | T | TTCTTTCT others(7): Show |
9 | a0001c0001t0003g0214 a0001c0003t0001g0138 a0001c0003t0001g0165 others(6): Show |
9 | HG01109.hp2 HG01361.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.330-4827_330-4826i others(16): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897727 | ||||||
| chr17:76897727 | T | TTCTTTCT others(11): Show |
4 | a0001c0001t0006g0270 a0002c0012t0001g0159 a0002c0015t0003g0111 others(1): Show |
4 | HG02630.hp2 HG02738.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.330-4827_330-4826i others(20): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897727 | ||||||
| chr17:76897728 | T | C | 1 | a0001c0008t0001g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.330-4827T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897728 | |||||||
| chr17:76897728 | T | TC | 3 | a0001c0005t0002g0019 a0002c0006t0002g0076 a0004c0035t0004g0155 |
3 | HG01109.hp1 HG01358.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.330-4827_330-4826i others(3): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897728 | |||||||
| chr17:76897728 | T | TCTTTCTT others(6): Show |
1 | a0001c0003t0029g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.330-4827_330-4826i others(15): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897728 | |||||||
| chr17:76897729 | T | C | 1 | a0002c0002t0003g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.330-4826T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897729 | |||||||
| chr17:76897731 | C | CT | 10 | a0001c0001t0003g0036 a0001c0001t0004g0156 a0001c0003t0001g0151 others(7): Show |
10 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.330-4806dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897731 | ||||||
| chr17:76897731 | C | T | 21 | a0001c0001t0004g0160 a0001c0001t0005g0043 a0001c0001t0006g0134 others(18): Show |
21 | HG01099.hp1 HG01106.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.330-4824C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897731 | |||||||
| chr17:76897731 | CT | C | 6 | a0001c0001t0002g0205 a0001c0007t0002g0203 a0002c0002t0005g0164 others(3): Show |
6 | HG00099.hp1 HG00423.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-4806delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897731 | ||||||
| chr17:76897731 | CTT | C | 15 | a0001c0003t0001g0183 a0001c0013t0001g0131 a0001c0018t0004g0191 others(12): Show |
16 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.330-4807_330-4806d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897731 | ||||||
| chr17:76897731 | CTTT | C | 7 | a0001c0030t0001g0154 a0002c0002t0006g0185 a0002c0009t0001g0092 others(4): Show |
7 | HG00673.hp2 HG02723.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.330-4808_330-4806d others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897731 | ||||||
| chr17:76897731 | CTTTT | C | 25 | a0001c0003t0001g0204 a0001c0005t0003g0212 a0001c0005t0008g0264 others(22): Show |
25 | HG00639.hp2 HG01099.hp2 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.330-4809_330-4806d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897731 | ||||||
| chr17:76897732 | T | C | 1 | a0002c0002t0008g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.330-4823T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897732 | |||||||
| chr17:76897733 | T | C | 17 | a0001c0001t0004g0160 a0001c0001t0005g0043 a0001c0001t0006g0134 others(14): Show |
17 | HG01099.hp1 HG01106.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.330-4822T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897733 | |||||||
| chr17:76897733 | T | TTCTTTCT others(17): Show |
2 | a0001c0007t0019g0180 a0002c0014t0001g0172 |
2 | HG00438.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.330-4821_330-4820i others(26): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897733 | ||||||
| chr17:76897733 | T | TTTTC | 26 | a0001c0001t0003g0157 a0001c0001t0005g0053 a0001c0001t0006g0049 others(23): Show |
26 | HG00408.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.330-4819_330-4818i others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897733 | ||||||
| chr17:76897734 | T | C | 6 | a0001c0005t0002g0019 a0001c0005t0004g0208 a0002c0002t0005g0238 others(3): Show |
6 | HG01109.hp1 HG01358.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.330-4821T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897734 | |||||||
| chr17:76897734 | T | TCTTTCTT others(16): Show |
2 | a0001c0001t0006g0228 a0002c0015t0003g0109 |
2 | HG00738.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.330-4821_330-4820i others(25): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897734 | |||||||
| chr17:76897734 | T | TTTC | 22 | a0001c0001t0003g0214 a0001c0003t0001g0138 a0001c0003t0001g0215 others(19): Show |
22 | HG00280.hp2 HG01928.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.330-4819_330-4818i others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76897734 | ||||||
| chr17:76897735 | T | C | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0002c0002t0002g0253 others(46): Show |
49 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.330-4820T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897735 | |||||||
| chr17:76897777 | C | T | 1 | a0002c0042t0004g0168 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.330-4778C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897777 | |||||||
| chr17:76897788 | G | C | 55 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(52): Show |
55 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.330-4767G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897788 | |||||||
| chr17:76897936 | A | G | 1 | a0002c0017t0002g0273 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.330-4619A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76897936 | |||||||
| chr17:76898014 | T | C | 189 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0003g0214 others(186): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.330-4541T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898014 | |||||||
| chr17:76898056 | CA | C | 148 | a0001c0001t0003g0157 a0001c0001t0003g0214 a0001c0001t0004g0160 others(145): Show |
149 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.330-4488delA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76898056 | ||||||
| chr17:76898067 | AG | A | 30 | a0001c0003t0001g0204 a0001c0005t0003g0212 a0001c0005t0008g0264 others(27): Show |
30 | HG00639.hp2 HG01106.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.330-4487delG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898067 | |||||||
| chr17:76898137 | G | T | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.330-4418G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898137 | |||||||
| chr17:76898193 | C | T | 75 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0003t0001g0204 others(72): Show |
75 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.330-4362C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898193 | |||||||
| chr17:76898326 | C | CT | 4 | a0001c0003t0001g0204 a0002c0016t0007g0063 a0002c0021t0001g0266 others(1): Show |
4 | HG02647.hp1 HG02738.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-4224dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76898326 | ||||||
| chr17:76898330 | TTA | T | 133 | a0001c0001t0003g0157 a0001c0001t0003g0214 a0001c0001t0004g0160 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.330-4223_330-4222d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76898330 | ||||||
| chr17:76898331 | TA | T | 13 | a0001c0001t0006g0049 a0001c0001t0006g0134 a0001c0001t0007g0233 others(10): Show |
13 | HG01109.hp1 HG01358.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.330-4223delA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898331 | |||||||
| chr17:76898332 | A | T | 30 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(27): Show |
30 | HG00639.hp2 HG01106.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.330-4223A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898332 | |||||||
| chr17:76898398 | G | A | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-4157G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898398 | |||||||
| chr17:76898476 | G | A | 83 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(80): Show |
83 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.330-4079G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898476 | |||||||
| chr17:76898477 | C | T | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.330-4078C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898477 | |||||||
| chr17:76898478 | A | G | 83 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(80): Show |
83 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.330-4077A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898478 | |||||||
| chr17:76898486 | A | G | 90 | a0001c0001t0003g0157 a0001c0001t0003g0214 a0001c0001t0004g0156 others(87): Show |
91 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.330-4069A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898486 | |||||||
| chr17:76898495 | A | AT | 7 | a0001c0001t0005g0053 a0001c0013t0001g0189 a0001c0049t0010g0067 others(4): Show |
7 | HG00438.hp2 HG02148.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.330-4048dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76898495 | ||||||
| chr17:76898598 | C | T | 2 | a0002c0002t0025g0274 a0002c0017t0002g0273 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.330-3957C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898598 | |||||||
| chr17:76898687 | A | T | 2 | a0001c0025t0014g0071 a0002c0006t0007g0069 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.330-3868A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898687 | |||||||
| chr17:76898729 | T | G | 2 | a0001c0025t0014g0071 a0002c0006t0007g0069 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.330-3826T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898729 | |||||||
| chr17:76898739 | A | G | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.330-3816A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898739 | |||||||
| chr17:76898835 | A | C | 1 | a0001c0010t0007g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.330-3720A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898835 | |||||||
| chr17:76898907 | G | A | 52 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(49): Show |
52 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.330-3648G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898907 | |||||||
| chr17:76898930 | A | G | 98 | a0001c0001t0004g0160 a0001c0001t0006g0270 a0001c0001t0008g0107 others(95): Show |
98 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.330-3625A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898930 | |||||||
| chr17:76898931 | T | C | 232 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.330-3624T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898931 | |||||||
| chr17:76898955 | G | T | 37 | a0001c0001t0003g0157 a0001c0001t0005g0043 a0001c0001t0006g0134 others(34): Show |
38 | HG00408.hp2 HG00738.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.330-3600G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76898955 | |||||||
| chr17:76899069 | G | A | 37 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(34): Show |
37 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.330-3486G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899069 | |||||||
| chr17:76899118 | G | A | 68 | a0001c0001t0005g0053 a0001c0001t0006g0049 a0001c0001t0006g0175 others(65): Show |
68 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.330-3437G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899118 | |||||||
| chr17:76899134 | C | T | 36 | a0001c0001t0003g0157 a0001c0001t0005g0043 a0001c0001t0006g0134 others(33): Show |
37 | HG00408.hp2 HG00738.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.330-3421C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899134 | |||||||
| chr17:76899158 | G | C | 1 | a0001c0007t0002g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.330-3397G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899158 | |||||||
| chr17:76899478 | T | A | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.330-3077T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899478 | |||||||
| chr17:76899532 | G | A | 2 | a0001c0055t0007g0073 a0001c0056t0008g0108 |
2 | HG01069.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.330-3023G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899532 | |||||||
| chr17:76899641 | C | T | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.330-2914C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899641 | |||||||
| chr17:76899704 | A | C | 140 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(137): Show |
141 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.330-2851A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899704 | |||||||
| chr17:76899805 | G | T | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-2750G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899805 | |||||||
| chr17:76899819 | C | G | 9 | a0001c0001t0003g0192 a0002c0002t0004g0105 a0002c0006t0004g0241 others(6): Show |
9 | HG00438.hp1 HG01891.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.330-2736C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76899819 | |||||||
| chr17:76900020 | G | A | 36 | a0001c0001t0003g0157 a0001c0001t0005g0043 a0001c0001t0006g0134 others(33): Show |
37 | HG00408.hp2 HG00738.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.330-2535G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900020 | |||||||
| chr17:76900130 | G | T | 1 | a0002c0028t0004g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.330-2425G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900130 | |||||||
| chr17:76900131 | G | A | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.330-2424G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900131 | |||||||
| chr17:76900144 | T | C | 36 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(33): Show |
36 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.330-2411T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900144 | |||||||
| chr17:76900237 | T | G | 87 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(84): Show |
87 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.330-2318T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900237 | |||||||
| chr17:76900263 | G | T | 141 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(138): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.330-2292G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900263 | |||||||
| chr17:76900277 | C | T | 143 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(140): Show |
144 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.330-2278C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900277 | |||||||
| chr17:76900278 | G | C | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-2277G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900278 | |||||||
| chr17:76900304 | C | G | 1 | a0002c0002t0011g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.330-2251C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900304 | |||||||
| chr17:76900353 | G | A | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-2202G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900353 | |||||||
| chr17:76900384 | C | T | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-2171C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900384 | |||||||
| chr17:76900641 | G | A | 3 | a0001c0005t0008g0264 a0002c0002t0005g0164 a0002c0002t0008g0013 |
3 | HG00099.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.330-1914G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900641 | |||||||
| chr17:76900656 | A | G | 90 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(87): Show |
90 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.330-1899A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900656 | |||||||
| chr17:76900662 | C | T | 66 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0221 others(63): Show |
66 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.330-1893C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900662 | |||||||
| chr17:76900705 | T | C | 50 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0221 others(47): Show |
50 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.330-1850T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900705 | |||||||
| chr17:76900798 | T | G | 53 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(50): Show |
53 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.330-1757T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900798 | |||||||
| chr17:76900869 | G | T | 1 | a0002c0004t0001g0077 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.330-1686G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900869 | |||||||
| chr17:76900871 | ATGTGTGC others(3): Show |
A | 5 | a0001c0003t0001g0204 a0001c0005t0003g0212 a0002c0015t0007g0268 others(2): Show |
5 | HG02738.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.330-1676_330-1667d others(12): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76900871 | ||||||
| chr17:76900879 | GTGTGTGT others(3): Show |
G | 68 | a0001c0001t0003g0157 a0001c0001t0005g0043 a0001c0001t0006g0134 others(65): Show |
69 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.330-1657_330-1648d others(12): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76900879 | ||||||
| chr17:76900893 | GTGTGCAT others(21): Show |
G | 1 | a0002c0002t0011g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.330-1657_330-1630d others(30): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76900893 | ||||||
| chr17:76900903 | GTGTGTGT others(11): Show |
G | 52 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(49): Show |
52 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.330-1645_330-1628d others(20): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76900903 | ||||||
| chr17:76900932 | C | T | 53 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(50): Show |
53 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.330-1623C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900932 | |||||||
| chr17:76900933 | G | T | 53 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(50): Show |
53 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.330-1622G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900933 | |||||||
| chr17:76900936 | T | C | 53 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(50): Show |
53 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.330-1619T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900936 | |||||||
| chr17:76900936 | T | TTTGC | 35 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(32): Show |
35 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.330-1616_330-1615i others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76900936 | ||||||
| chr17:76900943 | G | A | 2 | a0002c0004t0001g0123 a0002c0015t0003g0150 |
2 | HG00544.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.330-1612G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900943 | |||||||
| chr17:76900962 | CGCCTGTG others(5): Show |
C | 53 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(50): Show |
53 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.330-1591_330-1580d others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76900962 | ||||||
| chr17:76900965 | C | G | 35 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(32): Show |
35 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.330-1590C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900965 | |||||||
| chr17:76900985 | A | G | 37 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(34): Show |
37 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.330-1570A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76900985 | |||||||
| chr17:76901069 | G | A | 2 | a0001c0005t0008g0264 a0002c0002t0008g0013 |
2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.330-1486G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901069 | |||||||
| chr17:76901255 | G | A | 26 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(23): Show |
26 | HG00639.hp2 HG01106.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.330-1300G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901255 | |||||||
| chr17:76901331 | A | G | 3 | a0001c0003t0001g0181 a0001c0003t0001g0187 a0001c0011t0002g0186 |
3 | HG02083.hp2 HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.330-1224A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901331 | |||||||
| chr17:76901335 | G | A | 9 | a0001c0001t0004g0160 a0001c0001t0006g0270 a0002c0002t0003g0009 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.330-1220G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901335 | |||||||
| chr17:76901402 | T | TA | 29 | a0001c0001t0003g0214 a0001c0001t0006g0228 a0001c0003t0001g0138 others(26): Show |
29 | HG00280.hp2 HG00738.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.330-1140dupA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76901402 | ||||||
| chr17:76901402 | T | TAA | 35 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(32): Show |
35 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.330-1141_330-1140d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76901402 | ||||||
| chr17:76901402 | T | TAAA | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-1142_330-1140d others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76901402 | ||||||
| chr17:76901736 | C | T | 50 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(47): Show |
50 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.330-819C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901736 | |||||||
| chr17:76901793 | G | A | 2 | a0001c0025t0014g0071 a0002c0006t0007g0069 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.330-762G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901793 | |||||||
| chr17:76901816 | A | G | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-739A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901816 | |||||||
| chr17:76901840 | C | T | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.330-715C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901840 | |||||||
| chr17:76901899 | T | C | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.330-656T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901899 | |||||||
| chr17:76901983 | C | T | 27 | a0001c0001t0003g0214 a0001c0001t0006g0228 a0001c0003t0001g0138 others(24): Show |
27 | HG00280.hp2 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.330-572C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76901983 | |||||||
| chr17:76902074 | G | GTGCAGTT others(11): Show |
1 | a0002c0006t0007g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.330-467_330-450dup others(18): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76902074 | ||||||
| chr17:76902108 | G | A | 48 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(45): Show |
48 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.330-447G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902108 | |||||||
| chr17:76902146 | G | A | 75 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0221 others(72): Show |
75 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.330-409G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902146 | |||||||
| chr17:76902217 | C | T | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.330-338C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902217 | |||||||
| chr17:76902218 | A | G | 232 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.330-337A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902218 | |||||||
| chr17:76902227 | G | A | 1 | a0002c0012t0001g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.330-328G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902227 | |||||||
| chr17:76902279 | CACATGCA others(12): Show |
C | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.330-262_330-244del others(19): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 76902279 | ||||||
| chr17:76902338 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.330-217C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902338 | |||||||
| chr17:76902397 | G | A | 4 | a0002c0028t0004g0061 a0002c0028t0026g0060 a0002c0033t0001g0059 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-158G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902397 | |||||||
| chr17:76902466 | G | A | 1 | a0001c0007t0002g0216 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.330-89G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902466 | |||||||
| chr17:76902466 | G | T | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.330-89G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902466 | |||||||
| chr17:76902475 | T | C | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.330-80T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902475 | |||||||
| chr17:76902508 | G | A | 36 | a0001c0001t0003g0157 a0001c0001t0005g0043 a0001c0001t0006g0134 others(33): Show |
37 | HG00408.hp2 HG00738.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.330-47G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902508 | |||||||
| chr17:76902516 | G | A | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.330-39G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 3/17 | chr17 | 76902516 | |||||||
| chr17:76902684 | G | T | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445+14G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902684 | |||||||
| chr17:76902731 | G | C | 48 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(45): Show |
48 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.445+61G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902731 | |||||||
| chr17:76902761 | T | C | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.445+91T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902761 | |||||||
| chr17:76902800 | C | T | 1 | a0001c0001t0007g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.445+130C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902800 | |||||||
| chr17:76902844 | T | TC | 88 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(85): Show |
88 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.445+177dupC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr17 | 76902844 | ||||||
| chr17:76902848 | T | C | 240 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.445+178T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902848 | |||||||
| chr17:76902952 | G | A | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.445+282G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902952 | |||||||
| chr17:76902989 | T | TCCAA | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.446-314_446-313ins others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902989 | |||||||
| chr17:76902990 | G | T | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.446-313G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902990 | |||||||
| chr17:76902992 | G | A | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.446-311G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76902992 | |||||||
| chr17:76903041 | C | T | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.446-262C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903041 | |||||||
| chr17:76903044 | G | A | 2 | a0002c0002t0025g0274 a0002c0017t0002g0273 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.446-259G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903044 | |||||||
| chr17:76903152 | T | A | 232 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.446-151T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903152 | |||||||
| chr17:76903180 | A | C | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.446-123A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903180 | |||||||
| chr17:76903216 | T | G | 2 | a0001c0055t0007g0073 a0001c0056t0008g0108 |
2 | HG01069.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.446-87T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903216 | |||||||
| chr17:76903235 | C | T | 1 | a0001c0005t0002g0235 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.446-68C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903235 | |||||||
| chr17:76903238 | G | C | 232 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.446-65G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903238 | |||||||
| chr17:76903291 | C | T | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.446-12C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 4/17 | chr17 | 76903291 | |||||||
| chr17:76903533 | A | G | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.519+157A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903533 | |||||||
| chr17:76903553 | C | T | 8 | a0001c0001t0003g0192 a0002c0002t0004g0105 a0002c0006t0004g0241 others(5): Show |
8 | HG00438.hp1 HG01891.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+177C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903553 | |||||||
| chr17:76903614 | C | T | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519+238C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903614 | |||||||
| chr17:76903657 | C | T | 1 | a0001c0001t0007g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.519+281C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903657 | |||||||
| chr17:76903681 | C | T | 1 | a0001c0005t0002g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.519+305C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903681 | |||||||
| chr17:76903715 | A | G | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.519+339A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903715 | |||||||
| chr17:76903758 | G | A | 35 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(32): Show |
35 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.519+382G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903758 | |||||||
| chr17:76903789 | C | T | 3 | a0001c0055t0007g0073 a0001c0056t0008g0108 a0002c0002t0005g0238 |
3 | HG01069.hp2 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.519+413C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903789 | |||||||
| chr17:76903881 | G | A | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.520-371G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76903881 | |||||||
| chr17:76904023 | C | T | 138 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(135): Show |
139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.520-229C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76904023 | |||||||
| chr17:76904167 | G | A | 48 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(45): Show |
48 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.520-85G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76904167 | |||||||
| chr17:76904180 | G | A | 1 | a0002c0015t0007g0268 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.520-72G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76904180 | |||||||
| chr17:76904183 | C | T | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.520-69C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76904183 | |||||||
| chr17:76904218 | C | T | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.520-34C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 5/17 | chr17 | 76904218 | |||||||
| chr17:76904446 | C | T | 1 | a0001c0023t0004g0227 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.690+24C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904446 | |||||||
| chr17:76904500 | G | A | 37 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(34): Show |
37 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.690+78G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904500 | |||||||
| chr17:76904503 | C | A | 86 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.690+81C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904503 | |||||||
| chr17:76904535 | G | T | 4 | a0002c0028t0004g0061 a0002c0028t0026g0060 a0002c0033t0001g0059 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.690+113G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904535 | |||||||
| chr17:76904548 | C | T | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.690+126C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904548 | |||||||
| chr17:76904570 | C | T | 1 | a0002c0029t0001g0149 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.690+148C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904570 | |||||||
| chr17:76904600 | C | A | 1 | a0002c0004t0001g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.690+178C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904600 | |||||||
| chr17:76904690 | G | A | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.690+268G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904690 | |||||||
| chr17:76904723 | A | C | 1 | a0002c0006t0004g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.690+301A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904723 | |||||||
| chr17:76904853 | C | T | 86 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.691-316C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904853 | |||||||
| chr17:76904862 | G | A | 86 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0003t0001g0044 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.691-307G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76904862 | |||||||
| chr17:76905095 | C | G | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.691-74C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76905095 | |||||||
| chr17:76905137 | G | A | 4 | a0002c0028t0004g0061 a0002c0028t0026g0060 a0002c0033t0001g0059 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-32G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 6/17 | chr17 | 76905137 | |||||||
| chr17:76905478 | C | T | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.855+145C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905478 | |||||||
| chr17:76905526 | A | G | 1 | a0001c0001t0007g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.855+193A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905526 | |||||||
| chr17:76905607 | G | A | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.855+274G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905607 | |||||||
| chr17:76905776 | G | T | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.856-242G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905776 | |||||||
| chr17:76905819 | ATGAGGGC others(16): Show |
A | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.856-196_856-174del others(23): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 76905819 | ||||||
| chr17:76905852 | G | A | 1 | a0002c0014t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.856-166G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905852 | |||||||
| chr17:76905877 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.856-141C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905877 | |||||||
| chr17:76905887 | G | A | 1 | a0002c0006t0004g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.856-131G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905887 | |||||||
| chr17:76905958 | G | C | 1 | a0002c0002t0005g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.856-60G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905958 | |||||||
| chr17:76905987 | T | C | 50 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(47): Show |
50 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.856-31T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905987 | |||||||
| chr17:76905991 | C | T | 8 | a0001c0001t0003g0192 a0002c0002t0004g0105 a0002c0006t0004g0241 others(5): Show |
8 | HG00438.hp1 HG01891.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-27C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76905991 | |||||||
| chr17:76906006 | C | T | 2 | a0001c0018t0004g0226 a0001c0025t0010g0229 |
2 | HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.856-12C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76906006 | |||||||
| chr17:76906007 | C | T | 1 | a0002c0006t0032g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.856-11C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76906007 | |||||||
| chr17:76906008 | G | A | 1 | a0002c0002t0011g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.856-10G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 7/17 | chr17 | 76906008 | |||||||
| chr17:76906276 | C | T | 27 | a0001c0001t0003g0214 a0001c0001t0006g0228 a0001c0003t0001g0138 others(24): Show |
27 | HG00280.hp2 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1025+89C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906276 | |||||||
| chr17:76906301 | G | A | 1 | a0001c0010t0007g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1025+114G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906301 | |||||||
| chr17:76906366 | C | A | 1 | a0002c0017t0002g0273 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1025+179C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906366 | |||||||
| chr17:76906373 | G | A | 8 | a0001c0001t0003g0192 a0002c0002t0004g0105 a0002c0006t0004g0241 others(5): Show |
8 | HG00438.hp1 HG01891.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+186G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906373 | |||||||
| chr17:76906376 | C | G | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+189C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906376 | |||||||
| chr17:76906412 | G | A | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+225G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906412 | |||||||
| chr17:76906427 | C | T | 1 | a0002c0016t0002g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1025+240C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906427 | |||||||
| chr17:76906458 | G | T | 1 | a0002c0016t0002g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1025+271G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906458 | |||||||
| chr17:76906536 | G | T | 8 | a0001c0001t0003g0192 a0002c0002t0004g0105 a0002c0006t0004g0241 others(5): Show |
8 | HG00438.hp1 HG01891.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+349G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906536 | |||||||
| chr17:76906611 | G | A | 2 | a0001c0055t0007g0073 a0001c0056t0008g0108 |
2 | HG01069.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1025+424G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906611 | |||||||
| chr17:76906614 | C | G | 8 | a0001c0001t0003g0192 a0002c0002t0004g0105 a0002c0006t0004g0241 others(5): Show |
8 | HG00438.hp1 HG01891.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+427C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906614 | |||||||
| chr17:76906865 | T | C | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1025+678T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906865 | |||||||
| chr17:76906993 | A | G | 51 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(48): Show |
51 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1025+806A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76906993 | |||||||
| chr17:76907055 | CT | C | 5 | a0002c0006t0002g0006 a0002c0012t0001g0012 a0002c0014t0001g0066 others(2): Show |
5 | HG03209.hp1 NA18954.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+883delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76907055 | ||||||
| chr17:76907070 | T | A | 48 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(45): Show |
48 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1025+883T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907070 | |||||||
| chr17:76907091 | C | G | 57 | a0001c0001t0003g0192 a0001c0001t0008g0107 a0001c0003t0001g0044 others(54): Show |
57 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1025+904C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907091 | |||||||
| chr17:76907138 | G | A | 33 | a0001c0001t0011g0065 a0001c0003t0001g0204 a0001c0005t0003g0212 others(30): Show |
33 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1025+951G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907138 | |||||||
| chr17:76907154 | C | T | 1 | a0002c0019t0004g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1025+967C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907154 | |||||||
| chr17:76907196 | C | G | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+1009C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907196 | |||||||
| chr17:76907202 | C | T | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1025+1015C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907202 | |||||||
| chr17:76907249 | G | C | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+1062G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907249 | |||||||
| chr17:76907302 | C | T | 1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1025+1115C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907302 | |||||||
| chr17:76907495 | ACT | A | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+1311_1025+131 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76907495 | ||||||
| chr17:76907528 | T | G | 48 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(45): Show |
48 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1025+1341T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907528 | |||||||
| chr17:76907573 | C | G | 8 | a0001c0001t0003g0192 a0002c0002t0004g0105 a0002c0006t0004g0241 others(5): Show |
8 | HG00438.hp1 HG01891.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+1386C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907573 | |||||||
| chr17:76907618 | C | T | 2 | a0001c0001t0005g0053 a0009c0058t0003g0050 |
2 | HG02148.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1025+1431C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907618 | |||||||
| chr17:76907640 | A | C | 1 | a0002c0017t0002g0273 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1025+1453A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907640 | |||||||
| chr17:76907695 | T | C | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+1508T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907695 | |||||||
| chr17:76907727 | G | C | 2 | a0001c0003t0001g0138 a0002c0012t0001g0159 |
2 | HG03831.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1025+1540G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907727 | |||||||
| chr17:76907836 | C | T | 3 | a0001c0005t0008g0264 a0002c0002t0005g0164 a0002c0002t0008g0013 |
3 | HG00099.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1025+1649C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907836 | |||||||
| chr17:76907837 | G | A | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1025+1650G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76907837 | |||||||
| chr17:76908062 | A | G | 1 | a0002c0038t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1025+1875A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76908062 | |||||||
| chr17:76908249 | T | C | 232 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1025+2062T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76908249 | |||||||
| chr17:76908272 | CTTCT | C | 48 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(45): Show |
48 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1025+2088_1025+209 others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76908272 | ||||||
| chr17:76908275 | CT | C | 182 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(179): Show |
183 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1025+2105delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76908275 | ||||||
| chr17:76908306 | G | A | 1 | a0002c0006t0009g0001 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1025+2119G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76908306 | |||||||
| chr17:76908373 | C | A | 1 | a0002c0002t0011g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1025+2186C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76908373 | |||||||
| chr17:76908424 | G | A | 1 | a0001c0001t0007g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1025+2237G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76908424 | |||||||
| chr17:76908811 | C | CT | 30 | a0001c0001t0003g0214 a0001c0001t0006g0228 a0001c0003t0001g0138 others(27): Show |
30 | HG00280.hp2 HG00738.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1025+2637dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76908811 | ||||||
| chr17:76908823 | TTGA | T | 47 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(44): Show |
47 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1025+2637_1025+263 others(7): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76908823 | |||||||
| chr17:76908831 | G | T | 4 | a0001c0001t0006g0034 a0001c0003t0001g0035 a0001c0003t0023g0040 others(1): Show |
4 | HG00140.hp1 HG01074.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025+2644G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76908831 | |||||||
| chr17:76909015 | C | T | 74 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0221 others(71): Show |
74 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1025+2828C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909015 | |||||||
| chr17:76909161 | G | A | 47 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0030t0001g0154 others(44): Show |
47 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1025+2974G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909161 | |||||||
| chr17:76909190 | G | A | 49 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0007t0002g0064 others(46): Show |
49 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1025+3003G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909190 | |||||||
| chr17:76909205 | C | T | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1025+3018C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909205 | |||||||
| chr17:76909302 | T | C | 1 | a0001c0003t0001g0094 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1025+3115T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909302 | |||||||
| chr17:76909513 | T | G | 193 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1025+3326T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909513 | |||||||
| chr17:76909569 | G | T | 1 | a0001c0003t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1025+3382G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909569 | |||||||
| chr17:76909656 | C | A | 1 | a0001c0025t0014g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1025+3469C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76909656 | |||||||
| chr17:76910099 | C | A | 1 | a0001c0013t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1025+3912C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910099 | |||||||
| chr17:76910227 | A | C | 192 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1025+4040A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910227 | |||||||
| chr17:76910387 | G | A | 3 | a0001c0005t0008g0264 a0002c0002t0005g0164 a0002c0002t0008g0013 |
3 | HG00099.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1025+4200G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910387 | |||||||
| chr17:76910389 | A | G | 2 | a0001c0055t0007g0073 a0001c0056t0008g0108 |
2 | HG01069.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1025+4202A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910389 | |||||||
| chr17:76910391 | A | G | 1 | a0001c0023t0004g0227 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1025+4204A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910391 | |||||||
| chr17:76910425 | C | T | 1 | a0002c0002t0003g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1025+4238C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910425 | |||||||
| chr17:76910503 | A | G | 51 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0221 others(48): Show |
51 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.1025+4316A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910503 | |||||||
| chr17:76910852 | C | T | 3 | a0001c0005t0015g0031 a0001c0011t0002g0033 a0001c0053t0001g0032 |
3 | HG01243.hp1 HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1025+4665C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910852 | |||||||
| chr17:76910887 | C | T | 1 | a0002c0020t0022g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1025+4700C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76910887 | |||||||
| chr17:76911213 | T | C | 1 | a0002c0002t0005g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1025+5026T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911213 | |||||||
| chr17:76911270 | C | T | 2 | a0002c0002t0025g0274 a0002c0017t0002g0273 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1025+5083C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911270 | |||||||
| chr17:76911316 | T | C | 3 | a0001c0001t0007g0233 a0001c0005t0008g0264 a0002c0002t0008g0013 |
3 | HG03017.hp2 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1025+5129T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911316 | |||||||
| chr17:76911425 | T | C | 139 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(136): Show |
140 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1025+5238T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911425 | |||||||
| chr17:76911505 | G | A | 3 | a0001c0003t0001g0181 a0001c0003t0001g0187 a0001c0011t0002g0186 |
3 | HG02083.hp2 HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1025+5318G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911505 | |||||||
| chr17:76911577 | T | C | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1025+5390T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911577 | |||||||
| chr17:76911713 | C | T | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1025+5526C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911713 | |||||||
| chr17:76911957 | T | C | 11 | a0001c0025t0014g0071 a0001c0055t0007g0073 a0001c0056t0008g0108 others(8): Show |
11 | HG00099.hp1 HG01069.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025+5770T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911957 | |||||||
| chr17:76911957 | T | G | 229 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(226): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1025+5770T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911957 | |||||||
| chr17:76911975 | T | G | 1 | a0006c0059t0007g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1025+5788T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76911975 | |||||||
| chr17:76912017 | G | T | 4 | a0002c0028t0004g0061 a0002c0028t0026g0060 a0002c0033t0001g0059 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+5830G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912017 | |||||||
| chr17:76912070 | C | T | 9 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0002t0025g0274 others(6): Show |
9 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+5883C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912070 | |||||||
| chr17:76912138 | C | T | 56 | a0001c0001t0008g0107 a0001c0003t0001g0044 a0001c0025t0014g0071 others(53): Show |
56 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1025+5951C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912138 | |||||||
| chr17:76912232 | G | A | 151 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(148): Show |
152 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1025+6045G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912232 | |||||||
| chr17:76912235 | G | A | 11 | a0001c0025t0014g0071 a0001c0055t0007g0073 a0001c0056t0008g0108 others(8): Show |
11 | HG00099.hp1 HG01069.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1025+6048G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912235 | |||||||
| chr17:76912254 | A | G | 2 | a0001c0025t0014g0071 a0002c0006t0007g0069 |
2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1025+6067A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912254 | |||||||
| chr17:76912458 | G | A | 1 | a0001c0013t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1025+6271G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912458 | |||||||
| chr17:76912494 | C | T | 1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1025+6307C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912494 | |||||||
| chr17:76912503 | C | T | 1 | a0002c0017t0002g0273 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1025+6316C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912503 | |||||||
| chr17:76912546 | C | T | 9 | a0001c0001t0004g0160 a0001c0001t0006g0270 a0002c0002t0003g0009 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+6359C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912546 | |||||||
| chr17:76912620 | C | G | 1 | a0002c0016t0002g0085 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1025+6433C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912620 | |||||||
| chr17:76912630 | C | T | 8 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0006t0007g0069 others(5): Show |
8 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+6443C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912630 | |||||||
| chr17:76912686 | C | A | 1 | a0002c0004t0001g0091 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1025+6499C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912686 | |||||||
| chr17:76912703 | G | A | 8 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0006t0007g0069 others(5): Show |
8 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+6516G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912703 | |||||||
| chr17:76912722 | G | T | 8 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0006t0007g0069 others(5): Show |
8 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+6535G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912722 | |||||||
| chr17:76912738 | G | A | 1 | a0001c0007t0002g0203 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1025+6551G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912738 | |||||||
| chr17:76912814 | G | A | 1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1025+6627G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912814 | |||||||
| chr17:76912825 | G | A | 12 | a0001c0001t0002g0205 a0001c0007t0002g0201 a0001c0007t0002g0219 others(9): Show |
12 | HG00408.hp1 HG02040.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1025+6638G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76912825 | |||||||
| chr17:76913017 | T | C | 160 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1025+6830T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913017 | |||||||
| chr17:76913018 | C | A | 1 | a0002c0009t0001g0119 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1025+6831C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913018 | |||||||
| chr17:76913048 | G | A | 1 | a0001c0001t0027g0220 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1025+6861G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913048 | |||||||
| chr17:76913089 | A | G | 8 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0006t0007g0069 others(5): Show |
8 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+6902A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913089 | |||||||
| chr17:76913247 | C | T | 152 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(149): Show |
153 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1025+7060C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913247 | |||||||
| chr17:76913257 | A | G | 8 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0006t0007g0069 others(5): Show |
8 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+7070A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913257 | |||||||
| chr17:76913323 | G | T | 27 | a0001c0001t0003g0214 a0001c0001t0006g0228 a0001c0003t0001g0138 others(24): Show |
27 | HG00280.hp2 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1025+7136G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913323 | |||||||
| chr17:76913335 | C | G | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1025+7148C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913335 | |||||||
| chr17:76913394 | G | A | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1025+7207G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913394 | |||||||
| chr17:76913427 | G | A | 1 | a0001c0007t0002g0216 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1025+7240G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913427 | |||||||
| chr17:76913489 | G | A | 30 | a0001c0001t0007g0233 a0001c0001t0011g0065 a0001c0003t0001g0204 others(27): Show |
30 | HG00639.hp2 HG01106.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1025+7302G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913489 | |||||||
| chr17:76913552 | A | G | 8 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0006t0007g0069 others(5): Show |
8 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+7365A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913552 | |||||||
| chr17:76913782 | C | T | 4 | a0002c0028t0004g0061 a0002c0028t0026g0060 a0002c0033t0001g0059 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+7595C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913782 | |||||||
| chr17:76913793 | G | A | 1 | a0001c0018t0004g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1025+7606G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913793 | |||||||
| chr17:76913849 | T | C | 10 | a0001c0025t0014g0071 a0001c0055t0007g0073 a0001c0056t0008g0108 others(7): Show |
10 | HG00099.hp1 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+7662T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913849 | |||||||
| chr17:76913882 | G | A | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1025+7695G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913882 | |||||||
| chr17:76913923 | C | G | 1 | a0001c0023t0004g0227 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1025+7736C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76913923 | |||||||
| chr17:76914033 | C | T | 1 | a0001c0001t0006g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1025+7846C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914033 | |||||||
| chr17:76914091 | A | ACT | 196 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1025+7905_1025+790 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76914091 | ||||||
| chr17:76914108 | AGAG | A | 25 | a0001c0001t0003g0214 a0001c0001t0006g0228 a0001c0003t0001g0215 others(22): Show |
25 | HG00738.hp2 HG01109.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.1025+7922_1025+792 others(7): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914108 | |||||||
| chr17:76914208 | A | C | 1 | a0001c0008t0001g0230 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1025+8021A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914208 | |||||||
| chr17:76914272 | C | T | 10 | a0001c0025t0014g0071 a0001c0055t0007g0073 a0001c0056t0008g0108 others(7): Show |
10 | HG00099.hp1 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+8085C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914272 | |||||||
| chr17:76914381 | G | A | 6 | a0001c0055t0007g0073 a0001c0056t0008g0108 a0002c0028t0004g0061 others(3): Show |
6 | HG01069.hp2 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025+8194G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914381 | |||||||
| chr17:76914398 | G | C | 1 | a0002c0021t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1025+8211G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914398 | |||||||
| chr17:76914427 | G | T | 1 | a0001c0007t0019g0180 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1025+8240G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914427 | |||||||
| chr17:76914523 | C | T | 3 | a0001c0001t0007g0233 a0001c0005t0008g0264 a0002c0002t0008g0013 |
3 | HG03017.hp2 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1025+8336C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914523 | |||||||
| chr17:76914550 | C | T | 10 | a0001c0025t0014g0071 a0001c0055t0007g0073 a0001c0056t0008g0108 others(7): Show |
10 | HG00099.hp1 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+8363C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914550 | |||||||
| chr17:76914574 | T | C | 10 | a0001c0025t0014g0071 a0001c0055t0007g0073 a0001c0056t0008g0108 others(7): Show |
10 | HG00099.hp1 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+8387T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914574 | |||||||
| chr17:76914644 | C | CTTTTTTT others(3): Show |
6 | a0001c0055t0007g0073 a0001c0056t0008g0108 a0002c0006t0007g0069 others(3): Show |
6 | HG01069.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025+8461_1025+847 others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76914644 | ||||||
| chr17:76914644 | C | CTTTTTTT others(4): Show |
3 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0017t0002g0273 |
3 | HG00099.hp1 HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1025+8460_1025+847 others(15): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76914644 | ||||||
| chr17:76914644 | CT | C | 74 | a0001c0001t0003g0024 a0001c0001t0003g0029 a0001c0001t0004g0156 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1025+8470delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76914644 | ||||||
| chr17:76914691 | C | T | 7 | a0001c0055t0007g0073 a0001c0056t0008g0108 a0002c0002t0005g0164 others(4): Show |
7 | HG00099.hp1 HG01069.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1025+8504C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914691 | |||||||
| chr17:76914720 | C | T | 1 | a0002c0002t0005g0258 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1025+8533C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914720 | |||||||
| chr17:76914793 | A | G | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1025+8606A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914793 | |||||||
| chr17:76914798 | C | T | 3 | a0002c0028t0004g0061 a0002c0028t0026g0060 a0002c0033t0001g0059 |
3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1025+8611C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914798 | |||||||
| chr17:76914861 | C | T | 31 | a0001c0001t0003g0024 a0001c0001t0003g0029 a0001c0001t0004g0156 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.1025+8674C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914861 | |||||||
| chr17:76914882 | C | T | 134 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0192 others(131): Show |
135 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1025+8695C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914882 | |||||||
| chr17:76914934 | G | A | 33 | a0001c0003t0001g0044 a0001c0003t0001g0135 a0002c0002t0003g0084 others(30): Show |
33 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.1025+8747G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914934 | |||||||
| chr17:76914969 | A | G | 1 | a0001c0011t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1025+8782A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76914969 | |||||||
| chr17:76915060 | G | C | 9 | a0001c0025t0014g0071 a0002c0002t0005g0164 a0002c0006t0007g0069 others(6): Show |
10 | HG00099.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025+8873G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915060 | |||||||
| chr17:76915105 | C | T | 17 | a0001c0001t0004g0160 a0001c0001t0005g0043 a0001c0003t0001g0187 others(14): Show |
17 | HG00438.hp2 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1025+8918C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915105 | |||||||
| chr17:76915117 | T | C | 35 | a0001c0001t0003g0157 a0001c0001t0005g0021 a0001c0001t0005g0041 others(32): Show |
35 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1025+8930T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915117 | |||||||
| chr17:76915135 | G | C | 2 | a0001c0001t0005g0043 a0001c0011t0012g0174 |
2 | HG01106.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1025+8948G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915135 | |||||||
| chr17:76915209 | GGA | G | 4 | a0001c0001t0003g0157 a0001c0013t0001g0101 a0002c0006t0004g0241 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+9028_1025+902 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76915209 | ||||||
| chr17:76915325 | C | T | 2 | a0002c0002t0005g0258 a0002c0006t0007g0069 |
2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1025+9138C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915325 | |||||||
| chr17:76915376 | G | A | 1 | a0001c0011t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1025+9189G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915376 | |||||||
| chr17:76915397 | G | A | 1 | a0002c0020t0001g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1025+9210G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915397 | |||||||
| chr17:76915408 | G | C | 1 | a0002c0016t0007g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1025+9221G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915408 | |||||||
| chr17:76915445 | C | T | 2 | a0001c0001t0003g0192 a0002c0014t0001g0172 |
2 | HG00438.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1025+9258C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915445 | |||||||
| chr17:76915445 | CG | C | 3 | a0001c0010t0003g0132 a0001c0010t0003g0133 a0001c0030t0001g0272 |
3 | HG00408.hp2 HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1025+9259delG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915445 | |||||||
| chr17:76915561 | T | C | 274 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(271): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1025+9374T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915561 | |||||||
| chr17:76915693 | T | C | 159 | a0001c0001t0002g0038 a0001c0001t0002g0209 a0001c0001t0003g0024 others(156): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1026-9273T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915693 | |||||||
| chr17:76915703 | C | T | 11 | a0001c0003t0029g0051 a0001c0005t0002g0235 a0001c0007t0002g0216 others(8): Show |
11 | HG00597.hp1 HG00673.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1026-9263C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915703 | |||||||
| chr17:76915726 | C | T | 8 | a0001c0003t0029g0051 a0001c0005t0002g0235 a0001c0007t0002g0216 others(5): Show |
8 | HG00597.hp1 HG00673.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026-9240C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915726 | |||||||
| chr17:76915779 | G | A | 1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1026-9187G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915779 | |||||||
| chr17:76915852 | G | A | 1 | a0001c0051t0001g0171 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1026-9114G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915852 | |||||||
| chr17:76915914 | A | G | 3 | a0001c0031t0001g0252 a0002c0006t0007g0072 a0002c0012t0001g0012 |
3 | HG03209.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1026-9052A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76915914 | |||||||
| chr17:76916023 | G | A | 1 | a0001c0031t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1026-8943G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916023 | |||||||
| chr17:76916032 | G | A | 1 | a0002c0021t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1026-8934G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916032 | |||||||
| chr17:76916039 | C | T | 1 | a0001c0001t0003g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1026-8927C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916039 | |||||||
| chr17:76916040 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1026-8926G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916040 | |||||||
| chr17:76916050 | G | A | 78 | a0001c0001t0002g0209 a0001c0001t0003g0157 a0001c0001t0005g0021 others(75): Show |
78 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.1026-8916G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916050 | |||||||
| chr17:76916079 | G | C | 1 | a0001c0005t0007g0045 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1026-8887G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916079 | |||||||
| chr17:76916145 | A | AG | 14 | a0001c0001t0004g0156 a0001c0001t0008g0107 a0001c0030t0001g0154 others(11): Show |
14 | HG01069.hp2 HG01891.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1026-8819dupG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76916145 | ||||||
| chr17:76916152 | G | A | 15 | a0001c0001t0005g0053 a0001c0001t0005g0210 a0002c0002t0005g0039 others(12): Show |
15 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1026-8814G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916152 | |||||||
| chr17:76916161 | T | C | 23 | a0001c0001t0004g0156 a0001c0001t0008g0107 a0001c0005t0007g0045 others(20): Show |
23 | HG01069.hp2 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1026-8805T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916161 | |||||||
| chr17:76916167 | C | T | 1 | a0001c0031t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1026-8799C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916167 | |||||||
| chr17:76916172 | TA | T | 23 | a0001c0001t0004g0156 a0001c0001t0008g0107 a0001c0005t0007g0045 others(20): Show |
23 | HG01069.hp2 HG01243.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1026-8793delA | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916172 | |||||||
| chr17:76916189 | C | T | 1 | a0002c0006t0007g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1026-8777C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916189 | |||||||
| chr17:76916203 | T | C | 2 | a0002c0006t0008g0198 a0002c0020t0001g0008 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1026-8763T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916203 | |||||||
| chr17:76916266 | C | T | 4 | a0001c0013t0001g0101 a0002c0006t0007g0069 a0002c0020t0022g0153 others(1): Show |
4 | HG02280.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-8700C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916266 | |||||||
| chr17:76916278 | G | A | 48 | a0001c0001t0003g0157 a0001c0001t0003g0221 a0001c0001t0004g0156 others(45): Show |
48 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1026-8688G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916278 | |||||||
| chr17:76916316 | G | A | 9 | a0001c0005t0007g0045 a0001c0007t0002g0219 a0001c0011t0002g0033 others(6): Show |
9 | HG01243.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026-8650G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916316 | |||||||
| chr17:76916365 | G | A | 1 | a0001c0030t0001g0272 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1026-8601G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916365 | |||||||
| chr17:76916370 | G | A | 114 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0003g0214 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1026-8596G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916370 | |||||||
| chr17:76916403 | G | A | 17 | a0001c0001t0003g0024 a0001c0001t0003g0036 a0001c0001t0006g0248 others(14): Show |
18 | HG01123.hp1 HG01175.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.1026-8563G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916403 | |||||||
| chr17:76916407 | G | C | 1 | a0002c0020t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1026-8559G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916407 | |||||||
| chr17:76916424 | A | G | 107 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0003g0214 others(104): Show |
107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1026-8542A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916424 | |||||||
| chr17:76916507 | T | C | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1026-8459T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916507 | |||||||
| chr17:76916683 | G | A | 4 | a0001c0001t0031g0256 a0002c0002t0004g0257 a0002c0002t0004g0260 others(1): Show |
4 | HG01243.hp2 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-8283G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916683 | |||||||
| chr17:76916710 | G | A | 4 | a0001c0001t0031g0256 a0002c0002t0004g0257 a0002c0002t0004g0260 others(1): Show |
4 | HG01243.hp2 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-8256G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916710 | |||||||
| chr17:76916871 | G | A | 49 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(46): Show |
49 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1026-8095G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916871 | |||||||
| chr17:76916898 | C | T | 89 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0049 others(86): Show |
89 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1026-8068C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916898 | |||||||
| chr17:76916942 | G | T | 42 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(39): Show |
42 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.1026-8024G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76916942 | |||||||
| chr17:76917026 | G | A | 1 | a0002c0006t0008g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1026-7940G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917026 | |||||||
| chr17:76917032 | G | A | 1 | a0001c0001t0006g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1026-7934G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917032 | |||||||
| chr17:76917065 | G | A | 1 | a0001c0024t0001g0141 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1026-7901G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917065 | |||||||
| chr17:76917072 | G | A | 1 | a0001c0005t0002g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1026-7894G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917072 | |||||||
| chr17:76917125 | C | T | 3 | a0001c0011t0002g0188 a0001c0055t0007g0073 a0002c0006t0007g0072 |
3 | HG03471.hp2 NA19043.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1026-7841C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917125 | |||||||
| chr17:76917127 | G | A | 47 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(44): Show |
47 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1026-7839G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917127 | |||||||
| chr17:76917146 | G | A | 1 | a0001c0025t0014g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1026-7820G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917146 | |||||||
| chr17:76917210 | G | A | 1 | a0002c0012t0001g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1026-7756G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917210 | |||||||
| chr17:76917272 | G | C | 1 | a0001c0003t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1026-7694G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917272 | |||||||
| chr17:76917286 | C | T | 4 | a0001c0001t0031g0256 a0001c0056t0008g0108 a0002c0002t0004g0257 others(1): Show |
4 | HG01069.hp2 HG01243.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026-7680C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917286 | |||||||
| chr17:76917287 | G | A | 1 | a0002c0038t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1026-7679G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917287 | |||||||
| chr17:76917337 | C | T | 1 | a0002c0004t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1026-7629C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917337 | |||||||
| chr17:76917365 | C | T | 41 | a0001c0001t0006g0049 a0001c0001t0006g0134 a0001c0003t0029g0051 others(38): Show |
42 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1026-7601C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917365 | |||||||
| chr17:76917623 | C | G | 50 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(47): Show |
50 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1026-7343C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917623 | |||||||
| chr17:76917636 | G | A | 88 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0049 others(85): Show |
88 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1026-7330G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917636 | |||||||
| chr17:76917769 | G | A | 51 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0178 others(48): Show |
51 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1026-7197G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917769 | |||||||
| chr17:76917781 | G | A | 92 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0049 others(89): Show |
93 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1026-7185G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917781 | |||||||
| chr17:76917796 | C | T | 1 | a0001c0013t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1026-7170C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917796 | |||||||
| chr17:76917799 | C | T | 2 | a0001c0005t0007g0045 a0001c0007t0002g0219 |
2 | HG03492.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1026-7167C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917799 | |||||||
| chr17:76917838 | G | A | 2 | a0001c0031t0001g0252 a0002c0014t0017g0004 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1026-7128G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917838 | |||||||
| chr17:76917855 | G | T | 44 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(41): Show |
44 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1026-7111G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917855 | |||||||
| chr17:76917992 | C | T | 1 | a0001c0001t0004g0160 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1026-6974C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917992 | |||||||
| chr17:76917993 | G | A | 3 | a0001c0018t0004g0190 a0001c0018t0004g0191 a0002c0019t0004g0242 |
3 | HG00140.hp2 HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1026-6973G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76917993 | |||||||
| chr17:76918007 | C | T | 7 | a0001c0001t0004g0156 a0001c0005t0008g0264 a0001c0025t0010g0047 others(4): Show |
7 | HG01255.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-6959C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918007 | |||||||
| chr17:76918008 | G | A | 5 | a0001c0013t0001g0101 a0002c0020t0001g0011 a0002c0020t0022g0153 others(2): Show |
5 | HG02976.hp2 HG03225.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-6958G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918008 | |||||||
| chr17:76918020 | T | C | 156 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(153): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1026-6946T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918020 | |||||||
| chr17:76918076 | G | A | 92 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0049 others(89): Show |
93 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1026-6890G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918076 | |||||||
| chr17:76918116 | C | T | 1 | a0002c0002t0005g0086 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1026-6850C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918116 | |||||||
| chr17:76918182 | T | TC | 76 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0049 others(73): Show |
77 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1026-6777dupC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76918182 | ||||||
| chr17:76918182 | T | TCC | 16 | a0001c0001t0006g0178 a0001c0003t0001g0183 a0001c0011t0002g0184 others(13): Show |
16 | HG00621.hp2 HG01993.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1026-6778_1026-677 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76918182 | ||||||
| chr17:76918220 | C | T | 146 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(143): Show |
147 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1026-6746C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918220 | |||||||
| chr17:76918224 | C | T | 92 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0049 others(89): Show |
93 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1026-6742C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918224 | |||||||
| chr17:76918355 | C | T | 2 | a0001c0005t0004g0126 a0002c0006t0032g0070 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1026-6611C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918355 | |||||||
| chr17:76918440 | A | G | 148 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(145): Show |
149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1026-6526A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918440 | |||||||
| chr17:76918445 | G | A | 148 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(145): Show |
149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1026-6521G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918445 | |||||||
| chr17:76918446 | T | C | 1 | a0002c0012t0001g0271 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1026-6520T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918446 | |||||||
| chr17:76918483 | G | A | 148 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(145): Show |
149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1026-6483G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918483 | |||||||
| chr17:76918569 | C | T | 148 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(145): Show |
149 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1026-6397C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918569 | |||||||
| chr17:76918859 | A | G | 55 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(52): Show |
55 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1026-6107A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918859 | |||||||
| chr17:76918896 | AAG | A | 92 | a0001c0001t0003g0192 a0001c0001t0004g0156 a0001c0001t0006g0049 others(89): Show |
93 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1026-6060_1026-605 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76918896 | ||||||
| chr17:76918991 | G | A | 1 | a0001c0001t0006g0025 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1026-5975G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76918991 | |||||||
| chr17:76919014 | G | A | 6 | a0001c0005t0007g0045 a0001c0007t0002g0219 a0001c0011t0002g0033 others(3): Show |
6 | HG01243.hp1 HG03471.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-5952G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919014 | |||||||
| chr17:76919043 | A | T | 8 | a0001c0001t0003g0192 a0001c0001t0006g0270 a0001c0001t0011g0065 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026-5923A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919043 | |||||||
| chr17:76919065 | G | A | 2 | a0002c0002t0004g0105 a0002c0034t0014g0058 |
2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1026-5901G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919065 | |||||||
| chr17:76919163 | C | T | 2 | a0002c0002t0011g0199 a0002c0020t0001g0008 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1026-5803C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919163 | |||||||
| chr17:76919481 | G | A | 1 | a0002c0006t0008g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1026-5485G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919481 | |||||||
| chr17:76919482 | T | G | 2 | a0002c0002t0011g0199 a0002c0020t0001g0008 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1026-5484T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919482 | |||||||
| chr17:76919514 | T | A | 1 | a0001c0003t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1026-5452T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919514 | |||||||
| chr17:76919523 | A | G | 146 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(143): Show |
147 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1026-5443A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919523 | |||||||
| chr17:76919626 | T | C | 5 | a0001c0001t0031g0256 a0001c0056t0008g0108 a0002c0002t0004g0257 others(2): Show |
5 | HG01069.hp2 HG01243.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-5340T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919626 | |||||||
| chr17:76919724 | C | G | 1 | a0001c0003t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1026-5242C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919724 | |||||||
| chr17:76919740 | C | A | 141 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(138): Show |
142 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1026-5226C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919740 | |||||||
| chr17:76919850 | C | G | 12 | a0001c0001t0003g0024 a0001c0001t0003g0036 a0001c0005t0003g0212 others(9): Show |
12 | HG01099.hp2 HG01175.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026-5116C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919850 | |||||||
| chr17:76919898 | C | A | 58 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(55): Show |
58 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1026-5068C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919898 | |||||||
| chr17:76919925 | G | A | 100 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1026-5041G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919925 | |||||||
| chr17:76919930 | G | A | 43 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(40): Show |
43 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1026-5036G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919930 | |||||||
| chr17:76919949 | T | A | 1 | a0002c0020t0001g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1026-5017T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919949 | |||||||
| chr17:76919958 | G | A | 1 | a0001c0001t0012g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1026-5008G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76919958 | |||||||
| chr17:76920005 | C | A | 60 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0024 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1026-4961C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920005 | |||||||
| chr17:76920020 | C | CCCTACCC others(19): Show |
1 | a0003c0027t0001g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1026-4945_1026-492 others(30): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76920020 | ||||||
| chr17:76920088 | A | G | 49 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(46): Show |
49 | HG00621.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.1026-4878A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920088 | |||||||
| chr17:76920112 | A | G | 7 | a0001c0001t0004g0156 a0001c0005t0008g0264 a0001c0025t0010g0047 others(4): Show |
7 | HG01255.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-4854A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920112 | |||||||
| chr17:76920155 | G | T | 1 | a0001c0003t0001g0094 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1026-4811G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920155 | |||||||
| chr17:76920225 | A | G | 105 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(102): Show |
105 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1026-4741A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920225 | |||||||
| chr17:76920226 | C | G | 1 | a0002c0004t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026-4740C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920226 | |||||||
| chr17:76920260 | C | T | 2 | a0001c0001t0005g0043 a0001c0001t0027g0220 |
2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1026-4706C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920260 | |||||||
| chr17:76920267 | C | G | 113 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(110): Show |
113 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1026-4699C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920267 | |||||||
| chr17:76920288 | CAAGAGAA others(6): Show |
C | 42 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(39): Show |
42 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.1026-4676_1026-466 others(17): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76920288 | ||||||
| chr17:76920289 | AAGAGAAA others(7): Show |
A | 1 | a0002c0004t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026-4676_1026-466 others(18): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920289 | |||||||
| chr17:76920303 | C | G | 42 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(39): Show |
42 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.1026-4663C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920303 | |||||||
| chr17:76920304 | T | G | 1 | a0002c0004t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026-4662T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920304 | |||||||
| chr17:76920306 | G | T | 1 | a0002c0004t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1026-4660G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920306 | |||||||
| chr17:76920385 | C | G | 10 | a0001c0001t0003g0024 a0001c0001t0003g0036 a0001c0005t0003g0212 others(7): Show |
10 | HG01175.hp1 HG01361.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026-4581C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920385 | |||||||
| chr17:76920418 | C | T | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1026-4548C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920418 | |||||||
| chr17:76920422 | A | G | 196 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(193): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1026-4544A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920422 | |||||||
| chr17:76920428 | A | C | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1026-4538A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920428 | |||||||
| chr17:76920475 | G | A | 99 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(96): Show |
99 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1026-4491G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920475 | |||||||
| chr17:76920672 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1026-4294C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920672 | |||||||
| chr17:76920860 | C | A | 1 | a0001c0024t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1026-4106C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920860 | |||||||
| chr17:76920897 | C | T | 43 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(40): Show |
43 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1026-4069C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76920897 | |||||||
| chr17:76921042 | G | A | 43 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(40): Show |
43 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1026-3924G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921042 | |||||||
| chr17:76921109 | A | G | 136 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0005g0021 others(133): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1026-3857A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921109 | |||||||
| chr17:76921288 | C | T | 1 | a0001c0018t0004g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1026-3678C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921288 | |||||||
| chr17:76921312 | A | G | 136 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0005g0021 others(133): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1026-3654A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921312 | |||||||
| chr17:76921373 | T | A | 1 | a0001c0011t0002g0223 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1026-3593T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921373 | |||||||
| chr17:76921422 | A | G | 7 | a0001c0001t0031g0256 a0001c0056t0008g0108 a0002c0002t0004g0257 others(4): Show |
7 | HG01069.hp2 HG01243.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-3544A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921422 | |||||||
| chr17:76921444 | A | C | 131 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0005g0021 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1026-3522A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921444 | |||||||
| chr17:76921444 | A | G | 3 | a0001c0025t0014g0071 a0002c0002t0005g0086 a0002c0004t0001g0102 |
3 | HG01071.hp2 HG02145.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1026-3522A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921444 | |||||||
| chr17:76921444 | A | T | 2 | a0002c0002t0011g0199 a0002c0020t0001g0008 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1026-3522A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921444 | |||||||
| chr17:76921450 | C | G | 135 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0005g0021 others(132): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1026-3516C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921450 | |||||||
| chr17:76921530 | C | T | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1026-3436C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921530 | |||||||
| chr17:76921589 | C | T | 1 | a0001c0003t0001g0044 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1026-3377C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921589 | |||||||
| chr17:76921771 | C | A | 82 | a0001c0001t0002g0038 a0001c0001t0005g0021 a0001c0001t0005g0041 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.1026-3195C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921771 | |||||||
| chr17:76921782 | T | C | 1 | a0001c0001t0005g0043 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1026-3184T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921782 | |||||||
| chr17:76921818 | G | A | 14 | a0001c0001t0006g0134 a0001c0003t0029g0051 a0001c0007t0002g0064 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1026-3148G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921818 | |||||||
| chr17:76921902 | G | C | 1 | a0001c0025t0014g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1026-3064G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921902 | |||||||
| chr17:76921943 | A | C | 137 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0005g0021 others(134): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1026-3023A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921943 | |||||||
| chr17:76921968 | T | C | 137 | a0001c0001t0002g0038 a0001c0001t0003g0192 a0001c0001t0005g0021 others(134): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1026-2998T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76921968 | |||||||
| chr17:76922209 | C | A | 7 | a0001c0001t0004g0156 a0001c0005t0008g0264 a0001c0025t0010g0047 others(4): Show |
7 | HG01255.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1026-2757C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922209 | |||||||
| chr17:76922249 | G | A | 37 | a0001c0001t0002g0038 a0001c0001t0005g0021 a0001c0001t0005g0041 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1026-2717G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922249 | |||||||
| chr17:76922317 | C | G | 44 | a0001c0001t0003g0192 a0001c0001t0006g0178 a0001c0001t0006g0270 others(41): Show |
44 | HG00621.hp1 HG01099.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1026-2649C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922317 | |||||||
| chr17:76922371 | GTGTGGTT others(3): Show |
G | 1 | a0001c0013t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1026-2594_1026-258 others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922371 | |||||||
| chr17:76922410 | G | T | 1 | a0001c0011t0002g0223 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1026-2556G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922410 | |||||||
| chr17:76922511 | A | T | 1 | a0001c0031t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1026-2455A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922511 | |||||||
| chr17:76922600 | T | C | 4 | a0001c0005t0009g0162 a0001c0005t0009g0163 a0001c0005t0009g0170 others(1): Show |
5 | HG02109.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-2366T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922600 | |||||||
| chr17:76922688 | G | C | 1 | a0001c0025t0014g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1026-2278G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922688 | |||||||
| chr17:76922885 | C | T | 5 | a0001c0013t0001g0101 a0002c0020t0001g0011 a0002c0020t0022g0153 others(2): Show |
5 | HG02976.hp2 HG03225.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-2081C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922885 | |||||||
| chr17:76922969 | C | A | 46 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(43): Show |
46 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1026-1997C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76922969 | |||||||
| chr17:76923084 | A | G | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1026-1882A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923084 | |||||||
| chr17:76923094 | C | T | 47 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0157 others(44): Show |
47 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.1026-1872C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923094 | |||||||
| chr17:76923095 | G | A | 6 | a0001c0001t0004g0156 a0001c0005t0008g0264 a0001c0025t0010g0047 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-1871G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923095 | |||||||
| chr17:76923120 | C | T | 1 | a0002c0016t0007g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1026-1846C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923120 | |||||||
| chr17:76923130 | C | T | 87 | a0001c0001t0002g0038 a0001c0001t0005g0021 a0001c0001t0005g0041 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.1026-1836C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923130 | |||||||
| chr17:76923131 | G | A | 37 | a0001c0001t0002g0038 a0001c0001t0005g0021 a0001c0001t0005g0041 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.1026-1835G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923131 | |||||||
| chr17:76923217 | T | G | 2 | a0002c0002t0011g0199 a0002c0020t0001g0008 |
2 | HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1026-1749T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923217 | |||||||
| chr17:76923218 | TCAAGGAG others(8): Show |
T | 1 | a0002c0004t0001g0103 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1026-1745_1026-173 others(19): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76923218 | ||||||
| chr17:76923381 | AGCTG | A | 118 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0024 others(115): Show |
118 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1026-1578_1026-157 others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76923381 | ||||||
| chr17:76923394 | C | A | 129 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(126): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1026-1572C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923394 | |||||||
| chr17:76923438 | A | G | 200 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1026-1528A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923438 | |||||||
| chr17:76923461 | A | T | 1 | a0002c0002t0004g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1026-1505A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923461 | |||||||
| chr17:76923554 | C | T | 15 | a0001c0001t0006g0134 a0001c0003t0029g0051 a0001c0007t0002g0064 others(12): Show |
15 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026-1412C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923554 | |||||||
| chr17:76923642 | G | A | 2 | a0001c0025t0014g0071 a0002c0034t0014g0058 |
2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1026-1324G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923642 | |||||||
| chr17:76923690 | G | A | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1026-1276G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923690 | |||||||
| chr17:76923726 | G | A | 1 | a0002c0014t0001g0172 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1026-1240G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923726 | |||||||
| chr17:76923745 | G | A | 1 | a0002c0006t0007g0110 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1026-1221G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923745 | |||||||
| chr17:76923750 | A | C | 190 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1026-1216A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923750 | |||||||
| chr17:76923752 | A | G | 190 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1026-1214A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923752 | |||||||
| chr17:76923765 | G | A | 1 | a0001c0001t0006g0049 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1026-1201G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923765 | |||||||
| chr17:76923830 | T | G | 50 | a0001c0001t0003g0192 a0001c0001t0005g0210 a0001c0001t0006g0175 others(47): Show |
50 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1026-1136T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923830 | |||||||
| chr17:76923881 | G | A | 63 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0003g0024 others(60): Show |
64 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.1026-1085G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923881 | |||||||
| chr17:76923929 | C | T | 21 | a0001c0001t0006g0175 a0001c0005t0002g0235 a0001c0005t0007g0045 others(18): Show |
21 | HG00438.hp1 HG00438.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1026-1037C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923929 | |||||||
| chr17:76923949 | C | T | 45 | a0001c0001t0003g0192 a0001c0001t0006g0270 a0001c0001t0011g0065 others(42): Show |
45 | HG00621.hp1 HG01109.hp2 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.1026-1017C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76923949 | |||||||
| chr17:76924004 | G | A | 89 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0004g0156 others(86): Show |
90 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.1026-962G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924004 | |||||||
| chr17:76924099 | G | C | 57 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0005g0021 others(54): Show |
57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.1026-867G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924099 | |||||||
| chr17:76924115 | A | G | 195 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(192): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1026-851A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924115 | |||||||
| chr17:76924166 | CAGGGAGG others(17): Show |
C | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1026-799_1026-776d others(26): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924166 | |||||||
| chr17:76924288 | A | T | 8 | a0001c0001t0004g0156 a0001c0024t0001g0141 a0001c0025t0014g0071 others(5): Show |
8 | HG00639.hp2 HG01069.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026-678A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924288 | |||||||
| chr17:76924293 | CCAGCAGC others(35): Show |
C | 1 | a0001c0001t0012g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1026-671_1026-630d others(44): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76924293 | ||||||
| chr17:76924359 | C | T | 12 | a0001c0005t0002g0235 a0001c0005t0008g0264 a0001c0013t0001g0152 others(9): Show |
12 | HG00438.hp1 HG00438.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026-607C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924359 | |||||||
| chr17:76924364 | T | C | 2 | a0001c0003t0013g0249 a0001c0003t0013g0251 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1026-602T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924364 | |||||||
| chr17:76924411 | A | T | 1 | a0001c0013t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1026-555A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924411 | |||||||
| chr17:76924454 | G | C | 1 | a0002c0002t0008g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1026-512G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924454 | |||||||
| chr17:76924455 | G | C | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-511G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924455 | |||||||
| chr17:76924456 | G | A | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-510G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924456 | |||||||
| chr17:76924456 | GGTGGGAA others(11): Show |
G | 35 | a0001c0001t0002g0038 a0001c0001t0005g0021 a0001c0001t0005g0041 others(32): Show |
35 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1026-505_1026-488d others(20): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76924456 | ||||||
| chr17:76924457 | G | T | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-509G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924457 | |||||||
| chr17:76924457 | GTGGGAAG others(10): Show |
G | 2 | a0002c0002t0005g0086 a0002c0002t0008g0048 |
2 | HG01071.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1026-508_1026-492d others(19): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924457 | |||||||
| chr17:76924458 | T | A | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-508T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924458 | |||||||
| chr17:76924460 | G | A | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-506G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924460 | |||||||
| chr17:76924463 | A | G | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-503A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924463 | |||||||
| chr17:76924464 | G | A | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-502G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924464 | |||||||
| chr17:76924465 | C | T | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-501C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924465 | |||||||
| chr17:76924468 | G | T | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-498G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924468 | |||||||
| chr17:76924469 | T | A | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-497T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924469 | |||||||
| chr17:76924470 | A | T | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-496A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924470 | |||||||
| chr17:76924471 | A | T | 1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1026-495A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924471 | |||||||
| chr17:76924494 | G | A | 81 | a0001c0001t0002g0038 a0001c0001t0003g0036 a0001c0001t0003g0221 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1026-472G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924494 | |||||||
| chr17:76924497 | C | A | 1 | a0001c0053t0001g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1026-469C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924497 | |||||||
| chr17:76924506 | C | G | 1 | a0001c0007t0018g0176 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1026-460C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924506 | |||||||
| chr17:76924513 | C | T | 1 | a0001c0048t0003g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1026-453C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924513 | |||||||
| chr17:76924517 | A | G | 165 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(162): Show |
166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1026-449A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924517 | |||||||
| chr17:76924559 | G | A | 1 | a0002c0009t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1026-407G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924559 | |||||||
| chr17:76924578 | CCAGA | C | 4 | a0001c0005t0009g0162 a0001c0005t0009g0163 a0001c0005t0009g0170 others(1): Show |
5 | HG02109.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026-385_1026-382d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 76924578 | ||||||
| chr17:76924611 | G | A | 4 | a0002c0002t0005g0238 a0002c0002t0005g0239 a0002c0002t0005g0258 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-355G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924611 | |||||||
| chr17:76924676 | G | C | 5 | a0001c0052t0003g0137 a0002c0017t0002g0144 a0002c0022t0003g0082 others(2): Show |
5 | HG01496.hp1 HG01978.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026-290G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924676 | |||||||
| chr17:76924696 | G | A | 2 | a0001c0005t0007g0028 a0001c0005t0015g0031 |
2 | HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1026-270G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924696 | |||||||
| chr17:76924714 | T | G | 29 | a0001c0001t0002g0038 a0001c0001t0005g0021 a0001c0001t0005g0041 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1026-252T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924714 | |||||||
| chr17:76924715 | T | C | 1 | a0001c0001t0012g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1026-251T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924715 | |||||||
| chr17:76924741 | C | A | 15 | a0001c0005t0002g0019 a0001c0005t0003g0212 a0001c0013t0001g0237 others(12): Show |
15 | HG00140.hp2 HG00642.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1026-225C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924741 | |||||||
| chr17:76924800 | G | A | 1 | a0002c0002t0008g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1026-166G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924800 | |||||||
| chr17:76924806 | C | A | 1 | a0001c0053t0001g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1026-160C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924806 | |||||||
| chr17:76924810 | C | T | 2 | a0001c0011t0002g0186 a0001c0011t0002g0223 |
2 | HG02523.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1026-156C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924810 | |||||||
| chr17:76924817 | G | A | 6 | a0001c0001t0006g0270 a0002c0002t0006g0200 a0002c0012t0001g0012 others(3): Show |
6 | HG00639.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-149G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924817 | |||||||
| chr17:76924851 | G | A | 3 | a0001c0013t0001g0101 a0002c0033t0001g0059 a0010c0046t0001g0224 |
3 | HG03225.hp1 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1026-115G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924851 | |||||||
| chr17:76924875 | G | T | 170 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(167): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1026-91G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 8/17 | chr17 | 76924875 | |||||||
| chr17:76925103 | A | AG | 3 | a0001c0001t0012g0014 a0001c0011t0002g0223 a0002c0004t0001g0124 |
3 | HG00621.hp2 HG00642.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1157+9dupG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925103 | ||||||
| chr17:76925125 | G | A | 1 | a0002c0043t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1157+28G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925125 | |||||||
| chr17:76925141 | G | GGGAGAAA others(25): Show |
1 | a0002c0006t0002g0006 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1157+75_1157+76ins others(32): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925141 | ||||||
| chr17:76925162 | G | T | 6 | a0001c0001t0004g0156 a0001c0001t0011g0065 a0001c0025t0014g0071 others(3): Show |
6 | HG02145.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1157+65G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925162 | |||||||
| chr17:76925167 | G | GC | 10 | a0001c0001t0003g0157 a0001c0003t0001g0254 a0001c0005t0009g0162 others(7): Show |
10 | HG01106.hp1 HG01952.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1157+75dupC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925167 | ||||||
| chr17:76925175 | G | A | 121 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(118): Show |
121 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1157+78G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925175 | |||||||
| chr17:76925176 | T | TC | 5 | a0001c0001t0012g0014 a0001c0013t0001g0101 a0002c0009t0001g0148 others(2): Show |
5 | HG00642.hp1 HG01358.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157+83dupC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925176 | ||||||
| chr17:76925212 | T | G | 1 | a0002c0002t0008g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1157+115T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925212 | |||||||
| chr17:76925228 | G | GCCTCCGC others(741): Show |
1 | a0001c0053t0001g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1157+133_1157+134i others(750): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925228 | ||||||
| chr17:76925231 | C | T | 1 | a0001c0005t0007g0045 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1157+134C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925231 | |||||||
| chr17:76925233 | C | T | 15 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0003g0214 others(12): Show |
15 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1157+136C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925233 | |||||||
| chr17:76925235 | G | GCCCCTCC others(400): Show |
1 | a0001c0001t0006g0096 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1157+141_1157+142i others(409): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(928): Show |
1 | a0001c0005t0009g0162 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1157+146_1157+147i others(937): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(966): Show |
1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1157+146_1157+147i others(975): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(400): Show |
1 | a0001c0001t0006g0034 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1157+146_1157+147i others(409): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(687): Show |
1 | a0002c0017t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1157+146_1157+147i others(696): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(773): Show |
1 | a0002c0002t0005g0083 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1157+146_1157+147i others(782): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(788): Show |
1 | a0001c0011t0002g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1157+146_1157+147i others(797): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(933): Show |
1 | a0001c0013t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1157+151_1157+152i others(942): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(950): Show |
1 | a0001c0013t0001g0177 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1157+151_1157+152i others(959): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(773): Show |
1 | a0001c0001t0005g0041 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1157+151_1157+152i others(782): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(808): Show |
1 | a0001c0011t0002g0223 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1157+153_1157+154i others(817): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(951): Show |
1 | a0001c0018t0004g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(960): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(934): Show |
1 | a0002c0006t0002g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(943): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(630): Show |
1 | a0002c0041t0010g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(639): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(635): Show |
1 | a0002c0002t0006g0074 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(644): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(949): Show |
1 | a0001c0013t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(958): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(944): Show |
1 | a0001c0005t0002g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(953): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(960): Show |
1 | a0001c0005t0003g0212 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(969): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(969): Show |
1 | a0002c0006t0004g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(978): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(600): Show |
1 | a0001c0001t0003g0214 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(609): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(628): Show |
1 | a0002c0002t0003g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(637): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(938): Show |
1 | a0001c0013t0001g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(947): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(623): Show |
2 | a0002c0002t0004g0240 a0002c0028t0004g0061 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1157+156_1157+157i others(632): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(628): Show |
1 | a0002c0002t0003g0007 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(637): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(969): Show |
1 | a0002c0019t0004g0005 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(978): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(629): Show |
1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(638): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(929): Show |
1 | a0001c0005t0008g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(938): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(982): Show |
1 | a0004c0035t0004g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(991): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(969): Show |
1 | a0002c0034t0014g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(978): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(630): Show |
1 | a0001c0049t0010g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(639): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(638): Show |
1 | a0001c0030t0001g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(647): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(627): Show |
13 | a0001c0001t0003g0029 a0001c0001t0003g0192 a0001c0025t0010g0047 others(10): Show |
13 | HG00639.hp2 HG01255.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(636): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(957): Show |
1 | a0002c0014t0001g0172 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(966): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(912): Show |
1 | a0002c0006t0007g0110 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(921): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(963): Show |
1 | a0001c0001t0004g0160 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(972): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(894): Show |
1 | a0002c0014t0017g0004 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(903): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(970): Show |
1 | a0002c0037t0007g0166 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(979): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(999): Show |
1 | a0001c0005t0004g0208 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(1008): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(960): Show |
1 | a0002c0002t0004g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(969): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(934): Show |
1 | a0001c0005t0007g0028 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(943): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(936): Show |
1 | a0003c0026t0030g0269 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(945): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(933): Show |
1 | a0001c0045t0001g0231 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(942): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(894): Show |
1 | a0001c0013t0001g0152 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(903): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(934): Show |
1 | a0002c0014t0001g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(943): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(975): Show |
1 | a0002c0006t0007g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(984): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(949): Show |
1 | a0001c0001t0002g0209 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(958): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(932): Show |
3 | a0002c0002t0002g0253 a0002c0006t0002g0076 a0003c0032t0001g0261 |
3 | HG02056.hp1 NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1157+156_1157+157i others(941): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(928): Show |
1 | a0001c0001t0002g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(937): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(948): Show |
1 | a0001c0005t0002g0235 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(957): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(945): Show |
1 | a0006c0059t0007g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(954): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(992): Show |
1 | a0001c0055t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(1001): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(947): Show |
1 | a0001c0013t0001g0250 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(956): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(953): Show |
1 | a0002c0036t0001g0232 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(962): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(974): Show |
1 | a0002c0014t0001g0207 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(983): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(926): Show |
1 | a0003c0026t0002g0263 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(935): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(931): Show |
1 | a0001c0005t0015g0031 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(940): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(948): Show |
2 | a0001c0005t0009g0163 a0002c0006t0009g0001 |
2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1157+156_1157+157i others(957): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(948): Show |
1 | a0002c0006t0009g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(957): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(947): Show |
1 | a0001c0005t0007g0045 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(956): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(960): Show |
1 | a0001c0013t0001g0237 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(969): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(1007): Show |
1 | a0001c0023t0004g0244 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(1016): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(965): Show |
2 | a0002c0019t0004g0002 a0002c0019t0004g0003 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1157+156_1157+157i others(974): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(943): Show |
1 | a0001c0018t0004g0020 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(952): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(1002): Show |
1 | a0001c0023t0004g0227 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(1011): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(948): Show |
1 | a0001c0018t0004g0037 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(957): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(948): Show |
2 | a0001c0018t0004g0190 a0002c0019t0004g0242 |
2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1157+156_1157+157i others(957): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(984): Show |
1 | a0001c0018t0004g0226 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(993): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(947): Show |
2 | a0001c0005t0004g0126 a0002c0006t0032g0070 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1157+156_1157+157i others(956): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(810): Show |
1 | a0002c0033t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(819): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(812): Show |
1 | a0002c0006t0008g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(821): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(1037): Show |
1 | a0002c0014t0001g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(1046): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(929): Show |
1 | a0010c0046t0001g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(938): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(742): Show |
1 | a0001c0001t0002g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(751): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(970): Show |
1 | a0001c0025t0014g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(979): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(953): Show |
1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(962): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(1018): Show |
1 | a0002c0002t0011g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(1027): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(898): Show |
1 | a0001c0001t0011g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(907): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(400): Show |
1 | a0002c0012t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(409): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(883): Show |
1 | a0002c0014t0001g0088 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(892): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(750): Show |
1 | a0002c0021t0001g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(759): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(798): Show |
1 | a0002c0006t0007g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(807): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(997): Show |
1 | a0001c0023t0004g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(1006): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(400): Show |
1 | a0002c0029t0001g0149 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(409): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(400): Show |
1 | a0001c0001t0006g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(409): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(399): Show |
8 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0049 others(5): Show |
8 | HG00408.hp2 HG00738.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(408): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(399): Show |
1 | a0002c0002t0006g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(408): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(787): Show |
1 | a0001c0007t0002g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(796): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(799): Show |
1 | a0001c0056t0008g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(808): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(826): Show |
1 | a0002c0016t0002g0112 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(835): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(774): Show |
1 | a0002c0002t0005g0086 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(783): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(768): Show |
1 | a0001c0001t0012g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(777): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(773): Show |
1 | a0005c0044t0001g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(782): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(772): Show |
1 | a0001c0024t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(781): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(772): Show |
8 | a0001c0001t0005g0021 a0001c0001t0005g0043 a0001c0001t0008g0107 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(781): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(772): Show |
1 | a0002c0002t0016g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(781): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(772): Show |
1 | a0001c0047t0001g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(781): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(771): Show |
7 | a0001c0001t0005g0053 a0001c0001t0005g0210 a0002c0002t0005g0039 others(4): Show |
7 | HG00639.hp1 HG00735.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(780): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(771): Show |
1 | a0001c0001t0005g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(780): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(783): Show |
1 | a0002c0020t0022g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(792): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(767): Show |
1 | a0002c0002t0005g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(776): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(756): Show |
1 | a0002c0020t0001g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(765): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(755): Show |
1 | a0002c0020t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(764): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(756): Show |
1 | a0002c0020t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(765): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(755): Show |
1 | a0001c0031t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(764): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(827): Show |
1 | a0002c0016t0002g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(836): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(825): Show |
8 | a0001c0007t0002g0064 a0001c0007t0002g0136 a0001c0007t0002g0201 others(5): Show |
8 | HG00423.hp2 HG01975.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(834): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(826): Show |
1 | a0001c0007t0002g0216 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(835): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(847): Show |
1 | a0001c0007t0018g0176 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(856): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(780): Show |
1 | a0001c0007t0002g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(789): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(791): Show |
1 | a0001c0011t0002g0186 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(800): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(765): Show |
1 | a0001c0011t0012g0174 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(774): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(782): Show |
1 | a0009c0058t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(791): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(788): Show |
2 | a0002c0017t0002g0100 a0002c0017t0002g0195 |
2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1157+156_1157+157i others(797): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(787): Show |
1 | a0002c0017t0002g0144 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(796): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(787): Show |
8 | a0001c0011t0002g0184 a0001c0011t0002g0202 a0001c0011t0002g0276 others(5): Show |
8 | HG00408.hp1 HG01496.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(796): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(786): Show |
1 | a0001c0011t0002g0188 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(795): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(743): Show |
1 | a0002c0017t0002g0273 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(752): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(749): Show |
1 | a0002c0004t0001g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(758): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(755): Show |
1 | a0002c0004t0001g0091 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(764): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(748): Show |
1 | a0001c0010t0007g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(757): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(763): Show |
1 | a0002c0004t0001g0103 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(772): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(720): Show |
1 | a0001c0010t0003g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(729): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(717): Show |
1 | a0002c0015t0003g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(726): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(720): Show |
1 | a0002c0015t0003g0111 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(729): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(719): Show |
5 | a0001c0007t0003g0222 a0001c0010t0003g0130 a0001c0010t0003g0132 others(2): Show |
5 | HG00423.hp1 HG02132.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(728): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(714): Show |
1 | a0001c0010t0003g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(723): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(748): Show |
1 | a0001c0003t0001g0165 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(757): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(747): Show |
8 | a0001c0003t0001g0181 a0001c0003t0001g0204 a0001c0003t0001g0206 others(5): Show |
8 | HG00597.hp1 HG00738.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(756): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(747): Show |
1 | a0002c0004t0001g0115 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(756): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(746): Show |
1 | a0002c0016t0007g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(755): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(745): Show |
1 | a0002c0004t0001g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(754): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(742): Show |
1 | a0002c0004t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(751): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(743): Show |
1 | a0001c0003t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(752): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(751): Show |
1 | a0002c0004t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(760): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(747): Show |
1 | a0002c0015t0003g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(756): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(737): Show |
1 | a0001c0050t0033g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(746): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(748): Show |
1 | a0002c0004t0001g0077 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(757): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(747): Show |
18 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0044 others(15): Show |
18 | HG00544.hp2 HG00621.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1157+156_1157+157i others(756): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(746): Show |
1 | a0002c0004t0001g0139 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(755): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(747): Show |
1 | a0001c0003t0001g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(756): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(741): Show |
1 | a0001c0003t0013g0251 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(750): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(752): Show |
1 | a0002c0042t0004g0168 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(761): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(743): Show |
1 | a0002c0004t0001g0173 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(752): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(759): Show |
1 | a0001c0003t0001g0099 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(768): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(744): Show |
1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(753): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(744): Show |
1 | a0001c0003t0013g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(753): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(742): Show |
1 | a0002c0015t0005g0080 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(751): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(737): Show |
1 | a0002c0004t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(746): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(728): Show |
1 | a0003c0027t0001g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(737): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(398): Show |
2 | a0001c0001t0006g0270 a0002c0002t0006g0200 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1157+157_1157+158i others(407): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(744): Show |
1 | a0002c0021t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1157+150_1157+151i others(753): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(749): Show |
1 | a0002c0002t0005g0258 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(758): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(748): Show |
1 | a0001c0008t0001g0055 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1157+145_1157+146i others(757): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(751): Show |
1 | a0001c0008t0001g0246 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(760): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(745): Show |
1 | a0001c0008t0001g0247 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(754): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(742): Show |
1 | a0002c0009t0001g0092 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(751): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(747): Show |
19 | a0001c0001t0003g0024 a0001c0001t0003g0036 a0001c0001t0007g0233 others(16): Show |
19 | HG01175.hp1 HG01243.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.1157+145_1157+146i others(756): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(752): Show |
1 | a0007c0040t0002g0193 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(761): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(746): Show |
1 | a0001c0008t0001g0030 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(755): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(753): Show |
1 | a0001c0008t0001g0056 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(762): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(742): Show |
1 | a0001c0008t0001g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1157+145_1157+146i others(751): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(759): Show |
1 | a0001c0057t0004g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1157+145_1157+146i others(768): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(769): Show |
1 | a0001c0001t0003g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(778): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(752): Show |
1 | a0002c0012t0001g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(761): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(746): Show |
1 | a0002c0028t0026g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1157+145_1157+146i others(755): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(747): Show |
1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1157+145_1157+146i others(756): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCCTCCC others(734): Show |
1 | a0008c0039t0001g0117 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1157+145_1157+146i others(743): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925235 | G | GCCTCACC others(920): Show |
1 | a0002c0006t0002g0006 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1157+140_1157+141i others(929): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925235 | ||||||
| chr17:76925239 | T | TCCCCTCC others(642): Show |
1 | a0001c0001t0003g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(651): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925239 | ||||||
| chr17:76925239 | T | TCCCCTCC others(909): Show |
1 | a0001c0005t0009g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(918): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925239 | ||||||
| chr17:76925244 | T | TCCCCTCC others(400): Show |
1 | a0001c0001t0006g0134 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(409): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925244 | ||||||
| chr17:76925244 | T | TCCCCTCC others(789): Show |
1 | a0002c0002t0008g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(798): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925244 | ||||||
| chr17:76925244 | T | TCCCCTCC others(801): Show |
1 | a0001c0001t0012g0014 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1157+156_1157+157i others(810): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925244 | ||||||
| chr17:76925244 | T | TCCCCTCC others(826): Show |
1 | a0002c0015t0003g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1157+156_1157+157i others(835): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925244 | ||||||
| chr17:76925299 | A | T | 1 | a0002c0014t0001g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1157+202A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925299 | |||||||
| chr17:76925359 | C | T | 36 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(33): Show |
36 | HG00597.hp2 HG00673.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1157+262C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925359 | |||||||
| chr17:76925379 | G | A | 1 | a0002c0009t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1157+282G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925379 | |||||||
| chr17:76925407 | A | G | 246 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1157+310A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925407 | |||||||
| chr17:76925454 | T | C | 1 | a0002c0015t0003g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1157+357T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925454 | |||||||
| chr17:76925479 | A | AC | 4 | a0001c0001t0012g0014 a0001c0011t0002g0186 a0002c0002t0006g0185 others(1): Show |
4 | HG00642.hp1 HG02523.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1157+386dupC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925479 | ||||||
| chr17:76925605 | G | C | 28 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0007g0233 others(25): Show |
28 | HG00597.hp2 HG00673.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1157+508G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925605 | |||||||
| chr17:76925628 | TC | T | 3 | a0001c0008t0001g0246 a0001c0011t0002g0223 a0002c0002t0005g0164 |
3 | HG00099.hp1 NA18975.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1157+534delC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925628 | ||||||
| chr17:76925738 | TG | T | 5 | a0001c0003t0001g0135 a0001c0003t0013g0251 a0002c0014t0001g0121 others(2): Show |
5 | HG01081.hp2 HG01517.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157+646delG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925738 | ||||||
| chr17:76925805 | A | G | 1 | a0002c0002t0005g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1157+708A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925805 | |||||||
| chr17:76925868 | G | GGGAGGGC others(40): Show |
1 | a0002c0006t0004g0241 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1158-728_1158-682d others(49): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76925868 | ||||||
| chr17:76925963 | C | G | 1 | a0001c0007t0002g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1158-634C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925963 | |||||||
| chr17:76925995 | C | T | 88 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1158-602C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76925995 | |||||||
| chr17:76926020 | C | T | 1 | a0002c0002t0011g0199 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1158-577C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926020 | |||||||
| chr17:76926055 | C | T | 2 | a0001c0011t0002g0033 a0001c0011t0012g0174 |
2 | HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1158-542C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926055 | |||||||
| chr17:76926062 | A | G | 182 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1158-535A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926062 | |||||||
| chr17:76926164 | C | T | 5 | a0001c0008t0001g0054 a0001c0008t0001g0055 a0001c0008t0001g0056 others(2): Show |
5 | HG02027.hp1 NA18612.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1158-433C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926164 | |||||||
| chr17:76926196 | A | C | 182 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1158-401A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926196 | |||||||
| chr17:76926206 | A | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-391A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926206 | |||||||
| chr17:76926207 | T | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-390T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926207 | |||||||
| chr17:76926208 | G | A | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-389G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926208 | |||||||
| chr17:76926210 | C | A | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-387C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926210 | |||||||
| chr17:76926212 | C | T | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-385C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926212 | |||||||
| chr17:76926214 | C | A | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-383C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926214 | |||||||
| chr17:76926215 | T | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-382T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926215 | |||||||
| chr17:76926224 | A | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-373A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926224 | |||||||
| chr17:76926225 | G | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-372G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926225 | |||||||
| chr17:76926226 | A | T | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-371A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926226 | |||||||
| chr17:76926227 | T | A | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-370T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926227 | |||||||
| chr17:76926231 | A | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-366A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926231 | |||||||
| chr17:76926234 | T | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-363T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926234 | |||||||
| chr17:76926251 | G | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-346G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926251 | |||||||
| chr17:76926252 | G | A | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-345G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926252 | |||||||
| chr17:76926253 | A | T | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-344A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926253 | |||||||
| chr17:76926266 | A | AC | 11 | a0001c0003t0001g0204 a0001c0003t0013g0251 a0001c0007t0002g0136 others(8): Show |
11 | HG00438.hp1 HG01081.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1158-326dupC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76926266 | ||||||
| chr17:76926266 | A | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-331A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926266 | |||||||
| chr17:76926267 | C | A | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-330C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926267 | |||||||
| chr17:76926267 | C | T | 2 | a0001c0025t0010g0047 a0002c0002t0006g0074 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1158-330C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926267 | |||||||
| chr17:76926268 | C | T | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-329C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926268 | |||||||
| chr17:76926340 | T | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-257T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926340 | |||||||
| chr17:76926344 | T | C | 182 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1158-253T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926344 | |||||||
| chr17:76926367 | A | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-230A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926367 | |||||||
| chr17:76926383 | G | GT | 3 | a0002c0004t0001g0091 a0003c0026t0002g0263 a0004c0035t0004g0155 |
3 | HG01358.hp2 HG01952.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1158-209dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 76926383 | ||||||
| chr17:76926397 | A | T | 1 | a0001c0003t0001g0181 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1158-200A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926397 | |||||||
| chr17:76926425 | A | G | 182 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1158-172A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926425 | |||||||
| chr17:76926496 | T | C | 183 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(180): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1158-101T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926496 | |||||||
| chr17:76926517 | T | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-80T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926517 | |||||||
| chr17:76926518 | GCTCGTGG others(8): Show |
G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-78_1158-64del others(15): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926518 | |||||||
| chr17:76926554 | G | A | 182 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1158-43G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926554 | |||||||
| chr17:76926557 | G | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-40G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926557 | |||||||
| chr17:76926558 | A | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-39A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926558 | |||||||
| chr17:76926559 | G | A | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-38G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926559 | |||||||
| chr17:76926565 | T | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-32T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926565 | |||||||
| chr17:76926570 | C | T | 182 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1158-27C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926570 | |||||||
| chr17:76926571 | T | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-26T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926571 | |||||||
| chr17:76926576 | C | G | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-21C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926576 | |||||||
| chr17:76926578 | T | C | 1 | a0001c0025t0010g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1158-19T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 9/17 | chr17 | 76926578 | |||||||
| chr17:76926753 | G | T | 1 | a0004c0035t0004g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1291+23G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76926753 | |||||||
| chr17:76926754 | T | G | 1 | a0004c0035t0004g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1291+24T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76926754 | |||||||
| chr17:76926813 | G | A | 2 | a0001c0005t0004g0126 a0002c0006t0032g0070 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1291+83G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76926813 | |||||||
| chr17:76926972 | C | T | 51 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1291+242C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76926972 | |||||||
| chr17:76927035 | G | A | 51 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1291+305G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927035 | |||||||
| chr17:76927045 | G | T | 1 | a0002c0014t0001g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1291+315G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927045 | |||||||
| chr17:76927131 | C | T | 51 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1291+401C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927131 | |||||||
| chr17:76927177 | G | T | 1 | a0002c0014t0001g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1291+447G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927177 | |||||||
| chr17:76927179 | T | G | 187 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(184): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1291+449T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927179 | |||||||
| chr17:76927180 | T | G | 1 | a0003c0027t0001g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1291+450T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927180 | |||||||
| chr17:76927236 | ATTTG | A | 30 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(27): Show |
30 | HG00597.hp2 HG00673.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1291+518_1291+521d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76927236 | ||||||
| chr17:76927259 | C | A | 51 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.1291+529C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927259 | |||||||
| chr17:76927320 | G | A | 30 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(27): Show |
30 | HG00597.hp2 HG00673.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1291+590G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927320 | |||||||
| chr17:76927416 | T | C | 1 | a0002c0006t0008g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1291+686T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927416 | |||||||
| chr17:76927488 | C | T | 1 | a0001c0001t0006g0270 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1291+758C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927488 | |||||||
| chr17:76927518 | G | A | 2 | a0002c0006t0007g0069 a0002c0006t0007g0072 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1291+788G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927518 | |||||||
| chr17:76927530 | G | A | 6 | a0001c0001t0004g0156 a0001c0001t0011g0065 a0001c0025t0014g0071 others(3): Show |
6 | HG02145.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+800G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927530 | |||||||
| chr17:76927598 | C | T | 2 | a0001c0001t0004g0160 a0002c0002t0004g0105 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1291+868C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927598 | |||||||
| chr17:76927718 | G | A | 14 | a0001c0007t0002g0064 a0001c0007t0002g0127 a0001c0007t0002g0136 others(11): Show |
14 | HG00423.hp2 HG00673.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1291+988G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927718 | |||||||
| chr17:76927806 | C | T | 48 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(45): Show |
48 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1291+1076C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927806 | |||||||
| chr17:76927855 | T | C | 91 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1291+1125T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927855 | |||||||
| chr17:76927877 | G | A | 91 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1291+1147G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927877 | |||||||
| chr17:76927907 | A | G | 179 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(176): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1291+1177A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927907 | |||||||
| chr17:76927995 | A | G | 1 | a0002c0009t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1291+1265A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76927995 | |||||||
| chr17:76928158 | A | C | 1 | a0002c0020t0022g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1291+1428A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928158 | |||||||
| chr17:76928215 | G | A | 28 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(25): Show |
28 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+1485G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928215 | |||||||
| chr17:76928245 | G | C | 248 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1291+1515G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928245 | |||||||
| chr17:76928469 | G | A | 88 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1291+1739G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928469 | |||||||
| chr17:76928533 | C | T | 1 | a0001c0008t0001g0030 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1291+1803C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928533 | |||||||
| chr17:76928629 | C | T | 88 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1291+1899C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928629 | |||||||
| chr17:76928690 | G | A | 28 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(25): Show |
28 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291+1960G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928690 | |||||||
| chr17:76928708 | G | A | 1 | a0001c0003t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1291+1978G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928708 | |||||||
| chr17:76928744 | G | C | 1 | a0001c0005t0008g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1291+2014G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928744 | |||||||
| chr17:76928758 | T | C | 2 | a0001c0008t0001g0247 a0002c0009t0001g0092 |
2 | HG00673.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1291+2028T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928758 | |||||||
| chr17:76928815 | C | G | 1 | a0002c0014t0001g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1291+2085C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928815 | |||||||
| chr17:76928817 | A | C | 1 | a0002c0014t0001g0121 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1291+2087A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928817 | |||||||
| chr17:76928880 | A | AT | 138 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0192 others(135): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1291+2163dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76928880 | ||||||
| chr17:76928880 | A | ATT | 23 | a0001c0001t0003g0036 a0001c0001t0006g0023 a0001c0001t0006g0025 others(20): Show |
23 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291+2162_1291+216 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76928880 | ||||||
| chr17:76928880 | AT | A | 8 | a0001c0001t0011g0065 a0001c0025t0010g0229 a0002c0002t0002g0253 others(5): Show |
8 | HG01255.hp2 HG01256.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+2163delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76928880 | ||||||
| chr17:76928911 | G | T | 6 | a0001c0001t0004g0156 a0001c0001t0011g0065 a0001c0025t0014g0071 others(3): Show |
6 | HG02145.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291+2181G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928911 | |||||||
| chr17:76928920 | C | A | 2 | a0001c0025t0014g0071 a0002c0034t0014g0058 |
2 | HG02145.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1291+2190C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76928920 | |||||||
| chr17:76929038 | G | C | 88 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1291+2308G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929038 | |||||||
| chr17:76929045 | T | C | 1 | a0002c0017t0002g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1291+2315T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929045 | |||||||
| chr17:76929085 | T | C | 185 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(182): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1291+2355T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929085 | |||||||
| chr17:76929117 | C | T | 6 | a0001c0013t0001g0101 a0001c0024t0001g0141 a0001c0056t0008g0108 others(3): Show |
6 | HG01069.hp2 HG02897.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+2387C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929117 | |||||||
| chr17:76929222 | G | A | 88 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1291+2492G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929222 | |||||||
| chr17:76929251 | A | G | 88 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1291+2521A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929251 | |||||||
| chr17:76929277 | C | T | 1 | a0001c0007t0002g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1291+2547C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929277 | |||||||
| chr17:76929306 | G | C | 5 | a0001c0031t0001g0252 a0002c0020t0001g0008 a0002c0020t0001g0011 others(2): Show |
5 | HG02451.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+2576G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929306 | |||||||
| chr17:76929369 | C | G | 87 | a0001c0003t0001g0035 a0001c0003t0001g0042 a0001c0003t0001g0044 others(84): Show |
87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1291+2639C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929369 | |||||||
| chr17:76929370 | A | G | 1 | a0001c0003t0001g0017 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1291+2640A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929370 | |||||||
| chr17:76929439 | A | G | 116 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(113): Show |
116 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1291+2709A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929439 | |||||||
| chr17:76929638 | C | G | 1 | a0001c0003t0001g0187 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1291+2908C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929638 | |||||||
| chr17:76929669 | G | C | 48 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(45): Show |
48 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1291+2939G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929669 | |||||||
| chr17:76929692 | G | A | 1 | a0001c0030t0001g0272 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1292-2953G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929692 | |||||||
| chr17:76929778 | C | T | 130 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(127): Show |
130 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1292-2867C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929778 | |||||||
| chr17:76929789 | C | A | 4 | a0001c0001t0004g0156 a0001c0001t0011g0065 a0002c0002t0011g0199 others(1): Show |
4 | HG02258.hp2 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-2856C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929789 | |||||||
| chr17:76929798 | GC | G | 4 | a0001c0003t0001g0042 a0001c0003t0001g0135 a0001c0056t0008g0108 others(1): Show |
4 | HG01069.hp2 HG01516.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-2842delC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76929798 | ||||||
| chr17:76929842 | G | T | 1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-2803G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929842 | |||||||
| chr17:76929865 | T | C | 48 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(45): Show |
48 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1292-2780T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929865 | |||||||
| chr17:76929902 | C | T | 1 | a0002c0020t0001g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1292-2743C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929902 | |||||||
| chr17:76929968 | G | A | 48 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(45): Show |
48 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1292-2677G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76929968 | |||||||
| chr17:76930028 | C | G | 1 | a0002c0034t0014g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1292-2617C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930028 | |||||||
| chr17:76930030 | G | A | 1 | a0002c0012t0001g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1292-2615G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930030 | |||||||
| chr17:76930182 | C | T | 1 | a0002c0006t0008g0198 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1292-2463C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930182 | |||||||
| chr17:76930222 | T | C | 36 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(33): Show |
36 | HG00597.hp2 HG00673.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1292-2423T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930222 | |||||||
| chr17:76930346 | G | T | 35 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(32): Show |
35 | HG00597.hp2 HG00673.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.1292-2299G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930346 | |||||||
| chr17:76930386 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1292-2259G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930386 | |||||||
| chr17:76930408 | A | T | 36 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(33): Show |
36 | HG00597.hp2 HG00673.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1292-2237A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930408 | |||||||
| chr17:76930497 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1292-2148G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930497 | |||||||
| chr17:76930523 | C | T | 36 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(33): Show |
36 | HG00597.hp2 HG00673.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1292-2122C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930523 | |||||||
| chr17:76930570 | C | T | 15 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(12): Show |
15 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1292-2075C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930570 | |||||||
| chr17:76930587 | G | A | 4 | a0001c0001t0004g0156 a0001c0001t0011g0065 a0002c0002t0011g0199 others(1): Show |
4 | HG02258.hp2 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1292-2058G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930587 | |||||||
| chr17:76930620 | C | G | 191 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(188): Show |
192 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1292-2025C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930620 | |||||||
| chr17:76930690 | C | T | 5 | a0001c0031t0001g0252 a0002c0020t0001g0008 a0002c0020t0001g0011 others(2): Show |
5 | HG02451.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1292-1955C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930690 | |||||||
| chr17:76930746 | C | T | 70 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(67): Show |
71 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1292-1899C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930746 | |||||||
| chr17:76930828 | A | C | 226 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1292-1817A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930828 | |||||||
| chr17:76930848 | A | C | 1 | a0002c0043t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1292-1797A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930848 | |||||||
| chr17:76930922 | G | A | 17 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(14): Show |
17 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-1723G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76930922 | |||||||
| chr17:76931042 | G | A | 2 | a0001c0001t0006g0178 a0001c0001t0006g0248 |
2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1292-1603G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931042 | |||||||
| chr17:76931139 | C | A | 1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-1506C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931139 | |||||||
| chr17:76931140 | A | G | 1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-1505A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931140 | |||||||
| chr17:76931142 | G | C | 1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-1503G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931142 | |||||||
| chr17:76931157 | C | T | 23 | a0001c0005t0002g0019 a0001c0005t0003g0212 a0001c0005t0004g0126 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1292-1488C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931157 | |||||||
| chr17:76931197 | A | G | 1 | a0001c0001t0006g0175 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1292-1448A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931197 | |||||||
| chr17:76931207 | A | G | 23 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(20): Show |
23 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1292-1438A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931207 | |||||||
| chr17:76931258 | G | A | 4 | a0001c0010t0007g0140 a0001c0010t0007g0255 a0002c0015t0007g0268 others(1): Show |
4 | HG03710.hp1 HG03710.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-1387G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931258 | |||||||
| chr17:76931352 | C | G | 6 | a0001c0001t0004g0156 a0001c0001t0011g0065 a0001c0025t0014g0071 others(3): Show |
6 | HG02145.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1292-1293C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931352 | |||||||
| chr17:76931429 | T | G | 1 | a0003c0026t0002g0263 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1292-1216T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931429 | |||||||
| chr17:76931519 | A | T | 144 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(141): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1292-1126A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931519 | |||||||
| chr17:76931596 | G | A | 28 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(25): Show |
28 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1292-1049G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931596 | |||||||
| chr17:76931604 | A | G | 140 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1292-1041A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931604 | |||||||
| chr17:76931640 | CT | C | 61 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1292-1002delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76931640 | ||||||
| chr17:76931663 | G | A | 44 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1292-982G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931663 | |||||||
| chr17:76931696 | C | G | 60 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(57): Show |
60 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1292-949C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931696 | |||||||
| chr17:76931748 | G | A | 59 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(56): Show |
59 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1292-897G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931748 | |||||||
| chr17:76931790 | C | T | 2 | a0001c0001t0011g0065 a0002c0002t0011g0199 |
2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1292-855C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931790 | |||||||
| chr17:76931893 | T | C | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1292-752T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931893 | |||||||
| chr17:76931894 | C | T | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1292-751C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931894 | |||||||
| chr17:76931995 | G | C | 26 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.1292-650G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76931995 | |||||||
| chr17:76932052 | CTCCTCCT others(7): Show |
C | 1 | a0002c0014t0017g0004 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1292-582_1292-569d others(16): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76932052 | ||||||
| chr17:76932057 | C | CCTT | 18 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(15): Show |
18 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1292-586_1292-585i others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76932057 | ||||||
| chr17:76932060 | C | T | 64 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1292-585C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932060 | |||||||
| chr17:76932064 | T | C | 46 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1292-581T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932064 | |||||||
| chr17:76932068 | C | T | 46 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1292-577C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932068 | |||||||
| chr17:76932069 | C | T | 46 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1292-576C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932069 | |||||||
| chr17:76932085 | T | TC | 105 | a0001c0001t0003g0024 a0001c0001t0003g0192 a0001c0001t0003g0214 others(102): Show |
105 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1292-550dupC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76932085 | ||||||
| chr17:76932085 | T | TCC | 23 | a0001c0001t0002g0038 a0001c0001t0003g0036 a0001c0001t0003g0157 others(20): Show |
23 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1292-551_1292-550d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76932085 | ||||||
| chr17:76932085 | TC | T | 17 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(14): Show |
17 | HG00140.hp1 HG00408.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1292-550delC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76932085 | ||||||
| chr17:76932087 | C | CT | 46 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.1292-558_1292-557i others(3): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932087 | |||||||
| chr17:76932096 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-549T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932096 | |||||||
| chr17:76932098 | C | T | 1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-547C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932098 | |||||||
| chr17:76932099 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1292-546T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932099 | |||||||
| chr17:76932110 | C | G | 1 | a0002c0043t0001g0158 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1292-535C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932110 | |||||||
| chr17:76932123 | G | GTCTTCTC others(2): Show |
64 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(61): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1292-517_1292-509d others(11): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr17 | 76932123 | ||||||
| chr17:76932446 | A | C | 216 | a0001c0001t0002g0038 a0001c0001t0003g0024 a0001c0001t0003g0036 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1292-199A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932446 | |||||||
| chr17:76932463 | C | T | 1 | a0002c0038t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1292-182C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932463 | |||||||
| chr17:76932473 | G | A | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1292-172G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932473 | |||||||
| chr17:76932483 | A | G | 263 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1292-162A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932483 | |||||||
| chr17:76932551 | A | G | 2 | a0002c0006t0007g0069 a0002c0006t0007g0072 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1292-94A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 10/17 | chr17 | 76932551 | |||||||
| chr17:76932839 | C | T | 79 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(76): Show |
79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1422+64C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 11/17 | chr17 | 76932839 | |||||||
| chr17:76932849 | C | T | 143 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0006g0023 others(140): Show |
143 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1422+74C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 11/17 | chr17 | 76932849 | |||||||
| chr17:76932902 | C | T | 7 | a0001c0001t0003g0157 a0001c0001t0003g0192 a0001c0001t0003g0214 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1422+127C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 11/17 | chr17 | 76932902 | |||||||
| chr17:76933308 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1428+11C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933308 | |||||||
| chr17:76933332 | C | T | 1 | a0001c0003t0001g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1428+35C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933332 | |||||||
| chr17:76933360 | A | G | 145 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0004g0156 others(142): Show |
145 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.1428+63A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933360 | |||||||
| chr17:76933514 | T | C | 274 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(271): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1428+217T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933514 | |||||||
| chr17:76933728 | T | C | 144 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0006g0023 others(141): Show |
144 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1428+431T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933728 | |||||||
| chr17:76933802 | A | T | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1428+505A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933802 | |||||||
| chr17:76933805 | T | C | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1428+508T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933805 | |||||||
| chr17:76933824 | G | A | 30 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(27): Show |
30 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1428+527G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933824 | |||||||
| chr17:76933833 | T | G | 1 | a0001c0003t0029g0051 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1428+536T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933833 | |||||||
| chr17:76933839 | G | C | 1 | a0001c0005t0008g0264 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1428+542G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933839 | |||||||
| chr17:76933856 | C | G | 19 | a0001c0005t0002g0019 a0001c0005t0003g0212 a0001c0005t0004g0126 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1428+559C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933856 | |||||||
| chr17:76933916 | A | C | 174 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0004g0156 others(171): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1428+619A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933916 | |||||||
| chr17:76933917 | G | C | 4 | a0001c0025t0010g0047 a0001c0025t0010g0229 a0001c0025t0014g0071 others(1): Show |
4 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428+620G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76933917 | |||||||
| chr17:76934081 | G | C | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1428+784G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934081 | |||||||
| chr17:76934082 | C | G | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1428+785C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934082 | |||||||
| chr17:76934098 | A | G | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1428+801A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934098 | |||||||
| chr17:76934133 | G | C | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1428+836G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934133 | |||||||
| chr17:76934144 | A | G | 144 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0006g0023 others(141): Show |
144 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1428+847A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934144 | |||||||
| chr17:76934167 | C | T | 1 | a0002c0006t0007g0110 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1428+870C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934167 | |||||||
| chr17:76934284 | T | C | 174 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0004g0156 others(171): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1428+987T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934284 | |||||||
| chr17:76934338 | G | A | 4 | a0001c0025t0010g0047 a0001c0025t0010g0229 a0001c0025t0014g0071 others(1): Show |
4 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428+1041G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934338 | |||||||
| chr17:76934413 | C | T | 1 | a0002c0019t0004g0242 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1428+1116C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934413 | |||||||
| chr17:76934493 | A | G | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1428+1196A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934493 | |||||||
| chr17:76934546 | C | T | 1 | a0002c0002t0005g0039 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1428+1249C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934546 | |||||||
| chr17:76934592 | T | C | 174 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0004g0156 others(171): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1428+1295T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934592 | |||||||
| chr17:76934619 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1428+1322G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934619 | |||||||
| chr17:76934656 | G | C | 1 | a0002c0002t0003g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1428+1359G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934656 | |||||||
| chr17:76934711 | C | G | 115 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(112): Show |
115 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1428+1414C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934711 | |||||||
| chr17:76934712 | G | A | 1 | a0002c0002t0003g0084 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1428+1415G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934712 | |||||||
| chr17:76934809 | C | T | 222 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0004g0156 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1428+1512C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934809 | |||||||
| chr17:76934825 | A | G | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1428+1528A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934825 | |||||||
| chr17:76934832 | G | A | 1 | a0001c0018t0004g0020 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1428+1535G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934832 | |||||||
| chr17:76934847 | A | G | 1 | a0001c0001t0007g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1428+1550A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934847 | |||||||
| chr17:76934857 | A | T | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1428+1560A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934857 | |||||||
| chr17:76934863 | A | T | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1428+1566A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934863 | |||||||
| chr17:76934925 | G | A | 1 | a0004c0035t0004g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1428+1628G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76934925 | |||||||
| chr17:76935006 | G | T | 1 | a0002c0002t0020g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1428+1709G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935006 | |||||||
| chr17:76935007 | G | T | 78 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(75): Show |
78 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1428+1710G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935007 | |||||||
| chr17:76935223 | T | C | 8 | a0001c0030t0001g0154 a0001c0049t0010g0067 a0002c0012t0001g0012 others(5): Show |
8 | HG00639.hp2 HG02818.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1428+1926T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935223 | |||||||
| chr17:76935311 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1428+2014G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935311 | |||||||
| chr17:76935385 | A | C | 112 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(109): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1428+2088A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935385 | |||||||
| chr17:76935405 | G | A | 1 | a0002c0004t0001g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1428+2108G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935405 | |||||||
| chr17:76935420 | T | G | 3 | a0002c0020t0001g0008 a0002c0020t0001g0011 a0002c0020t0022g0153 |
3 | HG02976.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1428+2123T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935420 | |||||||
| chr17:76935425 | T | A | 1 | a0002c0015t0003g0109 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1428+2128T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935425 | |||||||
| chr17:76935429 | A | AAGGTG | 134 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(131): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1428+2132_1428+213 others(9): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935429 | |||||||
| chr17:76935431 | T | G | 2 | a0001c0013t0001g0250 a0002c0015t0003g0109 |
2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1428+2134T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935431 | |||||||
| chr17:76935432 | T | C | 134 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(131): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1428+2135T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935432 | |||||||
| chr17:76935432 | T | TGGTCATG others(22): Show |
2 | a0001c0013t0001g0250 a0002c0015t0003g0109 |
2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1428+2135_1428+213 others(33): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935432 | |||||||
| chr17:76935434 | T | TGCCATTT others(19): Show |
134 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(131): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1428+2137_1428+213 others(30): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935434 | |||||||
| chr17:76935544 | A | G | 174 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0004g0156 others(171): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1428+2247A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935544 | |||||||
| chr17:76935605 | C | CT | 26 | a0001c0001t0006g0023 a0001c0001t0006g0034 a0001c0001t0006g0049 others(23): Show |
26 | HG00140.hp1 HG00438.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1428+2325dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935605 | ||||||
| chr17:76935605 | C | CTT | 99 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(96): Show |
99 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1428+2324_1428+232 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935605 | ||||||
| chr17:76935605 | CT | C | 7 | a0001c0011t0002g0223 a0002c0002t0003g0009 a0002c0006t0007g0069 others(4): Show |
7 | HG01069.hp1 HG01975.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1428+2325delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935605 | ||||||
| chr17:76935687 | G | A | 13 | a0001c0001t0008g0107 a0001c0005t0008g0264 a0001c0013t0001g0101 others(10): Show |
13 | HG01069.hp2 HG01106.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1429-2301G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935687 | |||||||
| chr17:76935841 | C | CATTATAT others(15): Show |
1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1429-2138_1429-213 others(26): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935841 | ||||||
| chr17:76935843 | TTATATAT others(4): Show |
T | 2 | a0001c0003t0013g0249 a0001c0003t0013g0251 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1429-2137_1429-212 others(15): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935843 | ||||||
| chr17:76935850 | TAC | T | 81 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(78): Show |
81 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1429-2137_1429-213 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935850 | |||||||
| chr17:76935850 | TACTA | T | 90 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0005g0021 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1429-2137_1429-213 others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935850 | |||||||
| chr17:76935858 | AT | A | 81 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(78): Show |
81 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1429-2129delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935858 | |||||||
| chr17:76935861 | T | TTATATAC others(28): Show |
1 | a0001c0011t0002g0276 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1429-2084_1429-205 others(39): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935861 | ||||||
| chr17:76935861 | TTATATAC others(28): Show |
T | 1 | a0001c0001t0003g0214 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1429-2084_1429-205 others(39): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935861 | ||||||
| chr17:76935867 | AC | A | 92 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0005g0021 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1429-2120delC | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935867 | |||||||
| chr17:76935868 | C | T | 81 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(78): Show |
81 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1429-2120C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935868 | |||||||
| chr17:76935870 | T | C | 80 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(77): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1429-2118T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935870 | |||||||
| chr17:76935870 | TTATATAT others(19): Show |
T | 1 | a0003c0027t0001g0234 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1429-2111_1429-208 others(30): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935870 | ||||||
| chr17:76935879 | T | C | 92 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0005g0021 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1429-2109T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935879 | |||||||
| chr17:76935879 | TTATATAT others(10): Show |
T | 80 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(77): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1429-2102_1429-208 others(21): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935879 | ||||||
| chr17:76935886 | TTATATA | T | 90 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0005g0021 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1429-2101_1429-209 others(10): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935886 | |||||||
| chr17:76935886 | TTATATAA others(3): Show |
T | 2 | a0001c0003t0013g0249 a0001c0003t0013g0251 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1429-2095_1429-208 others(14): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935886 | ||||||
| chr17:76935894 | TTA | T | 90 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0001t0005g0021 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1429-2087_1429-208 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935894 | ||||||
| chr17:76935896 | A | ATATATAC others(9): Show |
1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1429-2085_1429-208 others(20): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935896 | ||||||
| chr17:76935897 | T | A | 2 | a0001c0003t0013g0249 a0001c0003t0013g0251 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1429-2091T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935897 | |||||||
| chr17:76935917 | T | C | 2 | a0001c0003t0001g0035 a0001c0003t0001g0042 |
2 | HG01516.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1429-2071T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76935917 | |||||||
| chr17:76935954 | T | TTA | 3 | a0001c0008t0001g0030 a0001c0053t0001g0032 a0002c0017t0002g0273 |
3 | HG01123.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1429-2020_1429-201 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76935954 | ||||||
| chr17:76936091 | C | T | 23 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1429-1897C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936091 | |||||||
| chr17:76936136 | G | A | 1 | a0001c0056t0008g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1429-1852G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936136 | |||||||
| chr17:76936244 | T | C | 1 | a0002c0015t0005g0080 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1429-1744T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936244 | |||||||
| chr17:76936284 | C | G | 83 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-1704C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936284 | |||||||
| chr17:76936284 | C | T | 18 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(15): Show |
18 | HG00140.hp1 HG00438.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1429-1704C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936284 | |||||||
| chr17:76936386 | C | A | 1 | a0001c0001t0003g0157 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1429-1602C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936386 | |||||||
| chr17:76936422 | A | G | 3 | a0002c0002t0003g0084 a0002c0002t0020g0087 a0002c0009t0001g0236 |
3 | HG01256.hp2 HG01261.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1429-1566A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936422 | |||||||
| chr17:76936502 | T | G | 1 | a0001c0048t0003g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1429-1486T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936502 | |||||||
| chr17:76936545 | C | T | 6 | a0001c0025t0010g0047 a0001c0025t0010g0229 a0001c0025t0014g0071 others(3): Show |
6 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1429-1443C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936545 | |||||||
| chr17:76936547 | T | C | 1 | a0006c0059t0007g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1429-1441T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936547 | |||||||
| chr17:76936674 | T | A | 83 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-1314T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936674 | |||||||
| chr17:76936687 | C | T | 83 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-1301C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936687 | |||||||
| chr17:76936822 | C | T | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1429-1166C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936822 | |||||||
| chr17:76936825 | A | G | 83 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-1163A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936825 | |||||||
| chr17:76936852 | G | T | 146 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(143): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1429-1136G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936852 | |||||||
| chr17:76936910 | G | A | 1 | a0002c0009t0001g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1429-1078G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76936910 | |||||||
| chr17:76937004 | G | GT | 35 | a0001c0001t0006g0025 a0001c0001t0006g0049 a0001c0001t0006g0096 others(32): Show |
35 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1429-969dupT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76937004 | ||||||
| chr17:76937004 | GT | G | 107 | a0001c0001t0006g0270 a0001c0003t0001g0017 a0001c0003t0001g0035 others(104): Show |
108 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1429-969delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76937004 | ||||||
| chr17:76937004 | GTT | G | 11 | a0001c0001t0008g0107 a0001c0003t0013g0249 a0001c0003t0013g0251 others(8): Show |
11 | HG01069.hp2 HG01106.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.1429-970_1429-969d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr17 | 76937004 | ||||||
| chr17:76937079 | A | G | 26 | a0001c0001t0002g0038 a0001c0001t0003g0221 a0001c0008t0001g0022 others(23): Show |
26 | HG00673.hp2 HG01123.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.1429-909A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937079 | |||||||
| chr17:76937117 | A | G | 83 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-871A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937117 | |||||||
| chr17:76937141 | G | A | 1 | a0001c0001t0012g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1429-847G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937141 | |||||||
| chr17:76937176 | T | C | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1429-812T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937176 | |||||||
| chr17:76937177 | G | A | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1429-811G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937177 | |||||||
| chr17:76937292 | G | A | 83 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-696G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937292 | |||||||
| chr17:76937341 | A | G | 83 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(80): Show |
83 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1429-647A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937341 | |||||||
| chr17:76937480 | C | T | 1 | a0001c0001t0008g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1429-508C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937480 | |||||||
| chr17:76937528 | T | C | 1 | a0001c0018t0004g0226 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1429-460T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937528 | |||||||
| chr17:76937762 | A | G | 19 | a0001c0005t0002g0019 a0001c0005t0003g0212 a0001c0005t0004g0126 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1429-226A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 12/17 | chr17 | 76937762 | |||||||
| chr17:76938161 | G | A | 5 | a0001c0001t0011g0065 a0002c0002t0011g0199 a0002c0020t0001g0008 others(2): Show |
5 | HG02809.hp2 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+18G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938161 | |||||||
| chr17:76938454 | C | T | 19 | a0001c0005t0002g0019 a0001c0005t0003g0212 a0001c0005t0004g0126 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1584+311C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938454 | |||||||
| chr17:76938568 | G | T | 85 | a0001c0001t0011g0065 a0001c0003t0001g0017 a0001c0003t0001g0035 others(82): Show |
85 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1584+425G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938568 | |||||||
| chr17:76938578 | C | T | 1 | a0002c0002t0003g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1584+435C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938578 | |||||||
| chr17:76938617 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1584+474C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938617 | |||||||
| chr17:76938799 | C | T | 1 | a0002c0009t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1584+656C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938799 | |||||||
| chr17:76938869 | G | A | 1 | a0001c0031t0001g0245 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1584+726G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938869 | |||||||
| chr17:76938919 | T | C | 271 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1584+776T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938919 | |||||||
| chr17:76938984 | C | G | 1 | a0001c0007t0018g0176 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1584+841C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76938984 | |||||||
| chr17:76939025 | T | TG | 10 | a0001c0003t0023g0040 a0001c0010t0003g0217 a0001c0010t0003g0218 others(7): Show |
10 | HG00639.hp2 HG01074.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.1584+887dupG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939025 | ||||||
| chr17:76939025 | T | TGGG | 26 | a0001c0003t0001g0187 a0001c0003t0001g0204 a0001c0003t0001g0206 others(23): Show |
26 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.1584+885_1584+887d others(5): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939025 | ||||||
| chr17:76939027 | GGGGT | G | 7 | a0001c0001t0003g0221 a0001c0005t0009g0162 a0001c0005t0009g0163 others(4): Show |
8 | HG02109.hp1 HG02965.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.1584+886_1584+889d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939027 | ||||||
| chr17:76939029 | G | GGGGT | 7 | a0001c0001t0005g0021 a0001c0024t0001g0026 a0001c0047t0001g0015 others(4): Show |
7 | HG01074.hp1 HG02738.hp1 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.1584+887_1584+888i others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939029 | ||||||
| chr17:76939029 | G | GGGGTGT | 8 | a0001c0001t0005g0041 a0001c0001t0005g0053 a0001c0001t0005g0210 others(5): Show |
8 | HG00099.hp1 HG00621.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+887_1584+888i others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939029 | ||||||
| chr17:76939029 | G | GGT | 24 | a0001c0001t0008g0107 a0001c0007t0002g0127 a0001c0007t0002g0201 others(21): Show |
24 | HG00408.hp1 HG00673.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.1584+931_1584+932d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939029 | ||||||
| chr17:76939029 | G | GGTGT | 10 | a0001c0001t0005g0043 a0001c0001t0027g0220 a0001c0005t0002g0019 others(7): Show |
10 | HG01106.hp2 HG01109.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1584+929_1584+932d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939029 | ||||||
| chr17:76939029 | G | GGTGTGT | 5 | a0001c0001t0003g0157 a0001c0001t0012g0014 a0001c0001t0012g0016 others(2): Show |
5 | HG00642.hp1 HG01175.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+927_1584+932d others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939029 | ||||||
| chr17:76939029 | G | T | 21 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(18): Show |
21 | HG00140.hp1 HG00438.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1584+886G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939029 | |||||||
| chr17:76939029 | GGT | G | 29 | a0001c0005t0002g0235 a0001c0005t0003g0212 a0001c0005t0007g0045 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.1584+931_1584+932d others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939029 | ||||||
| chr17:76939029 | GGTGT | G | 46 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(43): Show |
46 | HG00280.hp2 HG00438.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1584+929_1584+932d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939029 | ||||||
| chr17:76939030 | GT | G | 9 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(6): Show |
9 | HG00741.hp1 HG01081.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1584+888delT | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939030 | |||||||
| chr17:76939031 | T | G | 11 | a0001c0003t0001g0254 a0001c0003t0023g0040 a0001c0030t0001g0154 others(8): Show |
11 | HG00639.hp2 HG01074.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1584+888T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939031 | |||||||
| chr17:76939033 | T | G | 6 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(3): Show |
6 | HG01081.hp2 HG01256.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1584+890T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939033 | |||||||
| chr17:76939039 | T | G | 1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1584+896T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939039 | |||||||
| chr17:76939041 | T | G | 1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1584+898T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939041 | |||||||
| chr17:76939058 | G | GTA | 3 | a0002c0020t0001g0008 a0002c0020t0001g0011 a0002c0020t0022g0153 |
3 | HG02976.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1584+916_1584+917i others(4): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939058 | ||||||
| chr17:76939125 | C | T | 1 | a0001c0011t0002g0186 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1584+982C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939125 | |||||||
| chr17:76939383 | G | A | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1585-1019G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939383 | |||||||
| chr17:76939487 | C | T | 119 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(116): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1585-915C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939487 | |||||||
| chr17:76939512 | C | CAAAA | 123 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(120): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1585-889_1585-886d others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr17 | 76939512 | ||||||
| chr17:76939599 | T | G | 189 | a0001c0001t0002g0205 a0001c0001t0002g0209 a0001c0001t0004g0156 others(186): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1585-803T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939599 | |||||||
| chr17:76939663 | T | G | 47 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(44): Show |
47 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1585-739T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939663 | |||||||
| chr17:76939681 | C | T | 51 | a0001c0001t0004g0160 a0001c0001t0007g0233 a0001c0001t0031g0256 others(48): Show |
52 | HG00280.hp2 HG00673.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1585-721C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939681 | |||||||
| chr17:76939686 | T | C | 122 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(119): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1585-716T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939686 | |||||||
| chr17:76939687 | G | C | 1 | a0001c0013t0001g0250 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1585-715G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939687 | |||||||
| chr17:76939697 | A | C | 1 | a0001c0055t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1585-705A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939697 | |||||||
| chr17:76939705 | G | C | 27 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(24): Show |
27 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1585-697G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939705 | |||||||
| chr17:76939856 | T | TC | 150 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1585-546_1585-545i others(3): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939856 | |||||||
| chr17:76939886 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1585-516T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939886 | |||||||
| chr17:76939980 | T | C | 3 | a0001c0001t0011g0065 a0002c0002t0011g0057 a0002c0002t0011g0199 |
3 | HG02809.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1585-422T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76939980 | |||||||
| chr17:76940074 | G | T | 7 | a0001c0003t0001g0243 a0001c0013t0001g0131 a0001c0013t0001g0152 others(4): Show |
7 | HG01109.hp2 HG01928.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.1585-328G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76940074 | |||||||
| chr17:76940280 | C | T | 2 | a0002c0020t0001g0008 a0002c0020t0001g0011 |
2 | HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1585-122C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76940280 | |||||||
| chr17:76940347 | T | C | 30 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(27): Show |
30 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1585-55T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76940347 | |||||||
| chr17:76940385 | G | A | 2 | a0002c0002t0004g0240 a0002c0028t0004g0061 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1585-17G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 13/17 | chr17 | 76940385 | |||||||
| chr17:76940574 | G | A | 3 | a0001c0003t0013g0249 a0001c0003t0013g0251 a0001c0024t0001g0026 |
3 | HG01516.hp2 HG01517.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1731+26G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 14/17 | chr17 | 76940574 | |||||||
| chr17:76940587 | C | A | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1731+39C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 14/17 | chr17 | 76940587 | |||||||
| chr17:76940699 | G | A | 1 | a0001c0008t0001g0230 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1732-33G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 14/17 | chr17 | 76940699 | |||||||
| chr17:76940938 | A | C | 15 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(12): Show |
15 | HG00140.hp1 HG00738.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1848+90A>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76940938 | |||||||
| chr17:76940984 | C | G | 82 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(79): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1848+136C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76940984 | |||||||
| chr17:76941212 | G | C | 4 | a0001c0003t0001g0044 a0001c0003t0001g0151 a0001c0047t0001g0015 others(1): Show |
4 | HG00741.hp1 HG01358.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+364G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76941212 | |||||||
| chr17:76941316 | C | T | 82 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(79): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1848+468C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76941316 | |||||||
| chr17:76941695 | T | C | 140 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1848+847T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76941695 | |||||||
| chr17:76941999 | A | G | 138 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1848+1151A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76941999 | |||||||
| chr17:76942015 | C | T | 105 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(102): Show |
105 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1848+1167C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942015 | |||||||
| chr17:76942240 | A | G | 1 | a0002c0020t0022g0153 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1848+1392A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942240 | |||||||
| chr17:76942256 | A | G | 105 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(102): Show |
105 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1848+1408A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942256 | |||||||
| chr17:76942300 | G | A | 1 | a0002c0029t0001g0146 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1848+1452G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942300 | |||||||
| chr17:76942406 | G | A | 90 | a0001c0001t0004g0156 a0001c0003t0001g0017 a0001c0003t0001g0035 others(87): Show |
90 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1848+1558G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942406 | |||||||
| chr17:76942533 | A | T | 105 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(102): Show |
105 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1848+1685A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942533 | |||||||
| chr17:76942626 | G | T | 2 | a0002c0002t0003g0084 a0002c0002t0020g0087 |
2 | HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1848+1778G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942626 | |||||||
| chr17:76942651 | G | A | 90 | a0001c0001t0004g0156 a0001c0003t0001g0017 a0001c0003t0001g0035 others(87): Show |
90 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1848+1803G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942651 | |||||||
| chr17:76942655 | C | A | 1 | a0001c0008t0001g0277 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1848+1807C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942655 | |||||||
| chr17:76942699 | G | T | 1 | a0002c0009t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1848+1851G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942699 | |||||||
| chr17:76942751 | G | A | 33 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(30): Show |
33 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1848+1903G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942751 | |||||||
| chr17:76942858 | C | T | 1 | a0002c0002t0025g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1848+2010C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942858 | |||||||
| chr17:76942889 | T | C | 104 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(101): Show |
104 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1848+2041T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942889 | |||||||
| chr17:76942978 | C | T | 33 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(30): Show |
33 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1848+2130C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76942978 | |||||||
| chr17:76943037 | C | CCCCCA | 82 | a0001c0001t0004g0156 a0001c0003t0001g0017 a0001c0003t0001g0035 others(79): Show |
82 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1848+2193_1848+219 others(9): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr17 | 76943037 | ||||||
| chr17:76943037 | C | CCCCG | 14 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(11): Show |
14 | HG00140.hp1 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1848+2192_1848+219 others(8): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr17 | 76943037 | ||||||
| chr17:76943042 | G | C | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1848+2194G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943042 | |||||||
| chr17:76943089 | G | A | 81 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(78): Show |
81 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1848+2241G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943089 | |||||||
| chr17:76943093 | C | G | 136 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(133): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1848+2245C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943093 | |||||||
| chr17:76943107 | A | G | 104 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(101): Show |
104 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1848+2259A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943107 | |||||||
| chr17:76943146 | A | G | 15 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(12): Show |
15 | HG00140.hp1 HG00738.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1848+2298A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943146 | |||||||
| chr17:76943162 | G | A | 1 | a0002c0014t0001g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1848+2314G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943162 | |||||||
| chr17:76943198 | T | A | 1 | a0001c0003t0013g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1848+2350T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943198 | |||||||
| chr17:76943199 | G | GAT | 103 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(100): Show |
103 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1848+2351_1848+235 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943199 | |||||||
| chr17:76943199 | G | T | 1 | a0001c0003t0013g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1848+2351G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943199 | |||||||
| chr17:76943200 | G | T | 104 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(101): Show |
104 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1848+2352G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943200 | |||||||
| chr17:76943212 | A | G | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1848+2364A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943212 | |||||||
| chr17:76943331 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0027g0220 a0002c0015t0005g0080 |
3 | HG01081.hp2 HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1848+2483G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943331 | |||||||
| chr17:76943580 | T | A | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1848+2732T>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943580 | |||||||
| chr17:76943592 | T | C | 7 | a0001c0001t0004g0156 a0001c0025t0010g0047 a0001c0025t0010g0229 others(4): Show |
7 | HG01255.hp2 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1848+2744T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943592 | |||||||
| chr17:76943623 | T | TTG | 11 | a0001c0001t0008g0107 a0001c0001t0011g0065 a0001c0005t0008g0264 others(8): Show |
11 | HG01069.hp2 HG01106.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1849-2753_1849-275 others(6): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943623 | |||||||
| chr17:76943624 | G | T | 24 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.1849-2752G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943624 | |||||||
| chr17:76943627 | G | GGGT | 102 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(99): Show |
102 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1849-2747_1849-274 others(7): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr17 | 76943627 | ||||||
| chr17:76943692 | C | T | 5 | a0001c0001t0011g0065 a0002c0002t0011g0057 a0002c0002t0011g0199 others(2): Show |
5 | HG02809.hp2 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849-2684C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943692 | |||||||
| chr17:76943831 | G | A | 1 | a0002c0004t0001g0114 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1849-2545G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943831 | |||||||
| chr17:76943942 | C | T | 1 | a0001c0008t0001g0030 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1849-2434C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943942 | |||||||
| chr17:76943945 | G | A | 1 | a0002c0002t0028g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1849-2431G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76943945 | |||||||
| chr17:76944021 | A | G | 145 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(142): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1849-2355A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944021 | |||||||
| chr17:76944108 | C | T | 1 | a0001c0001t0006g0248 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1849-2268C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944108 | |||||||
| chr17:76944230 | G | A | 114 | a0001c0001t0011g0065 a0001c0003t0001g0017 a0001c0003t0001g0035 others(111): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1849-2146G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944230 | |||||||
| chr17:76944242 | A | ATGT | 5 | a0001c0013t0001g0101 a0001c0024t0001g0141 a0002c0020t0001g0161 others(2): Show |
5 | HG02451.hp1 HG02897.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1849-2134_1849-213 others(7): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944242 | |||||||
| chr17:76944249 | C | CGTT | 141 | a0001c0001t0004g0156 a0001c0001t0006g0023 a0001c0001t0006g0025 others(138): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1849-2125_1849-212 others(7): Show |
MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr17 | 76944249 | ||||||
| chr17:76944249 | C | T | 8 | a0001c0003t0001g0181 a0001c0013t0001g0101 a0001c0024t0001g0141 others(5): Show |
8 | HG00621.hp2 HG02083.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1849-2127C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944249 | |||||||
| chr17:76944255 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1849-2121C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944255 | |||||||
| chr17:76944350 | T | C | 14 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(11): Show |
14 | HG00140.hp1 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1849-2026T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944350 | |||||||
| chr17:76944409 | T | C | 5 | a0001c0031t0001g0252 a0002c0014t0017g0004 a0002c0020t0001g0008 others(2): Show |
5 | HG02965.hp2 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1849-1967T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944409 | |||||||
| chr17:76944426 | G | A | 1 | a0001c0001t0007g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1849-1950G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944426 | |||||||
| chr17:76944437 | G | A | 14 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(11): Show |
14 | HG00140.hp1 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1849-1939G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944437 | |||||||
| chr17:76944560 | A | G | 1 | a0001c0055t0007g0073 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1849-1816A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944560 | |||||||
| chr17:76944572 | C | T | 1 | a0002c0014t0001g0172 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1849-1804C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944572 | |||||||
| chr17:76944573 | A | G | 31 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(28): Show |
31 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1849-1803A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944573 | |||||||
| chr17:76944613 | A | G | 1 | a0001c0056t0008g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1849-1763A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944613 | |||||||
| chr17:76944633 | G | A | 1 | a0002c0002t0006g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1849-1743G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944633 | |||||||
| chr17:76944654 | C | T | 1 | a0001c0056t0008g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1849-1722C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944654 | |||||||
| chr17:76944702 | A | G | 114 | a0001c0001t0011g0065 a0001c0003t0001g0017 a0001c0003t0001g0035 others(111): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1849-1674A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944702 | |||||||
| chr17:76944775 | A | G | 31 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(28): Show |
31 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1849-1601A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944775 | |||||||
| chr17:76944779 | G | A | 14 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(11): Show |
14 | HG00140.hp1 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1849-1597G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944779 | |||||||
| chr17:76944800 | G | T | 1 | a0001c0001t0003g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1849-1576G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944800 | |||||||
| chr17:76944818 | G | A | 179 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1849-1558G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944818 | |||||||
| chr17:76944996 | G | A | 114 | a0001c0001t0011g0065 a0001c0003t0001g0017 a0001c0003t0001g0035 others(111): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1849-1380G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76944996 | |||||||
| chr17:76945036 | C | T | 2 | a0001c0011t0002g0276 a0002c0020t0022g0153 |
2 | NA18522.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1849-1340C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945036 | |||||||
| chr17:76945088 | T | C | 1 | a0001c0024t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1849-1288T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945088 | |||||||
| chr17:76945178 | AG | A | 30 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(27): Show |
30 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1849-1197delG | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945178 | |||||||
| chr17:76945490 | C | T | 114 | a0001c0001t0011g0065 a0001c0003t0001g0017 a0001c0003t0001g0035 others(111): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1849-886C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945490 | |||||||
| chr17:76945532 | G | A | 20 | a0001c0001t0004g0156 a0001c0005t0004g0126 a0001c0018t0004g0020 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1849-844G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945532 | |||||||
| chr17:76945588 | T | C | 181 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1849-788T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945588 | |||||||
| chr17:76945644 | G | T | 105 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(102): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1849-732G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945644 | |||||||
| chr17:76945754 | G | C | 14 | a0001c0001t0006g0023 a0001c0001t0006g0025 a0001c0001t0006g0034 others(11): Show |
14 | HG00140.hp1 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1849-622G>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945754 | |||||||
| chr17:76945878 | G | A | 1 | a0001c0013t0001g0250 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1849-498G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76945878 | |||||||
| chr17:76946073 | T | G | 180 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1849-303T>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76946073 | |||||||
| chr17:76946082 | C | G | 180 | a0001c0001t0004g0156 a0001c0001t0005g0021 a0001c0001t0005g0041 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1849-294C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76946082 | |||||||
| chr17:76946086 | G | T | 1 | a0001c0001t0003g0024 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1849-290G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76946086 | |||||||
| chr17:76946178 | C | T | 19 | a0001c0005t0004g0126 a0001c0018t0004g0020 a0001c0018t0004g0037 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1849-198C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76946178 | |||||||
| chr17:76946208 | G | A | 1 | a0001c0048t0003g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1849-168G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 15/17 | chr17 | 76946208 | |||||||
| chr17:76946529 | G | T | 7 | a0001c0005t0004g0126 a0001c0018t0004g0037 a0001c0018t0004g0190 others(4): Show |
7 | HG00140.hp2 HG00642.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1923+79G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76946529 | |||||||
| chr17:76946608 | G | A | 1 | a0001c0008t0001g0277 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1923+158G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76946608 | |||||||
| chr17:76946727 | G | A | 114 | a0001c0001t0011g0065 a0001c0003t0001g0017 a0001c0003t0001g0035 others(111): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1923+277G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76946727 | |||||||
| chr17:76946924 | G | T | 32 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1923+474G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76946924 | |||||||
| chr17:76946925 | A | T | 32 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1923+475A>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76946925 | |||||||
| chr17:76946938 | G | A | 2 | a0001c0005t0002g0019 a0001c0011t0002g0033 |
2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1923+488G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76946938 | |||||||
| chr17:76947030 | G | T | 1 | a0002c0004t0001g0052 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1923+580G>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947030 | |||||||
| chr17:76947103 | G | A | 171 | a0001c0001t0004g0156 a0001c0001t0004g0160 a0001c0001t0006g0023 others(168): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1923+653G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947103 | |||||||
| chr17:76947243 | A | G | 44 | a0001c0001t0004g0156 a0001c0001t0004g0160 a0001c0001t0007g0233 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1924-587A>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947243 | |||||||
| chr17:76947320 | T | C | 205 | a0001c0001t0004g0156 a0001c0001t0004g0160 a0001c0001t0005g0021 others(202): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1924-510T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947320 | |||||||
| chr17:76947326 | C | T | 1 | a0001c0003t0001g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1924-504C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947326 | |||||||
| chr17:76947364 | C | T | 105 | a0001c0003t0001g0017 a0001c0003t0001g0035 a0001c0003t0001g0042 others(102): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1924-466C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947364 | |||||||
| chr17:76947405 | C | T | 1 | a0001c0001t0007g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1924-425C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947405 | |||||||
| chr17:76947476 | T | C | 114 | a0001c0001t0011g0065 a0001c0003t0001g0017 a0001c0003t0001g0035 others(111): Show |
114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1924-354T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947476 | |||||||
| chr17:76947530 | C | T | 1 | a0002c0002t0005g0086 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1924-300C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947530 | |||||||
| chr17:76947610 | C | T | 1 | a0001c0007t0002g0127 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1924-220C>T | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947610 | |||||||
| chr17:76947618 | G | A | 44 | a0001c0001t0004g0156 a0001c0001t0004g0160 a0001c0001t0007g0233 others(41): Show |
45 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1924-212G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947618 | |||||||
| chr17:76947650 | G | A | 2 | a0002c0012t0001g0145 a0002c0012t0001g0147 |
2 | HG02818.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1924-180G>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 16/17 | chr17 | 76947650 | |||||||
| chr17:76948343 | C | A | 1 | a0001c0003t0013g0249 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2180+257C>A | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 17/17 | chr17 | 76948343 | |||||||
| chr17:76948503 | T | C | 100 | a0001c0001t0004g0156 a0001c0001t0004g0160 a0001c0001t0005g0021 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.2181-137T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 17/17 | chr17 | 76948503 | |||||||
| chr17:76948627 | T | C | 244 | a0001c0001t0002g0038 a0001c0001t0002g0205 a0001c0001t0002g0209 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.2181-13T>C | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 17/17 | chr17 | 76948627 | |||||||
| chr17:76948632 | C | G | 32 | a0001c0001t0005g0021 a0001c0001t0005g0041 a0001c0001t0005g0043 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(29): Show |
splice_region_variant&intron_variant | LOW | c.2181-8C>G | MGAT5B | ENSG00000167889.13 | transcript | ENST00000569840.7 | protein_coding | 17/17 | chr17 | 76948632 |