Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 116255 |
| ensemblid | ENSG00000124003.13 |
| hgncid | 18210 |
| symbol | MOGAT1 |
| name | monoacylglycerol O-acyltransferase 1 |
| refseq_nuc | NM_058165.3 |
| refseq_prot | NP_477513.2 |
| ensembl_nuc | ENST00000446656.4 |
| ensembl_prot | ENSP00000406674.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 222671658 |
| end | 222709930 |
| strand | + |
| ver | v1.2 |
| region | chr2:222671658-222709930 |
| region5000 | chr2:222666658-222714930 |
| regionname0 | MOGAT1_chr2_222671658_222709930 |
| regionname5000 | MOGAT1_chr2_222666658_222714930 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 335 | 218 | 49 | 36 | 99 | 11 | 23 | 75 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0002 | 0/0 | 335 | 60 | 28 | 14 | 12 | 1 | 5 | 9 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0003 | 0/0 | 335 | 14 | 9 | 3 | 1 | 0 | 1 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0004 | 0/0 | 335 | 8 | 1 | 3 | 0 | 0 | 4 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0005 | 0/0 | 335 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0006 | 0/0 | 335 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0007 | 0/0 | 158 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(153): Show |
chr2 | 222666658 | 222714930 |
| a0008 | 0/0 | 294 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(289): Show |
chr2 | 222666658 | 222714930 |
| a0009 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0010 | 0/0 | 335 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0011 | 0/0 | 335 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0012 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(330): Show |
chr2 | 222666658 | 222714930 |
| a0013 | 0/0 | 123 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | MKVEF others(118): Show |
chr2 | 222666658 | 222714930 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1005 | 217 | 49 | 36 | 99 | 11 | 22 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0001c0014 | 0/0 | 1005 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0002c0002 | 0/0 | 1005 | 60 | 28 | 14 | 12 | 1 | 5 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0003c0003 | 0/0 | 1005 | 14 | 9 | 3 | 1 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0004c0004 | 0/0 | 1005 | 8 | 1 | 3 | 0 | 0 | 4 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0005c0005 | 0/0 | 1005 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0006c0006 | 0/0 | 1005 | 3 | 2 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0007c0007 | 0/0 | 1013 | 3 | 0 | 0 | 3 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1008): Show |
chr2 | 222666658 | 222714930 | ||
| a0008c0012 | 0/0 | 1004 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(999): Show |
chr2 | 222666658 | 222714930 | ||
| a0009c0015 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0010c0010 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0011c0008 | 0/0 | 1005 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0012c0013 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(1000): Show |
chr2 | 222666658 | 222714930 | ||
| a0013c0009 | 0/0 | 1003 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | ATGAA others(998): Show |
chr2 | 222666658 | 222714930 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1176 | 198 | 38 | 33 | 97 | 11 | 19 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0001c0001t0002 | 0/0 | 1176 | 17 | 9 | 3 | 2 | 0 | 3 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0001c0001t0003 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0001c0001t0004 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0001c0014t0001 | 0/0 | 1176 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0002c0002t0001 | 0/0 | 1176 | 47 | 20 | 9 | 12 | 1 | 5 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0002c0002t0002 | 0/0 | 1176 | 13 | 8 | 5 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0003c0003t0001 | 0/0 | 1176 | 14 | 9 | 3 | 1 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0004c0004t0001 | 0/0 | 1176 | 8 | 1 | 3 | 0 | 0 | 4 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0005c0005t0001 | 0/0 | 1176 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0006c0006t0001 | 0/0 | 1176 | 3 | 2 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0007c0007t0001 | 0/0 | 1184 | 3 | 0 | 0 | 3 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1179): Show |
chr2 | 222666658 | 222714930 |
| a0008c0012t0001 | 0/0 | 1175 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1170): Show |
chr2 | 222666658 | 222714930 |
| a0009c0015t0001 | 0/0 | 1176 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0010c0010t0001 | 0/0 | 1176 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0011c0008t0001 | 0/0 | 1176 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0012c0013t0001 | 0/0 | 1176 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1171): Show |
chr2 | 222666658 | 222714930 |
| a0013c0009t0001 | 0/0 | 1174 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | GCCTT others(1169): Show |
chr2 | 222666658 | 222714930 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0001c0014t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0003c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0005c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0005c0005t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0005c0005t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0005c0005t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0006c0006t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0006c0006t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0006c0006t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0007c0007t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0007c0007t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0007c0007t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0008c0012t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0009c0015t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0010c0010t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0011c0008t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0012c0013t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| a0013c0009t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0278 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0176 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00735 | hp1 | a0006 | c0006 | t0001 | g0289 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01168 | hp1 | a0004 | c0004 | t0001 | g0241 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01169 | hp2 | a0004 | c0004 | t0001 | g0242 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0283 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01433 | hp2 | a0008 | c0012 | t0001 | g0145 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | CLM | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0239 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01884 | hp2 | a0005 | c0005 | t0001 | g0271 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0191 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0288 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02040 | hp2 | a0009 | c0015 | t0001 | g0231 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02572 | hp1 | a0005 | c0005 | t0001 | g0275 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0267 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02683 | hp1 | a0004 | c0004 | t0001 | g0269 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02717 | hp1 | a0005 | c0005 | t0001 | g0276 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02723 | hp1 | a0010 | c0010 | t0001 | g0126 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0286 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0256 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0190 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0290 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0291 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0279 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0284 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0272 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0280 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03490 | hp1 | a0004 | c0004 | t0001 | g0120 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03492 | hp1 | a0004 | c0004 | t0001 | g0121 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03540 | hp1 | a0006 | c0006 | t0001 | g0285 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0261 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0173 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03704 | hp2 | a0004 | c0004 | t0001 | g0236 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03942 | hp1 | a0011 | c0008 | t0001 | g0237 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18957 | hp1 | a0012 | c0013 | t0001 | g0196 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18962 | hp2 | a0007 | c0007 | t0001 | g0018 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18974 | hp2 | a0007 | c0007 | t0001 | g0168 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18995 | hp1 | a0007 | c0007 | t0001 | g0159 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0282 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0035 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19075 | hp1 | a0013 | c0009 | t0001 | g0147 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0277 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ASW | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA20905 | hp1 | a0001 | c0014 | t0001 | g0021 | SAS | GIH | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | GIH | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02109 | hp1 | a0005 | c0005 | t0001 | g0274 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0273 | AFR | MSL | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA20300 | hp1 | a0006 | c0006 | t0001 | g0281 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0287 | AFR | USA | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0268 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | MOGAT1_chr2_222666658_222714930 | MOGAT1 | chr2 | 222666658 | 222714930 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222671822 | G | A | 3 | a0003 a0005 a0006 |
21 | HG00639.hp1 HG00735.hp1 HG01361.hp1 others(18): Show |
missense_variant | MODERATE | c.37G>A | p.Ala13Thr | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/6 | 165/1176 | 37/1008 | 13/335 | chr2 | 222671822 | |||
| chr2:222671864 | A | C | 1 | a0009 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.79A>C | p.Lys27Gln | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/6 | 207/1176 | 79/1008 | 27/335 | chr2 | 222671864 | |||
| chr2:222688467 | G | T | 1 | a0012 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.218G>T | p.Ser73Ile | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/6 | 346/1176 | 218/1008 | 73/335 | chr2 | 222688467 | |||
| chr2:222689344 | C | A | 1 | a0011 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.353C>A | p.Ala118Asp | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/6 | 481/1176 | 353/1008 | 118/335 | chr2 | 222689344 | |||
| chr2:222689345 | CT | C | 1 | a0013 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.357delT | p.Phe119fs | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/6 | 485/1176 | 357/1008 | 119/335 | INFO_REALIGN_3_PRIME | chr2 | 222689345 | ||
| chr2:222689406 | T | TATCTTCA others(1): Show |
1 | a0007 | 3 | NA18962.hp2 NA18974.hp2 NA18995.hp1 |
frameshift_variant | HIGH | c.416_423dupATCTTCAC | p.Val142fs | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/6 | 552/1176 | 424/1008 | 142/335 | INFO_REALIGN_3_PRIME | chr2 | 222689406 | ||
| chr2:222689415 | G | C | 1 | a0004 | 8 | HG00639.hp2 HG01168.hp1 HG01169.hp2 others(5): Show |
missense_variant | MODERATE | c.424G>C | p.Val142Leu | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/6 | 552/1176 | 424/1008 | 142/335 | chr2 | 222689415 | |||
| chr2:222694370 | T | C | 4 | a0002 a0006 a0010 others(1): Show |
65 | HG00609.hp2 HG00642.hp1 HG00735.hp1 others(62): Show |
missense_variant | MODERATE | c.487T>C | p.Ser163Pro | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/6 | 615/1176 | 487/1008 | 163/335 | chr2 | 222694370 | |||
| chr2:222694392 | C | A | 1 | a0010 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.509C>A | p.Ser170Tyr | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/6 | 637/1176 | 509/1008 | 170/335 | chr2 | 222694392 | |||
| chr2:222694397 | A | C | 1 | a0005 | 4 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(1): Show |
missense_variant | MODERATE | c.514A>C | p.Met172Leu | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/6 | 642/1176 | 514/1008 | 172/335 | chr2 | 222694397 | |||
| chr2:222695090 | G | A | 1 | a0014 | 1 | homoSapiens_chm13v2.hp1 | missense_variant&splice_region_variant | MODERATE | c.655G>A | p.Ala219Thr | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/6 | 783/1176 | 655/1008 | 219/335 | chr2 | 222695090 | |||
| chr2:222695116 | TG | T | 1 | a0013 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.683delG | p.Gly228fs | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/6 | 811/1176 | 683/1008 | 228/335 | INFO_REALIGN_3_PRIME | chr2 | 222695116 | ||
| chr2:222695267 | AG | A | 1 | a0008 | 1 | HG01433.hp2 | frameshift_variant | HIGH | c.834delG | p.Ala280fs | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/6 | 962/1176 | 834/1008 | 278/335 | INFO_REALIGN_3_PRIME | chr2 | 222695267 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222688450 | A | G | 1 | a0001c0014 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.201A>G | p.Arg67Arg | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/6 | 329/1176 | 201/1008 | 67/335 | chr2 | 222688450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222671709 | G | A | 4 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(1): Show |
32 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/6 | 77 | chr2 | 222671709 | ||||||
| chr2:222709900 | A | T | 1 | a0001c0001t0004 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 6/6 | 10 | chr2 | 222709900 | ||||||
| chr2:222709919 | A | T | 1 | a0001c0001t0003 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*29A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 6/6 | 29 | chr2 | 222709919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:222671953 | C | T | 21 | a0003c0003t0001g0272 a0003c0003t0001g0273 a0003c0003t0001g0277 others(18): Show |
21 | HG00639.hp1 HG00735.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+74C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222671953 | |||||||
| chr2:222671958 | T | C | 1 | a0001c0014t0001g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.94+79T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222671958 | |||||||
| chr2:222672269 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.94+390A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672269 | |||||||
| chr2:222672379 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.94+500T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672379 | |||||||
| chr2:222672526 | T | C | 36 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0050 others(33): Show |
40 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.94+647T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672526 | |||||||
| chr2:222672556 | C | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(217): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+677C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672556 | |||||||
| chr2:222672563 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0002c0002t0001g0023 others(1): Show |
4 | HG01109.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+684T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672563 | |||||||
| chr2:222672609 | G | A | 30 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0002 others(27): Show |
34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+730G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672609 | |||||||
| chr2:222672642 | G | C | 30 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0002 others(27): Show |
34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+763G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672642 | |||||||
| chr2:222672645 | C | T | 30 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0002 others(27): Show |
34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+766C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672645 | |||||||
| chr2:222672742 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(217): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+863G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672742 | |||||||
| chr2:222672767 | C | T | 1 | a0004c0004t0001g0269 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.94+888C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672767 | |||||||
| chr2:222672856 | A | C | 1 | a0002c0002t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94+977A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672856 | |||||||
| chr2:222672859 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(217): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+980G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672859 | |||||||
| chr2:222672889 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.94+1010T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672889 | |||||||
| chr2:222672889 | T | TTTA | 20 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0113 others(17): Show |
22 | HG00280.hp2 HG00621.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1045_94+1047dup others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672889 | T | TTTATTA | 65 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(62): Show |
69 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.94+1042_94+1047dup others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672889 | T | TTTATTAT others(2): Show |
103 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0050 others(100): Show |
111 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.94+1039_94+1047dup others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672889 | T | TTTATTAT others(5): Show |
12 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1036_94+1047dup others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672889 | T | TTTTTTA | 3 | a0001c0001t0001g0025 a0002c0002t0001g0024 a0002c0002t0001g0256 |
3 | HG02280.hp1 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.94+1012_94+1013ins others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672889 | T | TTTTTTAT others(5): Show |
9 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0257 others(6): Show |
11 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+1012_94+1013ins others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672889 | T | TTTTTTAT others(8): Show |
4 | a0001c0001t0001g0264 a0002c0002t0001g0265 a0002c0002t0001g0266 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1012_94+1013ins others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672889 | TTTA | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
59 | HG00597.hp2 HG00609.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.94+1045_94+1047del others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222672889 | ||||||
| chr2:222672958 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.94+1079C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672958 | |||||||
| chr2:222672977 | C | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(217): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.94+1098C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672977 | |||||||
| chr2:222672982 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.94+1103C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222672982 | |||||||
| chr2:222673221 | G | C | 23 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0001g0180 others(20): Show |
23 | HG00639.hp1 HG01361.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+1342G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673221 | |||||||
| chr2:222673331 | C | CAAAAA | 18 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0002 others(15): Show |
22 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1463_94+1467dup others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673331 | C | CAAAAAA | 13 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0002g0028 others(10): Show |
13 | HG00642.hp1 HG01243.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+1462_94+1467dup others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673331 | C | CAAAAAAA | 18 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0136 others(15): Show |
19 | HG00639.hp2 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+1461_94+1467dup others(7): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673331 | C | CAAAAAAA others(1): Show |
110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(107): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+1460_94+1467dup others(8): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673331 | C | CAAAAAAA others(2): Show |
32 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(29): Show |
33 | HG01243.hp1 HG01361.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+1459_94+1467dup others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673331 | C | CAAAAAAA others(3): Show |
7 | a0001c0001t0001g0264 a0003c0003t0001g0278 a0003c0003t0001g0279 others(4): Show |
7 | HG00639.hp1 HG02145.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1458_94+1467dup others(10): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673331 | C | CAAAAAAA others(4): Show |
18 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0181 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+1457_94+1467dup others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673331 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0140 a0003c0003t0001g0272 |
2 | HG01884.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+1456_94+1467dup others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222673331 | ||||||
| chr2:222673472 | C | G | 14 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
14 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+1593C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673472 | |||||||
| chr2:222673597 | C | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(128): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.94+1718C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673597 | |||||||
| chr2:222673656 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94+1777C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673656 | |||||||
| chr2:222673673 | C | G | 1 | a0003c0003t0001g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94+1794C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673673 | |||||||
| chr2:222673676 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.94+1797T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673676 | |||||||
| chr2:222673703 | A | T | 2 | a0002c0002t0001g0173 a0011c0008t0001g0237 |
2 | HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.94+1824A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673703 | |||||||
| chr2:222673714 | G | C | 1 | a0003c0003t0001g0283 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.94+1835G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673714 | |||||||
| chr2:222673819 | T | G | 28 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0002 others(25): Show |
32 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+1940T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673819 | |||||||
| chr2:222673883 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.94+2004C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222673883 | |||||||
| chr2:222674156 | C | T | 1 | a0001c0014t0001g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.94+2277C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674156 | |||||||
| chr2:222674364 | C | T | 4 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0052 others(1): Show |
5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+2485C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674364 | |||||||
| chr2:222674424 | A | G | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0140 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+2545A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674424 | |||||||
| chr2:222674460 | T | A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+2581T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674460 | |||||||
| chr2:222674587 | T | G | 1 | a0003c0003t0001g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94+2708T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674587 | |||||||
| chr2:222674646 | G | A | 20 | a0003c0003t0001g0272 a0003c0003t0001g0273 a0003c0003t0001g0277 others(17): Show |
20 | HG00639.hp1 HG01361.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.94+2767G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674646 | |||||||
| chr2:222674880 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(1): Show |
5 | HG01243.hp1 HG02965.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+3001T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222674880 | |||||||
| chr2:222675229 | A | C | 1 | a0001c0001t0003g0054 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94+3350A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675229 | |||||||
| chr2:222675240 | A | T | 1 | a0003c0003t0001g0277 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.94+3361A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675240 | |||||||
| chr2:222675310 | G | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0257 others(11): Show |
16 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+3431G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675310 | |||||||
| chr2:222675353 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3474G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675353 | |||||||
| chr2:222675481 | C | CT | 125 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(122): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.94+3618dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222675481 | ||||||
| chr2:222675481 | CT | C | 22 | a0001c0001t0001g0062 a0001c0001t0001g0139 a0001c0001t0001g0179 others(19): Show |
22 | HG00639.hp1 HG01361.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+3618delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222675481 | ||||||
| chr2:222675487 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(5): Show |
9 | HG01496.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+3608T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675487 | |||||||
| chr2:222675511 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.94+3632A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675511 | |||||||
| chr2:222675580 | T | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(177): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.94+3701T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675580 | |||||||
| chr2:222675604 | T | C | 30 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0002 others(27): Show |
34 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.94+3725T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675604 | |||||||
| chr2:222675629 | A | G | 1 | a0004c0004t0001g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.94+3750A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675629 | |||||||
| chr2:222675635 | A | G | 1 | a0004c0004t0001g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.94+3756A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675635 | |||||||
| chr2:222675654 | T | C | 7 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0043 others(4): Show |
8 | HG01257.hp1 HG02145.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+3775T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675654 | |||||||
| chr2:222675693 | A | T | 1 | a0002c0002t0001g0171 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.94+3814A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675693 | |||||||
| chr2:222675920 | C | T | 15 | a0001c0001t0001g0056 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.94+4041C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675920 | |||||||
| chr2:222675955 | A | T | 4 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0052 others(1): Show |
5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+4076A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222675955 | |||||||
| chr2:222676080 | G | A | 24 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0001g0180 others(21): Show |
24 | HG00639.hp1 HG00735.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.94+4201G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676080 | |||||||
| chr2:222676122 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(5): Show |
9 | HG01496.hp2 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+4243C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676122 | |||||||
| chr2:222676146 | TCTC | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+4270_94+4272del others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222676146 | ||||||
| chr2:222676150 | C | CT | 23 | a0001c0001t0001g0172 a0001c0001t0001g0234 a0003c0003t0001g0272 others(20): Show |
23 | HG00597.hp1 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.94+4286dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222676150 | ||||||
| chr2:222676158 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG02027.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.94+4279T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676158 | |||||||
| chr2:222676166 | A | T | 2 | a0002c0002t0001g0235 a0002c0002t0001g0255 |
2 | NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.94+4287A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676166 | |||||||
| chr2:222676175 | C | T | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.94+4296C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676175 | |||||||
| chr2:222676662 | A | G | 2 | a0002c0002t0001g0235 a0002c0002t0001g0255 |
2 | NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.94+4783A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676662 | |||||||
| chr2:222676827 | G | T | 1 | a0003c0003t0001g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.94+4948G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222676827 | |||||||
| chr2:222677351 | T | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(193): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.94+5472T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677351 | |||||||
| chr2:222677397 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.94+5518G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677397 | |||||||
| chr2:222677512 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(140): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.94+5633A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677512 | |||||||
| chr2:222677996 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.94+6117C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222677996 | |||||||
| chr2:222678024 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+6145C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678024 | |||||||
| chr2:222678121 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.94+6242T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678121 | |||||||
| chr2:222678163 | A | T | 35 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0002 others(32): Show |
39 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.94+6284A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678163 | |||||||
| chr2:222678177 | A | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(139): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+6298A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678177 | |||||||
| chr2:222678393 | T | C | 1 | a0002c0002t0001g0256 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.94+6514T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678393 | |||||||
| chr2:222678461 | T | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0124 others(14): Show |
19 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+6582T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678461 | |||||||
| chr2:222678558 | T | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG02257.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+6679T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678558 | |||||||
| chr2:222678612 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94+6733T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678612 | |||||||
| chr2:222678714 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.94+6835G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678714 | |||||||
| chr2:222678757 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(140): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.94+6878A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678757 | |||||||
| chr2:222678762 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.94+6883G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678762 | |||||||
| chr2:222678766 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.94+6887C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678766 | |||||||
| chr2:222678913 | C | T | 14 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
14 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+7034C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678913 | |||||||
| chr2:222678914 | A | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(195): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.94+7035A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678914 | |||||||
| chr2:222678985 | T | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0181 a0001c0001t0001g0183 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7106T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222678985 | |||||||
| chr2:222679107 | A | G | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | NA18940.hp1 NA18950.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7228A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679107 | |||||||
| chr2:222679377 | C | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(139): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+7498C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679377 | |||||||
| chr2:222679392 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(139): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+7513C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679392 | |||||||
| chr2:222679393 | A | G | 15 | a0001c0001t0001g0056 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
15 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.94+7514A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679393 | |||||||
| chr2:222679532 | C | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | NA18940.hp1 NA18950.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7653C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679532 | |||||||
| chr2:222679818 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0150 a0001c0001t0001g0198 |
5 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+7939G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679818 | |||||||
| chr2:222679827 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.94+7948A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679827 | |||||||
| chr2:222679897 | T | A | 4 | a0001c0001t0002g0042 a0002c0002t0001g0135 a0002c0002t0001g0175 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+8018T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679897 | |||||||
| chr2:222679945 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.94+8066A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222679945 | |||||||
| chr2:222680026 | AG | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(8): Show |
12 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+8148delG | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680026 | |||||||
| chr2:222680244 | A | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(4): Show |
8 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-8100A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680244 | |||||||
| chr2:222680264 | G | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(148): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.95-8080G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680264 | |||||||
| chr2:222680442 | T | TAAAAGCA others(304): Show |
1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-7889_95-7888ins others(311): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222680442 | ||||||
| chr2:222680442 | T | TAAAAGCA others(305): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(4): Show |
8 | HG01496.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-7889_95-7888ins others(312): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222680442 | ||||||
| chr2:222680445 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.95-7899A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680445 | |||||||
| chr2:222680463 | A | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(150): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.95-7881A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680463 | |||||||
| chr2:222680625 | C | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(58): Show |
65 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.95-7719C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680625 | |||||||
| chr2:222680759 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-7585T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680759 | |||||||
| chr2:222680817 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.95-7527T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222680817 | |||||||
| chr2:222681087 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-7257G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681087 | |||||||
| chr2:222681134 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0158 others(8): Show |
13 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-7210C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681134 | |||||||
| chr2:222681251 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-7093C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681251 | |||||||
| chr2:222681327 | C | A | 4 | a0001c0001t0002g0042 a0002c0002t0001g0135 a0002c0002t0001g0175 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-7017C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681327 | |||||||
| chr2:222681328 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.95-7016G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681328 | |||||||
| chr2:222681683 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.95-6661G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681683 | |||||||
| chr2:222681744 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-6600G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222681744 | |||||||
| chr2:222682118 | C | CCA | 3 | a0001c0001t0001g0055 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG02572.hp2 NA18952.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.95-6209_95-6208dup others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222682118 | ||||||
| chr2:222682118 | CCA | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(129): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.95-6209_95-6208del others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222682118 | ||||||
| chr2:222682240 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(3): Show |
7 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-6104C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682240 | |||||||
| chr2:222682328 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-6016G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682328 | |||||||
| chr2:222682366 | C | G | 3 | a0003c0003t0001g0284 a0003c0003t0001g0287 a0003c0003t0001g0291 |
3 | HG03130.hp1 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.95-5978C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682366 | |||||||
| chr2:222682371 | A | G | 9 | a0001c0001t0001g0124 a0001c0001t0001g0263 a0002c0002t0001g0171 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-5973A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682371 | |||||||
| chr2:222682418 | C | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(146): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.95-5926C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682418 | |||||||
| chr2:222682452 | T | A | 9 | a0001c0001t0001g0124 a0001c0001t0001g0263 a0002c0002t0001g0171 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-5892T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682452 | |||||||
| chr2:222682497 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.95-5847A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682497 | |||||||
| chr2:222682545 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
12 | HG01496.hp2 HG01928.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-5799C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682545 | |||||||
| chr2:222682637 | G | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(113): Show |
123 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.95-5707G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682637 | |||||||
| chr2:222682640 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(140): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.95-5704C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682640 | |||||||
| chr2:222682690 | C | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(130): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.95-5654C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682690 | |||||||
| chr2:222682705 | T | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(141): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.95-5639T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682705 | |||||||
| chr2:222682713 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.95-5631C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682713 | |||||||
| chr2:222682811 | C | T | 3 | a0001c0001t0002g0002 a0001c0001t0002g0046 a0001c0001t0002g0049 |
6 | HG02622.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-5533C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682811 | |||||||
| chr2:222682984 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.95-5360G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682984 | |||||||
| chr2:222682992 | G | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(152): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.95-5352G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682992 | |||||||
| chr2:222682993 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.95-5351C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222682993 | |||||||
| chr2:222683001 | T | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(135): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.95-5343T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683001 | |||||||
| chr2:222683134 | G | A | 4 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0052 others(1): Show |
5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-5210G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683134 | |||||||
| chr2:222683182 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(62): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-5162T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683182 | |||||||
| chr2:222683205 | G | GA | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(132): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.95-5125dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683205 | ||||||
| chr2:222683273 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(6): Show |
10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-5071G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683273 | |||||||
| chr2:222683430 | T | TA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(4): Show |
8 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-4900dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | ||||||
| chr2:222683430 | T | TAA | 58 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(55): Show |
62 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.95-4901_95-4900dup others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | ||||||
| chr2:222683430 | TA | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0026 others(64): Show |
72 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.95-4900delA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | ||||||
| chr2:222683430 | TAA | T | 7 | a0001c0001t0001g0124 a0001c0001t0001g0263 a0003c0003t0001g0277 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-4901_95-4900del others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222683430 | ||||||
| chr2:222683453 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.95-4891C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683453 | |||||||
| chr2:222683465 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0001c0001t0003g0054 |
4 | HG02258.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4879C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683465 | |||||||
| chr2:222683556 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.95-4788C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683556 | |||||||
| chr2:222683618 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.95-4726C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683618 | |||||||
| chr2:222683758 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.95-4586C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222683758 | |||||||
| chr2:222684075 | T | C | 1 | a0008c0012t0001g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-4269T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684075 | |||||||
| chr2:222684299 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.95-4045G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684299 | |||||||
| chr2:222684337 | C | T | 7 | a0001c0001t0001g0124 a0001c0001t0001g0263 a0003c0003t0001g0277 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-4007C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684337 | |||||||
| chr2:222684338 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(62): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-4006G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684338 | |||||||
| chr2:222684368 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(62): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-3976C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684368 | |||||||
| chr2:222684517 | G | C | 3 | a0003c0003t0001g0284 a0003c0003t0001g0287 a0003c0003t0001g0291 |
3 | HG03130.hp1 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.95-3827G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684517 | |||||||
| chr2:222684578 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-3766C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684578 | |||||||
| chr2:222684586 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02165.hp1 NA18965.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3758T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684586 | |||||||
| chr2:222684631 | A | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(136): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.95-3713A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684631 | |||||||
| chr2:222684733 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-3611C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684733 | |||||||
| chr2:222684766 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(6): Show |
10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-3578G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684766 | |||||||
| chr2:222684855 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(62): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-3489G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222684855 | |||||||
| chr2:222685064 | T | C | 1 | a0002c0002t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.95-3280T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685064 | |||||||
| chr2:222685153 | G | T | 3 | a0002c0002t0001g0259 a0002c0002t0001g0265 a0002c0002t0001g0266 |
3 | HG02109.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.95-3191G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685153 | |||||||
| chr2:222685293 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.95-3051C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685293 | |||||||
| chr2:222685346 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-2998A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685346 | |||||||
| chr2:222685410 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-2934T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685410 | |||||||
| chr2:222685496 | T | C | 3 | a0002c0002t0001g0259 a0002c0002t0001g0265 a0002c0002t0001g0266 |
3 | HG02109.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.95-2848T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685496 | |||||||
| chr2:222685552 | T | C | 1 | a0002c0002t0002g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.95-2792T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685552 | |||||||
| chr2:222685556 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.95-2788C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685556 | |||||||
| chr2:222685598 | C | CT | 61 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0051 others(58): Show |
67 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.95-2726dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222685598 | ||||||
| chr2:222685598 | CT | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0058 others(21): Show |
26 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.95-2726delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222685598 | ||||||
| chr2:222685601 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-2743T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685601 | |||||||
| chr2:222685602 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0137 others(5): Show |
9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-2742T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685602 | |||||||
| chr2:222685634 | C | CTT | 4 | a0002c0002t0002g0044 a0002c0002t0002g0045 a0003c0003t0001g0288 others(1): Show |
4 | HG01975.hp1 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-2709_95-2708dup others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222685634 | ||||||
| chr2:222685725 | G | A | 49 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0055 others(46): Show |
52 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.95-2619G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685725 | |||||||
| chr2:222685729 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-2615T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685729 | |||||||
| chr2:222685745 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0158 others(9): Show |
14 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-2599C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685745 | |||||||
| chr2:222685746 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-2598A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685746 | |||||||
| chr2:222685802 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0158 others(10): Show |
15 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-2542T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685802 | |||||||
| chr2:222685881 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.95-2463C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685881 | |||||||
| chr2:222685895 | C | T | 1 | a0002c0002t0001g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.95-2449C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685895 | |||||||
| chr2:222685961 | C | T | 4 | a0001c0001t0001g0157 a0001c0001t0001g0192 a0001c0001t0001g0210 others(1): Show |
4 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2383C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222685961 | |||||||
| chr2:222686014 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0158 others(10): Show |
15 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-2330A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686014 | |||||||
| chr2:222686057 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(6): Show |
10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-2287T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686057 | |||||||
| chr2:222686138 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(6): Show |
10 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-2206C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686138 | |||||||
| chr2:222686266 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(85): Show |
94 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-2078C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686266 | |||||||
| chr2:222686320 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0248 |
2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.95-2024G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686320 | |||||||
| chr2:222686428 | A | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(62): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-1916A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686428 | |||||||
| chr2:222686451 | A | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(5): Show |
9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-1893A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686451 | |||||||
| chr2:222686497 | C | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(87): Show |
96 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.95-1847C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686497 | |||||||
| chr2:222686841 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.95-1503T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686841 | |||||||
| chr2:222686851 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(134): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-1493A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686851 | |||||||
| chr2:222686984 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-1360C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222686984 | |||||||
| chr2:222687113 | C | CA | 24 | a0001c0001t0001g0013 a0001c0001t0001g0057 a0001c0001t0001g0062 others(21): Show |
25 | HG00642.hp2 HG00735.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-1205dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | ||||||
| chr2:222687113 | CA | C | 11 | a0001c0001t0001g0208 a0002c0002t0001g0190 a0003c0003t0001g0273 others(8): Show |
11 | HG00639.hp1 HG01168.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-1205delA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | ||||||
| chr2:222687113 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-1215_95-1205del others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | ||||||
| chr2:222687113 | CAAAAAAA others(6): Show |
C | 4 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0052 others(1): Show |
5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1217_95-1205del others(13): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687113 | ||||||
| chr2:222687132 | AAAAAAAA others(11): Show |
A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0056 others(25): Show |
30 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-1208_95-1191del others(18): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687132 | ||||||
| chr2:222687133 | AAAAAAAG others(10): Show |
A | 51 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0090 others(48): Show |
54 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.95-1207_95-1191del others(17): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687133 | ||||||
| chr2:222687134 | AAAAAAGA others(9): Show |
A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(50): Show |
57 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.95-1206_95-1191del others(16): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687134 | ||||||
| chr2:222687135 | AAAAAGAA others(8): Show |
A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0170 a0001c0001t0001g0233 others(2): Show |
5 | HG01952.hp2 NA18995.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1205_95-1191del others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 222687135 | ||||||
| chr2:222687169 | T | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(149): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.95-1175T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687169 | |||||||
| chr2:222687341 | G | A | 4 | a0001c0001t0001g0213 a0001c0001t0002g0033 a0001c0001t0002g0034 others(1): Show |
4 | HG03041.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1003G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687341 | |||||||
| chr2:222687374 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-970C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687374 | |||||||
| chr2:222687633 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0139 a0001c0001t0001g0158 others(9): Show |
14 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.95-711C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687633 | |||||||
| chr2:222687705 | C | T | 9 | a0003c0003t0001g0273 a0003c0003t0001g0278 a0003c0003t0001g0279 others(6): Show |
9 | HG00639.hp1 HG03098.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-639C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687705 | |||||||
| chr2:222687989 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0195 |
2 | HG01928.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-355G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 1/5 | chr2 | 222687989 | |||||||
| chr2:222688565 | A | G | 52 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0026 others(49): Show |
56 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.273+43A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688565 | |||||||
| chr2:222688615 | G | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(3): Show |
7 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.273+93G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688615 | |||||||
| chr2:222688639 | C | T | 1 | a0002c0002t0002g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.273+117C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688639 | |||||||
| chr2:222688686 | A | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0026 others(49): Show |
56 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.273+164A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688686 | |||||||
| chr2:222688704 | T | C | 46 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0108 others(43): Show |
49 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.273+182T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688704 | |||||||
| chr2:222688806 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
148 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.273+284A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688806 | |||||||
| chr2:222688930 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.274-335A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222688930 | |||||||
| chr2:222689012 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0018 others(62): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.274-253G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689012 | |||||||
| chr2:222689020 | G | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0178 |
2 | NA18982.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.274-245G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689020 | |||||||
| chr2:222689058 | T | C | 4 | a0004c0004t0001g0120 a0004c0004t0001g0121 a0004c0004t0001g0191 others(1): Show |
4 | HG01891.hp1 HG02683.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-207T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689058 | |||||||
| chr2:222689238 | T | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(5): Show |
9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-27T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 2/5 | chr2 | 222689238 | |||||||
| chr2:222689473 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.478+4A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689473 | |||||||
| chr2:222689556 | T | C | 52 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0026 others(49): Show |
56 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.478+87T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689556 | |||||||
| chr2:222689624 | C | T | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.478+155C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689624 | |||||||
| chr2:222689625 | C | T | 1 | a0013c0009t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.478+156C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689625 | |||||||
| chr2:222689626 | T | C | 1 | a0013c0009t0001g0147 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.478+157T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689626 | |||||||
| chr2:222689706 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(5): Show |
9 | HG01496.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.478+237G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689706 | |||||||
| chr2:222689851 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.478+382G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689851 | |||||||
| chr2:222689970 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.478+501C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222689970 | |||||||
| chr2:222690007 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.478+538C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690007 | |||||||
| chr2:222690083 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.478+614T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690083 | |||||||
| chr2:222690181 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.478+712G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690181 | |||||||
| chr2:222690202 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.478+733C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690202 | |||||||
| chr2:222690280 | C | T | 1 | a0002c0002t0002g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.478+811C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690280 | |||||||
| chr2:222690454 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
148 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.478+985A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690454 | |||||||
| chr2:222690522 | A | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 others(3): Show |
7 | HG01243.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+1053A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690522 | |||||||
| chr2:222690571 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0188 others(6): Show |
11 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.478+1102G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690571 | |||||||
| chr2:222690575 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.478+1106A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222690575 | |||||||
| chr2:222691004 | G | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(4): Show |
8 | HG01496.hp2 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+1535G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691004 | |||||||
| chr2:222691051 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.478+1582C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691051 | |||||||
| chr2:222691067 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.478+1598A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691067 | |||||||
| chr2:222691111 | C | T | 8 | a0001c0001t0001g0124 a0001c0001t0001g0263 a0001c0001t0002g0049 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+1642C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691111 | |||||||
| chr2:222691174 | G | GTTTCTTT others(6): Show |
158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(155): Show |
169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.478+1714_478+1715i others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 222691174 | ||||||
| chr2:222691196 | T | A | 15 | a0001c0001t0001g0050 a0001c0001t0001g0124 a0001c0001t0001g0143 others(12): Show |
15 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.478+1727T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691196 | |||||||
| chr2:222691199 | A | T | 40 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0050 others(37): Show |
44 | HG00642.hp1 HG00738.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.478+1730A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691199 | |||||||
| chr2:222691214 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.478+1745A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691214 | |||||||
| chr2:222691534 | A | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
78 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.478+2065A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691534 | |||||||
| chr2:222691709 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.478+2240C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691709 | |||||||
| chr2:222691810 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.478+2341A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691810 | |||||||
| chr2:222691886 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.478+2417G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691886 | |||||||
| chr2:222691979 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.479-2383G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222691979 | |||||||
| chr2:222692033 | G | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0139 others(15): Show |
20 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.479-2329G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692033 | |||||||
| chr2:222692264 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.479-2098A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692264 | |||||||
| chr2:222692328 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(69): Show |
78 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.479-2034A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692328 | |||||||
| chr2:222692399 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.479-1963A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692399 | |||||||
| chr2:222692563 | C | T | 1 | a0002c0002t0002g0043 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.479-1799C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692563 | |||||||
| chr2:222692608 | T | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0139 others(12): Show |
17 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.479-1754T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692608 | |||||||
| chr2:222692662 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.479-1700T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692662 | |||||||
| chr2:222692766 | A | G | 1 | a0003c0003t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.479-1596A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692766 | |||||||
| chr2:222692810 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(143): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.479-1552G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692810 | |||||||
| chr2:222692814 | G | A | 2 | a0001c0001t0001g0025 a0002c0002t0001g0024 |
2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479-1548G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692814 | |||||||
| chr2:222692984 | C | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0195 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.479-1378C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222692984 | |||||||
| chr2:222693067 | A | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0139 others(12): Show |
17 | HG00140.hp2 HG00280.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.479-1295A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693067 | |||||||
| chr2:222693214 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(6): Show |
12 | HG00597.hp2 HG02083.hp2 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.479-1148A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693214 | |||||||
| chr2:222693339 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.479-1023A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693339 | |||||||
| chr2:222693344 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0162 a0001c0001t0001g0228 others(1): Show |
4 | HG00673.hp2 HG02129.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-1018G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693344 | |||||||
| chr2:222693448 | GT | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(108): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.479-894delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 222693448 | ||||||
| chr2:222693448 | GTT | G | 15 | a0001c0001t0001g0013 a0001c0001t0001g0130 a0001c0001t0001g0136 others(12): Show |
16 | HG01496.hp2 HG01884.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.479-895_479-894del others(2): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 222693448 | ||||||
| chr2:222693455 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.479-907T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693455 | |||||||
| chr2:222693492 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.479-870T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693492 | |||||||
| chr2:222693494 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.479-868A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693494 | |||||||
| chr2:222693637 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.479-725G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693637 | |||||||
| chr2:222693912 | A | C | 1 | a0003c0003t0001g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.479-450A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693912 | |||||||
| chr2:222693927 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.479-435G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693927 | |||||||
| chr2:222693956 | G | A | 20 | a0001c0001t0001g0087 a0001c0001t0002g0002 a0001c0001t0002g0028 others(17): Show |
23 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.479-406G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693956 | |||||||
| chr2:222693967 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0084 |
2 | NA18950.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.479-395C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222693967 | |||||||
| chr2:222694134 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.479-228G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694134 | |||||||
| chr2:222694171 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(119): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.479-191G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694171 | |||||||
| chr2:222694302 | T | A | 1 | a0003c0003t0001g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.479-60T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694302 | |||||||
| chr2:222694329 | G | T | 1 | a0002c0002t0002g0043 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.479-33G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 3/5 | chr2 | 222694329 | |||||||
| chr2:222694599 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.653+63G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694599 | |||||||
| chr2:222694633 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.653+97C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694633 | |||||||
| chr2:222694779 | C | T | 4 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0052 others(1): Show |
5 | HG02976.hp2 HG03139.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+243C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694779 | |||||||
| chr2:222694921 | A | G | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.654-168A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694921 | |||||||
| chr2:222694995 | T | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.654-94T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222694995 | |||||||
| chr2:222695070 | G | A | 1 | a0003c0003t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-19G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 4/5 | chr2 | 222695070 | |||||||
| chr2:222695621 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.853+333T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695621 | |||||||
| chr2:222695700 | T | C | 1 | a0005c0005t0001g0274 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.853+412T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695700 | |||||||
| chr2:222695702 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+414G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695702 | |||||||
| chr2:222695729 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+441G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695729 | |||||||
| chr2:222695783 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.853+495A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695783 | |||||||
| chr2:222695918 | C | G | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+630C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222695918 | |||||||
| chr2:222696163 | C | T | 1 | a0002c0002t0001g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.853+875C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696163 | |||||||
| chr2:222696225 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.853+937C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696225 | |||||||
| chr2:222696343 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.853+1055A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696343 | |||||||
| chr2:222696501 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+1213T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696501 | |||||||
| chr2:222696873 | T | C | 6 | a0001c0001t0001g0163 a0002c0002t0001g0023 a0002c0002t0001g0138 others(3): Show |
6 | HG01106.hp1 HG01109.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+1585T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696873 | |||||||
| chr2:222696968 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(50): Show |
57 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.853+1680A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696968 | |||||||
| chr2:222696987 | C | T | 35 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0100 others(32): Show |
36 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.853+1699C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222696987 | |||||||
| chr2:222697249 | T | C | 1 | a0003c0003t0001g0277 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.853+1961T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697249 | |||||||
| chr2:222697318 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.853+2030C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697318 | |||||||
| chr2:222697348 | C | T | 1 | a0005c0005t0001g0276 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.853+2060C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697348 | |||||||
| chr2:222697576 | C | CT | 16 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0066 others(13): Show |
17 | HG01109.hp1 HG01433.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.853+2311dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222697576 | ||||||
| chr2:222697576 | CT | C | 25 | a0001c0001t0001g0057 a0001c0001t0001g0068 a0001c0001t0001g0096 others(22): Show |
25 | HG00609.hp2 HG01106.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.853+2311delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222697576 | ||||||
| chr2:222697576 | CTT | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(75): Show |
84 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.853+2310_853+2311d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222697576 | ||||||
| chr2:222697631 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.853+2343G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697631 | |||||||
| chr2:222697659 | C | T | 1 | a0001c0001t0002g0036 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.853+2371C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697659 | |||||||
| chr2:222697960 | C | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0122 others(23): Show |
32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.853+2672C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222697960 | |||||||
| chr2:222698111 | G | GT | 115 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(112): Show |
121 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.853+2827dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222698111 | ||||||
| chr2:222698118 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0195 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.853+2830T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698118 | |||||||
| chr2:222698253 | G | A | 1 | a0002c0002t0002g0047 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.853+2965G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698253 | |||||||
| chr2:222698412 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.853+3124T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698412 | |||||||
| chr2:222698495 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+3207G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698495 | |||||||
| chr2:222698607 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.853+3319G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698607 | |||||||
| chr2:222698766 | T | A | 2 | a0001c0001t0001g0257 a0002c0002t0001g0024 |
2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.853+3478T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698766 | |||||||
| chr2:222698779 | G | T | 3 | a0002c0002t0001g0193 a0002c0002t0001g0211 a0002c0002t0001g0253 |
3 | HG01952.hp1 NA19010.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.853+3491G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698779 | |||||||
| chr2:222698812 | G | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0137 others(7): Show |
11 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.853+3524G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698812 | |||||||
| chr2:222698855 | G | A | 64 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0026 others(61): Show |
68 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.853+3567G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698855 | |||||||
| chr2:222698892 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0227 |
2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.853+3604C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698892 | |||||||
| chr2:222698925 | T | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(106): Show |
116 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.853+3637T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222698925 | |||||||
| chr2:222699002 | C | CT | 8 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0091 others(5): Show |
8 | HG02027.hp2 HG02738.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+3734dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | ||||||
| chr2:222699002 | CT | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0070 others(53): Show |
63 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.853+3734delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | ||||||
| chr2:222699002 | CTT | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0025 others(35): Show |
41 | HG00099.hp2 HG00609.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.853+3733_853+3734d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | ||||||
| chr2:222699002 | CTTT | C | 66 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0026 others(63): Show |
70 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.853+3732_853+3734d others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699002 | ||||||
| chr2:222699120 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0013 others(106): Show |
116 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.853+3832T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699120 | |||||||
| chr2:222699292 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.853+4004G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699292 | |||||||
| chr2:222699313 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(106): Show |
115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+4025T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699313 | |||||||
| chr2:222699392 | T | G | 5 | a0001c0001t0001g0163 a0002c0002t0001g0151 a0002c0002t0001g0256 others(2): Show |
5 | HG01106.hp1 HG01361.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+4104T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699392 | |||||||
| chr2:222699402 | A | G | 1 | a0002c0002t0001g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+4114A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699402 | |||||||
| chr2:222699475 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG02055.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.853+4187T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699475 | |||||||
| chr2:222699490 | C | CT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0025 others(46): Show |
52 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.853+4226dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | ||||||
| chr2:222699490 | C | CTT | 9 | a0001c0001t0001g0064 a0001c0001t0001g0081 a0001c0001t0001g0093 others(6): Show |
9 | HG01358.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+4225_853+4226d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | ||||||
| chr2:222699490 | C | CTTT | 53 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0055 others(50): Show |
56 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.853+4224_853+4226d others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | ||||||
| chr2:222699490 | C | CTTTT | 11 | a0001c0001t0001g0077 a0001c0001t0001g0133 a0001c0001t0001g0143 others(8): Show |
11 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.853+4223_853+4226d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | ||||||
| chr2:222699490 | CT | C | 6 | a0001c0001t0001g0058 a0001c0001t0001g0085 a0001c0001t0001g0115 others(3): Show |
6 | HG01167.hp1 HG02155.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+4226delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222699490 | ||||||
| chr2:222699520 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0127 others(17): Show |
23 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.853+4232G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699520 | |||||||
| chr2:222699645 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(101): Show |
110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+4357C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699645 | |||||||
| chr2:222699711 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(101): Show |
110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+4423G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699711 | |||||||
| chr2:222699832 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+4544T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699832 | |||||||
| chr2:222699840 | T | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(106): Show |
115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+4552T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699840 | |||||||
| chr2:222699859 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0177 |
2 | NA18952.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.853+4571C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699859 | |||||||
| chr2:222699952 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(101): Show |
110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+4664C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699952 | |||||||
| chr2:222699957 | T | C | 8 | a0001c0001t0001g0163 a0002c0002t0001g0138 a0002c0002t0001g0151 others(5): Show |
8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+4669T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699957 | |||||||
| chr2:222699963 | A | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(106): Show |
115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+4675A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222699963 | |||||||
| chr2:222700082 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.853+4794A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700082 | |||||||
| chr2:222700354 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.853+5066G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700354 | |||||||
| chr2:222700546 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+5258G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700546 | |||||||
| chr2:222700568 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.853+5280G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700568 | |||||||
| chr2:222700657 | C | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(106): Show |
115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+5369C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700657 | |||||||
| chr2:222700802 | T | C | 3 | a0002c0002t0001g0138 a0002c0002t0001g0262 a0003c0003t0001g0282 |
3 | HG02451.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.853+5514T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700802 | |||||||
| chr2:222700838 | A | T | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.853+5550A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700838 | |||||||
| chr2:222700872 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.853+5584G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700872 | |||||||
| chr2:222700905 | C | T | 67 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0055 others(64): Show |
70 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.853+5617C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222700905 | |||||||
| chr2:222701111 | G | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(106): Show |
115 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.853+5823G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701111 | |||||||
| chr2:222701141 | T | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0127 others(17): Show |
23 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.853+5853T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701141 | |||||||
| chr2:222701214 | C | T | 8 | a0001c0001t0001g0163 a0002c0002t0001g0138 a0002c0002t0001g0151 others(5): Show |
8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+5926C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701214 | |||||||
| chr2:222701282 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.853+5994G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701282 | |||||||
| chr2:222701287 | A | AGGAG | 3 | a0002c0002t0001g0138 a0002c0002t0001g0262 a0003c0003t0001g0282 |
3 | HG02451.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.853+6000_853+6001i others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701287 | ||||||
| chr2:222701287 | AGAG | A | 18 | a0001c0001t0001g0100 a0001c0001t0001g0140 a0001c0001t0001g0142 others(15): Show |
18 | HG00639.hp1 HG00738.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.853+6012_853+6014d others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701287 | ||||||
| chr2:222701296 | GGAGGA | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0143 a0001c0001t0001g0195 |
3 | HG02615.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.853+6012_853+6016d others(7): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701296 | ||||||
| chr2:222701296 | GGAGGAGA | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0132 others(11): Show |
15 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.853+6012_853+6018d others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701296 | ||||||
| chr2:222701298 | AG | A | 3 | a0001c0001t0001g0026 a0002c0002t0002g0031 a0002c0002t0002g0032 |
3 | HG00642.hp1 HG01261.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.853+6012delG | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701298 | ||||||
| chr2:222701299 | G | GA | 23 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0055 others(20): Show |
24 | HG00609.hp2 HG01192.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GAGA | 11 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0208 others(8): Show |
12 | HG00609.hp1 HG00735.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GAGAGA | 9 | a0001c0001t0001g0056 a0001c0001t0001g0077 a0001c0001t0001g0234 others(6): Show |
9 | HG01109.hp2 HG01928.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(7): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GAGAGAGA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0150 others(5): Show |
10 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GAGAGAGA others(2): Show |
11 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0094 others(8): Show |
11 | HG02257.hp1 HG02523.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GAGAGAGA others(4): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0093 others(5): Show |
9 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+6011_853+6012i others(13): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GAGAGAGA others(6): Show |
1 | a0003c0003t0001g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.853+6011_853+6012i others(15): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GAGAGAGA others(8): Show |
2 | a0001c0001t0001g0204 a0002c0002t0001g0152 |
2 | HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.853+6011_853+6012i others(17): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701299 | |||||||
| chr2:222701299 | G | GGA | 8 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0002c0002t0001g0123 others(5): Show |
9 | HG00597.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+6040_853+6041d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701299 | ||||||
| chr2:222701299 | G | GGAGAGAG others(5): Show |
1 | a0001c0001t0001g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.853+6030_853+6041d others(14): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701299 | ||||||
| chr2:222701299 | GGAGAGAG others(9): Show |
G | 2 | a0002c0002t0001g0135 a0002c0002t0001g0175 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.853+6026_853+6041d others(18): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701299 | ||||||
| chr2:222701301 | A | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0082 a0001c0001t0001g0085 others(3): Show |
7 | HG02080.hp2 HG02083.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+6013A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701301 | |||||||
| chr2:222701330 | T | G | 67 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0055 others(64): Show |
70 | HG00280.hp2 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.853+6042T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701330 | |||||||
| chr2:222701394 | A | G | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853+6106A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701394 | |||||||
| chr2:222701398 | A | AAG | 1 | a0001c0001t0001g0004 | 3 | HG02258.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.853+6124_853+6125d others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701398 | ||||||
| chr2:222701398 | A | G | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853+6110A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701398 | |||||||
| chr2:222701414 | A | G | 1 | a0010c0010t0001g0126 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.853+6126A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701414 | |||||||
| chr2:222701421 | A | T | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.853+6133A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701421 | |||||||
| chr2:222701487 | A | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(101): Show |
110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.853+6199A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701487 | |||||||
| chr2:222701497 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.853+6209G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701497 | |||||||
| chr2:222701537 | A | AAGAG | 120 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
126 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.853+6252_853+6253i others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701537 | ||||||
| chr2:222701546 | G | GA | 107 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.853+6264dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701546 | ||||||
| chr2:222701551 | A | AAAGAAAG | 9 | a0001c0001t0001g0163 a0002c0002t0001g0125 a0002c0002t0001g0138 others(6): Show |
9 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.853+6264_853+6265i others(9): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701551 | ||||||
| chr2:222701561 | G | GAAA | 8 | a0001c0001t0001g0163 a0002c0002t0001g0138 a0002c0002t0001g0151 others(5): Show |
8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+6274_853+6275i others(5): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701561 | ||||||
| chr2:222701571 | G | A | 8 | a0001c0001t0001g0163 a0002c0002t0001g0138 a0002c0002t0001g0151 others(5): Show |
8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+6283G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701571 | |||||||
| chr2:222701572 | A | AG | 8 | a0001c0001t0001g0163 a0002c0002t0001g0138 a0002c0002t0001g0151 others(5): Show |
8 | HG01106.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+6284_853+6285i others(3): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701572 | |||||||
| chr2:222701596 | A | AAAAGAAA others(11): Show |
2 | a0001c0001t0001g0257 a0002c0002t0001g0024 |
2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.853+6309_853+6310i others(20): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | ||||||
| chr2:222701596 | A | AAAAGAAA others(19): Show |
1 | a0001c0001t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.853+6309_853+6310i others(28): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | ||||||
| chr2:222701596 | A | AAAAGAGA others(9): Show |
2 | a0001c0001t0001g0204 a0002c0002t0001g0258 |
2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.853+6309_853+6310i others(18): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | ||||||
| chr2:222701596 | A | AAAAGAGA others(13): Show |
99 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(96): Show |
105 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.853+6309_853+6310i others(22): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | ||||||
| chr2:222701596 | A | AAAAGAGA others(17): Show |
3 | a0005c0005t0001g0274 a0005c0005t0001g0275 a0005c0005t0001g0276 |
3 | HG02109.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.853+6309_853+6310i others(26): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | ||||||
| chr2:222701596 | A | AAGAAAGA others(17): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+6310_853+6311i others(26): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222701596 | ||||||
| chr2:222701630 | C | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
126 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.853+6342C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701630 | |||||||
| chr2:222701733 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(105): Show |
114 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.853+6445G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222701733 | |||||||
| chr2:222702297 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(109): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.853+7009A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702297 | |||||||
| chr2:222702307 | C | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(154): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.853+7019C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702307 | |||||||
| chr2:222702576 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0240 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.854-7160G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702576 | |||||||
| chr2:222702832 | A | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0167 a0001c0001t0001g0225 others(1): Show |
4 | NA18971.hp2 NA19010.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-6904A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702832 | |||||||
| chr2:222702883 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0002g0049 a0002c0002t0001g0151 others(3): Show |
6 | HG01106.hp1 HG01361.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-6853C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702883 | |||||||
| chr2:222702934 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.854-6802A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222702934 | |||||||
| chr2:222703403 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0049 |
3 | HG02055.hp1 HG02717.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.854-6333T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703403 | |||||||
| chr2:222703437 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.854-6299C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703437 | |||||||
| chr2:222703523 | A | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0072 others(20): Show |
25 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.854-6213A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703523 | |||||||
| chr2:222703738 | C | T | 2 | a0005c0005t0001g0271 a0010c0010t0001g0126 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.854-5998C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222703738 | |||||||
| chr2:222703830 | AT | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(115): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.854-5895delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222703830 | ||||||
| chr2:222703917 | A | AC | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.854-5817dupC | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222703917 | ||||||
| chr2:222704054 | A | G | 1 | a0002c0002t0002g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.854-5682A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704054 | |||||||
| chr2:222704109 | T | C | 2 | a0005c0005t0001g0271 a0010c0010t0001g0126 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.854-5627T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704109 | |||||||
| chr2:222704183 | T | C | 2 | a0001c0001t0001g0213 a0003c0003t0001g0287 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.854-5553T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704183 | |||||||
| chr2:222704291 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(109): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.854-5445G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704291 | |||||||
| chr2:222704451 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0221 a0001c0001t0002g0037 |
3 | HG00280.hp2 HG01346.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.854-5285C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704451 | |||||||
| chr2:222704481 | G | A | 2 | a0005c0005t0001g0271 a0010c0010t0001g0126 |
2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.854-5255G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704481 | |||||||
| chr2:222704485 | G | A | 3 | a0002c0002t0001g0138 a0002c0002t0001g0262 a0003c0003t0001g0282 |
3 | HG02451.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.854-5251G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704485 | |||||||
| chr2:222704486 | T | A | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5250T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704486 | |||||||
| chr2:222704492 | T | C | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5244T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704492 | |||||||
| chr2:222704495 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5241A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704495 | |||||||
| chr2:222704503 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854-5233A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704503 | |||||||
| chr2:222704579 | G | C | 2 | a0002c0002t0001g0138 a0002c0002t0001g0262 |
2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.854-5157G>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704579 | |||||||
| chr2:222704618 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0007c0007t0001g0159 |
4 | HG02027.hp1 NA18972.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-5118C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704618 | |||||||
| chr2:222704627 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.854-5109A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704627 | |||||||
| chr2:222704856 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.854-4880G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704856 | |||||||
| chr2:222704909 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.854-4827C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704909 | |||||||
| chr2:222704989 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0180 a0003c0003t0001g0291 |
3 | HG02257.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.854-4747T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222704989 | |||||||
| chr2:222705138 | A | G | 1 | a0003c0003t0001g0282 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.854-4598A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705138 | |||||||
| chr2:222705161 | A | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.854-4575A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705161 | |||||||
| chr2:222705414 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.854-4322C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705414 | |||||||
| chr2:222705442 | C | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0233 |
4 | NA18954.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-4294C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705442 | |||||||
| chr2:222705473 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
12 | HG01106.hp1 HG01243.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.854-4263G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705473 | |||||||
| chr2:222705624 | GT | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 |
4 | HG01243.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-4109delT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222705624 | ||||||
| chr2:222705659 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.854-4077T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705659 | |||||||
| chr2:222705728 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | NA18950.hp1 NA18984.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.854-4008C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222705728 | |||||||
| chr2:222706023 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.854-3713G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706023 | |||||||
| chr2:222706114 | A | C | 1 | a0006c0006t0001g0285 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.854-3622A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706114 | |||||||
| chr2:222706294 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.854-3442G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706294 | |||||||
| chr2:222706344 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0127 a0001c0001t0001g0129 |
4 | HG01243.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-3392G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706344 | |||||||
| chr2:222706469 | T | C | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-3267T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706469 | |||||||
| chr2:222706471 | T | TA | 129 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(126): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.854-3249dupA | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222706471 | ||||||
| chr2:222706488 | T | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.854-3248T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706488 | |||||||
| chr2:222706496 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.854-3240A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706496 | |||||||
| chr2:222706511 | T | C | 4 | a0002c0002t0001g0125 a0002c0002t0001g0138 a0002c0002t0001g0262 others(1): Show |
4 | HG02451.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.854-3225T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706511 | |||||||
| chr2:222706518 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(109): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.854-3218T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706518 | |||||||
| chr2:222706691 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.854-3045A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706691 | |||||||
| chr2:222706726 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.854-3010A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706726 | |||||||
| chr2:222706850 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0195 a0001c0001t0002g0049 |
3 | HG02615.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.854-2886G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706850 | |||||||
| chr2:222706868 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.854-2868C>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706868 | |||||||
| chr2:222706966 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.854-2770A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222706966 | |||||||
| chr2:222707110 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.854-2626T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707110 | |||||||
| chr2:222707219 | C | CAAGG | 8 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0127 others(5): Show |
9 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.854-2500_854-2497d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707219 | ||||||
| chr2:222707281 | GGGAA | G | 3 | a0001c0001t0001g0163 a0004c0004t0001g0241 a0004c0004t0001g0242 |
3 | HG01168.hp1 HG01169.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.854-2438_854-2435d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707281 | ||||||
| chr2:222707337 | AAGAAAGA others(17): Show |
A | 1 | a0001c0001t0001g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.854-2387_854-2364d others(26): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707337 | ||||||
| chr2:222707339 | GAAAGAAA others(3): Show |
G | 15 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0192 others(12): Show |
16 | HG01433.hp1 HG01515.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.854-2385_854-2376d others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707339 | ||||||
| chr2:222707349 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0025 others(37): Show |
43 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.854-2387A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707349 | |||||||
| chr2:222707351 | A | G | 1 | a0003c0003t0001g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.854-2385A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707351 | |||||||
| chr2:222707351 | AAGAAAGA others(3): Show |
A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0025 others(38): Show |
44 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.854-2363_854-2354d others(12): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707351 | ||||||
| chr2:222707361 | G | GAGAA | 81 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0050 others(78): Show |
84 | HG00140.hp1 HG00280.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.854-2367_854-2364d others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707361 | ||||||
| chr2:222707361 | GAGAAAGA others(7): Show |
G | 1 | a0003c0003t0001g0283 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.854-2365_854-2352d others(16): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707361 | ||||||
| chr2:222707371 | G | GAAAT | 11 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0127 others(8): Show |
12 | HG01243.hp1 HG01496.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.854-2364_854-2363i others(6): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707371 | ||||||
| chr2:222707394 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0264 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.854-2342A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707394 | |||||||
| chr2:222707395 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0264 |
2 | HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.854-2341A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707395 | |||||||
| chr2:222707397 | GAGGGAGG others(2): Show |
G | 9 | a0001c0001t0001g0163 a0001c0001t0001g0257 a0002c0002t0001g0024 others(6): Show |
9 | HG01106.hp1 HG01361.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.854-2313_854-2305d others(11): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222707397 | ||||||
| chr2:222707457 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-2279A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707457 | |||||||
| chr2:222707672 | C | A | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-2064C>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707672 | |||||||
| chr2:222707698 | A | C | 5 | a0001c0001t0001g0163 a0002c0002t0001g0151 a0002c0002t0001g0256 others(2): Show |
5 | HG01106.hp1 HG01361.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.854-2038A>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707698 | |||||||
| chr2:222707892 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.854-1844T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707892 | |||||||
| chr2:222707909 | A | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0111 others(3): Show |
7 | HG02129.hp1 NA18945.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.854-1827A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222707909 | |||||||
| chr2:222708066 | C | CT | 15 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0124 others(12): Show |
15 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.854-1662dupT | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222708066 | ||||||
| chr2:222708142 | G | A | 1 | a0002c0002t0001g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.854-1594G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708142 | |||||||
| chr2:222708301 | A | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(146): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.854-1435A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708301 | |||||||
| chr2:222708367 | A | G | 2 | a0001c0001t0001g0213 a0003c0003t0001g0287 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.854-1369A>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708367 | |||||||
| chr2:222708460 | G | A | 5 | a0001c0001t0001g0163 a0002c0002t0001g0151 a0002c0002t0001g0256 others(2): Show |
5 | HG01106.hp1 HG01361.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.854-1276G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708460 | |||||||
| chr2:222708570 | G | T | 13 | a0001c0001t0001g0055 a0001c0001t0001g0124 a0001c0001t0001g0137 others(10): Show |
13 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.854-1166G>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708570 | |||||||
| chr2:222708591 | C | T | 3 | a0002c0002t0001g0023 a0003c0003t0001g0282 a0010c0010t0001g0126 |
3 | HG01109.hp2 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.854-1145C>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708591 | |||||||
| chr2:222708815 | TTGTG | T | 3 | a0001c0001t0001g0181 a0001c0001t0002g0002 a0001c0001t0002g0046 |
6 | HG02622.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-919_854-916del others(4): Show |
MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 222708815 | ||||||
| chr2:222708875 | T | C | 1 | a0001c0014t0001g0021 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.854-861T>C | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222708875 | |||||||
| chr2:222709026 | A | T | 107 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(104): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.854-710A>T | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709026 | |||||||
| chr2:222709107 | G | A | 1 | a0005c0005t0001g0271 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.854-629G>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709107 | |||||||
| chr2:222709358 | T | G | 1 | a0002c0002t0001g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.854-378T>G | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709358 | |||||||
| chr2:222709401 | T | A | 6 | a0001c0001t0001g0163 a0002c0002t0001g0119 a0002c0002t0001g0151 others(3): Show |
6 | HG01106.hp1 HG01361.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-335T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709401 | |||||||
| chr2:222709721 | T | A | 1 | a0002c0002t0001g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.854-15T>A | MOGAT1 | ENSG00000124003.13 | transcript | ENST00000446656.4 | protein_coding | 5/5 | chr2 | 222709721 |