Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2591 |
| ensemblid | ENSG00000115339.14 |
| hgncid | 4125 |
| symbol | GALNT3 |
| name | polypeptide N-acetylgalactosaminyltransferase 3 |
| refseq_nuc | NM_004482.4 |
| refseq_prot | NP_004473.2 |
| ensembl_nuc | ENST00000392701.8 |
| ensembl_prot | ENSP00000376465.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 165747588 |
| end | 165794247 |
| strand | - |
| ver | v1.2 |
| region | chr2:165747588-165794247 |
| region5000 | chr2:165742588-165799247 |
| regionname0 | GALNT3_chr2_165747588_165794247 |
| regionname5000 | GALNT3_chr2_165742588_165799247 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 633 | 378 | 85 | 66 | 172 | 12 | 41 | 130 | GALNT3_chr2_165742588_165799247 | GALNT3 | MAHLK others(628): Show |
chr2 | 165742588 | 165799247 |
| a0002 | 0/0 | 633 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | MAHLK others(628): Show |
chr2 | 165742588 | 165799247 |
| a0003 | 0/0 | 633 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | MAHLK others(628): Show |
chr2 | 165742588 | 165799247 |
| a0004 | 0/0 | 633 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | MAHLK others(628): Show |
chr2 | 165742588 | 165799247 |
| a0005 | 0/0 | 633 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | MAHLK others(628): Show |
chr2 | 165742588 | 165799247 |
| a0006 | 0/0 | 633 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | MAHLK others(628): Show |
chr2 | 165742588 | 165799247 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1899 | 373 | 82 | 65 | 171 | 12 | 41 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0001c0003 | 0/0 | 1899 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0001c0005 | 0/0 | 1899 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0001c0008 | 0/0 | 1899 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0002c0002 | 0/0 | 1899 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0003c0007 | 0/0 | 1899 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0004c0004 | 0/0 | 1899 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0005c0006 | 0/0 | 1899 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 | ||
| a0006c0009 | 0/0 | 1899 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | ATGGC others(1894): Show |
chr2 | 165742588 | 165799247 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3436 | 242 | 56 | 45 | 115 | 4 | 21 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0002 | 0/1 | 3436 | 110 | 16 | 16 | 55 | 5 | 17 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0003 | 0/0 | 3436 | 7 | 0 | 3 | 0 | 2 | 2 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0004 | 0/0 | 3436 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0005 | 0/0 | 3436 | 4 | 3 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0006 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0007 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0008 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0009 | 0/0 | 3436 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0010 | 0/0 | 3436 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0001t0011 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0003t0001 | 0/0 | 3436 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0005t0001 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0001c0008t0001 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0002c0002t0001 | 0/0 | 3436 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0003c0007t0002 | 0/0 | 3436 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0004c0004t0002 | 0/0 | 3436 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0005c0006t0001 | 0/0 | 3436 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| a0006c0009t0002 | 0/0 | 3436 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | AGCTC others(3431): Show |
chr2 | 165742588 | 165799247 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 5 | 6 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0009g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0001t0011g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0003t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0001c0008t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0003c0007t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0004c0004t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0005c0006t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| a0006c0009t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0042 | EUR | GBR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0097 | EUR | GBR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0190 | EUR | GBR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | FIN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | FIN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00423 | hp2 | a0001 | c0005 | t0001 | g0213 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00735 | hp2 | a0001 | c0001 | t0009 | g0140 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00738 | hp1 | a0003 | c0007 | t0002 | g0045 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01433 | hp1 | a0004 | c0004 | t0002 | g0082 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | IBS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CDX | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02615 | hp2 | a0005 | c0006 | t0001 | g0227 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0148 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0205 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03139 | hp2 | a0001 | c0008 | t0001 | g0210 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0249 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03654 | hp2 | a0006 | c0009 | t0002 | g0087 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | BEB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0269 | SAS | STU | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | YRI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | YRI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18969 | hp2 | a0001 | c0001 | t0011 | g0305 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | LWK | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ASW | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ASW | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | GIH | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | GIH | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | ACB | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | MSL | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0057 | REF | REF | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0215 | REF | REF | GALNT3_chr2_165742588_165799247 | GALNT3 | chr2 | 165742588 | 165799247 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:165749816 | C | T | 1 | a0003 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1705G>A | p.Val569Ile | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/11 | 2046/3436 | 1705/1902 | 569/633 | chr2 | 165749816 | |||
| chr2:165759508 | C | T | 1 | a0005 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.901G>A | p.Val301Ile | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 5/11 | 1242/3436 | 901/1902 | 301/633 | chr2 | 165759508 | |||
| chr2:165761944 | C | A | 1 | a0002 | 4 | HG02055.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
missense_variant | MODERATE | c.799G>T | p.Val267Phe | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/11 | 1140/3436 | 799/1902 | 267/633 | chr2 | 165761944 | |||
| chr2:165762010 | T | C | 1 | a0006 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.733A>G | p.Ile245Val | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/11 | 1074/3436 | 733/1902 | 245/633 | chr2 | 165762010 | |||
| chr2:165770300 | C | T | 1 | a0004 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.401G>A | p.Ser134Asn | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/11 | 742/3436 | 401/1902 | 134/633 | chr2 | 165770300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:165759512 | C | A | 1 | a0001c0008 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.897G>T | p.Thr299Thr | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 5/11 | 1238/3436 | 897/1902 | 299/633 | chr2 | 165759512 | |||
| chr2:165764903 | C | T | 1 | a0001c0003 | 3 | HG01106.hp1 HG02559.hp2 HG02630.hp2 |
synonymous_variant | LOW | c.669G>A | p.Val223Val | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/11 | 1010/3436 | 669/1902 | 223/633 | chr2 | 165764903 | |||
| chr2:165770197 | A | G | 1 | a0001c0005 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.504T>C | p.Thr168Thr | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/11 | 845/3436 | 504/1902 | 168/633 | chr2 | 165770197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:165747622 | C | G | 1 | a0001c0001t0008 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1159G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 1159 | chr2 | 165747622 | ||||||
| chr2:165747711 | C | T | 1 | a0001c0001t0007 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1070G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 1070 | chr2 | 165747711 | ||||||
| chr2:165747998 | T | C | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 |
6 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*783A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 783 | chr2 | 165747998 | ||||||
| chr2:165748154 | T | C | 1 | a0001c0001t0010 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*627A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 627 | chr2 | 165748154 | ||||||
| chr2:165748266 | C | T | 2 | a0001c0001t0004 a0001c0001t0007 |
5 | HG02615.hp1 HG02809.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*515G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 515 | chr2 | 165748266 | ||||||
| chr2:165748500 | A | T | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(3): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*281T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 281 | chr2 | 165748500 | ||||||
| chr2:165748509 | C | T | 1 | a0001c0001t0006 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 272 | chr2 | 165748509 | ||||||
| chr2:165748595 | G | A | 1 | a0001c0001t0005 | 4 | HG00140.hp2 HG02486.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*186C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 11/11 | 186 | chr2 | 165748595 | ||||||
| chr2:165794175 | C | A | 1 | a0001c0001t0011 | 1 | NA18969.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-269G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/11 | chr2 | 165794175 | |||||||
| chr2:165794201 | A | T | 1 | a0001c0001t0003 | 7 | HG00099.hp2 HG00280.hp2 HG01106.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-295T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/11 | 23501 | chr2 | 165794201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:165748931 | A | AT | 4 | a0001c0001t0004g0224 a0001c0001t0004g0226 a0001c0001t0004g0228 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1780-29_1780-28ins others(1): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165748931 | |||||||
| chr2:165749017 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1780-114C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749017 | |||||||
| chr2:165749270 | G | C | 1 | a0001c0001t0001g0300 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1780-367C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749270 | |||||||
| chr2:165749279 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1780-376T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749279 | |||||||
| chr2:165749290 | A | G | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1780-387T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749290 | |||||||
| chr2:165749307 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1780-404T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749307 | |||||||
| chr2:165749370 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1779+372T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749370 | |||||||
| chr2:165749417 | A | C | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1779+325T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749417 | |||||||
| chr2:165749435 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1779+307A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749435 | |||||||
| chr2:165749483 | C | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1779+259G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749483 | |||||||
| chr2:165749504 | A | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0138 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1779+238T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749504 | |||||||
| chr2:165749632 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1779+110C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 10/10 | chr2 | 165749632 | |||||||
| chr2:165749912 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1627-18G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165749912 | |||||||
| chr2:165749935 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1627-41A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165749935 | |||||||
| chr2:165750035 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1627-141G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165750035 | |||||||
| chr2:165750109 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(294): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1627-215C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165750109 | |||||||
| chr2:165750413 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0002g0050 |
2 | HG01099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1627-519C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165750413 | |||||||
| chr2:165750483 | G | T | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1627-589C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165750483 | |||||||
| chr2:165750505 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(6): Show |
14 | HG00544.hp2 HG00642.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1627-611G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165750505 | |||||||
| chr2:165750710 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1627-816T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165750710 | |||||||
| chr2:165750743 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1627-849A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165750743 | |||||||
| chr2:165751014 | A | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1627-1120T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751014 | |||||||
| chr2:165751015 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1627-1121A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751015 | |||||||
| chr2:165751056 | G | A | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1627-1162C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751056 | |||||||
| chr2:165751145 | C | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0225 |
3 | HG02723.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1627-1251G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751145 | |||||||
| chr2:165751203 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627-1309C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751203 | |||||||
| chr2:165751236 | T | C | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1627-1342A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751236 | |||||||
| chr2:165751277 | A | G | 4 | a0001c0001t0004g0224 a0001c0001t0004g0226 a0001c0001t0004g0228 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1627-1383T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751277 | |||||||
| chr2:165751888 | G | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02572.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1627-1994C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751888 | |||||||
| chr2:165751903 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1627-2009G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165751903 | |||||||
| chr2:165752119 | C | T | 4 | a0001c0001t0002g0118 a0001c0001t0002g0120 a0001c0001t0002g0176 others(1): Show |
4 | HG02071.hp2 NA18943.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627-2225G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165752119 | |||||||
| chr2:165752157 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1627-2263G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165752157 | |||||||
| chr2:165752405 | T | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0225 |
3 | HG02723.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1626+2222A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165752405 | |||||||
| chr2:165752649 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1626+1978G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165752649 | |||||||
| chr2:165752875 | A | G | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1626+1752T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165752875 | |||||||
| chr2:165752972 | G | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
8 | HG00597.hp1 HG02074.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.1626+1655C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165752972 | |||||||
| chr2:165753015 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1626+1612G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165753015 | |||||||
| chr2:165753213 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0214 a0001c0001t0001g0216 others(2): Show |
5 | HG02572.hp2 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+1414C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165753213 | |||||||
| chr2:165753282 | C | T | 5 | a0001c0001t0002g0097 a0001c0001t0002g0111 a0001c0001t0003g0003 others(2): Show |
9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626+1345G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165753282 | |||||||
| chr2:165753595 | G | A | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1626+1032C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165753595 | |||||||
| chr2:165753653 | G | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1626+974C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165753653 | |||||||
| chr2:165753902 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1626+725T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165753902 | |||||||
| chr2:165754159 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
108 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1626+468C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754159 | |||||||
| chr2:165754233 | G | T | 4 | a0001c0001t0004g0224 a0001c0001t0004g0226 a0001c0001t0004g0228 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1626+394C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754233 | |||||||
| chr2:165754250 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1626+377G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754250 | |||||||
| chr2:165754251 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1626+376C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754251 | |||||||
| chr2:165754271 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0218 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1626+356C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754271 | |||||||
| chr2:165754317 | C | T | 94 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1626+310G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754317 | |||||||
| chr2:165754392 | CT | C | 9 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0203 others(6): Show |
9 | HG01358.hp2 HG02074.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1626+234delA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754392 | |||||||
| chr2:165754392 | CTT | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1626+233_1626+234d others(4): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754392 | |||||||
| chr2:165754392 | CTTT | C | 38 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0079 others(35): Show |
45 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1626+232_1626+234d others(5): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754392 | |||||||
| chr2:165754392 | CTTTT | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(21): Show |
33 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1626+231_1626+234d others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754392 | |||||||
| chr2:165754462 | CA | C | 94 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1626+164delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754462 | |||||||
| chr2:165754496 | C | T | 94 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1626+131G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754496 | |||||||
| chr2:165754576 | C | T | 94 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1626+51G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 9/10 | chr2 | 165754576 | |||||||
| chr2:165754758 | T | C | 1 | a0001c0001t0007g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1525-30A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 8/10 | chr2 | 165754758 | |||||||
| chr2:165754886 | G | C | 1 | a0001c0001t0002g0064 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1524+46C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 8/10 | chr2 | 165754886 | |||||||
| chr2:165755165 | T | A | 1 | a0001c0001t0001g0257 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1393-102A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165755165 | |||||||
| chr2:165755264 | C | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(294): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1393-201G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165755264 | |||||||
| chr2:165755456 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1393-393A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165755456 | |||||||
| chr2:165755670 | T | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0108 others(3): Show |
10 | HG02129.hp1 NA18951.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.1393-607A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165755670 | |||||||
| chr2:165755767 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1393-704C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165755767 | |||||||
| chr2:165755828 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1393-765G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165755828 | |||||||
| chr2:165755995 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1393-932A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165755995 | |||||||
| chr2:165756146 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1392+901C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165756146 | |||||||
| chr2:165756639 | A | T | 1 | a0001c0001t0002g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1392+408T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165756639 | |||||||
| chr2:165756733 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
198 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(195): Show |
intron_variant | MODIFIER | c.1392+314C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165756733 | |||||||
| chr2:165756862 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1392+185A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165756862 | |||||||
| chr2:165756919 | T | C | 7 | a0001c0001t0001g0216 a0001c0001t0004g0139 a0001c0001t0004g0224 others(4): Show |
7 | HG00735.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1392+128A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 7/10 | chr2 | 165756919 | |||||||
| chr2:165757331 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1192-84A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757331 | |||||||
| chr2:165757458 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0218 |
2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1192-211A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757458 | |||||||
| chr2:165757584 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0162 |
2 | HG00673.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1192-337T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757584 | |||||||
| chr2:165757599 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1192-352C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757599 | |||||||
| chr2:165757611 | T | C | 4 | a0001c0001t0002g0010 a0001c0001t0002g0048 a0001c0001t0002g0071 others(1): Show |
6 | HG00438.hp2 HG00544.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-364A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757611 | |||||||
| chr2:165757765 | A | T | 1 | a0001c0001t0002g0116 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1192-518T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757765 | |||||||
| chr2:165757809 | CA | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1192-563delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757809 | |||||||
| chr2:165757907 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0096 |
2 | HG00323.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.1192-660A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757907 | |||||||
| chr2:165757978 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1192-731T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165757978 | |||||||
| chr2:165758067 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
211 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(208): Show |
intron_variant | MODIFIER | c.1191+680A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758067 | |||||||
| chr2:165758269 | G | A | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1191+478C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758269 | |||||||
| chr2:165758382 | T | C | 4 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0052 others(1): Show |
6 | HG02027.hp2 HG02080.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1191+365A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758382 | |||||||
| chr2:165758514 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1191+233G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758514 | |||||||
| chr2:165758558 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1191+189G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758558 | |||||||
| chr2:165758588 | T | G | 1 | a0001c0001t0002g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1191+159A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758588 | |||||||
| chr2:165758594 | G | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0138 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1191+153C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758594 | |||||||
| chr2:165758604 | T | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0066 others(12): Show |
20 | HG00597.hp2 HG01192.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.1191+143A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 6/10 | chr2 | 165758604 | |||||||
| chr2:165759045 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
206 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.1074-181G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 5/10 | chr2 | 165759045 | |||||||
| chr2:165759601 | T | C | 1 | a0001c0001t0004g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.839-31A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165759601 | |||||||
| chr2:165759854 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.839-284C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165759854 | |||||||
| chr2:165759980 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.839-410T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165759980 | |||||||
| chr2:165760050 | T | C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0035 others(13): Show |
20 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.839-480A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760050 | |||||||
| chr2:165760144 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0004g0139 |
2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.839-574A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760144 | |||||||
| chr2:165760157 | A | G | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.839-587T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760157 | |||||||
| chr2:165760261 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.839-691A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760261 | |||||||
| chr2:165760282 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.839-712C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760282 | |||||||
| chr2:165760305 | G | C | 1 | a0001c0001t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.839-735C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760305 | |||||||
| chr2:165760428 | G | T | 1 | a0001c0001t0002g0100 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.839-858C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760428 | |||||||
| chr2:165760483 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.839-913G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760483 | |||||||
| chr2:165760722 | G | A | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.839-1152C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760722 | |||||||
| chr2:165760726 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0241 a0001c0001t0001g0259 |
4 | NA18949.hp1 NA18971.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.839-1156A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760726 | |||||||
| chr2:165760782 | C | G | 1 | a0001c0001t0002g0069 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.838+1123G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760782 | |||||||
| chr2:165760885 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.838+1020C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165760885 | |||||||
| chr2:165761005 | G | T | 4 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+900C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761005 | |||||||
| chr2:165761014 | C | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.838+891G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761014 | |||||||
| chr2:165761073 | G | A | 7 | a0001c0001t0001g0141 a0001c0001t0001g0192 a0001c0001t0001g0193 others(4): Show |
7 | HG02572.hp2 HG02723.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.838+832C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761073 | |||||||
| chr2:165761116 | T | TA | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
258 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(255): Show |
intron_variant | MODIFIER | c.838+788dupT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761116 | |||||||
| chr2:165761147 | A | G | 93 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(90): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.838+758T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761147 | |||||||
| chr2:165761172 | G | A | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.838+733C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761172 | |||||||
| chr2:165761215 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.838+690A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761215 | |||||||
| chr2:165761510 | C | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.838+395G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761510 | |||||||
| chr2:165761526 | A | G | 8 | a0001c0001t0001g0141 a0001c0001t0001g0192 a0001c0001t0001g0193 others(5): Show |
8 | HG02572.hp2 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.838+379T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761526 | |||||||
| chr2:165761563 | AAAAC | A | 105 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(102): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.838+338_838+341del others(4): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761563 | |||||||
| chr2:165761617 | G | GA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
205 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.838+287dupT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761617 | |||||||
| chr2:165761632 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0186 |
2 | NA19003.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.838+273C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761632 | |||||||
| chr2:165761680 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.838+225A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761680 | |||||||
| chr2:165761752 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(118): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.838+153G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761752 | |||||||
| chr2:165761791 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.838+114G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 4/10 | chr2 | 165761791 | |||||||
| chr2:165762124 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.689-70C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762124 | |||||||
| chr2:165762233 | C | A | 1 | a0001c0001t0007g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.689-179G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762233 | |||||||
| chr2:165762278 | C | CATAAGTA others(5): Show |
1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.689-225_689-224ins others(12): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762278 | |||||||
| chr2:165762280 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.689-226A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762280 | |||||||
| chr2:165762283 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.689-229A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762283 | |||||||
| chr2:165762284 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.689-230G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762284 | |||||||
| chr2:165762288 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.689-234T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762288 | |||||||
| chr2:165762293 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.689-239A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762293 | |||||||
| chr2:165762295 | C | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0171 a0001c0001t0001g0201 |
3 | HG01071.hp2 HG02040.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.689-241G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762295 | |||||||
| chr2:165762298 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.689-244A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762298 | |||||||
| chr2:165762314 | G | A | 40 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0016 others(37): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(48): Show |
intron_variant | MODIFIER | c.689-260C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762314 | |||||||
| chr2:165762451 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01496.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.689-397C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762451 | |||||||
| chr2:165762685 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.689-631T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762685 | |||||||
| chr2:165762697 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.689-643T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762697 | |||||||
| chr2:165762876 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.689-822C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762876 | |||||||
| chr2:165762893 | A | G | 1 | a0001c0005t0001g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.689-839T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762893 | |||||||
| chr2:165762968 | CT | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(281): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.689-915delA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762968 | |||||||
| chr2:165762989 | C | T | 4 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 others(1): Show |
4 | HG02055.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-935G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762989 | |||||||
| chr2:165762997 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.689-943G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165762997 | |||||||
| chr2:165763458 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0084 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.689-1404C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165763458 | |||||||
| chr2:165764013 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0161 |
2 | HG02040.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.688+871A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764013 | |||||||
| chr2:165764022 | G | A | 1 | a0005c0006t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.688+862C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764022 | |||||||
| chr2:165764126 | C | G | 96 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.688+758G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764126 | |||||||
| chr2:165764182 | G | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+702C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764182 | |||||||
| chr2:165764354 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0240 a0004c0004t0002g0082 |
4 | HG01433.hp1 HG02602.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+530C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764354 | |||||||
| chr2:165764512 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.688+372A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764512 | |||||||
| chr2:165764549 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.688+335G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764549 | |||||||
| chr2:165764678 | T | G | 4 | a0001c0001t0004g0224 a0001c0001t0004g0226 a0001c0001t0004g0228 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+206A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764678 | |||||||
| chr2:165764726 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
125 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.688+158C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764726 | |||||||
| chr2:165764780 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.688+104A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764780 | |||||||
| chr2:165764794 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.688+90A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764794 | |||||||
| chr2:165764803 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.688+81C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764803 | |||||||
| chr2:165764852 | G | C | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.688+32C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764852 | |||||||
| chr2:165764860 | T | A | 1 | a0001c0001t0011g0305 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.688+24A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 3/10 | chr2 | 165764860 | |||||||
| chr2:165765359 | A | C | 8 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0044 others(5): Show |
11 | HG02258.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-303T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765359 | |||||||
| chr2:165765497 | AT | A | 102 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0046 others(99): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.516-442delA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765497 | |||||||
| chr2:165765508 | TTTATGGA others(9): Show |
T | 1 | a0001c0001t0002g0067 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.516-468_516-453del others(16): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765508 | |||||||
| chr2:165765526 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.516-470C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765526 | |||||||
| chr2:165765542 | T | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0024 others(61): Show |
76 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.516-486A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765542 | |||||||
| chr2:165765590 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0301 others(4): Show |
10 | HG00423.hp2 NA18940.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-534G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765590 | |||||||
| chr2:165765599 | C | T | 91 | a0001c0001t0001g0046 a0001c0001t0002g0009 a0001c0001t0002g0010 others(88): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.516-543G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765599 | |||||||
| chr2:165765665 | T | A | 1 | a0001c0001t0004g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.516-609A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765665 | |||||||
| chr2:165765978 | G | C | 1 | a0001c0001t0002g0194 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.516-922C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165765978 | |||||||
| chr2:165766027 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.516-971G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766027 | |||||||
| chr2:165766088 | C | G | 94 | a0001c0001t0001g0046 a0001c0001t0002g0009 a0001c0001t0002g0010 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.516-1032G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766088 | |||||||
| chr2:165766236 | A | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0225 |
3 | HG02723.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.516-1180T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766236 | |||||||
| chr2:165766439 | C | T | 1 | a0001c0001t0007g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.516-1383G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766439 | |||||||
| chr2:165766454 | A | T | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(297): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.516-1398T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766454 | |||||||
| chr2:165766652 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.516-1596T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766652 | |||||||
| chr2:165766661 | T | TGGCTGTA others(121): Show |
94 | a0001c0001t0001g0046 a0001c0001t0002g0009 a0001c0001t0002g0010 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.516-1606_516-1605i others(130): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766661 | |||||||
| chr2:165766678 | T | A | 94 | a0001c0001t0001g0046 a0001c0001t0002g0009 a0001c0001t0002g0010 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.516-1622A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766678 | |||||||
| chr2:165766720 | G | A | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.516-1664C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766720 | |||||||
| chr2:165766768 | T | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0035 others(12): Show |
19 | HG01255.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.516-1712A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165766768 | |||||||
| chr2:165767015 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516-1959G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767015 | |||||||
| chr2:165767028 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.516-1972G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767028 | |||||||
| chr2:165767037 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0185 |
3 | NA18961.hp1 NA19057.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.516-1981G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767037 | |||||||
| chr2:165767171 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0079 others(4): Show |
8 | HG01255.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.516-2115A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767171 | |||||||
| chr2:165767299 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.516-2243T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767299 | |||||||
| chr2:165767381 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.516-2325A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767381 | |||||||
| chr2:165767484 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.516-2428C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767484 | |||||||
| chr2:165767537 | C | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(280): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.516-2481G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767537 | |||||||
| chr2:165767678 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.515+2508A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767678 | |||||||
| chr2:165767681 | C | A | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.515+2505G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767681 | |||||||
| chr2:165767766 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(299): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.515+2420C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767766 | |||||||
| chr2:165767786 | C | G | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.515+2400G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767786 | |||||||
| chr2:165767865 | A | C | 1 | a0005c0006t0001g0227 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.515+2321T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767865 | |||||||
| chr2:165767868 | TC | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | HG01256.hp2 HG01258.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.515+2317delG | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767868 | |||||||
| chr2:165767869 | C | CT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0091 others(10): Show |
17 | HG00597.hp2 HG00735.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.515+2316dupA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767869 | |||||||
| chr2:165767869 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0114 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.515+2307_515+2316d others(12): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767869 | |||||||
| chr2:165767869 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0122 |
2 | NA18970.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.515+2306_515+2316d others(13): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767869 | |||||||
| chr2:165767869 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.515+2317G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767869 | |||||||
| chr2:165767869 | CT | C | 97 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0020 others(94): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.515+2316delA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767869 | |||||||
| chr2:165767869 | CTT | C | 94 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(91): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.515+2315_515+2316d others(4): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767869 | |||||||
| chr2:165767959 | C | T | 76 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0117 others(73): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.515+2227G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165767959 | |||||||
| chr2:165768019 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(294): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.515+2167C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768019 | |||||||
| chr2:165768067 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.515+2119A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768067 | |||||||
| chr2:165768228 | A | G | 1 | a0001c0001t0005g0298 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.515+1958T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768228 | |||||||
| chr2:165768233 | T | G | 10 | a0001c0001t0001g0199 a0001c0001t0001g0212 a0001c0001t0001g0216 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.515+1953A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768233 | |||||||
| chr2:165768287 | T | C | 4 | a0001c0001t0001g0225 a0001c0001t0004g0139 a0001c0001t0009g0140 others(1): Show |
4 | HG00735.hp2 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+1899A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768287 | |||||||
| chr2:165768397 | A | G | 1 | a0001c0001t0009g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.515+1789T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768397 | |||||||
| chr2:165768439 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(6): Show |
10 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.515+1747T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768439 | |||||||
| chr2:165768472 | CT | C | 41 | a0001c0001t0001g0091 a0001c0001t0001g0188 a0001c0001t0002g0009 others(38): Show |
49 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.515+1713delA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768472 | |||||||
| chr2:165768554 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(296): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.515+1632G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768554 | |||||||
| chr2:165768630 | T | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0301 others(4): Show |
10 | HG00423.hp2 NA18940.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+1556A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768630 | |||||||
| chr2:165768766 | T | C | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.515+1420A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768766 | |||||||
| chr2:165768792 | CT | C | 129 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0020 others(126): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.515+1393delA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768792 | |||||||
| chr2:165768792 | CTT | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(167): Show |
220 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.515+1392_515+1393d others(4): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768792 | |||||||
| chr2:165768825 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.515+1361C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768825 | |||||||
| chr2:165768852 | C | T | 1 | a0001c0001t0004g0224 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.515+1334G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165768852 | |||||||
| chr2:165769222 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.515+964T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769222 | |||||||
| chr2:165769278 | T | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.515+908A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769278 | |||||||
| chr2:165769298 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.515+888G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769298 | |||||||
| chr2:165769321 | G | A | 4 | a0001c0001t0002g0010 a0001c0001t0002g0048 a0001c0001t0002g0071 others(1): Show |
6 | HG00438.hp2 HG00544.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.515+865C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769321 | |||||||
| chr2:165769322 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.515+864G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769322 | |||||||
| chr2:165769376 | A | G | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.515+810T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769376 | |||||||
| chr2:165769407 | A | AAAT | 69 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(66): Show |
86 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.515+776_515+778dup others(3): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769407 | |||||||
| chr2:165769407 | A | AAATAAT | 63 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0068 others(60): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.515+773_515+778dup others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769407 | |||||||
| chr2:165769407 | A | AAATAATA others(2): Show |
21 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0091 others(18): Show |
24 | HG00099.hp1 HG00099.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.515+770_515+778dup others(9): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769407 | |||||||
| chr2:165769407 | A | AAATAATA others(5): Show |
2 | a0001c0001t0002g0092 a0001c0001t0002g0116 |
2 | HG01884.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.515+767_515+778dup others(12): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769407 | |||||||
| chr2:165769407 | AAAT | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(64): Show |
98 | HG00597.hp1 HG00609.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.515+776_515+778del others(3): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769407 | |||||||
| chr2:165769407 | AAATAATA others(2): Show |
A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0301 others(9): Show |
15 | HG00423.hp2 NA18940.hp1 NA18948.hp1 others(12): Show |
intron_variant | MODIFIER | c.515+770_515+778del others(9): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769407 | |||||||
| chr2:165769437 | T | TAATAATA others(6): Show |
6 | a0001c0001t0002g0021 a0001c0001t0002g0055 a0001c0001t0002g0062 others(3): Show |
7 | HG00438.hp1 HG02071.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+748_515+749ins others(13): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769437 | |||||||
| chr2:165769437 | TAATA | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.515+745_515+748del others(4): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769437 | |||||||
| chr2:165769440 | TA | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0088 others(12): Show |
22 | HG00597.hp2 HG00621.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.515+745delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769440 | |||||||
| chr2:165769441 | A | AAT | 13 | a0001c0001t0001g0066 a0001c0001t0001g0108 a0001c0001t0001g0112 others(10): Show |
13 | HG02040.hp2 HG02615.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.515+744_515+745ins others(2): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769441 | |||||||
| chr2:165769441 | A | AATAAT | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0002c0002t0001g0204 |
3 | HG02486.hp2 HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.515+744_515+745ins others(5): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769441 | |||||||
| chr2:165769445 | A | AAT | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.515+740_515+741ins others(2): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769445 | |||||||
| chr2:165769449 | A | G | 1 | a0001c0001t0001g0302 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.515+737T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769449 | |||||||
| chr2:165769463 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.515+723A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769463 | |||||||
| chr2:165769643 | T | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01358.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.515+543A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769643 | |||||||
| chr2:165769837 | T | C | 1 | a0001c0001t0002g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.515+349A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769837 | |||||||
| chr2:165769909 | T | A | 1 | a0001c0001t0001g0035 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.515+277A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165769909 | |||||||
| chr2:165770096 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(73): Show |
107 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.515+90C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165770096 | |||||||
| chr2:165770109 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.515+77A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 2/10 | chr2 | 165770109 | |||||||
| chr2:165771510 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-108-702C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165771510 | |||||||
| chr2:165771605 | AC | A | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-798delG | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165771605 | |||||||
| chr2:165772004 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-108-1196T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772004 | |||||||
| chr2:165772304 | G | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0026 others(57): Show |
72 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.-108-1496C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772304 | |||||||
| chr2:165772375 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-108-1567T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772375 | |||||||
| chr2:165772538 | T | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01358.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-108-1730A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772538 | |||||||
| chr2:165772584 | C | CA | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(148): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-108-1777dupT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772584 | |||||||
| chr2:165772584 | C | CAA | 35 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0035 others(32): Show |
44 | HG00280.hp1 HG00438.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-108-1778_-108-177 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772584 | |||||||
| chr2:165772584 | C | CAAA | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(48): Show |
65 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-108-1779_-108-177 others(7): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772584 | |||||||
| chr2:165772584 | C | CAAAA | 22 | a0001c0001t0001g0029 a0001c0001t0001g0142 a0001c0001t0001g0147 others(19): Show |
23 | HG00423.hp2 HG00621.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-108-1780_-108-177 others(8): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772584 | |||||||
| chr2:165772584 | CA | C | 7 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0217 others(4): Show |
7 | HG01496.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-108-1777delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772584 | |||||||
| chr2:165772584 | CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-108-1786_-108-177 others(14): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772584 | |||||||
| chr2:165772584 | CAAAAAAA others(4): Show |
C | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-108-1787_-108-177 others(15): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772584 | |||||||
| chr2:165772619 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-108-1811T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772619 | |||||||
| chr2:165772632 | G | C | 1 | a0001c0001t0005g0190 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-108-1824C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772632 | |||||||
| chr2:165772842 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-108-2034T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165772842 | |||||||
| chr2:165773125 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-108-2317A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773125 | |||||||
| chr2:165773325 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-108-2517A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773325 | |||||||
| chr2:165773451 | A | G | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-2643T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773451 | |||||||
| chr2:165773797 | T | TA | 39 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0035 others(36): Show |
46 | HG01123.hp2 HG01243.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.-108-2990dupT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773797 | |||||||
| chr2:165773797 | T | TAA | 15 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(12): Show |
24 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-108-2991_-108-299 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773797 | |||||||
| chr2:165773803 | A | C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-108-2995T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773803 | |||||||
| chr2:165773871 | C | A | 7 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0044 others(4): Show |
10 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-3063G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773871 | |||||||
| chr2:165773977 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-108-3169C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165773977 | |||||||
| chr2:165774000 | T | G | 2 | a0001c0001t0001g0225 a0005c0006t0001g0227 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-108-3192A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774000 | |||||||
| chr2:165774033 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-108-3225G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774033 | |||||||
| chr2:165774075 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-108-3267G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774075 | |||||||
| chr2:165774174 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-108-3366C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774174 | |||||||
| chr2:165774197 | C | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
85 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.-108-3389G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774197 | |||||||
| chr2:165774221 | A | C | 7 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0044 others(4): Show |
10 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-3413T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774221 | |||||||
| chr2:165774411 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0145 |
3 | HG00544.hp2 HG02165.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-108-3603C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774411 | |||||||
| chr2:165774564 | CA | C | 4 | a0001c0001t0001g0225 a0001c0001t0004g0139 a0001c0001t0009g0140 others(1): Show |
4 | HG00735.hp2 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-3757delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774564 | |||||||
| chr2:165774706 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-108-3898T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774706 | |||||||
| chr2:165774909 | C | CT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(87): Show |
119 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.-108-4102dupA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774909 | |||||||
| chr2:165774909 | C | CTT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0209 a0001c0001t0001g0293 others(11): Show |
20 | HG00642.hp1 HG00735.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-108-4103_-108-410 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774909 | |||||||
| chr2:165774909 | C | CTTT | 12 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0291 others(9): Show |
15 | HG00423.hp2 HG02451.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-4104_-108-410 others(7): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774909 | |||||||
| chr2:165774911 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0084 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-108-4103A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774911 | |||||||
| chr2:165774913 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0084 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-108-4105A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774913 | |||||||
| chr2:165774936 | A | T | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-108-4128T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774936 | |||||||
| chr2:165774962 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-108-4154G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165774962 | |||||||
| chr2:165775028 | T | G | 1 | a0001c0001t0002g0081 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-108-4220A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775028 | |||||||
| chr2:165775083 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-108-4275C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775083 | |||||||
| chr2:165775255 | GA | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(15): Show |
27 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.-108-4448delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775255 | |||||||
| chr2:165775315 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0084 |
2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-108-4507A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775315 | |||||||
| chr2:165775354 | A | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-108-4546T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775354 | |||||||
| chr2:165775508 | T | C | 1 | a0004c0004t0002g0082 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-108-4700A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775508 | |||||||
| chr2:165775537 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-4729C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775537 | |||||||
| chr2:165775548 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-108-4740A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775548 | |||||||
| chr2:165775675 | A | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-108-4867T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775675 | |||||||
| chr2:165775985 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-108-5177T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165775985 | |||||||
| chr2:165776016 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-108-5208A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776016 | |||||||
| chr2:165776106 | G | T | 1 | a0006c0009t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-108-5298C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776106 | |||||||
| chr2:165776193 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-108-5385G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776193 | |||||||
| chr2:165776201 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-108-5393G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776201 | |||||||
| chr2:165776254 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-108-5446G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776254 | |||||||
| chr2:165776364 | A | G | 4 | a0001c0001t0001g0225 a0001c0001t0004g0139 a0001c0001t0009g0140 others(1): Show |
4 | HG00735.hp2 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-5556T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776364 | |||||||
| chr2:165776713 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-108-5905C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776713 | |||||||
| chr2:165776745 | T | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0142 a0001c0001t0001g0191 others(7): Show |
13 | HG00140.hp2 HG01261.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-108-5937A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165776745 | |||||||
| chr2:165777095 | GA | G | 4 | a0001c0001t0001g0225 a0001c0001t0004g0139 a0001c0001t0009g0140 others(1): Show |
4 | HG00735.hp2 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-6288delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777095 | |||||||
| chr2:165777217 | G | A | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-108-6409C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777217 | |||||||
| chr2:165777399 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-6591G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777399 | |||||||
| chr2:165777459 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-108-6651G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777459 | |||||||
| chr2:165777504 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-108-6696G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777504 | |||||||
| chr2:165777536 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0047 |
3 | HG01255.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-108-6728T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777536 | |||||||
| chr2:165777647 | T | G | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-108-6839A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777647 | |||||||
| chr2:165777793 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-108-6985C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165777793 | |||||||
| chr2:165778024 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0044 others(4): Show |
10 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-7216G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778024 | |||||||
| chr2:165778029 | A | C | 1 | a0001c0001t0004g0228 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-108-7221T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778029 | |||||||
| chr2:165778133 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-108-7325A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778133 | |||||||
| chr2:165778153 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-108-7345T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778153 | |||||||
| chr2:165778173 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108-7365G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778173 | |||||||
| chr2:165778203 | C | G | 1 | a0001c0001t0002g0163 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-108-7395G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778203 | |||||||
| chr2:165778735 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-108-7927G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778735 | |||||||
| chr2:165778762 | G | C | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-7954C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778762 | |||||||
| chr2:165778890 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-108-8082C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778890 | |||||||
| chr2:165778910 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-108-8102C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778910 | |||||||
| chr2:165778933 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-8125C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778933 | |||||||
| chr2:165778935 | GT | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(294): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-108-8128delA | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165778935 | |||||||
| chr2:165779025 | C | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-108-8217G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165779025 | |||||||
| chr2:165779229 | CCAGTGCC others(5): Show |
C | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-8433_-108-842 others(16): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165779229 | |||||||
| chr2:165779704 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-108-8896A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165779704 | |||||||
| chr2:165779850 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-108-9042G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165779850 | |||||||
| chr2:165780159 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-108-9351T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780159 | |||||||
| chr2:165780190 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-108-9382A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780190 | |||||||
| chr2:165780398 | T | G | 7 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0044 others(4): Show |
10 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-9590A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780398 | |||||||
| chr2:165780413 | T | C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-108-9605A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780413 | |||||||
| chr2:165780477 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-108-9669C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780477 | |||||||
| chr2:165780555 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-108-9747G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780555 | |||||||
| chr2:165780606 | T | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-108-9798A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780606 | |||||||
| chr2:165780610 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-108-9802A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780610 | |||||||
| chr2:165780641 | G | T | 4 | a0001c0001t0002g0067 a0002c0002t0001g0204 a0002c0002t0001g0205 others(1): Show |
4 | HG02135.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-9833C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780641 | |||||||
| chr2:165780646 | T | TTTG | 9 | a0001c0001t0001g0256 a0001c0001t0001g0291 a0001c0001t0001g0292 others(6): Show |
9 | HG00099.hp1 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-9841_-108-983 others(7): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780646 | |||||||
| chr2:165780646 | TTTGTTG | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0191 a0001c0001t0001g0244 others(1): Show |
6 | HG00609.hp2 HG02922.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-9844_-108-983 others(10): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780646 | |||||||
| chr2:165780648 | TG | T | 6 | a0001c0001t0001g0141 a0001c0001t0001g0146 a0001c0001t0001g0162 others(3): Show |
6 | HG00673.hp1 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-9841delC | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780648 | |||||||
| chr2:165780649 | G | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.-108-9841C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780649 | |||||||
| chr2:165780652 | G | T | 16 | a0001c0001t0001g0066 a0001c0001t0001g0088 a0001c0001t0001g0108 others(13): Show |
16 | HG00738.hp1 HG01978.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.-108-9844C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780652 | |||||||
| chr2:165780655 | G | T | 6 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-9847C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780655 | |||||||
| chr2:165780673 | G | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0301 others(3): Show |
9 | NA18940.hp1 NA18948.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-9865C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780673 | |||||||
| chr2:165780676 | G | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-108-9868C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780676 | |||||||
| chr2:165780752 | C | T | 4 | a0001c0001t0001g0225 a0001c0001t0004g0139 a0001c0001t0009g0140 others(1): Show |
4 | HG00735.hp2 HG02615.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-9944G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780752 | |||||||
| chr2:165780837 | G | C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0265 a0001c0001t0001g0278 |
3 | HG02683.hp2 HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-108-10029C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780837 | |||||||
| chr2:165780875 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-10067G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780875 | |||||||
| chr2:165780920 | T | C | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-108-10112A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780920 | |||||||
| chr2:165780955 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-108-10147T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780955 | |||||||
| chr2:165780977 | C | A | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-108-10169G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165780977 | |||||||
| chr2:165781101 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-108-10293C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781101 | |||||||
| chr2:165781106 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-108-10298G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781106 | |||||||
| chr2:165781121 | T | C | 5 | a0001c0001t0002g0061 a0001c0001t0002g0109 a0001c0001t0002g0123 others(2): Show |
5 | HG01074.hp2 HG01123.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-10313A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781121 | |||||||
| chr2:165781124 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-108-10316G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781124 | |||||||
| chr2:165781163 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-108-10355A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781163 | |||||||
| chr2:165781182 | G | A | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-108-10374C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781182 | |||||||
| chr2:165781263 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
5 | HG00597.hp1 HG02074.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.-108-10455C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781263 | |||||||
| chr2:165781335 | C | T | 10 | a0001c0001t0002g0012 a0001c0001t0002g0094 a0001c0001t0002g0096 others(7): Show |
16 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-108-10527G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781335 | |||||||
| chr2:165781454 | G | A | 2 | a0001c0001t0004g0139 a0001c0001t0009g0140 |
2 | HG00735.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-108-10646C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781454 | |||||||
| chr2:165781459 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-108-10651A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781459 | |||||||
| chr2:165781509 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-108-10701T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781509 | |||||||
| chr2:165781807 | C | T | 5 | a0001c0001t0002g0021 a0001c0001t0002g0055 a0001c0001t0002g0062 others(2): Show |
6 | HG00438.hp1 HG02071.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-10999G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781807 | |||||||
| chr2:165781833 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-108-11025T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781833 | |||||||
| chr2:165781885 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01496.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-108-11077T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781885 | |||||||
| chr2:165781961 | G | A | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-108-11153C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781961 | |||||||
| chr2:165781965 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0301 others(3): Show |
9 | NA18940.hp1 NA18948.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.-108-11157G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781965 | |||||||
| chr2:165781971 | G | C | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG01175.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-108-11163C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165781971 | |||||||
| chr2:165782078 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-108-11270C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782078 | |||||||
| chr2:165782229 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0244 |
4 | NA18955.hp2 NA19064.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-11421A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782229 | |||||||
| chr2:165782257 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-108-11449G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782257 | |||||||
| chr2:165782357 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-108-11549G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782357 | |||||||
| chr2:165782392 | CA | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(287): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-108-11585delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782392 | |||||||
| chr2:165782486 | G | A | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-109+11529C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782486 | |||||||
| chr2:165782815 | T | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+11200A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782815 | |||||||
| chr2:165782837 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-109+11178C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782837 | |||||||
| chr2:165782862 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+11153T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782862 | |||||||
| chr2:165782914 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-109+11101A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782914 | |||||||
| chr2:165782928 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-109+11087G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782928 | |||||||
| chr2:165782966 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+11049G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165782966 | |||||||
| chr2:165783009 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-109+11006A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165783009 | |||||||
| chr2:165783184 | A | C | 1 | a0001c0001t0002g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-109+10831T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165783184 | |||||||
| chr2:165783702 | A | C | 1 | a0001c0001t0002g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-109+10313T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165783702 | |||||||
| chr2:165783857 | T | G | 1 | a0001c0001t0001g0225 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-109+10158A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165783857 | |||||||
| chr2:165784062 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-109+9953C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784062 | |||||||
| chr2:165784064 | T | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0024 others(102): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-109+9951A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784064 | |||||||
| chr2:165784065 | C | A | 105 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0024 others(102): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-109+9950G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784065 | |||||||
| chr2:165784133 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-109+9882G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784133 | |||||||
| chr2:165784199 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-109+9816C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784199 | |||||||
| chr2:165784287 | C | T | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-109+9728G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784287 | |||||||
| chr2:165784522 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0047 |
3 | HG01255.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+9493G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784522 | |||||||
| chr2:165784523 | G | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0026 others(54): Show |
69 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-109+9492C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784523 | |||||||
| chr2:165784640 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-109+9375T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784640 | |||||||
| chr2:165784784 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG01891.hp1 HG02040.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-109+9231A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784784 | |||||||
| chr2:165784999 | T | C | 2 | a0001c0001t0002g0104 a0001c0001t0002g0107 |
2 | NA18974.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-109+9016A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165784999 | |||||||
| chr2:165785281 | T | C | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+8734A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785281 | |||||||
| chr2:165785314 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-109+8701C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785314 | |||||||
| chr2:165785541 | G | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(81): Show |
112 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.-109+8474C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785541 | |||||||
| chr2:165785638 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-109+8377C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785638 | |||||||
| chr2:165785639 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0044 others(4): Show |
10 | HG02258.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+8376G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785639 | |||||||
| chr2:165785744 | A | C | 1 | a0001c0001t0001g0156 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-109+8271T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785744 | |||||||
| chr2:165785811 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-109+8204A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785811 | |||||||
| chr2:165785999 | C | A | 4 | a0001c0001t0001g0141 a0001c0001t0004g0224 a0001c0001t0004g0226 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+8016G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165785999 | |||||||
| chr2:165786022 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-109+7993A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786022 | |||||||
| chr2:165786046 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0281 |
2 | NA19000.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-109+7969G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786046 | |||||||
| chr2:165786066 | GCAAA | G | 53 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0046 others(50): Show |
69 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(66): Show |
intron_variant | MODIFIER | c.-109+7945_-109+794 others(8): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786066 | |||||||
| chr2:165786081 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG01175.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-109+7934C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786081 | |||||||
| chr2:165786134 | G | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(280): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-109+7881C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786134 | |||||||
| chr2:165786192 | A | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0246 |
2 | HG01123.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-109+7823T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786192 | |||||||
| chr2:165786336 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-109+7679A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786336 | |||||||
| chr2:165786362 | A | G | 1 | a0002c0002t0001g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+7653T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786362 | |||||||
| chr2:165786648 | A | T | 7 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0056 others(4): Show |
7 | HG00323.hp2 HG01099.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+7367T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786648 | |||||||
| chr2:165786697 | C | T | 1 | a0001c0001t0004g0228 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-109+7318G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786697 | |||||||
| chr2:165786769 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+7246T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165786769 | |||||||
| chr2:165787004 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(81): Show |
112 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.-109+7011A>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165787004 | |||||||
| chr2:165787202 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-109+6813G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165787202 | |||||||
| chr2:165787251 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-109+6764C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165787251 | |||||||
| chr2:165787456 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0141 |
2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-109+6559A>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165787456 | |||||||
| chr2:165787586 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-109+6429T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165787586 | |||||||
| chr2:165787782 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-109+6233G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165787782 | |||||||
| chr2:165787901 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-109+6114C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165787901 | |||||||
| chr2:165788079 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-109+5936T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788079 | |||||||
| chr2:165788221 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-109+5794C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788221 | |||||||
| chr2:165788296 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-109+5719C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788296 | |||||||
| chr2:165788298 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-109+5717A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788298 | |||||||
| chr2:165788304 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-109+5711T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788304 | |||||||
| chr2:165788309 | A | T | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-109+5706T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788309 | |||||||
| chr2:165788310 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-109+5705A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788310 | |||||||
| chr2:165788311 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-109+5704G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788311 | |||||||
| chr2:165788313 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-109+5702G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788313 | |||||||
| chr2:165788316 | C | CA | 18 | a0001c0001t0001g0029 a0001c0001t0001g0183 a0001c0001t0001g0199 others(15): Show |
19 | HG00673.hp2 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+5698dupT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788316 | |||||||
| chr2:165788316 | CA | C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0079 a0001c0001t0001g0084 others(20): Show |
27 | HG00323.hp1 HG01255.hp1 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.-109+5698delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788316 | |||||||
| chr2:165788316 | CAAA | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0207 others(3): Show |
8 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+5696_-109+569 others(7): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788316 | |||||||
| chr2:165788316 | CAAAA | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0299 others(9): Show |
20 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+5695_-109+569 others(8): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788316 | |||||||
| chr2:165788441 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+5574C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788441 | |||||||
| chr2:165788466 | G | GGT | 134 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
163 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-109+5547_-109+554 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788466 | |||||||
| chr2:165788466 | G | GGTGT | 46 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0136 others(43): Show |
58 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(55): Show |
intron_variant | MODIFIER | c.-109+5545_-109+554 others(8): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788466 | |||||||
| chr2:165788466 | G | GGTGTGT | 7 | a0001c0001t0001g0091 a0001c0001t0001g0144 a0001c0001t0001g0230 others(4): Show |
7 | HG00280.hp1 HG01884.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+5543_-109+554 others(10): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788466 | |||||||
| chr2:165788466 | GGT | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0130 a0001c0001t0001g0138 others(11): Show |
15 | HG00609.hp1 HG01071.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-109+5547_-109+554 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788466 | |||||||
| chr2:165788466 | GGTGT | G | 5 | a0001c0001t0001g0084 a0001c0001t0001g0196 a0001c0001t0001g0219 others(2): Show |
5 | HG02145.hp1 HG02647.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+5545_-109+554 others(8): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788466 | |||||||
| chr2:165788466 | GGTGTGT | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG01496.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-109+5543_-109+554 others(10): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788466 | |||||||
| chr2:165788466 | GGTGTGTG others(3): Show |
G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0288 others(4): Show |
10 | HG00597.hp1 NA18940.hp1 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.-109+5539_-109+554 others(14): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788466 | |||||||
| chr2:165788482 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-109+5533A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788482 | |||||||
| chr2:165788507 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02738.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-109+5508T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788507 | |||||||
| chr2:165788621 | C | G | 1 | a0001c0001t0002g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-109+5394G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788621 | |||||||
| chr2:165788891 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-109+5124T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788891 | |||||||
| chr2:165788899 | TGA | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
6 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+5114_-109+511 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788899 | |||||||
| chr2:165788934 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-109+5081G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788934 | |||||||
| chr2:165788949 | G | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-109+5066C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165788949 | |||||||
| chr2:165789084 | A | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0026 others(58): Show |
73 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-109+4931T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789084 | |||||||
| chr2:165789103 | G | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+4912C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789103 | |||||||
| chr2:165789131 | C | T | 1 | a0001c0001t0007g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-109+4884G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789131 | |||||||
| chr2:165789233 | G | A | 2 | a0001c0001t0002g0085 a0001c0001t0002g0086 |
2 | HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-109+4782C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789233 | |||||||
| chr2:165789334 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+4681T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789334 | |||||||
| chr2:165789370 | C | T | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-109+4645G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789370 | |||||||
| chr2:165789433 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-109+4582T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789433 | |||||||
| chr2:165789661 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01074.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-109+4354C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789661 | |||||||
| chr2:165789704 | TAA | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(204): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-109+4309_-109+431 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789704 | |||||||
| chr2:165789704 | TAAA | T | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
90 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.-109+4308_-109+431 others(7): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789704 | |||||||
| chr2:165789831 | C | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
87 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-109+4184G>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165789831 | |||||||
| chr2:165790003 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-109+4012A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165790003 | |||||||
| chr2:165790018 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-109+3997A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165790018 | |||||||
| chr2:165790027 | TGA | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0047 |
3 | HG01255.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+3986_-109+398 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165790027 | |||||||
| chr2:165790399 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-109+3616A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165790399 | |||||||
| chr2:165790537 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-109+3478C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165790537 | |||||||
| chr2:165790542 | T | C | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-109+3473A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165790542 | |||||||
| chr2:165790754 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+3261A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165790754 | |||||||
| chr2:165791179 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(82): Show |
115 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.-109+2836G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791179 | |||||||
| chr2:165791180 | A | G | 1 | a0006c0009t0002g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-109+2835T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791180 | |||||||
| chr2:165791255 | C | CTG | 61 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(58): Show |
76 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-109+2758_-109+275 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791255 | |||||||
| chr2:165791255 | C | CTGTG | 3 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0002g0048 |
4 | HG01255.hp1 HG02280.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+2756_-109+275 others(8): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791255 | |||||||
| chr2:165791255 | CTG | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(68): Show |
86 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-109+2758_-109+275 others(6): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791255 | |||||||
| chr2:165791380 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-109+2635A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791380 | |||||||
| chr2:165791517 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0002g0231 a0001c0001t0002g0232 |
3 | HG00280.hp1 HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-109+2498G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791517 | |||||||
| chr2:165791530 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(7): Show |
19 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+2485T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791530 | |||||||
| chr2:165791577 | GA | G | 4 | a0001c0001t0005g0229 a0002c0002t0001g0204 a0002c0002t0001g0205 others(1): Show |
4 | HG02486.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+2437delT | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791577 | |||||||
| chr2:165791816 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-109+2199T>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791816 | |||||||
| chr2:165791921 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-109+2094C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791921 | |||||||
| chr2:165791934 | T | C | 7 | a0001c0001t0001g0225 a0001c0001t0004g0139 a0001c0001t0004g0224 others(4): Show |
7 | HG00735.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+2081A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165791934 | |||||||
| chr2:165792026 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-109+1989G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792026 | |||||||
| chr2:165792049 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-109+1966C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792049 | |||||||
| chr2:165792161 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(84): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.-109+1854C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792161 | |||||||
| chr2:165792192 | T | C | 3 | a0002c0002t0001g0204 a0002c0002t0001g0205 a0002c0002t0001g0206 |
3 | HG02486.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-109+1823A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792192 | |||||||
| chr2:165792282 | A | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(204): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-109+1733T>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792282 | |||||||
| chr2:165792600 | T | C | 5 | a0001c0001t0001g0225 a0001c0001t0004g0224 a0001c0001t0004g0226 others(2): Show |
5 | HG02615.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+1415A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792600 | |||||||
| chr2:165792759 | A | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
92 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-109+1256T>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792759 | |||||||
| chr2:165792916 | C | T | 1 | a0003c0007t0002g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-109+1099G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792916 | |||||||
| chr2:165792941 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(84): Show |
117 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.-109+1074A>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165792941 | |||||||
| chr2:165793105 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-109+910C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793105 | |||||||
| chr2:165793105 | G | T | 2 | a0001c0001t0004g0139 a0001c0001t0009g0140 |
2 | HG00735.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-109+910C>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793105 | |||||||
| chr2:165793302 | G | A | 8 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(5): Show |
8 | HG02258.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+713C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793302 | |||||||
| chr2:165793433 | G | C | 1 | a0001c0001t0005g0298 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+582C>G | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793433 | |||||||
| chr2:165793447 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-109+568G>A | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793447 | |||||||
| chr2:165793815 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0041 others(6): Show |
18 | HG00642.hp1 HG01081.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.-109+200C>T | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793815 | |||||||
| chr2:165793860 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-109+155G>C | GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793860 | |||||||
| chr2:165793912 | A | ACCGTAGC | 110 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0024 others(107): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-109+96_-109+102du others(8): Show |
GALNT3 | ENSG00000115339.14 | transcript | ENST00000392701.8 | protein_coding | 1/10 | chr2 | 165793912 |