Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 727936 |
| ensemblid | ENSG00000172986.13 |
| hgncid | 33383 |
| symbol | GXYLT2 |
| name | glucoside xylosyltransferase 2 |
| refseq_nuc | NM_001080393.2 |
| refseq_prot | NP_001073862.1 |
| ensembl_nuc | ENST00000389617.9 |
| ensembl_prot | ENSP00000374268.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 72888046 |
| end | 72976915 |
| strand | + |
| ver | v1.2 |
| region | chr3:72888046-72976915 |
| region5000 | chr3:72883046-72981915 |
| regionname0 | GXYLT2_chr3_72888046_72976915 |
| regionname5000 | GXYLT2_chr3_72883046_72981915 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 443 | 282 | 85 | 67 | 88 | 6 | 34 | 60 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | MKLRS others(438): Show |
chr3 | 72883046 | 72981915 |
| a0002 | 0/0 | 443 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | MKLRS others(438): Show |
chr3 | 72883046 | 72981915 |
| a0003 | 0/0 | 443 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | MKLRS others(438): Show |
chr3 | 72883046 | 72981915 |
| a0004 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | MKLRS others(438): Show |
chr3 | 72883046 | 72981915 |
| a0005 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | MKLRS others(438): Show |
chr3 | 72883046 | 72981915 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1329 | 254 | 59 | 66 | 88 | 6 | 33 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0001c0002 | 0/0 | 1329 | 14 | 14 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0001c0004 | 0/0 | 1329 | 8 | 7 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0001c0005 | 0/0 | 1329 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0001c0007 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0001c0010 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0001c0012 | 0/0 | 1329 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0002c0003 | 0/0 | 1329 | 9 | 9 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0002c0006 | 0/0 | 1329 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0003c0008 | 0/0 | 1329 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0004c0011 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 | ||
| a0005c0009 | 0/0 | 1329 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | ATGAA others(1324): Show |
chr3 | 72883046 | 72981915 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3274 | 139 | 41 | 36 | 42 | 4 | 15 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0002 | 1/0 | 3276 | 58 | 2 | 14 | 29 | 2 | 10 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0003 | 0/0 | 3278 | 9 | 9 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0004 | 0/0 | 3273 | 11 | 0 | 10 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0005 | 0/0 | 3274 | 7 | 1 | 0 | 6 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0006 | 0/0 | 3277 | 7 | 3 | 1 | 2 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3272): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0007 | 0/0 | 3275 | 7 | 0 | 1 | 4 | 0 | 2 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3270): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0009 | 0/0 | 3273 | 3 | 1 | 1 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0010 | 0/0 | 3274 | 2 | 1 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0011 | 0/0 | 3273 | 2 | 0 | 0 | 1 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0012 | 0/0 | 3274 | 2 | 0 | 0 | 1 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0013 | 0/0 | 3273 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0016 | 0/0 | 3277 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3272): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0017 | 0/0 | 3274 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0022 | 0/0 | 3277 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3272): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0023 | 0/0 | 3276 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0024 | 0/0 | 3276 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0001c0001t0028 | 0/0 | 3278 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0001 | 0/0 | 3274 | 6 | 6 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0013 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0014 | 0/0 | 3276 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0018 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0020 | 0/0 | 3277 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3272): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0021 | 0/0 | 3278 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0025 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0001c0002t0027 | 0/0 | 3274 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0004t0008 | 0/0 | 3274 | 5 | 4 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0001c0004t0015 | 0/0 | 3276 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0001c0004t0029 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0001c0005t0003 | 0/0 | 3278 | 3 | 3 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| a0001c0007t0003 | 0/0 | 3278 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| a0001c0010t0031 | 0/0 | 3278 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| a0001c0012t0001 | 0/0 | 3274 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0002c0003t0001 | 0/0 | 3274 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0002c0003t0002 | 0/0 | 3276 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0002c0003t0005 | 0/0 | 3274 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0002c0003t0006 | 0/0 | 3277 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3272): Show |
chr3 | 72883046 | 72981915 |
| a0002c0003t0009 | 0/0 | 3273 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3268): Show |
chr3 | 72883046 | 72981915 |
| a0002c0003t0019 | 0/0 | 3278 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| a0002c0003t0026 | 0/0 | 3277 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3272): Show |
chr3 | 72883046 | 72981915 |
| a0002c0006t0008 | 0/0 | 3274 | 2 | 2 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0003c0008t0002 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3271): Show |
chr3 | 72883046 | 72981915 |
| a0004c0011t0001 | 0/0 | 3274 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3269): Show |
chr3 | 72883046 | 72981915 |
| a0005c0009t0030 | 0/0 | 3278 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | CTCTC others(3273): Show |
chr3 | 72883046 | 72981915 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0009g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0010g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0011g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0012g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0012g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0013g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0016g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0017g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0022g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0023g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0024g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0001t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0018g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0020g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0021g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0025g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0002t0027g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0008g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0015g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0015g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0004t0029g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0005t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0005t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0005t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0007t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0010t0031g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0001c0012t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0019g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0003t0026g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0006t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0002c0006t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0003c0008t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0004c0011t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| a0005c0009t0030g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0028 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01109 | hp1 | a0001 | c0001 | t0017 | g0280 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01109 | hp2 | a0001 | c0004 | t0008 | g0281 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01169 | hp2 | a0001 | c0001 | t0016 | g0215 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01256 | hp1 | a0001 | c0001 | t0007 | g0122 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01891 | hp1 | a0001 | c0001 | t0028 | g0003 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01891 | hp2 | a0002 | c0003 | t0009 | g0105 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0183 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02080 | hp2 | a0001 | c0001 | t0022 | g0152 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | CDX | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02280 | hp1 | a0001 | c0002 | t0014 | g0005 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0149 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02572 | hp1 | a0002 | c0003 | t0002 | g0269 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02630 | hp1 | a0001 | c0010 | t0031 | g0286 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0104 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02717 | hp1 | a0001 | c0005 | t0003 | g0091 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02717 | hp2 | a0001 | c0002 | t0020 | g0070 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02723 | hp1 | a0001 | c0005 | t0003 | g0052 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0185 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02818 | hp2 | a0001 | c0002 | t0018 | g0188 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02886 | hp2 | a0001 | c0004 | t0008 | g0287 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02895 | hp1 | a0002 | c0003 | t0002 | g0015 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02895 | hp2 | a0001 | c0004 | t0008 | g0282 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02896 | hp2 | a0001 | c0002 | t0021 | g0071 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02897 | hp1 | a0001 | c0004 | t0029 | g0283 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02922 | hp1 | a0001 | c0004 | t0015 | g0285 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02922 | hp2 | a0001 | c0004 | t0015 | g0290 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02965 | hp2 | a0004 | c0011 | t0001 | g0023 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03041 | hp2 | a0001 | c0002 | t0027 | g0048 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03098 | hp1 | a0002 | c0003 | t0005 | g0072 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03139 | hp2 | a0001 | c0002 | t0025 | g0006 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03195 | hp1 | a0002 | c0006 | t0008 | g0288 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03195 | hp2 | a0001 | c0002 | t0013 | g0041 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03209 | hp2 | a0001 | c0007 | t0003 | g0007 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03225 | hp1 | a0001 | c0005 | t0003 | g0069 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0088 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03453 | hp2 | a0005 | c0009 | t0030 | g0291 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0106 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03491 | hp2 | a0001 | c0012 | t0001 | g0162 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03540 | hp1 | a0002 | c0003 | t0026 | g0182 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03654 | hp2 | a0001 | c0001 | t0024 | g0078 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0169 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03704 | hp2 | a0001 | c0001 | t0023 | g0171 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03710 | hp1 | a0001 | c0001 | t0012 | g0168 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0193 | SAS | BEB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | BEB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | YRI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | CHB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CHB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18906 | hp1 | a0001 | c0004 | t0008 | g0284 | AFR | YRI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | YRI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18943 | hp1 | a0001 | c0001 | t0013 | g0187 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0272 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18957 | hp1 | a0001 | c0001 | t0007 | g0120 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18962 | hp1 | a0001 | c0001 | t0012 | g0252 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18970 | hp1 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18982 | hp2 | a0001 | c0001 | t0011 | g0256 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19030 | hp2 | a0002 | c0003 | t0006 | g0037 | AFR | LWK | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | LWK | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | LWK | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19077 | hp1 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19240 | hp1 | a0001 | c0004 | t0008 | g0292 | AFR | YRI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | YRI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ASW | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0102 | AFR | ASW | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | TSI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01123 | hp1 | a0003 | c0008 | t0002 | g0009 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02109 | hp1 | a0001 | c0002 | t0014 | g0039 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02559 | hp1 | a0002 | c0006 | t0008 | g0289 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | USA | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | USA | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA20300 | hp2 | a0002 | c0003 | t0019 | g0014 | AFR | USA | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | LWK | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0154 | REF | REF | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0148 | REF | REF | GXYLT2_chr3_72883046_72981915 | GXYLT2 | chr3 | 72883046 | 72981915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72888352 | C | G | 1 | a0004 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.119C>G | p.Ala40Gly | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/7 | 307/3276 | 119/1332 | 40/443 | chr3 | 72888352 | |||
| chr3:72888474 | C | A | 1 | a0005 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.241C>A | p.Arg81Ser | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/7 | 429/3276 | 241/1332 | 81/443 | chr3 | 72888474 | |||
| chr3:72922258 | A | G | 1 | a0002 | 11 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
missense_variant | MODERATE | c.523A>G | p.Ile175Val | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/7 | 711/3276 | 523/1332 | 175/443 | chr3 | 72922258 | |||
| chr3:72957245 | C | T | 1 | a0003 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.869C>T | p.Thr290Ile | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/7 | 1057/3276 | 869/1332 | 290/443 | chr3 | 72957245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72888305 | C | G | 1 | a0001c0012 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.72C>G | p.Ser24Ser | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/7 | 260/3276 | 72/1332 | 24/443 | chr3 | 72888305 | |||
| chr3:72888374 | C | T | 4 | a0001c0004 a0001c0010 a0002c0006 others(1): Show |
12 | HG01109.hp2 HG02559.hp1 HG02630.hp1 others(9): Show |
synonymous_variant | LOW | c.141C>T | p.Pro47Pro | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/7 | 329/3276 | 141/1332 | 47/443 | chr3 | 72888374 | |||
| chr3:72922263 | A | G | 2 | a0001c0002 a0001c0010 |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
synonymous_variant | LOW | c.528A>G | p.Thr176Thr | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/7 | 716/3276 | 528/1332 | 176/443 | chr3 | 72922263 | |||
| chr3:72955121 | A | C | 1 | a0001c0005 | 3 | HG02717.hp1 HG02723.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.624A>C | p.Ser208Ser | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/7 | 812/3276 | 624/1332 | 208/443 | chr3 | 72955121 | |||
| chr3:72957306 | G | T | 1 | a0001c0007 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.930G>T | p.Thr310Thr | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/7 | 1118/3276 | 930/1332 | 310/443 | chr3 | 72957306 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72888069 | C | T | 6 | a0001c0004t0008 a0001c0004t0015 a0001c0004t0029 others(3): Show |
12 | HG01109.hp2 HG02559.hp1 HG02630.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-165C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/7 | chr3 | 72888069 | |||||||
| chr3:72888081 | C | T | 2 | a0001c0001t0028 a0001c0002t0027 |
2 | HG01891.hp1 HG03041.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-153C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/7 | chr3 | 72888081 | |||||||
| chr3:72975199 | C | A | 15 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(12): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 40 | chr3 | 72975199 | ||||||
| chr3:72975369 | G | A | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*210G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 210 | chr3 | 72975369 | ||||||
| chr3:72975369 | G | GA | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(24): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*222dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 223 | INFO_REALIGN_3_PRIME | chr3 | 72975369 | |||||
| chr3:72975458 | A | T | 15 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(12): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*299A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 299 | chr3 | 72975458 | ||||||
| chr3:72975521 | T | C | 1 | a0001c0001t0023 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*362T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 362 | chr3 | 72975521 | ||||||
| chr3:72975542 | C | A | 1 | a0001c0001t0024 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 383 | chr3 | 72975542 | ||||||
| chr3:72975573 | T | G | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(31): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*414T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 414 | chr3 | 72975573 | ||||||
| chr3:72975599 | G | A | 1 | a0005c0009t0030 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 440 | chr3 | 72975599 | ||||||
| chr3:72975695 | C | G | 1 | a0001c0001t0017 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*536C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 536 | chr3 | 72975695 | ||||||
| chr3:72975702 | T | C | 1 | a0001c0001t0010 | 2 | HG01952.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*543T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 543 | chr3 | 72975702 | ||||||
| chr3:72975807 | T | C | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*648T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 648 | chr3 | 72975807 | ||||||
| chr3:72975926 | C | CT | 11 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0028 others(8): Show |
27 | HG01261.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*790dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 791 | INFO_REALIGN_3_PRIME | chr3 | 72975926 | |||||
| chr3:72975926 | CT | C | 1 | a0001c0001t0007 | 7 | HG01256.hp1 HG03704.hp1 HG03834.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*790delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 790 | INFO_REALIGN_3_PRIME | chr3 | 72975926 | |||||
| chr3:72975926 | CTTT | C | 18 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(15): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*790delTTT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 788 | INFO_REALIGN_3_PRIME | chr3 | 72975926 | |||||
| chr3:72975926 | CTTTT | C | 3 | a0001c0001t0004 a0001c0001t0011 a0001c0004t0029 |
14 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*787_*790delTTTT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 787 | INFO_REALIGN_3_PRIME | chr3 | 72975926 | |||||
| chr3:72975946 | T | C | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(19): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*787T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 787 | chr3 | 72975946 | ||||||
| chr3:72976032 | A | G | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*873A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 873 | chr3 | 72976032 | ||||||
| chr3:72976062 | G | C | 1 | a0001c0001t0012 | 2 | HG03710.hp1 NA18962.hp1 |
3_prime_UTR_variant | MODIFIER | c.*903G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 903 | chr3 | 72976062 | ||||||
| chr3:72976080 | T | C | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*921T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 921 | chr3 | 72976080 | ||||||
| chr3:72976118 | G | A | 3 | a0001c0002t0020 a0001c0002t0021 a0002c0003t0019 |
3 | HG02717.hp2 HG02896.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 959 | chr3 | 72976118 | ||||||
| chr3:72976137 | G | T | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*978G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 978 | chr3 | 72976137 | ||||||
| chr3:72976177 | C | T | 2 | a0001c0002t0014 a0002c0003t0026 |
3 | HG02109.hp1 HG02280.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1018C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 1018 | chr3 | 72976177 | ||||||
| chr3:72976487 | G | T | 1 | a0001c0002t0027 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1328G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 1328 | chr3 | 72976487 | ||||||
| chr3:72976543 | C | A | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1384C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 1384 | chr3 | 72976543 | ||||||
| chr3:72976657 | T | C | 1 | a0001c0002t0025 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1498T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 1498 | chr3 | 72976657 | ||||||
| chr3:72976681 | C | T | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1522C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 1522 | chr3 | 72976681 | ||||||
| chr3:72976814 | T | C | 1 | a0001c0002t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1655T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 7/7 | 1655 | chr3 | 72976814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:72888535 | A | G | 2 | a0001c0001t0002g0295 a0001c0001t0002g0296 |
2 | NA18962.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.275+27A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72888535 | |||||||
| chr3:72888542 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.275+34G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72888542 | |||||||
| chr3:72888547 | GTGTCTCG others(73): Show |
G | 1 | a0001c0001t0001g0002 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.275+42_275+121delT others(79): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72888547 | ||||||
| chr3:72888548 | T | G | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.275+40T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72888548 | |||||||
| chr3:72888584 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.275+76G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72888584 | |||||||
| chr3:72888787 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.275+279A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72888787 | |||||||
| chr3:72888981 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.275+473G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72888981 | |||||||
| chr3:72889169 | A | G | 12 | a0001c0004t0008g0281 a0001c0004t0008g0282 a0001c0004t0008g0284 others(9): Show |
12 | HG01109.hp2 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.275+661A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889169 | |||||||
| chr3:72889180 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.275+672C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889180 | |||||||
| chr3:72889325 | C | T | 1 | a0001c0001t0017g0280 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.275+817C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889325 | |||||||
| chr3:72889401 | T | G | 1 | a0001c0001t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.275+893T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889401 | |||||||
| chr3:72889407 | A | C | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+899A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889407 | |||||||
| chr3:72889583 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.275+1075A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889583 | |||||||
| chr3:72889585 | C | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+1077C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889585 | |||||||
| chr3:72889795 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.275+1287G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889795 | |||||||
| chr3:72889803 | C | T | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1295C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889803 | |||||||
| chr3:72889868 | CT | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(115): Show |
118 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.275+1362delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72889868 | ||||||
| chr3:72889896 | G | GT | 11 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
11 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.275+1398dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72889896 | ||||||
| chr3:72889896 | G | GTT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(7): Show |
10 | HG00558.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.275+1397_275+1398d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72889896 | ||||||
| chr3:72889896 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.275+1388G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889896 | |||||||
| chr3:72889907 | G | GGTT | 3 | a0001c0001t0001g0004 a0001c0002t0014g0005 a0001c0002t0025g0006 |
3 | HG02280.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.275+1399_275+1400i others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889907 | |||||||
| chr3:72889907 | G | GT | 24 | a0001c0001t0001g0044 a0001c0001t0001g0076 a0001c0001t0001g0081 others(21): Show |
24 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.275+1415dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72889907 | ||||||
| chr3:72889907 | G | T | 11 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0053 others(8): Show |
11 | HG00140.hp2 HG01891.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.275+1399G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889907 | |||||||
| chr3:72889907 | GT | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(46): Show |
49 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.275+1415delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72889907 | ||||||
| chr3:72889908 | T | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG00140.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.275+1400T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889908 | |||||||
| chr3:72889922 | T | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01884.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.275+1414T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889922 | |||||||
| chr3:72889955 | G | T | 3 | a0001c0001t0002g0264 a0001c0001t0002g0295 a0001c0001t0002g0296 |
3 | NA18962.hp2 NA18979.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.275+1447G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72889955 | |||||||
| chr3:72890031 | GTGCCTCA others(3): Show |
G | 1 | a0001c0001t0002g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.275+1528_275+1537d others(12): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72890031 | ||||||
| chr3:72890047 | G | C | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.275+1539G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890047 | |||||||
| chr3:72890144 | C | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.275+1636C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890144 | |||||||
| chr3:72890190 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.275+1682A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890190 | |||||||
| chr3:72890215 | A | AC | 62 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.275+1707_275+1708i others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890215 | |||||||
| chr3:72890320 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(115): Show |
118 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.275+1812A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890320 | |||||||
| chr3:72890616 | C | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.275+2108C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890616 | |||||||
| chr3:72890714 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.275+2206C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890714 | |||||||
| chr3:72890825 | C | T | 6 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0006g0092 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+2317C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890825 | |||||||
| chr3:72890846 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0002t0014g0005 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.275+2338T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890846 | |||||||
| chr3:72890857 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+2349C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72890857 | |||||||
| chr3:72891080 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.275+2572G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72891080 | |||||||
| chr3:72891172 | A | G | 6 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0006g0092 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+2664A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72891172 | |||||||
| chr3:72891184 | C | T | 3 | a0001c0001t0001g0081 a0001c0002t0001g0079 a0001c0002t0001g0080 |
3 | HG01884.hp1 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.275+2676C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72891184 | |||||||
| chr3:72891327 | C | T | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.275+2819C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72891327 | |||||||
| chr3:72891439 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.275+2931T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72891439 | |||||||
| chr3:72891575 | C | T | 1 | a0001c0001t0003g0260 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.275+3067C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72891575 | |||||||
| chr3:72891703 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.275+3195T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72891703 | |||||||
| chr3:72892056 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.275+3548G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892056 | |||||||
| chr3:72892078 | C | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG02027.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.275+3570C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892078 | |||||||
| chr3:72892138 | G | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.275+3630G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892138 | |||||||
| chr3:72892178 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.275+3670A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892178 | |||||||
| chr3:72892207 | G | A | 3 | a0001c0001t0001g0004 a0001c0002t0014g0005 a0001c0002t0025g0006 |
3 | HG02280.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.275+3699G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892207 | |||||||
| chr3:72892301 | G | C | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.275+3793G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892301 | |||||||
| chr3:72892429 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275+3921A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892429 | |||||||
| chr3:72892539 | T | TTGGGGA | 5 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0002t0014g0005 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.275+4033_275+4034i others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72892539 | ||||||
| chr3:72892729 | A | G | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.275+4221A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892729 | |||||||
| chr3:72892803 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.275+4295A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892803 | |||||||
| chr3:72892819 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0002t0014g0005 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.275+4311T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892819 | |||||||
| chr3:72892880 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+4372C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892880 | |||||||
| chr3:72892949 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0002t0014g0005 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.275+4441C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72892949 | |||||||
| chr3:72893040 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.275+4532G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893040 | |||||||
| chr3:72893159 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0002t0014g0005 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.275+4651G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893159 | |||||||
| chr3:72893256 | T | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
85 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.275+4748T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893256 | |||||||
| chr3:72893406 | T | C | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+4898T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893406 | |||||||
| chr3:72893434 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.275+4926G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893434 | |||||||
| chr3:72893504 | T | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0002t0020g0070 others(3): Show |
6 | HG02258.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.275+4996T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893504 | |||||||
| chr3:72893521 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG00099.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.275+5013G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893521 | |||||||
| chr3:72893545 | T | G | 1 | a0001c0005t0003g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.275+5037T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893545 | |||||||
| chr3:72893587 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.275+5079C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893587 | |||||||
| chr3:72893829 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0005g0045 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+5321T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893829 | |||||||
| chr3:72893837 | T | A | 6 | a0001c0001t0001g0044 a0001c0001t0005g0045 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+5329T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893837 | |||||||
| chr3:72893846 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0005g0045 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+5338T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72893846 | |||||||
| chr3:72894105 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.275+5597A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894105 | |||||||
| chr3:72894140 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.275+5632C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894140 | |||||||
| chr3:72894173 | A | T | 3 | a0001c0001t0001g0004 a0001c0002t0014g0005 a0001c0002t0025g0006 |
3 | HG02280.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.275+5665A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894173 | |||||||
| chr3:72894265 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.275+5757T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894265 | |||||||
| chr3:72894655 | G | A | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+6147G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894655 | |||||||
| chr3:72894726 | TG | T | 5 | a0001c0001t0001g0261 a0001c0001t0002g0253 a0001c0001t0005g0254 others(2): Show |
5 | HG02083.hp2 HG02165.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+6221delG | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72894726 | ||||||
| chr3:72894769 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+6261A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894769 | |||||||
| chr3:72894787 | A | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0081 a0001c0001t0005g0045 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+6279A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894787 | |||||||
| chr3:72894820 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.275+6312T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894820 | |||||||
| chr3:72894941 | C | T | 1 | a0001c0001t0012g0252 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.275+6433C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894941 | |||||||
| chr3:72894958 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.275+6450A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72894958 | |||||||
| chr3:72895240 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+6732C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895240 | |||||||
| chr3:72895596 | A | G | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.275+7088A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895596 | |||||||
| chr3:72895622 | A | G | 3 | a0001c0001t0001g0081 a0001c0002t0001g0079 a0001c0002t0001g0080 |
3 | HG01884.hp1 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.275+7114A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895622 | |||||||
| chr3:72895630 | T | C | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.275+7122T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895630 | |||||||
| chr3:72895734 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7226A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895734 | |||||||
| chr3:72895784 | A | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7276A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895784 | |||||||
| chr3:72895791 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7283C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895791 | |||||||
| chr3:72895864 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7356C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895864 | |||||||
| chr3:72895882 | G | A | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7374G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895882 | |||||||
| chr3:72895933 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.275+7425A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72895933 | |||||||
| chr3:72896037 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7529A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896037 | |||||||
| chr3:72896047 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7539A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896047 | |||||||
| chr3:72896195 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7687A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896195 | |||||||
| chr3:72896380 | C | A | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7872C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896380 | |||||||
| chr3:72896507 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+7999A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896507 | |||||||
| chr3:72896549 | T | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8041T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896549 | |||||||
| chr3:72896584 | T | C | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8076T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896584 | |||||||
| chr3:72896597 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8089C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896597 | |||||||
| chr3:72896611 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.275+8103G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896611 | |||||||
| chr3:72896616 | A | C | 4 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+8108A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896616 | |||||||
| chr3:72896647 | G | A | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8139G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896647 | |||||||
| chr3:72896667 | G | A | 3 | a0001c0001t0001g0004 a0001c0002t0014g0005 a0001c0002t0025g0006 |
3 | HG02280.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.275+8159G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896667 | |||||||
| chr3:72896674 | C | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8166C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896674 | |||||||
| chr3:72896854 | TA | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0076 others(40): Show |
43 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.275+8359delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72896854 | ||||||
| chr3:72896880 | G | A | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8372G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896880 | |||||||
| chr3:72896891 | T | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8383T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896891 | |||||||
| chr3:72896915 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8407C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72896915 | |||||||
| chr3:72897103 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8595C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897103 | |||||||
| chr3:72897126 | AGGTAGGA others(4): Show |
A | 1 | a0001c0001t0001g0250 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.275+8619_275+8629d others(13): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897126 | |||||||
| chr3:72897171 | G | A | 12 | a0001c0004t0008g0281 a0001c0004t0008g0282 a0001c0004t0008g0284 others(9): Show |
12 | HG01109.hp2 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.275+8663G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897171 | |||||||
| chr3:72897271 | C | G | 6 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0006g0092 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.275+8763C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897271 | |||||||
| chr3:72897365 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8857A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897365 | |||||||
| chr3:72897380 | T | C | 1 | a0001c0001t0005g0115 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.275+8872T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897380 | |||||||
| chr3:72897384 | T | C | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8876T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897384 | |||||||
| chr3:72897409 | C | A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.275+8901C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897409 | |||||||
| chr3:72897500 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.275+8992A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897500 | |||||||
| chr3:72897501 | A | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.275+8993A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897501 | |||||||
| chr3:72897502 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0005t0003g0052 |
3 | HG02559.hp2 HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+8994G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897502 | |||||||
| chr3:72897620 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+9112A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897620 | |||||||
| chr3:72897682 | G | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+9174G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897682 | |||||||
| chr3:72897707 | G | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+9199G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72897707 | |||||||
| chr3:72897905 | G | GT | 37 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.275+9403dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72897905 | ||||||
| chr3:72898040 | A | C | 3 | a0001c0001t0001g0081 a0001c0002t0001g0079 a0001c0002t0001g0080 |
3 | HG01884.hp1 HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.275+9532A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898040 | |||||||
| chr3:72898071 | A | G | 14 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(11): Show |
14 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.275+9563A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898071 | |||||||
| chr3:72898139 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.275+9631T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898139 | |||||||
| chr3:72898276 | T | C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0081 a0001c0002t0001g0079 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+9768T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898276 | |||||||
| chr3:72898365 | G | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01099.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.275+9857G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898365 | |||||||
| chr3:72898384 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.275+9876C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898384 | |||||||
| chr3:72898399 | T | G | 4 | a0001c0001t0001g0084 a0001c0001t0003g0082 a0001c0001t0003g0083 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.275+9891T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898399 | |||||||
| chr3:72898455 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.276-9912A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898455 | |||||||
| chr3:72898466 | G | C | 4 | a0001c0001t0001g0084 a0001c0001t0003g0082 a0001c0001t0003g0083 others(1): Show |
4 | HG02451.hp1 HG02809.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.276-9901G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898466 | |||||||
| chr3:72898626 | C | A | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.276-9741C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898626 | |||||||
| chr3:72898711 | T | C | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.276-9656T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898711 | |||||||
| chr3:72898744 | T | C | 59 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.276-9623T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898744 | |||||||
| chr3:72898813 | C | T | 50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.276-9554C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898813 | |||||||
| chr3:72898824 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01099.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.276-9543C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898824 | |||||||
| chr3:72898830 | A | C | 50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.276-9537A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898830 | |||||||
| chr3:72898890 | C | G | 50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.276-9477C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898890 | |||||||
| chr3:72898893 | G | A | 50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.276-9474G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898893 | |||||||
| chr3:72898922 | G | A | 6 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0006g0092 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.276-9445G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898922 | |||||||
| chr3:72898982 | T | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.276-9385T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898982 | |||||||
| chr3:72898983 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.276-9384G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72898983 | |||||||
| chr3:72899011 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.276-9356G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899011 | |||||||
| chr3:72899021 | G | A | 50 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.276-9346G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899021 | |||||||
| chr3:72899022 | C | T | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.276-9345C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899022 | |||||||
| chr3:72899061 | T | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0085 others(8): Show |
11 | HG01891.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.276-9306T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899061 | |||||||
| chr3:72899174 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0009g0088 |
2 | HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.276-9193T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899174 | |||||||
| chr3:72899364 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-9003T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899364 | |||||||
| chr3:72899428 | C | T | 5 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01261.hp2 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-8939C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899428 | |||||||
| chr3:72899547 | T | C | 1 | a0001c0010t0031g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.276-8820T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899547 | |||||||
| chr3:72899558 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.276-8809C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899558 | |||||||
| chr3:72899659 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.276-8708A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899659 | |||||||
| chr3:72899675 | G | A | 1 | a0001c0001t0007g0120 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.276-8692G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899675 | |||||||
| chr3:72899757 | T | A | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-8610T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899757 | |||||||
| chr3:72899819 | T | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0006g0092 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.276-8548T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899819 | |||||||
| chr3:72899828 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.276-8539C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899828 | |||||||
| chr3:72899844 | G | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-8523G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899844 | |||||||
| chr3:72899845 | G | A | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-8522G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899845 | |||||||
| chr3:72899889 | A | G | 109 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(106): Show |
109 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.276-8478A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899889 | |||||||
| chr3:72899986 | T | C | 1 | a0001c0002t0027g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.276-8381T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72899986 | |||||||
| chr3:72900032 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.276-8335C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900032 | |||||||
| chr3:72900046 | C | A | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-8321C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900046 | |||||||
| chr3:72900047 | G | A | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-8320G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900047 | |||||||
| chr3:72900104 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.276-8263C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900104 | |||||||
| chr3:72900224 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-8143T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900224 | |||||||
| chr3:72900295 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.276-8072T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900295 | |||||||
| chr3:72900378 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.276-7989G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900378 | |||||||
| chr3:72900563 | C | T | 2 | a0002c0003t0001g0104 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.276-7804C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900563 | |||||||
| chr3:72900575 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.276-7792C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900575 | |||||||
| chr3:72900642 | T | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-7725T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900642 | |||||||
| chr3:72900704 | T | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-7663T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900704 | |||||||
| chr3:72900706 | C | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-7661C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900706 | |||||||
| chr3:72900710 | A | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-7657A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900710 | |||||||
| chr3:72900818 | AT | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0002g0008 others(2): Show |
5 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.276-7546delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72900818 | ||||||
| chr3:72900820 | T | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0002g0008 others(2): Show |
5 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.276-7547T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900820 | |||||||
| chr3:72900824 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0002g0008 others(2): Show |
5 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.276-7543T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900824 | |||||||
| chr3:72900824 | T | TAAC | 48 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
48 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.276-7542_276-7540d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72900824 | ||||||
| chr3:72900872 | G | C | 6 | a0001c0001t0001g0044 a0001c0001t0005g0045 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.276-7495G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900872 | |||||||
| chr3:72900893 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.276-7474G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900893 | |||||||
| chr3:72900916 | A | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-7451A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900916 | |||||||
| chr3:72900982 | A | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-7385A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72900982 | |||||||
| chr3:72901050 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.276-7317A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901050 | |||||||
| chr3:72901267 | T | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-7100T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901267 | |||||||
| chr3:72901268 | G | A | 43 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(40): Show |
43 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.276-7099G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901268 | |||||||
| chr3:72901288 | C | CA | 50 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0054 others(47): Show |
50 | HG00558.hp1 HG00597.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.276-7062dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901288 | ||||||
| chr3:72901288 | C | CAA | 6 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0125 others(3): Show |
6 | HG01243.hp2 HG01978.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-7063_276-7062d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901288 | ||||||
| chr3:72901288 | CA | C | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(45): Show |
48 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.276-7062delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901288 | ||||||
| chr3:72901458 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-6909T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901458 | |||||||
| chr3:72901468 | G | GA | 14 | a0001c0001t0001g0044 a0001c0001t0001g0076 a0001c0001t0001g0081 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.276-6888dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901468 | ||||||
| chr3:72901468 | G | GAA | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-6889_276-6888d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901468 | ||||||
| chr3:72901468 | GA | G | 7 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0001g0266 others(4): Show |
7 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-6888delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901468 | ||||||
| chr3:72901546 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.276-6821C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901546 | |||||||
| chr3:72901554 | C | CT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0044 others(93): Show |
96 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.276-6789dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901554 | ||||||
| chr3:72901554 | C | CTT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0081 a0001c0001t0001g0085 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.276-6790_276-6789d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901554 | ||||||
| chr3:72901554 | CT | C | 13 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0002g0035 others(10): Show |
13 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.276-6789delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901554 | ||||||
| chr3:72901554 | CTT | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(39): Show |
42 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.276-6790_276-6789d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901554 | ||||||
| chr3:72901647 | G | A | 1 | a0001c0001t0004g0013 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.276-6720G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901647 | |||||||
| chr3:72901664 | A | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-6703A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901664 | |||||||
| chr3:72901672 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-6695T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901672 | |||||||
| chr3:72901673 | G | A | 5 | a0001c0004t0008g0281 a0001c0004t0008g0282 a0001c0004t0008g0284 others(2): Show |
5 | HG01109.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.276-6694G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901673 | |||||||
| chr3:72901700 | ACAGGCAT others(4): Show |
A | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-6664_276-6654d others(13): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72901700 | ||||||
| chr3:72901803 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.276-6564C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901803 | |||||||
| chr3:72901850 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0206 |
2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.276-6517C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901850 | |||||||
| chr3:72901856 | C | T | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-6511C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901856 | |||||||
| chr3:72901857 | A | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-6510A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901857 | |||||||
| chr3:72901892 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.276-6475G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901892 | |||||||
| chr3:72901910 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.276-6457A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901910 | |||||||
| chr3:72901933 | G | A | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-6434G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901933 | |||||||
| chr3:72901984 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.276-6383A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72901984 | |||||||
| chr3:72902095 | A | AT | 14 | a0001c0001t0001g0044 a0001c0001t0001g0076 a0001c0001t0001g0081 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.276-6269dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72902095 | ||||||
| chr3:72902122 | G | A | 2 | a0001c0001t0028g0003 a0001c0002t0027g0048 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.276-6245G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902122 | |||||||
| chr3:72902131 | TGC | T | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-6235_276-6234d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902131 | |||||||
| chr3:72902366 | ATCAGAAA others(11): Show |
A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(2): Show |
5 | HG00597.hp2 HG02080.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-5996_276-5979d others(20): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72902366 | ||||||
| chr3:72902473 | T | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0138 a0001c0001t0001g0147 others(1): Show |
4 | HG00558.hp2 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-5894T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902473 | |||||||
| chr3:72902514 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.276-5853T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902514 | |||||||
| chr3:72902590 | A | G | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.276-5777A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902590 | |||||||
| chr3:72902685 | TAAATA | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0002t0020g0070 others(3): Show |
6 | HG02258.hp2 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.276-5674_276-5670d others(7): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72902685 | ||||||
| chr3:72902689 | T | A | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-5678T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902689 | |||||||
| chr3:72902690 | A | T | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-5677A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902690 | |||||||
| chr3:72902712 | T | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.276-5655T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902712 | |||||||
| chr3:72902715 | GGTGGCTC others(26): Show |
G | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-5651_276-5619d others(35): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902715 | |||||||
| chr3:72902722 | C | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.276-5645C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902722 | |||||||
| chr3:72902731 | A | T | 2 | a0001c0001t0001g0053 a0001c0005t0003g0052 |
2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.276-5636A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902731 | |||||||
| chr3:72902741 | A | G | 22 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0076 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.276-5626A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902741 | |||||||
| chr3:72902750 | C | A | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-5617C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902750 | |||||||
| chr3:72902752 | TG | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-5614delG | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902752 | |||||||
| chr3:72902760 | A | G | 2 | a0002c0006t0008g0288 a0002c0006t0008g0289 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.276-5607A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902760 | |||||||
| chr3:72902797 | G | A | 6 | a0001c0001t0001g0087 a0001c0001t0001g0090 a0001c0001t0006g0092 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.276-5570G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902797 | |||||||
| chr3:72902810 | T | C | 59 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.276-5557T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902810 | |||||||
| chr3:72902897 | C | T | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-5470C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902897 | |||||||
| chr3:72902993 | C | T | 59 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.276-5374C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72902993 | |||||||
| chr3:72903035 | T | G | 59 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.276-5332T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903035 | |||||||
| chr3:72903058 | TAAA | T | 8 | a0001c0001t0001g0053 a0001c0001t0001g0087 a0001c0001t0001g0090 others(5): Show |
8 | HG02055.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.276-5306_276-5304d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72903058 | ||||||
| chr3:72903076 | G | A | 51 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.276-5291G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903076 | |||||||
| chr3:72903224 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(290): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.276-5143A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903224 | |||||||
| chr3:72903237 | A | G | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.276-5130A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903237 | |||||||
| chr3:72903249 | A | G | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(58): Show |
61 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.276-5118A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903249 | |||||||
| chr3:72903336 | A | G | 2 | a0001c0001t0002g0123 a0001c0001t0007g0122 |
2 | HG01256.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.276-5031A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903336 | |||||||
| chr3:72903350 | C | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0076 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.276-5017C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903350 | |||||||
| chr3:72903372 | T | C | 1 | a0001c0001t0002g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.276-4995T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903372 | |||||||
| chr3:72903414 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0076 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.276-4953T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903414 | |||||||
| chr3:72903527 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0076 others(19): Show |
22 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.276-4840G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903527 | |||||||
| chr3:72903629 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0053 others(27): Show |
30 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.276-4738G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903629 | |||||||
| chr3:72903715 | A | C | 2 | a0001c0001t0001g0205 a0001c0001t0002g0180 |
2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.276-4652A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903715 | |||||||
| chr3:72903731 | G | C | 2 | a0001c0001t0001g0294 a0001c0001t0003g0293 |
2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.276-4636G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903731 | |||||||
| chr3:72903831 | G | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0005g0045 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.276-4536G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72903831 | |||||||
| chr3:72904264 | T | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(159): Show |
162 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.276-4103T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904264 | |||||||
| chr3:72904325 | G | A | 3 | a0001c0001t0001g0004 a0001c0002t0014g0005 a0001c0002t0025g0006 |
3 | HG02280.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.276-4042G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904325 | |||||||
| chr3:72904380 | T | G | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.276-3987T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904380 | |||||||
| chr3:72904644 | TA | T | 7 | a0001c0001t0001g0081 a0001c0001t0001g0179 a0001c0001t0002g0012 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-3710delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72904644 | ||||||
| chr3:72904755 | A | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0086 a0001c0001t0009g0088 others(7): Show |
10 | HG02280.hp1 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.276-3612A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904755 | |||||||
| chr3:72904838 | C | T | 2 | a0001c0001t0005g0045 a0001c0001t0006g0092 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.276-3529C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904838 | |||||||
| chr3:72904877 | C | CA | 51 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0093 others(48): Show |
51 | HG00597.hp2 HG00741.hp2 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.276-3469dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72904877 | ||||||
| chr3:72904877 | C | CAA | 7 | a0001c0001t0001g0139 a0001c0001t0001g0230 a0001c0001t0001g0231 others(4): Show |
7 | HG00597.hp1 HG02572.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.276-3470_276-3469d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72904877 | ||||||
| chr3:72904887 | A | AT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0002g0134 others(4): Show |
7 | HG01106.hp2 HG02004.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.276-3480_276-3479i others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904887 | |||||||
| chr3:72904891 | A | AT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.276-3476_276-3475i others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904891 | |||||||
| chr3:72904891 | A | T | 10 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0001g0178 others(7): Show |
10 | HG01106.hp2 HG01167.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.276-3476A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904891 | |||||||
| chr3:72904895 | A | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.276-3472A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904895 | |||||||
| chr3:72904921 | G | A | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-3446G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72904921 | |||||||
| chr3:72905064 | C | CA | 17 | a0001c0001t0001g0050 a0001c0001t0001g0142 a0001c0001t0001g0155 others(14): Show |
17 | HG01169.hp2 HG01261.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.276-3279dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72905064 | ||||||
| chr3:72905064 | CA | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0060 others(30): Show |
33 | HG00099.hp1 HG00639.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.276-3279delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72905064 | ||||||
| chr3:72905064 | CAA | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0056 others(17): Show |
20 | HG01952.hp1 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.276-3280_276-3279d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72905064 | ||||||
| chr3:72905064 | CAAAA | C | 8 | a0001c0001t0006g0063 a0001c0004t0008g0281 a0001c0004t0008g0284 others(5): Show |
8 | HG01109.hp2 HG02897.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.276-3282_276-3279d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72905064 | ||||||
| chr3:72905123 | G | T | 1 | a0001c0002t0027g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.276-3244G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905123 | |||||||
| chr3:72905129 | G | C | 1 | a0001c0001t0004g0032 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.276-3238G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905129 | |||||||
| chr3:72905205 | T | C | 10 | a0001c0001t0001g0081 a0001c0002t0001g0040 a0001c0002t0001g0042 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.276-3162T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905205 | |||||||
| chr3:72905230 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
5 | HG02717.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-3137G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905230 | |||||||
| chr3:72905422 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.276-2945C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905422 | |||||||
| chr3:72905449 | T | G | 10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG01884.hp2 HG02451.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.276-2918T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905449 | |||||||
| chr3:72905649 | T | C | 28 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(25): Show |
28 | HG01109.hp2 HG01952.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.276-2718T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905649 | |||||||
| chr3:72905664 | G | C | 25 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0064 others(22): Show |
25 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.276-2703G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905664 | |||||||
| chr3:72905701 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.276-2666C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905701 | |||||||
| chr3:72905703 | A | C | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.276-2664A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905703 | |||||||
| chr3:72905750 | C | T | 20 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(17): Show |
20 | HG01109.hp2 HG01952.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.276-2617C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905750 | |||||||
| chr3:72905751 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.276-2616G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905751 | |||||||
| chr3:72905776 | C | G | 1 | a0001c0001t0002g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.276-2591C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905776 | |||||||
| chr3:72905988 | T | C | 2 | a0001c0001t0002g0143 a0001c0001t0007g0156 |
2 | NA18944.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.276-2379T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72905988 | |||||||
| chr3:72906132 | T | A | 1 | a0001c0001t0009g0216 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.276-2235T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906132 | |||||||
| chr3:72906298 | G | T | 9 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.276-2069G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906298 | |||||||
| chr3:72906323 | G | A | 2 | a0001c0001t0002g0190 a0001c0001t0002g0251 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.276-2044G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906323 | |||||||
| chr3:72906332 | G | T | 1 | a0001c0005t0003g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276-2035G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906332 | |||||||
| chr3:72906380 | C | A | 29 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(26): Show |
29 | HG01109.hp2 HG01952.hp1 HG02451.hp1 others(26): Show |
intron_variant | MODIFIER | c.276-1987C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906380 | |||||||
| chr3:72906529 | T | C | 9 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.276-1838T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906529 | |||||||
| chr3:72906586 | TGCAGGC | T | 34 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0064 others(31): Show |
34 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.276-1779_276-1774d others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72906586 | ||||||
| chr3:72906592 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.276-1775C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906592 | |||||||
| chr3:72906696 | G | A | 1 | a0001c0001t0009g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.276-1671G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906696 | |||||||
| chr3:72906696 | G | C | 25 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(22): Show |
25 | HG01109.hp2 HG01952.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.276-1671G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906696 | |||||||
| chr3:72906739 | T | C | 1 | a0001c0001t0002g0110 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.276-1628T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72906739 | |||||||
| chr3:72907043 | C | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02965.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.276-1324C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907043 | |||||||
| chr3:72907342 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.276-1025A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907342 | |||||||
| chr3:72907509 | CT | C | 3 | a0001c0004t0008g0292 a0001c0004t0015g0290 a0005c0009t0030g0291 |
3 | HG02922.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.276-856delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 72907509 | ||||||
| chr3:72907649 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.276-718A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907649 | |||||||
| chr3:72907747 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0064 others(46): Show |
49 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.276-620C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907747 | |||||||
| chr3:72907815 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | NA18971.hp2 NA18983.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-552G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907815 | |||||||
| chr3:72907821 | G | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
13 | HG00735.hp1 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.276-546G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907821 | |||||||
| chr3:72907823 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(59): Show |
62 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.276-544G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907823 | |||||||
| chr3:72907836 | T | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(60): Show |
63 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.276-531T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72907836 | |||||||
| chr3:72908100 | C | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
93 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.276-267C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72908100 | |||||||
| chr3:72908333 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.276-34A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 1/6 | chr3 | 72908333 | |||||||
| chr3:72908583 | C | CAGTGTTT others(1): Show |
63 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(60): Show |
63 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.468+25_468+32dupAG others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72908583 | ||||||
| chr3:72908758 | A | T | 1 | a0001c0001t0002g0012 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.468+199A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72908758 | |||||||
| chr3:72908802 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.468+243A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72908802 | |||||||
| chr3:72908819 | C | A | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
13 | HG00735.hp1 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+260C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72908819 | |||||||
| chr3:72908850 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.468+291G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72908850 | |||||||
| chr3:72908967 | C | G | 1 | a0001c0002t0021g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.468+408C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72908967 | |||||||
| chr3:72908974 | C | T | 33 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0103 others(30): Show |
33 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.468+415C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72908974 | |||||||
| chr3:72909062 | C | CT | 42 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0073 others(39): Show |
42 | HG00140.hp1 HG00597.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.468+527dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72909062 | ||||||
| chr3:72909062 | C | CTT | 13 | a0001c0001t0001g0085 a0001c0001t0001g0247 a0001c0002t0001g0040 others(10): Show |
13 | HG01934.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.468+526_468+527dup others(2): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72909062 | ||||||
| chr3:72909062 | C | CTTT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(20): Show |
23 | HG00735.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+525_468+527dup others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72909062 | ||||||
| chr3:72909062 | CT | C | 8 | a0001c0001t0001g0093 a0001c0001t0001g0175 a0001c0001t0001g0217 others(5): Show |
8 | HG01256.hp1 HG01257.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+527delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72909062 | ||||||
| chr3:72909062 | CTTTTTT | C | 22 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(19): Show |
22 | HG01109.hp2 HG01952.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+522_468+527del others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72909062 | ||||||
| chr3:72909062 | CTTTTTTT | C | 26 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0103 others(23): Show |
26 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.468+521_468+527del others(7): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72909062 | ||||||
| chr3:72909105 | G | T | 1 | a0001c0001t0002g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.468+546G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72909105 | |||||||
| chr3:72909132 | G | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
13 | HG00735.hp1 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+573G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72909132 | |||||||
| chr3:72909382 | C | A | 27 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(24): Show |
27 | HG01109.hp2 HG01952.hp1 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.468+823C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72909382 | |||||||
| chr3:72909726 | C | T | 33 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0103 others(30): Show |
33 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.468+1167C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72909726 | |||||||
| chr3:72909899 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.468+1340G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72909899 | |||||||
| chr3:72909927 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.468+1368A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72909927 | |||||||
| chr3:72910081 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(91): Show |
94 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.468+1522G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72910081 | |||||||
| chr3:72910195 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.468+1636A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72910195 | |||||||
| chr3:72910224 | G | A | 3 | a0001c0001t0002g0213 a0001c0001t0002g0229 a0001c0001t0006g0214 |
3 | NA18982.hp1 NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.468+1665G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72910224 | |||||||
| chr3:72910321 | C | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(60): Show |
63 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.468+1762C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72910321 | |||||||
| chr3:72910617 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0003g0059 a0001c0001t0003g0061 |
3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.468+2058C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72910617 | |||||||
| chr3:72910697 | C | T | 5 | a0001c0002t0014g0039 a0002c0003t0001g0104 a0002c0003t0002g0015 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+2138C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72910697 | |||||||
| chr3:72910740 | C | T | 9 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+2181C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72910740 | |||||||
| chr3:72911041 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.468+2482C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911041 | |||||||
| chr3:72911067 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.468+2508G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911067 | |||||||
| chr3:72911185 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0003g0062 a0001c0001t0003g0068 |
3 | HG02055.hp2 HG02109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.468+2626G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911185 | |||||||
| chr3:72911325 | A | G | 1 | a0001c0004t0008g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.468+2766A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911325 | |||||||
| chr3:72911329 | G | A | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+2770G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911329 | |||||||
| chr3:72911377 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0064 others(42): Show |
45 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.468+2818A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911377 | |||||||
| chr3:72911400 | C | T | 3 | a0001c0005t0003g0069 a0002c0006t0008g0288 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.468+2841C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911400 | |||||||
| chr3:72911512 | C | T | 1 | a0001c0001t0009g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.468+2953C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911512 | |||||||
| chr3:72911584 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0007g0169 |
2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.468+3025A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911584 | |||||||
| chr3:72911613 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.468+3054A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911613 | |||||||
| chr3:72911932 | T | A | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.468+3373T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911932 | |||||||
| chr3:72911991 | G | GTATATA | 4 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0003g0062 others(1): Show |
4 | HG02055.hp2 HG02976.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3433_468+3434i others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72911991 | ||||||
| chr3:72911991 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468+3433_468+3434i others(14): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72911991 | ||||||
| chr3:72911993 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0055 others(46): Show |
49 | HG01109.hp2 HG01243.hp2 HG01952.hp1 others(46): Show |
intron_variant | MODIFIER | c.468+3434G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911993 | |||||||
| chr3:72911993 | G | GTATATAT others(3): Show |
5 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0013g0041 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3446_468+3455d others(12): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72911993 | ||||||
| chr3:72911993 | G | GTGTATAT others(3): Show |
2 | a0001c0002t0001g0043 a0001c0002t0001g0079 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.468+3435_468+3436i others(12): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72911993 | ||||||
| chr3:72911993 | G | GTGTGTAT others(5): Show |
2 | a0001c0002t0001g0080 a0001c0002t0018g0188 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.468+3435_468+3436i others(14): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72911993 | ||||||
| chr3:72911995 | A | G | 1 | a0001c0001t0012g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.468+3436A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72911995 | |||||||
| chr3:72912009 | A | ATT | 3 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02965.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.468+3451_468+3452i others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912009 | ||||||
| chr3:72912009 | A | ATTT | 3 | a0001c0001t0001g0259 a0001c0005t0003g0091 a0004c0011t0001g0023 |
3 | HG02647.hp2 HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.468+3451_468+3452i others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912009 | ||||||
| chr3:72912009 | A | ATTTTTT | 3 | a0001c0004t0008g0292 a0001c0004t0015g0290 a0005c0009t0030g0291 |
3 | HG02922.hp2 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.468+3451_468+3452i others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912009 | ||||||
| chr3:72912011 | A | ATTT | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0076 others(5): Show |
8 | HG00735.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+3453_468+3454i others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912011 | ||||||
| chr3:72912011 | A | ATTTT | 11 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(8): Show |
11 | HG02293.hp2 HG02559.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+3453_468+3454i others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912011 | ||||||
| chr3:72912011 | A | ATTTTTT | 8 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0101 others(5): Show |
8 | HG01952.hp1 HG02451.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+3453_468+3454i others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912011 | ||||||
| chr3:72912011 | A | T | 9 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3452A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912011 | |||||||
| chr3:72912013 | A | AT | 6 | a0001c0001t0001g0233 a0001c0001t0001g0271 a0001c0001t0001g0279 others(3): Show |
6 | HG01243.hp2 HG02056.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+3469dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912013 | ||||||
| chr3:72912013 | A | ATTTT | 16 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0103 others(13): Show |
16 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.468+3466_468+3469d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912013 | ||||||
| chr3:72912013 | A | T | 53 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(50): Show |
53 | HG00597.hp1 HG00735.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.468+3454A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912013 | |||||||
| chr3:72912013 | AT | A | 11 | a0001c0001t0001g0117 a0001c0001t0001g0179 a0001c0001t0001g0226 others(8): Show |
11 | HG00558.hp1 HG00741.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+3469delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912013 | ||||||
| chr3:72912014 | T | TA | 11 | a0001c0001t0001g0031 a0001c0001t0001g0113 a0001c0001t0001g0128 others(8): Show |
11 | HG00639.hp1 HG01358.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+3455_468+3456i others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912014 | |||||||
| chr3:72912015 | T | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0111 others(20): Show |
23 | HG00099.hp1 HG00423.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.468+3456T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912015 | |||||||
| chr3:72912016 | T | A | 5 | a0001c0001t0001g0117 a0001c0001t0002g0098 a0001c0001t0002g0157 others(2): Show |
5 | HG00558.hp1 HG00639.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3457T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912016 | |||||||
| chr3:72912017 | T | A | 1 | a0001c0002t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.468+3458T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912017 | |||||||
| chr3:72912042 | GCT | G | 9 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.468+3486_468+3487d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72912042 | ||||||
| chr3:72912102 | C | T | 1 | a0001c0001t0004g0013 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.468+3543C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912102 | |||||||
| chr3:72912116 | T | G | 36 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0053 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.468+3557T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912116 | |||||||
| chr3:72912159 | G | A | 1 | a0001c0005t0003g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.468+3600G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912159 | |||||||
| chr3:72912206 | C | T | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+3647C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912206 | |||||||
| chr3:72912248 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.468+3689A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912248 | |||||||
| chr3:72912290 | A | G | 1 | a0001c0001t0005g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.468+3731A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912290 | |||||||
| chr3:72912340 | C | T | 4 | a0001c0005t0003g0069 a0001c0010t0031g0286 a0002c0006t0008g0288 others(1): Show |
4 | HG02559.hp1 HG02630.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+3781C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912340 | |||||||
| chr3:72912346 | C | G | 1 | a0001c0001t0009g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.468+3787C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912346 | |||||||
| chr3:72912450 | G | A | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+3891G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912450 | |||||||
| chr3:72912464 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0002g0109 a0001c0001t0005g0254 |
3 | HG02027.hp2 HG02165.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.468+3905G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912464 | |||||||
| chr3:72912527 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.468+3968T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912527 | |||||||
| chr3:72912562 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.468+4003A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912562 | |||||||
| chr3:72912764 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.468+4205G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72912764 | |||||||
| chr3:72913024 | G | GT | 6 | a0001c0001t0001g0081 a0001c0001t0001g0279 a0001c0001t0002g0110 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+4475dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72913024 | ||||||
| chr3:72913024 | G | GTT | 20 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0065 others(17): Show |
20 | HG01109.hp2 HG01952.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.468+4474_468+4475d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72913024 | ||||||
| chr3:72913024 | G | T | 3 | a0001c0005t0003g0069 a0002c0006t0008g0288 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.468+4465G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913024 | |||||||
| chr3:72913024 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0007g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.468+4485_468+4496d others(14): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72913024 | ||||||
| chr3:72913035 | G | GT | 14 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(11): Show |
14 | HG00558.hp2 HG00735.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.468+4487dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72913035 | ||||||
| chr3:72913035 | G | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0166 a0001c0001t0001g0202 |
3 | HG01069.hp1 HG01071.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.468+4476G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913035 | |||||||
| chr3:72913102 | A | G | 13 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
13 | HG00735.hp1 HG02622.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+4543A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913102 | |||||||
| chr3:72913189 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0084 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+4630C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913189 | |||||||
| chr3:72913198 | C | T | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+4639C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913198 | |||||||
| chr3:72913200 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.468+4641G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913200 | |||||||
| chr3:72913267 | T | C | 1 | a0001c0001t0005g0254 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.468+4708T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913267 | |||||||
| chr3:72913281 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.468+4722G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913281 | |||||||
| chr3:72913373 | A | G | 3 | a0001c0005t0003g0069 a0002c0006t0008g0288 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.468+4814A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913373 | |||||||
| chr3:72913462 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0084 others(8): Show |
11 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+4903A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913462 | |||||||
| chr3:72913509 | A | T | 1 | a0001c0004t0008g0287 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.468+4950A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913509 | |||||||
| chr3:72913515 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(1): Show |
4 | HG02717.hp1 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+4956C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913515 | |||||||
| chr3:72913652 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0096 others(42): Show |
45 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.468+5093G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913652 | |||||||
| chr3:72913992 | G | A | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+5433G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72913992 | |||||||
| chr3:72914301 | G | A | 1 | a0001c0001t0006g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.468+5742G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914301 | |||||||
| chr3:72914425 | G | A | 6 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
6 | HG00597.hp2 HG02071.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+5866G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914425 | |||||||
| chr3:72914503 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.468+5944T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914503 | |||||||
| chr3:72914507 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0170 a0001c0005t0003g0052 |
3 | HG02723.hp1 NA18612.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.468+5948A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914507 | |||||||
| chr3:72914527 | A | ATG | 3 | a0001c0001t0001g0198 a0001c0001t0002g0273 a0001c0010t0031g0286 |
3 | HG02630.hp1 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.468+5987_468+5988d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72914527 | ||||||
| chr3:72914527 | A | ATGTG | 4 | a0001c0001t0001g0250 a0001c0002t0014g0005 a0001c0002t0025g0006 others(1): Show |
4 | HG02280.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+5985_468+5988d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72914527 | ||||||
| chr3:72914527 | A | G | 10 | a0001c0001t0001g0075 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG00099.hp1 HG01123.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+5968A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914527 | |||||||
| chr3:72914527 | ATG | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0031 others(51): Show |
54 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.468+5987_468+5988d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72914527 | ||||||
| chr3:72914527 | ATGTG | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0076 others(4): Show |
7 | HG01952.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+5985_468+5988d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72914527 | ||||||
| chr3:72914538 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.468+5979T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914538 | |||||||
| chr3:72914544 | T | C | 1 | a0001c0005t0003g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.468+5985T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914544 | |||||||
| chr3:72914546 | T | C | 66 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0055 others(63): Show |
66 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.468+5987T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914546 | |||||||
| chr3:72914546 | T | TGC | 4 | a0001c0001t0002g0108 a0001c0001t0002g0213 a0001c0001t0002g0229 others(1): Show |
4 | NA18948.hp2 NA18982.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+5998_468+5999d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72914546 | ||||||
| chr3:72914546 | T | TGTGCGC | 4 | a0001c0001t0001g0279 a0002c0003t0001g0102 a0002c0003t0002g0269 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+5988_468+5989i others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72914546 | ||||||
| chr3:72914549 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.468+5990G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914549 | |||||||
| chr3:72914551 | G | A | 65 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0055 others(62): Show |
65 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.468+5992G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914551 | |||||||
| chr3:72914559 | T | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(94): Show |
97 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.468+6000T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914559 | |||||||
| chr3:72914567 | G | A | 10 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+6008G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914567 | |||||||
| chr3:72914618 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(99): Show |
102 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.468+6059A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914618 | |||||||
| chr3:72914677 | G | C | 8 | a0001c0004t0008g0281 a0001c0004t0008g0282 a0001c0004t0008g0284 others(5): Show |
8 | HG01109.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+6118G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914677 | |||||||
| chr3:72914749 | CAGATTGA others(2): Show |
C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(17): Show |
20 | HG01243.hp2 HG02257.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.468+6195_468+6203d others(11): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72914749 | ||||||
| chr3:72914753 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.468+6194T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914753 | |||||||
| chr3:72914766 | G | A | 1 | a0001c0001t0009g0088 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.468+6207G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914766 | |||||||
| chr3:72914793 | A | G | 69 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0050 others(66): Show |
69 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.468+6234A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914793 | |||||||
| chr3:72914906 | C | T | 42 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0084 others(39): Show |
42 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.468+6347C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914906 | |||||||
| chr3:72914982 | G | T | 2 | a0001c0001t0001g0085 a0001c0005t0003g0052 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.468+6423G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914982 | |||||||
| chr3:72914993 | A | G | 7 | a0001c0004t0008g0287 a0002c0003t0001g0102 a0002c0003t0002g0269 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+6434A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72914993 | |||||||
| chr3:72915020 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.468+6461A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915020 | |||||||
| chr3:72915109 | C | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.468+6550C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915109 | |||||||
| chr3:72915176 | G | C | 5 | a0001c0004t0008g0281 a0001c0004t0008g0282 a0001c0004t0008g0284 others(2): Show |
5 | HG01109.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+6617G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915176 | |||||||
| chr3:72915205 | C | A | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+6646C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915205 | |||||||
| chr3:72915240 | T | C | 3 | a0002c0003t0005g0072 a0002c0006t0008g0288 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.468+6681T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915240 | |||||||
| chr3:72915254 | GA | G | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+6703delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72915254 | ||||||
| chr3:72915294 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.468+6735G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915294 | |||||||
| chr3:72915309 | G | A | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.468+6750G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915309 | |||||||
| chr3:72915338 | C | CT | 36 | a0001c0001t0001g0031 a0001c0001t0001g0051 a0001c0001t0001g0058 others(33): Show |
36 | HG00673.hp1 HG00673.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.468+6795dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72915338 | ||||||
| chr3:72915338 | C | CTT | 13 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0084 others(10): Show |
13 | HG02451.hp1 HG02622.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.468+6794_468+6795d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72915338 | ||||||
| chr3:72915354 | T | G | 1 | a0001c0001t0002g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.468+6795T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915354 | |||||||
| chr3:72915354 | T | TTGC | 8 | a0001c0001t0001g0125 a0001c0001t0001g0130 a0001c0001t0001g0147 others(5): Show |
8 | HG00558.hp2 HG01071.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+6795_468+6796i others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915354 | |||||||
| chr3:72915354 | T | TTTGC | 11 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0060 others(8): Show |
11 | HG00735.hp1 HG01952.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+6795_468+6796i others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915354 | |||||||
| chr3:72915354 | TG | T | 8 | a0001c0001t0001g0085 a0001c0002t0001g0040 a0001c0002t0013g0041 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+6796delG | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915354 | |||||||
| chr3:72915355 | G | C | 1 | a0001c0001t0002g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.468+6796G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915355 | |||||||
| chr3:72915355 | G | T | 4 | a0001c0001t0001g0228 a0001c0001t0007g0221 a0001c0002t0001g0043 others(1): Show |
4 | HG02145.hp1 HG02165.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+6796G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915355 | |||||||
| chr3:72915356 | C | CG | 88 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
88 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.468+6810dupG | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72915356 | ||||||
| chr3:72915356 | C | CGG | 23 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0094 others(20): Show |
23 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+6809_468+6810d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72915356 | ||||||
| chr3:72915356 | C | G | 27 | a0001c0001t0001g0026 a0001c0001t0001g0055 a0001c0001t0001g0060 others(24): Show |
27 | HG00558.hp2 HG00735.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.468+6797C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915356 | |||||||
| chr3:72915356 | C | T | 8 | a0001c0001t0001g0085 a0001c0002t0001g0040 a0001c0002t0013g0041 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+6797C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915356 | |||||||
| chr3:72915356 | CGG | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
21 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.468+6809_468+6810d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72915356 | ||||||
| chr3:72915357 | G | C | 4 | a0001c0001t0001g0228 a0001c0001t0007g0221 a0001c0002t0001g0043 others(1): Show |
4 | HG02145.hp1 HG02165.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+6798G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915357 | |||||||
| chr3:72915358 | G | C | 8 | a0001c0001t0001g0085 a0001c0002t0001g0040 a0001c0002t0013g0041 others(5): Show |
8 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+6799G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915358 | |||||||
| chr3:72915361 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.468+6802G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915361 | |||||||
| chr3:72915361 | G | GT | 25 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0084 others(22): Show |
25 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.468+6802_468+6803i others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915361 | |||||||
| chr3:72915361 | G | T | 3 | a0001c0001t0005g0045 a0001c0001t0006g0063 a0001c0001t0028g0003 |
3 | HG01891.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.468+6802G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915361 | |||||||
| chr3:72915362 | G | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0012 |
2 | HG01081.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.468+6803G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915362 | |||||||
| chr3:72915362 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468+6803G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915362 | |||||||
| chr3:72915367 | G | T | 3 | a0001c0001t0007g0156 a0001c0002t0001g0080 a0001c0002t0018g0188 |
3 | HG02818.hp2 HG03516.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.468+6808G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915367 | |||||||
| chr3:72915368 | G | C | 1 | a0001c0001t0003g0061 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.468+6809G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915368 | |||||||
| chr3:72915370 | A | T | 1 | a0001c0001t0002g0097 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.468+6811A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915370 | |||||||
| chr3:72915378 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468+6819A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915378 | |||||||
| chr3:72915455 | C | A | 4 | a0001c0001t0001g0258 a0001c0001t0003g0293 a0001c0001t0009g0088 others(1): Show |
4 | HG02486.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-6749C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915455 | |||||||
| chr3:72915589 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.469-6615C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915589 | |||||||
| chr3:72915596 | G | A | 16 | a0001c0001t0001g0085 a0001c0002t0001g0040 a0001c0002t0001g0042 others(13): Show |
16 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.469-6608G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915596 | |||||||
| chr3:72915823 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.469-6381A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915823 | |||||||
| chr3:72915827 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02965.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.469-6377T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915827 | |||||||
| chr3:72915832 | CA | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0126 a0001c0001t0001g0173 others(3): Show |
6 | HG01081.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-6359delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72915832 | ||||||
| chr3:72915899 | G | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(94): Show |
97 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.469-6305G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915899 | |||||||
| chr3:72915934 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.469-6270C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915934 | |||||||
| chr3:72915980 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.469-6224G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72915980 | |||||||
| chr3:72916185 | T | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0076 others(4): Show |
7 | HG02258.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-6019T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916185 | |||||||
| chr3:72916209 | T | C | 24 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0084 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.469-5995T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916209 | |||||||
| chr3:72916226 | C | A | 1 | a0001c0005t0003g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.469-5978C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916226 | |||||||
| chr3:72916226 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.469-5978C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916226 | |||||||
| chr3:72916261 | G | C | 4 | a0001c0001t0001g0258 a0001c0001t0003g0293 a0001c0001t0009g0088 others(1): Show |
4 | HG02486.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-5943G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916261 | |||||||
| chr3:72916262 | C | A | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.469-5942C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916262 | |||||||
| chr3:72916322 | A | G | 2 | a0001c0001t0002g0190 a0001c0001t0002g0251 |
2 | HG02735.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.469-5882A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916322 | |||||||
| chr3:72916482 | C | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(60): Show |
63 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.469-5722C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916482 | |||||||
| chr3:72916582 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(12): Show |
15 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.469-5622C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916582 | |||||||
| chr3:72916824 | A | G | 1 | a0002c0003t0002g0015 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.469-5380A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916824 | |||||||
| chr3:72916826 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0011g0256 |
2 | NA18982.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.469-5378T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916826 | |||||||
| chr3:72916946 | T | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0001c0001t0001g0111 others(9): Show |
12 | HG00099.hp1 HG01123.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.469-5258T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72916946 | |||||||
| chr3:72917202 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.469-5002C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917202 | |||||||
| chr3:72917217 | G | A | 6 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-4987G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917217 | |||||||
| chr3:72917234 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02965.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.469-4970G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917234 | |||||||
| chr3:72917304 | C | T | 48 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(45): Show |
48 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.469-4900C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917304 | |||||||
| chr3:72917426 | G | C | 23 | a0001c0001t0001g0026 a0001c0001t0001g0053 a0001c0001t0001g0055 others(20): Show |
23 | HG00735.hp1 HG01109.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.469-4778G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917426 | |||||||
| chr3:72917513 | A | C | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-4691A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917513 | |||||||
| chr3:72917593 | T | C | 24 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0084 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.469-4611T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917593 | |||||||
| chr3:72917625 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.469-4579C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917625 | |||||||
| chr3:72917644 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.469-4560C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917644 | |||||||
| chr3:72917757 | C | CA | 9 | a0001c0001t0001g0270 a0001c0001t0002g0227 a0001c0001t0006g0017 others(6): Show |
9 | HG01192.hp1 HG01261.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-4431dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72917757 | ||||||
| chr3:72917856 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.469-4348C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917856 | |||||||
| chr3:72917931 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.469-4273A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72917931 | |||||||
| chr3:72918234 | C | A | 2 | a0001c0001t0009g0088 a0001c0005t0003g0069 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.469-3970C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72918234 | |||||||
| chr3:72918432 | A | G | 2 | a0001c0001t0002g0077 a0001c0001t0024g0078 |
2 | HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.469-3772A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72918432 | |||||||
| chr3:72918701 | T | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(95): Show |
98 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.469-3503T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72918701 | |||||||
| chr3:72919028 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0003g0062 a0001c0001t0003g0068 others(2): Show |
5 | HG02055.hp1 HG02055.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-3176T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919028 | |||||||
| chr3:72919065 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.469-3139C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919065 | |||||||
| chr3:72919088 | C | T | 8 | a0002c0003t0001g0102 a0002c0003t0001g0104 a0002c0003t0002g0015 others(5): Show |
8 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-3116C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919088 | |||||||
| chr3:72919140 | C | A | 47 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.469-3064C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919140 | |||||||
| chr3:72919158 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.469-3046A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919158 | |||||||
| chr3:72919275 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.469-2929T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919275 | |||||||
| chr3:72919440 | A | G | 1 | a0001c0005t0003g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.469-2764A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919440 | |||||||
| chr3:72919451 | CTA | C | 84 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0044 others(81): Show |
84 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.469-2748_469-2747d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72919451 | ||||||
| chr3:72919490 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.469-2714C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919490 | |||||||
| chr3:72919492 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.469-2712C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919492 | |||||||
| chr3:72919543 | T | C | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.469-2661T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919543 | |||||||
| chr3:72919650 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.469-2554G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919650 | |||||||
| chr3:72919674 | G | C | 1 | a0001c0005t0003g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.469-2530G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919674 | |||||||
| chr3:72919712 | G | A | 17 | a0001c0001t0001g0258 a0001c0001t0003g0293 a0001c0002t0001g0040 others(14): Show |
17 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.469-2492G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919712 | |||||||
| chr3:72919744 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0170 |
2 | NA18612.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.469-2460G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919744 | |||||||
| chr3:72919856 | A | G | 1 | a0002c0003t0005g0072 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.469-2348A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72919856 | |||||||
| chr3:72920119 | C | G | 2 | a0001c0001t0002g0123 a0001c0001t0007g0122 |
2 | HG01256.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.469-2085C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920119 | |||||||
| chr3:72920228 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.469-1976G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920228 | |||||||
| chr3:72920515 | C | T | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG00735.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.469-1689C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920515 | |||||||
| chr3:72920702 | G | A | 14 | a0001c0001t0001g0031 a0001c0001t0001g0113 a0001c0001t0001g0128 others(11): Show |
14 | HG01358.hp1 HG01891.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.469-1502G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920702 | |||||||
| chr3:72920777 | C | A | 1 | a0001c0001t0002g0114 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.469-1427C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920777 | |||||||
| chr3:72920799 | C | CAT | 5 | a0001c0001t0002g0143 a0001c0001t0002g0267 a0001c0001t0007g0156 others(2): Show |
5 | HG03225.hp1 HG03453.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-1390_469-1389d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72920799 | ||||||
| chr3:72920799 | C | CATAT | 4 | a0001c0001t0001g0139 a0001c0001t0001g0170 a0001c0001t0001g0258 others(1): Show |
4 | HG02486.hp2 NA18612.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1392_469-1389d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72920799 | ||||||
| chr3:72920801 | T | C | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.469-1403T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920801 | |||||||
| chr3:72920816 | G | A | 21 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
21 | HG01891.hp2 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.469-1388G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920816 | |||||||
| chr3:72920818 | A | ATATG | 10 | a0002c0003t0001g0102 a0002c0003t0001g0104 a0002c0003t0002g0015 others(7): Show |
10 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-1385_469-1384i others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72920818 | ||||||
| chr3:72920818 | A | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-1386A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920818 | |||||||
| chr3:72920818 | AT | A | 71 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0050 others(68): Show |
71 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.469-1371delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72920818 | ||||||
| chr3:72920819 | T | TA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-1385_469-1384i others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920819 | |||||||
| chr3:72920820 | T | A | 10 | a0002c0003t0001g0102 a0002c0003t0001g0104 a0002c0003t0002g0015 others(7): Show |
10 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-1384T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920820 | |||||||
| chr3:72920874 | G | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG00099.hp1 HG01123.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1330G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920874 | |||||||
| chr3:72920930 | C | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0087 |
3 | HG02622.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.469-1274C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920930 | |||||||
| chr3:72920973 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.469-1231C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72920973 | |||||||
| chr3:72921017 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0002g0244 |
2 | HG01256.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.469-1187C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921017 | |||||||
| chr3:72921117 | G | A | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.469-1087G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921117 | |||||||
| chr3:72921179 | T | TA | 47 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(44): Show |
47 | HG00735.hp1 HG01109.hp2 HG01952.hp1 others(44): Show |
intron_variant | MODIFIER | c.469-1012dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 72921179 | ||||||
| chr3:72921180 | A | T | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.469-1024A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921180 | |||||||
| chr3:72921193 | T | A | 25 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0084 others(22): Show |
25 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.469-1011T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921193 | |||||||
| chr3:72921737 | G | A | 1 | a0001c0002t0021g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.469-467G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921737 | |||||||
| chr3:72921872 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.469-332A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921872 | |||||||
| chr3:72921890 | TG | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(77): Show |
80 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.469-313delG | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921890 | |||||||
| chr3:72921988 | C | A | 11 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.469-216C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72921988 | |||||||
| chr3:72922141 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
16 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.469-63C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72922141 | |||||||
| chr3:72922190 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(94): Show |
97 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.469-14C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 2/6 | chr3 | 72922190 | |||||||
| chr3:72922535 | G | A | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(49): Show |
52 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.600+200G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922535 | |||||||
| chr3:72922537 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.600+202G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922537 | |||||||
| chr3:72922598 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(63): Show |
66 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.600+263C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922598 | |||||||
| chr3:72922689 | G | C | 8 | a0002c0003t0001g0102 a0002c0003t0001g0104 a0002c0003t0002g0015 others(5): Show |
8 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+354G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922689 | |||||||
| chr3:72922842 | G | A | 1 | a0001c0001t0006g0185 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.600+507G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922842 | |||||||
| chr3:72922863 | A | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(64): Show |
67 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.600+528A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922863 | |||||||
| chr3:72922898 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0006g0092 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.600+563C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922898 | |||||||
| chr3:72922936 | G | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(89): Show |
92 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.600+601G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922936 | |||||||
| chr3:72922971 | T | C | 4 | a0001c0002t0014g0005 a0001c0002t0025g0006 a0001c0002t0027g0048 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+636T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922971 | |||||||
| chr3:72922975 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.600+640C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72922975 | |||||||
| chr3:72923026 | G | A | 1 | a0001c0001t0006g0063 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.600+691G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923026 | |||||||
| chr3:72923191 | C | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(96): Show |
99 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.600+856C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923191 | |||||||
| chr3:72923218 | G | T | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0101 |
3 | HG02451.hp1 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.600+883G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923218 | |||||||
| chr3:72923283 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(63): Show |
66 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.600+948C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923283 | |||||||
| chr3:72923400 | C | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(93): Show |
96 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.600+1065C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923400 | |||||||
| chr3:72923450 | AAAT | A | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+1124_600+1126d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72923450 | ||||||
| chr3:72923504 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.600+1169T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923504 | |||||||
| chr3:72923535 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.600+1200T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923535 | |||||||
| chr3:72923610 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.600+1275T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923610 | |||||||
| chr3:72923612 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.600+1277G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923612 | |||||||
| chr3:72923844 | T | G | 11 | a0002c0003t0001g0102 a0002c0003t0001g0104 a0002c0003t0002g0015 others(8): Show |
11 | HG01891.hp2 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.600+1509T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923844 | |||||||
| chr3:72923877 | C | T | 15 | a0001c0002t0001g0040 a0001c0002t0001g0042 a0001c0002t0001g0043 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+1542C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923877 | |||||||
| chr3:72923896 | A | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0076 others(5): Show |
8 | HG02258.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+1561A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923896 | |||||||
| chr3:72923926 | T | C | 1 | a0001c0005t0003g0091 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.600+1591T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72923926 | |||||||
| chr3:72924149 | G | A | 2 | a0001c0001t0003g0062 a0001c0001t0003g0068 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.600+1814G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72924149 | |||||||
| chr3:72924192 | C | CT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
21 | HG00639.hp1 HG01106.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.600+1874dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72924192 | ||||||
| chr3:72924192 | C | CTT | 47 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.600+1873_600+1874d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72924192 | ||||||
| chr3:72924368 | A | AT | 3 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | HG02965.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.600+2039dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72924368 | ||||||
| chr3:72924571 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.600+2236T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72924571 | |||||||
| chr3:72924581 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(127): Show |
130 | HG00558.hp2 HG00597.hp2 HG00733.hp2 others(127): Show |
intron_variant | MODIFIER | c.600+2246G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72924581 | |||||||
| chr3:72924630 | G | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.600+2295G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72924630 | |||||||
| chr3:72924692 | C | T | 3 | a0001c0002t0027g0048 a0002c0006t0008g0288 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.600+2357C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72924692 | |||||||
| chr3:72924867 | G | A | 3 | a0002c0006t0008g0288 a0002c0006t0008g0289 a0003c0008t0002g0009 |
3 | HG01123.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.600+2532G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72924867 | |||||||
| chr3:72925002 | G | A | 3 | a0001c0002t0001g0080 a0001c0002t0014g0039 a0005c0009t0030g0291 |
3 | HG02109.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.600+2667G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925002 | |||||||
| chr3:72925008 | T | C | 1 | a0001c0001t0009g0028 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.600+2673T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925008 | |||||||
| chr3:72925014 | G | A | 3 | a0001c0002t0001g0080 a0001c0002t0014g0039 a0005c0009t0030g0291 |
3 | HG02109.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.600+2679G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925014 | |||||||
| chr3:72925156 | C | CT | 31 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0056 others(28): Show |
31 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.600+2824dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72925156 | ||||||
| chr3:72925160 | C | CT | 7 | a0001c0001t0001g0142 a0001c0001t0001g0275 a0001c0001t0001g0277 others(4): Show |
7 | HG02055.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+2839dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72925160 | ||||||
| chr3:72925160 | C | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0056 others(38): Show |
41 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.600+2825C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925160 | |||||||
| chr3:72925300 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0002t0001g0042 others(1): Show |
4 | HG02257.hp2 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+2965C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925300 | |||||||
| chr3:72925398 | C | T | 1 | a0001c0001t0007g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.600+3063C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925398 | |||||||
| chr3:72925410 | C | A | 8 | a0001c0001t0002g0131 a0001c0001t0003g0082 a0001c0001t0003g0083 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+3075C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925410 | |||||||
| chr3:72925430 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0002g0124 a0001c0001t0002g0195 |
3 | NA18951.hp2 NA18952.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.600+3095A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925430 | |||||||
| chr3:72925480 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.600+3145C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925480 | |||||||
| chr3:72925490 | T | C | 15 | a0001c0001t0001g0064 a0001c0001t0001g0189 a0001c0001t0004g0013 others(12): Show |
15 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+3155T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925490 | |||||||
| chr3:72925498 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.600+3163C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925498 | |||||||
| chr3:72925513 | G | C | 1 | a0001c0001t0023g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.600+3178G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925513 | |||||||
| chr3:72925619 | A | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0090 |
3 | HG02615.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.600+3284A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925619 | |||||||
| chr3:72925760 | A | T | 1 | a0002c0003t0002g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.600+3425A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72925760 | |||||||
| chr3:72926118 | A | G | 2 | a0001c0001t0006g0063 a0001c0001t0006g0092 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+3783A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926118 | |||||||
| chr3:72926294 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.600+3959C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926294 | |||||||
| chr3:72926354 | C | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0092 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+4019C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926354 | |||||||
| chr3:72926418 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.600+4083T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926418 | |||||||
| chr3:72926627 | T | G | 1 | a0001c0001t0009g0216 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.600+4292T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926627 | |||||||
| chr3:72926665 | C | T | 3 | a0001c0001t0002g0264 a0001c0001t0002g0295 a0001c0001t0002g0296 |
3 | NA18962.hp2 NA18979.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.600+4330C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926665 | |||||||
| chr3:72926676 | G | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0081 others(1): Show |
4 | HG01884.hp1 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+4341G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926676 | |||||||
| chr3:72926963 | G | C | 1 | a0002c0003t0002g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.600+4628G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72926963 | |||||||
| chr3:72927369 | G | T | 5 | a0001c0001t0003g0062 a0001c0001t0003g0068 a0001c0005t0003g0052 others(2): Show |
5 | HG02055.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+5034G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72927369 | |||||||
| chr3:72927458 | A | C | 3 | a0001c0001t0001g0279 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG01243.hp2 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+5123A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72927458 | |||||||
| chr3:72927490 | G | A | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.600+5155G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72927490 | |||||||
| chr3:72927687 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(221): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.600+5352C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72927687 | |||||||
| chr3:72927850 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG01243.hp2 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+5515A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72927850 | |||||||
| chr3:72928094 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+5759A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928094 | |||||||
| chr3:72928262 | C | A | 1 | a0001c0001t0011g0106 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.600+5927C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928262 | |||||||
| chr3:72928335 | G | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(227): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.600+6000G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928335 | |||||||
| chr3:72928348 | C | T | 3 | a0001c0001t0001g0259 a0002c0003t0001g0102 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.600+6013C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928348 | |||||||
| chr3:72928369 | C | G | 1 | a0001c0001t0002g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.600+6034C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928369 | |||||||
| chr3:72928476 | G | C | 34 | a0001c0001t0001g0191 a0001c0001t0001g0205 a0001c0001t0002g0008 others(31): Show |
34 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.600+6141G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928476 | |||||||
| chr3:72928607 | A | T | 1 | a0001c0001t0002g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.600+6272A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928607 | |||||||
| chr3:72928689 | A | G | 11 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(8): Show |
11 | HG00735.hp1 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.600+6354A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928689 | |||||||
| chr3:72928755 | G | C | 14 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(11): Show |
14 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+6420G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928755 | |||||||
| chr3:72928785 | C | CA | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.600+6459dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72928785 | ||||||
| chr3:72928785 | C | CAA | 24 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(21): Show |
24 | HG00735.hp1 HG01109.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.600+6458_600+6459d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72928785 | ||||||
| chr3:72928795 | C | A | 6 | a0001c0001t0003g0260 a0001c0001t0003g0293 a0001c0004t0015g0285 others(3): Show |
6 | HG02572.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+6460C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928795 | |||||||
| chr3:72928902 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.600+6567A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928902 | |||||||
| chr3:72928964 | C | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+6629C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928964 | |||||||
| chr3:72928979 | G | A | 1 | a0001c0010t0031g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.600+6644G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928979 | |||||||
| chr3:72928994 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.600+6659G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72928994 | |||||||
| chr3:72929217 | A | C | 5 | a0001c0001t0001g0073 a0001c0002t0001g0040 a0001c0002t0001g0043 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+6882A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929217 | |||||||
| chr3:72929283 | T | C | 41 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0084 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.600+6948T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929283 | |||||||
| chr3:72929366 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0017g0280 |
2 | HG01109.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.600+7031A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929366 | |||||||
| chr3:72929374 | AT | A | 23 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(20): Show |
23 | HG00735.hp1 HG01109.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+7040delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929374 | |||||||
| chr3:72929375 | T | A | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.600+7040T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929375 | |||||||
| chr3:72929443 | T | C | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+7108T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929443 | |||||||
| chr3:72929509 | A | G | 7 | a0001c0001t0003g0062 a0001c0001t0003g0068 a0001c0001t0009g0088 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+7174A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929509 | |||||||
| chr3:72929649 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0002g0180 a0001c0001t0002g0203 others(2): Show |
5 | HG01243.hp1 HG02293.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+7314G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929649 | |||||||
| chr3:72929943 | G | T | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+7608G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72929943 | |||||||
| chr3:72930174 | C | CA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(123): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.600+7850dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930174 | ||||||
| chr3:72930174 | CA | C | 40 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0084 others(37): Show |
40 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.600+7850delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930174 | ||||||
| chr3:72930198 | T | G | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+7863T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930198 | |||||||
| chr3:72930270 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.600+7935T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930270 | |||||||
| chr3:72930273 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0081 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+7938G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930273 | |||||||
| chr3:72930502 | CA | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.600+8181delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930502 | ||||||
| chr3:72930502 | CAA | C | 7 | a0001c0001t0001g0166 a0001c0001t0001g0175 a0001c0001t0001g0202 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+8180_600+8181d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930502 | ||||||
| chr3:72930571 | C | T | 7 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+8236C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930571 | |||||||
| chr3:72930580 | TTTC | T | 7 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+8257_600+8259d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930580 | ||||||
| chr3:72930592 | C | CT | 20 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0055 others(17): Show |
20 | HG01109.hp2 HG02027.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.600+8276dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930592 | ||||||
| chr3:72930592 | C | CTT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.600+8275_600+8276d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930592 | ||||||
| chr3:72930592 | C | CTTT | 8 | a0001c0001t0001g0024 a0001c0001t0001g0058 a0001c0001t0001g0066 others(5): Show |
8 | HG01109.hp1 HG02056.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.600+8274_600+8276d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930592 | ||||||
| chr3:72930592 | CT | C | 39 | a0001c0001t0001g0025 a0001c0001t0001g0084 a0001c0001t0001g0087 others(36): Show |
39 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.600+8276delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72930592 | ||||||
| chr3:72930595 | T | C | 1 | a0001c0001t0003g0260 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.600+8260T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930595 | |||||||
| chr3:72930705 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0081 others(4): Show |
7 | HG01884.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+8370C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930705 | |||||||
| chr3:72930814 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.600+8479G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930814 | |||||||
| chr3:72930903 | T | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0002t0018g0188 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+8568T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930903 | |||||||
| chr3:72930917 | A | G | 5 | a0001c0001t0003g0062 a0001c0001t0003g0068 a0001c0005t0003g0052 others(2): Show |
5 | HG02055.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+8582A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930917 | |||||||
| chr3:72930948 | G | C | 6 | a0001c0001t0003g0260 a0001c0001t0003g0293 a0001c0004t0015g0285 others(3): Show |
6 | HG02572.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+8613G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72930948 | |||||||
| chr3:72931020 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.600+8685G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931020 | |||||||
| chr3:72931026 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.600+8691G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931026 | |||||||
| chr3:72931087 | A | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0217 a0001c0001t0002g0242 others(1): Show |
4 | HG03490.hp2 HG03834.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+8752A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931087 | |||||||
| chr3:72931236 | A | AT | 41 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0084 others(38): Show |
41 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.600+8911dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72931236 | ||||||
| chr3:72931236 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.600+8901A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931236 | |||||||
| chr3:72931246 | T | C | 7 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+8911T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931246 | |||||||
| chr3:72931265 | G | C | 5 | a0001c0001t0003g0260 a0001c0001t0003g0293 a0001c0004t0015g0285 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+8930G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931265 | |||||||
| chr3:72931297 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0057 others(9): Show |
12 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.600+8962C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931297 | |||||||
| chr3:72931333 | C | A | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+8998C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931333 | |||||||
| chr3:72931365 | G | A | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.600+9030G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931365 | |||||||
| chr3:72931370 | C | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+9035C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931370 | |||||||
| chr3:72931379 | G | A | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+9044G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931379 | |||||||
| chr3:72931396 | AT | A | 14 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(11): Show |
14 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+9067delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72931396 | ||||||
| chr3:72931407 | T | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+9072T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931407 | |||||||
| chr3:72931472 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.600+9137A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931472 | |||||||
| chr3:72931475 | T | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+9140T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931475 | |||||||
| chr3:72931508 | C | T | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+9173C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931508 | |||||||
| chr3:72931518 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(123): Show |
126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.600+9183C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931518 | |||||||
| chr3:72931577 | A | T | 3 | a0001c0001t0001g0279 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG01243.hp2 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+9242A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931577 | |||||||
| chr3:72931598 | A | G | 20 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(17): Show |
20 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.600+9263A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931598 | |||||||
| chr3:72931613 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.600+9278A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931613 | |||||||
| chr3:72931673 | G | A | 1 | a0001c0010t0031g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.600+9338G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931673 | |||||||
| chr3:72931780 | T | G | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+9445T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931780 | |||||||
| chr3:72931922 | A | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+9587A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931922 | |||||||
| chr3:72931949 | A | G | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+9614A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72931949 | |||||||
| chr3:72932031 | T | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0081 others(1): Show |
4 | HG01884.hp1 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+9696T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932031 | |||||||
| chr3:72932070 | CT | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0057 others(15): Show |
18 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.600+9750delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72932070 | ||||||
| chr3:72932094 | G | A | 3 | a0001c0004t0015g0285 a0002c0003t0002g0015 a0002c0003t0006g0037 |
3 | HG02895.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.600+9759G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932094 | |||||||
| chr3:72932138 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0173 others(1): Show |
4 | HG00642.hp1 HG01081.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+9803C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932138 | |||||||
| chr3:72932260 | G | A | 1 | a0001c0002t0027g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.600+9925G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932260 | |||||||
| chr3:72932281 | C | T | 3 | a0001c0002t0020g0070 a0001c0002t0021g0071 a0002c0003t0019g0014 |
3 | HG02717.hp2 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.600+9946C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932281 | |||||||
| chr3:72932288 | C | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+9953C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932288 | |||||||
| chr3:72932419 | A | G | 9 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
9 | HG01884.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+10084A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932419 | |||||||
| chr3:72932601 | G | C | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+10266G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932601 | |||||||
| chr3:72932817 | T | G | 1 | a0001c0002t0014g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.600+10482T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72932817 | |||||||
| chr3:72933100 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.600+10765A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933100 | |||||||
| chr3:72933121 | AT | A | 39 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0084 others(36): Show |
39 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.600+10793delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72933121 | ||||||
| chr3:72933290 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.600+10955A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933290 | |||||||
| chr3:72933327 | T | C | 5 | a0001c0001t0003g0260 a0001c0001t0003g0293 a0001c0004t0015g0285 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+10992T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933327 | |||||||
| chr3:72933410 | A | G | 1 | a0001c0001t0002g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.600+11075A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933410 | |||||||
| chr3:72933424 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.600+11089A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933424 | |||||||
| chr3:72933525 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0002t0018g0188 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+11190A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933525 | |||||||
| chr3:72933629 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0002t0018g0188 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+11294C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933629 | |||||||
| chr3:72933652 | T | C | 5 | a0001c0001t0003g0062 a0001c0001t0003g0068 a0001c0005t0003g0052 others(2): Show |
5 | HG02055.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+11317T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933652 | |||||||
| chr3:72933714 | G | T | 6 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(3): Show |
6 | HG01891.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+11379G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933714 | |||||||
| chr3:72933734 | C | A | 2 | a0001c0001t0001g0096 a0001c0001t0007g0169 |
2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.600+11399C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933734 | |||||||
| chr3:72933795 | G | A | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.600+11460G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933795 | |||||||
| chr3:72933795 | G | C | 1 | a0002c0003t0002g0015 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.600+11460G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933795 | |||||||
| chr3:72933802 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG01243.hp2 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+11467C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933802 | |||||||
| chr3:72933993 | G | T | 7 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+11658G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72933993 | |||||||
| chr3:72934080 | CT | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(59): Show |
62 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.600+11764delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72934080 | ||||||
| chr3:72934080 | CTT | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(133): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.600+11763_600+1176 others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72934080 | ||||||
| chr3:72934080 | CTTT | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0057 others(4): Show |
7 | HG00735.hp1 HG01358.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+11762_600+1176 others(7): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72934080 | ||||||
| chr3:72934259 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.600+11924A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934259 | |||||||
| chr3:72934259 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.600+11924A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934259 | |||||||
| chr3:72934261 | T | C | 1 | a0001c0010t0031g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.600+11926T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934261 | |||||||
| chr3:72934337 | C | CA | 4 | a0001c0002t0020g0070 a0001c0002t0021g0071 a0001c0007t0003g0007 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+12003dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72934337 | ||||||
| chr3:72934355 | G | A | 5 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0002t0018g0188 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+12020G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934355 | |||||||
| chr3:72934378 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.600+12043A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934378 | |||||||
| chr3:72934451 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.600+12116G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934451 | |||||||
| chr3:72934486 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.600+12151A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934486 | |||||||
| chr3:72934605 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.600+12270C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934605 | |||||||
| chr3:72934715 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(140): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.600+12380G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934715 | |||||||
| chr3:72934724 | G | A | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.600+12389G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934724 | |||||||
| chr3:72934796 | C | G | 5 | a0001c0001t0003g0260 a0001c0001t0003g0293 a0001c0004t0015g0285 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+12461C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934796 | |||||||
| chr3:72934882 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0259 a0001c0004t0008g0292 others(2): Show |
5 | HG02559.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+12547A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72934882 | |||||||
| chr3:72935117 | G | A | 2 | a0001c0001t0006g0063 a0001c0001t0006g0092 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+12782G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72935117 | |||||||
| chr3:72935249 | A | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(116): Show |
119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.600+12914A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72935249 | |||||||
| chr3:72935301 | C | CT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0275 a0001c0001t0001g0277 others(5): Show |
8 | HG02615.hp2 HG03041.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+12969dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72935301 | ||||||
| chr3:72935602 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG01243.hp2 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.600+13267C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72935602 | |||||||
| chr3:72935860 | A | G | 18 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(15): Show |
18 | HG00735.hp1 HG01109.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.600+13525A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72935860 | |||||||
| chr3:72936204 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.600+13869A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936204 | |||||||
| chr3:72936291 | CAAAAAAA others(9): Show |
C | 29 | a0001c0001t0001g0205 a0001c0001t0002g0008 a0001c0001t0002g0012 others(26): Show |
29 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.600+13971_600+1398 others(20): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72936291 | ||||||
| chr3:72936300 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.600+13965G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936300 | |||||||
| chr3:72936300 | G | GA | 26 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(23): Show |
26 | HG00735.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+13980dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72936300 | ||||||
| chr3:72936300 | GA | G | 10 | a0001c0001t0001g0031 a0001c0001t0001g0093 a0001c0001t0001g0125 others(7): Show |
10 | HG01256.hp1 HG01975.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+13980delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72936300 | ||||||
| chr3:72936301 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.600+13966A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936301 | |||||||
| chr3:72936317 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+13982A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936317 | |||||||
| chr3:72936441 | A | G | 1 | a0002c0003t0002g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.600+14106A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936441 | |||||||
| chr3:72936655 | C | A | 1 | a0001c0001t0002g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.600+14320C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936655 | |||||||
| chr3:72936666 | CA | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.600+14340delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72936666 | ||||||
| chr3:72936813 | T | C | 2 | a0001c0002t0014g0039 a0005c0009t0030g0291 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600+14478T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936813 | |||||||
| chr3:72936950 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.600+14615C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72936950 | |||||||
| chr3:72937038 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.600+14703A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937038 | |||||||
| chr3:72937039 | T | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0057 others(12): Show |
15 | HG01884.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+14704T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937039 | |||||||
| chr3:72937183 | G | A | 1 | a0001c0002t0013g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.600+14848G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937183 | |||||||
| chr3:72937296 | T | C | 2 | a0001c0001t0003g0062 a0001c0001t0003g0068 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.600+14961T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937296 | |||||||
| chr3:72937328 | C | A | 5 | a0001c0001t0003g0293 a0001c0004t0015g0285 a0002c0003t0002g0015 others(2): Show |
5 | HG02572.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+14993C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937328 | |||||||
| chr3:72937328 | C | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0057 others(12): Show |
15 | HG01884.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+14993C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937328 | |||||||
| chr3:72937333 | T | C | 1 | a0001c0010t0031g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.600+14998T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937333 | |||||||
| chr3:72937625 | T | G | 18 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(15): Show |
18 | HG00735.hp1 HG01109.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.600+15290T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937625 | |||||||
| chr3:72937793 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.600+15458C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72937793 | |||||||
| chr3:72938070 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(117): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.600+15735C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72938070 | |||||||
| chr3:72938106 | T | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0231 a0001c0001t0001g0257 others(1): Show |
4 | HG00673.hp2 HG01069.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+15771T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72938106 | |||||||
| chr3:72938144 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.600+15809G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72938144 | |||||||
| chr3:72938199 | T | C | 1 | a0002c0003t0002g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.600+15864T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72938199 | |||||||
| chr3:72938215 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.600+15880G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72938215 | |||||||
| chr3:72938710 | A | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0217 |
2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.600+16375A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72938710 | |||||||
| chr3:72939164 | A | C | 3 | a0001c0001t0001g0279 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG01243.hp2 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-15934A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939164 | |||||||
| chr3:72939219 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.601-15879A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939219 | |||||||
| chr3:72939276 | G | T | 3 | a0001c0001t0001g0279 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG01243.hp2 HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-15822G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939276 | |||||||
| chr3:72939290 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.601-15808T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939290 | |||||||
| chr3:72939376 | A | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0085 a0001c0001t0001g0258 |
3 | HG02486.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.601-15722A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939376 | |||||||
| chr3:72939413 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(162): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.601-15685T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939413 | |||||||
| chr3:72939420 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.601-15678G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939420 | |||||||
| chr3:72939468 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.601-15630A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939468 | |||||||
| chr3:72939574 | CAG | C | 3 | a0001c0001t0001g0259 a0002c0003t0001g0102 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.601-15522_601-1552 others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72939574 | ||||||
| chr3:72939575 | A | G | 4 | a0001c0004t0008g0281 a0001c0004t0008g0282 a0001c0004t0008g0284 others(1): Show |
4 | HG01109.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-15523A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939575 | |||||||
| chr3:72939684 | C | CT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.601-15400dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72939684 | ||||||
| chr3:72939729 | G | A | 1 | a0001c0010t0031g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.601-15369G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939729 | |||||||
| chr3:72939749 | G | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(225): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.601-15349G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939749 | |||||||
| chr3:72939772 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.601-15326C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939772 | |||||||
| chr3:72939907 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.601-15191C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72939907 | |||||||
| chr3:72940219 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0002t0018g0188 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-14879A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940219 | |||||||
| chr3:72940563 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.601-14535G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940563 | |||||||
| chr3:72940642 | A | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0081 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-14456A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940642 | |||||||
| chr3:72940704 | C | T | 7 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-14394C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940704 | |||||||
| chr3:72940746 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.601-14352A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940746 | |||||||
| chr3:72940776 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.601-14322A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940776 | |||||||
| chr3:72940815 | G | A | 2 | a0001c0001t0001g0067 a0001c0002t0018g0188 |
2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601-14283G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940815 | |||||||
| chr3:72940824 | C | G | 1 | a0001c0001t0004g0013 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.601-14274C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940824 | |||||||
| chr3:72940861 | T | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0002t0018g0188 others(2): Show |
5 | HG02630.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-14237T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940861 | |||||||
| chr3:72940891 | G | A | 2 | a0001c0002t0014g0039 a0005c0009t0030g0291 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.601-14207G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940891 | |||||||
| chr3:72940898 | C | G | 3 | a0001c0002t0020g0070 a0001c0002t0021g0071 a0002c0003t0019g0014 |
3 | HG02717.hp2 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.601-14200C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940898 | |||||||
| chr3:72940936 | T | A | 1 | a0001c0001t0023g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.601-14162T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72940936 | |||||||
| chr3:72941084 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.601-14014G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941084 | |||||||
| chr3:72941107 | G | A | 3 | a0001c0001t0001g0259 a0002c0003t0001g0102 a0002c0003t0002g0269 |
3 | HG02572.hp1 HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.601-13991G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941107 | |||||||
| chr3:72941135 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.601-13963G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941135 | |||||||
| chr3:72941240 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.601-13858C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941240 | |||||||
| chr3:72941370 | A | G | 16 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(13): Show |
16 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-13728A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941370 | |||||||
| chr3:72941371 | T | C | 1 | a0001c0001t0011g0106 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.601-13727T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941371 | |||||||
| chr3:72941607 | C | G | 2 | a0001c0001t0001g0191 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.601-13491C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941607 | |||||||
| chr3:72941618 | C | T | 1 | a0002c0003t0002g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.601-13480C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941618 | |||||||
| chr3:72941636 | A | T | 1 | a0001c0001t0002g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.601-13462A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941636 | |||||||
| chr3:72941776 | T | TG | 12 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-13321dupG | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72941776 | ||||||
| chr3:72941787 | A | G | 1 | a0002c0003t0009g0105 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.601-13311A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941787 | |||||||
| chr3:72941979 | G | A | 12 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-13119G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941979 | |||||||
| chr3:72941998 | G | A | 4 | a0001c0002t0020g0070 a0001c0002t0021g0071 a0001c0007t0003g0007 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-13100G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72941998 | |||||||
| chr3:72942031 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.601-13067A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942031 | |||||||
| chr3:72942126 | G | A | 12 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-12972G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942126 | |||||||
| chr3:72942173 | C | G | 5 | a0001c0001t0003g0260 a0001c0001t0003g0293 a0001c0004t0015g0285 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-12925C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942173 | |||||||
| chr3:72942270 | A | C | 1 | a0001c0001t0002g0134 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.601-12828A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942270 | |||||||
| chr3:72942490 | G | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.601-12608G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942490 | |||||||
| chr3:72942602 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.601-12496G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942602 | |||||||
| chr3:72942745 | A | G | 3 | a0001c0001t0003g0293 a0001c0001t0006g0063 a0001c0001t0006g0092 |
3 | HG02055.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-12353A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942745 | |||||||
| chr3:72942751 | T | TA | 8 | a0001c0001t0001g0056 a0001c0001t0001g0259 a0001c0001t0003g0082 others(5): Show |
8 | HG02451.hp1 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-12332dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72942751 | ||||||
| chr3:72942788 | C | A | 13 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0057 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-12310C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942788 | |||||||
| chr3:72942815 | A | G | 6 | a0001c0001t0001g0054 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-12283A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942815 | |||||||
| chr3:72942823 | A | C | 3 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG00735.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601-12275A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942823 | |||||||
| chr3:72942901 | T | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.601-12197T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72942901 | |||||||
| chr3:72943028 | T | C | 3 | a0001c0002t0020g0070 a0001c0002t0021g0071 a0002c0003t0019g0014 |
3 | HG02717.hp2 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.601-12070T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943028 | |||||||
| chr3:72943182 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(119): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.601-11916G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943182 | |||||||
| chr3:72943379 | C | CT | 7 | a0001c0001t0001g0191 a0001c0001t0002g0110 a0001c0001t0007g0169 others(4): Show |
7 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-11705dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72943379 | ||||||
| chr3:72943379 | CT | C | 10 | a0001c0001t0001g0056 a0001c0001t0001g0259 a0001c0001t0003g0293 others(7): Show |
10 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-11705delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72943379 | ||||||
| chr3:72943544 | CTT | C | 22 | a0001c0001t0001g0064 a0001c0001t0001g0189 a0001c0001t0004g0013 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.601-11550_601-1154 others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72943544 | ||||||
| chr3:72943569 | G | T | 60 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0066 others(57): Show |
60 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.601-11529G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943569 | |||||||
| chr3:72943593 | T | C | 1 | a0001c0001t0002g0264 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.601-11505T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943593 | |||||||
| chr3:72943623 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.601-11475T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943623 | |||||||
| chr3:72943624 | G | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.601-11474G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943624 | |||||||
| chr3:72943632 | C | T | 1 | a0002c0003t0019g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.601-11466C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943632 | |||||||
| chr3:72943666 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.601-11432G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943666 | |||||||
| chr3:72943671 | C | A | 1 | a0001c0001t0002g0190 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.601-11427C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943671 | |||||||
| chr3:72943677 | C | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0279 |
3 | HG01243.hp2 HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.601-11421C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943677 | |||||||
| chr3:72943721 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0029 others(7): Show |
10 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-11377G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943721 | |||||||
| chr3:72943823 | G | C | 27 | a0001c0001t0001g0064 a0001c0001t0001g0189 a0001c0001t0004g0013 others(24): Show |
27 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.601-11275G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943823 | |||||||
| chr3:72943854 | A | AT | 8 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0087 others(5): Show |
8 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-11232dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72943854 | ||||||
| chr3:72943854 | AT | A | 9 | a0001c0001t0001g0075 a0001c0001t0001g0111 a0001c0001t0001g0112 others(6): Show |
9 | HG00099.hp1 HG01123.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.601-11232delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72943854 | ||||||
| chr3:72943963 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.601-11135C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72943963 | |||||||
| chr3:72944087 | C | CT | 59 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(56): Show |
59 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.601-11006dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72944087 | ||||||
| chr3:72944093 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(238): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.601-11005G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72944093 | |||||||
| chr3:72944104 | T | TAAAGACA others(317): Show |
1 | a0001c0002t0021g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.601-10981_601-1098 others(328): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72944104 | ||||||
| chr3:72944104 | T | TAAAGACA others(318): Show |
2 | a0001c0001t0001g0191 a0001c0002t0020g0070 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.601-10981_601-1098 others(329): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72944104 | ||||||
| chr3:72944104 | T | TAAAGACA others(319): Show |
1 | a0002c0003t0019g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.601-10981_601-1098 others(330): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72944104 | ||||||
| chr3:72944263 | C | CT | 241 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(238): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.601-10824dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72944263 | ||||||
| chr3:72944446 | G | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-10652G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72944446 | |||||||
| chr3:72944499 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.601-10599C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72944499 | |||||||
| chr3:72944501 | C | T | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.601-10597C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72944501 | |||||||
| chr3:72944570 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-10528G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72944570 | |||||||
| chr3:72944622 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.601-10476T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72944622 | |||||||
| chr3:72944634 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.601-10464T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72944634 | |||||||
| chr3:72945055 | C | T | 4 | a0001c0001t0005g0115 a0001c0001t0005g0167 a0001c0001t0005g0255 others(1): Show |
4 | NA18943.hp1 NA18946.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-10043C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945055 | |||||||
| chr3:72945095 | G | A | 54 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(51): Show |
54 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.601-10003G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945095 | |||||||
| chr3:72945122 | C | CA | 118 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.601-9960dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72945122 | ||||||
| chr3:72945122 | C | CAA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(59): Show |
62 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.601-9961_601-9960d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72945122 | ||||||
| chr3:72945123 | A | C | 4 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0002g0251 others(1): Show |
4 | HG02735.hp2 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-9975A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945123 | |||||||
| chr3:72945145 | G | A | 1 | a0002c0003t0002g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.601-9953G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945145 | |||||||
| chr3:72945183 | G | A | 48 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0076 others(45): Show |
48 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.601-9915G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945183 | |||||||
| chr3:72945188 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.601-9910T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945188 | |||||||
| chr3:72945282 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601-9816C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945282 | |||||||
| chr3:72945303 | A | AAAAAT | 104 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(101): Show |
104 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.601-9782_601-9778d others(7): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72945303 | ||||||
| chr3:72945303 | A | AAAAT | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.601-9792_601-9791i others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72945303 | ||||||
| chr3:72945303 | A | AAAATAAA others(2): Show |
15 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-9792_601-9791i others(11): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72945303 | ||||||
| chr3:72945319 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.601-9779A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945319 | |||||||
| chr3:72945393 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.601-9705T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945393 | |||||||
| chr3:72945443 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(240): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.601-9655A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945443 | |||||||
| chr3:72945450 | C | T | 6 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(3): Show |
6 | HG02451.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-9648C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945450 | |||||||
| chr3:72945566 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | HG00597.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.601-9532T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945566 | |||||||
| chr3:72945593 | G | A | 3 | a0001c0001t0002g0212 a0001c0001t0002g0227 a0001c0001t0002g0232 |
3 | HG00597.hp1 HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.601-9505G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945593 | |||||||
| chr3:72945739 | G | A | 81 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(78): Show |
81 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.601-9359G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945739 | |||||||
| chr3:72945884 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.601-9214T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72945884 | |||||||
| chr3:72946155 | C | T | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-8943C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946155 | |||||||
| chr3:72946193 | G | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.601-8905G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946193 | |||||||
| chr3:72946254 | G | A | 2 | a0001c0002t0020g0070 a0001c0002t0021g0071 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.601-8844G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946254 | |||||||
| chr3:72946276 | G | GA | 9 | a0001c0001t0002g0035 a0001c0001t0002g0098 a0001c0001t0002g0172 others(6): Show |
9 | HG00558.hp1 HG00597.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-8794dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GA | G | 8 | a0001c0001t0001g0076 a0001c0001t0001g0279 a0001c0001t0002g0143 others(5): Show |
8 | HG01243.hp2 HG01993.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-8794delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GAA | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0051 others(66): Show |
69 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.601-8795_601-8794d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GAAA | G | 51 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.601-8796_601-8794d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GAAAA | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0001t0001g0240 others(6): Show |
9 | HG01975.hp2 HG02083.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-8797_601-8794d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0003g0082 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601-8803_601-8794d others(12): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GAAAAAAA others(4): Show |
G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0031 others(100): Show |
103 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.601-8804_601-8794d others(13): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GAAAAAAA others(5): Show |
G | 2 | a0001c0001t0001g0055 a0001c0002t0014g0039 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.601-8805_601-8794d others(14): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946276 | GAAAAAAA others(7): Show |
G | 2 | a0001c0001t0004g0021 a0001c0001t0004g0022 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601-8807_601-8794d others(16): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72946276 | ||||||
| chr3:72946433 | G | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.601-8665G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946433 | |||||||
| chr3:72946434 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.601-8664C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946434 | |||||||
| chr3:72946582 | C | G | 1 | a0001c0001t0004g0036 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.601-8516C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946582 | |||||||
| chr3:72946629 | G | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-8469G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946629 | |||||||
| chr3:72946654 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0075 others(66): Show |
69 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.601-8444T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946654 | |||||||
| chr3:72946747 | T | C | 3 | a0001c0001t0006g0063 a0001c0001t0006g0092 a0001c0001t0006g0210 |
3 | HG02055.hp1 HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-8351T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946747 | |||||||
| chr3:72946998 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-8100C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72946998 | |||||||
| chr3:72947034 | A | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-8064A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947034 | |||||||
| chr3:72947143 | A | G | 1 | a0001c0002t0014g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-7955A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947143 | |||||||
| chr3:72947186 | A | T | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-7912A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947186 | |||||||
| chr3:72947200 | C | T | 48 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0076 others(45): Show |
48 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.601-7898C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947200 | |||||||
| chr3:72947235 | C | T | 3 | a0001c0002t0020g0070 a0001c0002t0021g0071 a0002c0003t0019g0014 |
3 | HG02717.hp2 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.601-7863C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947235 | |||||||
| chr3:72947263 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0076 a0001c0001t0001g0087 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7835G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947263 | |||||||
| chr3:72947264 | T | C | 1 | a0001c0002t0014g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-7834T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947264 | |||||||
| chr3:72947266 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0075 others(77): Show |
80 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.601-7832G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947266 | |||||||
| chr3:72947281 | A | G | 3 | a0001c0002t0020g0070 a0001c0002t0021g0071 a0002c0003t0019g0014 |
3 | HG02717.hp2 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.601-7817A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947281 | |||||||
| chr3:72947427 | A | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-7671A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947427 | |||||||
| chr3:72947461 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.601-7637T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947461 | |||||||
| chr3:72947582 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-7516T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947582 | |||||||
| chr3:72947626 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.601-7472C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947626 | |||||||
| chr3:72947716 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0240 |
2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.601-7382G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947716 | |||||||
| chr3:72947939 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.601-7159G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947939 | |||||||
| chr3:72947995 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.601-7103G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72947995 | |||||||
| chr3:72948052 | T | G | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601-7046T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948052 | |||||||
| chr3:72948204 | G | A | 1 | a0001c0002t0014g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-6894G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948204 | |||||||
| chr3:72948212 | C | G | 81 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(78): Show |
81 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.601-6886C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948212 | |||||||
| chr3:72948216 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601-6882G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948216 | |||||||
| chr3:72948356 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.601-6742G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948356 | |||||||
| chr3:72948621 | G | A | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(84): Show |
87 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.601-6477G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948621 | |||||||
| chr3:72948735 | G | T | 1 | a0001c0001t0003g0083 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601-6363G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948735 | |||||||
| chr3:72948804 | T | C | 1 | a0001c0002t0014g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-6294T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948804 | |||||||
| chr3:72948835 | C | CA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(80): Show |
83 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.601-6242dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72948835 | ||||||
| chr3:72948835 | C | CAA | 15 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0142 others(12): Show |
15 | HG00639.hp1 HG01358.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-6243_601-6242d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72948835 | ||||||
| chr3:72948835 | CA | C | 33 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0044 others(30): Show |
33 | HG00639.hp2 HG01069.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.601-6242delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72948835 | ||||||
| chr3:72948946 | G | A | 27 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(24): Show |
27 | HG00735.hp1 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.601-6152G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72948946 | |||||||
| chr3:72949083 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.601-6015G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949083 | |||||||
| chr3:72949225 | A | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0057 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-5873A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949225 | |||||||
| chr3:72949246 | T | G | 2 | a0001c0001t0001g0067 a0001c0002t0018g0188 |
2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601-5852T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949246 | |||||||
| chr3:72949305 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0047 others(67): Show |
70 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.601-5793T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949305 | |||||||
| chr3:72949502 | C | CT | 14 | a0001c0001t0002g0035 a0001c0001t0002g0077 a0001c0001t0002g0109 others(11): Show |
14 | HG01106.hp2 HG01346.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-5568dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72949502 | ||||||
| chr3:72949502 | CT | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(50): Show |
53 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.601-5568delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72949502 | ||||||
| chr3:72949502 | CTT | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(159): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.601-5569_601-5568d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72949502 | ||||||
| chr3:72949502 | CTTT | C | 10 | a0001c0001t0001g0057 a0001c0001t0001g0173 a0001c0001t0002g0176 others(7): Show |
10 | HG01081.hp2 HG01168.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-5570_601-5568d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72949502 | ||||||
| chr3:72949502 | CTTTTTTT others(1): Show |
C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0050 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-5575_601-5568d others(10): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72949502 | ||||||
| chr3:72949502 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-5577_601-5568d others(12): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72949502 | ||||||
| chr3:72949549 | A | G | 91 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(88): Show |
91 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.601-5549A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949549 | |||||||
| chr3:72949553 | C | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0279 |
3 | HG01243.hp2 HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.601-5545C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949553 | |||||||
| chr3:72949598 | G | A | 37 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0057 others(34): Show |
37 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.601-5500G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949598 | |||||||
| chr3:72949684 | C | T | 37 | a0001c0001t0001g0024 a0001c0001t0001g0044 a0001c0001t0001g0057 others(34): Show |
37 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.601-5414C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949684 | |||||||
| chr3:72949986 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.601-5112C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72949986 | |||||||
| chr3:72950063 | A | ATGGTGGC others(7): Show |
256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-5033_601-5032i others(16): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72950063 | ||||||
| chr3:72950132 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.601-4966G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950132 | |||||||
| chr3:72950178 | C | T | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-4920C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950178 | |||||||
| chr3:72950231 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.601-4867C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950231 | |||||||
| chr3:72950359 | G | A | 9 | a0001c0001t0001g0056 a0001c0001t0001g0081 a0001c0001t0001g0090 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-4739G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950359 | |||||||
| chr3:72950393 | A | G | 88 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(85): Show |
88 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.601-4705A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950393 | |||||||
| chr3:72950440 | G | A | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-4658G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950440 | |||||||
| chr3:72950572 | G | A | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-4526G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950572 | |||||||
| chr3:72950580 | T | C | 1 | a0001c0002t0014g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-4518T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950580 | |||||||
| chr3:72950628 | T | TA | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(84): Show |
87 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.601-4458dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72950628 | ||||||
| chr3:72950697 | C | T | 2 | a0001c0001t0001g0064 a0001c0004t0008g0287 |
2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.601-4401C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950697 | |||||||
| chr3:72950753 | C | T | 88 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(85): Show |
88 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.601-4345C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950753 | |||||||
| chr3:72950768 | C | T | 51 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0076 others(48): Show |
51 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.601-4330C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950768 | |||||||
| chr3:72950960 | G | C | 1 | a0001c0001t0004g0019 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.601-4138G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72950960 | |||||||
| chr3:72951191 | A | AT | 88 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0057 others(85): Show |
88 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.601-3897dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72951191 | ||||||
| chr3:72951348 | G | A | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(84): Show |
87 | HG00423.hp2 HG00673.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.601-3750G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951348 | |||||||
| chr3:72951415 | AAC | A | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-3679_601-3678d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72951415 | ||||||
| chr3:72951460 | A | C | 1 | a0001c0001t0002g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.601-3638A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951460 | |||||||
| chr3:72951548 | G | A | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-3550G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951548 | |||||||
| chr3:72951573 | C | G | 1 | a0001c0001t0006g0165 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.601-3525C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951573 | |||||||
| chr3:72951581 | C | A | 2 | a0001c0001t0003g0062 a0001c0001t0003g0068 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.601-3517C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951581 | |||||||
| chr3:72951616 | C | T | 66 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0044 others(63): Show |
66 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.601-3482C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951616 | |||||||
| chr3:72951635 | C | G | 1 | a0001c0012t0001g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.601-3463C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951635 | |||||||
| chr3:72951654 | C | G | 1 | a0001c0012t0001g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.601-3444C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951654 | |||||||
| chr3:72951928 | G | A | 1 | a0001c0002t0014g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.601-3170G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72951928 | |||||||
| chr3:72952005 | CT | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.601-3078delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72952005 | ||||||
| chr3:72952043 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.601-3055C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952043 | |||||||
| chr3:72952084 | C | T | 6 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0082 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-3014C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952084 | |||||||
| chr3:72952229 | C | T | 4 | a0001c0004t0015g0285 a0001c0004t0015g0290 a0002c0003t0002g0015 others(1): Show |
4 | HG02895.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-2869C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952229 | |||||||
| chr3:72952439 | G | A | 1 | a0001c0001t0002g0229 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.601-2659G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952439 | |||||||
| chr3:72952440 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.601-2658A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952440 | |||||||
| chr3:72952449 | G | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.601-2649G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952449 | |||||||
| chr3:72952476 | C | T | 1 | a0001c0001t0006g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.601-2622C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952476 | |||||||
| chr3:72952544 | G | A | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-2554G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952544 | |||||||
| chr3:72952551 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.601-2547C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952551 | |||||||
| chr3:72952552 | G | A | 1 | a0001c0001t0002g0229 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.601-2546G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952552 | |||||||
| chr3:72952710 | A | G | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-2388A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952710 | |||||||
| chr3:72952777 | C | T | 23 | a0001c0001t0001g0064 a0001c0001t0004g0013 a0001c0001t0004g0019 others(20): Show |
23 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.601-2321C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952777 | |||||||
| chr3:72952843 | T | C | 1 | a0001c0001t0002g0204 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.601-2255T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952843 | |||||||
| chr3:72952873 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(97): Show |
100 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.601-2225T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952873 | |||||||
| chr3:72952972 | A | G | 1 | a0001c0001t0007g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.601-2126A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72952972 | |||||||
| chr3:72953045 | C | G | 1 | a0001c0001t0004g0013 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.601-2053C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72953045 | |||||||
| chr3:72953329 | G | A | 1 | a0001c0001t0006g0210 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.601-1769G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72953329 | |||||||
| chr3:72953381 | C | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.601-1717C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72953381 | |||||||
| chr3:72953497 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.601-1601C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72953497 | |||||||
| chr3:72953751 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.601-1347G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72953751 | |||||||
| chr3:72953802 | A | T | 3 | a0001c0001t0001g0259 a0001c0004t0008g0287 a0002c0003t0001g0102 |
3 | HG02647.hp2 HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.601-1296A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72953802 | |||||||
| chr3:72953971 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0277 |
2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.601-1127G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72953971 | |||||||
| chr3:72954002 | G | A | 2 | a0001c0002t0018g0188 a0001c0007t0003g0007 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.601-1096G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954002 | |||||||
| chr3:72954038 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.601-1060C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954038 | |||||||
| chr3:72954352 | T | G | 2 | a0001c0002t0018g0188 a0001c0007t0003g0007 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.601-746T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954352 | |||||||
| chr3:72954399 | C | CTG | 3 | a0001c0001t0001g0044 a0001c0001t0002g0194 a0001c0001t0002g0223 |
3 | HG03239.hp2 HG06807.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.601-665_601-664dup others(2): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTG | 4 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0002t0020g0070 others(1): Show |
4 | HG00741.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-667_601-664dup others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTG | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(43): Show |
46 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.601-669_601-664dup others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(1): Show |
37 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0081 others(34): Show |
37 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.601-671_601-664dup others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(3): Show |
35 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0090 others(32): Show |
35 | HG00558.hp2 HG00733.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.601-673_601-664dup others(10): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(5): Show |
63 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0095 others(60): Show |
63 | HG00423.hp1 HG00423.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.601-675_601-664dup others(12): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(7): Show |
26 | a0001c0001t0001g0025 a0001c0001t0001g0047 a0001c0001t0001g0066 others(23): Show |
26 | HG00099.hp1 HG01081.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.601-677_601-664dup others(14): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(9): Show |
19 | a0001c0001t0001g0026 a0001c0001t0001g0053 a0001c0001t0001g0055 others(16): Show |
19 | HG00735.hp1 HG01257.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.601-679_601-664dup others(16): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(11): Show |
12 | a0001c0001t0001g0050 a0001c0001t0003g0059 a0001c0001t0003g0260 others(9): Show |
12 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-681_601-664dup others(18): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(13): Show |
2 | a0001c0001t0001g0064 a0001c0002t0013g0041 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.601-683_601-664dup others(20): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | C | CTGTGTGT others(15): Show |
2 | a0001c0001t0003g0293 a0002c0003t0002g0269 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.601-685_601-664dup others(22): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | CTG | C | 13 | a0001c0001t0002g0114 a0001c0001t0002g0151 a0001c0001t0002g0163 others(10): Show |
13 | HG00597.hp1 HG00639.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-665_601-664del others(2): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954399 | CTGTGTGT others(7): Show |
C | 4 | a0001c0004t0015g0285 a0001c0004t0015g0290 a0002c0003t0002g0015 others(1): Show |
4 | HG02895.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-677_601-664del others(14): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954399 | ||||||
| chr3:72954485 | A | G | 26 | a0001c0001t0001g0064 a0001c0001t0004g0013 a0001c0001t0004g0019 others(23): Show |
26 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.601-613A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954485 | |||||||
| chr3:72954502 | T | C | 1 | a0001c0005t0003g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-596T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954502 | |||||||
| chr3:72954531 | C | T | 1 | a0001c0002t0027g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.601-567C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954531 | |||||||
| chr3:72954614 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-484C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954614 | |||||||
| chr3:72954637 | A | AAAAT | 103 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.601-423_601-420dup others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954637 | ||||||
| chr3:72954637 | A | AAAATAAA others(1): Show |
35 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0064 others(32): Show |
35 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.601-427_601-420dup others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954637 | ||||||
| chr3:72954637 | A | AAAATAAA others(5): Show |
13 | a0001c0001t0001g0025 a0001c0001t0001g0100 a0001c0001t0001g0103 others(10): Show |
13 | HG00733.hp2 HG01257.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-431_601-420dup others(12): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954637 | ||||||
| chr3:72954637 | AAAAT | A | 15 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(12): Show |
15 | HG00735.hp1 HG01891.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-423_601-420del others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 72954637 | ||||||
| chr3:72954804 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0004t0008g0292 |
3 | HG02965.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.601-294C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954804 | |||||||
| chr3:72954813 | G | T | 1 | a0001c0001t0001g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.601-285G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954813 | |||||||
| chr3:72954824 | C | A | 14 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-274C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954824 | |||||||
| chr3:72954854 | T | C | 5 | a0001c0001t0003g0293 a0001c0001t0006g0063 a0001c0001t0006g0092 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-244T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954854 | |||||||
| chr3:72954906 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.601-192T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72954906 | |||||||
| chr3:72955006 | T | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.601-92T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72955006 | |||||||
| chr3:72955038 | C | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-60C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 3/6 | chr3 | 72955038 | |||||||
| chr3:72955429 | T | A | 23 | a0001c0001t0001g0064 a0001c0001t0004g0013 a0001c0001t0004g0019 others(20): Show |
23 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+80T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72955429 | |||||||
| chr3:72955666 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.852+317G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72955666 | |||||||
| chr3:72955733 | A | C | 1 | a0001c0001t0013g0187 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.852+384A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72955733 | |||||||
| chr3:72955741 | G | C | 3 | a0001c0001t0001g0170 a0001c0001t0002g0197 a0001c0001t0006g0165 |
3 | HG00423.hp2 NA18612.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.852+392G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72955741 | |||||||
| chr3:72955809 | G | C | 1 | a0001c0002t0001g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.852+460G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72955809 | |||||||
| chr3:72955958 | G | A | 20 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(17): Show |
20 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.852+609G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72955958 | |||||||
| chr3:72956125 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.852+776G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956125 | |||||||
| chr3:72956195 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.852+846A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956195 | |||||||
| chr3:72956245 | AAAAG | A | 15 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.852+912_852+915del others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 72956245 | ||||||
| chr3:72956274 | C | G | 23 | a0001c0001t0001g0064 a0001c0001t0004g0013 a0001c0001t0004g0019 others(20): Show |
23 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.852+925C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956274 | |||||||
| chr3:72956276 | A | G | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.852+927A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956276 | |||||||
| chr3:72956317 | C | T | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.853-912C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956317 | |||||||
| chr3:72956343 | T | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(51): Show |
54 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.853-886T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956343 | |||||||
| chr3:72956452 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.853-777A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956452 | |||||||
| chr3:72956484 | C | T | 23 | a0001c0001t0001g0064 a0001c0001t0004g0013 a0001c0001t0004g0019 others(20): Show |
23 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.853-745C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956484 | |||||||
| chr3:72956610 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.853-619G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956610 | |||||||
| chr3:72956633 | G | A | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.853-596G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956633 | |||||||
| chr3:72956757 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.853-472G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956757 | |||||||
| chr3:72956805 | G | T | 1 | a0002c0003t0002g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.853-424G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956805 | |||||||
| chr3:72956875 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.853-354G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956875 | |||||||
| chr3:72956888 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.853-341T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956888 | |||||||
| chr3:72956889 | C | CAAAACA | 9 | a0001c0001t0001g0056 a0001c0001t0001g0081 a0001c0001t0001g0090 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.853-321_853-316dup others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 72956889 | ||||||
| chr3:72956922 | A | AAGGG | 6 | a0001c0001t0001g0205 a0001c0001t0002g0180 a0001c0001t0002g0203 others(3): Show |
6 | HG01123.hp1 HG01243.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-289_853-286dup others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 72956922 | ||||||
| chr3:72956936 | G | C | 3 | a0001c0001t0001g0004 a0001c0002t0027g0048 a0002c0003t0001g0104 |
3 | HG02647.hp1 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.853-293G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72956936 | |||||||
| chr3:72957208 | T | A | 1 | a0001c0001t0002g0296 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.853-21T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 4/6 | chr3 | 72957208 | |||||||
| chr3:72957420 | A | G | 1 | a0001c0012t0001g0162 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.976+68A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72957420 | |||||||
| chr3:72957616 | A | G | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+264A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72957616 | |||||||
| chr3:72957737 | G | C | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+385G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72957737 | |||||||
| chr3:72957860 | A | G | 1 | a0001c0001t0005g0167 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.976+508A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72957860 | |||||||
| chr3:72957864 | G | T | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.976+512G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72957864 | |||||||
| chr3:72957923 | G | A | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+571G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72957923 | |||||||
| chr3:72957928 | G | A | 1 | a0001c0001t0005g0115 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.976+576G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72957928 | |||||||
| chr3:72958061 | G | A | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.976+709G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958061 | |||||||
| chr3:72958116 | CA | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(97): Show |
100 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.976+772delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72958116 | ||||||
| chr3:72958272 | C | CA | 8 | a0001c0001t0001g0276 a0001c0001t0002g0213 a0001c0001t0002g0264 others(5): Show |
8 | HG02055.hp2 HG02572.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.976+938dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72958272 | ||||||
| chr3:72958272 | CA | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.976+938delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72958272 | ||||||
| chr3:72958272 | CAAA | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(97): Show |
100 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.976+936_976+938del others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72958272 | ||||||
| chr3:72958351 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.976+999C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958351 | |||||||
| chr3:72958412 | AC | A | 45 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0076 others(42): Show |
45 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.976+1061delC | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958412 | |||||||
| chr3:72958493 | A | G | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+1141A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958493 | |||||||
| chr3:72958600 | A | T | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.976+1248A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958600 | |||||||
| chr3:72958629 | C | CT | 27 | a0001c0001t0001g0010 a0001c0001t0001g0044 a0001c0001t0001g0047 others(24): Show |
27 | HG00597.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.976+1297dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72958629 | ||||||
| chr3:72958629 | CT | C | 99 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0075 others(96): Show |
99 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.976+1297delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72958629 | ||||||
| chr3:72958630 | T | G | 2 | a0001c0001t0002g0124 a0001c0001t0002g0223 |
2 | NA18951.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.976+1278T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958630 | |||||||
| chr3:72958631 | T | G | 1 | a0001c0001t0002g0195 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.976+1279T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958631 | |||||||
| chr3:72958775 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.976+1423G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72958775 | |||||||
| chr3:72958942 | C | CT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.976+1602dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72958942 | ||||||
| chr3:72959024 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.976+1672C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959024 | |||||||
| chr3:72959106 | C | CT | 83 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0031 others(80): Show |
83 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.976+1783dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72959106 | ||||||
| chr3:72959106 | C | CTT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0054 others(39): Show |
42 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.976+1782_976+1783d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72959106 | ||||||
| chr3:72959106 | C | CTTT | 31 | a0001c0001t0001g0073 a0001c0001t0001g0096 a0001c0001t0001g0112 others(28): Show |
31 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.976+1781_976+1783d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72959106 | ||||||
| chr3:72959106 | C | CTTTT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0111 a0001c0001t0001g0201 others(4): Show |
7 | HG01123.hp2 HG01952.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.976+1780_976+1783d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72959106 | ||||||
| chr3:72959106 | CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0001g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.976+1773_976+1783d others(13): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72959106 | ||||||
| chr3:72959106 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0002t0001g0042 others(1): Show |
4 | HG02257.hp2 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.976+1772_976+1783d others(14): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72959106 | ||||||
| chr3:72959175 | T | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.976+1823T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959175 | |||||||
| chr3:72959186 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(98): Show |
101 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.976+1834C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959186 | |||||||
| chr3:72959369 | C | T | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.976+2017C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959369 | |||||||
| chr3:72959399 | T | G | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+2047T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959399 | |||||||
| chr3:72959419 | A | C | 4 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0002g0251 others(1): Show |
4 | HG02735.hp2 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.976+2067A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959419 | |||||||
| chr3:72959450 | G | A | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+2098G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959450 | |||||||
| chr3:72959511 | T | A | 15 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.976+2159T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959511 | |||||||
| chr3:72959567 | T | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.976+2215T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959567 | |||||||
| chr3:72959712 | G | A | 2 | a0001c0002t0020g0070 a0001c0002t0021g0071 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.976+2360G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959712 | |||||||
| chr3:72959930 | C | T | 16 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(13): Show |
16 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.976+2578C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72959930 | |||||||
| chr3:72960047 | G | A | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+2695G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960047 | |||||||
| chr3:72960048 | C | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.976+2696C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960048 | |||||||
| chr3:72960133 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.976+2781T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960133 | |||||||
| chr3:72960180 | A | G | 2 | a0001c0002t0014g0005 a0002c0003t0026g0182 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.976+2828A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960180 | |||||||
| chr3:72960184 | C | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(70): Show |
73 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.976+2832C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960184 | |||||||
| chr3:72960312 | C | G | 1 | a0001c0002t0027g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.976+2960C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960312 | |||||||
| chr3:72960396 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.976+3044T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960396 | |||||||
| chr3:72960694 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG02056.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.976+3342C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960694 | |||||||
| chr3:72960731 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.976+3379A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72960731 | |||||||
| chr3:72960741 | G | GTT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(145): Show |
148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.976+3391_976+3392d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72960741 | ||||||
| chr3:72961086 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.976+3734C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961086 | |||||||
| chr3:72961186 | G | C | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.976+3834G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961186 | |||||||
| chr3:72961212 | A | G | 22 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(19): Show |
22 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.976+3860A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961212 | |||||||
| chr3:72961244 | T | C | 3 | a0001c0004t0015g0285 a0002c0003t0002g0015 a0002c0003t0006g0037 |
3 | HG02895.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.976+3892T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961244 | |||||||
| chr3:72961393 | T | C | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.976+4041T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961393 | |||||||
| chr3:72961468 | A | G | 11 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(8): Show |
11 | HG00735.hp1 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.976+4116A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961468 | |||||||
| chr3:72961483 | C | T | 2 | a0001c0002t0014g0039 a0001c0007t0003g0007 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.976+4131C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961483 | |||||||
| chr3:72961585 | C | T | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.976+4233C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961585 | |||||||
| chr3:72961659 | C | CA | 58 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0076 others(55): Show |
58 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.976+4323dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72961659 | ||||||
| chr3:72961674 | A | AAAAAAAG | 66 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.976+4323_976+4324i others(9): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72961674 | ||||||
| chr3:72961674 | AAG | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0047 others(64): Show |
67 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.976+4336_976+4337d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72961674 | ||||||
| chr3:72961675 | AG | A | 27 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0044 others(24): Show |
27 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.976+4324delG | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961675 | |||||||
| chr3:72961676 | G | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0056 others(79): Show |
82 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(79): Show |
intron_variant | MODIFIER | c.976+4324G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961676 | |||||||
| chr3:72961709 | A | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.976+4357A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961709 | |||||||
| chr3:72961770 | A | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.976+4418A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961770 | |||||||
| chr3:72961905 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.976+4553C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961905 | |||||||
| chr3:72961964 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.976+4612C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72961964 | |||||||
| chr3:72962381 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0047 others(64): Show |
67 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.976+5029A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72962381 | |||||||
| chr3:72962497 | A | G | 5 | a0001c0001t0003g0062 a0001c0001t0003g0068 a0001c0005t0003g0052 others(2): Show |
5 | HG02055.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.977-5050A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72962497 | |||||||
| chr3:72962569 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.977-4978G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72962569 | |||||||
| chr3:72962691 | G | T | 2 | a0001c0002t0014g0005 a0002c0003t0026g0182 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.977-4856G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72962691 | |||||||
| chr3:72962926 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.977-4621A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72962926 | |||||||
| chr3:72962954 | T | TA | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(106): Show |
109 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.977-4581dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72962954 | ||||||
| chr3:72962964 | A | AAC | 52 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.977-4582_977-4581i others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72962964 | ||||||
| chr3:72962964 | A | AC | 24 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.977-4583_977-4582i others(3): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72962964 | |||||||
| chr3:72963003 | G | A | 2 | a0001c0002t0014g0005 a0002c0003t0026g0182 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.977-4544G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72963003 | |||||||
| chr3:72963033 | C | T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0227 |
2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.977-4514C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72963033 | |||||||
| chr3:72963090 | T | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.977-4457T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72963090 | |||||||
| chr3:72963507 | G | GT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(106): Show |
109 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.977-4027dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72963507 | ||||||
| chr3:72963507 | G | GTT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.977-4028_977-4027d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72963507 | ||||||
| chr3:72963549 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.977-3998C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72963549 | |||||||
| chr3:72963669 | A | AT | 62 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(59): Show |
62 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.977-3859dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72963669 | ||||||
| chr3:72963669 | A | ATT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(110): Show |
113 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.977-3860_977-3859d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72963669 | ||||||
| chr3:72963669 | A | ATTT | 6 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0161 others(3): Show |
6 | HG00140.hp2 HG00741.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.977-3861_977-3859d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72963669 | ||||||
| chr3:72963749 | C | A | 2 | a0001c0001t0001g0219 a0001c0001t0016g0215 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.977-3798C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72963749 | |||||||
| chr3:72963894 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(49): Show |
52 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.977-3653C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72963894 | |||||||
| chr3:72963930 | G | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.977-3617G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72963930 | |||||||
| chr3:72964108 | C | T | 12 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(9): Show |
12 | HG02055.hp2 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.977-3439C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72964108 | |||||||
| chr3:72964504 | G | A | 3 | a0001c0001t0001g0056 a0001c0004t0008g0292 a0002c0006t0008g0289 |
3 | HG02559.hp1 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.977-3043G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72964504 | |||||||
| chr3:72964568 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.977-2979G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72964568 | |||||||
| chr3:72964652 | T | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.977-2895T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72964652 | |||||||
| chr3:72964747 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0057 others(6): Show |
9 | HG02615.hp2 HG02647.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.977-2800A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72964747 | |||||||
| chr3:72964881 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.977-2666G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72964881 | |||||||
| chr3:72965078 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.977-2469C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965078 | |||||||
| chr3:72965081 | A | G | 2 | a0001c0002t0020g0070 a0001c0002t0021g0071 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.977-2466A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965081 | |||||||
| chr3:72965135 | A | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.977-2412A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965135 | |||||||
| chr3:72965146 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.977-2401G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965146 | |||||||
| chr3:72965230 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.977-2317A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965230 | |||||||
| chr3:72965238 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.977-2309C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965238 | |||||||
| chr3:72965292 | A | G | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.977-2255A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965292 | |||||||
| chr3:72965297 | T | A | 1 | a0001c0002t0027g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.977-2250T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965297 | |||||||
| chr3:72965461 | G | A | 3 | a0001c0001t0002g0143 a0001c0001t0002g0267 a0001c0001t0007g0156 |
3 | NA18944.hp1 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.977-2086G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965461 | |||||||
| chr3:72965507 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0107 others(11): Show |
14 | HG00140.hp1 HG00673.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.977-2040C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965507 | |||||||
| chr3:72965545 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.977-2002G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965545 | |||||||
| chr3:72965748 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
78 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.977-1799G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965748 | |||||||
| chr3:72965967 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
78 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.977-1580T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965967 | |||||||
| chr3:72965973 | T | G | 1 | a0001c0001t0005g0254 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.977-1574T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72965973 | |||||||
| chr3:72966005 | G | A | 1 | a0001c0001t0002g0253 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.977-1542G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966005 | |||||||
| chr3:72966088 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(94): Show |
97 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.977-1459C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966088 | |||||||
| chr3:72966278 | C | T | 50 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0081 others(47): Show |
50 | HG00423.hp2 HG00673.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.977-1269C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966278 | |||||||
| chr3:72966298 | GT | G | 88 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.977-1236delT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966298 | ||||||
| chr3:72966298 | GTT | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0093 others(60): Show |
63 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.977-1237_977-1236d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966298 | ||||||
| chr3:72966299 | T | G | 1 | a0005c0009t0030g0291 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.977-1248T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966299 | |||||||
| chr3:72966310 | T | C | 1 | a0004c0011t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.977-1237T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966310 | |||||||
| chr3:72966328 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
78 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.977-1219G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966328 | |||||||
| chr3:72966458 | C | CT | 131 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.977-1068dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966458 | ||||||
| chr3:72966458 | C | CTT | 48 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0001g0075 others(45): Show |
48 | HG00597.hp1 HG00642.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.977-1069_977-1068d others(4): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966458 | ||||||
| chr3:72966458 | C | CTTT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0031 others(66): Show |
69 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.977-1070_977-1068d others(5): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966458 | ||||||
| chr3:72966458 | C | CTTTT | 32 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0026 others(29): Show |
32 | HG00597.hp2 HG00735.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.977-1071_977-1068d others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966458 | ||||||
| chr3:72966501 | ACAGGCTA others(94): Show |
A | 1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.977-1045_977-945de others(1): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966501 | |||||||
| chr3:72966597 | C | G | 1 | a0001c0001t0023g0171 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.977-950C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966597 | |||||||
| chr3:72966605 | A | ATTTTTTT others(94): Show |
1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.977-939_977-938ins others(101): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966605 | ||||||
| chr3:72966616 | T | C | 3 | a0001c0001t0006g0063 a0001c0001t0006g0092 a0001c0001t0006g0210 |
3 | HG02055.hp1 HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.977-931T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966616 | |||||||
| chr3:72966635 | G | A | 1 | a0002c0006t0008g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.977-912G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966635 | |||||||
| chr3:72966635 | G | GT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
84 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.977-903dupT | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966635 | ||||||
| chr3:72966666 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.977-881G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966666 | |||||||
| chr3:72966692 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0057 |
2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.977-855C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966692 | |||||||
| chr3:72966792 | A | ATTTTTGT others(193): Show |
1 | a0001c0001t0005g0254 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.977-742_977-741ins others(200): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 72966792 | ||||||
| chr3:72966842 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.977-705C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966842 | |||||||
| chr3:72966905 | G | T | 1 | a0001c0001t0001g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.977-642G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966905 | |||||||
| chr3:72966915 | A | G | 1 | a0001c0005t0003g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.977-632A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966915 | |||||||
| chr3:72966968 | T | A | 15 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(12): Show |
15 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.977-579T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966968 | |||||||
| chr3:72966969 | A | G | 15 | a0001c0001t0003g0059 a0001c0001t0003g0061 a0001c0001t0003g0062 others(12): Show |
15 | HG01891.hp1 HG02055.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.977-578A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72966969 | |||||||
| chr3:72967032 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.977-515C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72967032 | |||||||
| chr3:72967109 | A | C | 1 | a0001c0001t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.977-438A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72967109 | |||||||
| chr3:72967182 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0030 others(32): Show |
35 | HG00140.hp1 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.977-365A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72967182 | |||||||
| chr3:72967332 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.977-215G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72967332 | |||||||
| chr3:72967433 | G | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0096 a0001c0001t0001g0119 others(42): Show |
45 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.977-114G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72967433 | |||||||
| chr3:72967484 | C | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.977-63C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72967484 | |||||||
| chr3:72967489 | T | C | 24 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.977-58T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 5/6 | chr3 | 72967489 | |||||||
| chr3:72967823 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1149+104A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72967823 | |||||||
| chr3:72968062 | C | T | 11 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(8): Show |
11 | HG00735.hp1 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+343C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968062 | |||||||
| chr3:72968074 | A | C | 3 | a0001c0005t0003g0052 a0001c0005t0003g0069 a0001c0005t0003g0091 |
3 | HG02717.hp1 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1149+355A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968074 | |||||||
| chr3:72968105 | C | A | 3 | a0001c0002t0014g0005 a0001c0002t0014g0039 a0002c0003t0026g0182 |
3 | HG02109.hp1 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1149+386C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968105 | |||||||
| chr3:72968121 | G | A | 2 | a0001c0001t0001g0004 a0002c0003t0001g0104 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1149+402G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968121 | |||||||
| chr3:72968419 | C | G | 1 | a0001c0001t0002g0131 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1149+700C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968419 | |||||||
| chr3:72968463 | T | G | 1 | a0001c0001t0001g0266 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1149+744T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968463 | |||||||
| chr3:72968799 | T | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(51): Show |
54 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1149+1080T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968799 | |||||||
| chr3:72968843 | C | T | 1 | a0001c0001t0004g0034 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1149+1124C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968843 | |||||||
| chr3:72968857 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1149+1138C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968857 | |||||||
| chr3:72968902 | CA | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
16 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1149+1193delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72968902 | ||||||
| chr3:72968911 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1149+1192A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968911 | |||||||
| chr3:72968940 | G | A | 2 | a0001c0001t0012g0168 a0001c0001t0012g0252 |
2 | HG03710.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1149+1221G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72968940 | |||||||
| chr3:72969002 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1149+1283C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969002 | |||||||
| chr3:72969080 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(95): Show |
98 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1149+1361A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969080 | |||||||
| chr3:72969267 | G | GC | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1149+1549dupC | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72969267 | ||||||
| chr3:72969332 | G | T | 2 | a0001c0002t0020g0070 a0001c0002t0021g0071 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1149+1613G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969332 | |||||||
| chr3:72969392 | C | CA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(121): Show |
124 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1149+1690dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72969392 | ||||||
| chr3:72969479 | G | C | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1149+1760G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969479 | |||||||
| chr3:72969531 | C | G | 3 | a0001c0005t0003g0052 a0001c0005t0003g0069 a0001c0005t0003g0091 |
3 | HG02717.hp1 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1149+1812C>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969531 | |||||||
| chr3:72969597 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1149+1878A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969597 | |||||||
| chr3:72969751 | AAGTT | A | 3 | a0001c0002t0014g0005 a0001c0002t0014g0039 a0002c0003t0026g0182 |
3 | HG02109.hp1 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1149+2035_1149+203 others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72969751 | ||||||
| chr3:72969909 | G | GAAA | 40 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0053 others(37): Show |
40 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1149+2200_1149+220 others(7): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72969909 | ||||||
| chr3:72969909 | G | GAAAA | 28 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(25): Show |
28 | HG01081.hp2 HG01255.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1149+2199_1149+220 others(8): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72969909 | ||||||
| chr3:72969909 | G | GAAAAA | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(43): Show |
46 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1149+2198_1149+220 others(9): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72969909 | ||||||
| chr3:72969922 | C | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1149+2203C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969922 | |||||||
| chr3:72969927 | A | AAAAAAC | 6 | a0001c0001t0001g0125 a0001c0001t0001g0192 a0001c0001t0001g0206 others(3): Show |
6 | HG00423.hp1 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+2208_1149+220 others(10): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969927 | |||||||
| chr3:72969927 | A | AAAAAC | 57 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0047 others(54): Show |
57 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1149+2208_1149+220 others(9): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72969927 | |||||||
| chr3:72970011 | G | C | 2 | a0001c0002t0014g0005 a0002c0003t0026g0182 |
2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1149+2292G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72970011 | |||||||
| chr3:72970179 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1149+2460C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72970179 | |||||||
| chr3:72970267 | C | T | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1149+2548C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72970267 | |||||||
| chr3:72970432 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1149+2713T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72970432 | |||||||
| chr3:72970519 | A | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1149+2800A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72970519 | |||||||
| chr3:72970671 | C | T | 25 | a0001c0001t0001g0240 a0001c0001t0004g0013 a0001c0001t0004g0019 others(22): Show |
25 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.1149+2952C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72970671 | |||||||
| chr3:72971100 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0179 a0001c0001t0001g0226 others(1): Show |
4 | HG01099.hp2 HG02145.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+3381C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971100 | |||||||
| chr3:72971137 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1149+3418G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971137 | |||||||
| chr3:72971147 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1149+3428C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971147 | |||||||
| chr3:72971520 | C | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01884.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1150-3457C>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971520 | |||||||
| chr3:72971613 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1150-3364T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971613 | |||||||
| chr3:72971746 | C | T | 3 | a0001c0002t0014g0005 a0001c0002t0014g0039 a0002c0003t0026g0182 |
3 | HG02109.hp1 HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1150-3231C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971746 | |||||||
| chr3:72971854 | TAGG | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1150-3120_1150-311 others(7): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72971854 | ||||||
| chr3:72971945 | T | A | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-3032T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971945 | |||||||
| chr3:72971947 | TAA | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0066 a0001c0001t0001g0076 others(6): Show |
9 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150-3014_1150-301 others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72971947 | ||||||
| chr3:72971955 | A | G | 1 | a0001c0007t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1150-3022A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72971955 | |||||||
| chr3:72972159 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1150-2818C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972159 | |||||||
| chr3:72972218 | G | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1150-2759G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972218 | |||||||
| chr3:72972297 | T | C | 4 | a0001c0001t0001g0191 a0001c0002t0020g0070 a0001c0002t0021g0071 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-2680T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972297 | |||||||
| chr3:72972386 | C | CTGTAA | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(277): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1150-2590_1150-258 others(9): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72972386 | ||||||
| chr3:72972595 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0057 others(5): Show |
8 | HG02615.hp2 HG02647.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-2382C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972595 | |||||||
| chr3:72972642 | G | GA | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(202): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1150-2316dupA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72972642 | ||||||
| chr3:72972642 | G | GAA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(42): Show |
45 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.1150-2317_1150-231 others(6): Show |
GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72972642 | ||||||
| chr3:72972696 | A | T | 6 | a0001c0001t0003g0062 a0001c0001t0003g0068 a0001c0005t0003g0052 others(3): Show |
6 | HG02055.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-2281A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972696 | |||||||
| chr3:72972699 | G | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1150-2278G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972699 | |||||||
| chr3:72972701 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0004t0008g0292 |
3 | HG02965.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1150-2276T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972701 | |||||||
| chr3:72972762 | TA | T | 23 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0049 others(20): Show |
23 | HG01070.hp1 HG01256.hp2 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150-2197delA | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 72972762 | ||||||
| chr3:72972881 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1150-2096G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972881 | |||||||
| chr3:72972901 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1150-2076T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72972901 | |||||||
| chr3:72973092 | T | G | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150-1885T>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973092 | |||||||
| chr3:72973281 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1150-1696G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973281 | |||||||
| chr3:72973324 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(111): Show |
114 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.1150-1653C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973324 | |||||||
| chr3:72973336 | T | C | 2 | a0001c0001t0009g0088 a0002c0003t0009g0105 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1150-1641T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973336 | |||||||
| chr3:72973511 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1150-1466G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973511 | |||||||
| chr3:72973550 | G | A | 24 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1150-1427G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973550 | |||||||
| chr3:72973653 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1150-1324G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973653 | |||||||
| chr3:72973690 | G | T | 1 | a0001c0001t0003g0059 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1150-1287G>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973690 | |||||||
| chr3:72973804 | A | G | 1 | a0001c0001t0003g0059 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1150-1173A>G | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973804 | |||||||
| chr3:72973812 | G | A | 4 | a0001c0004t0008g0281 a0001c0004t0008g0282 a0001c0004t0008g0284 others(1): Show |
4 | HG01109.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-1165G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72973812 | |||||||
| chr3:72974002 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1150-975T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974002 | |||||||
| chr3:72974025 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1150-952C>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974025 | |||||||
| chr3:72974127 | A | T | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150-850A>T | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974127 | |||||||
| chr3:72974234 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0002t0001g0040 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-743G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974234 | |||||||
| chr3:72974470 | T | C | 24 | a0001c0001t0004g0013 a0001c0001t0004g0019 a0001c0001t0004g0020 others(21): Show |
24 | HG00733.hp2 HG00735.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1150-507T>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974470 | |||||||
| chr3:72974509 | A | C | 1 | a0001c0001t0001g0024 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1150-468A>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974509 | |||||||
| chr3:72974516 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1150-461G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974516 | |||||||
| chr3:72974598 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1150-379T>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974598 | |||||||
| chr3:72974783 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.1150-194G>A | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974783 | |||||||
| chr3:72974810 | G | C | 1 | a0001c0002t0018g0188 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150-167G>C | GXYLT2 | ENSG00000172986.13 | transcript | ENST00000389617.9 | protein_coding | 6/6 | chr3 | 72974810 |