Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9956 |
| ensemblid | ENSG00000122254.7 |
| hgncid | 5195 |
| symbol | HS3ST2 |
| name | heparan sulfate-glucosamine 3-sulfotransferase 2 |
| refseq_nuc | NM_006043.2 |
| refseq_prot | NP_006034.1 |
| ensembl_nuc | ENST00000261374.4 |
| ensembl_prot | ENSP00000261374.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 22814162 |
| end | 22916338 |
| strand | + |
| ver | v1.2 |
| region | chr16:22814162-22916338 |
| region5000 | chr16:22809162-22921338 |
| regionname0 | HS3ST2_chr16_22814162_22916338 |
| regionname5000 | HS3ST2_chr16_22809162_22921338 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 367 | 341 | 91 | 73 | 123 | 12 | 40 | 90 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | MAYRV others(362): Show |
chr16 | 22809162 | 22921338 |
| a0002 | 0/0 | 367 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | MAYRV others(362): Show |
chr16 | 22809162 | 22921338 |
| a0003 | 0/0 | 367 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | MAYRV others(362): Show |
chr16 | 22809162 | 22921338 |
| a0004 | 0/0 | 367 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | MAYRV others(362): Show |
chr16 | 22809162 | 22921338 |
| a0005 | 0/0 | 367 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | MAYRV others(362): Show |
chr16 | 22809162 | 22921338 |
| a0006 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | MAYRV others(362): Show |
chr16 | 22809162 | 22921338 |
| a0007 | 0/0 | 367 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | MAYRV others(362): Show |
chr16 | 22809162 | 22921338 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1101 | 180 | 40 | 26 | 78 | 5 | 30 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0001c0002 | 0/1 | 1101 | 107 | 15 | 35 | 45 | 5 | 6 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0001c0003 | 0/0 | 1101 | 17 | 15 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0001c0004 | 0/0 | 1101 | 17 | 9 | 4 | 0 | 1 | 3 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0001c0005 | 0/0 | 1101 | 13 | 5 | 6 | 0 | 1 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0001c0006 | 0/0 | 1101 | 6 | 6 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0001c0011 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0002c0007 | 0/0 | 1101 | 2 | 0 | 1 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0003c0008 | 0/0 | 1101 | 2 | 0 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0004c0009 | 0/0 | 1101 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0005c0010 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0006c0013 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 | ||
| a0007c0012 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | ATGGC others(1096): Show |
chr16 | 22809162 | 22921338 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2329 | 168 | 39 | 24 | 74 | 5 | 25 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0001t0004 | 0/0 | 2329 | 6 | 0 | 2 | 1 | 0 | 3 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0001t0007 | 0/0 | 2330 | 3 | 1 | 0 | 1 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2325): Show |
chr16 | 22809162 | 22921338 |
| a0001c0001t0009 | 0/0 | 2329 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0001t0013 | 0/0 | 2329 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0001 | 0/1 | 2329 | 77 | 11 | 16 | 39 | 5 | 5 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0003 | 0/0 | 2329 | 2 | 2 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0004 | 0/0 | 2329 | 9 | 0 | 6 | 2 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0005 | 0/0 | 2329 | 9 | 1 | 8 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0007 | 0/0 | 2330 | 3 | 0 | 0 | 3 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2325): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0008 | 0/0 | 2329 | 5 | 0 | 5 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0010 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0002t0012 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0003t0003 | 0/0 | 2329 | 16 | 14 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0003t0015 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0004t0002 | 0/0 | 2329 | 16 | 8 | 4 | 0 | 1 | 3 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0004t0014 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0005t0002 | 0/0 | 2329 | 11 | 4 | 5 | 0 | 1 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0005t0006 | 0/0 | 2329 | 2 | 1 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0006t0006 | 0/0 | 2329 | 6 | 6 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0001c0011t0011 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0002c0007t0001 | 0/0 | 2329 | 2 | 0 | 1 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0003c0008t0002 | 0/0 | 2329 | 2 | 0 | 2 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0004c0009t0001 | 0/0 | 2329 | 2 | 0 | 0 | 2 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0005c0010t0001 | 0/0 | 2329 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0006c0013t0002 | 0/0 | 2329 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| a0007c0012t0001 | 0/0 | 2329 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | GGCAT others(2324): Show |
chr16 | 22809162 | 22921338 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0001t0013g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0002t0012g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0003t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0004t0014g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0005t0006g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0006t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0001c0011t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0002c0007t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0002c0007t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0003c0008t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0003c0008t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0004c0009t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0004c0009t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0005c0010t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0006c0013t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| a0007c0012t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0339 | EUR | GBR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0138 | EUR | GBR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0135 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0078 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | FIN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00438 | hp2 | a0001 | c0001 | t0009 | g0234 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00544 | hp1 | a0001 | c0002 | t0007 | g0044 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | CHS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00639 | hp1 | a0001 | c0005 | t0002 | g0011 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00639 | hp2 | a0002 | c0007 | t0001 | g0231 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0083 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00738 | hp2 | a0001 | c0005 | t0002 | g0089 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01070 | hp2 | a0003 | c0008 | t0002 | g0229 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01071 | hp1 | a0003 | c0008 | t0002 | g0230 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0102 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01081 | hp1 | a0001 | c0004 | t0002 | g0270 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01106 | hp1 | a0001 | c0004 | t0002 | g0236 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0302 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01167 | hp2 | a0001 | c0005 | t0006 | g0040 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0101 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01255 | hp1 | a0001 | c0002 | t0005 | g0128 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01256 | hp1 | a0001 | c0005 | t0002 | g0005 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0125 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01346 | hp1 | a0001 | c0005 | t0002 | g0004 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0165 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01361 | hp2 | a0001 | c0004 | t0002 | g0155 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0086 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0030 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0309 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0308 | EUR | IBS | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01884 | hp1 | a0001 | c0005 | t0006 | g0038 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01928 | hp1 | a0001 | c0002 | t0008 | g0131 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0134 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0033 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01943 | hp2 | a0001 | c0002 | t0005 | g0126 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01952 | hp1 | a0001 | c0002 | t0005 | g0121 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01952 | hp2 | a0001 | c0002 | t0008 | g0130 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0202 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01975 | hp2 | a0001 | c0002 | t0005 | g0127 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01978 | hp1 | a0001 | c0002 | t0005 | g0129 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01978 | hp2 | a0001 | c0002 | t0004 | g0137 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01981 | hp2 | a0001 | c0002 | t0008 | g0141 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0049 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02040 | hp2 | a0001 | c0001 | t0009 | g0182 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0287 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02071 | hp1 | a0001 | c0002 | t0004 | g0059 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02071 | hp2 | a0001 | c0002 | t0007 | g0058 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02148 | hp1 | a0001 | c0002 | t0008 | g0143 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CDX | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02258 | hp1 | a0001 | c0002 | t0010 | g0043 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02273 | hp2 | a0001 | c0002 | t0005 | g0132 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02293 | hp1 | a0001 | c0002 | t0004 | g0097 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02293 | hp2 | a0001 | c0002 | t0008 | g0133 | AMR | PEL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0276 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0002 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02622 | hp1 | a0001 | c0003 | t0015 | g0032 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02622 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02647 | hp1 | a0005 | c0010 | t0001 | g0042 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0212 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0140 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02717 | hp2 | a0001 | c0003 | t0003 | g0023 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0290 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0281 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0035 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0039 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02886 | hp2 | a0001 | c0003 | t0003 | g0034 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0015 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02970 | hp1 | a0001 | c0006 | t0006 | g0022 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02970 | hp2 | a0001 | c0004 | t0002 | g0305 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0019 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02976 | hp2 | a0001 | c0006 | t0006 | g0016 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0017 | AFR | GWD | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0181 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03195 | hp2 | a0001 | c0006 | t0006 | g0027 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0041 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0029 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03225 | hp1 | a0001 | c0006 | t0006 | g0031 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03239 | hp1 | a0002 | c0007 | t0001 | g0232 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03486 | hp1 | a0001 | c0006 | t0006 | g0025 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0268 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03516 | hp1 | a0001 | c0005 | t0002 | g0010 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0037 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0018 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0331 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03704 | hp2 | a0001 | c0005 | t0002 | g0091 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03831 | hp2 | a0001 | c0004 | t0002 | g0258 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0349 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0334 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03942 | hp1 | a0001 | c0004 | t0002 | g0186 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0267 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04199 | hp2 | a0001 | c0001 | t0013 | g0273 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04204 | hp1 | a0006 | c0013 | t0002 | g0272 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18747 | hp1 | a0007 | c0012 | t0001 | g0348 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18953 | hp1 | a0001 | c0002 | t0012 | g0100 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18959 | hp2 | a0001 | c0002 | t0004 | g0069 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18962 | hp2 | a0004 | c0009 | t0001 | g0341 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19030 | hp1 | a0001 | c0004 | t0014 | g0237 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19030 | hp2 | a0001 | c0005 | t0002 | g0009 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0144 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0154 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19054 | hp1 | a0001 | c0002 | t0007 | g0047 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19065 | hp2 | a0004 | c0009 | t0001 | g0336 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0142 | AFR | ASW | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20129 | hp2 | a0001 | c0006 | t0006 | g0024 | AFR | ASW | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20752 | hp1 | a0001 | c0004 | t0002 | g0152 | EUR | TSI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0104 | EUR | TSI | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0136 | SAS | GIH | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02486 | hp2 | a0001 | c0005 | t0002 | g0060 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0036 | AFR | ACB | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03471 | hp1 | a0001 | c0011 | t0011 | g0003 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | USA | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA21309 | hp1 | a0001 | c0004 | t0002 | g0149 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | LWK | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0064 | REF | REF | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0257 | REF | REF | HS3ST2_chr16_22809162_22921338 | HS3ST2 | chr16 | 22809162 | 22921338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22814725 | T | G | 1 | a0002 | 2 | HG00639.hp2 HG03239.hp1 |
missense_variant | MODERATE | c.115T>G | p.Cys39Gly | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 564/2329 | 115/1104 | 39/367 | chr16 | 22814725 | |||
| chr16:22814741 | T | C | 1 | a0003 | 2 | HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.131T>C | p.Leu44Pro | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 580/2329 | 131/1104 | 44/367 | chr16 | 22814741 | |||
| chr16:22814756 | T | C | 1 | a0004 | 2 | NA18962.hp2 NA19065.hp2 |
missense_variant | MODERATE | c.146T>C | p.Leu49Pro | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 595/2329 | 146/1104 | 49/367 | chr16 | 22814756 | |||
| chr16:22814794 | G | A | 1 | a0005 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.184G>A | p.Gly62Ser | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 633/2329 | 184/1104 | 62/367 | chr16 | 22814794 | |||
| chr16:22814853 | C | G | 1 | a0006 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.243C>G | p.Ser81Arg | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 692/2329 | 243/1104 | 81/367 | chr16 | 22814853 | |||
| chr16:22814900 | G | T | 1 | a0007 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.290G>T | p.Arg97Leu | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 739/2329 | 290/1104 | 97/367 | chr16 | 22814900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22815000 | G | A | 2 | a0001c0003 a0001c0006 |
23 | HG01496.hp2 HG01891.hp1 HG01934.hp1 others(20): Show |
synonymous_variant | LOW | c.390G>A | p.Val130Val | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 839/2329 | 390/1104 | 130/367 | chr16 | 22815000 | |||
| chr16:22815018 | A | G | 6 | a0001c0002 a0001c0003 a0001c0005 others(3): Show |
144 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(141): Show |
synonymous_variant | LOW | c.408A>G | p.Val136Val | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 857/2329 | 408/1104 | 136/367 | chr16 | 22815018 | |||
| chr16:22915190 | A | G | 6 | a0001c0004 a0001c0005 a0001c0006 others(3): Show |
40 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
synonymous_variant | LOW | c.732A>G | p.Ser244Ser | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 1181/2329 | 732/1104 | 244/367 | chr16 | 22915190 | |||
| chr16:22915361 | G | A | 1 | a0001c0011 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.903G>A | p.Lys301Lys | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 1352/2329 | 903/1104 | 301/367 | chr16 | 22915361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22814223 | G | T | 1 | a0001c0003t0015 | 1 | HG02622.hp1 | 5_prime_UTR_variant | MODIFIER | c.-388G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 388 | chr16 | 22814223 | ||||||
| chr16:22814254 | C | A | 1 | a0001c0002t0010 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-357C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 357 | chr16 | 22814254 | ||||||
| chr16:22814317 | G | A | 6 | a0001c0002t0003 a0001c0003t0003 a0001c0003t0015 others(3): Show |
28 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-294G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 294 | chr16 | 22814317 | ||||||
| chr16:22814428 | C | G | 2 | a0001c0002t0005 a0001c0002t0008 |
14 | HG01255.hp1 HG01261.hp1 HG01928.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-183C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 183 | chr16 | 22814428 | ||||||
| chr16:22814507 | C | G | 6 | a0001c0002t0003 a0001c0003t0003 a0001c0003t0015 others(3): Show |
28 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-104C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 104 | chr16 | 22814507 | ||||||
| chr16:22814539 | C | T | 1 | a0001c0004t0014 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-72C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | chr16 | 22814539 | |||||||
| chr16:22814568 | G | GC | 2 | a0001c0001t0007 a0001c0002t0007 |
6 | HG00544.hp1 HG02055.hp2 HG02071.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-38dupC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/2 | 37 | INFO_REALIGN_3_PRIME | chr16 | 22814568 | |||||
| chr16:22915635 | G | T | 7 | a0001c0004t0002 a0001c0004t0014 a0001c0005t0002 others(4): Show |
39 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*73G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 73 | chr16 | 22915635 | ||||||
| chr16:22915736 | C | T | 7 | a0001c0004t0002 a0001c0004t0014 a0001c0005t0002 others(4): Show |
39 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*174C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 174 | chr16 | 22915736 | ||||||
| chr16:22915801 | T | C | 1 | a0001c0002t0012 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*239T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 239 | chr16 | 22915801 | ||||||
| chr16:22915891 | G | T | 1 | a0001c0001t0009 | 2 | HG00438.hp2 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*329G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 329 | chr16 | 22915891 | ||||||
| chr16:22915893 | T | C | 10 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0008 others(7): Show |
59 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*331T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 331 | chr16 | 22915893 | ||||||
| chr16:22915934 | A | G | 1 | a0001c0001t0013 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 372 | chr16 | 22915934 | ||||||
| chr16:22915968 | G | A | 1 | a0001c0011t0011 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 2/2 | 406 | chr16 | 22915968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:22815145 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.485+50T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815145 | |||||||
| chr16:22815277 | G | A | 2 | a0001c0002t0003g0002 a0001c0011t0011g0003 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+182G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815277 | |||||||
| chr16:22815442 | G | A | 11 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0008 others(8): Show |
11 | HG00639.hp1 HG01256.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+347G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815442 | |||||||
| chr16:22815612 | C | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0311 a0001c0001t0001g0312 others(38): Show |
41 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.485+517C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815612 | |||||||
| chr16:22815732 | G | A | 31 | a0001c0002t0003g0002 a0001c0002t0003g0039 a0001c0002t0010g0043 others(28): Show |
31 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.485+637G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815732 | |||||||
| chr16:22815840 | C | A | 26 | a0001c0002t0003g0039 a0001c0003t0003g0015 a0001c0003t0003g0017 others(23): Show |
26 | HG01167.hp2 HG01496.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.485+745C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815840 | |||||||
| chr16:22815847 | G | A | 141 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0008 others(138): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.485+752G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22815847 | |||||||
| chr16:22816051 | A | C | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+956A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816051 | |||||||
| chr16:22816140 | T | A | 2 | a0001c0002t0003g0002 a0001c0011t0011g0003 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+1045T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816140 | |||||||
| chr16:22816196 | A | C | 150 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0288 others(147): Show |
150 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.485+1101A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816196 | |||||||
| chr16:22816256 | G | A | 2 | a0001c0002t0003g0002 a0001c0011t0011g0003 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+1161G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816256 | |||||||
| chr16:22816315 | T | G | 25 | a0001c0002t0001g0006 a0001c0003t0003g0017 a0001c0003t0003g0018 others(22): Show |
25 | HG01256.hp1 HG01346.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.485+1220T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816315 | |||||||
| chr16:22816392 | A | G | 26 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(23): Show |
26 | HG00140.hp2 HG00280.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.485+1297A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816392 | |||||||
| chr16:22816415 | A | G | 22 | a0001c0003t0003g0017 a0001c0003t0003g0018 a0001c0003t0003g0019 others(19): Show |
22 | HG01496.hp2 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.485+1320A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816415 | |||||||
| chr16:22816423 | C | T | 11 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(8): Show |
11 | HG01106.hp2 NA18966.hp1 NA18979.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+1328C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816423 | |||||||
| chr16:22816464 | G | A | 2 | a0001c0001t0001g0145 a0001c0004t0002g0144 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.485+1369G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816464 | |||||||
| chr16:22816585 | A | G | 1 | a0001c0001t0001g0349 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.485+1490A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22816585 | |||||||
| chr16:22817015 | A | T | 1 | a0001c0002t0004g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.485+1920A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817015 | |||||||
| chr16:22817031 | T | C | 2 | a0001c0002t0003g0002 a0001c0011t0011g0003 |
2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+1936T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817031 | |||||||
| chr16:22817125 | T | A | 27 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(24): Show |
27 | HG00741.hp2 HG01243.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.485+2030T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817125 | |||||||
| chr16:22817281 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.485+2186C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817281 | |||||||
| chr16:22817290 | C | G | 3 | a0001c0002t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0109 |
3 | NA18967.hp1 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.485+2195C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817290 | |||||||
| chr16:22817299 | A | G | 1 | a0001c0002t0008g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.485+2204A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817299 | |||||||
| chr16:22817476 | T | G | 1 | a0001c0003t0003g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.485+2381T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817476 | |||||||
| chr16:22817550 | T | C | 19 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0288 others(16): Show |
19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+2455T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817550 | |||||||
| chr16:22817689 | T | C | 120 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(117): Show |
120 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.485+2594T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817689 | |||||||
| chr16:22817892 | GC | G | 98 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(95): Show |
98 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.485+2798delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817892 | |||||||
| chr16:22817917 | T | A | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+2822T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817917 | |||||||
| chr16:22817918 | A | T | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+2823A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817918 | |||||||
| chr16:22817968 | A | C | 1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+2873A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22817968 | |||||||
| chr16:22818137 | G | A | 88 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(85): Show |
88 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.485+3042G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818137 | |||||||
| chr16:22818147 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.485+3052C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818147 | |||||||
| chr16:22818164 | C | T | 3 | a0001c0001t0001g0298 a0001c0003t0003g0036 a0001c0003t0003g0037 |
3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+3069C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818164 | |||||||
| chr16:22818316 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.485+3221C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818316 | |||||||
| chr16:22818555 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 others(1): Show |
4 | HG01175.hp2 HG01952.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3460G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818555 | |||||||
| chr16:22818649 | T | G | 3 | a0001c0002t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0109 |
3 | NA18967.hp1 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.485+3554T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818649 | |||||||
| chr16:22818665 | T | TTCCTTCC others(9): Show |
9 | a0001c0001t0001g0216 a0001c0001t0001g0292 a0001c0001t0001g0293 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3582_485+3583i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818665 | ||||||
| chr16:22818666 | TCCTTCCT others(21): Show |
T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3583_485+3610d others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818666 | ||||||
| chr16:22818669 | T | TTCCTTCC others(5): Show |
7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+3582_485+3583i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818669 | ||||||
| chr16:22818674 | T | TCCTTCCC others(294): Show |
1 | a0001c0001t0007g0287 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.485+3582_485+3583i others(303): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818674 | ||||||
| chr16:22818674 | T | TCCTTCCC others(293): Show |
2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485+3582_485+3583i others(302): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818674 | ||||||
| chr16:22818678 | C | T | 7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+3583C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818678 | |||||||
| chr16:22818686 | CCTTGCCT others(413): Show |
C | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+3593_485+4012d others(2): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818686 | ||||||
| chr16:22818688 | T | C | 19 | a0001c0001t0001g0216 a0001c0001t0001g0285 a0001c0001t0001g0286 others(16): Show |
19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3593T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818688 | |||||||
| chr16:22818690 | G | C | 10 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0288 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+3595G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818690 | |||||||
| chr16:22818690 | G | T | 9 | a0001c0001t0001g0216 a0001c0001t0001g0292 a0001c0001t0001g0293 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3595G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818690 | |||||||
| chr16:22818694 | G | T | 19 | a0001c0001t0001g0216 a0001c0001t0001g0285 a0001c0001t0001g0286 others(16): Show |
19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3599G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818694 | |||||||
| chr16:22818705 | T | C | 1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+3610T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818705 | |||||||
| chr16:22818709 | C | T | 17 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(14): Show |
17 | HG01243.hp2 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.485+3614C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818709 | |||||||
| chr16:22818715 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3620C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818715 | |||||||
| chr16:22818720 | CT | C | 12 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 others(9): Show |
12 | HG01109.hp2 HG01175.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+3627delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818720 | ||||||
| chr16:22818721 | T | C | 1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+3626T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818721 | |||||||
| chr16:22818724 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3629C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818724 | |||||||
| chr16:22818725 | C | T | 19 | a0001c0001t0001g0216 a0001c0001t0001g0285 a0001c0001t0001g0286 others(16): Show |
19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3630C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818725 | |||||||
| chr16:22818729 | C | T | 20 | a0001c0001t0001g0216 a0001c0001t0001g0219 a0001c0001t0001g0285 others(17): Show |
20 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+3634C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818729 | |||||||
| chr16:22818732 | C | A | 16 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(13): Show |
16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3637C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818732 | |||||||
| chr16:22818733 | C | T | 17 | a0001c0001t0001g0216 a0001c0001t0001g0219 a0001c0001t0001g0288 others(14): Show |
17 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.485+3638C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818733 | |||||||
| chr16:22818733 | CTCCT | C | 17 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(14): Show |
17 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.485+3642_485+3645d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818733 | ||||||
| chr16:22818734 | T | TC | 6 | a0001c0002t0001g0046 a0001c0002t0001g0079 a0001c0002t0001g0080 others(3): Show |
6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3641dupC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818734 | ||||||
| chr16:22818737 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(299): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.485+3642T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818737 | |||||||
| chr16:22818738 | TC | T | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0007g0287 |
3 | HG02055.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485+3646delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818738 | ||||||
| chr16:22818739 | C | CCTTCCTT others(76): Show |
6 | a0001c0002t0001g0046 a0001c0002t0001g0079 a0001c0002t0001g0080 others(3): Show |
6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3645_485+3646i others(85): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818739 | ||||||
| chr16:22818739 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(299): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.485+3644C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818739 | |||||||
| chr16:22818741 | CT | C | 16 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(13): Show |
16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3648delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818741 | ||||||
| chr16:22818749 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3654C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818749 | |||||||
| chr16:22818753 | C | A | 3 | a0001c0002t0001g0122 a0001c0005t0002g0004 a0001c0005t0002g0041 |
3 | HG01346.hp1 HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+3658C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818753 | |||||||
| chr16:22818754 | T | TTCCC | 44 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0221 others(41): Show |
44 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.485+3662_485+3663i others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818754 | ||||||
| chr16:22818758 | T | C | 19 | a0001c0001t0001g0216 a0001c0001t0001g0285 a0001c0001t0001g0286 others(16): Show |
19 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3663T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818758 | |||||||
| chr16:22818761 | A | ATTCCTTC others(17): Show |
1 | a0001c0002t0007g0044 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.485+3678_485+3679i others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818761 | ||||||
| chr16:22818761 | A | ATTCCTTC others(309): Show |
1 | a0001c0004t0002g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+3678_485+3679i others(318): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818761 | ||||||
| chr16:22818761 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(71): Show |
74 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.485+3666A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818761 | |||||||
| chr16:22818766 | TTCCTTCC others(32): Show |
T | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3672_485+3710d others(41): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818766 | |||||||
| chr16:22818769 | C | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01175.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3674C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818769 | |||||||
| chr16:22818770 | TTCCC | T | 6 | a0001c0002t0001g0046 a0001c0002t0001g0079 a0001c0002t0001g0080 others(3): Show |
6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3679_485+3682d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818770 | ||||||
| chr16:22818773 | C | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02258.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+3678C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818773 | |||||||
| chr16:22818774 | C | G | 9 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(6): Show |
9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3679C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818774 | |||||||
| chr16:22818774 | C | T | 88 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(85): Show |
88 | HG00323.hp1 HG00323.hp2 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.485+3679C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818774 | |||||||
| chr16:22818775 | T | C | 6 | a0001c0002t0001g0046 a0001c0002t0001g0079 a0001c0002t0001g0080 others(3): Show |
6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3680T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818775 | |||||||
| chr16:22818778 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01175.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3683T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818778 | |||||||
| chr16:22818782 | T | C | 91 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(88): Show |
91 | HG00323.hp1 HG00323.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.485+3687T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818782 | |||||||
| chr16:22818785 | CT | C | 13 | a0001c0001t0001g0216 a0001c0001t0001g0285 a0001c0001t0001g0286 others(10): Show |
13 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.485+3692delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818785 | ||||||
| chr16:22818786 | T | TCCC | 7 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0291 others(4): Show |
7 | HG00544.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+3691_485+3692i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818786 | |||||||
| chr16:22818786 | T | TTCCCTCC others(8): Show |
4 | a0001c0001t0001g0200 a0001c0002t0001g0074 a0001c0002t0001g0076 others(1): Show |
4 | HG02109.hp1 HG03710.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3698_485+3699i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818786 | ||||||
| chr16:22818790 | C | T | 98 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(95): Show |
98 | HG00323.hp1 HG00323.hp2 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.485+3695C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818790 | |||||||
| chr16:22818791 | TCCCTC | T | 6 | a0001c0002t0001g0046 a0001c0002t0001g0079 a0001c0002t0001g0080 others(3): Show |
6 | HG01978.hp2 HG03239.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3699_485+3703d others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818791 | ||||||
| chr16:22818792 | C | CCTTCCTT others(48): Show |
2 | a0001c0002t0001g0065 a0001c0002t0001g0066 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485+3698_485+3699i others(57): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818792 | ||||||
| chr16:22818794 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(128): Show |
131 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.485+3699C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818794 | |||||||
| chr16:22818796 | C | CCTTCCTC others(64): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0221 others(32): Show |
35 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.485+3702_485+3703i others(73): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818796 | ||||||
| chr16:22818796 | C | CCTTCCTT others(260): Show |
4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02258.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3702_485+3703i others(269): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818796 | ||||||
| chr16:22818798 | C | T | 5 | a0001c0002t0001g0075 a0001c0002t0001g0117 a0001c0002t0001g0308 others(2): Show |
5 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+3703C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818798 | |||||||
| chr16:22818799 | TC | T | 10 | a0001c0001t0001g0299 a0001c0001t0001g0303 a0001c0001t0001g0304 others(7): Show |
10 | HG01109.hp2 HG01256.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3707delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818799 | ||||||
| chr16:22818800 | C | CCCTT | 115 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0148 others(112): Show |
115 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.485+3736_485+3739d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCCTTCCT others(1): Show |
4 | a0001c0001t0001g0238 a0001c0001t0001g0262 a0001c0001t0001g0324 others(1): Show |
4 | HG01123.hp1 HG02165.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3732_485+3739d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTCCCTC others(60): Show |
5 | a0001c0002t0001g0075 a0001c0002t0001g0117 a0001c0002t0001g0308 others(2): Show |
5 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(69): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(316): Show |
11 | a0001c0001t0001g0170 a0001c0001t0001g0177 a0001c0001t0001g0178 others(8): Show |
11 | HG02280.hp2 HG02486.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(318): Show |
1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(327): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(320): Show |
1 | a0001c0002t0005g0134 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(296): Show |
2 | a0001c0002t0001g0123 a0001c0002t0001g0124 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(305): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(296): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(305): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(316): Show |
1 | a0001c0001t0001g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(288): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0002t0005g0127 |
3 | HG01975.hp2 HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(297): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(300): Show |
2 | a0001c0004t0002g0152 a0001c0004t0002g0155 |
2 | HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(309): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(316): Show |
1 | a0001c0001t0001g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(304): Show |
4 | a0001c0001t0001g0174 a0001c0003t0003g0018 a0001c0003t0003g0021 others(1): Show |
4 | HG01891.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(313): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(316): Show |
4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0002t0001g0077 others(1): Show |
4 | HG00323.hp1 HG00323.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(320): Show |
39 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(36): Show |
39 | HG01255.hp1 HG01261.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(392): Show |
3 | a0001c0001t0001g0157 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG00738.hp1 HG01993.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(401): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(316): Show |
2 | a0001c0001t0001g0284 a0001c0001t0007g0156 |
2 | NA18942.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(320): Show |
1 | a0001c0001t0001g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(324): Show |
1 | a0001c0001t0009g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(333): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(316): Show |
1 | a0001c0001t0001g0189 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485+3706_485+3707i others(325): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(248): Show |
1 | a0001c0006t0006g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.485+3706_485+3707i others(257): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | CCTTCCTT others(320): Show |
1 | a0001c0001t0001g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.485+3706_485+3707i others(329): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818800 | ||||||
| chr16:22818800 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(57): Show |
60 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.485+3705C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818800 | |||||||
| chr16:22818803 | T | C | 67 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(64): Show |
67 | HG01255.hp1 HG01261.hp1 HG01361.hp1 others(64): Show |
intron_variant | MODIFIER | c.485+3708T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818803 | |||||||
| chr16:22818803 | T | TCCCTCCC others(289): Show |
1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+3708_485+3709i others(298): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818803 | |||||||
| chr16:22818803 | T | TCCCTCCC others(305): Show |
1 | a0001c0002t0001g0138 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.485+3708_485+3709i others(314): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818803 | |||||||
| chr16:22818807 | T | C | 12 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(9): Show |
12 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+3712T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818807 | |||||||
| chr16:22818810 | C | A | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3715C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818810 | |||||||
| chr16:22818811 | T | C | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG01175.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3716T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818811 | |||||||
| chr16:22818812 | T | C | 10 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(7): Show |
10 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3717T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818812 | |||||||
| chr16:22818815 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.485+3720T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818815 | |||||||
| chr16:22818816 | T | C | 10 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(7): Show |
10 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3721T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818816 | |||||||
| chr16:22818819 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0158 others(114): Show |
117 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.485+3724T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818819 | |||||||
| chr16:22818819 | T | TTCCTTCA others(529): Show |
3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0007g0287 |
3 | HG02055.hp2 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.485+3730_485+3731i others(538): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | ||||||
| chr16:22818819 | T | TTCCTTCC others(33): Show |
4 | a0001c0001t0001g0288 a0001c0001t0001g0292 a0001c0001t0001g0297 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3738_485+3739i others(42): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | ||||||
| chr16:22818819 | T | TTCCTTCC others(37): Show |
8 | a0001c0001t0001g0216 a0001c0001t0001g0289 a0001c0001t0001g0293 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+3739_485+3740i others(46): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | ||||||
| chr16:22818819 | T | TTCCTTCC others(41): Show |
4 | a0001c0001t0001g0291 a0001c0001t0001g0296 a0001c0001t0001g0300 others(1): Show |
4 | HG02723.hp2 HG02965.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3739_485+3740i others(50): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | ||||||
| chr16:22818819 | TTCCTTCC others(9): Show |
T | 1 | a0001c0005t0002g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.485+3737_485+3752d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818819 | ||||||
| chr16:22818820 | T | C | 11 | a0001c0001t0001g0219 a0001c0001t0001g0303 a0001c0001t0001g0304 others(8): Show |
11 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3725T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818820 | |||||||
| chr16:22818820 | TCCTTCCT others(29): Show |
T | 15 | a0001c0001t0001g0146 a0001c0003t0003g0020 a0001c0003t0003g0023 others(12): Show |
15 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3729_485+3764d others(38): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818820 | ||||||
| chr16:22818821 | C | CCTTCATT others(51): Show |
1 | a0001c0002t0001g0074 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.485+3730_485+3731i others(60): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818821 | ||||||
| chr16:22818823 | T | C | 18 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(15): Show |
18 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+3728T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818823 | |||||||
| chr16:22818823 | TTCCTTCC others(5): Show |
T | 1 | a0001c0002t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+3740_485+3751d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818823 | ||||||
| chr16:22818824 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0005t0002g0041 others(1): Show |
4 | HG01175.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3729T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818824 | |||||||
| chr16:22818824 | T | TCATTCCT others(148): Show |
1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+3730_485+3731i others(157): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818824 | ||||||
| chr16:22818825 | C | CATTCCTT others(291): Show |
1 | a0001c0001t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.485+3730_485+3731i others(300): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818825 | |||||||
| chr16:22818827 | TTCCTTCC others(1): Show |
T | 16 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
16 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3740_485+3747d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818827 | ||||||
| chr16:22818828 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01175.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3733T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818828 | |||||||
| chr16:22818831 | T | C | 1 | a0001c0001t0001g0299 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.485+3736T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818831 | |||||||
| chr16:22818832 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0002t0001g0012 others(1): Show |
4 | HG01175.hp2 HG02055.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3737T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818832 | |||||||
| chr16:22818834 | C | A | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3739C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818834 | |||||||
| chr16:22818835 | C | T | 37 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(34): Show |
37 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.485+3740C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818835 | |||||||
| chr16:22818836 | T | C | 6 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0282 others(3): Show |
6 | HG01175.hp2 HG02055.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+3741T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818836 | |||||||
| chr16:22818839 | T | C | 21 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(18): Show |
21 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.485+3744T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818839 | |||||||
| chr16:22818840 | T | C | 7 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0282 others(4): Show |
7 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3745T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818840 | |||||||
| chr16:22818840 | TCCTTCCT others(17): Show |
T | 1 | a0001c0006t0006g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.485+3753_485+3776d others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818840 | ||||||
| chr16:22818843 | T | C | 9 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(6): Show |
9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3748T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818843 | |||||||
| chr16:22818844 | T | C | 5 | a0001c0001t0001g0282 a0001c0002t0001g0006 a0001c0002t0001g0012 others(2): Show |
5 | HG02055.hp1 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3749T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818844 | |||||||
| chr16:22818846 | C | CTTCCCTC others(22): Show |
1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3752_485+3753i others(31): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818846 | ||||||
| chr16:22818848 | C | T | 32 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(29): Show |
32 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.485+3753C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818848 | |||||||
| chr16:22818850 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3755C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818850 | |||||||
| chr16:22818852 | C | T | 15 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(12): Show |
15 | HG01109.hp2 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+3757C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818852 | |||||||
| chr16:22818856 | C | T | 8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0282 others(5): Show |
8 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+3761C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818856 | |||||||
| chr16:22818858 | C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3763C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818858 | |||||||
| chr16:22818860 | C | T | 8 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0282 others(5): Show |
8 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+3765C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818860 | |||||||
| chr16:22818862 | C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3767C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818862 | |||||||
| chr16:22818864 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0157 others(94): Show |
97 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.485+3769C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818864 | |||||||
| chr16:22818868 | T | C | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+3773T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818868 | |||||||
| chr16:22818869 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.485+3774C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818869 | |||||||
| chr16:22818870 | C | A | 5 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 others(2): Show |
5 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3775C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818870 | |||||||
| chr16:22818872 | T | C | 16 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(13): Show |
16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3777T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818872 | |||||||
| chr16:22818874 | C | A | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+3779C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818874 | |||||||
| chr16:22818875 | T | C | 15 | a0001c0001t0001g0146 a0001c0003t0003g0020 a0001c0003t0003g0023 others(12): Show |
15 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3780T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818875 | |||||||
| chr16:22818876 | T | C | 16 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(13): Show |
16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+3781T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818876 | |||||||
| chr16:22818879 | T | C | 1 | a0001c0006t0006g0027 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.485+3784T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818879 | |||||||
| chr16:22818880 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3785T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818880 | |||||||
| chr16:22818882 | C | A | 1 | a0002c0007t0001g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.485+3787C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818882 | |||||||
| chr16:22818883 | T | C | 2 | a0001c0002t0007g0044 a0001c0005t0002g0041 |
2 | HG00544.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+3788T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818883 | |||||||
| chr16:22818886 | A | C | 25 | a0001c0001t0001g0146 a0001c0001t0001g0282 a0001c0002t0001g0006 others(22): Show |
25 | HG00544.hp1 HG01496.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.485+3791A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818886 | |||||||
| chr16:22818891 | T | C | 19 | a0001c0001t0001g0146 a0001c0001t0001g0282 a0001c0002t0001g0012 others(16): Show |
19 | HG01496.hp2 HG01934.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+3796T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818891 | |||||||
| chr16:22818891 | T | TTCCGTCC others(5): Show |
1 | a0002c0007t0001g0232 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.485+3799_485+3800i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818891 | ||||||
| chr16:22818895 | T | C | 21 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(18): Show |
21 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+3800T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818895 | |||||||
| chr16:22818899 | T | C | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3804T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818899 | |||||||
| chr16:22818899 | T | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0221 others(34): Show |
37 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.485+3804T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818899 | |||||||
| chr16:22818907 | C | T | 21 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(18): Show |
21 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+3812C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818907 | |||||||
| chr16:22818908 | T | TCCTTCCT others(13): Show |
2 | a0001c0001t0001g0288 a0001c0004t0002g0290 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.485+3820_485+3821i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818908 | ||||||
| chr16:22818911 | T | C | 9 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0282 others(6): Show |
9 | HG01175.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3816T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818911 | |||||||
| chr16:22818914 | CT | C | 14 | a0001c0001t0001g0216 a0001c0001t0001g0289 a0001c0001t0001g0291 others(11): Show |
14 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3821delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818914 | ||||||
| chr16:22818915 | T | C | 7 | a0001c0001t0001g0282 a0001c0002t0001g0006 a0001c0002t0001g0012 others(4): Show |
7 | HG02055.hp1 HG02523.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3820T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818915 | |||||||
| chr16:22818919 | T | C | 21 | a0001c0001t0001g0216 a0001c0001t0001g0282 a0001c0001t0001g0289 others(18): Show |
21 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.485+3824T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818919 | |||||||
| chr16:22818919 | T | TCCC | 15 | a0001c0001t0001g0146 a0001c0003t0003g0020 a0001c0003t0003g0023 others(12): Show |
15 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3824_485+3825i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818919 | |||||||
| chr16:22818919 | T | TTCCC | 71 | a0001c0001t0001g0148 a0001c0001t0001g0220 a0001c0001t0001g0238 others(68): Show |
71 | HG00140.hp1 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.485+3842_485+3845d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | ||||||
| chr16:22818919 | T | TTCCCTCC others(5): Show |
1 | a0001c0001t0001g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.485+3834_485+3845d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | ||||||
| chr16:22818919 | T | TTCCCTCC others(8): Show |
1 | a0001c0001t0001g0284 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.485+3831_485+3832i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | ||||||
| chr16:22818919 | T | TTCCCTCC others(12): Show |
1 | a0001c0001t0007g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.485+3831_485+3832i others(21): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | ||||||
| chr16:22818919 | T | TTCCCTCC others(13): Show |
3 | a0001c0002t0001g0103 a0001c0002t0001g0105 a0001c0002t0001g0106 |
3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.485+3831_485+3832i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818919 | ||||||
| chr16:22818920 | TC | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3828delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818920 | ||||||
| chr16:22818921 | C | CCCTCCTT others(4): Show |
135 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(132): Show |
135 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.485+3831_485+3832i others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818921 | ||||||
| chr16:22818923 | C | T | 4 | a0001c0001t0001g0288 a0001c0002t0001g0076 a0001c0002t0007g0044 others(1): Show |
4 | HG00544.hp1 HG01891.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3828C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818923 | |||||||
| chr16:22818925 | C | CCTTCCTT | 11 | a0001c0002t0001g0065 a0001c0002t0001g0066 a0001c0002t0001g0110 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3831_485+3832i others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818925 | ||||||
| chr16:22818929 | C | CCTTCCTT others(68): Show |
1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+3835_485+3836i others(77): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818929 | ||||||
| chr16:22818929 | C | CCTTCCTT others(20): Show |
1 | a0001c0002t0007g0044 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.485+3835_485+3836i others(29): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818929 | ||||||
| chr16:22818929 | C | T | 3 | a0001c0001t0001g0228 a0001c0005t0002g0041 a0001c0006t0006g0027 |
3 | HG01175.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.485+3834C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818929 | |||||||
| chr16:22818933 | C | T | 6 | a0001c0001t0001g0288 a0001c0002t0001g0076 a0001c0002t0007g0044 others(3): Show |
6 | HG00544.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3838C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818933 | |||||||
| chr16:22818937 | C | CCCTCCCT others(9): Show |
1 | a0001c0001t0001g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.485+3845_485+3846i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | ||||||
| chr16:22818937 | C | CCCTCCCT others(13): Show |
1 | a0001c0005t0002g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.485+3845_485+3846i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | ||||||
| chr16:22818937 | C | CCCTCCCT others(5): Show |
14 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(11): Show |
14 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3845_485+3846i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | ||||||
| chr16:22818937 | C | CCCTCCCT others(1): Show |
3 | a0001c0001t0001g0213 a0001c0002t0003g0002 a0001c0003t0003g0015 |
3 | HG02615.hp2 HG02738.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.485+3845_485+3846i others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | ||||||
| chr16:22818937 | C | CCCTCCCT others(9): Show |
1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+3845_485+3846i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818937 | ||||||
| chr16:22818937 | C | T | 40 | a0001c0001t0001g0146 a0001c0001t0001g0216 a0001c0001t0001g0282 others(37): Show |
40 | HG00544.hp1 HG01243.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.485+3842C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818937 | |||||||
| chr16:22818941 | T | C | 28 | a0001c0001t0001g0145 a0001c0001t0001g0219 a0001c0001t0001g0228 others(25): Show |
28 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.485+3846T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818941 | |||||||
| chr16:22818945 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.485+3850T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818945 | |||||||
| chr16:22818948 | T | C | 2 | a0001c0001t0001g0288 a0001c0004t0002g0290 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.485+3853T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818948 | |||||||
| chr16:22818948 | T | TTCCCTCC others(21): Show |
14 | a0001c0001t0001g0216 a0001c0001t0001g0289 a0001c0001t0001g0291 others(11): Show |
14 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3856_485+3857i others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818948 | ||||||
| chr16:22818949 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3854T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818949 | |||||||
| chr16:22818951 | C | A | 2 | a0001c0001t0007g0156 a0001c0002t0007g0044 |
2 | HG00544.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.485+3856C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818951 | |||||||
| chr16:22818951 | C | CTTCA | 6 | a0001c0001t0001g0146 a0001c0003t0003g0020 a0001c0003t0003g0033 others(3): Show |
6 | HG01934.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+3859_485+3860i others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | ||||||
| chr16:22818951 | C | CTTCCCTC others(89): Show |
1 | a0001c0001t0001g0316 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485+3860_485+3861i others(98): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | ||||||
| chr16:22818951 | C | CTTCCCTC others(93): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0317 |
2 | HG01993.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.485+3860_485+3861i others(102): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | ||||||
| chr16:22818951 | C | CTTCCTCA | 35 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0221 others(32): Show |
35 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.485+3861_485+3862i others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | ||||||
| chr16:22818951 | C | CTTCCTTC others(1): Show |
4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0284 others(1): Show |
4 | HG01256.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3863_485+3864i others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | ||||||
| chr16:22818951 | C | CTTCCTTC others(5): Show |
86 | a0001c0001t0001g0153 a0001c0001t0001g0159 a0001c0001t0001g0160 others(83): Show |
86 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.485+3867_485+3868i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818951 | ||||||
| chr16:22818952 | T | TTCCTCAT others(124): Show |
1 | a0001c0002t0001g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.485+3861_485+3862i others(133): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818952 | ||||||
| chr16:22818952 | T | TTCCTTCC others(25): Show |
5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3867_485+3868i others(34): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818952 | ||||||
| chr16:22818953 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3858T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818953 | |||||||
| chr16:22818955 | C | A | 10 | a0001c0003t0003g0023 a0001c0003t0003g0026 a0001c0003t0003g0028 others(7): Show |
10 | HG01496.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+3860C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818955 | |||||||
| chr16:22818956 | T | TTCCTTCA others(145): Show |
1 | a0001c0001t0001g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+3867_485+3868i others(154): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818956 | ||||||
| chr16:22818963 | C | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 others(1): Show |
4 | HG01175.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3868C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818963 | |||||||
| chr16:22818967 | C | A | 13 | a0001c0001t0001g0228 a0001c0002t0001g0065 a0001c0002t0001g0066 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.485+3872C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818967 | |||||||
| chr16:22818972 | C | T | 19 | a0001c0001t0001g0228 a0001c0001t0001g0349 a0001c0002t0001g0065 others(16): Show |
19 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+3877C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818972 | |||||||
| chr16:22818976 | T | C | 4 | a0001c0001t0001g0349 a0001c0002t0001g0084 a0001c0004t0002g0331 others(1): Show |
4 | HG01123.hp1 HG03669.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+3881T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818976 | |||||||
| chr16:22818977 | T | TCCTCCCT others(9): Show |
35 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0221 others(32): Show |
35 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.485+3885_485+3886i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818977 | ||||||
| chr16:22818980 | T | G | 11 | a0001c0002t0001g0065 a0001c0002t0001g0066 a0001c0002t0001g0110 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3885T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818980 | |||||||
| chr16:22818984 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.485+3889T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818984 | |||||||
| chr16:22818988 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0217 others(39): Show |
42 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.485+3893C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818988 | |||||||
| chr16:22818992 | T | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0221 others(36): Show |
39 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.485+3897T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818992 | |||||||
| chr16:22818992 | T | TTCCTTCC others(108): Show |
11 | a0001c0002t0001g0065 a0001c0002t0001g0066 a0001c0002t0001g0110 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+3905_485+3906i others(117): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818992 | ||||||
| chr16:22818993 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3898T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818993 | |||||||
| chr16:22818997 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3902T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22818997 | |||||||
| chr16:22818997 | TCCTC | T | 7 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0002t0001g0103 others(4): Show |
7 | HG00735.hp2 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3922_485+3925d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818997 | ||||||
| chr16:22818999 | C | CT | 5 | a0001c0001t0001g0330 a0001c0002t0001g0122 a0001c0002t0003g0039 others(2): Show |
5 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+3905dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22818999 | ||||||
| chr16:22819001 | C | CCCTCCCT others(92): Show |
1 | a0001c0001t0001g0228 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.485+3921_485+3922i others(101): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819001 | ||||||
| chr16:22819001 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0219 others(48): Show |
51 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.485+3906C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819001 | |||||||
| chr16:22819005 | C | CCTT | 3 | a0001c0002t0003g0039 a0001c0005t0006g0038 a0001c0005t0006g0040 |
3 | HG01167.hp2 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.485+3911_485+3912i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819005 | ||||||
| chr16:22819007 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3912C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819007 | |||||||
| chr16:22819009 | C | T | 3 | a0001c0002t0003g0039 a0001c0005t0006g0038 a0001c0005t0006g0040 |
3 | HG01167.hp2 HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.485+3914C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819009 | |||||||
| chr16:22819011 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3916C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819011 | |||||||
| chr16:22819013 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3918C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819013 | |||||||
| chr16:22819015 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3920C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819015 | |||||||
| chr16:22819017 | C | T | 123 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(120): Show |
123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.485+3922C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819017 | |||||||
| chr16:22819021 | T | C | 4 | a0001c0002t0001g0122 a0001c0002t0003g0039 a0001c0005t0006g0038 others(1): Show |
4 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3926T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819021 | |||||||
| chr16:22819025 | T | C | 4 | a0001c0002t0001g0122 a0001c0002t0003g0039 a0001c0005t0006g0038 others(1): Show |
4 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3930T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819025 | |||||||
| chr16:22819028 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3933T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819028 | |||||||
| chr16:22819029 | T | C | 4 | a0001c0002t0001g0122 a0001c0002t0003g0039 a0001c0005t0006g0038 others(1): Show |
4 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3934T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819029 | |||||||
| chr16:22819032 | T | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
14 | HG01109.hp2 HG01256.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+3937T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819032 | |||||||
| chr16:22819039 | A | C | 18 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(15): Show |
18 | HG01109.hp2 HG01175.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+3944A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819039 | |||||||
| chr16:22819045 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+3950T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819045 | |||||||
| chr16:22819045 | T | TCCTC | 15 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3953_485+3954i others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819045 | ||||||
| chr16:22819049 | T | C | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+3954T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819049 | |||||||
| chr16:22819052 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3957T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819052 | |||||||
| chr16:22819056 | T | C | 9 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(6): Show |
9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3961T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819056 | |||||||
| chr16:22819060 | C | T | 15 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 others(12): Show |
15 | HG01081.hp2 HG01109.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+3965C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819060 | |||||||
| chr16:22819064 | T | C | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+3969T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819064 | |||||||
| chr16:22819076 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0197 others(72): Show |
75 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.485+3981C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819076 | |||||||
| chr16:22819078 | C | CCTT | 83 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(80): Show |
83 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.485+3984_485+3985i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819078 | ||||||
| chr16:22819078 | C | CCTTCCTT others(187): Show |
7 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0003t0003g0017 others(4): Show |
7 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+3984_485+3985i others(196): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819078 | ||||||
| chr16:22819080 | C | T | 9 | a0001c0001t0001g0200 a0001c0001t0001g0217 a0001c0001t0001g0218 others(6): Show |
9 | HG01081.hp2 HG01175.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+3985C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819080 | |||||||
| chr16:22819081 | TC | T | 6 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
6 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+3989delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819081 | ||||||
| chr16:22819082 | C | CCTT | 19 | a0001c0001t0001g0157 a0001c0001t0001g0216 a0001c0001t0001g0288 others(16): Show |
19 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3988_485+3989i others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | ||||||
| chr16:22819082 | C | CCTTCCTC others(161): Show |
1 | a0001c0001t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.485+3988_485+3989i others(170): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | ||||||
| chr16:22819082 | C | CCTTCCTT others(8): Show |
48 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0221 others(45): Show |
48 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.485+3988_485+3989i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | ||||||
| chr16:22819082 | C | CCTTCCTT others(183): Show |
2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.485+3988_485+3989i others(192): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819082 | ||||||
| chr16:22819082 | C | T | 90 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(87): Show |
90 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.485+3987C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819082 | |||||||
| chr16:22819084 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 others(1): Show |
4 | HG01175.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+3989C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819084 | |||||||
| chr16:22819086 | C | CCTTCCCT | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+3992_485+3993i others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819086 | ||||||
| chr16:22819086 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0197 others(81): Show |
84 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.485+3991C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819086 | |||||||
| chr16:22819088 | C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+3993C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819088 | |||||||
| chr16:22819090 | T | C | 91 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(88): Show |
91 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.485+3995T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819090 | |||||||
| chr16:22819093 | T | C | 19 | a0001c0001t0001g0157 a0001c0001t0001g0216 a0001c0001t0001g0288 others(16): Show |
19 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+3998T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819093 | |||||||
| chr16:22819094 | C | T | 29 | a0001c0001t0001g0157 a0001c0001t0001g0197 a0001c0001t0001g0198 others(26): Show |
29 | HG00544.hp1 HG00738.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.485+3999C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819094 | |||||||
| chr16:22819094 | CCCTCCCT others(9): Show |
C | 4 | a0001c0003t0003g0020 a0001c0003t0003g0033 a0001c0003t0003g0034 others(1): Show |
4 | HG01934.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+4003_485+4018d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819094 | ||||||
| chr16:22819094 | CCCTCCCT others(13): Show |
C | 12 | a0001c0001t0001g0146 a0001c0003t0003g0023 a0001c0003t0003g0026 others(9): Show |
12 | HG01496.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+4003_485+4022d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819094 | ||||||
| chr16:22819097 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+4002T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819097 | |||||||
| chr16:22819098 | C | T | 26 | a0001c0001t0001g0157 a0001c0001t0001g0197 a0001c0001t0001g0198 others(23): Show |
26 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.485+4003C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819098 | |||||||
| chr16:22819101 | T | C | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+4006T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819101 | |||||||
| chr16:22819102 | C | T | 109 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(106): Show |
109 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.485+4007C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819102 | |||||||
| chr16:22819102 | CCCTT | C | 5 | a0001c0001t0001g0148 a0001c0001t0001g0277 a0001c0002t0003g0002 others(2): Show |
5 | HG00741.hp2 HG02071.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+4033_485+4036d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819102 | ||||||
| chr16:22819104 | C | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+4009C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819104 | |||||||
| chr16:22819106 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0200 a0001c0001t0001g0211 others(53): Show |
56 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+4011T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819106 | |||||||
| chr16:22819110 | T | C | 2 | a0001c0001t0001g0310 a0001c0002t0001g0076 |
2 | HG02258.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.485+4015T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819110 | |||||||
| chr16:22819113 | T | C | 15 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+4018T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819113 | |||||||
| chr16:22819114 | T | C | 3 | a0001c0001t0001g0310 a0001c0002t0001g0008 a0001c0002t0001g0076 |
3 | HG02258.hp2 HG03710.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.485+4019T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819114 | |||||||
| chr16:22819117 | T | C | 84 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(81): Show |
84 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.485+4022T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819117 | |||||||
| chr16:22819118 | T | C | 3 | a0001c0002t0001g0008 a0001c0002t0001g0076 a0001c0005t0002g0041 |
3 | HG03209.hp1 HG03710.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.485+4023T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819118 | |||||||
| chr16:22819122 | T | C | 2 | a0001c0002t0001g0008 a0001c0002t0001g0076 |
2 | HG03710.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.485+4027T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819122 | |||||||
| chr16:22819122 | T | TCCTTCCC others(21): Show |
15 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(12): Show |
15 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+4033_485+4034i others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819122 | ||||||
| chr16:22819125 | T | C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG00544.hp1 HG00738.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+4030T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819125 | |||||||
| chr16:22819126 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+4031T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819126 | |||||||
| chr16:22819126 | T | TCCTCATT others(84): Show |
1 | a0001c0002t0001g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.485+4034_485+4035i others(93): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819126 | ||||||
| chr16:22819130 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+4035T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819130 | |||||||
| chr16:22819132 | A | C | 123 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 others(120): Show |
123 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.485+4037A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819132 | |||||||
| chr16:22819134 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 others(1): Show |
4 | HG01175.hp2 HG02109.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+4039T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819134 | |||||||
| chr16:22819134 | T | TCCCTCCT others(465): Show |
1 | a0001c0001t0001g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+4041_485+4042i others(474): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(466): Show |
1 | a0001c0005t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485+4045_485+4046i others(475): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(467): Show |
1 | a0001c0001t0001g0159 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.485+4045_485+4046i others(476): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(465): Show |
2 | a0001c0002t0001g0062 a0001c0004t0002g0152 |
2 | HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(474): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(281): Show |
1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+4045_485+4046i others(290): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(465): Show |
2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(474): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(469): Show |
69 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(66): Show |
69 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(66): Show |
intron_variant | MODIFIER | c.485+4045_485+4046i others(478): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(468): Show |
1 | a0001c0001t0001g0350 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.485+4045_485+4046i others(477): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(469): Show |
2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18946.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(478): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCC others(449): Show |
2 | a0001c0002t0001g0077 a0001c0002t0001g0078 |
2 | HG00323.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.485+4045_485+4046i others(458): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCT others(201): Show |
1 | a0001c0001t0001g0316 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.485+4053_485+4054i others(210): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCT others(205): Show |
3 | a0001c0001t0001g0157 a0001c0001t0001g0317 a0001c0002t0007g0044 |
3 | HG00544.hp1 HG01993.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.485+4053_485+4054i others(214): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCT others(65): Show |
9 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0306 others(6): Show |
9 | HG01109.hp2 HG01256.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+4057_485+4058i others(74): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCT others(121): Show |
5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+4057_485+4058i others(130): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819134 | T | TCCTTCCT others(300): Show |
1 | a0001c0001t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.485+4057_485+4058i others(309): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819134 | ||||||
| chr16:22819138 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+4043T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819138 | |||||||
| chr16:22819138 | T | TCCTTCCT others(188): Show |
1 | a0001c0001t0001g0328 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.485+4061_485+4062i others(197): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819138 | ||||||
| chr16:22819141 | T | C | 17 | a0001c0001t0001g0146 a0001c0001t0001g0194 a0001c0003t0003g0020 others(14): Show |
17 | HG01496.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.485+4046T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819141 | |||||||
| chr16:22819142 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+4047T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819142 | |||||||
| chr16:22819142 | T | TCCTTCCC others(57): Show |
1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+4053_485+4054i others(66): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819142 | ||||||
| chr16:22819148 | C | A | 16 | a0001c0001t0001g0216 a0001c0001t0001g0288 a0001c0001t0001g0289 others(13): Show |
16 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+4053C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819148 | |||||||
| chr16:22819151 | C | CCTTCCTT others(468): Show |
1 | a0001c0001t0001g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.485+4061_485+4062i others(477): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819151 | ||||||
| chr16:22819157 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0216 others(65): Show |
68 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.485+4062C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819157 | |||||||
| chr16:22819161 | T | C | 2 | a0001c0002t0001g0075 a0001c0002t0001g0076 |
2 | HG01081.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.485+4066T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819161 | |||||||
| chr16:22819161 | T | TTCCTTCA others(196): Show |
3 | a0001c0001t0001g0221 a0001c0002t0001g0067 a0001c0002t0001g0117 |
3 | HG01106.hp2 NA18953.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.485+4072_485+4073i others(205): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819161 | T | TTCCTTCC others(200): Show |
5 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(2): Show |
5 | NA18979.hp1 NA18995.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+4076_485+4077i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819161 | T | TTCCTTCC others(200): Show |
10 | a0001c0001t0001g0211 a0001c0001t0001g0326 a0001c0001t0001g0327 others(7): Show |
10 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+4076_485+4077i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819161 | T | TTCCTTCC others(208): Show |
3 | a0001c0001t0001g0222 a0001c0002t0001g0065 a0001c0002t0001g0066 |
3 | HG02895.hp1 HG02897.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.485+4077_485+4078i others(217): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819161 | T | TTCCTTCC others(200): Show |
1 | a0001c0002t0001g0079 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.485+4077_485+4078i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819161 | T | TTCCTTCC others(204): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0223 a0001c0001t0001g0224 others(20): Show |
23 | HG00609.hp2 HG00639.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.485+4077_485+4078i others(213): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819161 | T | TTCCTTCC others(200): Show |
1 | a0001c0001t0001g0228 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.485+4077_485+4078i others(209): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819161 | T | TTCCTTCC others(208): Show |
1 | a0001c0002t0001g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.485+4077_485+4078i others(217): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22819161 | ||||||
| chr16:22819186 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+4091C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819186 | |||||||
| chr16:22819191 | C | A | 10 | a0001c0003t0003g0023 a0001c0003t0003g0026 a0001c0003t0003g0028 others(7): Show |
10 | HG01496.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+4096C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819191 | |||||||
| chr16:22819293 | T | C | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
6 | HG02165.hp1 NA18955.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+4198T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819293 | |||||||
| chr16:22819587 | A | G | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.485+4492A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819587 | |||||||
| chr16:22819769 | C | T | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+4674C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819769 | |||||||
| chr16:22819781 | G | A | 2 | a0001c0002t0001g0122 a0001c0005t0002g0041 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+4686G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22819781 | |||||||
| chr16:22820100 | C | A | 6 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 others(3): Show |
6 | HG01109.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+5005C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820100 | |||||||
| chr16:22820125 | C | T | 3 | a0001c0001t0001g0298 a0001c0003t0003g0036 a0001c0003t0003g0037 |
3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+5030C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820125 | |||||||
| chr16:22820137 | A | G | 85 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(82): Show |
85 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.485+5042A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820137 | |||||||
| chr16:22820169 | A | C | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+5074A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820169 | |||||||
| chr16:22820172 | C | G | 3 | a0001c0001t0001g0349 a0001c0002t0001g0063 a0001c0005t0002g0060 |
3 | HG02486.hp2 HG03834.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.485+5077C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820172 | |||||||
| chr16:22820178 | C | A | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.485+5083C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820178 | |||||||
| chr16:22820392 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.485+5297A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820392 | |||||||
| chr16:22820583 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.485+5488A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820583 | |||||||
| chr16:22820840 | G | A | 65 | a0001c0001t0001g0146 a0001c0001t0001g0201 a0001c0001t0001g0203 others(62): Show |
65 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.485+5745G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22820840 | |||||||
| chr16:22821145 | A | G | 2 | a0001c0002t0004g0101 a0001c0002t0004g0102 |
2 | HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.485+6050A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821145 | |||||||
| chr16:22821252 | C | T | 1 | a0001c0003t0015g0032 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485+6157C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821252 | |||||||
| chr16:22821257 | C | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.485+6162C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821257 | |||||||
| chr16:22821284 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+6189G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821284 | |||||||
| chr16:22821456 | G | A | 89 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(86): Show |
89 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.485+6361G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821456 | |||||||
| chr16:22821640 | A | C | 1 | a0001c0002t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+6545A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821640 | |||||||
| chr16:22821706 | G | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(139): Show |
142 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.485+6611G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22821706 | |||||||
| chr16:22822097 | C | T | 43 | a0001c0001t0001g0146 a0001c0001t0001g0201 a0001c0001t0001g0203 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+7002C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822097 | |||||||
| chr16:22822348 | G | T | 2 | a0001c0002t0001g0122 a0001c0005t0002g0041 |
2 | HG02109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.485+7253G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822348 | |||||||
| chr16:22822377 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(145): Show |
148 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.485+7282A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822377 | |||||||
| chr16:22822384 | T | C | 43 | a0001c0001t0001g0146 a0001c0001t0001g0201 a0001c0001t0001g0203 others(40): Show |
43 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+7289T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822384 | |||||||
| chr16:22822416 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.485+7321C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822416 | |||||||
| chr16:22822438 | G | A | 6 | a0001c0001t0001g0146 a0001c0003t0003g0020 a0001c0003t0003g0033 others(3): Show |
6 | HG01934.hp1 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+7343G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822438 | |||||||
| chr16:22822443 | C | T | 2 | a0001c0002t0005g0121 a0001c0002t0005g0134 |
2 | HG01928.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.485+7348C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822443 | |||||||
| chr16:22822449 | T | G | 3 | a0001c0001t0001g0304 a0001c0004t0002g0305 a0001c0005t0002g0005 |
3 | HG01256.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.485+7354T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822449 | |||||||
| chr16:22822482 | G | C | 19 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(16): Show |
19 | HG01175.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.485+7387G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822482 | |||||||
| chr16:22822746 | T | G | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+7651T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822746 | |||||||
| chr16:22822767 | G | A | 50 | a0001c0001t0001g0146 a0001c0001t0001g0201 a0001c0001t0001g0203 others(47): Show |
50 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+7672G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822767 | |||||||
| chr16:22822856 | G | GA | 22 | a0001c0001t0001g0146 a0001c0001t0001g0222 a0001c0001t0001g0298 others(19): Show |
22 | HG00544.hp1 HG01261.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.485+7775dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22822856 | ||||||
| chr16:22822856 | GA | G | 16 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(13): Show |
16 | HG01934.hp1 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+7775delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22822856 | ||||||
| chr16:22822875 | G | A | 8 | a0001c0001t0001g0238 a0001c0002t0001g0050 a0001c0002t0001g0051 others(5): Show |
8 | HG00741.hp1 HG01257.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+7780G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822875 | |||||||
| chr16:22822957 | C | T | 1 | a0001c0002t0001g0099 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.485+7862C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822957 | |||||||
| chr16:22822986 | A | G | 3 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0081 |
3 | NA18980.hp2 NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.485+7891A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22822986 | |||||||
| chr16:22823196 | A | G | 33 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(30): Show |
33 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.485+8101A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823196 | |||||||
| chr16:22823245 | A | T | 59 | a0001c0001t0001g0146 a0001c0001t0001g0201 a0001c0001t0001g0203 others(56): Show |
59 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.485+8150A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823245 | |||||||
| chr16:22823558 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+8463G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823558 | |||||||
| chr16:22823568 | C | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+8473C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823568 | |||||||
| chr16:22823571 | C | A | 1 | a0001c0001t0004g0165 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.485+8476C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823571 | |||||||
| chr16:22823618 | T | TA | 8 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0241 others(5): Show |
8 | HG01433.hp1 HG02080.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+8542dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823618 | ||||||
| chr16:22823618 | TA | T | 31 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0001g0200 others(28): Show |
31 | HG00323.hp1 HG00438.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.485+8542delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823618 | ||||||
| chr16:22823618 | TAA | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(170): Show |
173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.485+8541_485+8542d others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823618 | ||||||
| chr16:22823672 | AACT | A | 8 | a0001c0001t0001g0146 a0001c0003t0003g0023 a0001c0003t0003g0026 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+8581_485+8583d others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22823672 | ||||||
| chr16:22823698 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+8603A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823698 | |||||||
| chr16:22823731 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+8636A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22823731 | |||||||
| chr16:22824000 | T | C | 1 | a0001c0005t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.485+8905T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824000 | |||||||
| chr16:22824054 | CACGTATC others(5): Show |
C | 1 | a0001c0002t0001g0074 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.485+8964_485+8975d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22824054 | ||||||
| chr16:22824057 | G | A | 97 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(94): Show |
97 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.485+8962G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824057 | |||||||
| chr16:22824068 | C | T | 34 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0203 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.485+8973C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824068 | |||||||
| chr16:22824142 | G | C | 1 | a0001c0002t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+9047G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824142 | |||||||
| chr16:22824178 | G | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9083G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824178 | |||||||
| chr16:22824213 | A | C | 2 | a0001c0001t0001g0192 a0001c0005t0002g0009 |
2 | HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485+9118A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824213 | |||||||
| chr16:22824243 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485+9148C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824243 | |||||||
| chr16:22824248 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9153A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824248 | |||||||
| chr16:22824275 | G | A | 36 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0203 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+9180G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824275 | |||||||
| chr16:22824276 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9181T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824276 | |||||||
| chr16:22824284 | C | T | 6 | a0001c0001t0001g0216 a0001c0001t0001g0293 a0001c0001t0001g0294 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+9189C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824284 | |||||||
| chr16:22824303 | C | A | 18 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(15): Show |
18 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+9208C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824303 | |||||||
| chr16:22824325 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9230G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824325 | |||||||
| chr16:22824339 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.485+9244G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824339 | |||||||
| chr16:22824341 | G | T | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+9246G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824341 | |||||||
| chr16:22824471 | C | T | 1 | a0001c0002t0001g0045 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.485+9376C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824471 | |||||||
| chr16:22824542 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9447G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824542 | |||||||
| chr16:22824547 | A | AAAGC | 91 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(88): Show |
91 | HG00140.hp2 HG00544.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.485+9459_485+9462d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22824547 | ||||||
| chr16:22824558 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0223 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.485+9463A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824558 | |||||||
| chr16:22824629 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9534C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824629 | |||||||
| chr16:22824634 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9539G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824634 | |||||||
| chr16:22824743 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9648G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824743 | |||||||
| chr16:22824804 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0223 others(47): Show |
50 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.485+9709T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824804 | |||||||
| chr16:22824928 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9833G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824928 | |||||||
| chr16:22824992 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+9897T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22824992 | |||||||
| chr16:22825071 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+9976T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825071 | |||||||
| chr16:22825129 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0197 others(53): Show |
56 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.485+10034G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825129 | |||||||
| chr16:22825161 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+10066A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825161 | |||||||
| chr16:22825253 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+10158A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825253 | |||||||
| chr16:22825322 | G | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0299 |
3 | HG01175.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.485+10227G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825322 | |||||||
| chr16:22825440 | T | C | 34 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0203 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.485+10345T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825440 | |||||||
| chr16:22825639 | T | A | 4 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
4 | HG02132.hp1 NA18942.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+10544T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825639 | |||||||
| chr16:22825662 | A | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+10567A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825662 | |||||||
| chr16:22825741 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+10646T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825741 | |||||||
| chr16:22825762 | A | C | 36 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0203 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+10667A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825762 | |||||||
| chr16:22825821 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+10726G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825821 | |||||||
| chr16:22825891 | C | T | 1 | a0001c0002t0001g0111 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.485+10796C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825891 | |||||||
| chr16:22825903 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+10808T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825903 | |||||||
| chr16:22825962 | G | T | 36 | a0001c0001t0001g0193 a0001c0001t0001g0201 a0001c0001t0001g0203 others(33): Show |
36 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+10867G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22825962 | |||||||
| chr16:22826127 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+11032G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826127 | |||||||
| chr16:22826169 | G | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+11074G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826169 | |||||||
| chr16:22826178 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+11083C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826178 | |||||||
| chr16:22826226 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+11131T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826226 | |||||||
| chr16:22826227 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0197 a0001c0001t0001g0198 others(52): Show |
55 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.485+11132G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826227 | |||||||
| chr16:22826271 | A | G | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00323.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+11176A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826271 | |||||||
| chr16:22826374 | T | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0193 a0001c0001t0001g0197 others(86): Show |
89 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.485+11279T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826374 | |||||||
| chr16:22826423 | A | C | 1 | a0007c0012t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.485+11328A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826423 | |||||||
| chr16:22826608 | C | T | 3 | a0001c0001t0001g0298 a0001c0003t0003g0036 a0001c0003t0003g0037 |
3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+11513C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826608 | |||||||
| chr16:22826637 | A | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0150 others(206): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.485+11542A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826637 | |||||||
| chr16:22826680 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0150 others(207): Show |
210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.485+11585A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826680 | |||||||
| chr16:22826837 | C | T | 91 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(88): Show |
91 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.485+11742C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826837 | |||||||
| chr16:22826887 | G | T | 3 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0005t0002g0010 |
3 | HG02055.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.485+11792G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826887 | |||||||
| chr16:22826955 | T | C | 2 | a0001c0003t0003g0021 a0005c0010t0001g0042 |
2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.485+11860T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22826955 | |||||||
| chr16:22827000 | C | T | 7 | a0001c0001t0001g0159 a0001c0001t0001g0278 a0001c0001t0001g0279 others(4): Show |
7 | HG01433.hp1 HG01496.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+11905C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827000 | |||||||
| chr16:22827411 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.485+12316T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827411 | |||||||
| chr16:22827468 | T | C | 3 | a0001c0001t0001g0298 a0001c0003t0003g0036 a0001c0003t0003g0037 |
3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.485+12373T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827468 | |||||||
| chr16:22827469 | G | A | 8 | a0001c0001t0001g0280 a0001c0002t0001g0122 a0001c0002t0003g0002 others(5): Show |
8 | HG01496.hp2 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+12374G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827469 | |||||||
| chr16:22827607 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.485+12512C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827607 | |||||||
| chr16:22827686 | G | A | 3 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0081 |
3 | NA18980.hp2 NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.485+12591G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827686 | |||||||
| chr16:22827710 | C | CT | 29 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0233 others(26): Show |
29 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+12634dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | ||||||
| chr16:22827710 | C | CTT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0198 a0001c0001t0001g0199 others(52): Show |
55 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.485+12633_485+1263 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | ||||||
| chr16:22827710 | CT | C | 116 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 others(113): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.485+12634delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | ||||||
| chr16:22827710 | CTT | C | 11 | a0001c0001t0001g0158 a0001c0001t0001g0167 a0001c0001t0001g0168 others(8): Show |
11 | HG01169.hp1 HG02280.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+12633_485+1263 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22827710 | ||||||
| chr16:22827721 | T | C | 2 | a0001c0002t0001g0115 a0001c0002t0001g0116 |
2 | NA18966.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.485+12626T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827721 | |||||||
| chr16:22827932 | A | G | 1 | a0001c0002t0001g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.485+12837A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827932 | |||||||
| chr16:22827996 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.485+12901C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22827996 | |||||||
| chr16:22828065 | A | C | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+12970A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828065 | |||||||
| chr16:22828100 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0220 a0001c0001t0001g0223 others(50): Show |
53 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.485+13005T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828100 | |||||||
| chr16:22828378 | A | G | 32 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(29): Show |
32 | HG00280.hp1 HG00544.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.485+13283A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828378 | |||||||
| chr16:22828554 | C | T | 1 | a0001c0002t0001g0120 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+13459C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828554 | |||||||
| chr16:22828672 | C | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+13577C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828672 | |||||||
| chr16:22828763 | A | T | 1 | a0001c0002t0001g0120 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+13668A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828763 | |||||||
| chr16:22828798 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0169 others(61): Show |
64 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.485+13703C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828798 | |||||||
| chr16:22828799 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.485+13704G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828799 | |||||||
| chr16:22828806 | C | A | 1 | a0001c0002t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.485+13711C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828806 | |||||||
| chr16:22828857 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18955.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.485+13762A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828857 | |||||||
| chr16:22828937 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.485+13842A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22828937 | |||||||
| chr16:22829058 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0304 a0001c0002t0001g0007 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+13963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829058 | |||||||
| chr16:22829070 | C | G | 3 | a0001c0001t0001g0274 a0001c0002t0001g0074 a0001c0002t0004g0059 |
3 | HG02071.hp1 HG04184.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.485+13975C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829070 | |||||||
| chr16:22829278 | G | A | 1 | a0001c0004t0002g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.485+14183G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829278 | |||||||
| chr16:22829342 | T | C | 4 | a0001c0002t0001g0122 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+14247T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829342 | |||||||
| chr16:22829383 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(133): Show |
136 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.485+14288G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829383 | |||||||
| chr16:22829425 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0304 a0001c0002t0001g0007 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+14330C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829425 | |||||||
| chr16:22829479 | C | CT | 10 | a0001c0001t0001g0216 a0001c0001t0001g0293 a0001c0001t0001g0294 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+14392dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22829479 | ||||||
| chr16:22829480 | T | A | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.485+14385T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829480 | |||||||
| chr16:22829487 | T | A | 67 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0157 others(64): Show |
67 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.485+14392T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829487 | |||||||
| chr16:22829487 | T | TA | 7 | a0001c0002t0001g0110 a0001c0002t0001g0111 a0001c0002t0001g0112 others(4): Show |
7 | HG02451.hp2 HG02615.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+14397dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22829487 | ||||||
| chr16:22829506 | A | G | 51 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 others(48): Show |
51 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.485+14411A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829506 | |||||||
| chr16:22829534 | A | G | 17 | a0001c0001t0001g0216 a0001c0001t0001g0293 a0001c0001t0001g0294 others(14): Show |
17 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.485+14439A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829534 | |||||||
| chr16:22829603 | G | T | 1 | a0001c0001t0013g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.485+14508G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829603 | |||||||
| chr16:22829622 | A | C | 2 | a0001c0003t0003g0017 a0001c0004t0014g0237 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+14527A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829622 | |||||||
| chr16:22829626 | G | T | 1 | a0001c0002t0003g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.485+14531G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829626 | |||||||
| chr16:22829670 | A | G | 1 | a0001c0002t0001g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.485+14575A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829670 | |||||||
| chr16:22829674 | G | C | 10 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0306 others(7): Show |
10 | HG02886.hp1 HG02922.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+14579G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829674 | |||||||
| chr16:22829738 | C | G | 1 | a0001c0002t0004g0137 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.485+14643C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829738 | |||||||
| chr16:22829787 | C | T | 49 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+14692C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829787 | |||||||
| chr16:22829882 | G | A | 2 | a0001c0001t0001g0322 a0001c0002t0001g0135 |
2 | HG00280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.485+14787G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22829882 | |||||||
| chr16:22830112 | GACTCGCT others(59): Show |
G | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15021_485+1508 others(70): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22830112 | ||||||
| chr16:22830135 | T | G | 1 | a0001c0002t0008g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.485+15040T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830135 | |||||||
| chr16:22830171 | T | G | 50 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15076T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830171 | |||||||
| chr16:22830181 | T | A | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15086T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830181 | |||||||
| chr16:22830184 | G | T | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15089G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830184 | |||||||
| chr16:22830188 | T | A | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15093T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830188 | |||||||
| chr16:22830189 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15094T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830189 | |||||||
| chr16:22830191 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15096C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830191 | |||||||
| chr16:22830192 | C | A | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15097C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830192 | |||||||
| chr16:22830194 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15099C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830194 | |||||||
| chr16:22830198 | C | A | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15103C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830198 | |||||||
| chr16:22830199 | T | A | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+15104T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830199 | |||||||
| chr16:22830236 | A | G | 4 | a0001c0002t0001g0122 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+15141A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830236 | |||||||
| chr16:22830275 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0223 others(45): Show |
48 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.485+15180G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830275 | |||||||
| chr16:22830371 | A | C | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.485+15276A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830371 | |||||||
| chr16:22830402 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0282 |
2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.485+15307G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830402 | |||||||
| chr16:22830403 | G | A | 50 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15308G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830403 | |||||||
| chr16:22830487 | G | A | 50 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15392G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830487 | |||||||
| chr16:22830490 | A | G | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+15395A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830490 | |||||||
| chr16:22830537 | A | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | NA18966.hp2 NA18995.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+15442A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830537 | |||||||
| chr16:22830627 | A | G | 50 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+15532A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830627 | |||||||
| chr16:22830722 | A | G | 4 | a0001c0001t0001g0296 a0001c0002t0001g0007 a0001c0004t0002g0144 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+15627A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830722 | |||||||
| chr16:22830948 | A | G | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.485+15853A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22830948 | |||||||
| chr16:22831042 | G | T | 1 | a0001c0002t0005g0142 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.485+15947G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831042 | |||||||
| chr16:22831104 | A | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(162): Show |
165 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.485+16009A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831104 | |||||||
| chr16:22831107 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+16012C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831107 | |||||||
| chr16:22831160 | G | A | 1 | a0001c0002t0003g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.485+16065G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831160 | |||||||
| chr16:22831224 | A | C | 2 | a0001c0001t0004g0334 a0001c0002t0001g0136 |
2 | HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.485+16129A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831224 | |||||||
| chr16:22831282 | A | C | 2 | a0001c0003t0003g0026 a0001c0006t0006g0025 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.485+16187A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831282 | |||||||
| chr16:22831481 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.485+16386G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831481 | |||||||
| chr16:22831537 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+16442G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831537 | |||||||
| chr16:22831593 | A | AT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0170 others(102): Show |
105 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(102): Show |
intron_variant | MODIFIER | c.485+16510dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22831593 | ||||||
| chr16:22831593 | A | ATT | 55 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(52): Show |
55 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.485+16509_485+1651 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22831593 | ||||||
| chr16:22831615 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(157): Show |
160 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.485+16520G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831615 | |||||||
| chr16:22831627 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.485+16532G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831627 | |||||||
| chr16:22831690 | T | A | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+16595T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831690 | |||||||
| chr16:22831879 | T | C | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+16784T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22831879 | |||||||
| chr16:22832004 | A | G | 10 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
10 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+16909A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832004 | |||||||
| chr16:22832151 | C | CT | 38 | a0001c0001t0001g0157 a0001c0001t0001g0168 a0001c0001t0001g0193 others(35): Show |
38 | HG00738.hp1 HG01175.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.485+17074dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | ||||||
| chr16:22832151 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0158 a0001c0001t0001g0315 a0001c0002t0001g0136 others(1): Show |
4 | HG01168.hp2 HG02965.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+17065_485+1707 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | ||||||
| chr16:22832151 | C | CTTTTTTT others(4): Show |
28 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0160 others(25): Show |
28 | HG00140.hp2 HG00323.hp2 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.485+17064_485+1707 others(15): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | ||||||
| chr16:22832151 | C | CTTTTTTT others(5): Show |
15 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0173 others(12): Show |
15 | HG00544.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+17063_485+1707 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | ||||||
| chr16:22832151 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0194 a0001c0002t0001g0333 |
2 | HG02074.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.485+17062_485+1707 others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | ||||||
| chr16:22832151 | CT | C | 21 | a0001c0001t0001g0147 a0001c0001t0001g0203 a0001c0001t0001g0210 others(18): Show |
21 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+17074delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22832151 | ||||||
| chr16:22832169 | T | A | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+17074T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832169 | |||||||
| chr16:22832175 | T | G | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+17080T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832175 | |||||||
| chr16:22832181 | G | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0225 a0001c0002t0001g0063 |
3 | NA18953.hp2 NA19054.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.485+17086G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832181 | |||||||
| chr16:22832208 | G | A | 49 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17113G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832208 | |||||||
| chr16:22832257 | A | G | 2 | a0001c0004t0002g0276 a0001c0011t0011g0003 |
2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.485+17162A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832257 | |||||||
| chr16:22832343 | A | G | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+17248A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832343 | |||||||
| chr16:22832435 | G | C | 49 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17340G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832435 | |||||||
| chr16:22832522 | C | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0217 others(1): Show |
4 | HG01175.hp2 HG02451.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+17427C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832522 | |||||||
| chr16:22832526 | C | T | 1 | a0001c0002t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.485+17431C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832526 | |||||||
| chr16:22832733 | G | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0170 others(91): Show |
94 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.485+17638G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832733 | |||||||
| chr16:22832780 | G | A | 1 | a0001c0004t0002g0155 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.485+17685G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832780 | |||||||
| chr16:22832922 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+17827G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832922 | |||||||
| chr16:22832932 | A | T | 49 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17837A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832932 | |||||||
| chr16:22832998 | C | T | 49 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17903C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22832998 | |||||||
| chr16:22833062 | G | C | 49 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+17967G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833062 | |||||||
| chr16:22833294 | G | T | 6 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
6 | HG02486.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+18199G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833294 | |||||||
| chr16:22833304 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0342 |
2 | HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.485+18209C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833304 | |||||||
| chr16:22833323 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0007g0156 |
2 | NA18942.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.485+18228A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833323 | |||||||
| chr16:22833372 | A | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(146): Show |
149 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.485+18277A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833372 | |||||||
| chr16:22833374 | T | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(141): Show |
144 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.485+18279T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833374 | |||||||
| chr16:22833406 | G | A | 1 | a0001c0006t0006g0022 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.485+18311G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833406 | |||||||
| chr16:22833424 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0223 others(52): Show |
55 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.485+18329G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833424 | |||||||
| chr16:22833656 | A | G | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+18561A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833656 | |||||||
| chr16:22833662 | G | T | 2 | a0001c0001t0001g0322 a0001c0002t0001g0135 |
2 | HG00280.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.485+18567G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833662 | |||||||
| chr16:22833711 | A | G | 1 | a0001c0002t0001g0054 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.485+18616A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833711 | |||||||
| chr16:22833852 | C | T | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+18757C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833852 | |||||||
| chr16:22833910 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0178 others(71): Show |
74 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.485+18815A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833910 | |||||||
| chr16:22833920 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.485+18825G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833920 | |||||||
| chr16:22833934 | AC | A | 10 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0197 others(7): Show |
10 | HG01175.hp2 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+18840delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22833934 | |||||||
| chr16:22834107 | A | G | 4 | a0001c0001t0001g0288 a0001c0003t0003g0019 a0001c0004t0002g0281 others(1): Show |
4 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+19012A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834107 | |||||||
| chr16:22834195 | C | G | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+19100C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834195 | |||||||
| chr16:22834211 | A | G | 49 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(46): Show |
49 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+19116A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834211 | |||||||
| chr16:22834323 | T | G | 1 | a0001c0001t0001g0223 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.485+19228T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834323 | |||||||
| chr16:22834423 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(134): Show |
137 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.485+19328G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834423 | |||||||
| chr16:22834538 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0170 others(91): Show |
94 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.485+19443G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834538 | |||||||
| chr16:22834677 | T | TAAAAAGT others(307): Show |
43 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(40): Show |
43 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.485+19601_485+1960 others(318): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | ||||||
| chr16:22834677 | T | TAAAAAGT others(308): Show |
1 | a0006c0013t0002g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.485+19601_485+1960 others(319): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | ||||||
| chr16:22834677 | T | TAAAAAGT others(312): Show |
4 | a0001c0003t0003g0020 a0001c0003t0003g0033 a0001c0003t0003g0034 others(1): Show |
4 | HG01934.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+19601_485+1960 others(323): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | ||||||
| chr16:22834677 | T | TAAAAAGT others(313): Show |
1 | a0001c0002t0001g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.485+19601_485+1960 others(324): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834677 | ||||||
| chr16:22834717 | C | T | 3 | a0001c0001t0001g0227 a0001c0001t0001g0251 a0001c0001t0001g0350 |
3 | NA18969.hp1 NA19006.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.485+19622C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834717 | |||||||
| chr16:22834724 | C | T | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+19629C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834724 | |||||||
| chr16:22834742 | A | T | 1 | a0001c0004t0002g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.485+19647A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834742 | |||||||
| chr16:22834752 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0304 a0001c0002t0001g0007 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+19657C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834752 | |||||||
| chr16:22834929 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(161): Show |
164 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.485+19834G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22834929 | |||||||
| chr16:22834953 | A | ATTTC | 90 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0170 others(87): Show |
90 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.485+19863_485+1986 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834953 | ||||||
| chr16:22834955 | T | TTCTG | 4 | a0001c0001t0001g0288 a0001c0003t0003g0019 a0001c0004t0002g0281 others(1): Show |
4 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+19863_485+1986 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22834955 | ||||||
| chr16:22835043 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.485+19948G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835043 | |||||||
| chr16:22835091 | G | A | 1 | a0001c0003t0003g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.485+19996G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835091 | |||||||
| chr16:22835115 | A | AAGTCTTA others(186): Show |
1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+20034_485+2003 others(197): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22835115 | ||||||
| chr16:22835138 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.485+20043G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835138 | |||||||
| chr16:22835180 | A | AT | 20 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(17): Show |
20 | HG01175.hp2 HG02451.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+20094dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22835180 | ||||||
| chr16:22835255 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.485+20160C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835255 | |||||||
| chr16:22835280 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.485+20185A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835280 | |||||||
| chr16:22835296 | T | TTTTG | 101 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0170 others(98): Show |
101 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.485+20209_485+2021 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22835296 | ||||||
| chr16:22835378 | C | T | 1 | a0001c0002t0004g0069 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.485+20283C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835378 | |||||||
| chr16:22835485 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.485+20390G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835485 | |||||||
| chr16:22835637 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0170 others(98): Show |
101 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(98): Show |
intron_variant | MODIFIER | c.485+20542C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835637 | |||||||
| chr16:22835677 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.485+20582A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835677 | |||||||
| chr16:22835692 | C | G | 3 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG02922.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.485+20597C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835692 | |||||||
| chr16:22835854 | T | A | 1 | a0001c0001t0001g0313 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.485+20759T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835854 | |||||||
| chr16:22835886 | A | G | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+20791A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22835886 | |||||||
| chr16:22836025 | A | C | 1 | a0001c0001t0001g0280 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.485+20930A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836025 | |||||||
| chr16:22836467 | C | T | 10 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
10 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+21372C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836467 | |||||||
| chr16:22836535 | T | C | 10 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+21440T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836535 | |||||||
| chr16:22836619 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485+21524A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836619 | |||||||
| chr16:22836620 | G | A | 2 | a0001c0002t0001g0065 a0001c0002t0001g0066 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485+21525G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836620 | |||||||
| chr16:22836640 | T | G | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0004t0002g0154 others(1): Show |
4 | HG00323.hp2 HG01168.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+21545T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836640 | |||||||
| chr16:22836738 | G | A | 4 | a0001c0001t0001g0288 a0001c0003t0003g0019 a0001c0004t0002g0281 others(1): Show |
4 | HG01891.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+21643G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836738 | |||||||
| chr16:22836797 | C | T | 1 | a0001c0004t0002g0270 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.485+21702C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836797 | |||||||
| chr16:22836801 | G | A | 2 | a0003c0008t0002g0229 a0003c0008t0002g0230 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.485+21706G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836801 | |||||||
| chr16:22836872 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0170 a0001c0001t0001g0174 others(99): Show |
102 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.485+21777A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22836872 | |||||||
| chr16:22837119 | G | GT | 238 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(235): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.485+22036dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837119 | ||||||
| chr16:22837119 | G | GTT | 11 | a0001c0001t0001g0159 a0001c0001t0001g0187 a0001c0001t0001g0269 others(8): Show |
11 | HG01256.hp1 HG02074.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+22035_485+2203 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837119 | ||||||
| chr16:22837119 | GT | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0167 a0001c0001t0001g0168 others(77): Show |
80 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.485+22036delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837119 | ||||||
| chr16:22837172 | T | C | 2 | a0001c0001t0001g0289 a0001c0001t0001g0291 |
2 | HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.485+22077T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837172 | |||||||
| chr16:22837327 | T | G | 3 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0014g0237 |
3 | HG02965.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+22232T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837327 | |||||||
| chr16:22837358 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.485+22263T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837358 | |||||||
| chr16:22837405 | G | A | 15 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0197 others(12): Show |
15 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+22310G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837405 | |||||||
| chr16:22837410 | T | C | 2 | a0001c0002t0001g0095 a0001c0004t0002g0258 |
2 | HG01255.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.485+22315T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837410 | |||||||
| chr16:22837446 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.485+22351C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837446 | |||||||
| chr16:22837473 | T | G | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0280 others(4): Show |
7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+22378T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837473 | |||||||
| chr16:22837479 | TC | T | 10 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0197 others(7): Show |
10 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+22386delC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837479 | ||||||
| chr16:22837483 | A | ATG | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0280 others(5): Show |
8 | HG02129.hp1 NA18955.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.485+22404_485+2240 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837483 | ||||||
| chr16:22837483 | A | ATGTG | 56 | a0001c0001t0001g0001 a0001c0001t0001g0188 a0001c0001t0001g0223 others(53): Show |
56 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.485+22402_485+2240 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837483 | ||||||
| chr16:22837483 | A | ATGTGTG | 13 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
13 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+22400_485+2240 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837483 | ||||||
| chr16:22837501 | A | G | 3 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0014g0237 |
3 | HG02965.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+22406A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837501 | |||||||
| chr16:22837509 | G | GTGTATAT others(37): Show |
1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+22429_485+2247 others(48): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837509 | ||||||
| chr16:22837513 | A | G | 16 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(13): Show |
16 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+22418A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837513 | |||||||
| chr16:22837538 | GATATATG others(3): Show |
G | 2 | a0001c0001t0001g0310 a0001c0002t0001g0014 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.485+22460_485+2246 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837538 | ||||||
| chr16:22837544 | T | G | 16 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0004g0165 others(13): Show |
16 | HG00423.hp1 HG00738.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+22449T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837544 | |||||||
| chr16:22837566 | CAT | C | 14 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(11): Show |
14 | HG01934.hp1 HG02055.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+22483_485+2248 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837566 | ||||||
| chr16:22837566 | CATAT | C | 10 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0197 others(7): Show |
10 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+22481_485+2248 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837566 | ||||||
| chr16:22837576 | TATAC | T | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0280 others(4): Show |
7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+22483_485+2248 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837576 | ||||||
| chr16:22837578 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0188 a0001c0001t0001g0223 others(53): Show |
56 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.485+22483T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837578 | |||||||
| chr16:22837590 | C | CAT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0188 a0001c0001t0001g0223 others(53): Show |
56 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.485+22495_485+2249 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837590 | |||||||
| chr16:22837590 | C | T | 14 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(11): Show |
14 | HG01934.hp1 HG02055.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+22495C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837590 | |||||||
| chr16:22837591 | G | A | 2 | a0004c0009t0001g0336 a0004c0009t0001g0341 |
2 | NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.485+22496G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837591 | |||||||
| chr16:22837630 | A | AAC | 102 | a0001c0001t0001g0001 a0001c0001t0001g0167 a0001c0001t0001g0168 others(99): Show |
102 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.485+22545_485+2254 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837630 | ||||||
| chr16:22837630 | A | AACAC | 5 | a0001c0002t0001g0122 a0001c0003t0003g0028 a0001c0003t0003g0029 others(2): Show |
5 | HG00639.hp1 HG01496.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+22543_485+2254 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22837630 | ||||||
| chr16:22837834 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.485+22739G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837834 | |||||||
| chr16:22837845 | G | A | 16 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(13): Show |
16 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+22750G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837845 | |||||||
| chr16:22837878 | G | A | 9 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+22783G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837878 | |||||||
| chr16:22837879 | A | G | 15 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0197 others(12): Show |
15 | HG01934.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+22784A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22837879 | |||||||
| chr16:22838024 | G | GA | 16 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.485+22938dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22838024 | ||||||
| chr16:22838177 | C | T | 8 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+23082C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838177 | |||||||
| chr16:22838256 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.485+23161G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838256 | |||||||
| chr16:22838276 | C | T | 2 | a0001c0004t0002g0152 a0001c0005t0002g0104 |
2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.485+23181C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838276 | |||||||
| chr16:22838280 | G | A | 1 | a0001c0002t0008g0141 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.485+23185G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838280 | |||||||
| chr16:22838338 | C | T | 2 | a0001c0002t0001g0072 a0001c0002t0001g0081 |
2 | NA18980.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.485+23243C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838338 | |||||||
| chr16:22838352 | G | A | 16 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(13): Show |
16 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+23257G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838352 | |||||||
| chr16:22838379 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG02559.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+23284G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838379 | |||||||
| chr16:22838401 | G | A | 9 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+23306G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838401 | |||||||
| chr16:22838522 | G | A | 1 | a0001c0005t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485+23427G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838522 | |||||||
| chr16:22838620 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(148): Show |
151 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.485+23525T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838620 | |||||||
| chr16:22838810 | G | A | 4 | a0001c0002t0001g0122 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+23715G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838810 | |||||||
| chr16:22838908 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.485+23813A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22838908 | |||||||
| chr16:22839175 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.485+24080G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839175 | |||||||
| chr16:22839193 | T | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+24098T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839193 | |||||||
| chr16:22839406 | T | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0304 a0001c0002t0001g0007 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+24311T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839406 | |||||||
| chr16:22839615 | T | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0001g0188 others(68): Show |
71 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.485+24520T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839615 | |||||||
| chr16:22839663 | A | G | 14 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(11): Show |
14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+24568A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839663 | |||||||
| chr16:22839677 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0208 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.485+24582A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839677 | |||||||
| chr16:22839727 | C | T | 46 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(43): Show |
46 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.485+24632C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839727 | |||||||
| chr16:22839852 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+24757C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839852 | |||||||
| chr16:22839914 | A | G | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+24819A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839914 | |||||||
| chr16:22839978 | T | C | 5 | a0001c0001t0001g0296 a0001c0001t0001g0304 a0001c0002t0001g0007 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+24883T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22839978 | |||||||
| chr16:22840139 | G | T | 3 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0014g0237 |
3 | HG02965.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+25044G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840139 | |||||||
| chr16:22840155 | G | A | 45 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(42): Show |
45 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.485+25060G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840155 | |||||||
| chr16:22840384 | C | CT | 15 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(12): Show |
15 | HG02486.hp1 HG02559.hp1 HG03225.hp2 others(12): Show |
intron_variant | MODIFIER | c.485+25302dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22840384 | ||||||
| chr16:22840515 | T | G | 13 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
13 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+25420T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840515 | |||||||
| chr16:22840556 | T | G | 14 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(11): Show |
14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+25461T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840556 | |||||||
| chr16:22840727 | T | C | 1 | a0001c0002t0001g0116 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.485+25632T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840727 | |||||||
| chr16:22840754 | G | A | 4 | a0001c0002t0001g0122 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+25659G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840754 | |||||||
| chr16:22840903 | T | C | 14 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(11): Show |
14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+25808T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840903 | |||||||
| chr16:22840938 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.485+25843A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840938 | |||||||
| chr16:22840962 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+25867C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840962 | |||||||
| chr16:22840963 | C | A | 3 | a0001c0002t0001g0117 a0001c0002t0001g0308 a0001c0002t0001g0309 |
3 | HG01106.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.485+25868C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840963 | |||||||
| chr16:22840981 | C | T | 1 | a0001c0002t0004g0097 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.485+25886C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840981 | |||||||
| chr16:22840994 | G | A | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+25899G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22840994 | |||||||
| chr16:22841003 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.485+25908C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841003 | |||||||
| chr16:22841125 | G | A | 1 | a0001c0002t0001g0045 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.485+26030G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841125 | |||||||
| chr16:22841164 | C | T | 4 | a0001c0002t0001g0122 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+26069C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841164 | |||||||
| chr16:22841175 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.485+26080C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841175 | |||||||
| chr16:22841215 | G | A | 1 | a0001c0004t0002g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+26120G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841215 | |||||||
| chr16:22841254 | C | G | 1 | a0001c0002t0001g0139 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.485+26159C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841254 | |||||||
| chr16:22841274 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485+26179G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841274 | |||||||
| chr16:22841330 | G | C | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0280 others(4): Show |
7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+26235G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841330 | |||||||
| chr16:22841368 | C | A | 12 | a0001c0001t0001g0177 a0001c0001t0001g0193 a0001c0001t0001g0197 others(9): Show |
12 | HG02451.hp1 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+26273C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841368 | |||||||
| chr16:22841627 | T | G | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+26532T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841627 | |||||||
| chr16:22841793 | T | C | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0280 others(4): Show |
7 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+26698T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841793 | |||||||
| chr16:22841824 | A | G | 15 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(12): Show |
15 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+26729A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841824 | |||||||
| chr16:22841850 | C | T | 12 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+26755C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22841850 | |||||||
| chr16:22842062 | CT | C | 68 | a0001c0001t0001g0145 a0001c0001t0001g0177 a0001c0001t0001g0178 others(65): Show |
68 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.485+26986delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22842062 | ||||||
| chr16:22842062 | CTT | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0167 a0001c0001t0001g0168 others(72): Show |
75 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.485+26985_485+2698 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22842062 | ||||||
| chr16:22842062 | CTTT | C | 42 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+26984_485+2698 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22842062 | ||||||
| chr16:22842068 | T | C | 14 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(11): Show |
14 | HG02486.hp1 HG02559.hp1 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.485+26973T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842068 | |||||||
| chr16:22842187 | G | A | 11 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
11 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+27092G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842187 | |||||||
| chr16:22842244 | C | T | 5 | a0001c0002t0001g0117 a0001c0002t0001g0308 a0001c0002t0001g0309 others(2): Show |
5 | HG00639.hp2 HG01106.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+27149C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842244 | |||||||
| chr16:22842295 | T | C | 1 | a0001c0002t0001g0071 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.485+27200T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842295 | |||||||
| chr16:22842309 | C | T | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+27214C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842309 | |||||||
| chr16:22842345 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.485+27250G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842345 | |||||||
| chr16:22842398 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.485+27303T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842398 | |||||||
| chr16:22842525 | C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+27430C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842525 | |||||||
| chr16:22842553 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0150 others(153): Show |
156 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.485+27458G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842553 | |||||||
| chr16:22842555 | C | A | 13 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(10): Show |
13 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.485+27460C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842555 | |||||||
| chr16:22842621 | C | T | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.485+27526C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842621 | |||||||
| chr16:22842704 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.485+27609C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842704 | |||||||
| chr16:22842810 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.485+27715C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842810 | |||||||
| chr16:22842921 | T | C | 15 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(12): Show |
15 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+27826T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22842921 | |||||||
| chr16:22843138 | CTG | C | 42 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+28046_485+2804 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843138 | ||||||
| chr16:22843154 | G | GCA | 3 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0030 |
3 | HG01496.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485+28059_485+2806 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843154 | |||||||
| chr16:22843155 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485+28060T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843155 | |||||||
| chr16:22843156 | A | ATG | 62 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(59): Show |
62 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.485+28080_485+2808 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843156 | ||||||
| chr16:22843156 | A | G | 3 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0030 |
3 | HG01496.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485+28061A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843156 | |||||||
| chr16:22843156 | ATG | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0304 a0001c0002t0001g0007 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+28080_485+2808 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843156 | ||||||
| chr16:22843236 | A | G | 15 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(12): Show |
15 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+28141A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843236 | |||||||
| chr16:22843284 | A | G | 4 | a0001c0001t0001g0183 a0001c0001t0001g0218 a0001c0005t0006g0040 others(1): Show |
4 | HG01167.hp2 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+28189A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843284 | |||||||
| chr16:22843362 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.485+28267G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843362 | |||||||
| chr16:22843402 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0185 a0001c0001t0001g0223 others(48): Show |
51 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.485+28307G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843402 | |||||||
| chr16:22843574 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.485+28479T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843574 | |||||||
| chr16:22843609 | T | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18955.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.485+28514T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843609 | |||||||
| chr16:22843621 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.485+28526G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843621 | |||||||
| chr16:22843621 | G | T | 1 | a0001c0004t0002g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+28526G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843621 | |||||||
| chr16:22843647 | T | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0150 others(153): Show |
156 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.485+28552T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843647 | |||||||
| chr16:22843806 | A | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0256 a0001c0003t0003g0015 |
3 | HG01175.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.485+28711A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843806 | |||||||
| chr16:22843906 | AAGAAAC | A | 42 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+28815_485+2882 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22843906 | ||||||
| chr16:22843958 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0185 a0001c0001t0001g0223 others(48): Show |
51 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.485+28863C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22843958 | |||||||
| chr16:22844008 | T | TAC | 21 | a0001c0001t0001g0213 a0001c0001t0001g0233 a0001c0001t0001g0235 others(18): Show |
21 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+28940_485+2894 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | ||||||
| chr16:22844008 | TAC | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(8): Show |
11 | HG01884.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+28940_485+2894 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | ||||||
| chr16:22844008 | TACAC | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+28938_485+2894 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | ||||||
| chr16:22844008 | TACACAC | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0150 others(104): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.485+28936_485+2894 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | ||||||
| chr16:22844008 | TACACACA others(1): Show |
T | 7 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+28934_485+2894 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844008 | ||||||
| chr16:22844029 | ACACACAC others(1): Show |
A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0304 a0001c0002t0001g0007 others(2): Show |
5 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+28942_485+2894 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844029 | ||||||
| chr16:22844039 | A | G | 6 | a0001c0001t0001g0253 a0001c0001t0001g0296 a0001c0001t0001g0304 others(3): Show |
6 | HG02145.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+28944A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22844039 | |||||||
| chr16:22844356 | C | A | 32 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(29): Show |
32 | HG02145.hp2 HG02451.hp1 HG02451.hp2 others(29): Show |
intron_variant | MODIFIER | c.485+29261C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22844356 | |||||||
| chr16:22844410 | G | A | 1 | a0004c0009t0001g0336 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.485+29315G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22844410 | |||||||
| chr16:22844859 | CT | C | 6 | a0001c0001t0001g0178 a0001c0001t0001g0247 a0001c0001t0001g0300 others(3): Show |
6 | HG01257.hp2 HG01516.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+29777delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844859 | ||||||
| chr16:22844980 | AAGTAGCT others(490): Show |
A | 33 | a0001c0001t0001g0146 a0001c0001t0001g0167 a0001c0001t0001g0168 others(30): Show |
33 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(30): Show |
intron_variant | MODIFIER | c.485+29904_485+3040 others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22844980 | ||||||
| chr16:22845001 | C | T | 2 | a0001c0001t0001g0214 a0001c0002t0001g0084 |
2 | HG01123.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.485+29906C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845001 | |||||||
| chr16:22845058 | G | A | 1 | a0001c0002t0001g0084 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.485+29963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845058 | |||||||
| chr16:22845083 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0185 a0001c0001t0001g0223 others(47): Show |
50 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.485+29988T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845083 | |||||||
| chr16:22845354 | A | AT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(109): Show |
112 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.485+30274dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22845354 | ||||||
| chr16:22845354 | A | ATT | 16 | a0001c0001t0004g0165 a0001c0002t0001g0062 a0001c0002t0001g0071 others(13): Show |
16 | HG01071.hp2 HG01081.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+30273_485+3027 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22845354 | ||||||
| chr16:22845624 | TA | T | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+30530delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845624 | |||||||
| chr16:22845630 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.485+30535C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845630 | |||||||
| chr16:22845641 | C | T | 8 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+30546C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845641 | |||||||
| chr16:22845671 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.485+30576C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845671 | |||||||
| chr16:22845733 | T | C | 3 | a0001c0003t0003g0028 a0001c0003t0003g0029 a0001c0003t0003g0030 |
3 | HG01496.hp2 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485+30638T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845733 | |||||||
| chr16:22845761 | G | A | 8 | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG02486.hp1 HG02559.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+30666G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22845761 | |||||||
| chr16:22846017 | C | A | 13 | a0001c0001t0001g0146 a0001c0001t0001g0177 a0001c0001t0001g0193 others(10): Show |
13 | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.485+30922C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846017 | |||||||
| chr16:22846027 | C | T | 1 | a0001c0002t0001g0120 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+30932C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846027 | |||||||
| chr16:22846059 | C | T | 1 | a0001c0004t0002g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.485+30964C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846059 | |||||||
| chr16:22846138 | A | G | 1 | a0001c0002t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.485+31043A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846138 | |||||||
| chr16:22846214 | T | C | 11 | a0001c0001t0001g0216 a0001c0001t0001g0293 a0001c0001t0001g0294 others(8): Show |
11 | HG01106.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.485+31119T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846214 | |||||||
| chr16:22846275 | T | TA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0150 a0001c0001t0001g0151 others(115): Show |
118 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.485+31194dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22846275 | ||||||
| chr16:22846275 | TA | T | 9 | a0001c0001t0001g0277 a0001c0001t0001g0296 a0001c0001t0001g0304 others(6): Show |
9 | HG00323.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.485+31194delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22846275 | ||||||
| chr16:22846391 | C | G | 4 | a0001c0002t0001g0122 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+31296C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846391 | |||||||
| chr16:22846415 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.485+31320A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846415 | |||||||
| chr16:22846600 | G | A | 1 | a0001c0002t0001g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.485+31505G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846600 | |||||||
| chr16:22846630 | G | A | 2 | a0001c0001t0001g0238 a0001c0002t0001g0054 |
2 | NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.485+31535G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846630 | |||||||
| chr16:22846798 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0150 others(151): Show |
154 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.485+31703G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846798 | |||||||
| chr16:22846799 | T | A | 53 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(50): Show |
53 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.485+31704T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846799 | |||||||
| chr16:22846914 | G | A | 1 | a0001c0001t0004g0334 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.485+31819G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846914 | |||||||
| chr16:22846975 | G | C | 60 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(57): Show |
60 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.485+31880G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22846975 | |||||||
| chr16:22847001 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0178 a0001c0001t0001g0179 others(74): Show |
77 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.485+31906T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847001 | |||||||
| chr16:22847038 | C | T | 21 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(18): Show |
21 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+31943C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847038 | |||||||
| chr16:22847045 | T | C | 64 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0158 others(61): Show |
64 | HG00140.hp2 HG00544.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.485+31950T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847045 | |||||||
| chr16:22847045 | T | G | 21 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(18): Show |
21 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+31950T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847045 | |||||||
| chr16:22847050 | G | A | 4 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0306 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+31955G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847050 | |||||||
| chr16:22847258 | G | A | 1 | a0001c0005t0002g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.485+32163G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847258 | |||||||
| chr16:22847531 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.485+32436A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847531 | |||||||
| chr16:22847546 | T | G | 1 | a0001c0001t0001g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.485+32451T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847546 | |||||||
| chr16:22847598 | C | G | 3 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG02922.hp1 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.485+32503C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847598 | |||||||
| chr16:22847661 | T | A | 5 | a0001c0002t0001g0012 a0001c0003t0003g0020 a0001c0003t0003g0033 others(2): Show |
5 | HG01934.hp1 HG02055.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+32566T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847661 | |||||||
| chr16:22847681 | C | T | 1 | a0001c0004t0002g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.485+32586C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847681 | |||||||
| chr16:22847682 | G | A | 140 | a0001c0001t0001g0145 a0001c0001t0001g0150 a0001c0001t0001g0151 others(137): Show |
140 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.485+32587G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847682 | |||||||
| chr16:22847840 | AAAGG | A | 8 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+32759_485+3276 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22847840 | ||||||
| chr16:22847864 | GA | G | 6 | a0001c0001t0001g0303 a0001c0001t0001g0306 a0001c0001t0001g0307 others(3): Show |
6 | HG02040.hp2 HG02109.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+32778delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22847864 | ||||||
| chr16:22847903 | A | G | 2 | a0001c0002t0001g0013 a0001c0005t0002g0010 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.485+32808A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22847903 | |||||||
| chr16:22848142 | TA | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(146): Show |
149 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.485+33049delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22848142 | ||||||
| chr16:22848300 | A | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(278): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.485+33205A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848300 | |||||||
| chr16:22848363 | A | G | 2 | a0001c0001t0001g0218 a0001c0006t0006g0016 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.485+33268A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848363 | |||||||
| chr16:22848521 | AT | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(92): Show |
95 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.485+33433delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22848521 | ||||||
| chr16:22848722 | C | T | 1 | a0001c0004t0002g0305 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.485+33627C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848722 | |||||||
| chr16:22848803 | T | C | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+33708T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848803 | |||||||
| chr16:22848829 | G | A | 5 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0002g0305 others(2): Show |
5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+33734G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22848829 | |||||||
| chr16:22849076 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.485+33981G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849076 | |||||||
| chr16:22849089 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.485+33994G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849089 | |||||||
| chr16:22849097 | T | C | 29 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(26): Show |
29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+34002T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849097 | |||||||
| chr16:22849377 | T | C | 10 | a0001c0001t0001g0145 a0001c0001t0001g0292 a0001c0002t0003g0039 others(7): Show |
10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+34282T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849377 | |||||||
| chr16:22849479 | G | A | 2 | a0001c0002t0001g0007 a0001c0005t0002g0041 |
2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.485+34384G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849479 | |||||||
| chr16:22849581 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0285 a0001c0004t0002g0181 |
3 | HG02280.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.485+34486C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849581 | |||||||
| chr16:22849605 | T | C | 8 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(5): Show |
8 | NA18747.hp1 NA18968.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+34510T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849605 | |||||||
| chr16:22849651 | A | C | 2 | a0001c0002t0001g0065 a0001c0002t0001g0066 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485+34556A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849651 | |||||||
| chr16:22849654 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(113): Show |
116 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.485+34559A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849654 | |||||||
| chr16:22849692 | T | A | 6 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+34597T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849692 | |||||||
| chr16:22849704 | A | G | 4 | a0001c0001t0001g0264 a0001c0004t0002g0186 a0001c0005t0002g0104 others(1): Show |
4 | HG01099.hp1 HG03942.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+34609A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849704 | |||||||
| chr16:22849872 | C | T | 5 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0002g0305 others(2): Show |
5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+34777C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849872 | |||||||
| chr16:22849888 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(113): Show |
116 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.485+34793T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849888 | |||||||
| chr16:22849899 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.485+34804G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22849899 | |||||||
| chr16:22850021 | C | T | 30 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(27): Show |
30 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.485+34926C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850021 | |||||||
| chr16:22850070 | A | AG | 19 | a0001c0001t0001g0146 a0001c0001t0001g0158 a0001c0001t0001g0228 others(16): Show |
19 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+34975_485+3497 others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850070 | |||||||
| chr16:22850120 | C | T | 6 | a0001c0001t0001g0192 a0001c0001t0001g0217 a0001c0001t0001g0256 others(3): Show |
6 | HG01175.hp2 HG02572.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+35025C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850120 | |||||||
| chr16:22850185 | A | C | 1 | a0001c0001t0001g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.485+35090A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850185 | |||||||
| chr16:22850252 | C | T | 4 | a0001c0001t0001g0174 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+35157C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850252 | |||||||
| chr16:22850320 | G | A | 6 | a0001c0001t0001g0216 a0001c0002t0001g0012 a0001c0003t0003g0020 others(3): Show |
6 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+35225G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850320 | |||||||
| chr16:22850343 | C | T | 3 | a0001c0001t0001g0263 a0001c0002t0001g0046 a0001c0002t0001g0107 |
3 | HG00558.hp2 NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.485+35248C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850343 | |||||||
| chr16:22850429 | G | A | 2 | a0001c0001t0001g0171 a0001c0006t0006g0027 |
2 | HG02735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.485+35334G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850429 | |||||||
| chr16:22850512 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.485+35417C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850512 | |||||||
| chr16:22850842 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.485+35747A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22850842 | |||||||
| chr16:22851014 | G | A | 68 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(65): Show |
68 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.485+35919G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851014 | |||||||
| chr16:22851178 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.485+36083G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851178 | |||||||
| chr16:22851248 | G | A | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+36153G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851248 | |||||||
| chr16:22851278 | A | G | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+36183A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851278 | |||||||
| chr16:22851293 | C | A | 1 | a0005c0010t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.485+36198C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851293 | |||||||
| chr16:22851414 | C | T | 40 | a0001c0001t0001g0145 a0001c0001t0001g0161 a0001c0001t0001g0162 others(37): Show |
40 | HG00140.hp2 HG01109.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.485+36319C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851414 | |||||||
| chr16:22851426 | G | A | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+36331G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851426 | |||||||
| chr16:22851441 | A | G | 1 | a0001c0004t0002g0236 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.485+36346A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851441 | |||||||
| chr16:22851584 | G | A | 11 | a0001c0001t0001g0145 a0001c0001t0001g0292 a0001c0001t0001g0310 others(8): Show |
11 | HG01243.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.485+36489G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851584 | |||||||
| chr16:22851607 | C | G | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+36512C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851607 | |||||||
| chr16:22851655 | T | C | 1 | a0001c0002t0001g0333 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.485+36560T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851655 | |||||||
| chr16:22851956 | A | G | 1 | a0001c0004t0002g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.485+36861A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22851956 | |||||||
| chr16:22852096 | G | C | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37001G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852096 | |||||||
| chr16:22852153 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.485+37058A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852153 | |||||||
| chr16:22852226 | G | A | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37131G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852226 | |||||||
| chr16:22852263 | T | C | 5 | a0001c0001t0001g0192 a0001c0001t0001g0217 a0001c0001t0001g0256 others(2): Show |
5 | HG01175.hp2 HG02572.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37168T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852263 | |||||||
| chr16:22852294 | T | C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0003t0003g0018 |
3 | HG02559.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.485+37199T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852294 | |||||||
| chr16:22852362 | A | G | 12 | a0001c0001t0001g0193 a0001c0001t0001g0249 a0001c0001t0001g0293 others(9): Show |
12 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.485+37267A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852362 | |||||||
| chr16:22852406 | A | G | 6 | a0001c0001t0001g0216 a0001c0002t0001g0012 a0001c0003t0003g0020 others(3): Show |
6 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+37311A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852406 | |||||||
| chr16:22852451 | T | C | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+37356T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852451 | |||||||
| chr16:22852453 | T | C | 2 | a0001c0001t0001g0315 a0001c0002t0001g0117 |
2 | HG01106.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.485+37358T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852453 | |||||||
| chr16:22852544 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0322 a0001c0002t0001g0139 |
3 | HG01261.hp2 HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.485+37449C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852544 | |||||||
| chr16:22852671 | G | A | 19 | a0001c0001t0001g0146 a0001c0001t0001g0158 a0001c0001t0001g0228 others(16): Show |
19 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.485+37576G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852671 | |||||||
| chr16:22852771 | C | A | 29 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(26): Show |
29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+37676C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852771 | |||||||
| chr16:22852897 | C | T | 29 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(26): Show |
29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+37802C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852897 | |||||||
| chr16:22852945 | T | TA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(111): Show |
114 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.485+37850_485+3785 others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852945 | |||||||
| chr16:22852949 | G | A | 29 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(26): Show |
29 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+37854G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852949 | |||||||
| chr16:22852985 | C | T | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37890C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22852985 | |||||||
| chr16:22853005 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.485+37910C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853005 | |||||||
| chr16:22853087 | T | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(137): Show |
140 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.485+37992T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853087 | |||||||
| chr16:22853088 | G | A | 5 | a0001c0001t0001g0228 a0001c0003t0015g0032 a0001c0004t0002g0152 others(2): Show |
5 | HG01106.hp1 HG01175.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+37993G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853088 | |||||||
| chr16:22853231 | C | A | 10 | a0001c0001t0001g0145 a0001c0001t0001g0292 a0001c0002t0003g0039 others(7): Show |
10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+38136C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853231 | |||||||
| chr16:22853561 | A | G | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+38466A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853561 | |||||||
| chr16:22853651 | C | T | 16 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0176 others(13): Show |
16 | HG00639.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+38556C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853651 | |||||||
| chr16:22853815 | C | T | 15 | a0001c0001t0001g0183 a0001c0001t0001g0197 a0001c0001t0001g0199 others(12): Show |
15 | HG02258.hp1 HG02647.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.485+38720C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853815 | |||||||
| chr16:22853913 | G | T | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+38818G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22853913 | |||||||
| chr16:22854135 | G | A | 6 | a0001c0001t0001g0192 a0001c0001t0001g0217 a0001c0001t0001g0256 others(3): Show |
6 | HG01175.hp2 HG02572.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+39040G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854135 | |||||||
| chr16:22854290 | A | C | 1 | a0001c0001t0001g0349 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.485+39195A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854290 | |||||||
| chr16:22854619 | ATC | A | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+39526_485+3952 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22854619 | ||||||
| chr16:22854639 | CT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0158 others(132): Show |
135 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.485+39561delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22854639 | ||||||
| chr16:22854664 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.485+39569G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854664 | |||||||
| chr16:22854742 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.485+39647G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854742 | |||||||
| chr16:22854884 | C | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+39789C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854884 | |||||||
| chr16:22854903 | G | A | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+39808G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22854903 | |||||||
| chr16:22855043 | G | A | 26 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0176 others(23): Show |
26 | HG00639.hp1 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.485+39948G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855043 | |||||||
| chr16:22855283 | G | A | 1 | a0001c0002t0001g0054 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.485+40188G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855283 | |||||||
| chr16:22855362 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(109): Show |
112 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.485+40267T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855362 | |||||||
| chr16:22855372 | C | A | 10 | a0001c0001t0001g0177 a0001c0001t0001g0198 a0001c0001t0001g0286 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+40277C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855372 | |||||||
| chr16:22855581 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.485+40486T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855581 | |||||||
| chr16:22855696 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485+40601G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855696 | |||||||
| chr16:22855696 | G | GTC | 28 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(25): Show |
28 | HG00438.hp2 HG01167.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.485+40633_485+4063 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTC | 47 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0150 others(44): Show |
47 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.485+40631_485+4063 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTCTC | 46 | a0001c0001t0001g0001 a0001c0001t0001g0167 a0001c0001t0001g0168 others(43): Show |
46 | HG00609.hp1 HG00639.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.485+40629_485+4063 others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTCTCT others(1): Show |
18 | a0001c0001t0001g0145 a0001c0001t0001g0280 a0001c0001t0001g0343 others(15): Show |
18 | HG00423.hp1 HG00558.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+40627_485+4063 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTCTCT others(3): Show |
18 | a0001c0001t0001g0169 a0001c0001t0001g0198 a0001c0001t0001g0261 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+40625_485+4063 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTCTCT others(5): Show |
20 | a0001c0001t0001g0190 a0001c0001t0001g0211 a0001c0001t0001g0223 others(17): Show |
20 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.485+40623_485+4063 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTCTCT others(7): Show |
9 | a0001c0001t0001g0220 a0001c0001t0001g0239 a0001c0001t0001g0260 others(6): Show |
9 | HG01099.hp2 HG02040.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.485+40621_485+4063 others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTCTCT others(9): Show |
1 | a0001c0001t0013g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.485+40619_485+4063 others(20): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | G | GTCTCTCT others(13): Show |
1 | a0001c0001t0001g0195 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.485+40615_485+4063 others(24): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | GTC | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0259 a0001c0001t0001g0269 others(7): Show |
10 | HG01516.hp1 HG02109.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.485+40633_485+4063 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | GTCTC | G | 6 | a0001c0001t0001g0166 a0001c0001t0001g0174 a0001c0002t0001g0135 others(3): Show |
6 | HG00280.hp1 HG01496.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+40631_485+4063 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855696 | GTCTCTCT others(3): Show |
G | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+40625_485+4063 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22855696 | ||||||
| chr16:22855729 | T | TCTCTCTC others(6): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0262 |
2 | HG02155.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.485+40634_485+4063 others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855729 | |||||||
| chr16:22855729 | T | TCTCTCTC others(8): Show |
1 | a0006c0013t0002g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.485+40634_485+4063 others(19): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855729 | |||||||
| chr16:22855729 | T | TCTCTCTC others(12): Show |
1 | a0001c0002t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.485+40634_485+4063 others(23): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855729 | |||||||
| chr16:22855879 | T | A | 1 | a0001c0003t0003g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.485+40784T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855879 | |||||||
| chr16:22855978 | C | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+40883C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22855978 | |||||||
| chr16:22856009 | A | G | 4 | a0001c0001t0001g0198 a0001c0001t0001g0286 a0001c0001t0001g0288 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+40914A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856009 | |||||||
| chr16:22856162 | G | A | 6 | a0001c0001t0001g0158 a0001c0001t0001g0228 a0001c0003t0015g0032 others(3): Show |
6 | HG01106.hp1 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+41067G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856162 | |||||||
| chr16:22856188 | T | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0199 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.485+41093T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856188 | |||||||
| chr16:22856296 | G | A | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+41201G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856296 | |||||||
| chr16:22856317 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(187): Show |
190 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.485+41222G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856317 | |||||||
| chr16:22856387 | G | A | 6 | a0001c0001t0001g0185 a0001c0001t0001g0318 a0001c0001t0001g0319 others(3): Show |
6 | HG00544.hp2 HG02132.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+41292G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856387 | |||||||
| chr16:22856500 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0158 others(43): Show |
46 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.485+41405A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856500 | |||||||
| chr16:22856548 | C | T | 3 | a0001c0003t0003g0017 a0001c0004t0014g0237 a0001c0005t0006g0040 |
3 | HG01167.hp2 HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.485+41453C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856548 | |||||||
| chr16:22856714 | T | C | 21 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0214 others(18): Show |
21 | HG00140.hp1 HG00738.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+41619T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856714 | |||||||
| chr16:22856721 | A | C | 10 | a0001c0001t0001g0145 a0001c0001t0001g0292 a0001c0002t0003g0039 others(7): Show |
10 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.485+41626A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856721 | |||||||
| chr16:22856817 | C | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+41722C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856817 | |||||||
| chr16:22856866 | G | A | 21 | a0001c0001t0001g0174 a0001c0001t0001g0192 a0001c0001t0001g0217 others(18): Show |
21 | HG01167.hp2 HG01175.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.485+41771G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22856866 | |||||||
| chr16:22857005 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.485+41910C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857005 | |||||||
| chr16:22857089 | G | A | 5 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0002g0305 others(2): Show |
5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+41994G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857089 | |||||||
| chr16:22857137 | G | A | 1 | a0001c0002t0003g0002 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.485+42042G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857137 | |||||||
| chr16:22857282 | G | A | 6 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(3): Show |
6 | NA18968.hp2 NA18973.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+42187G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857282 | |||||||
| chr16:22857303 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0286 a0001c0001t0001g0288 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+42208G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857303 | |||||||
| chr16:22857444 | C | A | 1 | a0001c0001t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485+42349C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857444 | |||||||
| chr16:22857444 | C | T | 5 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0002t0001g0093 others(2): Show |
5 | NA18955.hp2 NA18957.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+42349C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857444 | |||||||
| chr16:22857655 | C | G | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+42560C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857655 | |||||||
| chr16:22857697 | T | A | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485+42602T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857697 | |||||||
| chr16:22857706 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(182): Show |
185 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.485+42611C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857706 | |||||||
| chr16:22857860 | C | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+42765C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857860 | |||||||
| chr16:22857990 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0299 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.485+42895A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857990 | |||||||
| chr16:22857999 | A | G | 4 | a0001c0001t0001g0174 a0001c0003t0003g0028 a0001c0003t0003g0029 others(1): Show |
4 | HG01496.hp2 HG02622.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+42904A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22857999 | |||||||
| chr16:22858094 | AT | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(160): Show |
163 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.485+43003delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22858094 | ||||||
| chr16:22858183 | C | A | 5 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0002g0305 others(2): Show |
5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+43088C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858183 | |||||||
| chr16:22858191 | G | T | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+43096G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858191 | |||||||
| chr16:22858344 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(133): Show |
136 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.485+43249T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858344 | |||||||
| chr16:22858345 | T | A | 5 | a0001c0001t0001g0259 a0001c0001t0001g0269 a0001c0001t0001g0338 others(2): Show |
5 | HG01516.hp1 HG02109.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+43250T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858345 | |||||||
| chr16:22858346 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485+43251A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858346 | |||||||
| chr16:22858555 | T | TTTTG | 119 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0158 others(116): Show |
119 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.485+43485_485+4348 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22858555 | ||||||
| chr16:22858555 | T | TTTTGTTT others(1): Show |
12 | a0001c0001t0001g0145 a0001c0001t0001g0269 a0001c0001t0001g0292 others(9): Show |
12 | HG01243.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+43481_485+4348 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22858555 | ||||||
| chr16:22858632 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.485+43537A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858632 | |||||||
| chr16:22858633 | G | A | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+43538G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858633 | |||||||
| chr16:22858639 | A | G | 7 | a0001c0001t0001g0249 a0001c0001t0001g0325 a0001c0001t0001g0335 others(4): Show |
7 | NA18968.hp2 NA18973.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+43544A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858639 | |||||||
| chr16:22858937 | G | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0180 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+43842G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22858937 | |||||||
| chr16:22859276 | A | G | 5 | a0001c0001t0001g0193 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+44181A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859276 | |||||||
| chr16:22859387 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(158): Show |
161 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.485+44292T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859387 | |||||||
| chr16:22859415 | C | G | 16 | a0001c0001t0001g0146 a0001c0001t0001g0197 a0001c0001t0001g0199 others(13): Show |
16 | HG01106.hp1 HG01175.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.485+44320C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859415 | |||||||
| chr16:22859534 | T | C | 1 | a0001c0006t0006g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.485+44439T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859534 | |||||||
| chr16:22859589 | C | A | 34 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(31): Show |
34 | HG01167.hp2 HG01496.hp2 HG02280.hp2 others(31): Show |
intron_variant | MODIFIER | c.485+44494C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859589 | |||||||
| chr16:22859820 | T | A | 20 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0180 others(17): Show |
20 | HG01516.hp1 HG02280.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.485+44725T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859820 | |||||||
| chr16:22859841 | T | C | 8 | a0001c0001t0001g0216 a0001c0002t0001g0012 a0001c0002t0001g0014 others(5): Show |
8 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+44746T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859841 | |||||||
| chr16:22859868 | A | G | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.485+44773A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859868 | |||||||
| chr16:22859902 | A | C | 1 | a0001c0005t0002g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.485+44807A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859902 | |||||||
| chr16:22859940 | C | A | 90 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(87): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.485+44845C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859940 | |||||||
| chr16:22859991 | G | A | 169 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.485+44896G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22859991 | |||||||
| chr16:22860072 | G | A | 169 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.485+44977G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860072 | |||||||
| chr16:22860105 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.485+45010T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860105 | |||||||
| chr16:22860226 | A | G | 5 | a0001c0001t0001g0300 a0001c0003t0003g0017 a0001c0004t0002g0305 others(2): Show |
5 | HG01167.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+45131A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860226 | |||||||
| chr16:22860246 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0007g0156 a0004c0009t0001g0336 others(1): Show |
4 | NA18953.hp2 NA18962.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+45151G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860246 | |||||||
| chr16:22860284 | G | A | 42 | a0001c0001t0001g0158 a0001c0001t0001g0167 a0001c0001t0001g0168 others(39): Show |
42 | HG00438.hp1 HG00558.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+45189G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860284 | |||||||
| chr16:22860317 | G | A | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.485+45222G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860317 | |||||||
| chr16:22860425 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.485+45330A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860425 | |||||||
| chr16:22860468 | G | A | 5 | a0001c0001t0001g0174 a0001c0002t0001g0013 a0001c0003t0003g0028 others(2): Show |
5 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+45373G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860468 | |||||||
| chr16:22860735 | T | C | 2 | a0001c0002t0001g0014 a0001c0002t0003g0002 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.485+45640T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860735 | |||||||
| chr16:22860745 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.485+45650A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860745 | |||||||
| chr16:22860750 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.485+45655A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860750 | |||||||
| chr16:22860817 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0170 others(101): Show |
104 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.485+45722C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860817 | |||||||
| chr16:22860826 | G | A | 43 | a0001c0001t0001g0170 a0001c0001t0001g0188 a0001c0001t0001g0189 others(40): Show |
43 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.485+45731G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860826 | |||||||
| chr16:22860856 | T | C | 2 | a0001c0001t0001g0296 a0001c0003t0003g0021 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.485+45761T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860856 | |||||||
| chr16:22860867 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0170 others(108): Show |
111 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.485+45772G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860867 | |||||||
| chr16:22860912 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0177 a0001c0001t0001g0178 others(29): Show |
32 | HG00621.hp2 HG01099.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.485+45817G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860912 | |||||||
| chr16:22860964 | C | T | 2 | a0001c0002t0001g0014 a0001c0002t0003g0002 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.485+45869C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22860964 | |||||||
| chr16:22861173 | G | A | 5 | a0001c0002t0001g0103 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+46078G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861173 | |||||||
| chr16:22861229 | G | A | 5 | a0001c0001t0001g0174 a0001c0002t0001g0013 a0001c0003t0003g0028 others(2): Show |
5 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+46134G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861229 | |||||||
| chr16:22861399 | G | T | 7 | a0001c0001t0001g0228 a0001c0003t0015g0032 a0001c0004t0002g0236 others(4): Show |
7 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+46304G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861399 | |||||||
| chr16:22861404 | T | C | 48 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0158 others(45): Show |
48 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.485+46309T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861404 | |||||||
| chr16:22861702 | C | A | 4 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0055 others(1): Show |
4 | NA18973.hp1 NA19065.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+46607C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861702 | |||||||
| chr16:22861729 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.485+46634G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861729 | |||||||
| chr16:22861774 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.485+46679A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861774 | |||||||
| chr16:22861838 | G | A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0254 a0001c0001t0001g0319 others(4): Show |
7 | HG02132.hp1 HG02523.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+46743G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861838 | |||||||
| chr16:22861926 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.485+46831A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22861926 | |||||||
| chr16:22862118 | C | T | 25 | a0001c0001t0001g0153 a0001c0001t0001g0169 a0001c0001t0001g0205 others(22): Show |
25 | HG00423.hp2 HG00609.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.485+47023C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862118 | |||||||
| chr16:22862190 | C | T | 24 | a0001c0001t0001g0153 a0001c0001t0001g0169 a0001c0001t0001g0205 others(21): Show |
24 | HG00423.hp2 HG00609.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.485+47095C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862190 | |||||||
| chr16:22862263 | G | C | 24 | a0001c0001t0001g0153 a0001c0001t0001g0169 a0001c0001t0001g0205 others(21): Show |
24 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.485+47168G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862263 | |||||||
| chr16:22862275 | C | CT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0168 others(53): Show |
56 | HG00544.hp2 HG01099.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.485+47199dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22862275 | ||||||
| chr16:22862275 | CT | C | 35 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0001g0179 others(32): Show |
35 | HG00323.hp1 HG01106.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.485+47199delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22862275 | ||||||
| chr16:22862275 | CTT | C | 24 | a0001c0001t0001g0153 a0001c0001t0001g0169 a0001c0001t0001g0205 others(21): Show |
24 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.485+47198_485+4719 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22862275 | ||||||
| chr16:22862348 | G | T | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.485+47253G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862348 | |||||||
| chr16:22862418 | G | C | 1 | a0001c0002t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.485+47323G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862418 | |||||||
| chr16:22862493 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0153 others(162): Show |
165 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.485+47398C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862493 | |||||||
| chr16:22862510 | G | A | 29 | a0001c0001t0001g0177 a0001c0001t0001g0198 a0001c0001t0001g0256 others(26): Show |
29 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.485+47415G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862510 | |||||||
| chr16:22862521 | G | A | 3 | a0001c0001t0001g0314 a0002c0007t0001g0231 a0002c0007t0001g0232 |
3 | HG00323.hp2 HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.485+47426G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862521 | |||||||
| chr16:22862550 | G | A | 6 | a0001c0001t0001g0174 a0001c0002t0001g0013 a0001c0003t0003g0028 others(3): Show |
6 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+47455G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862550 | |||||||
| chr16:22862787 | T | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.485+47692T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862787 | |||||||
| chr16:22862847 | G | A | 1 | a0001c0002t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.485+47752G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22862847 | |||||||
| chr16:22863006 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.485+47911C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863006 | |||||||
| chr16:22863047 | C | T | 1 | a0001c0002t0001g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.485+47952C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863047 | |||||||
| chr16:22863079 | T | C | 59 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0001g0166 others(56): Show |
59 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.485+47984T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863079 | |||||||
| chr16:22863204 | T | C | 59 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0001g0166 others(56): Show |
59 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.485+48109T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863204 | |||||||
| chr16:22863242 | C | G | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+48147C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863242 | |||||||
| chr16:22863271 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0001g0301 a0001c0003t0003g0023 others(1): Show |
4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+48176A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863271 | |||||||
| chr16:22863292 | G | A | 2 | a0001c0004t0002g0281 a0001c0006t0006g0016 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.485+48197G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863292 | |||||||
| chr16:22863375 | C | G | 4 | a0001c0002t0001g0065 a0001c0002t0001g0066 a0001c0005t0002g0009 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.485+48280C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863375 | |||||||
| chr16:22863467 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.485+48372G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863467 | |||||||
| chr16:22863470 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.485+48375C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863470 | |||||||
| chr16:22863477 | G | T | 18 | a0001c0001t0001g0316 a0001c0001t0004g0165 a0001c0002t0001g0085 others(15): Show |
18 | HG00738.hp1 HG01071.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.485+48382G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863477 | |||||||
| chr16:22863607 | T | C | 49 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0175 others(46): Show |
49 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.485+48512T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863607 | |||||||
| chr16:22863706 | G | A | 6 | a0001c0001t0001g0174 a0001c0002t0001g0013 a0001c0003t0003g0028 others(3): Show |
6 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+48611G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863706 | |||||||
| chr16:22863752 | C | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0350 |
2 | NA18969.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.485+48657C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863752 | |||||||
| chr16:22863807 | G | A | 5 | a0001c0001t0001g0335 a0001c0002t0001g0007 a0001c0002t0001g0045 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+48712G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863807 | |||||||
| chr16:22863832 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0301 a0001c0003t0003g0023 others(1): Show |
4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+48737C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863832 | |||||||
| chr16:22863917 | G | A | 132 | a0001c0001t0001g0145 a0001c0001t0001g0153 a0001c0001t0001g0160 others(129): Show |
132 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.485+48822G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863917 | |||||||
| chr16:22863975 | A | G | 342 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(339): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.485+48880A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22863975 | |||||||
| chr16:22864062 | G | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.485+48967G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864062 | |||||||
| chr16:22864079 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.485+48984C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864079 | |||||||
| chr16:22864113 | T | G | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+49018T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864113 | |||||||
| chr16:22864165 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.485+49070A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864165 | |||||||
| chr16:22864262 | C | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(2): Show |
5 | NA18955.hp1 NA18961.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.485+49167C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864262 | |||||||
| chr16:22864329 | C | T | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.485+49234C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864329 | |||||||
| chr16:22864421 | A | G | 73 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0001g0166 others(70): Show |
73 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.485+49326A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864421 | |||||||
| chr16:22864479 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0153 others(162): Show |
165 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.485+49384C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864479 | |||||||
| chr16:22864577 | G | A | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.485+49482G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864577 | |||||||
| chr16:22864720 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0153 others(165): Show |
168 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.485+49625T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864720 | |||||||
| chr16:22864855 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0185 others(22): Show |
25 | HG01081.hp2 HG02074.hp1 HG02132.hp1 others(22): Show |
intron_variant | MODIFIER | c.485+49760A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864855 | |||||||
| chr16:22864871 | C | A | 1 | a0001c0002t0001g0081 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.485+49776C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864871 | |||||||
| chr16:22864882 | C | CA | 14 | a0001c0001t0001g0172 a0001c0001t0001g0190 a0001c0001t0001g0195 others(11): Show |
14 | HG01123.hp2 HG02145.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.485+49807dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | ||||||
| chr16:22864882 | C | CAAAAAAA others(1): Show |
49 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0174 others(46): Show |
49 | HG00735.hp2 HG01081.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.485+49800_485+4980 others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | ||||||
| chr16:22864882 | C | CAAAAAAA others(2): Show |
36 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0192 others(33): Show |
36 | HG01175.hp1 HG01361.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.485+49799_485+4980 others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | ||||||
| chr16:22864882 | C | CAAAAAAA others(3): Show |
42 | a0001c0001t0001g0160 a0001c0001t0001g0179 a0001c0001t0001g0180 others(39): Show |
42 | HG00558.hp2 HG00741.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.485+49798_485+4980 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | ||||||
| chr16:22864882 | C | CAAAAAAA others(4): Show |
26 | a0001c0001t0001g0153 a0001c0001t0001g0166 a0001c0001t0001g0169 others(23): Show |
26 | HG00423.hp2 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.485+49797_485+4980 others(15): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | ||||||
| chr16:22864882 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0289 a0001c0005t0002g0011 |
2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.485+49794_485+4980 others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | ||||||
| chr16:22864882 | CAAAAA | C | 7 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0293 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.485+49803_485+4980 others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22864882 | ||||||
| chr16:22864928 | G | A | 3 | a0001c0001t0001g0291 a0001c0004t0002g0305 a0001c0006t0006g0027 |
3 | HG02970.hp2 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.485+49833G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864928 | |||||||
| chr16:22864970 | G | A | 2 | a0001c0001t0001g0330 a0001c0002t0001g0119 |
2 | NA18612.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.485+49875G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22864970 | |||||||
| chr16:22865004 | C | G | 67 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0175 others(64): Show |
67 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.485+49909C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865004 | |||||||
| chr16:22865010 | C | T | 1 | a0001c0002t0001g0120 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+49915C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865010 | |||||||
| chr16:22865028 | G | A | 4 | a0001c0001t0001g0211 a0001c0001t0001g0324 a0001c0002t0001g0072 others(1): Show |
4 | HG00438.hp1 HG02165.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-49916G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865028 | |||||||
| chr16:22865049 | C | CA | 7 | a0001c0001t0001g0251 a0001c0001t0001g0289 a0001c0001t0001g0327 others(4): Show |
7 | HG00639.hp1 HG01261.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-49873dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | ||||||
| chr16:22865049 | CA | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0169 a0001c0001t0001g0170 others(63): Show |
66 | HG00323.hp2 HG00544.hp2 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.486-49873delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | ||||||
| chr16:22865049 | CAA | C | 83 | a0001c0001t0001g0145 a0001c0001t0001g0153 a0001c0001t0001g0160 others(80): Show |
83 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.486-49874_486-4987 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | ||||||
| chr16:22865049 | CAAAA | C | 9 | a0001c0001t0001g0174 a0001c0001t0001g0296 a0001c0002t0001g0013 others(6): Show |
9 | HG01496.hp2 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-49876_486-4987 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22865049 | ||||||
| chr16:22865087 | C | A | 55 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0175 others(52): Show |
55 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.486-49857C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865087 | |||||||
| chr16:22865185 | C | G | 4 | a0001c0001t0001g0168 a0001c0001t0001g0265 a0001c0002t0001g0079 others(1): Show |
4 | NA18947.hp2 NA18955.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-49759C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865185 | |||||||
| chr16:22865232 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.486-49712T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865232 | |||||||
| chr16:22865261 | A | C | 1 | a0001c0002t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-49683A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865261 | |||||||
| chr16:22865339 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0160 others(90): Show |
93 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.486-49605G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865339 | |||||||
| chr16:22865488 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-49456G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865488 | |||||||
| chr16:22865527 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.486-49417G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865527 | |||||||
| chr16:22865758 | G | T | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-49186G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865758 | |||||||
| chr16:22865889 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.486-49055A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865889 | |||||||
| chr16:22865961 | A | G | 1 | a0001c0002t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.486-48983A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865961 | |||||||
| chr16:22865996 | C | G | 1 | a0001c0002t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-48948C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22865996 | |||||||
| chr16:22866142 | C | G | 1 | a0001c0002t0001g0084 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.486-48802C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866142 | |||||||
| chr16:22866201 | GT | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0160 others(90): Show |
93 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.486-48739delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866201 | ||||||
| chr16:22866291 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.486-48653A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866291 | |||||||
| chr16:22866302 | T | C | 4 | a0001c0002t0001g0065 a0001c0002t0001g0066 a0001c0005t0002g0009 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-48642T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866302 | |||||||
| chr16:22866306 | C | T | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-48638C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866306 | |||||||
| chr16:22866314 | C | T | 15 | a0001c0001t0001g0179 a0001c0001t0001g0192 a0001c0001t0001g0217 others(12): Show |
15 | HG01175.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.486-48630C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866314 | |||||||
| chr16:22866316 | T | TGC | 17 | a0001c0001t0001g0169 a0001c0001t0001g0187 a0001c0001t0001g0205 others(14): Show |
17 | HG01099.hp2 HG01496.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.486-48617_486-4861 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866316 | ||||||
| chr16:22866318 | C | T | 2 | a0001c0004t0002g0305 a0001c0006t0006g0027 |
2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.486-48626C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866318 | |||||||
| chr16:22866321 | G | A | 7 | a0001c0004t0002g0152 a0001c0004t0002g0155 a0001c0004t0002g0258 others(4): Show |
7 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-48623G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866321 | |||||||
| chr16:22866323 | G | A | 8 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0293 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-48621G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866323 | |||||||
| chr16:22866325 | G | GCA | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0003t0003g0018 others(2): Show |
5 | HG01109.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-48618_486-4861 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866325 | ||||||
| chr16:22866325 | G | T | 1 | a0001c0002t0001g0108 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.486-48619G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866325 | |||||||
| chr16:22866326 | C | A | 1 | a0001c0002t0001g0108 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.486-48618C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866326 | |||||||
| chr16:22866326 | C | T | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-48618C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866326 | |||||||
| chr16:22866327 | G | A | 43 | a0001c0001t0001g0145 a0001c0001t0001g0175 a0001c0001t0001g0176 others(40): Show |
43 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.486-48617G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866327 | |||||||
| chr16:22866327 | GCA | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0170 a0001c0001t0001g0174 others(35): Show |
38 | HG01081.hp2 HG01496.hp2 HG01943.hp2 others(35): Show |
intron_variant | MODIFIER | c.486-48601_486-4860 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866327 | ||||||
| chr16:22866329 | A | G | 69 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0001g0166 others(66): Show |
69 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.486-48615A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866329 | |||||||
| chr16:22866331 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0174 others(31): Show |
34 | HG01081.hp2 HG01496.hp2 HG02074.hp1 others(31): Show |
intron_variant | MODIFIER | c.486-48613A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866331 | |||||||
| chr16:22866333 | A | G | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-48611A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866333 | |||||||
| chr16:22866369 | C | CGT | 62 | a0001c0001t0001g0147 a0001c0001t0001g0157 a0001c0001t0001g0171 others(59): Show |
62 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.486-48538_486-4853 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | ||||||
| chr16:22866369 | C | CGTGT | 11 | a0001c0001t0001g0183 a0001c0001t0001g0222 a0001c0002t0001g0006 others(8): Show |
11 | HG00639.hp1 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-48540_486-4853 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | ||||||
| chr16:22866369 | C | CGTGTGTG others(3): Show |
2 | a0001c0004t0002g0281 a0001c0006t0006g0016 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.486-48546_486-4853 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | ||||||
| chr16:22866369 | C | T | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-48575C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866369 | |||||||
| chr16:22866369 | CGT | C | 61 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(58): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.486-48538_486-4853 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | ||||||
| chr16:22866369 | CGTGT | C | 55 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0161 others(52): Show |
55 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.486-48540_486-4853 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22866369 | ||||||
| chr16:22866373 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-48571T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866373 | |||||||
| chr16:22866386 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.486-48558G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866386 | |||||||
| chr16:22866388 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0160 others(88): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.486-48556G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866388 | |||||||
| chr16:22866408 | T | C | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.486-48536T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866408 | |||||||
| chr16:22866409 | G | T | 1 | a0001c0002t0001g0119 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.486-48535G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866409 | |||||||
| chr16:22866577 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.486-48367C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866577 | |||||||
| chr16:22866614 | A | G | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-48330A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866614 | |||||||
| chr16:22866621 | C | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0301 a0001c0003t0003g0023 others(1): Show |
4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-48323C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866621 | |||||||
| chr16:22866849 | A | G | 8 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0293 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-48095A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866849 | |||||||
| chr16:22866883 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.486-48061C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22866883 | |||||||
| chr16:22867102 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.486-47842G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867102 | |||||||
| chr16:22867107 | G | T | 49 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0175 others(46): Show |
49 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.486-47837G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867107 | |||||||
| chr16:22867324 | T | C | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-47620T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867324 | |||||||
| chr16:22867419 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.486-47525A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867419 | |||||||
| chr16:22867538 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.486-47406A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867538 | |||||||
| chr16:22867562 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.486-47382C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867562 | |||||||
| chr16:22867663 | G | A | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-47281G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22867663 | |||||||
| chr16:22868074 | C | T | 32 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0175 others(29): Show |
32 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.486-46870C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868074 | |||||||
| chr16:22868134 | A | G | 12 | a0001c0001t0001g0157 a0001c0001t0001g0191 a0001c0001t0001g0193 others(9): Show |
12 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-46810A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868134 | |||||||
| chr16:22868160 | C | T | 1 | a0001c0002t0001g0071 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.486-46784C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868160 | |||||||
| chr16:22868317 | G | A | 27 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0188 others(24): Show |
27 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.486-46627G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868317 | |||||||
| chr16:22868405 | C | CA | 36 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0178 others(33): Show |
36 | HG00735.hp2 HG01081.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-46514dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | ||||||
| chr16:22868405 | C | CAA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0159 others(36): Show |
39 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.486-46515_486-4651 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | ||||||
| chr16:22868405 | C | CAAA | 55 | a0001c0001t0001g0153 a0001c0001t0001g0160 a0001c0001t0001g0169 others(52): Show |
55 | HG00423.hp2 HG00558.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.486-46516_486-4651 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | ||||||
| chr16:22868405 | C | CAAAA | 12 | a0001c0001t0001g0180 a0001c0001t0001g0213 a0001c0001t0001g0221 others(9): Show |
12 | HG00544.hp2 HG00621.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-46517_486-4651 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | ||||||
| chr16:22868405 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0174 a0001c0002t0001g0013 a0001c0003t0003g0028 others(3): Show |
6 | HG01496.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-46522_486-4651 others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22868405 | ||||||
| chr16:22868526 | C | T | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-46418C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868526 | |||||||
| chr16:22868596 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0160 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.486-46348G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868596 | |||||||
| chr16:22868606 | C | T | 3 | a0001c0001t0001g0298 a0001c0003t0003g0036 a0001c0003t0003g0037 |
3 | HG02559.hp2 HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.486-46338C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868606 | |||||||
| chr16:22868715 | T | G | 1 | a0001c0002t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.486-46229T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868715 | |||||||
| chr16:22868742 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.486-46202G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868742 | |||||||
| chr16:22868759 | G | A | 1 | a0001c0002t0005g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.486-46185G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22868759 | |||||||
| chr16:22869021 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0160 others(93): Show |
96 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.486-45923T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869021 | |||||||
| chr16:22869055 | T | C | 6 | a0001c0001t0001g0194 a0001c0001t0001g0219 a0001c0001t0001g0278 others(3): Show |
6 | HG01934.hp2 NA18962.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-45889T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869055 | |||||||
| chr16:22869066 | G | T | 8 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0293 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-45878G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869066 | |||||||
| chr16:22869382 | C | T | 4 | a0001c0001t0001g0296 a0001c0001t0001g0301 a0001c0003t0003g0023 others(1): Show |
4 | HG02717.hp2 HG02895.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-45562C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869382 | |||||||
| chr16:22869601 | A | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0160 others(88): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.486-45343A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869601 | |||||||
| chr16:22869691 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0160 others(83): Show |
86 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.486-45253C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869691 | |||||||
| chr16:22869990 | T | C | 4 | a0001c0001t0001g0298 a0001c0003t0003g0021 a0001c0003t0003g0036 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-44954T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22869990 | |||||||
| chr16:22870035 | A | G | 4 | a0001c0001t0001g0298 a0001c0003t0003g0021 a0001c0003t0003g0036 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-44909A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870035 | |||||||
| chr16:22870122 | G | A | 1 | a0001c0002t0001g0094 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.486-44822G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870122 | |||||||
| chr16:22870125 | G | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0168 a0001c0001t0001g0175 others(40): Show |
43 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.486-44819G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870125 | |||||||
| chr16:22870257 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0148 others(153): Show |
156 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.486-44687A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870257 | |||||||
| chr16:22870276 | G | C | 1 | a0001c0001t0001g0239 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.486-44668G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870276 | |||||||
| chr16:22870318 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.486-44626C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870318 | |||||||
| chr16:22870319 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0148 a0001c0001t0001g0168 others(51): Show |
54 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.486-44625G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870319 | |||||||
| chr16:22870499 | A | G | 2 | a0001c0001t0001g0301 a0001c0003t0003g0023 |
2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.486-44445A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870499 | |||||||
| chr16:22870544 | A | G | 3 | a0001c0001t0001g0221 a0004c0009t0001g0336 a0004c0009t0001g0341 |
3 | NA18953.hp2 NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.486-44400A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870544 | |||||||
| chr16:22870628 | T | C | 2 | a0001c0001t0001g0301 a0001c0003t0003g0023 |
2 | HG02717.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.486-44316T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870628 | |||||||
| chr16:22870878 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0253 |
2 | NA18957.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.486-44066C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870878 | |||||||
| chr16:22870897 | C | T | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-44047C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870897 | |||||||
| chr16:22870898 | G | A | 1 | a0001c0004t0002g0236 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.486-44046G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870898 | |||||||
| chr16:22870929 | C | T | 1 | a0001c0002t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.486-44015C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22870929 | |||||||
| chr16:22871058 | T | C | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-43886T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871058 | |||||||
| chr16:22871138 | A | G | 91 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(88): Show |
91 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.486-43806A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871138 | |||||||
| chr16:22871211 | C | T | 3 | a0001c0001t0001g0274 a0001c0001t0001g0313 a0001c0002t0001g0068 |
3 | HG00423.hp1 HG04184.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.486-43733C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871211 | |||||||
| chr16:22871354 | CA | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0148 others(195): Show |
198 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.486-43576delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22871354 | ||||||
| chr16:22871680 | C | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0319 a0001c0002t0001g0333 |
3 | HG02074.hp1 HG02132.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.486-43264C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871680 | |||||||
| chr16:22871981 | G | A | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-42963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871981 | |||||||
| chr16:22871987 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.486-42957C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22871987 | |||||||
| chr16:22872161 | T | C | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-42783T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872161 | |||||||
| chr16:22872249 | A | G | 1 | a0001c0005t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.486-42695A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872249 | |||||||
| chr16:22872530 | T | C | 90 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(87): Show |
90 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.486-42414T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872530 | |||||||
| chr16:22872655 | C | T | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-42289C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872655 | |||||||
| chr16:22872683 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-42261G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872683 | |||||||
| chr16:22872690 | G | A | 94 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(91): Show |
94 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.486-42254G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872690 | |||||||
| chr16:22872732 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0147 others(279): Show |
282 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-42212T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872732 | |||||||
| chr16:22872906 | T | C | 3 | a0001c0001t0001g0146 a0001c0002t0003g0002 a0001c0003t0003g0015 |
3 | HG02109.hp2 HG02615.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.486-42038T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872906 | |||||||
| chr16:22872923 | A | G | 103 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(100): Show |
103 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.486-42021A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872923 | |||||||
| chr16:22872969 | T | TC | 3 | a0001c0001t0001g0301 a0001c0003t0003g0023 a0001c0004t0002g0181 |
3 | HG02717.hp2 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.486-41974dupC | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22872969 | ||||||
| chr16:22872995 | T | G | 96 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(93): Show |
96 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.486-41949T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22872995 | |||||||
| chr16:22873188 | C | T | 7 | a0001c0001t0001g0228 a0001c0002t0001g0006 a0001c0004t0002g0236 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-41756C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873188 | |||||||
| chr16:22873247 | C | A | 1 | a0001c0001t0001g0251 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.486-41697C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873247 | |||||||
| chr16:22873275 | C | A | 2 | a0002c0007t0001g0231 a0002c0007t0001g0232 |
2 | HG00639.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.486-41669C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873275 | |||||||
| chr16:22873276 | G | A | 4 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0001g0292 others(1): Show |
4 | HG01243.hp2 HG02280.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-41668G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873276 | |||||||
| chr16:22873326 | A | G | 7 | a0001c0001t0001g0191 a0001c0001t0001g0193 a0001c0001t0001g0293 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-41618A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873326 | |||||||
| chr16:22873493 | T | C | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-41451T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873493 | |||||||
| chr16:22873678 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-41266G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873678 | |||||||
| chr16:22873827 | A | G | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-41117A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873827 | |||||||
| chr16:22873977 | G | A | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-40967G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873977 | |||||||
| chr16:22873982 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0147 others(279): Show |
282 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-40962T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22873982 | |||||||
| chr16:22874100 | G | A | 129 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0151 others(126): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.486-40844G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874100 | |||||||
| chr16:22874130 | G | A | 2 | a0001c0001t0001g0216 a0001c0003t0003g0034 |
2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.486-40814G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874130 | |||||||
| chr16:22874196 | TTCC | T | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-40746_486-4074 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22874196 | ||||||
| chr16:22874214 | G | T | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-40730G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874214 | |||||||
| chr16:22874374 | C | T | 4 | a0001c0001t0001g0185 a0001c0001t0001g0319 a0001c0002t0001g0333 others(1): Show |
4 | HG02074.hp1 HG02132.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-40570C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874374 | |||||||
| chr16:22874442 | A | G | 1 | a0001c0002t0001g0070 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.486-40502A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874442 | |||||||
| chr16:22874617 | C | A | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-40327C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874617 | |||||||
| chr16:22874658 | C | A | 7 | a0001c0004t0002g0152 a0001c0004t0002g0155 a0001c0004t0002g0258 others(4): Show |
7 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-40286C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874658 | |||||||
| chr16:22874847 | G | A | 1 | a0001c0005t0002g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.486-40097G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874847 | |||||||
| chr16:22874919 | C | G | 131 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0151 others(128): Show |
131 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.486-40025C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22874919 | |||||||
| chr16:22875369 | A | AATTTATT others(5): Show |
5 | a0001c0001t0001g0289 a0001c0001t0001g0335 a0001c0002t0001g0045 others(2): Show |
5 | HG03471.hp1 NA19065.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-39557_486-3954 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22875369 | ||||||
| chr16:22875369 | A | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0350 |
2 | NA18969.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.486-39575A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875369 | |||||||
| chr16:22875419 | C | T | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-39525C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875419 | |||||||
| chr16:22875488 | C | T | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-39456C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875488 | |||||||
| chr16:22875539 | C | T | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-39405C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875539 | |||||||
| chr16:22875574 | G | A | 2 | a0001c0001t0001g0328 a0001c0002t0001g0110 |
2 | NA18980.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.486-39370G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875574 | |||||||
| chr16:22875612 | ACCT | A | 3 | a0001c0003t0003g0026 a0001c0004t0002g0276 a0001c0006t0006g0025 |
3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.486-39330_486-3932 others(7): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22875612 | ||||||
| chr16:22875694 | T | G | 3 | a0001c0005t0002g0091 a0003c0008t0002g0229 a0003c0008t0002g0230 |
3 | HG01070.hp2 HG01071.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.486-39250T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875694 | |||||||
| chr16:22875831 | C | A | 1 | a0001c0001t0001g0347 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.486-39113C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875831 | |||||||
| chr16:22875875 | C | T | 1 | a0001c0002t0004g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.486-39069C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875875 | |||||||
| chr16:22875981 | G | A | 98 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0151 others(95): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.486-38963G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22875981 | |||||||
| chr16:22876002 | G | T | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-38942G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876002 | |||||||
| chr16:22876048 | T | A | 95 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(92): Show |
95 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.486-38896T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876048 | |||||||
| chr16:22876185 | T | C | 96 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(93): Show |
96 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.486-38759T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876185 | |||||||
| chr16:22876201 | C | T | 64 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0160 others(61): Show |
64 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.486-38743C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876201 | |||||||
| chr16:22876269 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.486-38675C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876269 | |||||||
| chr16:22876278 | G | C | 4 | a0001c0001t0001g0207 a0001c0001t0001g0221 a0004c0009t0001g0336 others(1): Show |
4 | HG01943.hp1 NA18953.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-38666G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876278 | |||||||
| chr16:22876308 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-38636G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876308 | |||||||
| chr16:22876397 | A | G | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-38547A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876397 | |||||||
| chr16:22876437 | T | A | 1 | a0001c0002t0012g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.486-38507T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876437 | |||||||
| chr16:22876488 | A | G | 1 | a0001c0002t0010g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.486-38456A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876488 | |||||||
| chr16:22876516 | G | A | 1 | a0001c0003t0003g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.486-38428G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876516 | |||||||
| chr16:22876551 | C | T | 2 | a0001c0004t0002g0154 a0001c0004t0002g0258 |
2 | HG03831.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.486-38393C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876551 | |||||||
| chr16:22876558 | A | G | 1 | a0001c0002t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.486-38386A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876558 | |||||||
| chr16:22876724 | C | T | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-38220C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22876724 | |||||||
| chr16:22877108 | G | A | 89 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(86): Show |
89 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.486-37836G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877108 | |||||||
| chr16:22877197 | A | C | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.486-37747A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877197 | |||||||
| chr16:22877278 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.486-37666G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877278 | |||||||
| chr16:22877363 | C | T | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-37581C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877363 | |||||||
| chr16:22877428 | A | G | 1 | a0001c0002t0001g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.486-37516A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877428 | |||||||
| chr16:22877480 | G | T | 1 | a0001c0003t0003g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.486-37464G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877480 | |||||||
| chr16:22877495 | G | A | 9 | a0001c0004t0002g0152 a0001c0004t0002g0155 a0001c0004t0002g0258 others(6): Show |
9 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.486-37449G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877495 | |||||||
| chr16:22877819 | G | T | 14 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0171 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-37125G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877819 | |||||||
| chr16:22877865 | G | A | 109 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0151 others(106): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.486-37079G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877865 | |||||||
| chr16:22877909 | G | T | 1 | a0001c0005t0002g0009 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.486-37035G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877909 | |||||||
| chr16:22877919 | G | A | 1 | a0001c0002t0004g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.486-37025G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877919 | |||||||
| chr16:22877987 | T | C | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-36957T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22877987 | |||||||
| chr16:22878086 | G | A | 1 | a0001c0004t0002g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486-36858G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878086 | |||||||
| chr16:22878106 | A | G | 8 | a0001c0001t0001g0174 a0001c0001t0001g0296 a0001c0001t0001g0298 others(5): Show |
8 | HG01496.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-36838A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878106 | |||||||
| chr16:22878135 | G | A | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-36809G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878135 | |||||||
| chr16:22878199 | T | C | 1 | a0001c0004t0002g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486-36745T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878199 | |||||||
| chr16:22878609 | T | TA | 3 | a0001c0001t0001g0179 a0001c0005t0006g0038 a0005c0010t0001g0042 |
3 | HG01884.hp1 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.486-36335_486-3633 others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878609 | |||||||
| chr16:22878610 | C | A | 3 | a0001c0001t0001g0179 a0001c0005t0006g0038 a0005c0010t0001g0042 |
3 | HG01884.hp1 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.486-36334C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878610 | |||||||
| chr16:22878610 | C | CA | 87 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(84): Show |
87 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.486-36325dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22878610 | ||||||
| chr16:22878612 | A | C | 6 | a0001c0001t0001g0323 a0001c0001t0004g0184 a0001c0001t0004g0334 others(3): Show |
6 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-36332A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878612 | |||||||
| chr16:22878713 | T | C | 3 | a0001c0003t0003g0026 a0001c0004t0002g0276 a0001c0006t0006g0025 |
3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.486-36231T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878713 | |||||||
| chr16:22878748 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0217 |
2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.486-36196C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878748 | |||||||
| chr16:22878797 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.486-36147G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878797 | |||||||
| chr16:22878893 | T | A | 1 | a0001c0001t0001g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.486-36051T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878893 | |||||||
| chr16:22878921 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.486-36023G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878921 | |||||||
| chr16:22878982 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.486-35962G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22878982 | |||||||
| chr16:22879242 | T | A | 89 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(86): Show |
89 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.486-35702T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879242 | |||||||
| chr16:22879259 | T | C | 3 | a0001c0001t0001g0297 a0001c0002t0001g0012 a0001c0003t0003g0020 |
3 | HG02055.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.486-35685T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879259 | |||||||
| chr16:22879408 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.486-35536C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879408 | |||||||
| chr16:22879481 | G | A | 1 | a0001c0002t0001g0079 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.486-35463G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879481 | |||||||
| chr16:22879544 | G | T | 3 | a0001c0003t0003g0026 a0001c0004t0002g0276 a0001c0006t0006g0025 |
3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.486-35400G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879544 | |||||||
| chr16:22879563 | C | T | 1 | a0001c0002t0008g0141 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.486-35381C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879563 | |||||||
| chr16:22879676 | G | A | 86 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(83): Show |
86 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.486-35268G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879676 | |||||||
| chr16:22879732 | G | T | 2 | a0001c0001t0001g0320 a0001c0001t0001g0325 |
2 | NA18968.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.486-35212G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879732 | |||||||
| chr16:22879753 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.486-35191G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879753 | |||||||
| chr16:22879763 | C | T | 93 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(90): Show |
93 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.486-35181C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879763 | |||||||
| chr16:22879807 | G | T | 3 | a0001c0002t0001g0103 a0001c0002t0001g0105 a0001c0002t0001g0106 |
3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.486-35137G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879807 | |||||||
| chr16:22879880 | A | C | 3 | a0001c0001t0001g0335 a0001c0002t0001g0045 a0001c0002t0001g0094 |
3 | NA19065.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.486-35064A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22879880 | |||||||
| chr16:22880103 | C | G | 86 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0153 others(83): Show |
86 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.486-34841C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880103 | |||||||
| chr16:22880117 | CTTCTTTC others(3): Show |
C | 8 | a0001c0001t0001g0174 a0001c0001t0001g0296 a0001c0001t0001g0298 others(5): Show |
8 | HG01496.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-34825_486-3481 others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22880117 | ||||||
| chr16:22880140 | G | A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0296 a0001c0001t0001g0298 others(5): Show |
8 | HG01496.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-34804G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880140 | |||||||
| chr16:22880144 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.486-34800G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880144 | |||||||
| chr16:22880188 | G | C | 1 | a0001c0002t0004g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.486-34756G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880188 | |||||||
| chr16:22880226 | A | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-34718A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880226 | |||||||
| chr16:22880254 | A | C | 1 | a0001c0002t0008g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.486-34690A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880254 | |||||||
| chr16:22880285 | G | A | 14 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0171 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-34659G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880285 | |||||||
| chr16:22880381 | T | C | 239 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0148 others(236): Show |
239 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.486-34563T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880381 | |||||||
| chr16:22880528 | T | C | 13 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0180 others(10): Show |
13 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.486-34416T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880528 | |||||||
| chr16:22880552 | C | T | 2 | a0001c0001t0001g0312 a0001c0002t0007g0058 |
2 | HG02071.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.486-34392C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880552 | |||||||
| chr16:22880556 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-34388C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880556 | |||||||
| chr16:22880565 | G | T | 2 | a0001c0001t0001g0148 a0001c0002t0001g0084 |
2 | HG00741.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.486-34379G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880565 | |||||||
| chr16:22880598 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.486-34346C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880598 | |||||||
| chr16:22880647 | C | G | 2 | a0001c0001t0001g0289 a0001c0011t0011g0003 |
2 | HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-34297C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880647 | |||||||
| chr16:22880648 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.486-34296C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880648 | |||||||
| chr16:22880811 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-34133G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880811 | |||||||
| chr16:22880832 | G | A | 2 | a0001c0001t0001g0304 a0001c0003t0003g0035 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34112G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880832 | |||||||
| chr16:22880834 | A | T | 2 | a0001c0001t0001g0304 a0001c0003t0003g0035 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34110A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880834 | |||||||
| chr16:22880841 | G | A | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-34103G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880841 | |||||||
| chr16:22880845 | C | T | 2 | a0001c0001t0001g0304 a0001c0003t0003g0035 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34099C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880845 | |||||||
| chr16:22880846 | A | T | 2 | a0001c0001t0001g0304 a0001c0003t0003g0035 |
2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-34098A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22880846 | |||||||
| chr16:22881214 | A | C | 4 | a0001c0001t0001g0301 a0001c0003t0003g0023 a0001c0004t0002g0181 others(1): Show |
4 | HG02717.hp2 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-33730A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881214 | |||||||
| chr16:22881323 | C | T | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-33621C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881323 | |||||||
| chr16:22881349 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.486-33595C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881349 | |||||||
| chr16:22881362 | A | G | 2 | a0001c0004t0002g0276 a0001c0006t0006g0025 |
2 | HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.486-33582A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881362 | |||||||
| chr16:22881586 | A | G | 229 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(226): Show |
229 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.486-33358A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881586 | |||||||
| chr16:22881644 | T | C | 126 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0151 others(123): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.486-33300T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881644 | |||||||
| chr16:22881770 | C | A | 1 | a0001c0001t0001g0241 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.486-33174C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22881770 | |||||||
| chr16:22881956 | A | ATGTT | 7 | a0001c0001t0001g0177 a0001c0001t0001g0198 a0001c0001t0001g0286 others(4): Show |
7 | HG01891.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-32972_486-3296 others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22881956 | ||||||
| chr16:22882126 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.486-32818G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882126 | |||||||
| chr16:22882170 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(251): Show |
254 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.486-32774A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882170 | |||||||
| chr16:22882424 | G | A | 14 | a0001c0004t0002g0144 a0001c0004t0002g0152 a0001c0004t0002g0155 others(11): Show |
14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-32520G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882424 | |||||||
| chr16:22882554 | C | T | 1 | a0001c0006t0006g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.486-32390C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882554 | |||||||
| chr16:22882716 | G | C | 1 | a0001c0006t0006g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-32228G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882716 | |||||||
| chr16:22882761 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.486-32183G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22882761 | |||||||
| chr16:22883274 | C | G | 3 | a0001c0002t0001g0103 a0001c0002t0001g0105 a0001c0002t0001g0106 |
3 | HG01167.hp1 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.486-31670C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883274 | |||||||
| chr16:22883277 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.486-31667C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883277 | |||||||
| chr16:22883308 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.486-31636C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883308 | |||||||
| chr16:22883319 | C | T | 1 | a0001c0001t0004g0184 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.486-31625C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883319 | |||||||
| chr16:22883633 | G | A | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-31311G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883633 | |||||||
| chr16:22883649 | A | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-31295A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883649 | |||||||
| chr16:22883688 | T | C | 154 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0159 others(151): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.486-31256T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883688 | |||||||
| chr16:22883718 | T | TA | 4 | a0001c0004t0002g0181 a0001c0004t0002g0276 a0001c0004t0002g0281 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-31219dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22883718 | ||||||
| chr16:22883936 | G | A | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-31008G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22883936 | |||||||
| chr16:22884077 | C | A | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-30867C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884077 | |||||||
| chr16:22884077 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.486-30867C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884077 | |||||||
| chr16:22884101 | C | T | 1 | a0001c0004t0002g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-30843C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884101 | |||||||
| chr16:22884129 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486-30815T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884129 | |||||||
| chr16:22884141 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(243): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.486-30803A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884141 | |||||||
| chr16:22884188 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.486-30756G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884188 | |||||||
| chr16:22884406 | T | C | 153 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0159 others(150): Show |
153 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.486-30538T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884406 | |||||||
| chr16:22884458 | T | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0301 a0001c0003t0003g0018 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-30486T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884458 | |||||||
| chr16:22884653 | G | GA | 9 | a0001c0001t0001g0145 a0001c0001t0001g0168 a0001c0001t0001g0188 others(6): Show |
9 | HG02155.hp2 HG02809.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-30284dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884653 | ||||||
| chr16:22884658 | AAATATAT others(12): Show |
A | 6 | a0001c0004t0002g0236 a0001c0005t0002g0004 a0001c0005t0002g0089 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-30285_486-3026 others(23): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884658 | |||||||
| chr16:22884659 | A | T | 9 | a0001c0001t0001g0291 a0001c0004t0002g0144 a0001c0004t0002g0154 others(6): Show |
9 | HG00639.hp1 HG01109.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-30285A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884659 | |||||||
| chr16:22884660 | AT | A | 12 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0173 others(9): Show |
12 | HG01516.hp1 HG02040.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.486-30283delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884660 | |||||||
| chr16:22884661 | T | A | 111 | a0001c0001t0001g0145 a0001c0001t0001g0157 a0001c0001t0001g0158 others(108): Show |
111 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.486-30283T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884661 | |||||||
| chr16:22884663 | T | A | 33 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0163 others(30): Show |
33 | HG00544.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.486-30281T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884663 | |||||||
| chr16:22884665 | T | A | 1 | a0001c0002t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.486-30279T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22884665 | |||||||
| chr16:22884677 | T | TTA | 6 | a0001c0001t0001g0183 a0001c0001t0001g0199 a0001c0002t0001g0008 others(3): Show |
6 | HG01884.hp1 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-30251_486-3025 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884677 | ||||||
| chr16:22884677 | TTA | T | 9 | a0001c0004t0002g0149 a0001c0004t0002g0154 a0001c0004t0002g0290 others(6): Show |
9 | HG01109.hp2 HG01167.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-30251_486-3025 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884677 | ||||||
| chr16:22884846 | C | CT | 134 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0159 others(131): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.486-30085dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22884846 | ||||||
| chr16:22885158 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.486-29786T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885158 | |||||||
| chr16:22885333 | G | GA | 13 | a0001c0004t0002g0149 a0001c0004t0002g0154 a0001c0004t0002g0181 others(10): Show |
13 | HG01109.hp2 HG01167.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.486-29602dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22885333 | ||||||
| chr16:22885373 | A | C | 2 | a0001c0001t0001g0291 a0001c0011t0011g0003 |
2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-29571A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885373 | |||||||
| chr16:22885389 | A | G | 10 | a0001c0001t0001g0173 a0001c0001t0001g0323 a0001c0001t0004g0184 others(7): Show |
10 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-29555A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885389 | |||||||
| chr16:22885502 | C | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-29442C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885502 | |||||||
| chr16:22885580 | C | T | 11 | a0001c0001t0001g0174 a0001c0001t0001g0178 a0001c0001t0001g0296 others(8): Show |
11 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-29364C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885580 | |||||||
| chr16:22885655 | C | A | 2 | a0001c0001t0001g0291 a0001c0011t0011g0003 |
2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-29289C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885655 | |||||||
| chr16:22885656 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.486-29288G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885656 | |||||||
| chr16:22885708 | G | A | 115 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(112): Show |
115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.486-29236G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22885708 | |||||||
| chr16:22886047 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.486-28897G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886047 | |||||||
| chr16:22886064 | C | T | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-28880C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886064 | |||||||
| chr16:22886075 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.486-28869A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886075 | |||||||
| chr16:22886244 | C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-28700C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886244 | |||||||
| chr16:22886474 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(75): Show |
78 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.486-28470G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886474 | |||||||
| chr16:22886476 | G | A | 2 | a0001c0001t0001g0291 a0001c0002t0001g0139 |
2 | HG01261.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.486-28468G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886476 | |||||||
| chr16:22886586 | C | T | 7 | a0001c0001t0001g0222 a0001c0001t0001g0241 a0001c0001t0001g0244 others(4): Show |
7 | NA18979.hp1 NA18979.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-28358C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886586 | |||||||
| chr16:22886627 | A | G | 2 | a0001c0002t0001g0006 a0001c0002t0001g0014 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-28317A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886627 | |||||||
| chr16:22886776 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.486-28168T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22886776 | |||||||
| chr16:22887569 | G | C | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-27375G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887569 | |||||||
| chr16:22887606 | G | A | 117 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(114): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.486-27338G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887606 | |||||||
| chr16:22887623 | G | A | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-27321G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887623 | |||||||
| chr16:22887638 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.486-27306C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887638 | |||||||
| chr16:22887712 | C | T | 3 | a0001c0001t0001g0235 a0001c0001t0001g0320 a0001c0001t0001g0325 |
3 | HG02129.hp2 NA18968.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.486-27232C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887712 | |||||||
| chr16:22887786 | G | GA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(119): Show |
122 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.486-27145dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22887786 | ||||||
| chr16:22887786 | G | GAA | 121 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(118): Show |
121 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.486-27146_486-2714 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22887786 | ||||||
| chr16:22887787 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.486-27157A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887787 | |||||||
| chr16:22887803 | G | T | 1 | a0001c0006t0006g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-27141G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22887803 | |||||||
| chr16:22888030 | G | C | 151 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-26914G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888030 | |||||||
| chr16:22888373 | C | CT | 34 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0178 others(31): Show |
34 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.486-26552dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888373 | ||||||
| chr16:22888378 | T | C | 29 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0180 others(26): Show |
29 | HG01081.hp2 HG01243.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.486-26566T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888378 | |||||||
| chr16:22888384 | T | TTC | 115 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(112): Show |
115 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.486-26559_486-2655 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888384 | ||||||
| chr16:22888384 | T | TTCTTTTT others(4): Show |
127 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(124): Show |
127 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.486-26559_486-2655 others(15): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888384 | ||||||
| chr16:22888384 | T | TTTCTTTT others(5): Show |
4 | a0001c0001t0001g0222 a0001c0001t0001g0244 a0001c0002t0001g0114 others(1): Show |
4 | NA18953.hp1 NA18979.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-26558_486-2655 others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888384 | ||||||
| chr16:22888392 | T | C | 3 | a0001c0001t0001g0211 a0001c0002t0001g0072 a0001c0002t0001g0088 |
3 | HG00438.hp1 NA18612.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.486-26552T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888392 | |||||||
| chr16:22888393 | C | CT | 11 | a0001c0001t0001g0233 a0001c0001t0001g0249 a0001c0001t0001g0259 others(8): Show |
11 | HG00735.hp1 HG01099.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-26540dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22888393 | ||||||
| chr16:22888393 | C | T | 3 | a0001c0001t0001g0211 a0001c0002t0001g0072 a0001c0002t0001g0088 |
3 | HG00438.hp1 NA18612.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.486-26551C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888393 | |||||||
| chr16:22888411 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.486-26533G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888411 | |||||||
| chr16:22888438 | G | T | 10 | a0001c0001t0001g0173 a0001c0001t0001g0323 a0001c0001t0004g0184 others(7): Show |
10 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-26506G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888438 | |||||||
| chr16:22888531 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0350 |
2 | NA18969.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.486-26413C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888531 | |||||||
| chr16:22888533 | T | A | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.486-26411T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888533 | |||||||
| chr16:22888547 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(72): Show |
75 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.486-26397T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888547 | |||||||
| chr16:22888653 | G | A | 1 | a0001c0002t0007g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-26291G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888653 | |||||||
| chr16:22888678 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.486-26266C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888678 | |||||||
| chr16:22888686 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.486-26258C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888686 | |||||||
| chr16:22888687 | G | A | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-26257G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888687 | |||||||
| chr16:22888786 | G | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-26158G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888786 | |||||||
| chr16:22888812 | G | T | 1 | a0001c0001t0001g0324 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.486-26132G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22888812 | |||||||
| chr16:22889123 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.486-25821C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889123 | |||||||
| chr16:22889303 | C | T | 2 | a0001c0001t0001g0291 a0001c0011t0011g0003 |
2 | HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-25641C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889303 | |||||||
| chr16:22889350 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.486-25594T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889350 | |||||||
| chr16:22889543 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.486-25401G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889543 | |||||||
| chr16:22889590 | A | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-25354A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889590 | |||||||
| chr16:22889595 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.486-25349C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22889595 | |||||||
| chr16:22890100 | C | T | 1 | a0001c0002t0001g0119 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.486-24844C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890100 | |||||||
| chr16:22890305 | AT | A | 117 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(114): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.486-24632delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22890305 | ||||||
| chr16:22890393 | A | C | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-24551A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890393 | |||||||
| chr16:22890462 | T | TTAAAGCT others(356): Show |
1 | a0001c0004t0002g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-24469_486-2446 others(367): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22890462 | ||||||
| chr16:22890493 | A | G | 7 | a0001c0001t0001g0167 a0001c0001t0001g0194 a0001c0001t0001g0219 others(4): Show |
7 | HG02523.hp2 NA18957.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-24451A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890493 | |||||||
| chr16:22890530 | G | C | 151 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-24414G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890530 | |||||||
| chr16:22890746 | T | G | 147 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(144): Show |
147 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.486-24198T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890746 | |||||||
| chr16:22890861 | G | A | 15 | a0001c0001t0001g0150 a0001c0001t0001g0201 a0001c0001t0001g0203 others(12): Show |
15 | HG01106.hp2 HG01168.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.486-24083G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890861 | |||||||
| chr16:22890954 | C | T | 1 | a0001c0002t0001g0098 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.486-23990C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22890954 | |||||||
| chr16:22891072 | G | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0291 a0001c0011t0011g0003 |
3 | HG03471.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.486-23872G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891072 | |||||||
| chr16:22891156 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.486-23788G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891156 | |||||||
| chr16:22891173 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.486-23771C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891173 | |||||||
| chr16:22891477 | GA | G | 163 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(160): Show |
163 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.486-23456delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22891477 | ||||||
| chr16:22891572 | A | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0299 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.486-23372A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891572 | |||||||
| chr16:22891573 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.486-23371C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891573 | |||||||
| chr16:22891699 | G | A | 29 | a0001c0001t0001g0167 a0001c0001t0001g0175 a0001c0001t0001g0180 others(26): Show |
29 | HG01081.hp2 HG01243.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.486-23245G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891699 | |||||||
| chr16:22891701 | A | T | 36 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0178 others(33): Show |
36 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-23243A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891701 | |||||||
| chr16:22891886 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.486-23058G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22891886 | |||||||
| chr16:22892090 | C | T | 151 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-22854C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892090 | |||||||
| chr16:22892110 | T | TA | 10 | a0001c0001t0001g0216 a0001c0001t0001g0223 a0001c0001t0001g0228 others(7): Show |
10 | HG01175.hp1 HG02145.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.486-22813dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22892110 | ||||||
| chr16:22892110 | TA | T | 152 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(149): Show |
152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.486-22813delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22892110 | ||||||
| chr16:22892110 | TAA | T | 14 | a0001c0001t0001g0173 a0001c0001t0001g0323 a0001c0001t0004g0184 others(11): Show |
14 | HG00423.hp2 HG01257.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-22814_486-2281 others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22892110 | ||||||
| chr16:22892111 | A | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0250 a0001c0002t0001g0077 others(1): Show |
4 | HG00323.hp1 HG01243.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-22833A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892111 | |||||||
| chr16:22892147 | G | A | 1 | a0001c0002t0005g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.486-22797G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892147 | |||||||
| chr16:22892156 | G | A | 1 | a0001c0006t0006g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-22788G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892156 | |||||||
| chr16:22892167 | A | G | 167 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(164): Show |
167 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.486-22777A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892167 | |||||||
| chr16:22892397 | A | C | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-22547A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892397 | |||||||
| chr16:22892453 | C | T | 330 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(327): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.486-22491C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892453 | |||||||
| chr16:22892468 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0253 |
2 | NA18957.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.486-22476A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892468 | |||||||
| chr16:22892750 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.486-22194A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892750 | |||||||
| chr16:22892800 | T | C | 16 | a0001c0004t0002g0149 a0001c0004t0002g0154 a0001c0004t0002g0236 others(13): Show |
16 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.486-22144T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892800 | |||||||
| chr16:22892834 | G | A | 15 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0171 others(12): Show |
15 | HG00280.hp1 HG00323.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.486-22110G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892834 | |||||||
| chr16:22892864 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.486-22080A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22892864 | |||||||
| chr16:22893040 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.486-21904C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893040 | |||||||
| chr16:22893171 | A | T | 1 | a0001c0001t0001g0300 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.486-21773A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893171 | |||||||
| chr16:22893191 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.486-21753G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893191 | |||||||
| chr16:22893254 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.486-21690T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893254 | |||||||
| chr16:22893258 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.486-21686A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893258 | |||||||
| chr16:22893284 | T | C | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-21660T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893284 | |||||||
| chr16:22893340 | C | T | 4 | a0001c0001t0001g0176 a0001c0001t0001g0301 a0001c0003t0003g0018 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-21604C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893340 | |||||||
| chr16:22893436 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.486-21508C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893436 | |||||||
| chr16:22893634 | C | CT | 324 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(321): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.486-21295dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22893634 | ||||||
| chr16:22893650 | A | T | 3 | a0001c0001t0001g0188 a0001c0002t0001g0308 a0001c0002t0001g0309 |
3 | HG01516.hp2 HG01517.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.486-21294A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893650 | |||||||
| chr16:22893709 | A | G | 1 | a0001c0004t0014g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.486-21235A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893709 | |||||||
| chr16:22893723 | C | A | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-21221C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22893723 | |||||||
| chr16:22894093 | T | C | 1 | a0001c0002t0001g0117 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.486-20851T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894093 | |||||||
| chr16:22894256 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.486-20688C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894256 | |||||||
| chr16:22894302 | C | G | 7 | a0001c0004t0002g0152 a0001c0004t0002g0155 a0001c0004t0002g0258 others(4): Show |
7 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-20642C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894302 | |||||||
| chr16:22894592 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0291 a0001c0011t0011g0003 |
3 | HG02717.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.486-20352A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894592 | |||||||
| chr16:22894735 | T | TA | 7 | a0001c0001t0001g0350 a0001c0001t0004g0267 a0001c0001t0009g0182 others(4): Show |
7 | HG00438.hp2 HG02040.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-20192dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22894735 | ||||||
| chr16:22894959 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.486-19985T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22894959 | |||||||
| chr16:22895017 | G | A | 2 | a0004c0009t0001g0336 a0004c0009t0001g0341 |
2 | NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.486-19927G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895017 | |||||||
| chr16:22895070 | CT | C | 174 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(171): Show |
174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.486-19858delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22895070 | ||||||
| chr16:22895135 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(243): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.486-19809A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895135 | |||||||
| chr16:22895215 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.486-19729G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895215 | |||||||
| chr16:22895328 | G | C | 151 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-19616G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895328 | |||||||
| chr16:22895343 | G | C | 3 | a0001c0001t0001g0304 a0001c0003t0003g0026 a0001c0003t0003g0035 |
3 | HG02572.hp1 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.486-19601G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895343 | |||||||
| chr16:22895769 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.486-19175T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22895769 | |||||||
| chr16:22896061 | C | T | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-18883C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896061 | |||||||
| chr16:22896867 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.486-18077C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896867 | |||||||
| chr16:22896933 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0291 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.486-18011A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896933 | |||||||
| chr16:22896975 | T | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0291 a0001c0011t0011g0003 |
3 | HG03471.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.486-17969T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22896975 | |||||||
| chr16:22896982 | A | AT | 5 | a0001c0001t0001g0228 a0001c0001t0001g0310 a0001c0001t0001g0342 others(2): Show |
5 | HG01099.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.486-17955dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22896982 | ||||||
| chr16:22897106 | C | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-17838C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897106 | |||||||
| chr16:22897152 | C | T | 147 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(144): Show |
147 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.486-17792C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897152 | |||||||
| chr16:22897201 | A | G | 166 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(163): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.486-17743A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897201 | |||||||
| chr16:22897230 | G | A | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-17714G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897230 | |||||||
| chr16:22897347 | G | T | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-17597G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897347 | |||||||
| chr16:22897562 | T | C | 8 | a0001c0001t0001g0323 a0001c0001t0004g0184 a0001c0001t0004g0267 others(5): Show |
8 | HG00423.hp2 HG02071.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-17382T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897562 | |||||||
| chr16:22897650 | CATCTTTG others(270): Show |
C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(244): Show |
247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.486-17291_486-1701 others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22897650 | ||||||
| chr16:22897748 | A | G | 4 | a0001c0001t0001g0269 a0001c0001t0001g0275 a0001c0002t0001g0073 others(1): Show |
4 | HG00140.hp2 HG02683.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-17196A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897748 | |||||||
| chr16:22897930 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(244): Show |
247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.486-17014G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22897930 | |||||||
| chr16:22898240 | G | A | 1 | a0001c0002t0007g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-16704G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22898240 | |||||||
| chr16:22899008 | G | A | 30 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0178 others(27): Show |
30 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.486-15936G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899008 | |||||||
| chr16:22899052 | C | A | 1 | a0001c0003t0003g0021 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-15892C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899052 | |||||||
| chr16:22899647 | A | G | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-15297A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899647 | |||||||
| chr16:22899747 | G | A | 24 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0163 others(21): Show |
24 | HG00544.hp2 HG00621.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.486-15197G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899747 | |||||||
| chr16:22899950 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(237): Show |
240 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.486-14994A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22899950 | |||||||
| chr16:22900232 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(77): Show |
80 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.486-14712G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900232 | |||||||
| chr16:22900401 | G | A | 2 | a0001c0005t0002g0089 a0001c0005t0002g0091 |
2 | HG00738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.486-14543G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900401 | |||||||
| chr16:22900424 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-14520A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900424 | |||||||
| chr16:22900427 | C | T | 163 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(160): Show |
163 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.486-14517C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900427 | |||||||
| chr16:22900485 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.486-14459C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900485 | |||||||
| chr16:22900487 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.486-14457G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900487 | |||||||
| chr16:22900718 | C | T | 1 | a0001c0002t0001g0113 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.486-14226C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900718 | |||||||
| chr16:22900754 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.486-14190G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22900754 | |||||||
| chr16:22901085 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.486-13859G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901085 | |||||||
| chr16:22901183 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0219 a0001c0001t0001g0254 others(1): Show |
4 | HG02523.hp2 NA18962.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-13761A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901183 | |||||||
| chr16:22901453 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0301 a0001c0003t0003g0018 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-13491A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901453 | |||||||
| chr16:22901549 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(244): Show |
247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.486-13395A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901549 | |||||||
| chr16:22901714 | G | A | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-13230G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901714 | |||||||
| chr16:22901906 | A | T | 1 | a0001c0005t0002g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.486-13038A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22901906 | |||||||
| chr16:22902046 | A | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-12898A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902046 | |||||||
| chr16:22902146 | T | C | 11 | a0001c0001t0001g0173 a0001c0001t0001g0256 a0001c0001t0004g0184 others(8): Show |
11 | HG00639.hp1 HG02071.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-12798T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902146 | |||||||
| chr16:22902246 | T | C | 4 | a0001c0001t0001g0274 a0001c0002t0001g0055 a0001c0002t0001g0056 others(1): Show |
4 | HG00558.hp1 HG04184.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-12698T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902246 | |||||||
| chr16:22902277 | G | A | 14 | a0001c0004t0002g0144 a0001c0004t0002g0152 a0001c0004t0002g0155 others(11): Show |
14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-12667G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902277 | |||||||
| chr16:22902526 | A | T | 9 | a0001c0001t0001g0173 a0001c0001t0004g0184 a0001c0001t0004g0267 others(6): Show |
9 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-12418A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902526 | |||||||
| chr16:22902620 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0307 |
2 | HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.486-12324T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902620 | |||||||
| chr16:22902666 | T | C | 10 | a0001c0001t0001g0145 a0001c0001t0001g0179 a0001c0001t0001g0289 others(7): Show |
10 | HG02055.hp1 HG02647.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-12278T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902666 | |||||||
| chr16:22902721 | A | T | 153 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(150): Show |
153 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.486-12223A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902721 | |||||||
| chr16:22902721 | AT | A | 12 | a0001c0001t0001g0173 a0001c0001t0001g0256 a0001c0001t0004g0184 others(9): Show |
12 | HG00639.hp1 HG02071.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.486-12215delT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22902721 | ||||||
| chr16:22902722 | T | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0180 a0001c0001t0001g0193 others(1): Show |
4 | HG01243.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-12222T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902722 | |||||||
| chr16:22902990 | C | T | 1 | a0001c0004t0002g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-11954C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22902990 | |||||||
| chr16:22903339 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(76): Show |
79 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.486-11605G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903339 | |||||||
| chr16:22903387 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-11557G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903387 | |||||||
| chr16:22903568 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.486-11376G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903568 | |||||||
| chr16:22903605 | T | C | 34 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0178 others(31): Show |
34 | HG00140.hp2 HG01175.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.486-11339T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903605 | |||||||
| chr16:22903627 | A | G | 155 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(152): Show |
155 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.486-11317A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903627 | |||||||
| chr16:22903638 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-11306A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903638 | |||||||
| chr16:22903644 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.486-11300C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903644 | |||||||
| chr16:22903819 | G | A | 1 | a0001c0006t0006g0016 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.486-11125G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903819 | |||||||
| chr16:22903825 | C | T | 157 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(154): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.486-11119C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903825 | |||||||
| chr16:22903911 | A | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-11033A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903911 | |||||||
| chr16:22903924 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(244): Show |
247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.486-11020T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22903924 | |||||||
| chr16:22904006 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(342): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.486-10938A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904006 | |||||||
| chr16:22904293 | C | T | 1 | a0001c0001t0004g0267 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.486-10651C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904293 | |||||||
| chr16:22904298 | C | A | 2 | a0001c0004t0002g0305 a0001c0006t0006g0027 |
2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.486-10646C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904298 | |||||||
| chr16:22904320 | C | T | 9 | a0001c0001t0001g0173 a0001c0001t0004g0184 a0001c0001t0004g0267 others(6): Show |
9 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-10624C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904320 | |||||||
| chr16:22904321 | G | A | 1 | a0001c0004t0002g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-10623G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904321 | |||||||
| chr16:22904431 | G | A | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-10513G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904431 | |||||||
| chr16:22904468 | T | C | 172 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(169): Show |
172 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.486-10476T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904468 | |||||||
| chr16:22904511 | C | T | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-10433C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904511 | |||||||
| chr16:22904545 | A | T | 1 | a0001c0001t0001g0322 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.486-10399A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904545 | |||||||
| chr16:22904603 | C | T | 148 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(145): Show |
148 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.486-10341C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904603 | |||||||
| chr16:22904889 | C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-10055C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904889 | |||||||
| chr16:22904926 | C | A | 10 | a0001c0001t0001g0205 a0001c0001t0001g0210 a0001c0001t0001g0278 others(7): Show |
10 | HG00741.hp1 HG01070.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-10018C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904926 | |||||||
| chr16:22904941 | A | G | 3 | a0001c0001t0001g0211 a0001c0002t0001g0072 a0001c0002t0001g0088 |
3 | HG00438.hp1 NA18612.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.486-10003A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904941 | |||||||
| chr16:22904980 | T | C | 1 | a0001c0002t0004g0069 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.486-9964T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22904980 | |||||||
| chr16:22905162 | T | C | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9782T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905162 | |||||||
| chr16:22905241 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.486-9703G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905241 | |||||||
| chr16:22905251 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.486-9693C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905251 | |||||||
| chr16:22905330 | C | T | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9614C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905330 | |||||||
| chr16:22905343 | C | T | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9601C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905343 | |||||||
| chr16:22905369 | A | G | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-9575A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905369 | |||||||
| chr16:22905424 | G | T | 1 | a0001c0001t0009g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.486-9520G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905424 | |||||||
| chr16:22905459 | C | A | 1 | a0005c0010t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486-9485C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905459 | |||||||
| chr16:22905623 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0014 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-9321C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905623 | |||||||
| chr16:22905624 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.486-9320G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905624 | |||||||
| chr16:22905730 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.486-9214G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905730 | |||||||
| chr16:22905866 | G | A | 1 | a0001c0002t0004g0069 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.486-9078G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905866 | |||||||
| chr16:22905880 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.486-9064T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905880 | |||||||
| chr16:22905998 | C | T | 2 | a0001c0002t0001g0006 a0001c0002t0001g0014 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-8946C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22905998 | |||||||
| chr16:22906095 | G | A | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-8849G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906095 | |||||||
| chr16:22906113 | C | T | 150 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(147): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.486-8831C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906113 | |||||||
| chr16:22906197 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.486-8747C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906197 | |||||||
| chr16:22906268 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.486-8676G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906268 | |||||||
| chr16:22906367 | C | CTAAA | 3 | a0001c0001t0001g0291 a0001c0002t0001g0006 a0001c0002t0001g0014 |
3 | HG03225.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.486-8552_486-8549d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | ||||||
| chr16:22906367 | C | CTAAATAA others(1): Show |
4 | a0001c0001t0001g0306 a0001c0002t0001g0112 a0001c0002t0001g0115 others(1): Show |
4 | HG02886.hp1 HG03453.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-8556_486-8549d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | ||||||
| chr16:22906367 | C | CTAAATAA others(5): Show |
14 | a0001c0001t0001g0170 a0001c0001t0001g0213 a0001c0001t0001g0221 others(11): Show |
14 | HG01952.hp2 HG01975.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.486-8560_486-8549d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | ||||||
| chr16:22906367 | C | CTAAATAA others(9): Show |
243 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(240): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.486-8564_486-8549d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | ||||||
| chr16:22906367 | C | CTAAATAA others(13): Show |
63 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0180 others(60): Show |
63 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.486-8568_486-8549d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906367 | ||||||
| chr16:22906379 | A | ATAAATAA others(9): Show |
1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-8550_486-8549i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22906379 | ||||||
| chr16:22906461 | T | A | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-8483T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906461 | |||||||
| chr16:22906573 | G | A | 2 | a0001c0001t0001g0148 a0001c0002t0001g0084 |
2 | HG00741.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.486-8371G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906573 | |||||||
| chr16:22906585 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0299 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.486-8359T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906585 | |||||||
| chr16:22906595 | C | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-8349C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906595 | |||||||
| chr16:22906662 | C | G | 4 | a0001c0001t0001g0318 a0001c0001t0001g0321 a0001c0002t0001g0094 others(1): Show |
4 | NA18942.hp1 NA19009.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-8282C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906662 | |||||||
| chr16:22906818 | C | A | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-8126C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906818 | |||||||
| chr16:22906826 | G | T | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-8118G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906826 | |||||||
| chr16:22906876 | T | C | 3 | a0001c0001t0001g0291 a0001c0002t0001g0006 a0001c0002t0001g0014 |
3 | HG03225.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.486-8068T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22906876 | |||||||
| chr16:22907036 | G | T | 1 | a0001c0004t0002g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-7908G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907036 | |||||||
| chr16:22907427 | A | G | 151 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-7517A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907427 | |||||||
| chr16:22907472 | T | A | 14 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0001g0256 others(11): Show |
14 | HG02071.hp1 HG02080.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-7472T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907472 | |||||||
| chr16:22907531 | G | GT | 3 | a0001c0001t0001g0291 a0001c0002t0001g0006 a0001c0002t0001g0014 |
3 | HG03225.hp2 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.486-7411dupT | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22907531 | ||||||
| chr16:22907943 | G | C | 6 | a0001c0001t0001g0191 a0001c0001t0001g0293 a0001c0001t0001g0294 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-7001G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22907943 | |||||||
| chr16:22908031 | G | C | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-6913G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908031 | |||||||
| chr16:22908059 | C | T | 1 | a0001c0001t0004g0334 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.486-6885C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908059 | |||||||
| chr16:22908075 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.486-6869T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908075 | |||||||
| chr16:22908142 | A | G | 151 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-6802A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908142 | |||||||
| chr16:22908227 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.486-6717G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908227 | |||||||
| chr16:22908385 | GTGGGGTG others(4): Show |
G | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.486-6557_486-6547d others(13): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22908385 | ||||||
| chr16:22908461 | T | G | 19 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0162 others(16): Show |
19 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.486-6483T>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908461 | |||||||
| chr16:22908496 | C | G | 2 | a0001c0002t0001g0006 a0001c0002t0001g0014 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-6448C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908496 | |||||||
| chr16:22908565 | C | G | 1 | a0001c0002t0001g0112 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.486-6379C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908565 | |||||||
| chr16:22908657 | C | T | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-6287C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908657 | |||||||
| chr16:22908771 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0203 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.486-6173A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908771 | |||||||
| chr16:22908810 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0299 |
2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.486-6134G>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908810 | |||||||
| chr16:22908825 | A | C | 14 | a0001c0004t0002g0144 a0001c0004t0002g0152 a0001c0004t0002g0155 others(11): Show |
14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-6119A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908825 | |||||||
| chr16:22908844 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.486-6100A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908844 | |||||||
| chr16:22908990 | G | A | 4 | a0001c0004t0002g0181 a0001c0004t0002g0276 a0001c0004t0002g0281 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-5954G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22908990 | |||||||
| chr16:22909148 | C | G | 1 | a0001c0002t0001g0115 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.486-5796C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909148 | |||||||
| chr16:22909183 | T | C | 151 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(148): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.486-5761T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909183 | |||||||
| chr16:22909283 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(277): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.486-5661G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909283 | |||||||
| chr16:22909380 | G | T | 1 | a0001c0002t0001g0119 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.486-5564G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909380 | |||||||
| chr16:22909483 | T | C | 2 | a0001c0002t0001g0007 a0001c0002t0001g0122 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.486-5461T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909483 | |||||||
| chr16:22909531 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(72): Show |
75 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.486-5413C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909531 | |||||||
| chr16:22909740 | A | C | 1 | a0001c0001t0004g0184 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.486-5204A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909740 | |||||||
| chr16:22909898 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.486-5046G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909898 | |||||||
| chr16:22909953 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.486-4991C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22909953 | |||||||
| chr16:22910037 | C | CA | 11 | a0001c0001t0001g0176 a0001c0001t0001g0221 a0001c0001t0001g0256 others(8): Show |
11 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-4890dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | ||||||
| chr16:22910037 | C | CAA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(80): Show |
83 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.486-4891_486-4890d others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | ||||||
| chr16:22910037 | C | CAAA | 131 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(128): Show |
131 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.486-4892_486-4890d others(5): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | ||||||
| chr16:22910037 | C | CAAAA | 11 | a0001c0001t0001g0350 a0001c0001t0009g0182 a0001c0002t0001g0055 others(8): Show |
11 | HG00639.hp1 HG01361.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.486-4893_486-4890d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22910037 | ||||||
| chr16:22910159 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0322 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.486-4785A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910159 | |||||||
| chr16:22910258 | T | C | 8 | a0001c0001t0001g0210 a0001c0001t0001g0278 a0001c0002t0001g0050 others(5): Show |
8 | HG00741.hp1 HG01070.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-4686T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910258 | |||||||
| chr16:22910277 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.486-4667A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910277 | |||||||
| chr16:22910376 | A | C | 2 | a0001c0001t0001g0216 a0001c0003t0003g0034 |
2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.486-4568A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910376 | |||||||
| chr16:22910575 | T | C | 15 | a0001c0001t0001g0209 a0001c0001t0001g0316 a0001c0001t0004g0165 others(12): Show |
15 | HG00280.hp2 HG00738.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.486-4369T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910575 | |||||||
| chr16:22910690 | A | T | 2 | a0001c0001t0001g0335 a0001c0002t0001g0045 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.486-4254A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910690 | |||||||
| chr16:22910846 | C | T | 1 | a0001c0004t0002g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.486-4098C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910846 | |||||||
| chr16:22910897 | T | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0291 a0001c0001t0001g0301 others(2): Show |
5 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-4047T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22910897 | |||||||
| chr16:22911059 | G | T | 1 | a0001c0001t0001g0317 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.486-3885G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911059 | |||||||
| chr16:22911241 | A | G | 1 | a0001c0002t0001g0045 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.486-3703A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911241 | |||||||
| chr16:22911257 | T | C | 13 | a0001c0001t0001g0185 a0001c0001t0001g0211 a0001c0001t0001g0215 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.486-3687T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911257 | |||||||
| chr16:22911343 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-3601A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911343 | |||||||
| chr16:22911530 | A | G | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-3414A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911530 | |||||||
| chr16:22911579 | C | T | 4 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0225 others(1): Show |
4 | NA18946.hp1 NA18960.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-3365C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911579 | |||||||
| chr16:22911592 | C | T | 5 | a0001c0001t0001g0176 a0001c0001t0001g0291 a0001c0001t0001g0301 others(2): Show |
5 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-3352C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911592 | |||||||
| chr16:22911657 | C | A | 1 | a0001c0002t0001g0082 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.486-3287C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911657 | |||||||
| chr16:22911695 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486-3249A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911695 | |||||||
| chr16:22911771 | C | G | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-3173C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911771 | |||||||
| chr16:22911924 | C | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0148 a0001c0001t0001g0169 others(22): Show |
25 | HG00423.hp2 HG00609.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.486-3020C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911924 | |||||||
| chr16:22911948 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.486-2996C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911948 | |||||||
| chr16:22911990 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(74): Show |
77 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.486-2954T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911990 | |||||||
| chr16:22911996 | C | A | 14 | a0001c0004t0002g0144 a0001c0004t0002g0152 a0001c0004t0002g0155 others(11): Show |
14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-2948C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22911996 | |||||||
| chr16:22912144 | A | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(225): Show |
228 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.486-2800A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912144 | |||||||
| chr16:22912372 | T | C | 33 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0178 others(30): Show |
33 | HG00140.hp2 HG01175.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.486-2572T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912372 | |||||||
| chr16:22912464 | A | G | 10 | a0001c0001t0001g0173 a0001c0001t0001g0256 a0001c0001t0004g0184 others(7): Show |
10 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-2480A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912464 | |||||||
| chr16:22912486 | C | G | 2 | a0001c0002t0001g0006 a0001c0002t0001g0014 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-2458C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912486 | |||||||
| chr16:22912530 | G | A | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-2414G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912530 | |||||||
| chr16:22912538 | G | A | 14 | a0001c0004t0002g0144 a0001c0004t0002g0152 a0001c0004t0002g0155 others(11): Show |
14 | HG00735.hp2 HG01081.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.486-2406G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912538 | |||||||
| chr16:22912664 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.486-2280G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912664 | |||||||
| chr16:22912771 | T | A | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.486-2173T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912771 | |||||||
| chr16:22912807 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0217 |
2 | HG01175.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.486-2137C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912807 | |||||||
| chr16:22912951 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.486-1993G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22912951 | |||||||
| chr16:22913066 | T | C | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-1878T>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913066 | |||||||
| chr16:22913123 | A | AAAGG | 26 | a0001c0001t0001g0209 a0001c0001t0001g0213 a0001c0001t0001g0245 others(23): Show |
26 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.486-1796_486-1793d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | ||||||
| chr16:22913123 | A | AAAGGAAG others(1): Show |
74 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(71): Show |
74 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.486-1800_486-1793d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | ||||||
| chr16:22913123 | A | AAAGGAAG others(5): Show |
24 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(21): Show |
24 | HG00423.hp1 HG00609.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.486-1804_486-1793d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | ||||||
| chr16:22913123 | A | AAAGGAAG others(9): Show |
6 | a0001c0001t0001g0222 a0001c0001t0001g0242 a0001c0001t0001g0338 others(3): Show |
6 | HG00544.hp1 HG02451.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-1808_486-1793d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | ||||||
| chr16:22913123 | A | AAAGGAAG others(13): Show |
2 | a0001c0004t0002g0281 a0001c0005t0002g0041 |
2 | HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.486-1812_486-1793d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | ||||||
| chr16:22913123 | A | AAAGGAAG others(17): Show |
1 | a0001c0006t0006g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.486-1816_486-1793d others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | ||||||
| chr16:22913123 | AAAGG | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0264 a0001c0002t0001g0007 |
3 | HG01099.hp1 HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.486-1796_486-1793d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913123 | ||||||
| chr16:22913131 | G | T | 1 | a0001c0002t0001g0080 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.486-1813G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913131 | |||||||
| chr16:22913144 | A | AAGGGAGG others(1): Show |
16 | a0001c0001t0001g0147 a0001c0001t0001g0163 a0001c0001t0001g0168 others(13): Show |
16 | HG00544.hp2 HG02040.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.486-1797_486-1796i others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913144 | ||||||
| chr16:22913144 | A | AAGGGAGG others(5): Show |
3 | a0001c0001t0001g0160 a0001c0001t0001g0206 a0001c0001t0001g0224 |
3 | HG03704.hp1 HG03710.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.486-1797_486-1796i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913144 | ||||||
| chr16:22913144 | A | AAGGGAGG others(9): Show |
4 | a0001c0001t0001g0145 a0001c0001t0001g0326 a0001c0002t0001g0054 others(1): Show |
4 | HG02809.hp2 NA19004.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-1797_486-1796i others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913144 | ||||||
| chr16:22913144 | A | G | 1 | a0001c0002t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486-1800A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913144 | |||||||
| chr16:22913148 | A | AAGGAAGG others(8): Show |
1 | a0001c0002t0001g0095 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.486-1793_486-1792i others(17): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGAAGG others(29): Show |
1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-1793_486-1792i others(38): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGAAGG others(13): Show |
1 | a0001c0004t0002g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486-1793_486-1792i others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGAAGG others(5): Show |
1 | a0001c0001t0001g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.486-1793_486-1792i others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGG | 6 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0180 others(3): Show |
6 | HG01243.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-1763_486-1760d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGGAGG others(1): Show |
4 | a0001c0001t0001g0304 a0001c0002t0003g0039 a0001c0003t0003g0026 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1767_486-1760d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGGAGG others(5): Show |
3 | a0001c0001t0001g0282 a0001c0003t0003g0019 a0001c0003t0003g0021 |
3 | HG01891.hp1 HG02523.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.486-1771_486-1760d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGGAGG others(9): Show |
10 | a0001c0001t0001g0185 a0001c0001t0001g0197 a0001c0001t0001g0199 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-1775_486-1760d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGGAGG others(13): Show |
2 | a0001c0001t0001g0179 a0001c0001t0001g0289 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-1779_486-1760d others(22): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGGAGG others(17): Show |
1 | a0001c0002t0001g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.486-1783_486-1760d others(26): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | AAGGGAGG others(21): Show |
1 | a0005c0010t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.486-1787_486-1760d others(30): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913148 | A | G | 36 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0160 others(33): Show |
36 | HG00544.hp2 HG00621.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.486-1796A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913148 | |||||||
| chr16:22913148 | AAGGG | A | 19 | a0001c0001t0001g0167 a0001c0001t0001g0174 a0001c0001t0001g0178 others(16): Show |
19 | HG00438.hp1 HG01261.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.486-1763_486-1760d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913148 | ||||||
| chr16:22913152 | G | A | 114 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(111): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.486-1792G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913152 | |||||||
| chr16:22913156 | G | A | 24 | a0001c0001t0001g0213 a0001c0001t0001g0271 a0001c0004t0002g0144 others(21): Show |
24 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.486-1788G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913156 | |||||||
| chr16:22913160 | G | A | 4 | a0001c0004t0002g0144 a0001c0004t0002g0305 a0001c0006t0006g0016 others(1): Show |
4 | HG02970.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1784G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913160 | |||||||
| chr16:22913172 | GAGGGAGG others(9): Show |
G | 2 | a0001c0005t0002g0009 a0001c0005t0006g0038 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.486-1768_486-1753d others(18): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913172 | ||||||
| chr16:22913176 | GAGGGAGG others(5): Show |
G | 2 | a0001c0001t0001g0291 a0001c0004t0014g0237 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.486-1764_486-1753d others(14): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913176 | ||||||
| chr16:22913180 | GAGGGCGG others(1): Show |
G | 11 | a0001c0001t0001g0301 a0001c0001t0007g0212 a0001c0003t0003g0023 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-1760_486-1753d others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913180 | ||||||
| chr16:22913181 | AGGGC | A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0299 a0001c0001t0001g0306 |
3 | HG02451.hp1 HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.486-1760_486-1757d others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22913181 | ||||||
| chr16:22913185 | C | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(210): Show |
213 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.486-1759C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913185 | |||||||
| chr16:22913188 | A | G | 139 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(136): Show |
139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.486-1756A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913188 | |||||||
| chr16:22913220 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(76): Show |
79 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.486-1724C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913220 | |||||||
| chr16:22913253 | G | A | 9 | a0001c0004t0002g0149 a0001c0004t0002g0154 a0001c0004t0002g0290 others(6): Show |
9 | HG01109.hp2 HG01167.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.486-1691G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913253 | |||||||
| chr16:22913298 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(225): Show |
228 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.486-1646A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913298 | |||||||
| chr16:22913381 | G | T | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1563G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913381 | |||||||
| chr16:22913394 | A | T | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1550A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913394 | |||||||
| chr16:22913399 | A | T | 1 | a0001c0011t0011g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486-1545A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913399 | |||||||
| chr16:22913424 | A | T | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1520A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913424 | |||||||
| chr16:22913426 | C | A | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1518C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913426 | |||||||
| chr16:22913427 | C | A | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1517C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913427 | |||||||
| chr16:22913431 | C | G | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1513C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913431 | |||||||
| chr16:22913433 | C | G | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1511C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913433 | |||||||
| chr16:22913435 | T | A | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1509T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913435 | |||||||
| chr16:22913445 | C | T | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1499C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913445 | |||||||
| chr16:22913446 | C | A | 1 | a0001c0004t0002g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.486-1498C>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913446 | |||||||
| chr16:22913503 | G | A | 5 | a0001c0004t0002g0144 a0001c0005t0002g0009 a0001c0005t0002g0060 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-1441G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913503 | |||||||
| chr16:22913575 | A | C | 1 | a0001c0004t0002g0281 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.486-1369A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913575 | |||||||
| chr16:22913637 | T | A | 2 | a0001c0005t0002g0010 a0001c0005t0006g0040 |
2 | HG01167.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.486-1307T>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913637 | |||||||
| chr16:22913870 | C | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0301 a0001c0003t0003g0018 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-1074C>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913870 | |||||||
| chr16:22913892 | C | T | 5 | a0001c0004t0002g0144 a0001c0005t0002g0009 a0001c0005t0002g0060 others(2): Show |
5 | HG01884.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-1052C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913892 | |||||||
| chr16:22913900 | G | A | 39 | a0001c0004t0002g0144 a0001c0004t0002g0149 a0001c0004t0002g0152 others(36): Show |
39 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.486-1044G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913900 | |||||||
| chr16:22913961 | A | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(74): Show |
77 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.486-983A>C | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22913961 | |||||||
| chr16:22914022 | C | T | 1 | a0001c0006t0006g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.486-922C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914022 | |||||||
| chr16:22914486 | G | T | 10 | a0001c0001t0001g0173 a0001c0001t0001g0256 a0001c0001t0004g0184 others(7): Show |
10 | HG02071.hp1 HG02080.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.486-458G>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914486 | |||||||
| chr16:22914606 | G | GAGATGGG others(1): Show |
94 | a0001c0001t0001g0001 a0001c0001t0001g0145 a0001c0001t0001g0146 others(91): Show |
94 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.486-301_486-294dup others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914606 | ||||||
| chr16:22914606 | G | GAGATGGG others(9): Show |
2 | a0001c0006t0006g0024 a0001c0006t0006g0025 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.486-309_486-294dup others(16): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914606 | ||||||
| chr16:22914615 | A | T | 7 | a0001c0001t0001g0177 a0001c0001t0001g0198 a0001c0001t0001g0286 others(4): Show |
7 | HG01891.hp2 HG01934.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.486-329A>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914615 | |||||||
| chr16:22914649 | A | G | 2 | a0001c0002t0001g0006 a0001c0002t0001g0014 |
2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.486-295A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914649 | |||||||
| chr16:22914716 | G | A | 20 | a0001c0004t0002g0149 a0001c0004t0002g0154 a0001c0004t0002g0186 others(17): Show |
20 | HG00639.hp1 HG00738.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.486-228G>A | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914716 | |||||||
| chr16:22914736 | C | CA | 17 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0218 others(14): Show |
17 | HG00735.hp1 HG01943.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.486-180dupA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0160 a0001c0001t0001g0168 a0001c0001t0001g0297 others(5): Show |
8 | HG00544.hp2 HG02965.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-188_486-180dup others(9): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | C | CAAAAAAA others(3): Show |
18 | a0001c0001t0001g0147 a0001c0001t0001g0179 a0001c0001t0001g0188 others(15): Show |
18 | HG02040.hp1 HG02055.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.486-189_486-180dup others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0289 a0001c0001t0001g0337 a0001c0002t0001g0013 |
3 | HG03098.hp1 NA19006.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.486-190_486-180dup others(11): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.486-191_486-180dup others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | CA | C | 107 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.486-180delA | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | CAA | C | 8 | a0001c0001t0001g0162 a0001c0001t0001g0170 a0001c0001t0001g0183 others(5): Show |
8 | HG00738.hp1 HG01943.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-181_486-180del others(2): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | CAAA | C | 6 | a0001c0001t0001g0195 a0001c0001t0001g0284 a0001c0001t0007g0156 others(3): Show |
6 | HG03225.hp2 NA18942.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-182_486-180del others(3): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | CAAAA | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0146 a0001c0001t0001g0148 others(28): Show |
31 | HG00423.hp2 HG00609.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.486-183_486-180del others(4): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914736 | CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0001g0191 a0001c0001t0001g0293 a0001c0001t0001g0294 others(8): Show |
11 | HG00621.hp2 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-187_486-180del others(8): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914736 | ||||||
| chr16:22914763 | A | AAAAAAAA others(5): Show |
2 | a0001c0004t0002g0181 a0001c0004t0002g0276 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.486-180_486-179ins others(12): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | ||||||
| chr16:22914763 | A | AAAAAAAA others(4): Show |
3 | a0001c0004t0002g0258 a0001c0004t0002g0281 a0001c0006t0006g0025 |
3 | HG02809.hp1 HG03486.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.486-180_486-179ins others(11): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | ||||||
| chr16:22914763 | A | AAAAAAAA others(3): Show |
6 | a0001c0004t0002g0290 a0001c0004t0002g0302 a0001c0004t0014g0237 others(3): Show |
6 | HG01109.hp2 HG02486.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-180_486-179ins others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | ||||||
| chr16:22914763 | A | AAAAAAAA others(3): Show |
1 | a0001c0005t0006g0040 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.486-180_486-179ins others(10): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | ||||||
| chr16:22914763 | A | AAAAAAG | 7 | a0001c0004t0002g0186 a0001c0005t0002g0004 a0001c0005t0002g0091 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-180_486-179ins others(6): Show |
HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr16 | 22914763 | ||||||
| chr16:22914763 | A | G | 4 | a0001c0004t0002g0144 a0001c0006t0006g0016 a0001c0006t0006g0022 others(1): Show |
4 | HG02970.hp1 HG02976.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-181A>G | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914763 | |||||||
| chr16:22914894 | C | T | 2 | a0001c0001t0004g0267 a0001c0001t0004g0268 |
2 | HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.486-50C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914894 | |||||||
| chr16:22914936 | C | T | 13 | a0001c0001t0001g0185 a0001c0001t0001g0211 a0001c0001t0001g0215 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG01099.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.486-8C>T | HS3ST2 | ENSG00000122254.7 | transcript | ENST00000261374.4 | protein_coding | 1/1 | chr16 | 22914936 |