Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51251 |
| ensemblid | ENSG00000122643.23 |
| hgncid | 17820 |
| symbol | NT5C3A |
| name | 5'-nucleotidase, cytosolic IIIA |
| refseq_nuc | NM_001002010.5 |
| refseq_prot | NP_001002010.2 |
| ensembl_nuc | ENST00000610140.7 |
| ensembl_prot | ENSP00000476480.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 33014130 |
| end | 33062776 |
| strand | - |
| ver | v1.2 |
| region | chr7:33014130-33062776 |
| region5000 | chr7:33009130-33067776 |
| regionname0 | NT5C3A_chr7_33014130_33062776 |
| regionname5000 | NT5C3A_chr7_33009130_33067776 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 331 | 398 | 94 | 69 | 181 | 14 | 38 | 145 | NT5C3A_chr7_33009130_33067776 | NT5C3A | MDRAA others(326): Show |
chr7 | 33009130 | 33067776 |
| a0002 | 0/0 | 331 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | MDRAA others(326): Show |
chr7 | 33009130 | 33067776 |
| a0003 | 0/0 | 331 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | MDRAA others(326): Show |
chr7 | 33009130 | 33067776 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 993 | 224 | 61 | 46 | 84 | 10 | 22 | NT5C3A_chr7_33009130_33067776 | NT5C3A | ATGGA others(988): Show |
chr7 | 33009130 | 33067776 | ||
| a0001c0002 | 1/0 | 993 | 164 | 23 | 23 | 97 | 4 | 16 | NT5C3A_chr7_33009130_33067776 | NT5C3A | ATGGA others(988): Show |
chr7 | 33009130 | 33067776 | ||
| a0001c0003 | 0/0 | 993 | 9 | 9 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | ATGGA others(988): Show |
chr7 | 33009130 | 33067776 | ||
| a0001c0004 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | ATGGA others(988): Show |
chr7 | 33009130 | 33067776 | ||
| a0002c0005 | 0/0 | 993 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | ATGGA others(988): Show |
chr7 | 33009130 | 33067776 | ||
| a0003c0006 | 0/0 | 993 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | ATGGA others(988): Show |
chr7 | 33009130 | 33067776 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1671 | 220 | 61 | 45 | 81 | 10 | 22 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0001t0007 | 0/0 | 1671 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0001t0013 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0001t0014 | 0/0 | 1667 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1662): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0001 | 0/0 | 1671 | 30 | 2 | 1 | 27 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0002 | 1/0 | 1667 | 63 | 0 | 13 | 42 | 3 | 4 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1662): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0003 | 0/0 | 1665 | 50 | 8 | 7 | 22 | 1 | 12 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1660): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0004 | 0/0 | 1666 | 10 | 10 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1661): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0005 | 0/0 | 1666 | 5 | 3 | 2 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1661): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0006 | 0/0 | 1671 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0008 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0010 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1662): Show |
chr7 | 33009130 | 33067776 |
| a0001c0002t0011 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1662): Show |
chr7 | 33009130 | 33067776 |
| a0001c0003t0001 | 0/0 | 1671 | 8 | 8 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0003t0009 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0001c0004t0012 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1660): Show |
chr7 | 33009130 | 33067776 |
| a0002c0005t0001 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| a0003c0006t0001 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | GCTTC others(1666): Show |
chr7 | 33009130 | 33067776 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0352 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0007g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0013g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0014g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0001 | 1/0 | 5 | 0 | 2 | 0 | 2 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0006g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0006g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0006g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0010g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0004t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0002c0005t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0003c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0322 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0138 | EUR | FIN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00438 | hp2 | a0001 | c0002 | t0006 | g0380 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0301 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0144 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0177 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01069 | hp2 | a0002 | c0005 | t0001 | g0017 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0151 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0079 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0375 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0103 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01255 | hp1 | a0001 | c0002 | t0005 | g0110 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0054 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0074 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0154 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0106 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0113 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0008 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0122 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0120 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0134 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0107 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0285 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0133 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0130 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0123 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | CDX | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0373 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0102 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0311 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02523 | hp2 | a0001 | c0002 | t0010 | g0085 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0377 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0126 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0108 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0116 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0362 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0333 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0114 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0002 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0109 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0143 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0068 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03209 | hp1 | a0001 | c0004 | t0012 | g0016 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0069 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0115 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0053 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0124 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0145 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0002 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0372 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0129 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0155 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0156 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0150 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0279 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03579 | hp2 | a0001 | c0003 | t0009 | g0278 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0371 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0139 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0141 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0096 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0090 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0101 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0152 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0153 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0142 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0131 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18939 | hp2 | a0001 | c0002 | t0008 | g0035 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18940 | hp1 | a0001 | c0002 | t0011 | g0075 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0303 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18970 | hp2 | a0001 | c0002 | t0006 | g0378 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0117 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0119 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18987 | hp2 | a0003 | c0006 | t0001 | g0199 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18988 | hp1 | a0001 | c0001 | t0013 | g0287 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19091 | hp2 | a0001 | c0002 | t0006 | g0379 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ASW | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0332 | AFR | ASW | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0343 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0147 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0331 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0352 | REF | REF | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0001 | REF | REF | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33017477 | C | T | 1 | a0003 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.655G>A | p.Val219Ile | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/9 | 726/1667 | 655/996 | 219/331 | chr7 | 33017477 | |||
| chr7:33062615 | A | G | 1 | a0002 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.91T>C | p.Phe31Leu | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/9 | 162/1667 | 91/996 | 31/331 | chr7 | 33062615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33021304 | A | G | 1 | a0001c0003 | 9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
synonymous_variant | LOW | c.408T>C | p.Thr136Thr | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/9 | 479/1667 | 408/996 | 136/331 | chr7 | 33021304 | |||
| chr7:33021334 | A | G | 4 | a0001c0001 a0001c0003 a0002c0005 others(1): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
synonymous_variant | LOW | c.378T>C | p.Tyr126Tyr | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/9 | 449/1667 | 378/996 | 126/331 | chr7 | 33021334 | |||
| chr7:33062685 | C | T | 1 | a0001c0004 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.21G>A | p.Ala7Ala | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/9 | 92/1667 | 21/996 | 7/331 | chr7 | 33062685 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33014138 | G | T | 1 | a0001c0002t0011 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 592 | chr7 | 33014138 | ||||||
| chr7:33014248 | A | G | 1 | a0001c0002t0010 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 482 | chr7 | 33014248 | ||||||
| chr7:33014302 | T | C | 1 | a0001c0004t0012 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 428 | chr7 | 33014302 | ||||||
| chr7:33014321 | A | G | 1 | a0001c0002t0005 | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*409T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 409 | chr7 | 33014321 | ||||||
| chr7:33014415 | G | A | 2 | a0001c0001t0007 a0001c0001t0013 |
3 | HG00621.hp1 NA18967.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*315C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 315 | chr7 | 33014415 | ||||||
| chr7:33014429 | T | G | 1 | a0001c0001t0013 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 301 | chr7 | 33014429 | ||||||
| chr7:33014500 | A | G | 11 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(8): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*230T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 230 | chr7 | 33014500 | ||||||
| chr7:33014502 | CT | C | 2 | a0001c0002t0004 a0001c0002t0005 |
15 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*227delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 227 | chr7 | 33014502 | ||||||
| chr7:33014502 | CTT | C | 2 | a0001c0002t0003 a0001c0004t0012 |
51 | HG00280.hp2 HG00673.hp1 HG01070.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*226_*227delAA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 226 | chr7 | 33014502 | ||||||
| chr7:33014505 | T | TAAGA | 10 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(7): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*224_*225insTCTT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 224 | chr7 | 33014505 | ||||||
| chr7:33014506 | T | A | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*224A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 224 | chr7 | 33014506 | ||||||
| chr7:33014630 | C | T | 1 | a0001c0003t0009 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 100 | chr7 | 33014630 | ||||||
| chr7:33014674 | C | G | 1 | a0001c0002t0008 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 56 | chr7 | 33014674 | ||||||
| chr7:33062734 | G | C | 1 | a0001c0002t0006 | 3 | HG00438.hp2 NA18970.hp2 NA19091.hp2 |
5_prime_UTR_variant | MODIFIER | c.-29C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/9 | 29 | chr7 | 33062734 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33014869 | G | A | 3 | a0001c0002t0001g0027 a0001c0002t0001g0037 a0001c0002t0001g0038 |
3 | NA18951.hp1 NA18977.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.895-38C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33014869 | |||||||
| chr7:33014947 | C | A | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.895-116G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33014947 | |||||||
| chr7:33014964 | G | C | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.895-133C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33014964 | |||||||
| chr7:33015084 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.895-253C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015084 | |||||||
| chr7:33015098 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.895-267G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015098 | |||||||
| chr7:33015104 | G | C | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.895-273C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015104 | |||||||
| chr7:33015182 | T | C | 1 | a0001c0001t0001g0307 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.895-351A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015182 | |||||||
| chr7:33015200 | C | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0021 others(76): Show |
81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.895-369G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015200 | |||||||
| chr7:33015304 | C | T | 5 | a0001c0002t0004g0002 a0001c0002t0004g0053 a0001c0002t0004g0068 others(2): Show |
7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+366G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015304 | |||||||
| chr7:33015409 | A | T | 1 | a0001c0001t0001g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.894+261T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015409 | |||||||
| chr7:33015507 | G | A | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.894+163C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015507 | |||||||
| chr7:33015529 | C | T | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.894+141G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015529 | |||||||
| chr7:33015537 | T | C | 1 | a0001c0002t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.894+133A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015537 | |||||||
| chr7:33015552 | T | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.894+118A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015552 | |||||||
| chr7:33015557 | C | CA | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.894+112dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015557 | |||||||
| chr7:33015609 | T | C | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.894+61A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015609 | |||||||
| chr7:33016006 | G | C | 1 | a0001c0001t0001g0308 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.694-136C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016006 | |||||||
| chr7:33016046 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.694-176G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016046 | |||||||
| chr7:33016097 | C | T | 1 | a0001c0002t0002g0105 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.694-227G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016097 | |||||||
| chr7:33016293 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.694-423C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016293 | |||||||
| chr7:33016438 | A | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.694-568T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016438 | |||||||
| chr7:33016519 | A | G | 1 | a0001c0002t0002g0079 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.694-649T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016519 | |||||||
| chr7:33016530 | T | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.694-660A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016530 | |||||||
| chr7:33016540 | G | A | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-670C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016540 | |||||||
| chr7:33016669 | C | CA | 143 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(140): Show |
148 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.693+769dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016669 | |||||||
| chr7:33016669 | C | CAA | 42 | a0001c0001t0001g0200 a0001c0001t0001g0221 a0001c0001t0001g0222 others(39): Show |
44 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.693+768_693+769dup others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016669 | |||||||
| chr7:33016758 | A | G | 2 | a0001c0002t0003g0155 a0001c0002t0003g0156 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.693+681T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016758 | |||||||
| chr7:33016803 | G | C | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.693+636C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016803 | |||||||
| chr7:33017080 | G | A | 13 | a0001c0001t0001g0178 a0001c0001t0001g0282 a0001c0001t0001g0283 others(10): Show |
13 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.693+359C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017080 | |||||||
| chr7:33017182 | CA | C | 224 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.693+256delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017182 | |||||||
| chr7:33017182 | CAA | C | 40 | a0001c0001t0001g0159 a0001c0001t0001g0174 a0001c0001t0001g0184 others(37): Show |
41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.693+255_693+256del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017182 | |||||||
| chr7:33017284 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.693+155A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017284 | |||||||
| chr7:33017308 | G | A | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+131C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017308 | |||||||
| chr7:33017824 | C | T | 1 | a0001c0001t0001g0350 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.531-223G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017824 | |||||||
| chr7:33017896 | A | G | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.531-295T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017896 | |||||||
| chr7:33017982 | C | A | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.531-381G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017982 | |||||||
| chr7:33017985 | C | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.531-384G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017985 | |||||||
| chr7:33018008 | T | C | 1 | a0001c0002t0002g0080 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.531-407A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018008 | |||||||
| chr7:33018134 | C | T | 261 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.531-533G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018134 | |||||||
| chr7:33018139 | C | T | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.531-538G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018139 | |||||||
| chr7:33018438 | C | T | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.531-837G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018438 | |||||||
| chr7:33018572 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.531-971G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018572 | |||||||
| chr7:33018588 | C | T | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.531-987G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018588 | |||||||
| chr7:33018707 | G | A | 14 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(11): Show |
15 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+928C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018707 | |||||||
| chr7:33018719 | G | A | 100 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0157 others(97): Show |
102 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.530+916C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018719 | |||||||
| chr7:33018722 | C | T | 1 | a0001c0002t0002g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.530+913G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018722 | |||||||
| chr7:33018828 | C | T | 7 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0220 others(4): Show |
7 | HG00738.hp1 HG01106.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.530+807G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018828 | |||||||
| chr7:33018829 | A | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.530+806T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018829 | |||||||
| chr7:33018844 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.530+791C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018844 | |||||||
| chr7:33018844 | G | GA | 16 | a0001c0001t0001g0354 a0001c0002t0003g0010 a0001c0002t0003g0054 others(13): Show |
17 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.530+790dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018844 | |||||||
| chr7:33018857 | T | C | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.530+778A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018857 | |||||||
| chr7:33018914 | C | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.530+721G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018914 | |||||||
| chr7:33019003 | C | T | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.530+632G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019003 | |||||||
| chr7:33019034 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG01952.hp2 HG02273.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.530+601C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019034 | |||||||
| chr7:33019100 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.530+535G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019100 | |||||||
| chr7:33019179 | C | T | 1 | a0001c0002t0004g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.530+456G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019179 | |||||||
| chr7:33019237 | C | G | 1 | a0001c0002t0001g0042 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.530+398G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019237 | |||||||
| chr7:33019256 | TA | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0021 others(79): Show |
84 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.530+378delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019256 | |||||||
| chr7:33019276 | C | G | 2 | a0001c0001t0001g0293 a0001c0001t0001g0296 |
2 | HG01070.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.530+359G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019276 | |||||||
| chr7:33019354 | G | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.530+281C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019354 | |||||||
| chr7:33019795 | A | G | 283 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.441-71T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33019795 | |||||||
| chr7:33019939 | A | G | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.441-215T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33019939 | |||||||
| chr7:33020045 | T | C | 1 | a0001c0002t0002g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.441-321A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020045 | |||||||
| chr7:33020282 | G | C | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.441-558C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020282 | |||||||
| chr7:33020314 | ACT | A | 11 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0300 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.441-592_441-591del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020314 | |||||||
| chr7:33020362 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.441-638G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020362 | |||||||
| chr7:33020495 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441-771A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020495 | |||||||
| chr7:33020566 | G | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.440+706C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020566 | |||||||
| chr7:33020655 | T | C | 35 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(32): Show |
36 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(33): Show |
intron_variant | MODIFIER | c.440+617A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020655 | |||||||
| chr7:33020687 | C | T | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.440+585G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020687 | |||||||
| chr7:33020694 | A | C | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.440+578T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020694 | |||||||
| chr7:33020700 | G | C | 1 | a0001c0002t0002g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.440+572C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020700 | |||||||
| chr7:33020775 | A | AT | 259 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(256): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.440+496dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020775 | |||||||
| chr7:33020793 | C | T | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.440+479G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020793 | |||||||
| chr7:33020834 | C | T | 5 | a0001c0002t0004g0002 a0001c0002t0004g0053 a0001c0002t0004g0068 others(2): Show |
7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.440+438G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020834 | |||||||
| chr7:33020853 | G | A | 4 | a0001c0002t0005g0008 a0001c0002t0005g0108 a0001c0002t0005g0109 others(1): Show |
5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+419C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020853 | |||||||
| chr7:33020863 | TG | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.440+408delC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020863 | |||||||
| chr7:33020887 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.440+385G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020887 | |||||||
| chr7:33020984 | G | A | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.440+288C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020984 | |||||||
| chr7:33020991 | TCA | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.440+279_440+280del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020991 | |||||||
| chr7:33021143 | A | C | 31 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(28): Show |
32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.440+129T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33021143 | |||||||
| chr7:33021263 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.440+9A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33021263 | |||||||
| chr7:33021505 | T | A | 1 | a0001c0002t0003g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.355-148A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021505 | |||||||
| chr7:33021520 | A | C | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.355-163T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021520 | |||||||
| chr7:33021623 | T | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.355-266A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021623 | |||||||
| chr7:33021787 | T | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.354+266A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021787 | |||||||
| chr7:33021851 | C | T | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.354+202G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021851 | |||||||
| chr7:33022213 | C | T | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.308-114G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022213 | |||||||
| chr7:33022418 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.308-319A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022418 | |||||||
| chr7:33022433 | AAC | A | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.308-336_308-335del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022433 | |||||||
| chr7:33022641 | C | T | 1 | a0001c0002t0002g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.308-542G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022641 | |||||||
| chr7:33022851 | C | T | 1 | a0001c0002t0002g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.308-752G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022851 | |||||||
| chr7:33022866 | T | C | 5 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(2): Show |
5 | HG01361.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-767A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022866 | |||||||
| chr7:33022920 | G | GT | 9 | a0001c0001t0001g0021 a0001c0001t0001g0212 a0001c0001t0001g0231 others(6): Show |
9 | HG01099.hp2 HG01109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-822dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022920 | |||||||
| chr7:33022934 | T | TC | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG01952.hp2 HG02273.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.308-836dupG | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022934 | |||||||
| chr7:33023023 | C | T | 1 | a0001c0002t0002g0058 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.308-924G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023023 | |||||||
| chr7:33023211 | G | A | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.307+828C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023211 | |||||||
| chr7:33023268 | CT | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.307+770delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023268 | |||||||
| chr7:33023341 | C | T | 7 | a0001c0002t0002g0007 a0001c0002t0002g0061 a0001c0002t0002g0062 others(4): Show |
8 | HG00621.hp2 NA18944.hp1 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.307+698G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023341 | |||||||
| chr7:33023422 | C | T | 5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(2): Show |
5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+617G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023422 | |||||||
| chr7:33023451 | G | T | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.307+588C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023451 | |||||||
| chr7:33023585 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.307+454C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023585 | |||||||
| chr7:33023586 | T | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.307+453A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023586 | |||||||
| chr7:33023666 | T | G | 14 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(11): Show |
15 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.307+373A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023666 | |||||||
| chr7:33023725 | A | T | 5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(2): Show |
5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+314T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023725 | |||||||
| chr7:33023851 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.307+188G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023851 | |||||||
| chr7:33023880 | A | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.307+159T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023880 | |||||||
| chr7:33024004 | G | A | 7 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+35C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33024004 | |||||||
| chr7:33024309 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.238-201A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024309 | |||||||
| chr7:33024347 | A | G | 4 | a0001c0002t0005g0008 a0001c0002t0005g0108 a0001c0002t0005g0109 others(1): Show |
5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-239T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024347 | |||||||
| chr7:33024439 | AAATAAGA others(7): Show |
A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.238-345_238-332del others(14): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024439 | |||||||
| chr7:33024807 | G | A | 1 | a0001c0001t0001g0358 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.238-699C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024807 | |||||||
| chr7:33024912 | G | A | 6 | a0001c0001t0001g0163 a0001c0001t0001g0169 a0001c0001t0001g0240 others(3): Show |
6 | HG02630.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-804C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024912 | |||||||
| chr7:33025084 | A | C | 1 | a0001c0001t0001g0190 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.238-976T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025084 | |||||||
| chr7:33025097 | C | T | 5 | a0001c0002t0004g0002 a0001c0002t0004g0053 a0001c0002t0004g0068 others(2): Show |
7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-989G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025097 | |||||||
| chr7:33025162 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.238-1054T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025162 | |||||||
| chr7:33025236 | A | G | 7 | a0001c0002t0002g0007 a0001c0002t0002g0061 a0001c0002t0002g0062 others(4): Show |
8 | HG00621.hp2 NA18944.hp1 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-1128T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025236 | |||||||
| chr7:33025490 | T | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(124): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.237+1327A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025490 | |||||||
| chr7:33025521 | T | A | 5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(2): Show |
5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1296A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025521 | |||||||
| chr7:33025570 | C | T | 283 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.237+1247G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025570 | |||||||
| chr7:33025596 | T | A | 7 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0116 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+1221A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025596 | |||||||
| chr7:33025625 | A | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.237+1192T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025625 | |||||||
| chr7:33025685 | C | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.237+1132G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025685 | |||||||
| chr7:33025686 | T | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.237+1131A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025686 | |||||||
| chr7:33025708 | T | TA | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+1108dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025708 | |||||||
| chr7:33025960 | T | C | 1 | a0001c0002t0003g0145 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237+857A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025960 | |||||||
| chr7:33026003 | T | C | 3 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0116 |
3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.237+814A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026003 | |||||||
| chr7:33026241 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.237+576C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026241 | |||||||
| chr7:33026306 | G | A | 10 | a0001c0001t0001g0163 a0001c0001t0001g0264 a0001c0001t0001g0265 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+511C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026306 | |||||||
| chr7:33026353 | G | GAA | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+462_237+463dup others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | |||||||
| chr7:33026353 | G | GAAAA | 6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0334 others(3): Show |
6 | HG03041.hp2 NA18747.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+460_237+463dup others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | |||||||
| chr7:33026353 | G | GAAAAA | 106 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0159 others(103): Show |
109 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.237+459_237+463dup others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | |||||||
| chr7:33026353 | G | GAAAAAA | 130 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(127): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.237+458_237+463dup others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | |||||||
| chr7:33026353 | G | GAAAAAAA | 13 | a0001c0001t0001g0180 a0001c0001t0001g0200 a0001c0001t0001g0203 others(10): Show |
13 | HG00741.hp1 HG01106.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.237+457_237+463dup others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | |||||||
| chr7:33026353 | G | GGAAAAA | 4 | a0001c0001t0001g0169 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG02630.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+463_237+464ins others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | |||||||
| chr7:33026441 | G | A | 3 | a0001c0001t0001g0294 a0001c0001t0001g0305 a0001c0001t0001g0308 |
3 | NA18999.hp1 NA19079.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.237+376C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026441 | |||||||
| chr7:33026498 | GC | G | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+318delG | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026498 | |||||||
| chr7:33026516 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.237+301C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026516 | |||||||
| chr7:33026576 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237+241C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026576 | |||||||
| chr7:33026608 | C | T | 14 | a0001c0001t0001g0178 a0001c0001t0001g0282 a0001c0001t0001g0283 others(11): Show |
14 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+209G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026608 | |||||||
| chr7:33026611 | C | A | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+206G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026611 | |||||||
| chr7:33026653 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.237+164C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026653 | |||||||
| chr7:33026657 | A | AT | 8 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0176 others(5): Show |
8 | HG02738.hp1 HG04199.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.237+159dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026657 | |||||||
| chr7:33026714 | G | A | 2 | a0001c0002t0003g0011 a0001c0002t0003g0119 |
3 | HG03471.hp2 NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.237+103C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026714 | |||||||
| chr7:33026919 | A | C | 3 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0116 |
3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.139-4T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33026919 | |||||||
| chr7:33026946 | T | G | 1 | a0001c0002t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.139-31A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33026946 | |||||||
| chr7:33027152 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG01891.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.139-237G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027152 | |||||||
| chr7:33027213 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.139-298G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027213 | |||||||
| chr7:33027353 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG01952.hp2 HG02273.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.139-438C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027353 | |||||||
| chr7:33027482 | T | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0252 a0001c0001t0001g0255 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-567A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027482 | |||||||
| chr7:33027518 | C | A | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.139-603G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027518 | |||||||
| chr7:33027667 | C | CAG | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.139-754_139-753dup others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027667 | |||||||
| chr7:33027777 | T | A | 4 | a0001c0002t0003g0149 a0001c0002t0003g0151 a0001c0002t0003g0371 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-862A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027777 | |||||||
| chr7:33027788 | C | G | 4 | a0001c0002t0003g0149 a0001c0002t0003g0151 a0001c0002t0003g0371 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-873G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027788 | |||||||
| chr7:33027796 | C | T | 4 | a0001c0002t0003g0149 a0001c0002t0003g0151 a0001c0002t0003g0371 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-881G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027796 | |||||||
| chr7:33027798 | A | T | 4 | a0001c0002t0003g0149 a0001c0002t0003g0151 a0001c0002t0003g0371 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-883T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027798 | |||||||
| chr7:33027882 | T | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0317 |
3 | HG01070.hp2 HG02300.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.139-967A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027882 | |||||||
| chr7:33027918 | A | ATTT | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-1006_139-1004d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027918 | |||||||
| chr7:33028079 | C | T | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-1164G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028079 | |||||||
| chr7:33028253 | C | T | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.139-1338G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028253 | |||||||
| chr7:33028268 | T | A | 283 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.139-1353A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028268 | |||||||
| chr7:33028291 | C | T | 1 | a0001c0002t0002g0112 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.139-1376G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028291 | |||||||
| chr7:33028493 | T | G | 1 | a0001c0001t0001g0282 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.139-1578A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028493 | |||||||
| chr7:33028741 | C | T | 1 | a0001c0002t0002g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.139-1826G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028741 | |||||||
| chr7:33028761 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-1846A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028761 | |||||||
| chr7:33028852 | G | A | 1 | a0001c0002t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.139-1937C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028852 | |||||||
| chr7:33028879 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-1964A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028879 | |||||||
| chr7:33028887 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.139-1972G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028887 | |||||||
| chr7:33028892 | G | A | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.139-1977C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028892 | |||||||
| chr7:33028915 | C | T | 36 | a0001c0001t0001g0294 a0001c0001t0001g0305 a0001c0001t0001g0308 others(33): Show |
37 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.139-2000G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028915 | |||||||
| chr7:33028980 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.139-2065C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028980 | |||||||
| chr7:33029029 | C | G | 1 | a0001c0001t0001g0326 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.139-2114G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029029 | |||||||
| chr7:33029244 | A | AT | 260 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.139-2330dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029244 | |||||||
| chr7:33029341 | G | A | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-2426C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029341 | |||||||
| chr7:33029401 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.139-2486T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029401 | |||||||
| chr7:33029461 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | NA18989.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.139-2546A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029461 | |||||||
| chr7:33029521 | T | A | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-2606A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029521 | |||||||
| chr7:33029565 | T | C | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-2650A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029565 | |||||||
| chr7:33030017 | T | C | 5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(2): Show |
5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-3102A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030017 | |||||||
| chr7:33030060 | T | C | 1 | a0001c0002t0008g0035 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.139-3145A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030060 | |||||||
| chr7:33030430 | C | T | 2 | a0001c0002t0001g0027 a0001c0002t0001g0037 |
2 | NA18951.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.139-3515G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030430 | |||||||
| chr7:33030461 | A | G | 6 | a0001c0002t0003g0124 a0001c0002t0003g0126 a0001c0002t0003g0127 others(3): Show |
6 | HG00280.hp2 HG02083.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-3546T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030461 | |||||||
| chr7:33030471 | T | C | 1 | a0001c0002t0003g0125 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.139-3556A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030471 | |||||||
| chr7:33030563 | C | T | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.139-3648G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030563 | |||||||
| chr7:33030840 | C | A | 1 | a0001c0002t0003g0124 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.139-3925G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030840 | |||||||
| chr7:33030871 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.139-3956C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030871 | |||||||
| chr7:33030885 | G | A | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-3970C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030885 | |||||||
| chr7:33030925 | C | T | 100 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0157 others(97): Show |
102 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.139-4010G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030925 | |||||||
| chr7:33030971 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.139-4056G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030971 | |||||||
| chr7:33030993 | G | A | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.139-4078C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030993 | |||||||
| chr7:33031051 | G | A | 1 | a0001c0002t0008g0035 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.139-4136C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031051 | |||||||
| chr7:33031107 | C | CA | 241 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(238): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.139-4193dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031107 | |||||||
| chr7:33031107 | CA | C | 32 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(29): Show |
33 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-4193delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031107 | |||||||
| chr7:33031184 | T | C | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(1): Show |
4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-4269A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031184 | |||||||
| chr7:33031433 | C | A | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.139-4518G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031433 | |||||||
| chr7:33031561 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-4646A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031561 | |||||||
| chr7:33031578 | C | A | 1 | a0001c0002t0002g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.139-4663G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031578 | |||||||
| chr7:33031593 | A | T | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.139-4678T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031593 | |||||||
| chr7:33031605 | T | A | 1 | a0001c0001t0001g0325 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.139-4690A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031605 | |||||||
| chr7:33031654 | T | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(108): Show |
114 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.139-4739A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031654 | |||||||
| chr7:33031722 | T | C | 1 | a0001c0002t0002g0064 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.139-4807A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031722 | |||||||
| chr7:33031847 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.139-4932C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031847 | |||||||
| chr7:33031926 | A | G | 1 | a0001c0001t0001g0373 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.139-5011T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031926 | |||||||
| chr7:33031945 | T | C | 1 | a0001c0001t0001g0373 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.139-5030A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031945 | |||||||
| chr7:33032002 | G | GT | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-5088dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032002 | |||||||
| chr7:33032224 | G | T | 1 | a0001c0002t0003g0137 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.139-5309C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032224 | |||||||
| chr7:33032280 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-5365C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032280 | |||||||
| chr7:33032297 | C | G | 1 | a0001c0001t0001g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.139-5382G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032297 | |||||||
| chr7:33032423 | C | CA | 8 | a0001c0002t0002g0073 a0001c0002t0002g0087 a0001c0002t0003g0128 others(5): Show |
8 | HG02886.hp1 HG02897.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-5509dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | |||||||
| chr7:33032423 | C | CAA | 188 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.139-5510_139-5509d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | |||||||
| chr7:33032423 | C | CAAA | 33 | a0001c0001t0001g0023 a0001c0001t0001g0157 a0001c0001t0001g0162 others(30): Show |
33 | HG00140.hp2 HG00423.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-5511_139-5509d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | |||||||
| chr7:33032423 | C | CAAAAAA | 26 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0026 others(23): Show |
27 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.139-5514_139-5509d others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | |||||||
| chr7:33032423 | C | CAAAAAAA | 7 | a0001c0002t0001g0020 a0001c0002t0001g0032 a0001c0002t0001g0034 others(4): Show |
7 | HG03516.hp2 NA18943.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-5515_139-5509d others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | |||||||
| chr7:33032423 | CAAAA | C | 7 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-5512_139-5509d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | |||||||
| chr7:33032518 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0300 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.139-5603C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032518 | |||||||
| chr7:33032524 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.139-5609A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032524 | |||||||
| chr7:33032564 | C | T | 5 | a0001c0002t0001g0032 a0001c0002t0001g0039 a0001c0002t0001g0044 others(2): Show |
5 | HG02293.hp1 NA18939.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-5649G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032564 | |||||||
| chr7:33032596 | C | G | 131 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(128): Show |
134 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.139-5681G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032596 | |||||||
| chr7:33032897 | C | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-5982G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032897 | |||||||
| chr7:33032920 | T | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-6005A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032920 | |||||||
| chr7:33033100 | T | A | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-6185A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033100 | |||||||
| chr7:33033264 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.139-6349G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033264 | |||||||
| chr7:33033355 | T | C | 2 | a0001c0002t0003g0155 a0001c0002t0003g0156 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.139-6440A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033355 | |||||||
| chr7:33033387 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-6472A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033387 | |||||||
| chr7:33033483 | G | A | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-6568C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033483 | |||||||
| chr7:33033498 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-6583A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033498 | |||||||
| chr7:33033717 | A | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-6802T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033717 | |||||||
| chr7:33033763 | T | C | 4 | a0001c0003t0001g0015 a0001c0003t0001g0331 a0001c0003t0001g0333 others(1): Show |
5 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-6848A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033763 | |||||||
| chr7:33033788 | T | G | 34 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0179 others(31): Show |
35 | HG00609.hp2 HG00738.hp2 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.139-6873A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033788 | |||||||
| chr7:33033877 | C | CAT | 10 | a0001c0002t0002g0055 a0001c0002t0002g0057 a0001c0002t0002g0065 others(7): Show |
10 | HG02074.hp1 HG02523.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-6964_139-6963d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | |||||||
| chr7:33033877 | C | CATATATA others(5): Show |
5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp2 HG02273.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-6974_139-6963d others(14): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | |||||||
| chr7:33033877 | C | CATATATA others(7): Show |
7 | a0001c0001t0001g0178 a0001c0001t0001g0319 a0001c0001t0001g0320 others(4): Show |
7 | HG00733.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-6976_139-6963d others(16): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | |||||||
| chr7:33033877 | C | CATATATA others(9): Show |
2 | a0001c0001t0001g0282 a0001c0001t0001g0297 |
2 | HG03834.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.139-6978_139-6963d others(18): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | |||||||
| chr7:33033894 | A | ATAT | 175 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(172): Show |
179 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.139-6980_139-6979i others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033894 | |||||||
| chr7:33033894 | A | ATATAT | 26 | a0001c0001t0001g0219 a0001c0001t0001g0255 a0001c0001t0001g0260 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(24): Show |
intron_variant | MODIFIER | c.139-6980_139-6979i others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033894 | |||||||
| chr7:33033894 | A | ATATATAT | 7 | a0001c0001t0001g0334 a0001c0001t0001g0347 a0001c0001t0001g0348 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-6980_139-6979i others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033894 | |||||||
| chr7:33033895 | A | AT | 31 | a0001c0002t0001g0005 a0001c0002t0001g0020 a0001c0002t0001g0026 others(28): Show |
32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.139-6981dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033895 | |||||||
| chr7:33033895 | A | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0227 a0001c0001t0001g0351 others(1): Show |
4 | HG01943.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-6980T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033895 | |||||||
| chr7:33033896 | T | A | 213 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.139-6981A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033896 | |||||||
| chr7:33033922 | C | T | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-7007G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033922 | |||||||
| chr7:33033926 | T | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.139-7011A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033926 | |||||||
| chr7:33034015 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.139-7100G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034015 | |||||||
| chr7:33034039 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.139-7124G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034039 | |||||||
| chr7:33034081 | C | T | 3 | a0001c0001t0001g0294 a0001c0001t0001g0305 a0001c0001t0001g0308 |
3 | NA18999.hp1 NA19079.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.139-7166G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034081 | |||||||
| chr7:33034318 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0001g0337 |
2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.139-7403G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034318 | |||||||
| chr7:33034394 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0235 |
2 | HG00735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.139-7479A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034394 | |||||||
| chr7:33034629 | C | T | 17 | a0001c0001t0001g0178 a0001c0001t0001g0282 a0001c0001t0001g0283 others(14): Show |
19 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(16): Show |
intron_variant | MODIFIER | c.139-7714G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034629 | |||||||
| chr7:33034642 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.139-7727C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034642 | |||||||
| chr7:33034720 | A | T | 1 | a0001c0002t0006g0378 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.139-7805T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034720 | |||||||
| chr7:33034744 | C | T | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.139-7829G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034744 | |||||||
| chr7:33034768 | C | T | 5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(2): Show |
5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-7853G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034768 | |||||||
| chr7:33034792 | TAGAG | T | 7 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-7881_139-7878d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034792 | |||||||
| chr7:33034863 | A | C | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(1): Show |
4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-7948T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034863 | |||||||
| chr7:33035028 | T | TA | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-8114dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035028 | |||||||
| chr7:33035079 | G | T | 277 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(274): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.139-8164C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035079 | |||||||
| chr7:33035164 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.139-8249C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035164 | |||||||
| chr7:33035173 | A | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(107): Show |
113 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.139-8258T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035173 | |||||||
| chr7:33035189 | G | GT | 227 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.139-8275dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035189 | |||||||
| chr7:33035189 | G | GTT | 48 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0022 others(45): Show |
50 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-8276_139-8275d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035189 | |||||||
| chr7:33035189 | GT | G | 16 | a0001c0002t0002g0070 a0001c0002t0003g0010 a0001c0002t0003g0011 others(13): Show |
18 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.139-8275delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035189 | |||||||
| chr7:33035199 | T | TG | 6 | a0001c0002t0003g0120 a0001c0002t0003g0122 a0001c0002t0003g0134 others(3): Show |
6 | HG00673.hp1 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-8285_139-8284i others(3): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035199 | |||||||
| chr7:33035216 | C | T | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.139-8301G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035216 | |||||||
| chr7:33035354 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-8439G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035354 | |||||||
| chr7:33035387 | G | A | 1 | a0001c0001t0001g0358 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.139-8472C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035387 | |||||||
| chr7:33035443 | T | G | 1 | a0001c0002t0003g0129 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.139-8528A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035443 | |||||||
| chr7:33035497 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-8582G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035497 | |||||||
| chr7:33035636 | A | G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0170 others(59): Show |
63 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.139-8721T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035636 | |||||||
| chr7:33035728 | C | T | 1 | a0001c0002t0002g0112 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.139-8813G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035728 | |||||||
| chr7:33035795 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.139-8880A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035795 | |||||||
| chr7:33035961 | A | G | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-9046T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035961 | |||||||
| chr7:33036065 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0304 a0001c0001t0001g0318 others(1): Show |
4 | NA18971.hp1 NA18987.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-9150G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036065 | |||||||
| chr7:33036066 | C | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0304 a0001c0001t0001g0318 others(1): Show |
4 | NA18971.hp1 NA18987.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-9151G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036066 | |||||||
| chr7:33036081 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.139-9166A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036081 | |||||||
| chr7:33036167 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.139-9252A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036167 | |||||||
| chr7:33036183 | C | T | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-9268G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036183 | |||||||
| chr7:33036253 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-9338C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036253 | |||||||
| chr7:33036265 | G | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0377 |
3 | HG00738.hp2 HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.139-9350C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036265 | |||||||
| chr7:33036300 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.139-9385A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036300 | |||||||
| chr7:33036448 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0236 |
2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.139-9533G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036448 | |||||||
| chr7:33036458 | C | G | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.139-9543G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036458 | |||||||
| chr7:33036458 | CT | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-9544delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036458 | |||||||
| chr7:33036467 | T | A | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-9552A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036467 | |||||||
| chr7:33036571 | T | C | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-9656A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036571 | |||||||
| chr7:33036604 | C | T | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-9689G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036604 | |||||||
| chr7:33036676 | T | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0317 |
3 | HG01070.hp2 HG02300.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.139-9761A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036676 | |||||||
| chr7:33036702 | G | A | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-9787C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036702 | |||||||
| chr7:33036873 | A | G | 276 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.139-9958T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036873 | |||||||
| chr7:33036979 | T | G | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-10064A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036979 | |||||||
| chr7:33037045 | C | T | 62 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0170 others(59): Show |
63 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.139-10130G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037045 | |||||||
| chr7:33037105 | C | T | 14 | a0001c0001t0001g0178 a0001c0001t0001g0282 a0001c0001t0001g0283 others(11): Show |
14 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-10190G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037105 | |||||||
| chr7:33037144 | G | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-10229C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037144 | |||||||
| chr7:33037374 | TA | T | 100 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0157 others(97): Show |
102 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.139-10460delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037374 | |||||||
| chr7:33037452 | G | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-10537C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037452 | |||||||
| chr7:33037462 | A | G | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.139-10547T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037462 | |||||||
| chr7:33037586 | T | C | 1 | a0001c0002t0003g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-10671A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037586 | |||||||
| chr7:33037693 | G | A | 1 | a0001c0002t0001g0038 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.139-10778C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037693 | |||||||
| chr7:33037925 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-11010A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037925 | |||||||
| chr7:33037942 | T | C | 16 | a0001c0002t0003g0010 a0001c0002t0003g0011 a0001c0002t0003g0054 others(13): Show |
18 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.139-11027A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037942 | |||||||
| chr7:33037993 | CA | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-11079delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037993 | |||||||
| chr7:33038001 | A | G | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-11086T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038001 | |||||||
| chr7:33038004 | T | C | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-11089A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038004 | |||||||
| chr7:33038030 | T | C | 2 | a0001c0002t0003g0121 a0001c0002t0003g0132 |
2 | NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.139-11115A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038030 | |||||||
| chr7:33038164 | G | C | 34 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0179 others(31): Show |
35 | HG00609.hp2 HG00738.hp2 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.139-11249C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038164 | |||||||
| chr7:33038203 | C | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-11288G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038203 | |||||||
| chr7:33038212 | C | T | 5 | a0001c0002t0003g0152 a0001c0002t0003g0153 a0001c0002t0003g0154 others(2): Show |
5 | HG01361.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-11297G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038212 | |||||||
| chr7:33038456 | A | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0356 |
2 | NA19056.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.139-11541T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038456 | |||||||
| chr7:33038477 | T | C | 4 | a0001c0002t0003g0149 a0001c0002t0003g0151 a0001c0002t0003g0371 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-11562A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038477 | |||||||
| chr7:33038498 | CT | C | 34 | a0001c0001t0001g0227 a0001c0002t0001g0005 a0001c0002t0001g0019 others(31): Show |
35 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.139-11584delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038498 | |||||||
| chr7:33038961 | C | A | 2 | a0001c0001t0001g0180 a0003c0006t0001g0199 |
2 | NA18987.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.139-12046G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038961 | |||||||
| chr7:33039049 | T | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.139-12134A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039049 | |||||||
| chr7:33039086 | T | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.139-12171A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039086 | |||||||
| chr7:33039097 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.139-12182T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039097 | |||||||
| chr7:33039248 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.139-12333G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039248 | |||||||
| chr7:33039351 | G | A | 19 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0300 others(16): Show |
20 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-12436C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039351 | |||||||
| chr7:33039402 | G | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-12487C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039402 | |||||||
| chr7:33039555 | G | GT | 8 | a0001c0002t0002g0072 a0001c0002t0002g0076 a0001c0002t0002g0088 others(5): Show |
8 | HG02132.hp2 HG02293.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-12641dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTT | 4 | a0001c0001t0001g0261 a0001c0002t0002g0095 a0001c0002t0003g0011 others(1): Show |
5 | HG02055.hp2 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-12642_139-1264 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTT | 6 | a0001c0002t0001g0026 a0001c0002t0001g0028 a0001c0002t0001g0037 others(3): Show |
6 | HG00438.hp2 NA18951.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-12644_139-1264 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTTT | 22 | a0001c0001t0001g0343 a0001c0001t0001g0354 a0001c0002t0001g0005 others(19): Show |
23 | HG00423.hp1 HG00673.hp2 HG02293.hp1 others(20): Show |
intron_variant | MODIFIER | c.139-12645_139-1264 others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTTTT | 20 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0222 others(17): Show |
20 | HG01169.hp1 HG01943.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-12646_139-1264 others(10): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTTTTT | 139 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(136): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.139-12641_139-1264 others(11): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTTTTT others(1): Show |
52 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(49): Show |
53 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.139-12641_139-1264 others(12): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTTTTT others(2): Show |
8 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0205 others(5): Show |
8 | HG01123.hp1 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-12641_139-1264 others(13): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0257 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139-12641_139-1264 others(16): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039555 | G | GTTTTTTT others(6): Show |
1 | a0001c0001t0001g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.139-12641_139-1264 others(17): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | |||||||
| chr7:33039561 | TG | T | 15 | a0001c0002t0002g0094 a0001c0002t0002g0111 a0001c0002t0003g0054 others(12): Show |
16 | HG01255.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.139-12647delC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039561 | |||||||
| chr7:33039562 | G | T | 363 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(360): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.139-12647C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039562 | |||||||
| chr7:33039593 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0298 a0001c0001t0001g0319 |
3 | HG02451.hp1 HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.139-12678C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039593 | |||||||
| chr7:33039613 | A | G | 4 | a0001c0001t0001g0343 a0001c0001t0001g0353 a0001c0001t0001g0354 others(1): Show |
4 | HG03540.hp1 NA19240.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-12698T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039613 | |||||||
| chr7:33039702 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-12787C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039702 | |||||||
| chr7:33039737 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.139-12822T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039737 | |||||||
| chr7:33039869 | C | A | 1 | a0001c0002t0004g0002 | 3 | HG02622.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.139-12954G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039869 | |||||||
| chr7:33040023 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-13108A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040023 | |||||||
| chr7:33040077 | T | C | 4 | a0001c0002t0005g0008 a0001c0002t0005g0108 a0001c0002t0005g0109 others(1): Show |
5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-13162A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040077 | |||||||
| chr7:33040126 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139-13211G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040126 | |||||||
| chr7:33040140 | C | T | 1 | a0001c0001t0001g0373 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.139-13225G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040140 | |||||||
| chr7:33040236 | A | C | 261 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.139-13321T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040236 | |||||||
| chr7:33040544 | C | G | 1 | a0001c0002t0002g0061 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.139-13629G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040544 | |||||||
| chr7:33040626 | G | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-13711C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040626 | |||||||
| chr7:33040860 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-13945C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040860 | |||||||
| chr7:33040888 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0191 |
2 | HG00609.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.139-13973G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040888 | |||||||
| chr7:33041003 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.139-14088G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041003 | |||||||
| chr7:33041047 | C | T | 7 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-14132G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041047 | |||||||
| chr7:33041406 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-14491A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041406 | |||||||
| chr7:33041623 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.139-14708G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041623 | |||||||
| chr7:33041642 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0233 a0001c0001t0001g0342 others(1): Show |
5 | HG02630.hp2 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-14727A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041642 | |||||||
| chr7:33041668 | C | A | 1 | a0001c0001t0001g0326 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.139-14753G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041668 | |||||||
| chr7:33041702 | T | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-14787A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041702 | |||||||
| chr7:33041745 | T | A | 1 | a0001c0002t0002g0003 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.139-14830A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041745 | |||||||
| chr7:33041768 | G | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-14853C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041768 | |||||||
| chr7:33041876 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.139-14961T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041876 | |||||||
| chr7:33041902 | A | G | 93 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0021 others(90): Show |
95 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.139-14987T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041902 | |||||||
| chr7:33041921 | C | G | 32 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(29): Show |
33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-15006G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041921 | |||||||
| chr7:33042006 | T | C | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-15091A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042006 | |||||||
| chr7:33042145 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.139-15230A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042145 | |||||||
| chr7:33042174 | C | T | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-15259G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042174 | |||||||
| chr7:33042267 | T | C | 14 | a0001c0001t0001g0178 a0001c0001t0001g0282 a0001c0001t0001g0283 others(11): Show |
14 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-15352A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042267 | |||||||
| chr7:33042328 | C | CA | 6 | a0001c0002t0002g0057 a0001c0002t0004g0002 a0001c0002t0004g0053 others(3): Show |
8 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-15414dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042328 | |||||||
| chr7:33042356 | A | C | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-15441T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042356 | |||||||
| chr7:33042410 | T | C | 49 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(46): Show |
52 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.139-15495A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042410 | |||||||
| chr7:33042763 | A | G | 32 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.139-15848T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042763 | |||||||
| chr7:33042776 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0233 a0001c0001t0001g0370 |
4 | HG02630.hp2 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-15861T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042776 | |||||||
| chr7:33042836 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.139-15921T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042836 | |||||||
| chr7:33042877 | C | T | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.139-15962G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042877 | |||||||
| chr7:33042906 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-15991A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042906 | |||||||
| chr7:33043013 | C | G | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-16098G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043013 | |||||||
| chr7:33043048 | A | G | 1 | a0001c0001t0001g0327 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.139-16133T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043048 | |||||||
| chr7:33043119 | C | T | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.139-16204G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043119 | |||||||
| chr7:33043438 | A | G | 1 | a0001c0002t0003g0145 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-16523T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043438 | |||||||
| chr7:33043495 | T | C | 131 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(128): Show |
134 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.139-16580A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043495 | |||||||
| chr7:33043566 | A | C | 6 | a0001c0002t0003g0120 a0001c0002t0003g0122 a0001c0002t0003g0134 others(3): Show |
6 | HG00673.hp1 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-16651T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043566 | |||||||
| chr7:33043608 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139-16693T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043608 | |||||||
| chr7:33043612 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139-16697C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043612 | |||||||
| chr7:33043693 | G | C | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(1): Show |
4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-16778C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043693 | |||||||
| chr7:33043702 | G | C | 1 | a0001c0001t0001g0353 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.139-16787C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043702 | |||||||
| chr7:33043989 | A | G | 1 | a0001c0002t0002g0058 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.139-17074T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043989 | |||||||
| chr7:33044063 | G | A | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-17148C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044063 | |||||||
| chr7:33044088 | G | A | 1 | a0001c0002t0003g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.139-17173C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044088 | |||||||
| chr7:33044111 | C | G | 1 | a0001c0001t0001g0237 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.139-17196G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044111 | |||||||
| chr7:33044146 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-17231C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044146 | |||||||
| chr7:33044292 | T | C | 19 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0300 others(16): Show |
20 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-17377A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044292 | |||||||
| chr7:33044360 | G | T | 262 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-17445C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044360 | |||||||
| chr7:33044393 | A | AT | 260 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.139-17479dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044393 | |||||||
| chr7:33044413 | G | GA | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-17499dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044413 | |||||||
| chr7:33044481 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.139-17566T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044481 | |||||||
| chr7:33044552 | C | T | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-17637G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044552 | |||||||
| chr7:33044625 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-17710C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044625 | |||||||
| chr7:33044854 | A | G | 136 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(133): Show |
139 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.138+17714T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044854 | |||||||
| chr7:33044874 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.138+17694T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044874 | |||||||
| chr7:33044915 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.138+17653A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044915 | |||||||
| chr7:33045059 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0202 |
2 | NA18991.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.138+17509G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045059 | |||||||
| chr7:33045150 | A | G | 4 | a0001c0002t0005g0008 a0001c0002t0005g0108 a0001c0002t0005g0109 others(1): Show |
5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+17418T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045150 | |||||||
| chr7:33045173 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0319 |
2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138+17395A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045173 | |||||||
| chr7:33045380 | C | T | 259 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.138+17188G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045380 | |||||||
| chr7:33045462 | A | AT | 15 | a0001c0001t0001g0294 a0001c0002t0002g0060 a0001c0002t0003g0010 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+17105dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045462 | |||||||
| chr7:33045463 | T | A | 1 | a0001c0003t0001g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.138+17105A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045463 | |||||||
| chr7:33045585 | G | A | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+16983C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045585 | |||||||
| chr7:33045588 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.138+16980A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045588 | |||||||
| chr7:33045634 | A | G | 260 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.138+16934T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045634 | |||||||
| chr7:33045649 | G | A | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+16919C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045649 | |||||||
| chr7:33045726 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0312 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.138+16842C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045726 | |||||||
| chr7:33045752 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.138+16816G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045752 | |||||||
| chr7:33045760 | AT | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0021 others(91): Show |
96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.138+16807delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045760 | |||||||
| chr7:33045779 | A | T | 11 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0300 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+16789T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045779 | |||||||
| chr7:33045780 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.138+16788A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045780 | |||||||
| chr7:33045907 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.138+16661C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045907 | |||||||
| chr7:33046084 | G | A | 1 | a0001c0002t0003g0148 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138+16484C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046084 | |||||||
| chr7:33046227 | T | C | 1 | a0001c0002t0002g0105 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138+16341A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046227 | |||||||
| chr7:33046307 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | NA18948.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.138+16261A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046307 | |||||||
| chr7:33046315 | T | C | 14 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(11): Show |
15 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+16253A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046315 | |||||||
| chr7:33046531 | CA | C | 316 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(313): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.138+16036delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046531 | |||||||
| chr7:33046770 | C | T | 1 | a0001c0002t0004g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+15798G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046770 | |||||||
| chr7:33046779 | G | A | 40 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(37): Show |
40 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.138+15789C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046779 | |||||||
| chr7:33046805 | CT | C | 22 | a0001c0001t0001g0178 a0001c0001t0001g0243 a0001c0001t0001g0282 others(19): Show |
22 | HG00733.hp1 HG01169.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.138+15762delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046805 | |||||||
| chr7:33046838 | C | A | 3 | a0001c0002t0003g0121 a0001c0002t0003g0131 a0001c0002t0003g0132 |
3 | NA18939.hp1 NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.138+15730G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046838 | |||||||
| chr7:33046897 | G | A | 4 | a0001c0002t0002g0081 a0001c0002t0002g0084 a0001c0002t0002g0095 others(1): Show |
4 | HG02083.hp2 NA18953.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+15671C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046897 | |||||||
| chr7:33046935 | T | C | 199 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(196): Show |
205 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.138+15633A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046935 | |||||||
| chr7:33046936 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+15632C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046936 | |||||||
| chr7:33046970 | C | CT | 249 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.138+15597dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046970 | |||||||
| chr7:33046993 | C | CG | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+15574dupC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046993 | |||||||
| chr7:33047025 | T | C | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+15543A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047025 | |||||||
| chr7:33047067 | G | A | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.138+15501C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047067 | |||||||
| chr7:33047336 | C | T | 1 | a0001c0002t0002g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.138+15232G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047336 | |||||||
| chr7:33047538 | C | A | 31 | a0001c0002t0001g0005 a0001c0002t0001g0026 a0001c0002t0001g0027 others(28): Show |
32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+15030G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047538 | |||||||
| chr7:33047567 | T | C | 14 | a0001c0002t0002g0097 a0001c0002t0003g0010 a0001c0002t0003g0147 others(11): Show |
15 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+15001A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047567 | |||||||
| chr7:33047569 | G | A | 15 | a0001c0002t0002g0097 a0001c0002t0003g0010 a0001c0002t0003g0147 others(12): Show |
16 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+14999C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047569 | |||||||
| chr7:33047573 | T | C | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0276 others(1): Show |
4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+14995A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047573 | |||||||
| chr7:33047575 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.138+14993T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047575 | |||||||
| chr7:33047692 | G | A | 2 | a0001c0002t0003g0133 a0001c0002t0003g0141 |
2 | HG02056.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.138+14876C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047692 | |||||||
| chr7:33047777 | C | T | 1 | a0001c0001t0014g0177 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.138+14791G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047777 | |||||||
| chr7:33047799 | G | T | 17 | a0001c0001t0001g0281 a0001c0001t0001g0288 a0001c0001t0001g0302 others(14): Show |
17 | HG00621.hp1 HG02074.hp2 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+14769C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047799 | |||||||
| chr7:33047996 | ATG | A | 116 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0178 others(113): Show |
119 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.138+14570_138+1457 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047996 | |||||||
| chr7:33047996 | ATGTG | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0021 others(76): Show |
81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.138+14568_138+1457 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047996 | |||||||
| chr7:33048037 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+14531T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048037 | |||||||
| chr7:33048046 | A | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.138+14522T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048046 | |||||||
| chr7:33048176 | T | TTG | 9 | a0001c0002t0002g0006 a0001c0002t0002g0102 a0001c0002t0002g0103 others(6): Show |
12 | HG00639.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+14390_138+1439 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048176 | |||||||
| chr7:33048176 | TTG | T | 226 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(223): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.138+14390_138+1439 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048176 | |||||||
| chr7:33048176 | TTGTG | T | 33 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0020 others(30): Show |
34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.138+14388_138+1439 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048176 | |||||||
| chr7:33048196 | GT | G | 3 | a0001c0001t0001g0190 a0001c0001t0001g0294 a0001c0001t0001g0316 |
3 | NA19000.hp1 NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.138+14371delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048196 | |||||||
| chr7:33048199 | G | T | 3 | a0001c0001t0001g0190 a0001c0001t0001g0294 a0001c0001t0001g0316 |
3 | NA19000.hp1 NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.138+14369C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048199 | |||||||
| chr7:33048205 | T | A | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+14363A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048205 | |||||||
| chr7:33048341 | G | A | 3 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0116 |
3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138+14227C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048341 | |||||||
| chr7:33048625 | A | C | 1 | a0001c0002t0002g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.138+13943T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048625 | |||||||
| chr7:33048805 | C | G | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138+13763G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048805 | |||||||
| chr7:33049017 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.138+13551A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049017 | |||||||
| chr7:33049031 | C | T | 11 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0300 others(8): Show |
11 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+13537G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049031 | |||||||
| chr7:33049180 | ATTCT | A | 8 | a0001c0003t0001g0015 a0001c0003t0001g0279 a0001c0003t0001g0285 others(5): Show |
9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+13384_138+1338 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049180 | |||||||
| chr7:33049268 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.138+13300G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049268 | |||||||
| chr7:33049314 | G | A | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+13254C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049314 | |||||||
| chr7:33049327 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.138+13241A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049327 | |||||||
| chr7:33049518 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0165 |
2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+13050G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049518 | |||||||
| chr7:33049576 | A | G | 8 | a0001c0003t0001g0015 a0001c0003t0001g0279 a0001c0003t0001g0285 others(5): Show |
9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+12992T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049576 | |||||||
| chr7:33049661 | A | T | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.138+12907T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049661 | |||||||
| chr7:33049693 | G | T | 9 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(6): Show |
9 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+12875C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049693 | |||||||
| chr7:33049735 | C | T | 2 | a0001c0001t0001g0251 a0001c0002t0004g0069 |
2 | HG03209.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.138+12833G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049735 | |||||||
| chr7:33049736 | G | A | 1 | a0001c0002t0002g0104 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.138+12832C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049736 | |||||||
| chr7:33049774 | C | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+12794G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049774 | |||||||
| chr7:33049830 | C | T | 7 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0116 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+12738G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049830 | |||||||
| chr7:33049894 | C | T | 2 | a0001c0002t0002g0073 a0001c0002t0010g0085 |
2 | HG02523.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.138+12674G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049894 | |||||||
| chr7:33049966 | T | C | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+12602A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049966 | |||||||
| chr7:33049969 | C | CA | 71 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(68): Show |
75 | HG00280.hp2 HG00673.hp1 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.138+12598dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | |||||||
| chr7:33049969 | C | CAA | 28 | a0001c0001t0001g0262 a0001c0002t0001g0005 a0001c0002t0001g0027 others(25): Show |
29 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.138+12597_138+1259 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | |||||||
| chr7:33049969 | C | CAAA | 8 | a0001c0001t0001g0263 a0001c0002t0001g0019 a0001c0002t0001g0043 others(5): Show |
8 | HG02647.hp1 HG02886.hp1 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+12596_138+1259 others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | |||||||
| chr7:33049969 | CA | C | 31 | a0001c0001t0001g0013 a0001c0001t0001g0178 a0001c0001t0001g0209 others(28): Show |
33 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.138+12598delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | |||||||
| chr7:33049992 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.138+12576T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049992 | |||||||
| chr7:33050151 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.138+12417G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050151 | |||||||
| chr7:33050169 | A | G | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+12399T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050169 | |||||||
| chr7:33050186 | T | G | 1 | a0001c0002t0003g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.138+12382A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050186 | |||||||
| chr7:33050188 | G | C | 5 | a0001c0002t0004g0002 a0001c0002t0004g0053 a0001c0002t0004g0068 others(2): Show |
7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+12380C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050188 | |||||||
| chr7:33050205 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.138+12363C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050205 | |||||||
| chr7:33050748 | A | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0377 |
3 | HG00738.hp2 HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.138+11820T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050748 | |||||||
| chr7:33050794 | ACTTG | A | 6 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | NA18953.hp1 NA18970.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+11770_138+1177 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050794 | |||||||
| chr7:33050798 | G | A | 257 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.138+11770C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050798 | |||||||
| chr7:33050854 | C | T | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+11714G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050854 | |||||||
| chr7:33050866 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.138+11702T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050866 | |||||||
| chr7:33050869 | A | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+11699T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050869 | |||||||
| chr7:33050921 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.138+11647G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050921 | |||||||
| chr7:33051166 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0001g0340 |
2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.138+11402A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051166 | |||||||
| chr7:33051205 | C | T | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+11363G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051205 | |||||||
| chr7:33051384 | G | A | 6 | a0001c0002t0003g0147 a0001c0002t0003g0152 a0001c0002t0003g0153 others(3): Show |
6 | HG01361.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+11184C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051384 | |||||||
| chr7:33051409 | G | A | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.138+11159C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051409 | |||||||
| chr7:33051683 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+10885C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051683 | |||||||
| chr7:33051737 | C | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(276): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.138+10831G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051737 | |||||||
| chr7:33051952 | G | A | 3 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0116 |
3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138+10616C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051952 | |||||||
| chr7:33052058 | TTTTTG | T | 15 | a0001c0001t0001g0319 a0001c0002t0003g0010 a0001c0002t0003g0011 others(12): Show |
17 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.138+10505_138+1050 others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052058 | |||||||
| chr7:33052130 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+10438C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052130 | |||||||
| chr7:33052135 | C | T | 1 | a0001c0002t0002g0086 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.138+10433G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052135 | |||||||
| chr7:33052236 | C | T | 1 | a0001c0002t0003g0120 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.138+10332G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052236 | |||||||
| chr7:33052247 | GC | G | 15 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(12): Show |
16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.138+10320delG | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052247 | |||||||
| chr7:33052343 | C | T | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+10225G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052343 | |||||||
| chr7:33052387 | GCAC | G | 257 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(254): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.138+10178_138+1018 others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052387 | |||||||
| chr7:33052394 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+10174C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052394 | |||||||
| chr7:33052417 | C | T | 1 | a0001c0002t0003g0136 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.138+10151G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052417 | |||||||
| chr7:33052479 | C | T | 1 | a0001c0002t0002g0072 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.138+10089G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052479 | |||||||
| chr7:33052480 | G | A | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.138+10088C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052480 | |||||||
| chr7:33052485 | C | CA | 8 | a0001c0002t0002g0059 a0001c0002t0002g0060 a0001c0002t0002g0096 others(5): Show |
8 | HG00544.hp1 HG00673.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+10082dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | |||||||
| chr7:33052485 | C | CAA | 13 | a0001c0002t0003g0010 a0001c0002t0003g0054 a0001c0002t0003g0147 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.138+10081_138+1008 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | |||||||
| chr7:33052485 | CA | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
9 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+10082delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | |||||||
| chr7:33052485 | CAA | C | 10 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0001t0001g0202 others(7): Show |
10 | HG00741.hp2 HG01361.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+10081_138+1008 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | |||||||
| chr7:33052485 | CAAA | C | 242 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(239): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.138+10080_138+1008 others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | |||||||
| chr7:33052737 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+9831T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052737 | |||||||
| chr7:33052876 | G | C | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+9692C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052876 | |||||||
| chr7:33052943 | T | C | 1 | a0001c0002t0002g0105 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138+9625A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052943 | |||||||
| chr7:33053025 | C | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.138+9543G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053025 | |||||||
| chr7:33053064 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0165 |
2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+9504C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053064 | |||||||
| chr7:33053101 | G | T | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138+9467C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053101 | |||||||
| chr7:33053203 | T | C | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+9365A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053203 | |||||||
| chr7:33053227 | C | A | 1 | a0003c0006t0001g0199 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.138+9341G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053227 | |||||||
| chr7:33053254 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(276): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.138+9314A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053254 | |||||||
| chr7:33053344 | C | T | 1 | a0001c0002t0003g0148 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138+9224G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053344 | |||||||
| chr7:33053346 | C | T | 9 | a0001c0001t0001g0164 a0001c0001t0001g0211 a0001c0001t0001g0212 others(6): Show |
9 | NA18960.hp1 NA18975.hp2 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+9222G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053346 | |||||||
| chr7:33053562 | G | C | 2 | a0001c0001t0001g0269 a0001c0001t0001g0271 |
2 | HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.138+9006C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053562 | |||||||
| chr7:33053563 | A | AG | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+9004dupC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053563 | |||||||
| chr7:33053647 | T | C | 3 | a0001c0002t0001g0028 a0001c0002t0001g0030 a0001c0002t0001g0036 |
3 | HG00423.hp1 NA18941.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.138+8921A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053647 | |||||||
| chr7:33053683 | T | TGAAA | 34 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0174 others(31): Show |
35 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.138+8881_138+8884d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053683 | |||||||
| chr7:33053777 | T | C | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+8791A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053777 | |||||||
| chr7:33054011 | G | T | 31 | a0001c0002t0001g0005 a0001c0002t0001g0026 a0001c0002t0001g0027 others(28): Show |
32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+8557C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054011 | |||||||
| chr7:33054063 | T | TAA | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+8504_138+8505i others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054063 | |||||||
| chr7:33054064 | G | A | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+8504C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054064 | |||||||
| chr7:33054074 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+8494C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054074 | |||||||
| chr7:33054128 | G | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138+8440C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054128 | |||||||
| chr7:33054241 | C | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+8327G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054241 | |||||||
| chr7:33054286 | C | T | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+8282G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054286 | |||||||
| chr7:33054353 | CA | C | 252 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(249): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.138+8214delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054353 | |||||||
| chr7:33054525 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.138+8043C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054525 | |||||||
| chr7:33054650 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.138+7918A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054650 | |||||||
| chr7:33054663 | C | T | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+7905G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054663 | |||||||
| chr7:33054675 | G | T | 1 | a0001c0002t0003g0135 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.138+7893C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054675 | |||||||
| chr7:33054948 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+7620T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054948 | |||||||
| chr7:33055011 | A | G | 1 | a0001c0002t0005g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.138+7557T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055011 | |||||||
| chr7:33055047 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.138+7521C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055047 | |||||||
| chr7:33055140 | T | C | 1 | a0001c0002t0001g0037 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.138+7428A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055140 | |||||||
| chr7:33055370 | C | T | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.138+7198G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055370 | |||||||
| chr7:33055485 | C | T | 4 | a0001c0002t0005g0008 a0001c0002t0005g0108 a0001c0002t0005g0109 others(1): Show |
5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+7083G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055485 | |||||||
| chr7:33055626 | G | C | 1 | a0001c0002t0002g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.138+6942C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055626 | |||||||
| chr7:33055710 | C | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.138+6858G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055710 | |||||||
| chr7:33055804 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+6764T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055804 | |||||||
| chr7:33055809 | C | T | 5 | a0001c0002t0004g0002 a0001c0002t0004g0053 a0001c0002t0004g0068 others(2): Show |
7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+6759G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055809 | |||||||
| chr7:33055831 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0249 |
2 | HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.138+6737C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055831 | |||||||
| chr7:33055872 | AG | A | 31 | a0001c0002t0001g0005 a0001c0002t0001g0026 a0001c0002t0001g0027 others(28): Show |
32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+6695delC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055872 | |||||||
| chr7:33055908 | T | G | 13 | a0001c0001t0001g0178 a0001c0001t0001g0282 a0001c0001t0001g0283 others(10): Show |
13 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+6660A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055908 | |||||||
| chr7:33055909 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138+6659C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055909 | |||||||
| chr7:33055993 | C | G | 8 | a0001c0003t0001g0015 a0001c0003t0001g0279 a0001c0003t0001g0285 others(5): Show |
9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+6575G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055993 | |||||||
| chr7:33056045 | G | A | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+6523C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056045 | |||||||
| chr7:33056076 | T | C | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.138+6492A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056076 | |||||||
| chr7:33056182 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.138+6386T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056182 | |||||||
| chr7:33056206 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+6362T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056206 | |||||||
| chr7:33056227 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0165 |
2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+6341G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056227 | |||||||
| chr7:33056301 | A | G | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+6267T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056301 | |||||||
| chr7:33056354 | T | G | 132 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0018 others(129): Show |
135 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.138+6214A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056354 | |||||||
| chr7:33056377 | C | T | 5 | a0001c0002t0004g0002 a0001c0002t0004g0053 a0001c0002t0004g0068 others(2): Show |
7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+6191G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056377 | |||||||
| chr7:33056465 | G | A | 1 | a0001c0002t0001g0030 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.138+6103C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056465 | |||||||
| chr7:33056473 | C | CA | 15 | a0001c0002t0002g0003 a0001c0002t0002g0060 a0001c0002t0002g0086 others(12): Show |
17 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+6094dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | C | CAA | 12 | a0001c0001t0001g0341 a0001c0002t0002g0007 a0001c0002t0002g0061 others(9): Show |
13 | HG00621.hp2 HG01168.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.138+6093_138+6094d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | C | CAAAAA | 6 | a0001c0001t0001g0342 a0001c0002t0002g0063 a0001c0002t0002g0064 others(3): Show |
6 | HG01433.hp2 NA18952.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+6090_138+6094d others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0002g0067 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.138+6084_138+6094d others(13): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAA | C | 24 | a0001c0001t0001g0162 a0001c0001t0001g0173 a0001c0001t0001g0174 others(21): Show |
24 | HG00099.hp2 HG01981.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.138+6092_138+6094d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAA | C | 51 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0158 others(48): Show |
52 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.138+6091_138+6094d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAA | C | 48 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0168 others(45): Show |
49 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.138+6090_138+6094d others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAA | C | 46 | a0001c0001t0001g0013 a0001c0001t0001g0163 a0001c0001t0001g0166 others(43): Show |
48 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.138+6089_138+6094d others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA | C | 49 | a0001c0001t0001g0164 a0001c0001t0001g0176 a0001c0001t0001g0211 others(46): Show |
50 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+6088_138+6094d others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0002t0001g0028 others(9): Show |
12 | HG02293.hp1 HG02965.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+6087_138+6094d others(10): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(2): Show |
C | 13 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0027 others(10): Show |
14 | HG00423.hp1 HG02647.hp1 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+6086_138+6094d others(11): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0159 a0001c0002t0001g0020 others(2): Show |
5 | HG01167.hp2 HG02145.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+6085_138+6094d others(12): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
6 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+6084_138+6094d others(13): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0277 a0001c0002t0002g0070 |
3 | HG01109.hp2 HG02922.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.138+6083_138+6094d others(14): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0001g0276 a0001c0002t0003g0010 a0001c0002t0003g0152 others(7): Show |
11 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+6082_138+6094d others(15): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(7): Show |
C | 14 | a0001c0001t0001g0207 a0001c0001t0001g0272 a0001c0001t0001g0273 others(11): Show |
15 | HG00741.hp2 HG01071.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+6081_138+6094d others(16): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0002t0003g0148 others(1): Show |
4 | HG01070.hp1 HG01106.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+6080_138+6094d others(17): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG00140.hp2 HG00639.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+6079_138+6094d others(18): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0354 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.138+6078_138+6094d others(19): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0353 a0001c0002t0003g0119 |
2 | NA18986.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.138+6077_138+6094d others(20): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(13): Show |
C | 1 | a0001c0002t0001g0029 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.138+6075_138+6094d others(22): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(16): Show |
C | 4 | a0001c0002t0004g0002 a0001c0002t0004g0053 a0001c0002t0004g0069 others(1): Show |
6 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+6072_138+6094d others(25): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(17): Show |
C | 1 | a0001c0002t0004g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.138+6071_138+6094d others(26): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138+6070_138+6094d others(27): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(19): Show |
C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0165 a0001c0001t0001g0262 |
3 | HG02258.hp2 HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+6069_138+6094d others(28): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056473 | CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0001g0357 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.138+6068_138+6094d others(29): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | |||||||
| chr7:33056634 | T | A | 1 | a0001c0004t0012g0016 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+5934A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056634 | |||||||
| chr7:33056655 | G | A | 322 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.138+5913C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056655 | |||||||
| chr7:33056662 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.138+5906G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056662 | |||||||
| chr7:33056830 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.138+5738T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056830 | |||||||
| chr7:33056898 | G | A | 1 | a0001c0002t0003g0145 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+5670C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056898 | |||||||
| chr7:33057032 | C | T | 72 | a0001c0001t0001g0013 a0001c0001t0001g0159 a0001c0001t0001g0160 others(69): Show |
73 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.138+5536G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057032 | |||||||
| chr7:33057065 | G | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+5503C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057065 | |||||||
| chr7:33057081 | G | A | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+5487C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057081 | |||||||
| chr7:33057098 | C | G | 1 | a0001c0002t0003g0054 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+5470G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057098 | |||||||
| chr7:33057172 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.138+5396T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057172 | |||||||
| chr7:33057384 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.138+5184G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057384 | |||||||
| chr7:33057586 | T | TA | 7 | a0001c0002t0004g0114 a0001c0002t0004g0115 a0001c0002t0004g0116 others(4): Show |
8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+4981dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057586 | |||||||
| chr7:33058098 | T | C | 264 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(261): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.138+4470A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058098 | |||||||
| chr7:33058297 | G | A | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+4271C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058297 | |||||||
| chr7:33058340 | T | A | 1 | a0001c0002t0003g0011 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+4228A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058340 | |||||||
| chr7:33058340 | TTTTTA | T | 103 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0158 others(100): Show |
105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.138+4223_138+4227d others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058340 | |||||||
| chr7:33058440 | G | C | 31 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(28): Show |
32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+4128C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058440 | |||||||
| chr7:33058545 | T | C | 1 | a0001c0002t0001g0050 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.138+4023A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058545 | |||||||
| chr7:33058587 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+3981T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058587 | |||||||
| chr7:33058688 | C | T | 2 | a0001c0002t0003g0147 a0001c0004t0012g0016 |
2 | HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.138+3880G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058688 | |||||||
| chr7:33058812 | C | A | 2 | a0001c0001t0001g0363 a0001c0001t0001g0364 |
2 | HG00733.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.138+3756G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058812 | |||||||
| chr7:33058826 | C | T | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+3742G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058826 | |||||||
| chr7:33058906 | T | C | 31 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(28): Show |
32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+3662A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058906 | |||||||
| chr7:33058912 | T | C | 33 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0179 others(30): Show |
34 | HG00609.hp2 HG00738.hp2 HG02155.hp2 others(31): Show |
intron_variant | MODIFIER | c.138+3656A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058912 | |||||||
| chr7:33058919 | G | C | 4 | a0001c0001t0001g0176 a0001c0001t0001g0344 a0001c0001t0001g0345 others(1): Show |
4 | HG00423.hp2 HG00558.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+3649C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058919 | |||||||
| chr7:33059015 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138+3553G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059015 | |||||||
| chr7:33059151 | G | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(262): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.138+3417C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059151 | |||||||
| chr7:33059168 | A | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+3400T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059168 | |||||||
| chr7:33059188 | T | G | 7 | a0001c0001t0001g0347 a0001c0001t0001g0348 a0001c0001t0001g0349 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+3380A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059188 | |||||||
| chr7:33059193 | C | T | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+3375G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059193 | |||||||
| chr7:33059196 | C | G | 30 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0179 others(27): Show |
31 | HG00609.hp2 HG00738.hp2 HG02155.hp2 others(28): Show |
intron_variant | MODIFIER | c.138+3372G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059196 | |||||||
| chr7:33059320 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0165 |
2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+3248A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059320 | |||||||
| chr7:33059528 | A | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+3040T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059528 | |||||||
| chr7:33059768 | G | A | 224 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.138+2800C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059768 | |||||||
| chr7:33059782 | G | A | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+2786C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059782 | |||||||
| chr7:33059803 | C | T | 3 | a0001c0002t0004g0002 a0001c0002t0004g0068 a0001c0002t0004g0069 |
5 | HG02622.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+2765G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059803 | |||||||
| chr7:33059831 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.138+2737T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059831 | |||||||
| chr7:33060036 | C | T | 1 | a0001c0001t0014g0177 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.138+2532G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060036 | |||||||
| chr7:33060169 | T | C | 2 | a0001c0001t0001g0353 a0001c0001t0001g0354 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.138+2399A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060169 | |||||||
| chr7:33060344 | T | C | 1 | a0001c0001t0001g0355 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.138+2224A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060344 | |||||||
| chr7:33060353 | G | C | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+2215C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060353 | |||||||
| chr7:33060369 | C | CT | 30 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0001c0002t0002g0057 others(27): Show |
32 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+2198dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | |||||||
| chr7:33060369 | CT | C | 10 | a0001c0001t0001g0157 a0001c0001t0001g0165 a0001c0002t0001g0020 others(7): Show |
10 | HG01516.hp2 HG02129.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+2198delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | |||||||
| chr7:33060369 | CTT | C | 16 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(13): Show |
16 | HG01891.hp2 HG02976.hp2 HG03486.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+2197_138+2198d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | |||||||
| chr7:33060369 | CTTT | C | 230 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.138+2196_138+2198d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | |||||||
| chr7:33060369 | CTTTT | C | 13 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 others(10): Show |
14 | HG00733.hp1 HG01167.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+2195_138+2198d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | |||||||
| chr7:33060432 | T | G | 1 | a0001c0001t0001g0365 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138+2136A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060432 | |||||||
| chr7:33060495 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.138+2073G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060495 | |||||||
| chr7:33060546 | C | T | 13 | a0001c0002t0003g0010 a0001c0002t0003g0147 a0001c0002t0003g0148 others(10): Show |
14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+2022G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060546 | |||||||
| chr7:33060741 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.138+1827C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060741 | |||||||
| chr7:33060897 | A | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+1671T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060897 | |||||||
| chr7:33061166 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+1402G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061166 | |||||||
| chr7:33061252 | G | A | 31 | a0001c0002t0003g0009 a0001c0002t0003g0117 a0001c0002t0003g0118 others(28): Show |
32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+1316C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061252 | |||||||
| chr7:33061253 | T | A | 264 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(261): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.138+1315A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061253 | |||||||
| chr7:33061292 | A | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG00280.hp1 HG01167.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+1276T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061292 | |||||||
| chr7:33061461 | T | G | 1 | a0001c0001t0001g0367 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.138+1107A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061461 | |||||||
| chr7:33061496 | T | C | 278 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.138+1072A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061496 | |||||||
| chr7:33061539 | A | G | 1 | a0001c0002t0004g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+1029T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061539 | |||||||
| chr7:33061603 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.138+965G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061603 | |||||||
| chr7:33061619 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.138+949A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061619 | |||||||
| chr7:33061693 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+875T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061693 | |||||||
| chr7:33061724 | T | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+844A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061724 | |||||||
| chr7:33061736 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+832C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061736 | |||||||
| chr7:33061954 | G | A | 31 | a0001c0002t0001g0005 a0001c0002t0001g0026 a0001c0002t0001g0027 others(28): Show |
32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+614C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061954 | |||||||
| chr7:33062129 | G | A | 2 | a0001c0001t0001g0368 a0001c0001t0001g0369 |
2 | NA18946.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.138+439C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062129 | |||||||
| chr7:33062155 | G | A | 1 | a0001c0001t0001g0370 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.138+413C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062155 | |||||||
| chr7:33062175 | G | A | 263 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.138+393C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062175 | |||||||
| chr7:33062214 | C | A | 2 | a0001c0002t0003g0371 a0001c0002t0003g0372 |
2 | HG03490.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.138+354G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062214 | |||||||
| chr7:33062338 | G | A | 3 | a0001c0001t0001g0373 a0001c0001t0001g0374 a0001c0001t0001g0375 |
3 | HG01167.hp1 HG01169.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.138+230C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062338 | |||||||
| chr7:33062355 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+213G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062355 | |||||||
| chr7:33062378 | G | A | 1 | a0001c0001t0001g0376 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138+190C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062378 | |||||||
| chr7:33062459 | G | A | 1 | a0001c0001t0001g0377 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.138+109C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062459 | |||||||
| chr7:33062520 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.138+48G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062520 |