Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 151246 |
| ensemblid | ENSG00000163535.18 |
| hgncid | 30812 |
| symbol | SGO2 |
| name | shugoshin 2 |
| refseq_nuc | NM_152524.6 |
| refseq_prot | NP_689737.4 |
| ensembl_nuc | ENST00000357799.9 |
| ensembl_prot | ENSP00000350447.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 200526207 |
| end | 200584096 |
| strand | + |
| ver | v1.2 |
| region | chr2:200526207-200584096 |
| region5000 | chr2:200521207-200589096 |
| regionname0 | SGO2_chr2_200526207_200584096 |
| regionname5000 | SGO2_chr2_200521207_200589096 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1265 | 295 | 49 | 61 | 137 | 14 | 33 | 108 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0002 | 0/1 | 1265 | 29 | 0 | 9 | 17 | 2 | 0 | 15 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0003 | 0/0 | 1265 | 17 | 7 | 6 | 0 | 0 | 4 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0004 | 0/0 | 1265 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0005 | 0/0 | 1265 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0006 | 0/0 | 1265 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0007 | 0/0 | 1265 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0008 | 0/0 | 1265 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0009 | 0/0 | 1265 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0010 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0011 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0012 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0013 | 0/0 | 1258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1253): Show |
chr2 | 200521207 | 200589096 |
| a0014 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0015 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0016 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0017 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0018 | 0/0 | 1265 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| a0019 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | MECPV others(1260): Show |
chr2 | 200521207 | 200589096 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3795 | 100 | 14 | 18 | 54 | 4 | 10 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0001c0002 | 0/0 | 3795 | 87 | 15 | 13 | 48 | 5 | 6 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0001c0003 | 1/0 | 3795 | 54 | 11 | 19 | 13 | 2 | 8 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0001c0004 | 0/0 | 3795 | 47 | 8 | 8 | 19 | 3 | 9 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0001c0011 | 0/0 | 3795 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0001c0012 | 0/0 | 3795 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0001c0016 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0001c0022 | 0/0 | 3795 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0002c0005 | 0/1 | 3795 | 29 | 0 | 9 | 17 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0003c0006 | 0/0 | 3795 | 17 | 7 | 6 | 0 | 0 | 4 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0004c0008 | 0/0 | 3795 | 9 | 7 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0005c0007 | 0/0 | 3795 | 9 | 9 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0006c0009 | 0/0 | 3795 | 6 | 0 | 0 | 6 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0007c0010 | 0/0 | 3795 | 5 | 5 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0008c0013 | 0/0 | 3795 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0009c0014 | 0/0 | 3795 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0010c0020 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0011c0026 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0012c0015 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0013c0025 | 0/0 | 3774 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3769): Show |
chr2 | 200521207 | 200589096 | ||
| a0014c0019 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0015c0024 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0016c0018 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0017c0023 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0018c0017 | 0/0 | 3795 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 | ||
| a0019c0021 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | ATGGA others(3790): Show |
chr2 | 200521207 | 200589096 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4478 | 97 | 14 | 18 | 51 | 4 | 10 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0001t0003 | 0/0 | 4479 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4474): Show |
chr2 | 200521207 | 200589096 |
| a0001c0002t0001 | 0/0 | 4478 | 87 | 15 | 13 | 48 | 5 | 6 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0003t0001 | 1/0 | 4478 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0003t0002 | 0/0 | 4478 | 53 | 11 | 19 | 13 | 2 | 8 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0004t0001 | 0/0 | 4478 | 47 | 8 | 8 | 19 | 3 | 9 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0011t0001 | 0/0 | 4478 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0012t0001 | 0/0 | 4478 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0016t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0001c0022t0002 | 0/0 | 4478 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0002c0005t0003 | 0/1 | 4479 | 28 | 0 | 9 | 16 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4474): Show |
chr2 | 200521207 | 200589096 |
| a0002c0005t0007 | 0/0 | 4479 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4474): Show |
chr2 | 200521207 | 200589096 |
| a0003c0006t0001 | 0/0 | 4478 | 16 | 7 | 5 | 0 | 0 | 4 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0003c0006t0003 | 0/0 | 4479 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4474): Show |
chr2 | 200521207 | 200589096 |
| a0004c0008t0001 | 0/0 | 4478 | 9 | 7 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0005c0007t0001 | 0/0 | 4478 | 9 | 9 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0006c0009t0002 | 0/0 | 4478 | 6 | 0 | 0 | 6 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0007c0010t0001 | 0/0 | 4478 | 4 | 4 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0007c0010t0004 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0008c0013t0001 | 0/0 | 4478 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0009c0014t0001 | 0/0 | 4478 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0010c0020t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0011c0026t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0012c0015t0006 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0013c0025t0001 | 0/0 | 4457 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4452): Show |
chr2 | 200521207 | 200589096 |
| a0014c0019t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0015c0024t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0016c0018t0005 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0017c0023t0002 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0018c0017t0001 | 0/0 | 4478 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| a0019c0021t0001 | 0/0 | 4478 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | GCCGA others(4473): Show |
chr2 | 200521207 | 200589096 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0001g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0011t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0011t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0011t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0012t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0016t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0001c0022t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0002c0005t0007g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0003c0006t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0004c0008t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0005c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0006c0009t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0006c0009t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0006c0009t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0006c0009t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0007c0010t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0007c0010t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0007c0010t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0007c0010t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0007c0010t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0008c0013t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0008c0013t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0009c0014t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0009c0014t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0010c0020t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0011c0026t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0012c0015t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0013c0025t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0014c0019t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0015c0024t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0016c0018t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0017c0023t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0018c0017t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| a0019c0021t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0296 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0259 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0077 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00323 | hp1 | a0002 | c0005 | t0003 | g0104 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00323 | hp2 | a0002 | c0005 | t0003 | g0123 | EUR | FIN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0079 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00544 | hp2 | a0008 | c0013 | t0001 | g0210 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0024 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00609 | hp1 | a0002 | c0005 | t0003 | g0146 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0028 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00639 | hp2 | a0003 | c0006 | t0001 | g0032 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | CHS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00738 | hp1 | a0002 | c0005 | t0003 | g0105 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00741 | hp1 | a0002 | c0005 | t0003 | g0103 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01070 | hp1 | a0001 | c0012 | t0001 | g0039 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01071 | hp1 | a0001 | c0012 | t0001 | g0039 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0050 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0078 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0148 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01106 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01109 | hp2 | a0004 | c0008 | t0001 | g0087 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01167 | hp2 | a0003 | c0006 | t0001 | g0167 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01169 | hp1 | a0003 | c0006 | t0003 | g0032 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0117 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01175 | hp1 | a0001 | c0003 | t0002 | g0147 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0008 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01243 | hp1 | a0003 | c0006 | t0001 | g0168 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01243 | hp2 | a0004 | c0008 | t0001 | g0088 | AMR | PUR | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01256 | hp2 | a0001 | c0003 | t0002 | g0028 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01257 | hp1 | a0003 | c0006 | t0001 | g0163 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01257 | hp2 | a0002 | c0005 | t0003 | g0022 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01258 | hp1 | a0002 | c0005 | t0003 | g0022 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0133 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0093 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0025 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01433 | hp1 | a0001 | c0022 | t0002 | g0010 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01496 | hp1 | a0001 | c0004 | t0001 | g0068 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0026 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0081 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0054 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0026 | EUR | IBS | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01884 | hp1 | a0010 | c0020 | t0001 | g0092 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0132 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0080 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01943 | hp1 | a0001 | c0003 | t0002 | g0113 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01952 | hp1 | a0001 | c0003 | t0002 | g0143 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0059 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0010 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01975 | hp2 | a0002 | c0005 | t0003 | g0098 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01978 | hp1 | a0002 | c0005 | t0003 | g0100 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01981 | hp2 | a0003 | c0006 | t0001 | g0166 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02004 | hp2 | a0002 | c0005 | t0003 | g0102 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0067 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02055 | hp1 | a0003 | c0006 | t0001 | g0169 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02055 | hp2 | a0005 | c0007 | t0001 | g0155 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0062 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0027 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0060 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02129 | hp2 | a0001 | c0004 | t0001 | g0052 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02132 | hp1 | a0002 | c0005 | t0003 | g0126 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02145 | hp2 | a0007 | c0010 | t0001 | g0315 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02148 | hp1 | a0002 | c0005 | t0003 | g0099 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02148 | hp2 | a0001 | c0003 | t0002 | g0025 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | CDX | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02258 | hp1 | a0011 | c0026 | t0001 | g0316 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0137 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02293 | hp1 | a0002 | c0005 | t0003 | g0101 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02300 | hp1 | a0001 | c0004 | t0001 | g0058 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | PEL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0069 | EAS | KHV | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0091 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0131 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02615 | hp2 | a0004 | c0008 | t0001 | g0020 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02622 | hp1 | a0001 | c0003 | t0002 | g0140 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0109 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02647 | hp2 | a0003 | c0006 | t0001 | g0172 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02683 | hp1 | a0003 | c0006 | t0001 | g0170 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02723 | hp1 | a0005 | c0007 | t0001 | g0154 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02723 | hp2 | a0007 | c0010 | t0001 | g0314 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02735 | hp1 | a0003 | c0006 | t0001 | g0165 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0082 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02738 | hp2 | a0003 | c0006 | t0001 | g0164 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0076 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02818 | hp1 | a0003 | c0006 | t0001 | g0160 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02886 | hp1 | a0007 | c0010 | t0001 | g0313 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02886 | hp2 | a0013 | c0025 | t0001 | g0255 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02895 | hp1 | a0003 | c0006 | t0001 | g0031 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02895 | hp2 | a0007 | c0010 | t0001 | g0317 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0017 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02896 | hp2 | a0004 | c0008 | t0001 | g0085 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0017 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02897 | hp2 | a0003 | c0006 | t0001 | g0031 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02922 | hp1 | a0014 | c0019 | t0001 | g0005 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02922 | hp2 | a0005 | c0007 | t0001 | g0149 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02965 | hp1 | a0005 | c0007 | t0001 | g0152 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0075 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0009 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0118 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03041 | hp1 | a0007 | c0010 | t0004 | g0312 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03041 | hp2 | a0004 | c0008 | t0001 | g0090 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03130 | hp2 | a0005 | c0007 | t0001 | g0151 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0074 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03195 | hp1 | a0001 | c0016 | t0001 | g0182 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03209 | hp2 | a0001 | c0003 | t0002 | g0111 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03225 | hp1 | a0004 | c0008 | t0001 | g0089 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03225 | hp2 | a0005 | c0007 | t0001 | g0150 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03453 | hp1 | a0003 | c0006 | t0001 | g0161 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03453 | hp2 | a0015 | c0024 | t0001 | g0254 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03486 | hp1 | a0003 | c0006 | t0001 | g0162 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03491 | hp1 | a0003 | c0006 | t0001 | g0171 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0019 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03492 | hp1 | a0001 | c0004 | t0001 | g0019 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | ESN | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0110 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03540 | hp2 | a0005 | c0007 | t0001 | g0153 | AFR | GWD | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0293 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03579 | hp2 | a0017 | c0023 | t0002 | g0120 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03654 | hp2 | a0001 | c0004 | t0001 | g0253 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0135 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0096 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0252 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0274 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0107 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0301 | SAS | PJL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03831 | hp2 | a0001 | c0004 | t0001 | g0070 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0144 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0097 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | BEB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0112 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG04115 | hp2 | a0018 | c0017 | t0001 | g0261 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0278 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG04199 | hp2 | a0001 | c0004 | t0001 | g0053 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0057 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0061 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0145 | EAS | CHB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0128 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18939 | hp1 | a0002 | c0005 | t0003 | g0023 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18940 | hp1 | a0002 | c0005 | t0003 | g0124 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0114 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18943 | hp2 | a0002 | c0005 | t0003 | g0125 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18944 | hp1 | a0002 | c0005 | t0003 | g0003 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18947 | hp1 | a0006 | c0009 | t0002 | g0029 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18947 | hp2 | a0001 | c0011 | t0001 | g0237 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18948 | hp2 | a0006 | c0009 | t0002 | g0138 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18949 | hp1 | a0001 | c0003 | t0002 | g0115 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18949 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18952 | hp2 | a0006 | c0009 | t0002 | g0029 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18957 | hp1 | a0002 | c0005 | t0003 | g0003 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18961 | hp1 | a0008 | c0013 | t0001 | g0208 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18961 | hp2 | a0002 | c0005 | t0003 | g0127 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18963 | hp2 | a0002 | c0005 | t0007 | g0121 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18965 | hp1 | a0001 | c0003 | t0002 | g0116 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18965 | hp2 | a0001 | c0004 | t0001 | g0083 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18975 | hp1 | a0001 | c0011 | t0001 | g0238 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18975 | hp2 | a0001 | c0004 | t0001 | g0072 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18978 | hp1 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18979 | hp2 | a0002 | c0005 | t0003 | g0003 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18987 | hp2 | a0001 | c0003 | t0002 | g0108 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18988 | hp2 | a0002 | c0005 | t0003 | g0119 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18989 | hp2 | a0002 | c0005 | t0003 | g0003 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18994 | hp1 | a0002 | c0005 | t0003 | g0023 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0141 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19001 | hp1 | a0002 | c0005 | t0003 | g0122 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19004 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19005 | hp1 | a0002 | c0005 | t0003 | g0021 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19005 | hp2 | a0001 | c0004 | t0001 | g0064 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0130 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19010 | hp2 | a0002 | c0005 | t0003 | g0021 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0142 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19030 | hp1 | a0009 | c0014 | t0001 | g0158 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19043 | hp1 | a0005 | c0007 | t0001 | g0157 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19055 | hp2 | a0006 | c0009 | t0002 | g0030 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0018 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0065 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19064 | hp1 | a0006 | c0009 | t0002 | g0030 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19066 | hp2 | a0001 | c0004 | t0001 | g0055 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19072 | hp1 | a0002 | c0005 | t0003 | g0095 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19082 | hp2 | a0001 | c0004 | t0001 | g0018 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0129 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19085 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19087 | hp2 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19088 | hp1 | a0001 | c0004 | t0001 | g0066 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19091 | hp2 | a0001 | c0011 | t0001 | g0241 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA19240 | hp2 | a0004 | c0008 | t0001 | g0084 | AFR | YRI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0284 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0258 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | GIH | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0277 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0134 | AMR | CLM | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02109 | hp1 | a0009 | c0014 | t0001 | g0159 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02109 | hp2 | a0005 | c0007 | t0001 | g0156 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02486 | hp2 | a0012 | c0015 | t0006 | g0047 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG02559 | hp2 | a0004 | c0008 | t0001 | g0086 | AFR | ACB | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03471 | hp1 | a0004 | c0008 | t0001 | g0020 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG03471 | hp2 | a0016 | c0018 | t0005 | g0048 | AFR | MSL | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG06807 | hp1 | a0019 | c0021 | t0001 | g0106 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0304 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18955 | hp1 | a0006 | c0009 | t0002 | g0139 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0073 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | USA | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0071 | AFR | LWK | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| homoSapiens | chm13v2 | a0002 | c0005 | t0003 | g0094 | REF | REF | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0249 | REF | REF | SGO2_chr2_200521207_200589096 | SGO2 | chr2 | 200521207 | 200589096 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200533001 | G | A | 1 | a0002 | 28 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(25): Show |
missense_variant | MODERATE | c.26G>A | p.Gly9Asp | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/9 | 74/4478 | 26/3798 | 9/1265 | chr2 | 200533001 | |||
| chr2:200571173 | G | A | 1 | a0012 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.827G>A | p.Arg276His | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 875/4478 | 827/3798 | 276/1265 | chr2 | 200571173 | |||
| chr2:200571292 | A | G | 1 | a0009 | 2 | HG02109.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.946A>G | p.Asn316Asp | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 994/4478 | 946/3798 | 316/1265 | chr2 | 200571292 | |||
| chr2:200571374 | A | C | 2 | a0007 a0011 |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
missense_variant | MODERATE | c.1028A>C | p.Glu343Ala | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1076/4478 | 1028/3798 | 343/1265 | chr2 | 200571374 | |||
| chr2:200571375 | G | T | 1 | a0009 | 2 | HG02109.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.1029G>T | p.Glu343Asp | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1077/4478 | 1029/3798 | 343/1265 | chr2 | 200571375 | |||
| chr2:200571431 | A | C | 2 | a0013 a0015 |
2 | HG02886.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.1085A>C | p.Asp362Ala | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1133/4478 | 1085/3798 | 362/1265 | chr2 | 200571431 | |||
| chr2:200571602 | A | T | 1 | a0012 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1256A>T | p.Asn419Ile | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1304/4478 | 1256/3798 | 419/1265 | chr2 | 200571602 | |||
| chr2:200571705 | TAATGAAC others(14): Show |
T | 1 | a0013 | 1 | HG02886.hp2 | conservative_inframe_deletion | MODERATE | c.1378_1398delATGAAT others(15): Show |
p.Met460_Gln466del | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1426/4478 | 1378/3798 | 460/1265 | INFO_REALIGN_3_PRIME | chr2 | 200571705 | ||
| chr2:200571832 | A | G | 2 | a0003 a0004 |
26 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(23): Show |
missense_variant | MODERATE | c.1486A>G | p.Ile496Val | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1534/4478 | 1486/3798 | 496/1265 | chr2 | 200571832 | |||
| chr2:200572106 | A | G | 1 | a0017 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1760A>G | p.His587Arg | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1808/4478 | 1760/3798 | 587/1265 | chr2 | 200572106 | |||
| chr2:200572325 | A | G | 1 | a0003 | 17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
missense_variant | MODERATE | c.1979A>G | p.Asn660Ser | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2027/4478 | 1979/3798 | 660/1265 | chr2 | 200572325 | |||
| chr2:200572612 | G | A | 1 | a0008 | 2 | HG00544.hp2 NA18961.hp1 |
missense_variant | MODERATE | c.2266G>A | p.Gly756Arg | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2314/4478 | 2266/3798 | 756/1265 | chr2 | 200572612 | |||
| chr2:200572727 | T | C | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2381T>C | p.Met794Thr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2429/4478 | 2381/3798 | 794/1265 | chr2 | 200572727 | |||
| chr2:200572784 | G | A | 1 | a0012 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.2438G>A | p.Cys813Tyr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2486/4478 | 2438/3798 | 813/1265 | chr2 | 200572784 | |||
| chr2:200572801 | A | C | 1 | a0018 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.2455A>C | p.Ile819Leu | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2503/4478 | 2455/3798 | 819/1265 | chr2 | 200572801 | |||
| chr2:200573094 | A | G | 1 | a0006 | 6 | NA18947.hp1 NA18948.hp2 NA18952.hp2 others(3): Show |
missense_variant | MODERATE | c.2748A>G | p.Ile916Met | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2796/4478 | 2748/3798 | 916/1265 | chr2 | 200573094 | |||
| chr2:200573363 | C | T | 1 | a0019 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.3017C>T | p.Ala1006Val | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3065/4478 | 3017/3798 | 1006/1265 | chr2 | 200573363 | |||
| chr2:200573420 | A | C | 1 | a0011 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.3074A>C | p.His1025Pro | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3122/4478 | 3074/3798 | 1025/1265 | chr2 | 200573420 | |||
| chr2:200573426 | C | T | 1 | a0014 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.3080C>T | p.Thr1027Ile | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3128/4478 | 3080/3798 | 1027/1265 | chr2 | 200573426 | |||
| chr2:200573668 | A | G | 1 | a0016 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.3322A>G | p.Thr1108Ala | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3370/4478 | 3322/3798 | 1108/1265 | chr2 | 200573668 | |||
| chr2:200573774 | A | G | 3 | a0005 a0009 a0019 |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
missense_variant | MODERATE | c.3428A>G | p.His1143Arg | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3476/4478 | 3428/3798 | 1143/1265 | chr2 | 200573774 | |||
| chr2:200573845 | G | A | 1 | a0012 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.3499G>A | p.Gly1167Ser | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3547/4478 | 3499/3798 | 1167/1265 | chr2 | 200573845 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200569726 | T | C | 1 | a0012c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.537T>C | p.Asn179Asn | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/9 | 585/4478 | 537/3798 | 179/1265 | chr2 | 200569726 | |||
| chr2:200571615 | C | T | 1 | a0013c0025 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.1269C>T | p.Val423Val | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1317/4478 | 1269/3798 | 423/1265 | chr2 | 200571615 | |||
| chr2:200571756 | A | C | 1 | a0009c0014 | 2 | HG02109.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.1410A>C | p.Leu470Leu | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 1458/4478 | 1410/3798 | 470/1265 | chr2 | 200571756 | |||
| chr2:200572491 | A | G | 1 | a0001c0004 | 47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
synonymous_variant | LOW | c.2145A>G | p.Lys715Lys | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2193/4478 | 2145/3798 | 715/1265 | chr2 | 200572491 | |||
| chr2:200572587 | G | A | 1 | a0001c0016 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2241G>A | p.Thr747Thr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2289/4478 | 2241/3798 | 747/1265 | chr2 | 200572587 | |||
| chr2:200572587 | G | T | 1 | a0012c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.2241G>T | p.Thr747Thr | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2289/4478 | 2241/3798 | 747/1265 | chr2 | 200572587 | |||
| chr2:200572605 | C | A | 3 | a0001c0002 a0001c0012 a0018c0017 |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
synonymous_variant | LOW | c.2259C>A | p.Ile753Ile | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2307/4478 | 2259/3798 | 753/1265 | chr2 | 200572605 | |||
| chr2:200572611 | T | C | 17 | a0001c0001 a0001c0002 a0001c0004 others(14): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
synonymous_variant | LOW | c.2265T>C | p.Pro755Pro | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2313/4478 | 2265/3798 | 755/1265 | chr2 | 200572611 | |||
| chr2:200572695 | A | G | 1 | a0001c0022 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.2349A>G | p.Gln783Gln | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2397/4478 | 2349/3798 | 783/1265 | chr2 | 200572695 | |||
| chr2:200572770 | T | G | 1 | a0001c0011 | 3 | NA18947.hp2 NA18975.hp1 NA19091.hp2 |
synonymous_variant | LOW | c.2424T>G | p.Pro808Pro | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 2472/4478 | 2424/3798 | 808/1265 | chr2 | 200572770 | |||
| chr2:200573379 | A | G | 1 | a0001c0012 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.3033A>G | p.Glu1011Glu | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/9 | 3081/4478 | 3033/3798 | 1011/1265 | chr2 | 200573379 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200526228 | G | A | 4 | a0001c0003t0002 a0001c0022t0002 a0006c0009t0002 others(1): Show |
61 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/9 | 6748 | chr2 | 200526228 | ||||||
| chr2:200583560 | G | GT | 4 | a0001c0001t0003 a0002c0005t0003 a0002c0005t0007 others(1): Show |
32 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*106dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 107 | INFO_REALIGN_3_PRIME | chr2 | 200583560 | |||||
| chr2:200583602 | G | C | 1 | a0007c0010t0004 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 138 | chr2 | 200583602 | ||||||
| chr2:200583801 | T | C | 1 | a0016c0018t0005 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*337T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 337 | chr2 | 200583801 | ||||||
| chr2:200583963 | T | G | 1 | a0002c0005t0007 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 499 | chr2 | 200583963 | ||||||
| chr2:200584034 | T | C | 1 | a0012c0015t0006 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*570T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 9/9 | 570 | chr2 | 200584034 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:200526438 | T | C | 1 | a0001c0002t0001g0046 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+186T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526438 | |||||||
| chr2:200526591 | C | T | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+339C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526591 | |||||||
| chr2:200526768 | A | G | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-3+516A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526768 | |||||||
| chr2:200526826 | G | T | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+574G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200526826 | |||||||
| chr2:200527086 | T | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+834T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527086 | |||||||
| chr2:200527365 | C | G | 1 | a0013c0025t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-3+1113C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527365 | |||||||
| chr2:200527412 | G | T | 1 | a0001c0002t0001g0311 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-3+1160G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527412 | |||||||
| chr2:200527848 | G | A | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+1596G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200527848 | |||||||
| chr2:200528091 | T | C | 3 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0004g0312 |
3 | HG02723.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-3+1839T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528091 | |||||||
| chr2:200528107 | G | T | 1 | a0001c0004t0001g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-3+1855G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528107 | |||||||
| chr2:200528345 | G | C | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-3+2093G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528345 | |||||||
| chr2:200528490 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-3+2238G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528490 | |||||||
| chr2:200528498 | T | A | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+2246T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528498 | |||||||
| chr2:200528540 | G | T | 1 | a0001c0004t0001g0252 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-3+2288G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528540 | |||||||
| chr2:200528541 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+2289G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528541 | |||||||
| chr2:200528584 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-3+2332G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528584 | |||||||
| chr2:200528603 | C | A | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-3+2351C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528603 | |||||||
| chr2:200528900 | A | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-3+2648A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200528900 | |||||||
| chr2:200529062 | T | C | 1 | a0001c0003t0002g0050 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-3+2810T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529062 | |||||||
| chr2:200529284 | T | C | 229 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(226): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.-3+3032T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529284 | |||||||
| chr2:200529325 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0250 a0001c0001t0001g0251 |
4 | NA18956.hp2 NA18974.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+3073C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529325 | |||||||
| chr2:200529360 | C | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(315): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-3+3108C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529360 | |||||||
| chr2:200529504 | C | CGTTTT | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-3+3268_-3+3272dup others(5): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200529504 | ||||||
| chr2:200529504 | C | T | 1 | a0001c0001t0003g0247 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-3+3252C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529504 | |||||||
| chr2:200529510 | GTTTTGTT others(5): Show |
G | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3+3268_-3+3279del others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200529510 | ||||||
| chr2:200529612 | C | T | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-3+3360C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529612 | |||||||
| chr2:200529626 | A | G | 11 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-3348A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529626 | |||||||
| chr2:200529667 | C | T | 1 | a0001c0002t0001g0310 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-2-3307C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529667 | |||||||
| chr2:200529668 | G | A | 9 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-3306G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529668 | |||||||
| chr2:200529720 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-2-3254G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529720 | |||||||
| chr2:200529970 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-2-3004G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529970 | |||||||
| chr2:200529973 | C | T | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-3001C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200529973 | |||||||
| chr2:200530047 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2927C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530047 | |||||||
| chr2:200530129 | T | C | 1 | a0001c0003t0002g0051 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-2-2845T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530129 | |||||||
| chr2:200530438 | A | C | 229 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(226): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.-2-2536A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530438 | |||||||
| chr2:200530480 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2494T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530480 | |||||||
| chr2:200530509 | A | G | 8 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-2465A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530509 | |||||||
| chr2:200530587 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2387G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530587 | |||||||
| chr2:200530671 | T | A | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-2303T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530671 | |||||||
| chr2:200530922 | G | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-2052G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200530922 | |||||||
| chr2:200531107 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-2-1867T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531107 | |||||||
| chr2:200531108 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-2-1866T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531108 | |||||||
| chr2:200531110 | AGGAGGCA others(10): Show |
A | 84 | a0001c0001t0001g0173 a0001c0003t0002g0008 a0001c0003t0002g0009 others(81): Show |
102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.-2-1860_-2-1844del others(17): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200531110 | ||||||
| chr2:200531287 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-1687T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531287 | |||||||
| chr2:200531320 | G | C | 47 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(44): Show |
55 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(52): Show |
intron_variant | MODIFIER | c.-2-1654G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531320 | |||||||
| chr2:200531368 | C | T | 1 | a0001c0002t0001g0309 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-2-1606C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531368 | |||||||
| chr2:200531430 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-1544A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531430 | |||||||
| chr2:200531440 | G | A | 49 | a0001c0003t0002g0093 a0001c0004t0001g0006 a0001c0004t0001g0007 others(46): Show |
57 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.-2-1534G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531440 | |||||||
| chr2:200531525 | G | A | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-1449G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531525 | |||||||
| chr2:200531838 | A | T | 1 | a0013c0025t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-2-1136A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531838 | |||||||
| chr2:200531905 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-1069A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531905 | |||||||
| chr2:200531965 | A | G | 3 | a0001c0003t0002g0050 a0001c0003t0002g0147 a0001c0003t0002g0148 |
3 | HG01081.hp2 HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-2-1009A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531965 | |||||||
| chr2:200531969 | C | A | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2-1005C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200531969 | |||||||
| chr2:200532122 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-852G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532122 | |||||||
| chr2:200532182 | A | G | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-2-792A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532182 | |||||||
| chr2:200532263 | G | C | 8 | a0001c0002t0001g0012 a0001c0002t0001g0038 a0001c0002t0001g0256 others(5): Show |
12 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-711G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532263 | |||||||
| chr2:200532265 | GTTTTTTG others(4): Show |
G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-702_-2-692delGT others(9): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532265 | ||||||
| chr2:200532271 | TG | T | 2 | a0001c0012t0001g0039 a0016c0018t0005g0048 |
3 | HG01070.hp1 HG01071.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-2-702delG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532271 | |||||||
| chr2:200532272 | G | GTT | 7 | a0005c0007t0001g0149 a0005c0007t0001g0151 a0005c0007t0001g0152 others(4): Show |
7 | HG02109.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2-692_-2-691dupTT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532272 | ||||||
| chr2:200532272 | G | T | 18 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0179 others(15): Show |
18 | HG01884.hp1 HG01884.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-702G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532272 | |||||||
| chr2:200532272 | GT | G | 129 | a0001c0001t0001g0173 a0001c0003t0002g0008 a0001c0003t0002g0009 others(126): Show |
156 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-2-691delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532272 | ||||||
| chr2:200532273 | T | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-2-701T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532273 | |||||||
| chr2:200532278 | T | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-696T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532278 | |||||||
| chr2:200532278 | T | TG | 5 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-696_-2-695insG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532278 | |||||||
| chr2:200532279 | T | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-695T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532279 | |||||||
| chr2:200532281 | T | G | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0179 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-693T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532281 | |||||||
| chr2:200532283 | T | G | 6 | a0001c0003t0002g0096 a0001c0003t0002g0147 a0001c0004t0001g0052 others(3): Show |
6 | HG01175.hp1 HG02129.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-691T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532283 | |||||||
| chr2:200532283 | TG | T | 51 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0015 others(48): Show |
64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2-690delG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532283 | |||||||
| chr2:200532284 | G | GT | 11 | a0001c0001t0001g0037 a0001c0001t0001g0203 a0001c0001t0001g0229 others(8): Show |
12 | HG03831.hp1 NA18940.hp2 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-675dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532284 | ||||||
| chr2:200532284 | G | T | 47 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0038 others(44): Show |
54 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.-2-690G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532284 | |||||||
| chr2:200532285 | T | G | 5 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-689T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532285 | |||||||
| chr2:200532286 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-2-688T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532286 | |||||||
| chr2:200532287 | T | G | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0179 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-687T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532287 | |||||||
| chr2:200532289 | T | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-685T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532289 | |||||||
| chr2:200532290 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-2-684T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532290 | |||||||
| chr2:200532295 | T | G | 11 | a0001c0003t0002g0097 a0002c0005t0003g0021 a0002c0005t0003g0022 others(8): Show |
13 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-679T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532295 | |||||||
| chr2:200532402 | T | C | 1 | a0001c0002t0001g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-2-572T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532402 | |||||||
| chr2:200532440 | C | T | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-534C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532440 | |||||||
| chr2:200532519 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-455C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532519 | |||||||
| chr2:200532527 | G | A | 11 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-447G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532527 | |||||||
| chr2:200532531 | T | C | 9 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-443T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532531 | |||||||
| chr2:200532622 | T | C | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-2-352T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532622 | |||||||
| chr2:200532727 | T | C | 12 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-247T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532727 | |||||||
| chr2:200532746 | A | G | 1 | a0001c0002t0001g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-2-228A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532746 | |||||||
| chr2:200532757 | A | G | 1 | a0004c0008t0001g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-2-217A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532757 | |||||||
| chr2:200532846 | G | A | 229 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(226): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.-2-128G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532846 | |||||||
| chr2:200532860 | ATACT | A | 6 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-111_-2-108delCT others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 200532860 | ||||||
| chr2:200532924 | A | C | 217 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(214): Show |
264 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-2-50A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 1/8 | chr2 | 200532924 | |||||||
| chr2:200533359 | C | G | 1 | a0003c0006t0001g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133+251C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533359 | |||||||
| chr2:200533365 | C | T | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+257C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533365 | |||||||
| chr2:200533432 | A | G | 2 | a0009c0014t0001g0158 a0009c0014t0001g0159 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.133+324A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533432 | |||||||
| chr2:200533515 | GTA | G | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.133+411_133+412del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533515 | ||||||
| chr2:200533519 | A | ATG | 12 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0003t0002g0050 others(9): Show |
12 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+439_133+440dup others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533519 | ||||||
| chr2:200533519 | A | G | 49 | a0001c0001t0001g0245 a0001c0004t0001g0006 a0001c0004t0001g0007 others(46): Show |
57 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.133+411A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533519 | |||||||
| chr2:200533519 | ATG | A | 30 | a0001c0001t0001g0187 a0001c0001t0001g0227 a0001c0001t0001g0229 others(27): Show |
32 | HG02145.hp2 HG02258.hp1 HG02486.hp1 others(29): Show |
intron_variant | MODIFIER | c.133+439_133+440del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533519 | ||||||
| chr2:200533519 | ATGTG | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(124): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.133+437_133+440del others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533519 | ||||||
| chr2:200533547 | G | A | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.133+439G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200533547 | |||||||
| chr2:200533547 | G | GTGTGTGT others(3): Show |
13 | a0001c0004t0001g0006 a0001c0004t0001g0018 a0001c0004t0001g0052 others(10): Show |
16 | HG01952.hp2 HG02056.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.133+440_133+441ins others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | ||||||
| chr2:200533547 | G | GTGTGTGT others(3): Show |
24 | a0001c0004t0001g0007 a0001c0004t0001g0064 a0001c0004t0001g0065 others(21): Show |
27 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.133+440_133+441ins others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | ||||||
| chr2:200533547 | G | GTGTGTGT others(5): Show |
1 | a0001c0004t0001g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.133+440_133+441ins others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | ||||||
| chr2:200533547 | G | GTGTGTGT others(5): Show |
4 | a0001c0004t0001g0019 a0001c0004t0001g0053 a0001c0004t0001g0080 others(1): Show |
5 | HG01515.hp2 HG01934.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+440_133+441ins others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | ||||||
| chr2:200533547 | G | GTGTGTGT others(7): Show |
1 | a0001c0004t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.133+440_133+441ins others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | ||||||
| chr2:200533547 | G | GTGTGTGT others(7): Show |
2 | a0001c0004t0001g0083 a0001c0004t0001g0253 |
2 | HG03654.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.133+440_133+441ins others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533547 | ||||||
| chr2:200533641 | CA | C | 10 | a0001c0002t0001g0309 a0007c0010t0001g0313 a0007c0010t0001g0314 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+543delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 200533641 | ||||||
| chr2:200534033 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133+925A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534033 | |||||||
| chr2:200534204 | A | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-792A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534204 | |||||||
| chr2:200534335 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-661C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534335 | |||||||
| chr2:200534463 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-533A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534463 | |||||||
| chr2:200534521 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-475G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534521 | |||||||
| chr2:200534695 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134-301A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534695 | |||||||
| chr2:200534817 | A | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134-179A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534817 | |||||||
| chr2:200534877 | C | G | 12 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-119C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534877 | |||||||
| chr2:200534919 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.134-77C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 2/8 | chr2 | 200534919 | |||||||
| chr2:200535194 | G | T | 11 | a0003c0006t0001g0032 a0003c0006t0001g0163 a0003c0006t0001g0164 others(8): Show |
11 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+23G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535194 | |||||||
| chr2:200535251 | T | C | 1 | a0001c0003t0002g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.309+80T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535251 | |||||||
| chr2:200535495 | G | A | 1 | a0015c0024t0001g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+324G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535495 | |||||||
| chr2:200535693 | G | T | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.310-372G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535693 | |||||||
| chr2:200535728 | G | A | 1 | a0019c0021t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.310-337G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535728 | |||||||
| chr2:200535962 | A | G | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.310-103A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200535962 | |||||||
| chr2:200536008 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.310-57T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 3/8 | chr2 | 200536008 | |||||||
| chr2:200536326 | A | T | 2 | a0003c0006t0001g0170 a0003c0006t0001g0171 |
2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.387+184A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536326 | |||||||
| chr2:200536484 | A | G | 1 | a0002c0005t0003g0022 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.387+342A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536484 | |||||||
| chr2:200536571 | A | G | 1 | a0019c0021t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.387+429A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536571 | |||||||
| chr2:200536602 | T | A | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+460T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536602 | |||||||
| chr2:200536603 | T | C | 1 | a0001c0002t0001g0256 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.387+461T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536603 | |||||||
| chr2:200536615 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.387+473G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536615 | |||||||
| chr2:200536654 | C | G | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.387+512C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536654 | |||||||
| chr2:200536813 | G | A | 41 | a0001c0003t0002g0141 a0001c0004t0001g0006 a0001c0004t0001g0007 others(38): Show |
48 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.387+671G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536813 | |||||||
| chr2:200536870 | C | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+728C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200536870 | |||||||
| chr2:200537026 | A | G | 1 | a0001c0003t0002g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387+884A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537026 | |||||||
| chr2:200537216 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.387+1074T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537216 | |||||||
| chr2:200537323 | C | T | 10 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+1181C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537323 | |||||||
| chr2:200537338 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+1196C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537338 | |||||||
| chr2:200537517 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | HG02015.hp1 NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.387+1375T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537517 | |||||||
| chr2:200537546 | A | T | 1 | a0001c0003t0002g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.387+1404A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537546 | |||||||
| chr2:200537669 | T | C | 1 | a0001c0003t0002g0113 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.387+1527T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537669 | |||||||
| chr2:200537706 | T | C | 3 | a0001c0003t0002g0114 a0001c0003t0002g0115 a0001c0003t0002g0116 |
3 | NA18942.hp2 NA18949.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.387+1564T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200537706 | |||||||
| chr2:200538048 | T | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+1906T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538048 | |||||||
| chr2:200538103 | A | G | 1 | a0008c0013t0001g0208 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.387+1961A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538103 | |||||||
| chr2:200538270 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+2128A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538270 | |||||||
| chr2:200538283 | A | G | 1 | a0001c0004t0001g0052 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.387+2141A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538283 | |||||||
| chr2:200538536 | C | T | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+2394C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538536 | |||||||
| chr2:200538684 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.387+2542A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538684 | |||||||
| chr2:200538700 | C | A | 1 | a0001c0001t0001g0192 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.387+2558C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200538700 | |||||||
| chr2:200539098 | G | T | 1 | a0001c0002t0001g0301 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.387+2956G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539098 | |||||||
| chr2:200539257 | A | C | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+3115A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539257 | |||||||
| chr2:200539435 | A | G | 10 | a0002c0005t0003g0021 a0002c0005t0003g0022 a0002c0005t0003g0098 others(7): Show |
12 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.388-3144A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539435 | |||||||
| chr2:200539456 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.388-3123A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539456 | |||||||
| chr2:200539628 | A | C | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2951A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539628 | |||||||
| chr2:200539628 | A | T | 1 | a0002c0005t0003g0104 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.388-2951A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539628 | |||||||
| chr2:200539761 | A | G | 1 | a0001c0002t0001g0300 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-2818A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539761 | |||||||
| chr2:200539971 | C | T | 154 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(151): Show |
192 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.388-2608C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539971 | |||||||
| chr2:200539975 | C | T | 64 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(61): Show |
73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.388-2604C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200539975 | |||||||
| chr2:200540055 | C | T | 4 | a0006c0009t0002g0029 a0006c0009t0002g0030 a0006c0009t0002g0138 others(1): Show |
6 | NA18947.hp1 NA18948.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2524C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540055 | |||||||
| chr2:200540224 | C | T | 83 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(80): Show |
101 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.388-2355C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540224 | |||||||
| chr2:200540253 | G | T | 1 | a0001c0002t0001g0260 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.388-2326G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540253 | |||||||
| chr2:200540275 | G | T | 3 | a0001c0004t0001g0018 a0001c0004t0001g0063 a0001c0004t0001g0079 |
4 | HG00408.hp2 NA18979.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-2304G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540275 | |||||||
| chr2:200540290 | A | T | 1 | a0001c0002t0001g0299 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.388-2289A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540290 | |||||||
| chr2:200540434 | G | A | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.388-2145G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540434 | |||||||
| chr2:200540450 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-2129G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540450 | |||||||
| chr2:200540513 | T | C | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.388-2066T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540513 | |||||||
| chr2:200540514 | G | A | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2065G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540514 | |||||||
| chr2:200540524 | A | T | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.388-2055A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540524 | |||||||
| chr2:200540570 | G | A | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-2009G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540570 | |||||||
| chr2:200540665 | T | C | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.388-1914T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540665 | |||||||
| chr2:200540679 | G | A | 64 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(61): Show |
73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.388-1900G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540679 | |||||||
| chr2:200540837 | G | T | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.388-1742G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540837 | |||||||
| chr2:200540994 | G | T | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.388-1585G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200540994 | |||||||
| chr2:200541034 | A | AG | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.388-1543dupG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 200541034 | ||||||
| chr2:200541072 | T | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-1507T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541072 | |||||||
| chr2:200541242 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-1337G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541242 | |||||||
| chr2:200541339 | A | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.388-1240A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541339 | |||||||
| chr2:200541697 | G | C | 1 | a0002c0005t0003g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.388-882G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541697 | |||||||
| chr2:200541870 | C | G | 1 | a0015c0024t0001g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.388-709C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541870 | |||||||
| chr2:200541939 | C | T | 1 | a0001c0003t0002g0137 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.388-640C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200541939 | |||||||
| chr2:200542006 | T | C | 83 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(80): Show |
101 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.388-573T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542006 | |||||||
| chr2:200542034 | A | G | 2 | a0001c0003t0002g0110 a0001c0003t0002g0111 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.388-545A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542034 | |||||||
| chr2:200542194 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0186 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.388-385C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542194 | |||||||
| chr2:200542501 | G | C | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-78G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542501 | |||||||
| chr2:200542538 | A | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.388-41A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | chr2 | 200542538 | |||||||
| chr2:200542554 | TTTTC | T | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.388-21_388-18delCT others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 200542554 | ||||||
| chr2:200543030 | C | T | 4 | a0001c0004t0001g0054 a0001c0004t0001g0077 a0001c0004t0001g0078 others(1): Show |
4 | HG00280.hp2 HG01099.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+366C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543030 | |||||||
| chr2:200543087 | G | A | 1 | a0001c0003t0002g0117 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.473+423G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543087 | |||||||
| chr2:200543252 | C | T | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+588C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543252 | |||||||
| chr2:200543269 | G | A | 21 | a0001c0004t0001g0007 a0001c0004t0001g0019 a0001c0004t0001g0053 others(18): Show |
24 | HG00280.hp2 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.473+605G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543269 | |||||||
| chr2:200543773 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.473+1109T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543773 | |||||||
| chr2:200543940 | C | T | 48 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(45): Show |
56 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.473+1276C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543940 | |||||||
| chr2:200543983 | C | T | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+1319C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200543983 | |||||||
| chr2:200544099 | A | G | 1 | a0001c0002t0001g0300 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473+1435A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544099 | |||||||
| chr2:200544111 | A | G | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+1447A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544111 | |||||||
| chr2:200544134 | T | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0193 others(13): Show |
20 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.473+1470T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544134 | |||||||
| chr2:200544341 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.473+1677G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544341 | |||||||
| chr2:200544408 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.473+1744A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544408 | |||||||
| chr2:200544486 | T | G | 2 | a0001c0002t0001g0274 a0001c0002t0001g0301 |
2 | HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.473+1822T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544486 | |||||||
| chr2:200544497 | A | G | 10 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+1833A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544497 | |||||||
| chr2:200544568 | C | A | 64 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(61): Show |
73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.473+1904C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544568 | |||||||
| chr2:200544691 | A | AGATC | 19 | a0001c0003t0002g0024 a0001c0003t0002g0128 a0001c0003t0002g0129 others(16): Show |
25 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.473+2028_473+2031d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544691 | ||||||
| chr2:200544692 | G | GATCGATC others(1): Show |
8 | a0001c0003t0002g0118 a0002c0005t0003g0021 a0002c0005t0003g0099 others(5): Show |
9 | HG00738.hp1 HG01978.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.473+2031_473+2032i others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | ||||||
| chr2:200544692 | G | GATCT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(108): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.473+2069_473+2072d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | ||||||
| chr2:200544692 | G | GATCTATC others(1): Show |
77 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0177 others(74): Show |
80 | HG00280.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.473+2065_473+2072d others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | ||||||
| chr2:200544692 | G | GATCTATC others(5): Show |
12 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(9): Show |
13 | HG01081.hp1 HG01255.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.473+2061_473+2072d others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | ||||||
| chr2:200544692 | G | GATCTATC others(9): Show |
1 | a0001c0002t0001g0274 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.473+2057_473+2072d others(18): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | ||||||
| chr2:200544692 | GATCT | G | 38 | a0001c0001t0001g0225 a0001c0003t0002g0008 a0001c0003t0002g0009 others(35): Show |
48 | HG00609.hp2 HG00639.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.473+2069_473+2072d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | ||||||
| chr2:200544692 | GATCTATC others(1): Show |
G | 3 | a0001c0001t0001g0204 a0001c0003t0002g0107 a0006c0009t0002g0139 |
3 | HG03710.hp1 NA18955.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.473+2065_473+2072d others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200544692 | ||||||
| chr2:200544696 | T | G | 9 | a0001c0003t0002g0108 a0001c0003t0002g0112 a0001c0003t0002g0114 others(6): Show |
10 | HG02602.hp2 HG04115.hp1 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+2032T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544696 | |||||||
| chr2:200544700 | T | G | 33 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(30): Show |
43 | HG00639.hp1 HG01081.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.473+2036T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544700 | |||||||
| chr2:200544704 | T | G | 2 | a0001c0003t0002g0107 a0006c0009t0002g0139 |
2 | HG03710.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.473+2040T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544704 | |||||||
| chr2:200544804 | A | G | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.473+2140A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200544804 | |||||||
| chr2:200545437 | G | A | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+2773G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545437 | |||||||
| chr2:200545445 | G | A | 84 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(81): Show |
102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.473+2781G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545445 | |||||||
| chr2:200545500 | C | T | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+2836C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545500 | |||||||
| chr2:200545600 | A | C | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.473+2936A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545600 | |||||||
| chr2:200545623 | C | T | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.473+2959C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545623 | |||||||
| chr2:200545681 | A | G | 1 | a0001c0002t0001g0305 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.473+3017A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545681 | |||||||
| chr2:200545693 | C | T | 1 | a0001c0004t0001g0006 | 3 | NA18949.hp2 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.473+3029C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545693 | |||||||
| chr2:200545755 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.473+3091A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545755 | |||||||
| chr2:200545814 | G | A | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+3150G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545814 | |||||||
| chr2:200545975 | A | T | 1 | a0001c0002t0001g0304 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.473+3311A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200545975 | |||||||
| chr2:200546094 | C | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+3430C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546094 | |||||||
| chr2:200546106 | C | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0016t0001g0182 |
3 | HG03130.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.473+3442C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546106 | |||||||
| chr2:200546178 | T | TA | 10 | a0001c0001t0001g0232 a0007c0010t0001g0313 a0007c0010t0001g0314 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+3530dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546178 | ||||||
| chr2:200546178 | TA | T | 211 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(208): Show |
258 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.473+3530delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546178 | ||||||
| chr2:200546178 | TAA | T | 6 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+3529_473+3530d others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546178 | ||||||
| chr2:200546330 | G | A | 1 | a0001c0003t0002g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.473+3666G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546330 | |||||||
| chr2:200546339 | C | T | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+3675C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546339 | |||||||
| chr2:200546353 | G | GA | 42 | a0001c0001t0001g0185 a0001c0001t0001g0197 a0001c0001t0001g0203 others(39): Show |
43 | HG00408.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.473+3716dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | ||||||
| chr2:200546353 | GA | G | 26 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(23): Show |
28 | HG00323.hp2 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.473+3716delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | ||||||
| chr2:200546353 | GAA | G | 107 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(104): Show |
131 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.473+3715_473+3716d others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | ||||||
| chr2:200546353 | GAAAAAAA others(8): Show |
G | 2 | a0010c0020t0001g0092 a0016c0018t0005g0048 |
2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.473+3702_473+3716d others(17): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200546353 | ||||||
| chr2:200546503 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+3839G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546503 | |||||||
| chr2:200546517 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+3853A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546517 | |||||||
| chr2:200546567 | T | G | 10 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+3903T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546567 | |||||||
| chr2:200546659 | A | G | 1 | a0001c0002t0001g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.473+3995A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546659 | |||||||
| chr2:200546867 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.473+4203G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546867 | |||||||
| chr2:200546899 | A | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.473+4235A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546899 | |||||||
| chr2:200546931 | A | G | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+4267A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546931 | |||||||
| chr2:200546944 | A | G | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+4280A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200546944 | |||||||
| chr2:200547120 | C | T | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+4456C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547120 | |||||||
| chr2:200547131 | A | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0202 others(1): Show |
4 | HG01255.hp1 NA18957.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+4467A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547131 | |||||||
| chr2:200547145 | A | G | 1 | a0001c0002t0001g0275 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.473+4481A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547145 | |||||||
| chr2:200547146 | C | T | 229 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(226): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+4482C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547146 | |||||||
| chr2:200547245 | A | G | 2 | a0001c0002t0001g0275 a0001c0002t0001g0287 |
2 | NA18966.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.473+4581A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547245 | |||||||
| chr2:200547247 | G | A | 229 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(226): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+4583G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547247 | |||||||
| chr2:200547322 | A | T | 1 | a0001c0001t0001g0251 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.473+4658A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547322 | |||||||
| chr2:200547361 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+4697G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547361 | |||||||
| chr2:200547362 | A | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+4698A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547362 | |||||||
| chr2:200547427 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+4763A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547427 | |||||||
| chr2:200547479 | A | G | 3 | a0001c0003t0002g0109 a0001c0003t0002g0110 a0001c0003t0002g0111 |
3 | HG02622.hp2 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.473+4815A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547479 | |||||||
| chr2:200547563 | C | T | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+4899C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547563 | |||||||
| chr2:200547702 | C | T | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.473+5038C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547702 | |||||||
| chr2:200547888 | A | G | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+5224A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547888 | |||||||
| chr2:200547905 | G | T | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+5241G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547905 | |||||||
| chr2:200547932 | A | G | 4 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0260 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.473+5268A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200547932 | |||||||
| chr2:200548028 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0189 others(16): Show |
23 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.473+5364C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548028 | |||||||
| chr2:200548037 | A | G | 84 | a0001c0001t0001g0173 a0001c0003t0002g0008 a0001c0003t0002g0009 others(81): Show |
102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.473+5373A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548037 | |||||||
| chr2:200548050 | G | C | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.473+5386G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548050 | |||||||
| chr2:200548082 | A | T | 1 | a0001c0002t0001g0297 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.473+5418A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548082 | |||||||
| chr2:200548201 | G | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+5537G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548201 | |||||||
| chr2:200548228 | G | A | 1 | a0003c0006t0001g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.473+5564G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548228 | |||||||
| chr2:200548403 | G | A | 229 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(226): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+5739G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548403 | |||||||
| chr2:200548529 | A | G | 1 | a0001c0004t0001g0055 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.473+5865A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548529 | |||||||
| chr2:200548761 | A | G | 1 | a0001c0003t0002g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.473+6097A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548761 | |||||||
| chr2:200548855 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+6191T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200548855 | |||||||
| chr2:200549195 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+6531C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549195 | |||||||
| chr2:200549294 | G | T | 1 | a0001c0003t0002g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.473+6630G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549294 | |||||||
| chr2:200549392 | A | T | 1 | a0001c0002t0001g0298 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.473+6728A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549392 | |||||||
| chr2:200549447 | C | T | 2 | a0001c0003t0002g0135 a0002c0005t0003g0123 |
2 | HG00323.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.473+6783C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549447 | |||||||
| chr2:200549535 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+6871C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549535 | |||||||
| chr2:200549538 | T | C | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+6874T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549538 | |||||||
| chr2:200549701 | A | C | 1 | a0004c0008t0001g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473+7037A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549701 | |||||||
| chr2:200549727 | A | C | 1 | a0002c0005t0003g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.473+7063A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549727 | |||||||
| chr2:200549876 | A | T | 2 | a0001c0003t0002g0141 a0001c0003t0002g0142 |
2 | NA18998.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.473+7212A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549876 | |||||||
| chr2:200549981 | G | A | 1 | a0015c0024t0001g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+7317G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200549981 | |||||||
| chr2:200550105 | C | A | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.473+7441C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550105 | |||||||
| chr2:200550139 | C | G | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.473+7475C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550139 | |||||||
| chr2:200550184 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+7520T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550184 | |||||||
| chr2:200550294 | A | G | 1 | a0001c0003t0002g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.473+7630A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550294 | |||||||
| chr2:200550334 | A | T | 72 | a0001c0001t0001g0173 a0001c0003t0002g0008 a0001c0003t0002g0009 others(69): Show |
90 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.473+7670A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550334 | |||||||
| chr2:200550381 | C | G | 5 | a0001c0004t0001g0007 a0001c0004t0001g0068 a0001c0004t0001g0070 others(2): Show |
7 | HG01106.hp1 HG01261.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.473+7717C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550381 | |||||||
| chr2:200550624 | G | A | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG02280.hp1 HG02572.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.473+7960G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550624 | |||||||
| chr2:200550892 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+8228G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550892 | |||||||
| chr2:200550926 | G | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+8262G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550926 | |||||||
| chr2:200550991 | C | A | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.473+8327C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200550991 | |||||||
| chr2:200550991 | C | CA | 151 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(148): Show |
188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.473+8339dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200550991 | ||||||
| chr2:200551276 | A | G | 1 | a0015c0024t0001g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+8612A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551276 | |||||||
| chr2:200551284 | G | A | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.473+8620G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551284 | |||||||
| chr2:200551380 | G | A | 10 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.473+8716G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551380 | |||||||
| chr2:200551514 | A | T | 1 | a0001c0004t0001g0076 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.473+8850A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551514 | |||||||
| chr2:200551525 | G | A | 229 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0012 others(226): Show |
276 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.473+8861G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551525 | |||||||
| chr2:200551718 | T | C | 3 | a0002c0005t0003g0023 a0002c0005t0003g0119 a0002c0005t0003g0124 |
4 | NA18939.hp1 NA18940.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.473+9054T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551718 | |||||||
| chr2:200551989 | C | T | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.473+9325C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200551989 | |||||||
| chr2:200552059 | G | T | 1 | a0005c0007t0001g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.473+9395G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552059 | |||||||
| chr2:200552251 | G | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+9587G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552251 | |||||||
| chr2:200552255 | T | C | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.473+9591T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552255 | |||||||
| chr2:200552484 | C | T | 1 | a0002c0005t0003g0102 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.473+9820C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552484 | |||||||
| chr2:200552510 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+9846G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552510 | |||||||
| chr2:200552892 | C | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+10228C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552892 | |||||||
| chr2:200552944 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.473+10280C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200552944 | |||||||
| chr2:200553113 | G | A | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0179 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+10449G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553113 | |||||||
| chr2:200553156 | T | C | 3 | a0001c0002t0001g0276 a0001c0002t0001g0277 a0001c0002t0001g0279 |
3 | HG00733.hp1 HG01123.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.473+10492T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553156 | |||||||
| chr2:200553189 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+10525G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553189 | |||||||
| chr2:200553426 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.473+10762T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553426 | |||||||
| chr2:200553780 | G | A | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.473+11116G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553780 | |||||||
| chr2:200553821 | C | G | 9 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.473+11157C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553821 | |||||||
| chr2:200553976 | T | C | 1 | a0001c0003t0002g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.473+11312T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200553976 | |||||||
| chr2:200554041 | A | G | 1 | a0001c0001t0003g0247 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.473+11377A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554041 | |||||||
| chr2:200554102 | C | T | 1 | a0001c0004t0001g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.473+11438C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554102 | |||||||
| chr2:200554111 | A | C | 1 | a0003c0006t0001g0163 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.473+11447A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554111 | |||||||
| chr2:200554115 | T | C | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.473+11451T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554115 | |||||||
| chr2:200554399 | C | G | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.473+11735C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554399 | |||||||
| chr2:200554586 | C | T | 10 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0179 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+11922C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554586 | |||||||
| chr2:200554611 | A | G | 1 | a0003c0006t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.473+11947A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554611 | |||||||
| chr2:200554815 | A | G | 12 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.473+12151A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554815 | |||||||
| chr2:200554945 | T | A | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.473+12281T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200554945 | |||||||
| chr2:200555003 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+12339A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555003 | |||||||
| chr2:200555018 | A | G | 1 | a0001c0003t0002g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.473+12354A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555018 | |||||||
| chr2:200555020 | C | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+12356C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555020 | |||||||
| chr2:200555063 | G | A | 83 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(80): Show |
101 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.473+12399G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555063 | |||||||
| chr2:200555103 | C | T | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.473+12439C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555103 | |||||||
| chr2:200555107 | C | G | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.473+12443C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555107 | |||||||
| chr2:200555237 | G | A | 84 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(81): Show |
102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.473+12573G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555237 | |||||||
| chr2:200555307 | C | T | 3 | a0001c0003t0002g0050 a0001c0003t0002g0147 a0001c0003t0002g0148 |
3 | HG01081.hp2 HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.473+12643C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555307 | |||||||
| chr2:200555312 | G | A | 2 | a0001c0003t0002g0110 a0001c0003t0002g0111 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.473+12648G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555312 | |||||||
| chr2:200555484 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.473+12820C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555484 | |||||||
| chr2:200555591 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.473+12927A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555591 | |||||||
| chr2:200555673 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+13009G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555673 | |||||||
| chr2:200555683 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+13019A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555683 | |||||||
| chr2:200555955 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.473+13291T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555955 | |||||||
| chr2:200555959 | C | T | 1 | a0013c0025t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.473+13295C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555959 | |||||||
| chr2:200555962 | T | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.473+13298T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200555962 | |||||||
| chr2:200556013 | G | A | 4 | a0001c0002t0001g0015 a0001c0002t0001g0306 a0001c0002t0001g0307 others(1): Show |
6 | NA18942.hp1 NA18943.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.473+13349G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556013 | |||||||
| chr2:200556194 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.474-13469G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556194 | |||||||
| chr2:200556230 | T | C | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-13433T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556230 | |||||||
| chr2:200556303 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.474-13360T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556303 | |||||||
| chr2:200556328 | A | G | 3 | a0001c0004t0001g0077 a0001c0004t0001g0078 a0001c0004t0001g0081 |
3 | HG00280.hp2 HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.474-13335A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556328 | |||||||
| chr2:200556415 | A | G | 1 | a0013c0025t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.474-13248A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556415 | |||||||
| chr2:200556481 | T | C | 1 | a0001c0002t0001g0265 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.474-13182T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556481 | |||||||
| chr2:200556600 | C | T | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.474-13063C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556600 | |||||||
| chr2:200556678 | G | A | 1 | a0002c0005t0003g0146 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.474-12985G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556678 | |||||||
| chr2:200556711 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-12952A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556711 | |||||||
| chr2:200556821 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-12842G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556821 | |||||||
| chr2:200556865 | G | A | 1 | a0001c0003t0002g0133 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.474-12798G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200556865 | |||||||
| chr2:200557086 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-12577T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557086 | |||||||
| chr2:200557370 | C | G | 3 | a0001c0004t0001g0074 a0001c0004t0001g0075 a0001c0004t0001g0076 |
3 | HG02809.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.474-12293C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557370 | |||||||
| chr2:200557469 | A | C | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-12194A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557469 | |||||||
| chr2:200557470 | A | G | 4 | a0001c0003t0002g0096 a0001c0003t0002g0141 a0001c0003t0002g0142 others(1): Show |
4 | HG03688.hp2 NA18747.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-12193A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557470 | |||||||
| chr2:200557788 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-11875C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557788 | |||||||
| chr2:200557798 | ATTTG | A | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-11849_474-1184 others(8): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200557798 | ||||||
| chr2:200557864 | AC | A | 2 | a0001c0004t0001g0019 a0001c0004t0001g0253 |
3 | HG03491.hp2 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.474-11798delC | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557864 | |||||||
| chr2:200557865 | C | CT | 72 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(69): Show |
87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.474-11781dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200557865 | ||||||
| chr2:200557865 | CT | C | 47 | a0001c0001t0001g0232 a0001c0004t0001g0006 a0001c0004t0001g0007 others(44): Show |
54 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.474-11781delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200557865 | ||||||
| chr2:200557933 | G | A | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-11730G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557933 | |||||||
| chr2:200557989 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-11674G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200557989 | |||||||
| chr2:200558020 | C | T | 1 | a0015c0024t0001g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-11643C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558020 | |||||||
| chr2:200558021 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-11642A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558021 | |||||||
| chr2:200558115 | C | T | 1 | a0007c0010t0004g0312 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.474-11548C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558115 | |||||||
| chr2:200558159 | G | A | 12 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-11504G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558159 | |||||||
| chr2:200558246 | T | C | 1 | a0009c0014t0001g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.474-11417T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558246 | |||||||
| chr2:200558352 | A | C | 1 | a0001c0003t0002g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.474-11311A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558352 | |||||||
| chr2:200558361 | A | G | 3 | a0002c0005t0003g0122 a0002c0005t0003g0126 a0002c0005t0003g0127 |
3 | HG02132.hp1 NA18961.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.474-11302A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558361 | |||||||
| chr2:200558363 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.474-11300C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558363 | |||||||
| chr2:200558527 | A | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.474-11136A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558527 | |||||||
| chr2:200558658 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.474-11005G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558658 | |||||||
| chr2:200558664 | C | T | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.474-10999C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558664 | |||||||
| chr2:200558687 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-10976G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558687 | |||||||
| chr2:200558805 | C | CT | 6 | a0001c0001t0001g0225 a0001c0001t0003g0228 a0010c0020t0001g0092 others(3): Show |
6 | HG00609.hp2 HG01884.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-10844dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200558805 | ||||||
| chr2:200558805 | C | CTT | 7 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-10845_474-1084 others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200558805 | ||||||
| chr2:200558862 | G | A | 6 | a0001c0003t0002g0008 a0001c0003t0002g0025 a0001c0003t0002g0093 others(3): Show |
9 | HG01192.hp1 HG01358.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-10801G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558862 | |||||||
| chr2:200558929 | A | C | 1 | a0001c0003t0002g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.474-10734A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558929 | |||||||
| chr2:200558960 | G | A | 1 | a0001c0002t0001g0275 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.474-10703G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200558960 | |||||||
| chr2:200559205 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.474-10458A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559205 | |||||||
| chr2:200559281 | T | C | 1 | a0005c0007t0001g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-10382T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559281 | |||||||
| chr2:200559409 | T | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-10254T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559409 | |||||||
| chr2:200559458 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0016t0001g0182 |
3 | HG03130.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.474-10205C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559458 | |||||||
| chr2:200559539 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-10124A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559539 | |||||||
| chr2:200559597 | T | C | 2 | a0001c0004t0001g0064 a0001c0004t0001g0065 |
2 | NA19005.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.474-10066T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559597 | |||||||
| chr2:200559958 | T | A | 1 | a0005c0007t0001g0150 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-9705T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559958 | |||||||
| chr2:200559974 | A | G | 5 | a0001c0001t0001g0180 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
5 | HG02572.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-9689A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200559974 | |||||||
| chr2:200560006 | G | T | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.474-9657G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560006 | |||||||
| chr2:200560022 | C | T | 1 | a0001c0004t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.474-9641C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560022 | |||||||
| chr2:200560263 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-9400A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560263 | |||||||
| chr2:200560378 | T | G | 1 | a0002c0005t0003g0119 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.474-9285T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560378 | |||||||
| chr2:200560488 | T | G | 1 | a0001c0004t0001g0068 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.474-9175T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560488 | |||||||
| chr2:200560895 | T | C | 48 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(45): Show |
56 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.474-8768T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200560895 | |||||||
| chr2:200561206 | A | C | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.474-8457A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561206 | |||||||
| chr2:200561311 | T | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-8352T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561311 | |||||||
| chr2:200561314 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-8349A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561314 | |||||||
| chr2:200561355 | C | T | 1 | a0001c0002t0001g0305 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.474-8308C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561355 | |||||||
| chr2:200561405 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-8258C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561405 | |||||||
| chr2:200561538 | T | C | 1 | a0001c0002t0001g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-8125T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561538 | |||||||
| chr2:200561741 | G | A | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-7922G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561741 | |||||||
| chr2:200561744 | C | T | 1 | a0004c0008t0001g0088 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.474-7919C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561744 | |||||||
| chr2:200561768 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.474-7895G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200561768 | |||||||
| chr2:200562173 | G | GT | 28 | a0001c0003t0002g0009 a0001c0003t0002g0010 a0001c0003t0002g0024 others(25): Show |
35 | HG00597.hp2 HG00639.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.474-7484dupT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200562173 | ||||||
| chr2:200562247 | G | A | 228 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(225): Show |
275 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.474-7416G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562247 | |||||||
| chr2:200562274 | T | C | 1 | a0001c0004t0001g0070 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.474-7389T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562274 | |||||||
| chr2:200562410 | G | A | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.474-7253G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562410 | |||||||
| chr2:200562418 | C | G | 1 | a0001c0002t0001g0260 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.474-7245C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562418 | |||||||
| chr2:200562467 | G | A | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-7196G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562467 | |||||||
| chr2:200562617 | G | A | 2 | a0009c0014t0001g0158 a0009c0014t0001g0159 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.474-7046G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562617 | |||||||
| chr2:200562780 | G | A | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-6883G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562780 | |||||||
| chr2:200562782 | A | G | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-6881A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562782 | |||||||
| chr2:200562829 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-6834A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562829 | |||||||
| chr2:200562864 | G | A | 9 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-6799G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200562864 | |||||||
| chr2:200563041 | T | A | 1 | a0002c0005t0003g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.474-6622T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563041 | |||||||
| chr2:200563074 | T | G | 1 | a0019c0021t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474-6589T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563074 | |||||||
| chr2:200563300 | C | T | 1 | a0001c0004t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474-6363C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563300 | |||||||
| chr2:200563357 | C | T | 17 | a0001c0003t0002g0010 a0001c0003t0002g0024 a0001c0003t0002g0028 others(14): Show |
22 | HG00597.hp2 HG00639.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.474-6306C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563357 | |||||||
| chr2:200563376 | G | A | 2 | a0001c0004t0001g0070 a0001c0004t0001g0071 |
2 | HG03831.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.474-6287G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563376 | |||||||
| chr2:200563472 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-6191A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563472 | |||||||
| chr2:200563515 | T | A | 1 | a0015c0024t0001g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-6148T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563515 | |||||||
| chr2:200563650 | T | G | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-6013T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563650 | |||||||
| chr2:200563746 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-5917G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563746 | |||||||
| chr2:200563811 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.474-5852A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563811 | |||||||
| chr2:200563975 | G | T | 1 | a0013c0025t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.474-5688G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200563975 | |||||||
| chr2:200564345 | T | G | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.474-5318T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564345 | |||||||
| chr2:200564452 | A | C | 48 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(45): Show |
56 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.474-5211A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564452 | |||||||
| chr2:200564533 | T | G | 83 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(80): Show |
101 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.474-5130T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564533 | |||||||
| chr2:200564787 | G | T | 9 | a0001c0002t0001g0012 a0001c0002t0001g0038 a0001c0002t0001g0256 others(6): Show |
13 | HG00099.hp1 HG00140.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.474-4876G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564787 | |||||||
| chr2:200564964 | T | C | 1 | a0001c0011t0001g0241 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.474-4699T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200564964 | |||||||
| chr2:200564995 | TG | T | 6 | a0001c0002t0001g0014 a0001c0002t0001g0264 a0001c0002t0001g0265 others(3): Show |
8 | HG00423.hp2 HG00544.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.474-4665delG | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200564995 | ||||||
| chr2:200565039 | C | T | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-4624C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565039 | |||||||
| chr2:200565040 | C | T | 1 | a0001c0003t0002g0133 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.474-4623C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565040 | |||||||
| chr2:200565223 | C | T | 1 | a0005c0007t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.474-4440C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565223 | |||||||
| chr2:200565235 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.474-4428G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565235 | |||||||
| chr2:200565271 | G | A | 1 | a0008c0013t0001g0208 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.474-4392G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565271 | |||||||
| chr2:200565361 | C | A | 84 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(81): Show |
102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.474-4302C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565361 | |||||||
| chr2:200565646 | C | T | 1 | a0001c0004t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.474-4017C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565646 | |||||||
| chr2:200565861 | C | T | 1 | a0001c0004t0001g0019 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.474-3802C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565861 | |||||||
| chr2:200565912 | A | T | 1 | a0001c0003t0002g0116 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.474-3751A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565912 | |||||||
| chr2:200565940 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.474-3723T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200565940 | |||||||
| chr2:200566104 | G | A | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.474-3559G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566104 | |||||||
| chr2:200566215 | G | T | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-3448G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566215 | |||||||
| chr2:200566244 | G | T | 3 | a0003c0006t0001g0165 a0003c0006t0001g0170 a0003c0006t0001g0171 |
3 | HG02683.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.474-3419G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566244 | |||||||
| chr2:200566264 | T | C | 1 | a0001c0003t0002g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.474-3399T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566264 | |||||||
| chr2:200566331 | G | A | 1 | a0017c0023t0002g0120 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.474-3332G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566331 | |||||||
| chr2:200566381 | C | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-3282C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566381 | |||||||
| chr2:200566419 | C | T | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-3244C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566419 | |||||||
| chr2:200566474 | G | A | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.474-3189G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566474 | |||||||
| chr2:200566481 | A | G | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474-3182A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566481 | |||||||
| chr2:200566576 | G | C | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.474-3087G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566576 | |||||||
| chr2:200566580 | G | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-3083G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566580 | |||||||
| chr2:200566717 | C | T | 5 | a0003c0006t0001g0031 a0003c0006t0001g0160 a0003c0006t0001g0161 others(2): Show |
6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-2946C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566717 | |||||||
| chr2:200566779 | G | A | 41 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(38): Show |
48 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.474-2884G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566779 | |||||||
| chr2:200566849 | G | T | 68 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(65): Show |
86 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.474-2814G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566849 | |||||||
| chr2:200566857 | G | T | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.474-2806G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566857 | |||||||
| chr2:200566877 | G | A | 12 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-2786G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200566877 | |||||||
| chr2:200567028 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-2635G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567028 | |||||||
| chr2:200567046 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-2617A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567046 | |||||||
| chr2:200567147 | G | A | 7 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-2516G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567147 | |||||||
| chr2:200567149 | C | T | 84 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(81): Show |
102 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.474-2514C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567149 | |||||||
| chr2:200567156 | A | G | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.474-2507A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567156 | |||||||
| chr2:200567391 | G | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0186 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.474-2272G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567391 | |||||||
| chr2:200567618 | AC | A | 8 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(5): Show |
8 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-2039delC | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200567618 | ||||||
| chr2:200567622 | C | G | 3 | a0001c0004t0001g0077 a0001c0004t0001g0078 a0001c0004t0001g0081 |
3 | HG00280.hp2 HG01099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.474-2041C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567622 | |||||||
| chr2:200567623 | C | G | 1 | a0001c0003t0002g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.474-2040C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567623 | |||||||
| chr2:200567824 | G | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(313): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.474-1839G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200567824 | |||||||
| chr2:200568071 | C | T | 1 | a0015c0024t0001g0254 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-1592C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568071 | |||||||
| chr2:200568072 | G | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.474-1591G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568072 | |||||||
| chr2:200568122 | T | C | 1 | a0001c0002t0001g0263 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.474-1541T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568122 | |||||||
| chr2:200568359 | A | G | 1 | a0001c0003t0002g0145 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.474-1304A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568359 | |||||||
| chr2:200568382 | A | C | 1 | a0019c0021t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.474-1281A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568382 | |||||||
| chr2:200568515 | C | G | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-1148C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568515 | |||||||
| chr2:200568759 | C | T | 9 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0180 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-904C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568759 | |||||||
| chr2:200568817 | A | T | 1 | a0005c0007t0001g0154 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.474-846A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568817 | |||||||
| chr2:200568909 | TTATTTTT others(5): Show |
T | 70 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(67): Show |
87 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-753_474-742del others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568909 | |||||||
| chr2:200568913 | T | A | 1 | a0002c0005t0003g0021 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.474-750T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568913 | |||||||
| chr2:200568914 | TTTGTTAA others(8): Show |
T | 1 | a0002c0005t0003g0021 | 2 | NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.474-748_474-734del others(15): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568914 | |||||||
| chr2:200568923 | TTG | T | 70 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(67): Show |
87 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-738_474-737del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 200568923 | ||||||
| chr2:200568926 | T | A | 70 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(67): Show |
87 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-737T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568926 | |||||||
| chr2:200568928 | T | A | 70 | a0001c0003t0002g0008 a0001c0003t0002g0009 a0001c0003t0002g0010 others(67): Show |
87 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-735T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200568928 | |||||||
| chr2:200569093 | C | T | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.474-570C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200569093 | |||||||
| chr2:200569127 | T | C | 1 | a0001c0001t0003g0228 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.474-536T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 5/8 | chr2 | 200569127 | |||||||
| chr2:200570006 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0250 a0001c0001t0001g0251 |
4 | NA18956.hp2 NA18974.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+114G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570006 | |||||||
| chr2:200570153 | A | G | 1 | a0001c0004t0001g0060 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.703+261A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570153 | |||||||
| chr2:200570180 | C | T | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.703+288C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570180 | |||||||
| chr2:200570186 | A | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+294A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570186 | |||||||
| chr2:200570355 | A | G | 16 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(13): Show |
17 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.703+463A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570355 | |||||||
| chr2:200570405 | A | G | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.703+513A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570405 | |||||||
| chr2:200570431 | A | G | 1 | a0001c0004t0001g0073 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703+539A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570431 | |||||||
| chr2:200570478 | A | ATG | 26 | a0001c0002t0001g0012 a0001c0002t0001g0038 a0001c0002t0001g0256 others(23): Show |
32 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.704-541_704-540dup others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | A | ATGTG | 61 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0179 others(58): Show |
78 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.704-543_704-540dup others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | A | ATGTGTG | 51 | a0001c0001t0001g0188 a0001c0001t0001g0197 a0001c0001t0001g0198 others(48): Show |
58 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.704-545_704-540dup others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | A | ATGTGTGT others(1): Show |
61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.704-547_704-540dup others(8): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | A | ATGTGTGT others(3): Show |
18 | a0001c0001t0001g0035 a0001c0001t0001g0183 a0001c0001t0001g0187 others(15): Show |
19 | HG01255.hp1 HG03130.hp1 HG03492.hp2 others(16): Show |
intron_variant | MODIFIER | c.704-549_704-540dup others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | A | ATGTGTGT others(5): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0214 a0001c0016t0001g0182 |
3 | HG00642.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.704-551_704-540dup others(12): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0186 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.704-553_704-540dup others(14): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | ATG | A | 11 | a0001c0003t0002g0026 a0002c0005t0003g0100 a0005c0007t0001g0149 others(8): Show |
12 | HG01515.hp1 HG01517.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.704-541_704-540del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570478 | ATGTG | A | 5 | a0001c0003t0002g0110 a0001c0003t0002g0111 a0001c0003t0002g0144 others(2): Show |
5 | HG01243.hp2 HG03209.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-543_704-540del others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570478 | ||||||
| chr2:200570494 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-547_704-546ins others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570494 | ||||||
| chr2:200570510 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.704-540_704-539ins others(11): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570510 | |||||||
| chr2:200570552 | TAC | T | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.704-492_704-491del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570552 | ||||||
| chr2:200570631 | CAT | C | 64 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(61): Show |
73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.704-414_704-413del others(2): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 200570631 | ||||||
| chr2:200570698 | A | G | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-352A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570698 | |||||||
| chr2:200570732 | A | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-318A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570732 | |||||||
| chr2:200570778 | C | A | 1 | a0001c0002t0001g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704-272C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570778 | |||||||
| chr2:200570872 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-178T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570872 | |||||||
| chr2:200570886 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-164C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 6/8 | chr2 | 200570886 | |||||||
| chr2:200574058 | G | A | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3631+81G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574058 | |||||||
| chr2:200574279 | A | G | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3631+302A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574279 | |||||||
| chr2:200574501 | C | T | 1 | a0005c0007t0001g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3631+524C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574501 | |||||||
| chr2:200574536 | T | A | 1 | a0003c0006t0001g0168 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3631+559T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574536 | |||||||
| chr2:200574557 | A | G | 64 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(61): Show |
73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.3631+580A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574557 | |||||||
| chr2:200574570 | A | G | 12 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3631+593A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574570 | |||||||
| chr2:200574890 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3632-421C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574890 | |||||||
| chr2:200574911 | G | A | 71 | a0001c0001t0001g0231 a0001c0002t0001g0002 a0001c0002t0001g0012 others(68): Show |
91 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.3632-400G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200574911 | |||||||
| chr2:200574923 | T | TA | 2 | a0001c0001t0001g0016 a0001c0001t0001g0214 |
3 | HG00642.hp1 HG00733.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.3632-384dupA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 200574923 | ||||||
| chr2:200575081 | C | G | 1 | a0019c0021t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3632-230C>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200575081 | |||||||
| chr2:200575099 | T | C | 1 | a0001c0004t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3632-212T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200575099 | |||||||
| chr2:200575287 | G | C | 2 | a0001c0002t0001g0042 a0001c0002t0001g0262 |
3 | HG00673.hp2 NA18944.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3632-24G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 7/8 | chr2 | 200575287 | |||||||
| chr2:200575576 | A | G | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.3782+115A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575576 | |||||||
| chr2:200575581 | A | G | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+120A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575581 | |||||||
| chr2:200575643 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+182G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575643 | |||||||
| chr2:200575698 | T | TCTA | 64 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(61): Show |
73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.3782+243_3782+245d others(5): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200575698 | ||||||
| chr2:200575857 | C | T | 1 | a0001c0011t0001g0238 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3782+396C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575857 | |||||||
| chr2:200575913 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0206 a0001c0001t0001g0213 others(1): Show |
5 | HG00423.hp1 HG01070.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.3782+452G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575913 | |||||||
| chr2:200575934 | T | C | 1 | a0001c0004t0001g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3782+473T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200575934 | |||||||
| chr2:200576145 | A | C | 1 | a0001c0003t0002g0134 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3782+684A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576145 | |||||||
| chr2:200576216 | CT | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+765delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200576216 | ||||||
| chr2:200576223 | TTTTC | T | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+766_3782+769d others(6): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200576223 | ||||||
| chr2:200576225 | TTC | T | 55 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(52): Show |
62 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.3782+766_3782+767d others(4): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200576225 | ||||||
| chr2:200576237 | T | C | 1 | a0003c0006t0001g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3782+776T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576237 | |||||||
| chr2:200576240 | T | C | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+779T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576240 | |||||||
| chr2:200576310 | T | A | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3782+849T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576310 | |||||||
| chr2:200576410 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0187 others(13): Show |
20 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.3782+949T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576410 | |||||||
| chr2:200576449 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+988G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576449 | |||||||
| chr2:200576499 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3782+1038T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576499 | |||||||
| chr2:200576530 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1069T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576530 | |||||||
| chr2:200576560 | C | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3782+1099C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576560 | |||||||
| chr2:200576586 | A | T | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3782+1125A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576586 | |||||||
| chr2:200576706 | C | T | 64 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(61): Show |
73 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.3782+1245C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576706 | |||||||
| chr2:200576717 | A | G | 1 | a0019c0021t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3782+1256A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576717 | |||||||
| chr2:200576833 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1372T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576833 | |||||||
| chr2:200576856 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1395A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576856 | |||||||
| chr2:200576902 | T | A | 5 | a0003c0006t0001g0031 a0003c0006t0001g0160 a0003c0006t0001g0161 others(2): Show |
6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+1441T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576902 | |||||||
| chr2:200576903 | C | A | 5 | a0003c0006t0001g0031 a0003c0006t0001g0160 a0003c0006t0001g0161 others(2): Show |
6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+1442C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576903 | |||||||
| chr2:200576910 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1449G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576910 | |||||||
| chr2:200576966 | T | C | 1 | a0009c0014t0001g0159 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3782+1505T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576966 | |||||||
| chr2:200576971 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+1510C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200576971 | |||||||
| chr2:200577038 | T | G | 1 | a0001c0004t0001g0062 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3782+1577T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577038 | |||||||
| chr2:200577061 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3782+1600C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577061 | |||||||
| chr2:200577080 | A | C | 24 | a0003c0006t0001g0031 a0003c0006t0001g0032 a0003c0006t0001g0160 others(21): Show |
26 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.3782+1619A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577080 | |||||||
| chr2:200577151 | C | A | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3782+1690C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577151 | |||||||
| chr2:200577186 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3782+1725C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577186 | |||||||
| chr2:200577212 | T | C | 40 | a0001c0004t0001g0006 a0001c0004t0001g0007 a0001c0004t0001g0017 others(37): Show |
47 | HG00280.hp2 HG00408.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.3782+1751T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577212 | |||||||
| chr2:200577252 | GT | G | 70 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(67): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.3782+1795delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200577252 | ||||||
| chr2:200577300 | A | G | 1 | a0001c0002t0001g0040 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3782+1839A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577300 | |||||||
| chr2:200577321 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+1860G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577321 | |||||||
| chr2:200577466 | C | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+2005C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577466 | |||||||
| chr2:200577538 | A | G | 1 | a0013c0025t0001g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3782+2077A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577538 | |||||||
| chr2:200577678 | CT | C | 7 | a0003c0006t0001g0167 a0007c0010t0001g0313 a0007c0010t0001g0314 others(4): Show |
7 | HG01167.hp2 HG02145.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782+2231delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200577678 | ||||||
| chr2:200577699 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3782+2238T>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577699 | |||||||
| chr2:200577748 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+2287A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577748 | |||||||
| chr2:200577787 | G | T | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3782+2326G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577787 | |||||||
| chr2:200577861 | G | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3782+2400G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577861 | |||||||
| chr2:200577863 | G | A | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+2402G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577863 | |||||||
| chr2:200577941 | A | C | 1 | a0001c0003t0002g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3782+2480A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577941 | |||||||
| chr2:200577979 | T | C | 1 | a0019c0021t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3782+2518T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200577979 | |||||||
| chr2:200578150 | C | CTATAGA | 18 | a0001c0002t0001g0292 a0001c0003t0002g0028 a0001c0003t0002g0133 others(15): Show |
23 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.3782+2718_3782+272 others(10): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578150 | C | CTATAGAT others(5): Show |
20 | a0001c0001t0001g0179 a0002c0005t0003g0122 a0002c0005t0003g0125 others(17): Show |
21 | HG01243.hp2 HG01257.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.3782+2712_3782+272 others(16): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578150 | C | CTATAGAT others(11): Show |
35 | a0001c0001t0001g0016 a0001c0001t0001g0217 a0001c0001t0001g0218 others(32): Show |
41 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.3782+2706_3782+272 others(22): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578150 | C | CTATAGAT others(17): Show |
62 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0034 others(59): Show |
72 | HG00423.hp1 HG00609.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.3782+2700_3782+272 others(28): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578150 | C | CTATAGAT others(23): Show |
71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(68): Show |
93 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.3782+2694_3782+272 others(34): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578150 | C | CTATAGAT others(29): Show |
40 | a0001c0001t0001g0049 a0001c0001t0001g0174 a0001c0001t0001g0178 others(37): Show |
44 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(40): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578150 | C | CTATAGAT others(35): Show |
6 | a0001c0001t0001g0240 a0001c0001t0001g0246 a0001c0002t0001g0270 others(3): Show |
6 | HG00423.hp2 NA18747.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(46): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578150 | C | CTATAGAT others(41): Show |
5 | a0001c0002t0001g0043 a0001c0002t0001g0274 a0001c0002t0001g0282 others(2): Show |
6 | HG01934.hp1 HG03704.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(52): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578150 | ||||||
| chr2:200578163 | T | TATAGATA others(16): Show |
1 | a0001c0001t0001g0215 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3782+2723_3782+272 others(27): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578163 | ||||||
| chr2:200578177 | T | TAGATATA others(11): Show |
1 | a0001c0004t0001g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3782+2723_3782+272 others(22): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578177 | ||||||
| chr2:200578177 | T | TAGATATA others(17): Show |
3 | a0001c0004t0001g0018 a0001c0004t0001g0055 a0001c0004t0001g0059 |
4 | HG01952.hp2 NA19056.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(28): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578177 | ||||||
| chr2:200578177 | T | TAGATATA others(23): Show |
3 | a0001c0004t0001g0056 a0001c0004t0001g0063 a0001c0004t0001g0079 |
3 | HG00408.hp2 NA18979.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3782+2723_3782+272 others(34): Show |
SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200578177 | ||||||
| chr2:200578330 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3782+2869A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578330 | |||||||
| chr2:200578416 | G | T | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+2955G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578416 | |||||||
| chr2:200578450 | G | C | 5 | a0003c0006t0001g0031 a0003c0006t0001g0160 a0003c0006t0001g0161 others(2): Show |
6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+2989G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578450 | |||||||
| chr2:200578620 | G | A | 2 | a0001c0002t0001g0042 a0001c0002t0001g0262 |
3 | HG00673.hp2 NA18944.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3782+3159G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578620 | |||||||
| chr2:200578675 | A | C | 6 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3782+3214A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578675 | |||||||
| chr2:200578708 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.3782+3247A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578708 | |||||||
| chr2:200578761 | T | C | 61 | a0001c0002t0001g0002 a0001c0002t0001g0013 a0001c0002t0001g0014 others(58): Show |
77 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.3782+3300T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578761 | |||||||
| chr2:200578772 | A | G | 1 | a0005c0007t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3782+3311A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578772 | |||||||
| chr2:200578775 | G | A | 2 | a0013c0025t0001g0255 a0015c0024t0001g0254 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3782+3314G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578775 | |||||||
| chr2:200578909 | G | A | 11 | a0003c0006t0001g0032 a0003c0006t0001g0163 a0003c0006t0001g0164 others(8): Show |
11 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.3782+3448G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200578909 | |||||||
| chr2:200579065 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.3782+3604A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579065 | |||||||
| chr2:200579141 | T | C | 3 | a0001c0003t0002g0009 a0001c0003t0002g0051 a0001c0003t0002g0140 |
5 | HG02559.hp1 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3782+3680T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579141 | |||||||
| chr2:200579179 | A | G | 2 | a0001c0001t0001g0235 a0005c0007t0001g0154 |
2 | HG02723.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.3782+3718A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579179 | |||||||
| chr2:200579322 | T | C | 1 | a0001c0002t0001g0300 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3782+3861T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579322 | |||||||
| chr2:200579575 | G | T | 9 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3783-3874G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579575 | |||||||
| chr2:200579718 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3783-3731C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200579718 | |||||||
| chr2:200580082 | G | T | 8 | a0004c0008t0001g0020 a0004c0008t0001g0084 a0004c0008t0001g0085 others(5): Show |
9 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3783-3367G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580082 | |||||||
| chr2:200580096 | G | C | 5 | a0003c0006t0001g0031 a0003c0006t0001g0160 a0003c0006t0001g0161 others(2): Show |
6 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.3783-3353G>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580096 | |||||||
| chr2:200580263 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3783-3186C>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580263 | |||||||
| chr2:200580429 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.3783-3020C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580429 | |||||||
| chr2:200580478 | T | A | 9 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3783-2971T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580478 | |||||||
| chr2:200580545 | T | C | 1 | a0016c0018t0005g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3783-2904T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580545 | |||||||
| chr2:200580591 | G | A | 22 | a0002c0005t0003g0003 a0002c0005t0003g0021 a0002c0005t0003g0022 others(19): Show |
28 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.3783-2858G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580591 | |||||||
| chr2:200580860 | A | C | 2 | a0001c0001t0001g0250 a0016c0018t0005g0048 |
2 | HG03471.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.3783-2589A>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580860 | |||||||
| chr2:200580865 | AT | A | 7 | a0007c0010t0001g0313 a0007c0010t0001g0314 a0007c0010t0001g0315 others(4): Show |
7 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3783-2575delT | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200580865 | ||||||
| chr2:200580866 | T | A | 74 | a0001c0001t0001g0004 a0001c0002t0001g0002 a0001c0002t0001g0012 others(71): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.3783-2583T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580866 | |||||||
| chr2:200580894 | A | G | 1 | a0001c0002t0001g0291 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3783-2555A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200580894 | |||||||
| chr2:200581038 | T | C | 6 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.3783-2411T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581038 | |||||||
| chr2:200581175 | T | C | 1 | a0001c0002t0001g0296 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3783-2274T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581175 | |||||||
| chr2:200581379 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3783-2070G>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581379 | |||||||
| chr2:200581575 | A | G | 1 | a0007c0010t0001g0314 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3783-1874A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581575 | |||||||
| chr2:200581660 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.3783-1789A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200581660 | |||||||
| chr2:200582053 | TA | T | 3 | a0001c0004t0001g0074 a0001c0004t0001g0075 a0001c0004t0001g0076 |
3 | HG02809.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3783-1392delA | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 200582053 | ||||||
| chr2:200582065 | A | G | 1 | a0003c0006t0001g0164 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3783-1384A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582065 | |||||||
| chr2:200582075 | A | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-1374A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582075 | |||||||
| chr2:200582165 | T | C | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-1284T>C | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582165 | |||||||
| chr2:200582362 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3783-1087G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582362 | |||||||
| chr2:200582568 | C | T | 1 | a0001c0002t0001g0266 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3783-881C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582568 | |||||||
| chr2:200582637 | C | T | 2 | a0001c0002t0001g0015 a0001c0002t0001g0307 |
4 | NA18942.hp1 NA18943.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.3783-812C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582637 | |||||||
| chr2:200582821 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3783-628G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200582821 | |||||||
| chr2:200583041 | A | G | 12 | a0005c0007t0001g0149 a0005c0007t0001g0150 a0005c0007t0001g0151 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3783-408A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583041 | |||||||
| chr2:200583047 | T | A | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-402T>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583047 | |||||||
| chr2:200583063 | G | A | 1 | a0010c0020t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3783-386G>A | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583063 | |||||||
| chr2:200583180 | C | T | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-269C>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583180 | |||||||
| chr2:200583212 | A | G | 1 | a0012c0015t0006g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3783-237A>G | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583212 | |||||||
| chr2:200583212 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3783-237A>T | SGO2 | ENSG00000163535.18 | transcript | ENST00000357799.9 | protein_coding | 8/8 | chr2 | 200583212 |